Ligand source activities (1 row/activity)





Ligands Receptor Assay information Chemical information
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name
GPCRdb ID #Vendors Reference
ligand
Fold selectivity
(Potency)
# tested GPCRs
(Potency)
Species p-value
(-log)
Type Activity
Relation
Activity
Value
Assay Type Assay Description Source Mol
weight
Rot
Bonds
H don H acc LogP Smiles DOI
49783414 17495 0 None - 1 Human 9.8 pEC50 = 9.8 Functional
Agonist activity at 5HT4 receptor expressed in HEK293/L9 cells by cAMP assayAgonist activity at 5HT4 receptor expressed in HEK293/L9 cells by cAMP assay
ChEMBL 320 7 1 5 2.9 CCCCN1CCC(COC(=O)c2ccc(N)cc2OC)CC1 10.1021/jm100668r
CHEMBL1258451 17495 0 None - 1 Human 9.8 pEC50 = 9.8 Functional
Agonist activity at 5HT4 receptor expressed in HEK293/L9 cells by cAMP assayAgonist activity at 5HT4 receptor expressed in HEK293/L9 cells by cAMP assay
ChEMBL 320 7 1 5 2.9 CCCCN1CCC(COC(=O)c2ccc(N)cc2OC)CC1 10.1021/jm100668r
53354764 3015 30 None 1 2 Human 9.7 pEC50 = 9.7 Functional
Partial agonist activity at human 5HT4D receptor expressed in HEK293 cells assessed as cAMP production after 30 mins by HTRF assayPartial agonist activity at human 5HT4D receptor expressed in HEK293 cells assessed as cAMP production after 30 mins by HTRF assay
ChEMBL 432 7 1 8 2.6 OC1(CCOCC1)CN1CCC(CC1)COc1noc2c1c(ccc2)O[C@H]1COCC1 10.1021/jm300953p
9059 3015 30 None 1 2 Human 9.7 pEC50 = 9.7 Functional
Partial agonist activity at human 5HT4D receptor expressed in HEK293 cells assessed as cAMP production after 30 mins by HTRF assayPartial agonist activity at human 5HT4D receptor expressed in HEK293 cells assessed as cAMP production after 30 mins by HTRF assay
ChEMBL 432 7 1 8 2.6 OC1(CCOCC1)CN1CCC(CC1)COc1noc2c1c(ccc2)O[C@H]1COCC1 10.1021/jm300953p
CHEMBL2152922 3015 30 None 1 2 Human 9.7 pEC50 = 9.7 Functional
Partial agonist activity at human 5HT4D receptor expressed in HEK293 cells assessed as cAMP production after 30 mins by HTRF assayPartial agonist activity at human 5HT4D receptor expressed in HEK293 cells assessed as cAMP production after 30 mins by HTRF assay
ChEMBL 432 7 1 8 2.6 OC1(CCOCC1)CN1CCC(CC1)COc1noc2c1c(ccc2)O[C@H]1COCC1 10.1021/jm300953p
DB12675 3015 30 None 1 2 Human 9.7 pEC50 = 9.7 Functional
Partial agonist activity at human 5HT4D receptor expressed in HEK293 cells assessed as cAMP production after 30 mins by HTRF assayPartial agonist activity at human 5HT4D receptor expressed in HEK293 cells assessed as cAMP production after 30 mins by HTRF assay
ChEMBL 432 7 1 8 2.6 OC1(CCOCC1)CN1CCC(CC1)COc1noc2c1c(ccc2)O[C@H]1COCC1 10.1021/jm300953p
53354764 3015 30 None 1 2 Human 9.6 pEC50 = 9.6 Functional
Agonist activity at human 5HT4E receptor expressed in HEK293 cells assessed as increase in cAMP production after 30 mins by HTRF assayAgonist activity at human 5HT4E receptor expressed in HEK293 cells assessed as increase in cAMP production after 30 mins by HTRF assay
ChEMBL 432 7 1 8 2.6 OC1(CCOCC1)CN1CCC(CC1)COc1noc2c1c(ccc2)O[C@H]1COCC1 10.1021/jm300953p
9059 3015 30 None 1 2 Human 9.6 pEC50 = 9.6 Functional
Agonist activity at human 5HT4E receptor expressed in HEK293 cells assessed as increase in cAMP production after 30 mins by HTRF assayAgonist activity at human 5HT4E receptor expressed in HEK293 cells assessed as increase in cAMP production after 30 mins by HTRF assay
ChEMBL 432 7 1 8 2.6 OC1(CCOCC1)CN1CCC(CC1)COc1noc2c1c(ccc2)O[C@H]1COCC1 10.1021/jm300953p
CHEMBL2152922 3015 30 None 1 2 Human 9.6 pEC50 = 9.6 Functional
Agonist activity at human 5HT4E receptor expressed in HEK293 cells assessed as increase in cAMP production after 30 mins by HTRF assayAgonist activity at human 5HT4E receptor expressed in HEK293 cells assessed as increase in cAMP production after 30 mins by HTRF assay
ChEMBL 432 7 1 8 2.6 OC1(CCOCC1)CN1CCC(CC1)COc1noc2c1c(ccc2)O[C@H]1COCC1 10.1021/jm300953p
DB12675 3015 30 None 1 2 Human 9.6 pEC50 = 9.6 Functional
Agonist activity at human 5HT4E receptor expressed in HEK293 cells assessed as increase in cAMP production after 30 mins by HTRF assayAgonist activity at human 5HT4E receptor expressed in HEK293 cells assessed as increase in cAMP production after 30 mins by HTRF assay
ChEMBL 432 7 1 8 2.6 OC1(CCOCC1)CN1CCC(CC1)COc1noc2c1c(ccc2)O[C@H]1COCC1 10.1021/jm300953p
53354764 3015 30 None 1 2 Human 9.4 pEC50 = 9.4 Functional
Agonist activity at human 5HT4B receptor expressed in HEK293 cells assessed as increase in cAMP production after 30 mins by HTRF assayAgonist activity at human 5HT4B receptor expressed in HEK293 cells assessed as increase in cAMP production after 30 mins by HTRF assay
ChEMBL 432 7 1 8 2.6 OC1(CCOCC1)CN1CCC(CC1)COc1noc2c1c(ccc2)O[C@H]1COCC1 10.1021/jm300953p
9059 3015 30 None 1 2 Human 9.4 pEC50 = 9.4 Functional
Agonist activity at human 5HT4B receptor expressed in HEK293 cells assessed as increase in cAMP production after 30 mins by HTRF assayAgonist activity at human 5HT4B receptor expressed in HEK293 cells assessed as increase in cAMP production after 30 mins by HTRF assay
ChEMBL 432 7 1 8 2.6 OC1(CCOCC1)CN1CCC(CC1)COc1noc2c1c(ccc2)O[C@H]1COCC1 10.1021/jm300953p
CHEMBL2152922 3015 30 None 1 2 Human 9.4 pEC50 = 9.4 Functional
Agonist activity at human 5HT4B receptor expressed in HEK293 cells assessed as increase in cAMP production after 30 mins by HTRF assayAgonist activity at human 5HT4B receptor expressed in HEK293 cells assessed as increase in cAMP production after 30 mins by HTRF assay
ChEMBL 432 7 1 8 2.6 OC1(CCOCC1)CN1CCC(CC1)COc1noc2c1c(ccc2)O[C@H]1COCC1 10.1021/jm300953p
DB12675 3015 30 None 1 2 Human 9.4 pEC50 = 9.4 Functional
Agonist activity at human 5HT4B receptor expressed in HEK293 cells assessed as increase in cAMP production after 30 mins by HTRF assayAgonist activity at human 5HT4B receptor expressed in HEK293 cells assessed as increase in cAMP production after 30 mins by HTRF assay
ChEMBL 432 7 1 8 2.6 OC1(CCOCC1)CN1CCC(CC1)COc1noc2c1c(ccc2)O[C@H]1COCC1 10.1021/jm300953p
11166796 82264 0 None 1 2 Human 9.4 pEC50 = 9.4 Functional
Agonist activity at human 5HT4A receptor expressed in HEK293 cells assessed as increase in cAMP production after 30 mins by HTRF assayAgonist activity at human 5HT4A receptor expressed in HEK293 cells assessed as increase in cAMP production after 30 mins by HTRF assay
ChEMBL 448 5 2 7 2.3 CC(C)n1c(=O)n(C(=O)NCC2CCN(CC3(O)CCOCC3)CC2)c2cc(F)ccc21 10.1021/jm300953p
CHEMBL2179583 82264 0 None 1 2 Human 9.4 pEC50 = 9.4 Functional
Agonist activity at human 5HT4A receptor expressed in HEK293 cells assessed as increase in cAMP production after 30 mins by HTRF assayAgonist activity at human 5HT4A receptor expressed in HEK293 cells assessed as increase in cAMP production after 30 mins by HTRF assay
ChEMBL 448 5 2 7 2.3 CC(C)n1c(=O)n(C(=O)NCC2CCN(CC3(O)CCOCC3)CC2)c2cc(F)ccc21 10.1021/jm300953p
11504722 76069 0 None - 1 Human 9.4 pEC50 = 9.4 Functional
Agonist activity at human 5HT4C receptor expressed at 100 fold physiological-level in HEK293 cells assessed as cAMP accumulationAgonist activity at human 5HT4C receptor expressed at 100 fold physiological-level in HEK293 cells assessed as cAMP accumulation
ChEMBL 532 8 2 8 1.3 CC(C)n1nc(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3C[C@@H](O)CN2CCN(S(C)(=O)=O)CC2)c2ccccc21 10.1016/j.bmcl.2012.05.034
CHEMBL2059588 76069 0 None - 1 Human 9.4 pEC50 = 9.4 Functional
Agonist activity at human 5HT4C receptor expressed at 100 fold physiological-level in HEK293 cells assessed as cAMP accumulationAgonist activity at human 5HT4C receptor expressed at 100 fold physiological-level in HEK293 cells assessed as cAMP accumulation
ChEMBL 532 8 2 8 1.3 CC(C)n1nc(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3C[C@@H](O)CN2CCN(S(C)(=O)=O)CC2)c2ccccc21 10.1016/j.bmcl.2012.05.034
44224237 193122 7 None - 1 Human 9.4 pEC50 = 9.4 Functional
Agonist activity at human 5HT4C receptor expressed at 100 fold physiological-level in HEK293 cells assessed as cAMP accumulationAgonist activity at human 5HT4C receptor expressed at 100 fold physiological-level in HEK293 cells assessed as cAMP accumulation
ChEMBL 559 8 2 8 1.2 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3C[C@@H](O)CN2CCN(S(C)(=O)=O)CC2)cc2ccccc21 10.1016/j.bmcl.2012.05.034
CHEMBL538635 193122 7 None - 1 Human 9.4 pEC50 = 9.4 Functional
Agonist activity at human 5HT4C receptor expressed at 100 fold physiological-level in HEK293 cells assessed as cAMP accumulationAgonist activity at human 5HT4C receptor expressed at 100 fold physiological-level in HEK293 cells assessed as cAMP accumulation
ChEMBL 559 8 2 8 1.2 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3C[C@@H](O)CN2CCN(S(C)(=O)=O)CC2)cc2ccccc21 10.1016/j.bmcl.2012.05.034
44224237 193122 7 None - 1 Human 9.4 pEC50 = 9.4 Functional
Agonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assayAgonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assay
ChEMBL 559 8 2 8 1.2 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3C[C@@H](O)CN2CCN(S(C)(=O)=O)CC2)cc2ccccc21 10.1021/jm900881j
CHEMBL538635 193122 7 None - 1 Human 9.4 pEC50 = 9.4 Functional
Agonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assayAgonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assay
ChEMBL 559 8 2 8 1.2 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3C[C@@H](O)CN2CCN(S(C)(=O)=O)CC2)cc2ccccc21 10.1021/jm900881j
44248189 91900499 193177 0 None - 1 Human 9.4 pEC50 = 9.4 Functional
Agonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assayAgonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assay
ChEMBL 549 12 2 6 4.2 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CCCCCCCN2CCC[C@@H]2C(N)=O)cc2ccccc21 10.1021/jm900881j
CHEMBL539713 193177 0 None - 1 Human 9.4 pEC50 = 9.4 Functional
Agonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assayAgonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assay
ChEMBL 549 12 2 6 4.2 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CCCCCCCN2CCC[C@@H]2C(N)=O)cc2ccccc21 10.1021/jm900881j
71712463 90959 0 None - 1 Human 9.4 pEC50 = 9.4 Functional
Agonist activity at human recombinant 5HT4 receptor assessed as cAMP accumulationAgonist activity at human recombinant 5HT4 receptor assessed as cAMP accumulation
ChEMBL 465 9 3 6 1.4 CC(C)c1nc2c(C(=O)NCC3CCN(CC(O)CN(C)S(C)(=O)=O)CC3)cccc2[nH]1 10.1016/j.bmcl.2013.05.018
CHEMBL2402900 90959 0 None - 1 Human 9.4 pEC50 = 9.4 Functional
Agonist activity at human recombinant 5HT4 receptor assessed as cAMP accumulationAgonist activity at human recombinant 5HT4 receptor assessed as cAMP accumulation
ChEMBL 465 9 3 6 1.4 CC(C)c1nc2c(C(=O)NCC3CCN(CC(O)CN(C)S(C)(=O)=O)CC3)cccc2[nH]1 10.1016/j.bmcl.2013.05.018
53357011 82261 0 None - 1 Human 9.4 pEC50 = 9.4 Functional
Agonist activity at human 5HT4D receptor expressed in HEK293 cells assessed as cAMP production after 30 mins by HTRF assayAgonist activity at human 5HT4D receptor expressed in HEK293 cells assessed as cAMP production after 30 mins by HTRF assay
ChEMBL 446 7 2 8 2.8 O[C@@H]1CC[C@@H](Oc2cccc3onc(OCC4CCN(CC5(O)CCOCC5)CC4)c23)C1 10.1021/jm300953p
CHEMBL2179580 82261 0 None - 1 Human 9.4 pEC50 = 9.4 Functional
Agonist activity at human 5HT4D receptor expressed in HEK293 cells assessed as cAMP production after 30 mins by HTRF assayAgonist activity at human 5HT4D receptor expressed in HEK293 cells assessed as cAMP production after 30 mins by HTRF assay
ChEMBL 446 7 2 8 2.8 O[C@@H]1CC[C@@H](Oc2cccc3onc(OCC4CCN(CC5(O)CCOCC5)CC4)c23)C1 10.1021/jm300953p
53354764 3015 30 None 1 2 Human 9.3 pEC50 = 9.3 Functional
Agonist activity at human 5HT4A receptor expressed in HEK293 cells assessed as increase in cAMP production after 30 mins by HTRF assayAgonist activity at human 5HT4A receptor expressed in HEK293 cells assessed as increase in cAMP production after 30 mins by HTRF assay
ChEMBL 432 7 1 8 2.6 OC1(CCOCC1)CN1CCC(CC1)COc1noc2c1c(ccc2)O[C@H]1COCC1 10.1021/jm300953p
9059 3015 30 None 1 2 Human 9.3 pEC50 = 9.3 Functional
Agonist activity at human 5HT4A receptor expressed in HEK293 cells assessed as increase in cAMP production after 30 mins by HTRF assayAgonist activity at human 5HT4A receptor expressed in HEK293 cells assessed as increase in cAMP production after 30 mins by HTRF assay
ChEMBL 432 7 1 8 2.6 OC1(CCOCC1)CN1CCC(CC1)COc1noc2c1c(ccc2)O[C@H]1COCC1 10.1021/jm300953p
CHEMBL2152922 3015 30 None 1 2 Human 9.3 pEC50 = 9.3 Functional
Agonist activity at human 5HT4A receptor expressed in HEK293 cells assessed as increase in cAMP production after 30 mins by HTRF assayAgonist activity at human 5HT4A receptor expressed in HEK293 cells assessed as increase in cAMP production after 30 mins by HTRF assay
ChEMBL 432 7 1 8 2.6 OC1(CCOCC1)CN1CCC(CC1)COc1noc2c1c(ccc2)O[C@H]1COCC1 10.1021/jm300953p
DB12675 3015 30 None 1 2 Human 9.3 pEC50 = 9.3 Functional
Agonist activity at human 5HT4A receptor expressed in HEK293 cells assessed as increase in cAMP production after 30 mins by HTRF assayAgonist activity at human 5HT4A receptor expressed in HEK293 cells assessed as increase in cAMP production after 30 mins by HTRF assay
ChEMBL 432 7 1 8 2.6 OC1(CCOCC1)CN1CCC(CC1)COc1noc2c1c(ccc2)O[C@H]1COCC1 10.1021/jm300953p
11350913 136272 1 None - 1 Human 9.3 pEC50 = 9.3 Functional
Agonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assayAgonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assay
ChEMBL 430 5 2 7 2.2 CC(C)n1c(=O)n(C(=O)NCC2CCN(CC3(O)CCOCC3)CC2)c2ccccc21 10.1016/j.ejmech.2015.08.051
CHEMBL3741376 136272 1 None - 1 Human 9.3 pEC50 = 9.3 Functional
Agonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assayAgonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assay
ChEMBL 430 5 2 7 2.2 CC(C)n1c(=O)n(C(=O)NCC2CCN(CC3(O)CCOCC3)CC2)c2ccccc21 10.1016/j.ejmech.2015.08.051
11961293 3710 13 None 5 2 Human 9.3 pEC50 = 9.3 Functional
Agonist activity at human recombinant 5HT4 receptor assessed as cAMP accumulationAgonist activity at human recombinant 5HT4 receptor assessed as cAMP accumulation
ChEMBL 455 6 2 5 3.6 COC(=O)N1CCC(CC1)CN1CCC(CC1)CNC(=O)c1cccc2c1nc([nH]2)C(C)C 10.1016/j.bmcl.2013.05.018
8426 3710 13 None 5 2 Human 9.3 pEC50 = 9.3 Functional
Agonist activity at human recombinant 5HT4 receptor assessed as cAMP accumulationAgonist activity at human recombinant 5HT4 receptor assessed as cAMP accumulation
ChEMBL 455 6 2 5 3.6 COC(=O)N1CCC(CC1)CN1CCC(CC1)CNC(=O)c1cccc2c1nc([nH]2)C(C)C 10.1016/j.bmcl.2013.05.018
CHEMBL2402904 3710 13 None 5 2 Human 9.3 pEC50 = 9.3 Functional
Agonist activity at human recombinant 5HT4 receptor assessed as cAMP accumulationAgonist activity at human recombinant 5HT4 receptor assessed as cAMP accumulation
ChEMBL 455 6 2 5 3.6 COC(=O)N1CCC(CC1)CN1CCC(CC1)CNC(=O)c1cccc2c1nc([nH]2)C(C)C 10.1016/j.bmcl.2013.05.018
DB12725 3710 13 None 5 2 Human 9.3 pEC50 = 9.3 Functional
Agonist activity at human recombinant 5HT4 receptor assessed as cAMP accumulationAgonist activity at human recombinant 5HT4 receptor assessed as cAMP accumulation
ChEMBL 455 6 2 5 3.6 COC(=O)N1CCC(CC1)CN1CCC(CC1)CNC(=O)c1cccc2c1nc([nH]2)C(C)C 10.1016/j.bmcl.2013.05.018
53354764 3015 30 None -1 2 Rat 9.2 pEC50 = 9.2 Functional
Agonist activity at rat 5HT4S receptor expressed in HEK293 cells assessed as increase in cAMP production after 30 mins by HTRF assayAgonist activity at rat 5HT4S receptor expressed in HEK293 cells assessed as increase in cAMP production after 30 mins by HTRF assay
ChEMBL 432 7 1 8 2.6 OC1(CCOCC1)CN1CCC(CC1)COc1noc2c1c(ccc2)O[C@H]1COCC1 10.1021/jm300953p
9059 3015 30 None -1 2 Rat 9.2 pEC50 = 9.2 Functional
Agonist activity at rat 5HT4S receptor expressed in HEK293 cells assessed as increase in cAMP production after 30 mins by HTRF assayAgonist activity at rat 5HT4S receptor expressed in HEK293 cells assessed as increase in cAMP production after 30 mins by HTRF assay
ChEMBL 432 7 1 8 2.6 OC1(CCOCC1)CN1CCC(CC1)COc1noc2c1c(ccc2)O[C@H]1COCC1 10.1021/jm300953p
CHEMBL2152922 3015 30 None -1 2 Rat 9.2 pEC50 = 9.2 Functional
Agonist activity at rat 5HT4S receptor expressed in HEK293 cells assessed as increase in cAMP production after 30 mins by HTRF assayAgonist activity at rat 5HT4S receptor expressed in HEK293 cells assessed as increase in cAMP production after 30 mins by HTRF assay
ChEMBL 432 7 1 8 2.6 OC1(CCOCC1)CN1CCC(CC1)COc1noc2c1c(ccc2)O[C@H]1COCC1 10.1021/jm300953p
DB12675 3015 30 None -1 2 Rat 9.2 pEC50 = 9.2 Functional
Agonist activity at rat 5HT4S receptor expressed in HEK293 cells assessed as increase in cAMP production after 30 mins by HTRF assayAgonist activity at rat 5HT4S receptor expressed in HEK293 cells assessed as increase in cAMP production after 30 mins by HTRF assay
ChEMBL 432 7 1 8 2.6 OC1(CCOCC1)CN1CCC(CC1)COc1noc2c1c(ccc2)O[C@H]1COCC1 10.1021/jm300953p
53354764 3015 30 None -1 2 Rat 9.2 pEC50 = 9.2 Functional
Agonist activity at rat 5HT4E receptor expressed in HEK293 cells assessed as increase in cAMP production after 30 mins by HTRF assayAgonist activity at rat 5HT4E receptor expressed in HEK293 cells assessed as increase in cAMP production after 30 mins by HTRF assay
ChEMBL 432 7 1 8 2.6 OC1(CCOCC1)CN1CCC(CC1)COc1noc2c1c(ccc2)O[C@H]1COCC1 10.1021/jm300953p
9059 3015 30 None -1 2 Rat 9.2 pEC50 = 9.2 Functional
Agonist activity at rat 5HT4E receptor expressed in HEK293 cells assessed as increase in cAMP production after 30 mins by HTRF assayAgonist activity at rat 5HT4E receptor expressed in HEK293 cells assessed as increase in cAMP production after 30 mins by HTRF assay
ChEMBL 432 7 1 8 2.6 OC1(CCOCC1)CN1CCC(CC1)COc1noc2c1c(ccc2)O[C@H]1COCC1 10.1021/jm300953p
CHEMBL2152922 3015 30 None -1 2 Rat 9.2 pEC50 = 9.2 Functional
Agonist activity at rat 5HT4E receptor expressed in HEK293 cells assessed as increase in cAMP production after 30 mins by HTRF assayAgonist activity at rat 5HT4E receptor expressed in HEK293 cells assessed as increase in cAMP production after 30 mins by HTRF assay
ChEMBL 432 7 1 8 2.6 OC1(CCOCC1)CN1CCC(CC1)COc1noc2c1c(ccc2)O[C@H]1COCC1 10.1021/jm300953p
DB12675 3015 30 None -1 2 Rat 9.2 pEC50 = 9.2 Functional
Agonist activity at rat 5HT4E receptor expressed in HEK293 cells assessed as increase in cAMP production after 30 mins by HTRF assayAgonist activity at rat 5HT4E receptor expressed in HEK293 cells assessed as increase in cAMP production after 30 mins by HTRF assay
ChEMBL 432 7 1 8 2.6 OC1(CCOCC1)CN1CCC(CC1)COc1noc2c1c(ccc2)O[C@H]1COCC1 10.1021/jm300953p
11842633 3918 17 None 7 2 Human 9.2 pEC50 = 9.2 Functional
Agonist activity at 5HT4c receptor expressed in cells at 100-fold physiological level assessed as cAMP accumulationAgonist activity at 5HT4c receptor expressed in cells at 100-fold physiological level assessed as cAMP accumulation
ChEMBL 504 8 2 7 1.6 O[C@@H](CN(S(=O)(=O)C)C)CN1[C@@H]2CC[C@H]1CC(C2)NC(=O)c1cc2ccccc2n(c1=O)C(C)C 10.1016/j.bmcl.2012.08.051
8425 3918 17 None 7 2 Human 9.2 pEC50 = 9.2 Functional
Agonist activity at 5HT4c receptor expressed in cells at 100-fold physiological level assessed as cAMP accumulationAgonist activity at 5HT4c receptor expressed in cells at 100-fold physiological level assessed as cAMP accumulation
ChEMBL 504 8 2 7 1.6 O[C@@H](CN(S(=O)(=O)C)C)CN1[C@@H]2CC[C@H]1CC(C2)NC(=O)c1cc2ccccc2n(c1=O)C(C)C 10.1016/j.bmcl.2012.08.051
CHEMBL2087337 3918 17 None 7 2 Human 9.2 pEC50 = 9.2 Functional
Agonist activity at 5HT4c receptor expressed in cells at 100-fold physiological level assessed as cAMP accumulationAgonist activity at 5HT4c receptor expressed in cells at 100-fold physiological level assessed as cAMP accumulation
ChEMBL 504 8 2 7 1.6 O[C@@H](CN(S(=O)(=O)C)C)CN1[C@@H]2CC[C@H]1CC(C2)NC(=O)c1cc2ccccc2n(c1=O)C(C)C 10.1016/j.bmcl.2012.08.051
70686434 76064 0 None - 1 Human 9.2 pEC50 = 9.2 Functional
Agonist activity at human 5HT4C receptor expressed at 100 fold physiological-level in HEK293 cells assessed as cAMP accumulationAgonist activity at human 5HT4C receptor expressed at 100 fold physiological-level in HEK293 cells assessed as cAMP accumulation
ChEMBL 560 10 3 8 2.0 CC(C)n1nc(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CC(O)CN2CCC(CNS(C)(=O)=O)CC2)c2ccccc21 10.1016/j.bmcl.2012.05.034
CHEMBL2059583 76064 0 None - 1 Human 9.2 pEC50 = 9.2 Functional
Agonist activity at human 5HT4C receptor expressed at 100 fold physiological-level in HEK293 cells assessed as cAMP accumulationAgonist activity at human 5HT4C receptor expressed at 100 fold physiological-level in HEK293 cells assessed as cAMP accumulation
ChEMBL 560 10 3 8 2.0 CC(C)n1nc(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CC(O)CN2CCC(CNS(C)(=O)=O)CC2)c2ccccc21 10.1016/j.bmcl.2012.05.034
44248922 193231 0 None - 1 Human 9.2 pEC50 = 9.2 Functional
Agonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assayAgonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assay
ChEMBL 627 14 2 7 4.5 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CCCCCCCN2CCC(CNS(C)(=O)=O)CC2)cc2ccccc21 10.1021/jm900881j
CHEMBL540981 193231 0 None - 1 Human 9.2 pEC50 = 9.2 Functional
Agonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assayAgonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assay
ChEMBL 627 14 2 7 4.5 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CCCCCCCN2CCC(CNS(C)(=O)=O)CC2)cc2ccccc21 10.1021/jm900881j
44248319 193823 0 None - 1 Human 9.2 pEC50 = 9.2 Functional
Agonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assayAgonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assay
ChEMBL 615 16 1 7 4.5 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CCCCCCCN(C)CCCN(C)S(C)(=O)=O)cc2ccccc21 10.1021/jm900881j
CHEMBL553404 193823 0 None - 1 Human 9.2 pEC50 = 9.2 Functional
Agonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assayAgonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assay
ChEMBL 615 16 1 7 4.5 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CCCCCCCN(C)CCCN(C)S(C)(=O)=O)cc2ccccc21 10.1021/jm900881j
44247953 194145 0 None - 1 Human 9.2 pEC50 = 9.2 Functional
Agonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assayAgonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assay
ChEMBL 581 12 2 5 6.1 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CCCCCN(C)CCc2c[nH]c3ccccc23)cc2ccccc21 10.1021/jm900881j
CHEMBL558163 194145 0 None - 1 Human 9.2 pEC50 = 9.2 Functional
Agonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assayAgonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assay
ChEMBL 581 12 2 5 6.1 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CCCCCN(C)CCc2c[nH]c3ccccc23)cc2ccccc21 10.1021/jm900881j
71714541 90950 0 None - 1 Human 9.2 pEC50 = 9.2 Functional
Agonist activity at human recombinant 5HT4 receptor assessed as cAMP accumulationAgonist activity at human recombinant 5HT4 receptor assessed as cAMP accumulation
ChEMBL 520 9 3 7 1.1 CC(C)c1nc2c(C(=O)NCC3CCN(CC(O)CN4CCN(S(C)(=O)=O)CC4)CC3)cccc2[nH]1 10.1016/j.bmcl.2013.05.018
CHEMBL2402891 90950 0 None - 1 Human 9.2 pEC50 = 9.2 Functional
Agonist activity at human recombinant 5HT4 receptor assessed as cAMP accumulationAgonist activity at human recombinant 5HT4 receptor assessed as cAMP accumulation
ChEMBL 520 9 3 7 1.1 CC(C)c1nc2c(C(=O)NCC3CCN(CC(O)CN4CCN(S(C)(=O)=O)CC4)CC3)cccc2[nH]1 10.1016/j.bmcl.2013.05.018
71714542 90951 0 None - 1 Human 9.2 pEC50 = 9.2 Functional
Agonist activity at human recombinant 5HT4 receptor assessed as cAMP accumulationAgonist activity at human recombinant 5HT4 receptor assessed as cAMP accumulation
ChEMBL 518 9 3 7 0.8 CS(=O)(=O)N1CCN(CC(O)CN2CCC(CNC(=O)c3cccc4[nH]c(C5CC5)nc34)CC2)CC1 10.1016/j.bmcl.2013.05.018
CHEMBL2402892 90951 0 None - 1 Human 9.2 pEC50 = 9.2 Functional
Agonist activity at human recombinant 5HT4 receptor assessed as cAMP accumulationAgonist activity at human recombinant 5HT4 receptor assessed as cAMP accumulation
ChEMBL 518 9 3 7 0.8 CS(=O)(=O)N1CCN(CC(O)CN2CCC(CNC(=O)c3cccc4[nH]c(C5CC5)nc34)CC2)CC1 10.1016/j.bmcl.2013.05.018
53354764 3015 30 None -1 2 Rat 9.2 pEC50 = 9.2 Functional
Agonist activity at rat 5HT4L receptor expressed in HEK293 cells assessed as increase in cAMP production after 30 mins by HTRF assayAgonist activity at rat 5HT4L receptor expressed in HEK293 cells assessed as increase in cAMP production after 30 mins by HTRF assay
ChEMBL 432 7 1 8 2.6 OC1(CCOCC1)CN1CCC(CC1)COc1noc2c1c(ccc2)O[C@H]1COCC1 10.1021/jm300953p
9059 3015 30 None -1 2 Rat 9.2 pEC50 = 9.2 Functional
Agonist activity at rat 5HT4L receptor expressed in HEK293 cells assessed as increase in cAMP production after 30 mins by HTRF assayAgonist activity at rat 5HT4L receptor expressed in HEK293 cells assessed as increase in cAMP production after 30 mins by HTRF assay
ChEMBL 432 7 1 8 2.6 OC1(CCOCC1)CN1CCC(CC1)COc1noc2c1c(ccc2)O[C@H]1COCC1 10.1021/jm300953p
CHEMBL2152922 3015 30 None -1 2 Rat 9.2 pEC50 = 9.2 Functional
Agonist activity at rat 5HT4L receptor expressed in HEK293 cells assessed as increase in cAMP production after 30 mins by HTRF assayAgonist activity at rat 5HT4L receptor expressed in HEK293 cells assessed as increase in cAMP production after 30 mins by HTRF assay
ChEMBL 432 7 1 8 2.6 OC1(CCOCC1)CN1CCC(CC1)COc1noc2c1c(ccc2)O[C@H]1COCC1 10.1021/jm300953p
DB12675 3015 30 None -1 2 Rat 9.2 pEC50 = 9.2 Functional
Agonist activity at rat 5HT4L receptor expressed in HEK293 cells assessed as increase in cAMP production after 30 mins by HTRF assayAgonist activity at rat 5HT4L receptor expressed in HEK293 cells assessed as increase in cAMP production after 30 mins by HTRF assay
ChEMBL 432 7 1 8 2.6 OC1(CCOCC1)CN1CCC(CC1)COc1noc2c1c(ccc2)O[C@H]1COCC1 10.1021/jm300953p
70694780 76063 0 None - 1 Human 9.1 pEC50 = 9.1 Functional
Agonist activity at human 5HT4C receptor expressed at 100 fold physiological-level in HEK293 cells assessed as cAMP accumulationAgonist activity at human 5HT4C receptor expressed at 100 fold physiological-level in HEK293 cells assessed as cAMP accumulation
ChEMBL 509 12 1 6 5.0 COC[C@@H]1CCCN1CCCCCCN1[C@H]2CC[C@@H]1C[C@H](NC(=O)c1nn(C(C)C)c3ccccc13)C2 10.1016/j.bmcl.2012.05.034
CHEMBL2059582 76063 0 None - 1 Human 9.1 pEC50 = 9.1 Functional
Agonist activity at human 5HT4C receptor expressed at 100 fold physiological-level in HEK293 cells assessed as cAMP accumulationAgonist activity at human 5HT4C receptor expressed at 100 fold physiological-level in HEK293 cells assessed as cAMP accumulation
ChEMBL 509 12 1 6 5.0 COC[C@@H]1CCCN1CCCCCCN1[C@H]2CC[C@@H]1C[C@H](NC(=O)c1nn(C(C)C)c3ccccc13)C2 10.1016/j.bmcl.2012.05.034
11606227 76066 0 None - 1 Human 9.1 pEC50 = 9.1 Functional
Agonist activity at human 5HT4C receptor expressed at 100 fold physiological-level in HEK293 cells assessed as cAMP accumulationAgonist activity at human 5HT4C receptor expressed at 100 fold physiological-level in HEK293 cells assessed as cAMP accumulation
ChEMBL 532 8 2 8 1.3 CC(C)n1nc(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CC(O)CN2CCN(S(C)(=O)=O)CC2)c2ccccc21 10.1016/j.bmcl.2012.05.034
CHEMBL2059585 76066 0 None - 1 Human 9.1 pEC50 = 9.1 Functional
Agonist activity at human 5HT4C receptor expressed at 100 fold physiological-level in HEK293 cells assessed as cAMP accumulationAgonist activity at human 5HT4C receptor expressed at 100 fold physiological-level in HEK293 cells assessed as cAMP accumulation
ChEMBL 532 8 2 8 1.3 CC(C)n1nc(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CC(O)CN2CCN(S(C)(=O)=O)CC2)c2ccccc21 10.1016/j.bmcl.2012.05.034
11627949 76068 0 None - 1 Human 9.1 pEC50 = 9.1 Functional
Agonist activity at human 5HT4C receptor expressed at 100 fold physiological-level in HEK293 cells assessed as cAMP accumulationAgonist activity at human 5HT4C receptor expressed at 100 fold physiological-level in HEK293 cells assessed as cAMP accumulation
ChEMBL 532 8 2 8 1.3 CC(C)n1nc(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3C[C@H](O)CN2CCN(S(C)(=O)=O)CC2)c2ccccc21 10.1016/j.bmcl.2012.05.034
CHEMBL2059587 76068 0 None - 1 Human 9.1 pEC50 = 9.1 Functional
Agonist activity at human 5HT4C receptor expressed at 100 fold physiological-level in HEK293 cells assessed as cAMP accumulationAgonist activity at human 5HT4C receptor expressed at 100 fold physiological-level in HEK293 cells assessed as cAMP accumulation
ChEMBL 532 8 2 8 1.3 CC(C)n1nc(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3C[C@H](O)CN2CCN(S(C)(=O)=O)CC2)c2ccccc21 10.1016/j.bmcl.2012.05.034
44248921 193576 0 None - 1 Human 9.1 pEC50 = 9.1 Functional
Agonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assayAgonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assay
ChEMBL 520 11 1 5 5.7 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CCCCCCCN2CCCCC2)cc2ccccc21 10.1021/jm900881j
CHEMBL551013 193576 0 None - 1 Human 9.1 pEC50 = 9.1 Functional
Agonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assayAgonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assay
ChEMBL 520 11 1 5 5.7 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CCCCCCCN2CCCCC2)cc2ccccc21 10.1021/jm900881j
44248186 193790 0 None - 1 Human 9.1 pEC50 = 9.1 Functional
Agonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assayAgonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assay
ChEMBL 567 15 3 5 6.1 COc1cc(N)c(Cl)cc1C(=O)NC1CCN(CCCCCCCCN(C)CCc2c[nH]c3ccccc23)CC1 10.1021/jm900881j
CHEMBL552484 193790 0 None - 1 Human 9.1 pEC50 = 9.1 Functional
Agonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assayAgonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assay
ChEMBL 567 15 3 5 6.1 COc1cc(N)c(Cl)cc1C(=O)NC1CCN(CCCCCCCCN(C)CCc2c[nH]c3ccccc23)CC1 10.1021/jm900881j
11519716 193824 0 None - 1 Human 9.1 pEC50 = 9.1 Functional
Agonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assayAgonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assay
ChEMBL 559 8 2 8 1.2 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CC(O)CN2CCN(S(C)(=O)=O)CC2)cc2ccccc21 10.1021/jm900881j
CHEMBL553405 193824 0 None - 1 Human 9.1 pEC50 = 9.1 Functional
Agonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assayAgonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assay
ChEMBL 559 8 2 8 1.2 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CC(O)CN2CCN(S(C)(=O)=O)CC2)cc2ccccc21 10.1021/jm900881j
44248321 193908 0 None - 1 Human 9.1 pEC50 = 9.1 Functional
Agonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assayAgonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assay
ChEMBL 541 8 1 6 4.5 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CCCN2CCN(c3ccccc3)CC2)cc2ccccc21 10.1021/jm900881j
CHEMBL555222 193908 0 None - 1 Human 9.1 pEC50 = 9.1 Functional
Agonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assayAgonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assay
ChEMBL 541 8 1 6 4.5 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CCCN2CCN(c3ccccc3)CC2)cc2ccccc21 10.1021/jm900881j
71714544 90953 0 None - 1 Human 9.1 pEC50 = 9.1 Functional
Agonist activity at human recombinant 5HT4 receptor assessed as cAMP accumulationAgonist activity at human recombinant 5HT4 receptor assessed as cAMP accumulation
ChEMBL 542 9 3 7 1.1 CC(F)(F)c1nc2c(C(=O)NCC3CCN(CC(O)CN4CCN(S(C)(=O)=O)CC4)CC3)cccc2[nH]1 10.1016/j.bmcl.2013.05.018
CHEMBL2402894 90953 0 None - 1 Human 9.1 pEC50 = 9.1 Functional
Agonist activity at human recombinant 5HT4 receptor assessed as cAMP accumulationAgonist activity at human recombinant 5HT4 receptor assessed as cAMP accumulation
ChEMBL 542 9 3 7 1.1 CC(F)(F)c1nc2c(C(=O)NCC3CCN(CC(O)CN4CCN(S(C)(=O)=O)CC4)CC3)cccc2[nH]1 10.1016/j.bmcl.2013.05.018
71712327 90956 0 None - 1 Human 9.1 pEC50 = 9.1 Functional
Agonist activity at human recombinant 5HT4 receptor assessed as cAMP accumulationAgonist activity at human recombinant 5HT4 receptor assessed as cAMP accumulation
ChEMBL 490 8 2 6 1.7 CC(C)c1nc2c(C(=O)NCC3CCN(CCN4CCN(S(C)(=O)=O)CC4)CC3)cccc2[nH]1 10.1016/j.bmcl.2013.05.018
CHEMBL2402897 90956 0 None - 1 Human 9.1 pEC50 = 9.1 Functional
Agonist activity at human recombinant 5HT4 receptor assessed as cAMP accumulationAgonist activity at human recombinant 5HT4 receptor assessed as cAMP accumulation
ChEMBL 490 8 2 6 1.7 CC(C)c1nc2c(C(=O)NCC3CCN(CCN4CCN(S(C)(=O)=O)CC4)CC3)cccc2[nH]1 10.1016/j.bmcl.2013.05.018
71451950 82263 5 None 1 2 Human 9.1 pEC50 = 9.1 Functional
Agonist activity at human 5HT4A receptor expressed in HEK293 cells assessed as increase in cAMP production after 30 mins by HTRF assayAgonist activity at human 5HT4A receptor expressed in HEK293 cells assessed as increase in cAMP production after 30 mins by HTRF assay
ChEMBL 433 4 2 5 2.4 CC1(C)C(=O)N(C(=O)NCC2CCN(CC3(O)CCOCC3)CC2)c2cc(F)ccc21 10.1021/jm300953p
CHEMBL2179582 82263 5 None 1 2 Human 9.1 pEC50 = 9.1 Functional
Agonist activity at human 5HT4A receptor expressed in HEK293 cells assessed as increase in cAMP production after 30 mins by HTRF assayAgonist activity at human 5HT4A receptor expressed in HEK293 cells assessed as increase in cAMP production after 30 mins by HTRF assay
ChEMBL 433 4 2 5 2.4 CC1(C)C(=O)N(C(=O)NCC2CCN(CC3(O)CCOCC3)CC2)c2cc(F)ccc21 10.1021/jm300953p
71450132 82265 0 None - 1 Human 9.1 pEC50 = 9.1 Functional
Agonist activity at human 5HT4D receptor expressed in HEK293 cells assessed as cAMP production after 30 mins by HTRF assayAgonist activity at human 5HT4D receptor expressed in HEK293 cells assessed as cAMP production after 30 mins by HTRF assay
ChEMBL 358 8 0 5 4.7 CCCCN1CCC(COc2noc3cccc(OC4CCC4)c23)CC1 10.1021/jm300953p
CHEMBL2179584 82265 0 None - 1 Human 9.1 pEC50 = 9.1 Functional
Agonist activity at human 5HT4D receptor expressed in HEK293 cells assessed as cAMP production after 30 mins by HTRF assayAgonist activity at human 5HT4D receptor expressed in HEK293 cells assessed as cAMP production after 30 mins by HTRF assay
ChEMBL 358 8 0 5 4.7 CCCCN1CCC(COc2noc3cccc(OC4CCC4)c23)CC1 10.1021/jm300953p
71451950 82263 5 None 1 2 Human 9.1 pEC50 = 9.1 Functional
Agonist activity at human 5HT4D receptor expressed in HEK293 cells assessed as cAMP production after 30 mins by HTRF assayAgonist activity at human 5HT4D receptor expressed in HEK293 cells assessed as cAMP production after 30 mins by HTRF assay
ChEMBL 433 4 2 5 2.4 CC1(C)C(=O)N(C(=O)NCC2CCN(CC3(O)CCOCC3)CC2)c2cc(F)ccc21 10.1021/jm300953p
CHEMBL2179582 82263 5 None 1 2 Human 9.1 pEC50 = 9.1 Functional
Agonist activity at human 5HT4D receptor expressed in HEK293 cells assessed as cAMP production after 30 mins by HTRF assayAgonist activity at human 5HT4D receptor expressed in HEK293 cells assessed as cAMP production after 30 mins by HTRF assay
ChEMBL 433 4 2 5 2.4 CC1(C)C(=O)N(C(=O)NCC2CCN(CC3(O)CCOCC3)CC2)c2cc(F)ccc21 10.1021/jm300953p
11166796 82264 0 None 1 2 Human 9.1 pEC50 = 9.1 Functional
Agonist activity at human 5HT4D receptor expressed in HEK293 cells assessed as cAMP production after 30 mins by HTRF assayAgonist activity at human 5HT4D receptor expressed in HEK293 cells assessed as cAMP production after 30 mins by HTRF assay
ChEMBL 448 5 2 7 2.3 CC(C)n1c(=O)n(C(=O)NCC2CCN(CC3(O)CCOCC3)CC2)c2cc(F)ccc21 10.1021/jm300953p
CHEMBL2179583 82264 0 None 1 2 Human 9.1 pEC50 = 9.1 Functional
Agonist activity at human 5HT4D receptor expressed in HEK293 cells assessed as cAMP production after 30 mins by HTRF assayAgonist activity at human 5HT4D receptor expressed in HEK293 cells assessed as cAMP production after 30 mins by HTRF assay
ChEMBL 448 5 2 7 2.3 CC(C)n1c(=O)n(C(=O)NCC2CCN(CC3(O)CCOCC3)CC2)c2cc(F)ccc21 10.1021/jm300953p
11166796 82264 0 None -1 2 Rat 9.1 pEC50 = 9.1 Functional
Agonist activity at rat 5HT4S receptor expressed in HEK293 cells assessed as increase in cAMP production after 30 mins by HTRF assayAgonist activity at rat 5HT4S receptor expressed in HEK293 cells assessed as increase in cAMP production after 30 mins by HTRF assay
ChEMBL 448 5 2 7 2.3 CC(C)n1c(=O)n(C(=O)NCC2CCN(CC3(O)CCOCC3)CC2)c2cc(F)ccc21 10.1021/jm300953p
CHEMBL2179583 82264 0 None -1 2 Rat 9.1 pEC50 = 9.1 Functional
Agonist activity at rat 5HT4S receptor expressed in HEK293 cells assessed as increase in cAMP production after 30 mins by HTRF assayAgonist activity at rat 5HT4S receptor expressed in HEK293 cells assessed as increase in cAMP production after 30 mins by HTRF assay
ChEMBL 448 5 2 7 2.3 CC(C)n1c(=O)n(C(=O)NCC2CCN(CC3(O)CCOCC3)CC2)c2cc(F)ccc21 10.1021/jm300953p
11166796 82264 0 None -1 2 Rat 9.0 pEC50 = 9.0 Functional
Agonist activity at rat 5HT4L receptor expressed in HEK293 cells assessed as increase in cAMP production after 30 mins by HTRF assayAgonist activity at rat 5HT4L receptor expressed in HEK293 cells assessed as increase in cAMP production after 30 mins by HTRF assay
ChEMBL 448 5 2 7 2.3 CC(C)n1c(=O)n(C(=O)NCC2CCN(CC3(O)CCOCC3)CC2)c2cc(F)ccc21 10.1021/jm300953p
CHEMBL2179583 82264 0 None -1 2 Rat 9.0 pEC50 = 9.0 Functional
Agonist activity at rat 5HT4L receptor expressed in HEK293 cells assessed as increase in cAMP production after 30 mins by HTRF assayAgonist activity at rat 5HT4L receptor expressed in HEK293 cells assessed as increase in cAMP production after 30 mins by HTRF assay
ChEMBL 448 5 2 7 2.3 CC(C)n1c(=O)n(C(=O)NCC2CCN(CC3(O)CCOCC3)CC2)c2cc(F)ccc21 10.1021/jm300953p
53357029 82270 0 None - 1 Human 9.0 pEC50 = 9.0 Functional
Agonist activity at human 5HT4D receptor expressed in HEK293 cells assessed as cAMP production after 30 mins by HTRF assayAgonist activity at human 5HT4D receptor expressed in HEK293 cells assessed as cAMP production after 30 mins by HTRF assay
ChEMBL 418 8 1 7 3.5 CC(C)COc1cccc2onc(OCC3CCN(CC4(O)CCOCC4)CC3)c12 10.1021/jm300953p
CHEMBL2179589 82270 0 None - 1 Human 9.0 pEC50 = 9.0 Functional
Agonist activity at human 5HT4D receptor expressed in HEK293 cells assessed as cAMP production after 30 mins by HTRF assayAgonist activity at human 5HT4D receptor expressed in HEK293 cells assessed as cAMP production after 30 mins by HTRF assay
ChEMBL 418 8 1 7 3.5 CC(C)COc1cccc2onc(OCC3CCN(CC4(O)CCOCC4)CC3)c12 10.1021/jm300953p
11166796 82264 0 None 1 2 Human 9.0 pEC50 = 9.0 Functional
Agonist activity at human 5HT4E receptor expressed in HEK293 cells assessed as increase in cAMP production after 30 mins by HTRF assayAgonist activity at human 5HT4E receptor expressed in HEK293 cells assessed as increase in cAMP production after 30 mins by HTRF assay
ChEMBL 448 5 2 7 2.3 CC(C)n1c(=O)n(C(=O)NCC2CCN(CC3(O)CCOCC3)CC2)c2cc(F)ccc21 10.1021/jm300953p
CHEMBL2179583 82264 0 None 1 2 Human 9.0 pEC50 = 9.0 Functional
Agonist activity at human 5HT4E receptor expressed in HEK293 cells assessed as increase in cAMP production after 30 mins by HTRF assayAgonist activity at human 5HT4E receptor expressed in HEK293 cells assessed as increase in cAMP production after 30 mins by HTRF assay
ChEMBL 448 5 2 7 2.3 CC(C)n1c(=O)n(C(=O)NCC2CCN(CC3(O)CCOCC3)CC2)c2cc(F)ccc21 10.1021/jm300953p
135409453 3714 38 None 3 3 Human 9.0 pEC50 = 9 Functional
Agonist activity at human 5HT4C receptor expressed at 100 fold physiological-level in HEK293 cells assessed as cAMP accumulationAgonist activity at human 5HT4C receptor expressed at 100 fold physiological-level in HEK293 cells assessed as cAMP accumulation
ChEMBL 301 7 3 3 2.6 CCCCCN=C(N/N=C/c1c[nH]c2c1cc(OC)cc2)N 10.1016/j.bmcl.2012.05.034
226 3714 38 None 3 3 Human 9.0 pEC50 = 9 Functional
Agonist activity at human 5HT4C receptor expressed at 100 fold physiological-level in HEK293 cells assessed as cAMP accumulationAgonist activity at human 5HT4C receptor expressed at 100 fold physiological-level in HEK293 cells assessed as cAMP accumulation
ChEMBL 301 7 3 3 2.6 CCCCCN=C(N/N=C/c1c[nH]c2c1cc(OC)cc2)N 10.1016/j.bmcl.2012.05.034
CHEMBL76370 3714 38 None 3 3 Human 9.0 pEC50 = 9 Functional
Agonist activity at human 5HT4C receptor expressed at 100 fold physiological-level in HEK293 cells assessed as cAMP accumulationAgonist activity at human 5HT4C receptor expressed at 100 fold physiological-level in HEK293 cells assessed as cAMP accumulation
ChEMBL 301 7 3 3 2.6 CCCCCN=C(N/N=C/c1c[nH]c2c1cc(OC)cc2)N 10.1016/j.bmcl.2012.05.034
44248435 193907 0 None - 1 Human 9.0 pEC50 = 9 Functional
Agonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assayAgonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assay
ChEMBL 623 15 2 5 7.3 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CCCCCCCCN(C)CCc2c[nH]c3ccccc23)cc2ccccc21 10.1021/jm900881j
CHEMBL555210 193907 0 None - 1 Human 9.0 pEC50 = 9 Functional
Agonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assayAgonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assay
ChEMBL 623 15 2 5 7.3 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CCCCCCCCN(C)CCc2c[nH]c3ccccc23)cc2ccccc21 10.1021/jm900881j
44248680 193909 0 None - 1 Human 9.0 pEC50 = 9 Functional
Agonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assayAgonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assay
ChEMBL 571 10 2 7 3.0 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CCCN2CCC(CNS(C)(=O)=O)CC2)cc2ccccc21 10.1021/jm900881j
CHEMBL555223 193909 0 None - 1 Human 9.0 pEC50 = 9 Functional
Agonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assayAgonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assay
ChEMBL 571 10 2 7 3.0 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CCCN2CCC(CNS(C)(=O)=O)CC2)cc2ccccc21 10.1021/jm900881j
44248313 91900492 194191 0 None - 1 Human 9.0 pEC50 = 9 Functional
Agonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assayAgonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assay
ChEMBL 492 9 1 5 5.0 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CCCCCN2CCCCC2)cc2ccccc21 10.1021/jm900881j
CHEMBL558719 194191 0 None - 1 Human 9.0 pEC50 = 9 Functional
Agonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assayAgonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assay
ChEMBL 492 9 1 5 5.0 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CCCCCN2CCCCC2)cc2ccccc21 10.1021/jm900881j
71714540 90949 0 None - 1 Human 9.0 pEC50 = 9 Functional
Agonist activity at human recombinant 5HT4 receptor assessed as cAMP accumulationAgonist activity at human recombinant 5HT4 receptor assessed as cAMP accumulation
ChEMBL 506 9 3 7 0.5 CCc1nc2c(C(=O)NCC3CCN(CC(O)CN4CCN(S(C)(=O)=O)CC4)CC3)cccc2[nH]1 10.1016/j.bmcl.2013.05.018
CHEMBL2402890 90949 0 None - 1 Human 9.0 pEC50 = 9 Functional
Agonist activity at human recombinant 5HT4 receptor assessed as cAMP accumulationAgonist activity at human recombinant 5HT4 receptor assessed as cAMP accumulation
ChEMBL 506 9 3 7 0.5 CCc1nc2c(C(=O)NCC3CCN(CC(O)CN4CCN(S(C)(=O)=O)CC4)CC3)cccc2[nH]1 10.1016/j.bmcl.2013.05.018
66810955 90962 0 None - 1 Human 9.0 pEC50 = 9 Functional
Agonist activity at human recombinant 5HT4 receptor assessed as cAMP accumulationAgonist activity at human recombinant 5HT4 receptor assessed as cAMP accumulation
ChEMBL 475 7 2 5 2.8 CC(C)c1nc2c(C(=O)NCC3CCN(CC4CCN(S(C)(=O)=O)CC4)CC3)cccc2[nH]1 10.1016/j.bmcl.2013.05.018
CHEMBL2402903 90962 0 None - 1 Human 9.0 pEC50 = 9 Functional
Agonist activity at human recombinant 5HT4 receptor assessed as cAMP accumulationAgonist activity at human recombinant 5HT4 receptor assessed as cAMP accumulation
ChEMBL 475 7 2 5 2.8 CC(C)c1nc2c(C(=O)NCC3CCN(CC4CCN(S(C)(=O)=O)CC4)CC3)cccc2[nH]1 10.1016/j.bmcl.2013.05.018
71462650 82267 0 None - 1 Human 9.0 pEC50 = 9.0 Functional
Agonist activity at human 5HT4D receptor expressed in HEK293 cells assessed as cAMP production after 30 mins by HTRF assayAgonist activity at human 5HT4D receptor expressed in HEK293 cells assessed as cAMP production after 30 mins by HTRF assay
ChEMBL 372 9 0 5 4.9 CCCCN1CCC(COc2noc3cccc(OCC4CCC4)c23)CC1 10.1021/jm300953p
CHEMBL2179586 82267 0 None - 1 Human 9.0 pEC50 = 9.0 Functional
Agonist activity at human 5HT4D receptor expressed in HEK293 cells assessed as cAMP production after 30 mins by HTRF assayAgonist activity at human 5HT4D receptor expressed in HEK293 cells assessed as cAMP production after 30 mins by HTRF assay
ChEMBL 372 9 0 5 4.9 CCCCN1CCC(COc2noc3cccc(OCC4CCC4)c23)CC1 10.1021/jm300953p
71451950 82263 5 None -1 2 Rat 8.9 pEC50 = 8.9 Functional
Agonist activity at rat 5HT4S receptor expressed in HEK293 cells assessed as increase in cAMP production after 30 mins by HTRF assayAgonist activity at rat 5HT4S receptor expressed in HEK293 cells assessed as increase in cAMP production after 30 mins by HTRF assay
ChEMBL 433 4 2 5 2.4 CC1(C)C(=O)N(C(=O)NCC2CCN(CC3(O)CCOCC3)CC2)c2cc(F)ccc21 10.1021/jm300953p
CHEMBL2179582 82263 5 None -1 2 Rat 8.9 pEC50 = 8.9 Functional
Agonist activity at rat 5HT4S receptor expressed in HEK293 cells assessed as increase in cAMP production after 30 mins by HTRF assayAgonist activity at rat 5HT4S receptor expressed in HEK293 cells assessed as increase in cAMP production after 30 mins by HTRF assay
ChEMBL 433 4 2 5 2.4 CC1(C)C(=O)N(C(=O)NCC2CCN(CC3(O)CCOCC3)CC2)c2cc(F)ccc21 10.1021/jm300953p
11166796 82264 0 None 1 2 Human 8.9 pEC50 = 8.9 Functional
Agonist activity at human 5HT4B receptor expressed in HEK293 cells assessed as increase in cAMP production after 30 mins by HTRF assayAgonist activity at human 5HT4B receptor expressed in HEK293 cells assessed as increase in cAMP production after 30 mins by HTRF assay
ChEMBL 448 5 2 7 2.3 CC(C)n1c(=O)n(C(=O)NCC2CCN(CC3(O)CCOCC3)CC2)c2cc(F)ccc21 10.1021/jm300953p
CHEMBL2179583 82264 0 None 1 2 Human 8.9 pEC50 = 8.9 Functional
Agonist activity at human 5HT4B receptor expressed in HEK293 cells assessed as increase in cAMP production after 30 mins by HTRF assayAgonist activity at human 5HT4B receptor expressed in HEK293 cells assessed as increase in cAMP production after 30 mins by HTRF assay
ChEMBL 448 5 2 7 2.3 CC(C)n1c(=O)n(C(=O)NCC2CCN(CC3(O)CCOCC3)CC2)c2cc(F)ccc21 10.1021/jm300953p
71451951 82266 0 None - 1 Human 8.9 pEC50 = 8.9 Functional
Agonist activity at human 5HT4D receptor expressed in HEK293 cells assessed as cAMP production after 30 mins by HTRF assayAgonist activity at human 5HT4D receptor expressed in HEK293 cells assessed as cAMP production after 30 mins by HTRF assay
ChEMBL 372 8 0 5 5.0 CCCCN1CCC(COc2noc3cccc(OC4CCCC4)c23)CC1 10.1021/jm300953p
CHEMBL2179585 82266 0 None - 1 Human 8.9 pEC50 = 8.9 Functional
Agonist activity at human 5HT4D receptor expressed in HEK293 cells assessed as cAMP production after 30 mins by HTRF assayAgonist activity at human 5HT4D receptor expressed in HEK293 cells assessed as cAMP production after 30 mins by HTRF assay
ChEMBL 372 8 0 5 5.0 CCCCN1CCC(COc2noc3cccc(OC4CCCC4)c23)CC1 10.1021/jm300953p
71462651 82268 0 None - 1 Human 8.9 pEC50 = 8.9 Functional
Agonist activity at human 5HT4D receptor expressed in HEK293 cells assessed as cAMP production after 30 mins by HTRF assayAgonist activity at human 5HT4D receptor expressed in HEK293 cells assessed as cAMP production after 30 mins by HTRF assay
ChEMBL 360 9 0 5 4.8 CCCCN1CCC(COc2noc3cccc(OCC(C)C)c23)CC1 10.1021/jm300953p
CHEMBL2179587 82268 0 None - 1 Human 8.9 pEC50 = 8.9 Functional
Agonist activity at human 5HT4D receptor expressed in HEK293 cells assessed as cAMP production after 30 mins by HTRF assayAgonist activity at human 5HT4D receptor expressed in HEK293 cells assessed as cAMP production after 30 mins by HTRF assay
ChEMBL 360 9 0 5 4.8 CCCCN1CCC(COc2noc3cccc(OCC(C)C)c23)CC1 10.1021/jm300953p
71451950 82263 5 None 1 2 Human 8.9 pEC50 = 8.9 Functional
Agonist activity at human 5HT4E receptor expressed in HEK293 cells assessed as increase in cAMP production after 30 mins by HTRF assayAgonist activity at human 5HT4E receptor expressed in HEK293 cells assessed as increase in cAMP production after 30 mins by HTRF assay
ChEMBL 433 4 2 5 2.4 CC1(C)C(=O)N(C(=O)NCC2CCN(CC3(O)CCOCC3)CC2)c2cc(F)ccc21 10.1021/jm300953p
CHEMBL2179582 82263 5 None 1 2 Human 8.9 pEC50 = 8.9 Functional
Agonist activity at human 5HT4E receptor expressed in HEK293 cells assessed as increase in cAMP production after 30 mins by HTRF assayAgonist activity at human 5HT4E receptor expressed in HEK293 cells assessed as increase in cAMP production after 30 mins by HTRF assay
ChEMBL 433 4 2 5 2.4 CC1(C)C(=O)N(C(=O)NCC2CCN(CC3(O)CCOCC3)CC2)c2cc(F)ccc21 10.1021/jm300953p
44247820 91900493 193131 0 None - 1 Human 8.9 pEC50 = 8.9 Functional
Agonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assayAgonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assay
ChEMBL 534 12 1 5 6.1 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CCCCCCCCN2CCCCC2)cc2ccccc21 10.1021/jm900881j
CHEMBL538706 193131 0 None - 1 Human 8.9 pEC50 = 8.9 Functional
Agonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assayAgonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assay
ChEMBL 534 12 1 5 6.1 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CCCCCCCCN2CCCCC2)cc2ccccc21 10.1021/jm900881j
44247951 91900497 193243 0 None - 1 Human 8.9 pEC50 = 8.9 Functional
Agonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assayAgonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assay
ChEMBL 539 9 2 5 5.0 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CCN(C)CCc2c[nH]c3ccccc23)cc2ccccc21 10.1021/jm900881j
CHEMBL541223 193243 0 None - 1 Human 8.9 pEC50 = 8.9 Functional
Agonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assayAgonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assay
ChEMBL 539 9 2 5 5.0 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CCN(C)CCc2c[nH]c3ccccc23)cc2ccccc21 10.1021/jm900881j
44248923 193267 0 None - 1 Human 8.9 pEC50 = 8.9 Functional
Agonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assayAgonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assay
ChEMBL 559 8 2 8 1.2 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3C[C@H](O)CN2CCN(S(C)(=O)=O)CC2)cc2ccccc21 10.1021/jm900881j
CHEMBL541968 193267 0 None - 1 Human 8.9 pEC50 = 8.9 Functional
Agonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assayAgonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assay
ChEMBL 559 8 2 8 1.2 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3C[C@H](O)CN2CCN(S(C)(=O)=O)CC2)cc2ccccc21 10.1021/jm900881j
44247822 91900495 193843 0 None - 1 Human 8.9 pEC50 = 8.9 Functional
Agonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assayAgonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assay
ChEMBL 571 10 1 7 3.1 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CCCCCN2CCN(S(C)(=O)=O)CC2)cc2ccccc21 10.1021/jm900881j
CHEMBL553685 193843 0 None - 1 Human 8.9 pEC50 = 8.9 Functional
Agonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assayAgonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assay
ChEMBL 571 10 1 7 3.1 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CCCCCN2CCN(S(C)(=O)=O)CC2)cc2ccccc21 10.1021/jm900881j
44248184 194488 0 None - 1 Human 8.9 pEC50 = 8.9 Functional
Agonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assayAgonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assay
ChEMBL 525 12 3 5 5.0 COc1cc(N)c(Cl)cc1C(=O)NC1CCN(CCCCCN(C)CCc2c[nH]c3ccccc23)CC1 10.1021/jm900881j
CHEMBL561278 194488 0 None - 1 Human 8.9 pEC50 = 8.9 Functional
Agonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assayAgonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assay
ChEMBL 525 12 3 5 5.0 COc1cc(N)c(Cl)cc1C(=O)NC1CCN(CCCCCN(C)CCc2c[nH]c3ccccc23)CC1 10.1021/jm900881j
71451950 82263 5 None 1 2 Human 8.9 pEC50 = 8.9 Functional
Agonist activity at human 5HT4B receptor expressed in HEK293 cells assessed as increase in cAMP production after 30 mins by HTRF assayAgonist activity at human 5HT4B receptor expressed in HEK293 cells assessed as increase in cAMP production after 30 mins by HTRF assay
ChEMBL 433 4 2 5 2.4 CC1(C)C(=O)N(C(=O)NCC2CCN(CC3(O)CCOCC3)CC2)c2cc(F)ccc21 10.1021/jm300953p
CHEMBL2179582 82263 5 None 1 2 Human 8.9 pEC50 = 8.9 Functional
Agonist activity at human 5HT4B receptor expressed in HEK293 cells assessed as increase in cAMP production after 30 mins by HTRF assayAgonist activity at human 5HT4B receptor expressed in HEK293 cells assessed as increase in cAMP production after 30 mins by HTRF assay
ChEMBL 433 4 2 5 2.4 CC1(C)C(=O)N(C(=O)NCC2CCN(CC3(O)CCOCC3)CC2)c2cc(F)ccc21 10.1021/jm300953p
53354764 3015 30 None 1 2 Human 8.9 pEC50 = 8.9 Functional
Agonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assayAgonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assay
ChEMBL 432 7 1 8 2.6 OC1(CCOCC1)CN1CCC(CC1)COc1noc2c1c(ccc2)O[C@H]1COCC1 10.1016/j.ejmech.2015.08.051
9059 3015 30 None 1 2 Human 8.9 pEC50 = 8.9 Functional
Agonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assayAgonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assay
ChEMBL 432 7 1 8 2.6 OC1(CCOCC1)CN1CCC(CC1)COc1noc2c1c(ccc2)O[C@H]1COCC1 10.1016/j.ejmech.2015.08.051
CHEMBL2152922 3015 30 None 1 2 Human 8.9 pEC50 = 8.9 Functional
Agonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assayAgonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assay
ChEMBL 432 7 1 8 2.6 OC1(CCOCC1)CN1CCC(CC1)COc1noc2c1c(ccc2)O[C@H]1COCC1 10.1016/j.ejmech.2015.08.051
DB12675 3015 30 None 1 2 Human 8.9 pEC50 = 8.9 Functional
Agonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assayAgonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assay
ChEMBL 432 7 1 8 2.6 OC1(CCOCC1)CN1CCC(CC1)COc1noc2c1c(ccc2)O[C@H]1COCC1 10.1016/j.ejmech.2015.08.051
155565664 175030 0 None - 1 Human 8.9 pEC50 = 8.9 Functional
Partial agonist activity at human HA-tagged 5HT4 receptor expressed in COS7 cells assessed as induction of cAMP production measured after 10 mins by HTRF assayPartial agonist activity at human HA-tagged 5HT4 receptor expressed in COS7 cells assessed as induction of cAMP production measured after 10 mins by HTRF assay
ChEMBL 432 8 2 6 4.5 COc1ccc(CN2CCC(CCC(=O)c3cc(Cl)c(N)cc3OC)CC2)cc1O 10.1016/j.ejmech.2019.111596
CHEMBL4580044 175030 0 None - 1 Human 8.9 pEC50 = 8.9 Functional
Partial agonist activity at human HA-tagged 5HT4 receptor expressed in COS7 cells assessed as induction of cAMP production measured after 10 mins by HTRF assayPartial agonist activity at human HA-tagged 5HT4 receptor expressed in COS7 cells assessed as induction of cAMP production measured after 10 mins by HTRF assay
ChEMBL 432 8 2 6 4.5 COc1ccc(CN2CCC(CCC(=O)c3cc(Cl)c(N)cc3OC)CC2)cc1O 10.1016/j.ejmech.2019.111596
11493559 73066 0 None - 1 Rat 8.8 pEC50 = 8.8 Functional
Agonism at 5HT4 receptor in rat tunica muscularis mucosaAgonism at 5HT4 receptor in rat tunica muscularis mucosa
ChEMBL 324 4 1 5 2.6 COc1cc(N)c(Cl)cc1C(=O)OC[C@@H]1CCN2CCC[C@@H]12 10.1021/jm0509501
CHEMBL201621 73066 0 None - 1 Rat 8.8 pEC50 = 8.8 Functional
Agonism at 5HT4 receptor in rat tunica muscularis mucosaAgonism at 5HT4 receptor in rat tunica muscularis mucosa
ChEMBL 324 4 1 5 2.6 COc1cc(N)c(Cl)cc1C(=O)OC[C@@H]1CCN2CCC[C@@H]12 10.1021/jm0509501
11961293 3710 13 None 5 2 Human 8.8 pEC50 = 8.8 Functional
Agonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assayAgonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assay
ChEMBL 455 6 2 5 3.6 COC(=O)N1CCC(CC1)CN1CCC(CC1)CNC(=O)c1cccc2c1nc([nH]2)C(C)C 10.1016/j.ejmech.2015.08.051
8426 3710 13 None 5 2 Human 8.8 pEC50 = 8.8 Functional
Agonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assayAgonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assay
ChEMBL 455 6 2 5 3.6 COC(=O)N1CCC(CC1)CN1CCC(CC1)CNC(=O)c1cccc2c1nc([nH]2)C(C)C 10.1016/j.ejmech.2015.08.051
CHEMBL2402904 3710 13 None 5 2 Human 8.8 pEC50 = 8.8 Functional
Agonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assayAgonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assay
ChEMBL 455 6 2 5 3.6 COC(=O)N1CCC(CC1)CN1CCC(CC1)CNC(=O)c1cccc2c1nc([nH]2)C(C)C 10.1016/j.ejmech.2015.08.051
DB12725 3710 13 None 5 2 Human 8.8 pEC50 = 8.8 Functional
Agonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assayAgonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assay
ChEMBL 455 6 2 5 3.6 COC(=O)N1CCC(CC1)CN1CCC(CC1)CNC(=O)c1cccc2c1nc([nH]2)C(C)C 10.1016/j.ejmech.2015.08.051
71451950 82263 5 None -1 2 Rat 8.8 pEC50 = 8.8 Functional
Agonist activity at rat 5HT4L receptor expressed in HEK293 cells assessed as increase in cAMP production after 30 mins by HTRF assayAgonist activity at rat 5HT4L receptor expressed in HEK293 cells assessed as increase in cAMP production after 30 mins by HTRF assay
ChEMBL 433 4 2 5 2.4 CC1(C)C(=O)N(C(=O)NCC2CCN(CC3(O)CCOCC3)CC2)c2cc(F)ccc21 10.1021/jm300953p
CHEMBL2179582 82263 5 None -1 2 Rat 8.8 pEC50 = 8.8 Functional
Agonist activity at rat 5HT4L receptor expressed in HEK293 cells assessed as increase in cAMP production after 30 mins by HTRF assayAgonist activity at rat 5HT4L receptor expressed in HEK293 cells assessed as increase in cAMP production after 30 mins by HTRF assay
ChEMBL 433 4 2 5 2.4 CC1(C)C(=O)N(C(=O)NCC2CCN(CC3(O)CCOCC3)CC2)c2cc(F)ccc21 10.1021/jm300953p
70688535 76065 0 None - 1 Human 8.8 pEC50 = 8.8 Functional
Agonist activity at human 5HT4C receptor expressed at 100 fold physiological-level in HEK293 cells assessed as cAMP accumulationAgonist activity at human 5HT4C receptor expressed at 100 fold physiological-level in HEK293 cells assessed as cAMP accumulation
ChEMBL 586 13 2 7 4.2 CC(C)n1nc(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CCCCCCN2CCC(CNS(C)(=O)=O)CC2)c2ccccc21 10.1016/j.bmcl.2012.05.034
CHEMBL2059584 76065 0 None - 1 Human 8.8 pEC50 = 8.8 Functional
Agonist activity at human 5HT4C receptor expressed at 100 fold physiological-level in HEK293 cells assessed as cAMP accumulationAgonist activity at human 5HT4C receptor expressed at 100 fold physiological-level in HEK293 cells assessed as cAMP accumulation
ChEMBL 586 13 2 7 4.2 CC(C)n1nc(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CCCCCCN2CCC(CNS(C)(=O)=O)CC2)c2ccccc21 10.1016/j.bmcl.2012.05.034
44248076 193374 0 None - 1 Human 8.8 pEC50 = 8.8 Functional
Agonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assayAgonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assay
ChEMBL 543 8 1 7 2.3 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CCCN2CCN(S(C)(=O)=O)CC2)cc2ccccc21 10.1021/jm900881j
CHEMBL549449 193374 0 None - 1 Human 8.8 pEC50 = 8.8 Functional
Agonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assayAgonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assay
ChEMBL 543 8 1 7 2.3 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CCCN2CCN(S(C)(=O)=O)CC2)cc2ccccc21 10.1021/jm900881j
71712466 90810 0 None - 1 Human 8.8 pEC50 = 8.8 Functional
Agonist activity at human recombinant 5HT4 receptor assessed as cAMP accumulationAgonist activity at human recombinant 5HT4 receptor assessed as cAMP accumulation
ChEMBL 439 6 2 4 3.4 CC(=O)N1CCC(CN2CCC(CNC(=O)c3cccc4[nH]c(C(C)C)nc34)CC2)CC1 10.1016/j.bmcl.2013.05.018
CHEMBL2401750 90810 0 None - 1 Human 8.8 pEC50 = 8.8 Functional
Agonist activity at human recombinant 5HT4 receptor assessed as cAMP accumulationAgonist activity at human recombinant 5HT4 receptor assessed as cAMP accumulation
ChEMBL 439 6 2 4 3.4 CC(=O)N1CCC(CN2CCC(CNC(=O)c3cccc4[nH]c(C(C)C)nc34)CC2)CC1 10.1016/j.bmcl.2013.05.018
71712325 90954 0 None - 1 Human 8.8 pEC50 = 8.8 Functional
Agonist activity at human recombinant 5HT4 receptor assessed as cAMP accumulationAgonist activity at human recombinant 5HT4 receptor assessed as cAMP accumulation
ChEMBL 554 9 3 7 1.6 CS(=O)(=O)N1CCN(CC(O)CN2CCC(CNC(=O)c3cccc4[nH]c(-c5ccccc5)nc34)CC2)CC1 10.1016/j.bmcl.2013.05.018
CHEMBL2402895 90954 0 None - 1 Human 8.8 pEC50 = 8.8 Functional
Agonist activity at human recombinant 5HT4 receptor assessed as cAMP accumulationAgonist activity at human recombinant 5HT4 receptor assessed as cAMP accumulation
ChEMBL 554 9 3 7 1.6 CS(=O)(=O)N1CCN(CC(O)CN2CCC(CNC(=O)c3cccc4[nH]c(-c5ccccc5)nc34)CC2)CC1 10.1016/j.bmcl.2013.05.018
71712328 90957 0 None - 1 Human 8.8 pEC50 = 8.8 Functional
Agonist activity at human recombinant 5HT4 receptor assessed as cAMP accumulationAgonist activity at human recombinant 5HT4 receptor assessed as cAMP accumulation
ChEMBL 470 7 2 6 2.5 COC(=O)N1CCN(CCN2CCC(CNC(=O)c3cccc4[nH]c(C(C)C)nc34)CC2)CC1 10.1016/j.bmcl.2013.05.018
CHEMBL2402898 90957 0 None - 1 Human 8.8 pEC50 = 8.8 Functional
Agonist activity at human recombinant 5HT4 receptor assessed as cAMP accumulationAgonist activity at human recombinant 5HT4 receptor assessed as cAMP accumulation
ChEMBL 470 7 2 6 2.5 COC(=O)N1CCN(CCN2CCC(CNC(=O)c3cccc4[nH]c(C(C)C)nc34)CC2)CC1 10.1016/j.bmcl.2013.05.018
71712465 90961 0 None - 1 Human 8.8 pEC50 = 8.8 Functional
Agonist activity at human recombinant 5HT4 receptor assessed as cAMP accumulationAgonist activity at human recombinant 5HT4 receptor assessed as cAMP accumulation
ChEMBL 429 8 3 5 2.0 CC(=O)N(C)CC(O)CN1CCC(CNC(=O)c2cccc3[nH]c(C(C)C)nc23)CC1 10.1016/j.bmcl.2013.05.018
CHEMBL2402902 90961 0 None - 1 Human 8.8 pEC50 = 8.8 Functional
Agonist activity at human recombinant 5HT4 receptor assessed as cAMP accumulationAgonist activity at human recombinant 5HT4 receptor assessed as cAMP accumulation
ChEMBL 429 8 3 5 2.0 CC(=O)N(C)CC(O)CN1CCC(CNC(=O)c2cccc3[nH]c(C(C)C)nc23)CC1 10.1016/j.bmcl.2013.05.018
11166796 82264 0 None -1 2 Rat 8.8 pEC50 = 8.8 Functional
Agonist activity at rat 5HT4E receptor expressed in HEK293 cells assessed as increase in cAMP production after 30 mins by HTRF assayAgonist activity at rat 5HT4E receptor expressed in HEK293 cells assessed as increase in cAMP production after 30 mins by HTRF assay
ChEMBL 448 5 2 7 2.3 CC(C)n1c(=O)n(C(=O)NCC2CCN(CC3(O)CCOCC3)CC2)c2cc(F)ccc21 10.1021/jm300953p
CHEMBL2179583 82264 0 None -1 2 Rat 8.8 pEC50 = 8.8 Functional
Agonist activity at rat 5HT4E receptor expressed in HEK293 cells assessed as increase in cAMP production after 30 mins by HTRF assayAgonist activity at rat 5HT4E receptor expressed in HEK293 cells assessed as increase in cAMP production after 30 mins by HTRF assay
ChEMBL 448 5 2 7 2.3 CC(C)n1c(=O)n(C(=O)NCC2CCN(CC3(O)CCOCC3)CC2)c2cc(F)ccc21 10.1021/jm300953p
71462652 82271 0 None - 1 Human 8.8 pEC50 = 8.8 Functional
Agonist activity at human 5HT4D receptor expressed in HEK293 cells assessed as cAMP production after 30 mins by HTRF assayAgonist activity at human 5HT4D receptor expressed in HEK293 cells assessed as cAMP production after 30 mins by HTRF assay
ChEMBL 434 8 2 8 2.6 CC(C)(O)COc1cccc2onc(OCC3CCN(CC4(O)CCOCC4)CC3)c12 10.1021/jm300953p
CHEMBL2179590 82271 0 None - 1 Human 8.8 pEC50 = 8.8 Functional
Agonist activity at human 5HT4D receptor expressed in HEK293 cells assessed as cAMP production after 30 mins by HTRF assayAgonist activity at human 5HT4D receptor expressed in HEK293 cells assessed as cAMP production after 30 mins by HTRF assay
ChEMBL 434 8 2 8 2.6 CC(C)(O)COc1cccc2onc(OCC3CCN(CC4(O)CCOCC4)CC3)c12 10.1021/jm300953p
9952994 106487 0 None - 1 Rat 8.7 pEC50 = 8.7 Functional
In vitro relaxation of carbachol pre-contracted rat oesophageal TMM.In vitro relaxation of carbachol pre-contracted rat oesophageal TMM.
ChEMBL 366 6 1 5 3.5 CCCCN1CCC(COC(=O)c2cc(Cl)c(N)c3c2OCC3)CC1 10.1016/0960-894X(96)00002-9
CHEMBL315071 106487 0 None - 1 Rat 8.7 pEC50 = 8.7 Functional
In vitro relaxation of carbachol pre-contracted rat oesophageal TMM.In vitro relaxation of carbachol pre-contracted rat oesophageal TMM.
ChEMBL 366 6 1 5 3.5 CCCCN1CCC(COC(=O)c2cc(Cl)c(N)c3c2OCC3)CC1 10.1016/0960-894X(96)00002-9
53357016 82262 0 None - 1 Human 8.7 pEC50 = 8.7 Functional
Agonist activity at human 5HT4D receptor expressed in HEK293 cells assessed as cAMP production after 30 mins by HTRF assayAgonist activity at human 5HT4D receptor expressed in HEK293 cells assessed as cAMP production after 30 mins by HTRF assay
ChEMBL 446 7 1 8 3.0 OC1(CN2CCC(COc3noc4cccc(OC5CCOCC5)c34)CC2)CCOCC1 10.1021/jm300953p
CHEMBL2179581 82262 0 None - 1 Human 8.7 pEC50 = 8.7 Functional
Agonist activity at human 5HT4D receptor expressed in HEK293 cells assessed as cAMP production after 30 mins by HTRF assayAgonist activity at human 5HT4D receptor expressed in HEK293 cells assessed as cAMP production after 30 mins by HTRF assay
ChEMBL 446 7 1 8 3.0 OC1(CN2CCC(COc3noc4cccc(OC5CCOCC5)c34)CC2)CCOCC1 10.1021/jm300953p
70682173 76058 0 None - 1 Human 8.7 pEC50 = 8.7 Functional
Agonist activity at human 5HT4C receptor expressed at 100 fold physiological-level in HEK293 cells assessed as cAMP accumulationAgonist activity at human 5HT4C receptor expressed at 100 fold physiological-level in HEK293 cells assessed as cAMP accumulation
ChEMBL 453 7 2 6 3.2 CC(C)n1nc(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CC(O)CN2CCCCC2)c2ccccc21 10.1016/j.bmcl.2012.05.034
CHEMBL2059577 76058 0 None - 1 Human 8.7 pEC50 = 8.7 Functional
Agonist activity at human 5HT4C receptor expressed at 100 fold physiological-level in HEK293 cells assessed as cAMP accumulationAgonist activity at human 5HT4C receptor expressed at 100 fold physiological-level in HEK293 cells assessed as cAMP accumulation
ChEMBL 453 7 2 6 3.2 CC(C)n1nc(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CC(O)CN2CCCCC2)c2ccccc21 10.1016/j.bmcl.2012.05.034
44248439 194518 0 None - 1 Human 8.7 pEC50 = 8.7 Functional
Agonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assayAgonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assay
ChEMBL 464 7 1 5 4.2 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CCCN2CCCCC2)cc2ccccc21 10.1021/jm900881j
CHEMBL561398 194518 0 None - 1 Human 8.7 pEC50 = 8.7 Functional
Agonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assayAgonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assay
ChEMBL 464 7 1 5 4.2 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CCCN2CCCCC2)cc2ccccc21 10.1021/jm900881j
135409453 3714 38 None 3 3 Human 8.7 pEC50 = 8.7 Functional
Agonist activity at human 5HT4C receptor expressed in a cell line expressing receptor at 10 fold physiological-level assessed as cAMP accumulationAgonist activity at human 5HT4C receptor expressed in a cell line expressing receptor at 10 fold physiological-level assessed as cAMP accumulation
ChEMBL 301 7 3 3 2.6 CCCCCN=C(N/N=C/c1c[nH]c2c1cc(OC)cc2)N 10.1016/j.bmcl.2012.05.034
226 3714 38 None 3 3 Human 8.7 pEC50 = 8.7 Functional
Agonist activity at human 5HT4C receptor expressed in a cell line expressing receptor at 10 fold physiological-level assessed as cAMP accumulationAgonist activity at human 5HT4C receptor expressed in a cell line expressing receptor at 10 fold physiological-level assessed as cAMP accumulation
ChEMBL 301 7 3 3 2.6 CCCCCN=C(N/N=C/c1c[nH]c2c1cc(OC)cc2)N 10.1016/j.bmcl.2012.05.034
CHEMBL76370 3714 38 None 3 3 Human 8.7 pEC50 = 8.7 Functional
Agonist activity at human 5HT4C receptor expressed in a cell line expressing receptor at 10 fold physiological-level assessed as cAMP accumulationAgonist activity at human 5HT4C receptor expressed in a cell line expressing receptor at 10 fold physiological-level assessed as cAMP accumulation
ChEMBL 301 7 3 3 2.6 CCCCCN=C(N/N=C/c1c[nH]c2c1cc(OC)cc2)N 10.1016/j.bmcl.2012.05.034
44224237 193122 7 None - 1 Human 8.7 pEC50 = 8.7 Functional
Agonist activity at human 5HT4C receptor expressed in a cell line expressing receptor at 10 fold physiological-level assessed as cAMP accumulationAgonist activity at human 5HT4C receptor expressed in a cell line expressing receptor at 10 fold physiological-level assessed as cAMP accumulation
ChEMBL 559 8 2 8 1.2 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3C[C@@H](O)CN2CCN(S(C)(=O)=O)CC2)cc2ccccc21 10.1016/j.bmcl.2012.05.034
CHEMBL538635 193122 7 None - 1 Human 8.7 pEC50 = 8.7 Functional
Agonist activity at human 5HT4C receptor expressed in a cell line expressing receptor at 10 fold physiological-level assessed as cAMP accumulationAgonist activity at human 5HT4C receptor expressed in a cell line expressing receptor at 10 fold physiological-level assessed as cAMP accumulation
ChEMBL 559 8 2 8 1.2 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3C[C@@H](O)CN2CCN(S(C)(=O)=O)CC2)cc2ccccc21 10.1016/j.bmcl.2012.05.034
71712464 90960 0 None - 1 Human 8.7 pEC50 = 8.7 Functional
Agonist activity at human recombinant 5HT4 receptor assessed as cAMP accumulationAgonist activity at human recombinant 5HT4 receptor assessed as cAMP accumulation
ChEMBL 445 8 3 6 2.2 COC(=O)N(C)CC(O)CN1CCC(CNC(=O)c2cccc3[nH]c(C(C)C)nc23)CC1 10.1016/j.bmcl.2013.05.018
CHEMBL2402901 90960 0 None - 1 Human 8.7 pEC50 = 8.7 Functional
Agonist activity at human recombinant 5HT4 receptor assessed as cAMP accumulationAgonist activity at human recombinant 5HT4 receptor assessed as cAMP accumulation
ChEMBL 445 8 3 6 2.2 COC(=O)N(C)CC(O)CN1CCC(CNC(=O)c2cccc3[nH]c(C(C)C)nc23)CC1 10.1016/j.bmcl.2013.05.018
44224237 193122 7 None - 1 Human 8.7 pEC50 = 8.7 Functional
Agonist activity at human recombinant 5HT4c receptor expressed in HEK293 cells at 10-fold physiological level assessed as accumulation of cAMPAgonist activity at human recombinant 5HT4c receptor expressed in HEK293 cells at 10-fold physiological level assessed as accumulation of cAMP
ChEMBL 559 8 2 8 1.2 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3C[C@@H](O)CN2CCN(S(C)(=O)=O)CC2)cc2ccccc21 10.1016/j.bmcl.2012.08.051
CHEMBL538635 193122 7 None - 1 Human 8.7 pEC50 = 8.7 Functional
Agonist activity at human recombinant 5HT4c receptor expressed in HEK293 cells at 10-fold physiological level assessed as accumulation of cAMPAgonist activity at human recombinant 5HT4c receptor expressed in HEK293 cells at 10-fold physiological level assessed as accumulation of cAMP
ChEMBL 559 8 2 8 1.2 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3C[C@@H](O)CN2CCN(S(C)(=O)=O)CC2)cc2ccccc21 10.1016/j.bmcl.2012.08.051
15295138 50789 0 None - 1 Guinea pig 8.0 pEC50 = 8 Functional
5-hydroxytryptamine 4 receptor agonist activity, concentration which gave 50% increase in the response to electrically-stimulated myenteric plexus and longitudinal muscle of the guinea pig ileum5-hydroxytryptamine 4 receptor agonist activity, concentration which gave 50% increase in the response to electrically-stimulated myenteric plexus and longitudinal muscle of the guinea pig ileum
ChEMBL 328 5 2 6 1.5 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCCC(O)C1 10.1021/jm960320m
CHEMBL157880 50789 0 None - 1 Guinea pig 8.0 pEC50 = 8 Functional
5-hydroxytryptamine 4 receptor agonist activity, concentration which gave 50% increase in the response to electrically-stimulated myenteric plexus and longitudinal muscle of the guinea pig ileum5-hydroxytryptamine 4 receptor agonist activity, concentration which gave 50% increase in the response to electrically-stimulated myenteric plexus and longitudinal muscle of the guinea pig ileum
ChEMBL 328 5 2 6 1.5 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCCC(O)C1 10.1021/jm960320m
19081984 204238 0 None - 1 Human 8.0 pEC50 = 8 Functional
Agonist activity against 5-HT4 receptor in rat esophageal muscularis mucosaeAgonist activity against 5-HT4 receptor in rat esophageal muscularis mucosae
ChEMBL 336 7 1 4 3.8 C=CCN1CCC(CCC(=O)c2cc(Cl)c(N)cc2OC)CC1 10.1016/S0960-894X(01)80413-3
CHEMBL84398 204238 0 None - 1 Human 8.0 pEC50 = 8 Functional
Agonist activity against 5-HT4 receptor in rat esophageal muscularis mucosaeAgonist activity against 5-HT4 receptor in rat esophageal muscularis mucosae
ChEMBL 336 7 1 4 3.8 C=CCN1CCC(CCC(=O)c2cc(Cl)c(N)cc2OC)CC1 10.1016/S0960-894X(01)80413-3
49783210 17457 0 None - 1 Human 8.0 pEC50 = 8 Functional
Agonist activity at 5HT4 receptor expressed in HEK293/L9 cells by cAMP assayAgonist activity at 5HT4 receptor expressed in HEK293/L9 cells by cAMP assay
ChEMBL 440 7 1 6 3.9 CCCCN1CCC(COC(=O)c2cc(Br)c(NC)c3c2OCCO3)CC1 10.1021/jm100668r
CHEMBL1258338 17457 0 None - 1 Human 8.0 pEC50 = 8 Functional
Agonist activity at 5HT4 receptor expressed in HEK293/L9 cells by cAMP assayAgonist activity at 5HT4 receptor expressed in HEK293/L9 cells by cAMP assay
ChEMBL 440 7 1 6 3.9 CCCCN1CCC(COC(=O)c2cc(Br)c(NC)c3c2OCCO3)CC1 10.1021/jm100668r
5 139 66 None -13 27 Guinea pig 8.0 pEC50 = 8 Functional
Agonist activity at 5HT4 receptor in guinea pig colon assessed as longitudinal muscle plexus contractionAgonist activity at 5HT4 receptor in guinea pig colon assessed as longitudinal muscle plexus contraction
ChEMBL 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 10.1016/j.bmcl.2012.05.034
5202 139 66 None -13 27 Guinea pig 8.0 pEC50 = 8 Functional
Agonist activity at 5HT4 receptor in guinea pig colon assessed as longitudinal muscle plexus contractionAgonist activity at 5HT4 receptor in guinea pig colon assessed as longitudinal muscle plexus contraction
ChEMBL 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 10.1016/j.bmcl.2012.05.034
CHEMBL39 139 66 None -13 27 Guinea pig 8.0 pEC50 = 8 Functional
Agonist activity at 5HT4 receptor in guinea pig colon assessed as longitudinal muscle plexus contractionAgonist activity at 5HT4 receptor in guinea pig colon assessed as longitudinal muscle plexus contraction
ChEMBL 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 10.1016/j.bmcl.2012.05.034
DB08839 139 66 None -13 27 Guinea pig 8.0 pEC50 = 8 Functional
Agonist activity at 5HT4 receptor in guinea pig colon assessed as longitudinal muscle plexus contractionAgonist activity at 5HT4 receptor in guinea pig colon assessed as longitudinal muscle plexus contraction
ChEMBL 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 10.1016/j.bmcl.2012.05.034
11225102 76071 2 None -1 2 Guinea pig 8.0 pEC50 = 8 Functional
Agonist activity at 5HT4 receptor in guinea pig colon assessed as longitudinal muscle plexus contractionAgonist activity at 5HT4 receptor in guinea pig colon assessed as longitudinal muscle plexus contraction
ChEMBL 466 6 1 6 2.5 CC(=O)N1CCN(CCN2[C@H]3CC[C@@H]2C[C@H](NC(=O)c2nn(C(C)C)c4ccccc24)C3)CC1 10.1016/j.bmcl.2012.05.034
CHEMBL2059590 76071 2 None -1 2 Guinea pig 8.0 pEC50 = 8 Functional
Agonist activity at 5HT4 receptor in guinea pig colon assessed as longitudinal muscle plexus contractionAgonist activity at 5HT4 receptor in guinea pig colon assessed as longitudinal muscle plexus contraction
ChEMBL 466 6 1 6 2.5 CC(=O)N1CCN(CCN2[C@H]3CC[C@@H]2C[C@H](NC(=O)c2nn(C(C)C)c4ccccc24)C3)CC1 10.1016/j.bmcl.2012.05.034
10837280 91900491 194149 0 None - 1 Human 8.0 pEC50 = 8 Functional
Agonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assayAgonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assay
ChEMBL 450 6 1 5 3.8 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CCN2CCCCC2)cc2ccccc21 10.1021/jm900881j
CHEMBL558259 194149 0 None - 1 Human 8.0 pEC50 = 8 Functional
Agonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assayAgonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assay
ChEMBL 450 6 1 5 3.8 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CCN2CCCCC2)cc2ccccc21 10.1021/jm900881j
44248317 194225 0 None - 1 Human 8.0 pEC50 = 8 Functional
Agonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assayAgonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assay
ChEMBL 559 12 1 7 2.9 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CCCN(C)CCCN(C)S(C)(=O)=O)cc2ccccc21 10.1021/jm900881j
CHEMBL559050 194225 0 None - 1 Human 8.0 pEC50 = 8 Functional
Agonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assayAgonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assay
ChEMBL 559 12 1 7 2.9 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CCCN(C)CCCN(C)S(C)(=O)=O)cc2ccccc21 10.1021/jm900881j
11225102 76071 2 None 1 2 Human 8.0 pEC50 = 8 Functional
Agonist activity at human 5HT4C receptor expressed in a cell line expressing receptor at 10 fold physiological-level assessed as cAMP accumulationAgonist activity at human 5HT4C receptor expressed in a cell line expressing receptor at 10 fold physiological-level assessed as cAMP accumulation
ChEMBL 466 6 1 6 2.5 CC(=O)N1CCN(CCN2[C@H]3CC[C@@H]2C[C@H](NC(=O)c2nn(C(C)C)c4ccccc24)C3)CC1 10.1016/j.bmcl.2012.05.034
CHEMBL2059590 76071 2 None 1 2 Human 8.0 pEC50 = 8 Functional
Agonist activity at human 5HT4C receptor expressed in a cell line expressing receptor at 10 fold physiological-level assessed as cAMP accumulationAgonist activity at human 5HT4C receptor expressed in a cell line expressing receptor at 10 fold physiological-level assessed as cAMP accumulation
ChEMBL 466 6 1 6 2.5 CC(=O)N1CCN(CCN2[C@H]3CC[C@@H]2C[C@H](NC(=O)c2nn(C(C)C)c4ccccc24)C3)CC1 10.1016/j.bmcl.2012.05.034
127039167 136298 0 None - 1 Human 8.0 pEC50 = 8 Functional
Agonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assayAgonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assay
ChEMBL 398 6 1 5 3.3 CC(C)c1nc(C(=O)NCC2CCN(CC3CCOCC3)CC2)c2ccccn12 10.1016/j.ejmech.2015.08.051
CHEMBL3741608 136298 0 None - 1 Human 8.0 pEC50 = 8 Functional
Agonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assayAgonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assay
ChEMBL 398 6 1 5 3.3 CC(C)c1nc(C(=O)NCC2CCN(CC3CCOCC3)CC2)c2ccccn12 10.1016/j.ejmech.2015.08.051
71712611 90946 0 None - 1 Human 8.0 pEC50 = 8 Functional
Agonist activity at human recombinant 5HT4 receptor assessed as cAMP accumulationAgonist activity at human recombinant 5HT4 receptor assessed as cAMP accumulation
ChEMBL 478 8 3 7 -0.1 CS(=O)(=O)N1CCN(CC(O)CN2CCC(CNC(=O)c3cccc4[nH]cnc34)CC2)CC1 10.1016/j.bmcl.2013.05.018
CHEMBL2402887 90946 0 None - 1 Human 8.0 pEC50 = 8 Functional
Agonist activity at human recombinant 5HT4 receptor assessed as cAMP accumulationAgonist activity at human recombinant 5HT4 receptor assessed as cAMP accumulation
ChEMBL 478 8 3 7 -0.1 CS(=O)(=O)N1CCN(CC(O)CN2CCC(CNC(=O)c3cccc4[nH]cnc34)CC2)CC1 10.1016/j.bmcl.2013.05.018
11225102 76071 2 None 1 2 Human 8.0 pEC50 = 8 Functional
Agonist activity at human recombinant 5HT4c receptor expressed in HEK293 cells at 10-fold physiological level assessed as accumulation of cAMPAgonist activity at human recombinant 5HT4c receptor expressed in HEK293 cells at 10-fold physiological level assessed as accumulation of cAMP
ChEMBL 466 6 1 6 2.5 CC(=O)N1CCN(CCN2[C@H]3CC[C@@H]2C[C@H](NC(=O)c2nn(C(C)C)c4ccccc24)C3)CC1 10.1016/j.bmcl.2012.08.051
CHEMBL2059590 76071 2 None 1 2 Human 8.0 pEC50 = 8 Functional
Agonist activity at human recombinant 5HT4c receptor expressed in HEK293 cells at 10-fold physiological level assessed as accumulation of cAMPAgonist activity at human recombinant 5HT4c receptor expressed in HEK293 cells at 10-fold physiological level assessed as accumulation of cAMP
ChEMBL 466 6 1 6 2.5 CC(=O)N1CCN(CCN2[C@H]3CC[C@@H]2C[C@H](NC(=O)c2nn(C(C)C)c4ccccc24)C3)CC1 10.1016/j.bmcl.2012.08.051
70684790 77154 0 None - 1 Human 8.0 pEC50 = 8 Functional
Agonist activity at human recombinant 5HT4c receptor expressed in HEK293 cells at 10-fold physiological level assessed as accumulation of cAMPAgonist activity at human recombinant 5HT4c receptor expressed in HEK293 cells at 10-fold physiological level assessed as accumulation of cAMP
ChEMBL 484 7 2 7 2.4 COC(=O)N(C)CC(O)CN1[C@H]2CC[C@@H]1C[C@H](NC(=O)c1cc3ccccc3n(C(C)C)c1=O)C2 10.1016/j.bmcl.2012.08.051
CHEMBL2087333 77154 0 None - 1 Human 8.0 pEC50 = 8 Functional
Agonist activity at human recombinant 5HT4c receptor expressed in HEK293 cells at 10-fold physiological level assessed as accumulation of cAMPAgonist activity at human recombinant 5HT4c receptor expressed in HEK293 cells at 10-fold physiological level assessed as accumulation of cAMP
ChEMBL 484 7 2 7 2.4 COC(=O)N(C)CC(O)CN1[C@H]2CC[C@@H]1C[C@H](NC(=O)c1cc3ccccc3n(C(C)C)c1=O)C2 10.1016/j.bmcl.2012.08.051
11432106 77156 0 None - 1 Human 8.0 pEC50 = 8 Functional
Agonist activity at human recombinant 5HT4c receptor expressed in HEK293 cells at 10-fold physiological level assessed as accumulation of cAMPAgonist activity at human recombinant 5HT4c receptor expressed in HEK293 cells at 10-fold physiological level assessed as accumulation of cAMP
ChEMBL 504 8 2 7 1.6 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CC(O)CN(C)S(C)(=O)=O)cc2ccccc21 10.1016/j.bmcl.2012.08.051
CHEMBL2087335 77156 0 None - 1 Human 8.0 pEC50 = 8 Functional
Agonist activity at human recombinant 5HT4c receptor expressed in HEK293 cells at 10-fold physiological level assessed as accumulation of cAMPAgonist activity at human recombinant 5HT4c receptor expressed in HEK293 cells at 10-fold physiological level assessed as accumulation of cAMP
ChEMBL 504 8 2 7 1.6 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CC(O)CN(C)S(C)(=O)=O)cc2ccccc21 10.1016/j.bmcl.2012.08.051
71462777 82552 0 None - 1 Human 8.0 pEC50 = 8 Functional
Inverse agonist activity at human recombinant 5HT4R expressed in HEK293T cells assessed as Gs activationInverse agonist activity at human recombinant 5HT4R expressed in HEK293T cells assessed as Gs activation
ChEMBL 335 5 0 4 4.3 CCCN1CCC(COc2nc3ccccc3c3ncccc23)CC1 10.1021/jm300943r
CHEMBL2181171 82552 0 None - 1 Human 8.0 pEC50 = 8 Functional
Inverse agonist activity at human recombinant 5HT4R expressed in HEK293T cells assessed as Gs activationInverse agonist activity at human recombinant 5HT4R expressed in HEK293T cells assessed as Gs activation
ChEMBL 335 5 0 4 4.3 CCCN1CCC(COc2nc3ccccc3c3ncccc23)CC1 10.1021/jm300943r
130946 201070 2 None - 1 Rat 8.0 pEC50 = 8 Functional
Tested for its agonist potency against the 5-hydroxytryptamine 4 receptor located in the rat esophageal tunica muscularis mucosaeTested for its agonist potency against the 5-hydroxytryptamine 4 receptor located in the rat esophageal tunica muscularis mucosae
ChEMBL 328 2 1 5 2.0 CCn1c(=O)n(C(=O)NC2CC3CCC(C2)N3C)c2ccccc21 10.1016/S0960-894X(01)81243-9
CHEMBL62023 201070 2 None - 1 Rat 8.0 pEC50 = 8 Functional
Tested for its agonist potency against the 5-hydroxytryptamine 4 receptor located in the rat esophageal tunica muscularis mucosaeTested for its agonist potency against the 5-hydroxytryptamine 4 receptor located in the rat esophageal tunica muscularis mucosae
ChEMBL 328 2 1 5 2.0 CCn1c(=O)n(C(=O)NC2CC3CCC(C2)N3C)c2ccccc21 10.1016/S0960-894X(01)81243-9
5 139 66 None -138 27 Human 7.0 pEC50 = 7 Functional
Activity at SER4 receptor expressed in HEK293 cells assessed as increase in calcium by calcium imaging assayActivity at SER4 receptor expressed in HEK293 cells assessed as increase in calcium by calcium imaging assay
ChEMBL 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 10.1038/nature05991
5202 139 66 None -138 27 Human 7.0 pEC50 = 7 Functional
Activity at SER4 receptor expressed in HEK293 cells assessed as increase in calcium by calcium imaging assayActivity at SER4 receptor expressed in HEK293 cells assessed as increase in calcium by calcium imaging assay
ChEMBL 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 10.1038/nature05991
CHEMBL39 139 66 None -138 27 Human 7.0 pEC50 = 7 Functional
Activity at SER4 receptor expressed in HEK293 cells assessed as increase in calcium by calcium imaging assayActivity at SER4 receptor expressed in HEK293 cells assessed as increase in calcium by calcium imaging assay
ChEMBL 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 10.1038/nature05991
DB08839 139 66 None -138 27 Human 7.0 pEC50 = 7 Functional
Activity at SER4 receptor expressed in HEK293 cells assessed as increase in calcium by calcium imaging assayActivity at SER4 receptor expressed in HEK293 cells assessed as increase in calcium by calcium imaging assay
ChEMBL 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 10.1038/nature05991
44249186 193646 0 None - 1 Human 7.0 pEC50 = 7 Functional
Agonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assayAgonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assay
ChEMBL 327 4 2 4 2.3 CC(C)n1c(=O)c(C(=O)NCC2CCNCC2)cc2ccccc21 10.1021/jm900881j
CHEMBL551535 193646 0 None - 1 Human 7.0 pEC50 = 7 Functional
Agonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assayAgonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assay
ChEMBL 327 4 2 4 2.3 CC(C)n1c(=O)c(C(=O)NCC2CCNCC2)cc2ccccc21 10.1021/jm900881j
15231247 91900477 193979 0 None - 1 Human 7.0 pEC50 = 7 Functional
Agonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assayAgonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assay
ChEMBL 309 3 3 4 1.9 COc1cc(N)c(Cl)cc1C(=O)N[C@@H]1C[C@@H]2CC[C@H](C1)N2 10.1021/jm900881j
CHEMBL556438 193979 0 None - 1 Human 7.0 pEC50 = 7 Functional
Agonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assayAgonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assay
ChEMBL 309 3 3 4 1.9 COc1cc(N)c(Cl)cc1C(=O)N[C@@H]1C[C@@H]2CC[C@H](C1)N2 10.1021/jm900881j
44249053 194826 0 None - 1 Human 7.0 pEC50 = 7 Functional
Agonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assayAgonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assay
ChEMBL 394 6 2 5 2.6 COc1cc(N)c(Cl)cc1C(=O)NC1CCN(CCN2CCCCC2)CC1 10.1021/jm900881j
CHEMBL563445 194826 0 None - 1 Human 7.0 pEC50 = 7 Functional
Agonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assayAgonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assay
ChEMBL 394 6 2 5 2.6 COc1cc(N)c(Cl)cc1C(=O)NC1CCN(CCN2CCCCC2)CC1 10.1021/jm900881j
10545215 188395 0 None - 1 Guinea pig 7.0 pEC50 = 7 Functional
concentration which gave a 50% increase in the response to electrical stimulation against 5-hydroxytryptamine 4 receptor in the guinea pig ileum.concentration which gave a 50% increase in the response to electrical stimulation against 5-hydroxytryptamine 4 receptor in the guinea pig ileum.
ChEMBL 341 5 2 5 3.4 COc1cc(N)c(Cl)cc1NC(=O)OCCN1CCCCCC1 10.1021/jm960853v
CHEMBL50852 188395 0 None - 1 Guinea pig 7.0 pEC50 = 7 Functional
concentration which gave a 50% increase in the response to electrical stimulation against 5-hydroxytryptamine 4 receptor in the guinea pig ileum.concentration which gave a 50% increase in the response to electrical stimulation against 5-hydroxytryptamine 4 receptor in the guinea pig ileum.
ChEMBL 341 5 2 5 3.4 COc1cc(N)c(Cl)cc1NC(=O)OCCN1CCCCCC1 10.1021/jm960853v
44247949 193444 0 None - 1 Human 6.0 pEC50 = 6 Functional
Agonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assayAgonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assay
ChEMBL 475 12 3 6 3.4 COc1cc(N)c(Cl)cc1C(=O)NC1CCN(CCCCCCCCS(=O)(=O)O)CC1 10.1021/jm900881j
CHEMBL549998 193444 0 None - 1 Human 6.0 pEC50 = 6 Functional
Agonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assayAgonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assay
ChEMBL 475 12 3 6 3.4 COc1cc(N)c(Cl)cc1C(=O)NC1CCN(CCCCCCCCS(=O)(=O)O)CC1 10.1021/jm900881j
127037817 136085 0 None - 1 Human 6.0 pEC50 = 6.0 Functional
Agonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assayAgonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assay
ChEMBL 382 5 1 5 2.5 CC(C)c1nc(C(=O)NC2C3CN(CC4CCOCC4)CC32)c2ccccn12 10.1016/j.ejmech.2015.08.051
CHEMBL3739689 136085 0 None - 1 Human 6.0 pEC50 = 6.0 Functional
Agonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assayAgonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assay
ChEMBL 382 5 1 5 2.5 CC(C)c1nc(C(=O)NC2C3CN(CC4CCOCC4)CC32)c2ccccn12 10.1016/j.ejmech.2015.08.051
127041480 136104 0 None - 1 Human 8.0 pEC50 = 8.0 Functional
Agonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assayAgonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assay
ChEMBL 384 5 1 5 3.1 CC(C)c1nc(C(=O)NCC2CCN(C3CCOCC3)CC2)c2ccccn12 10.1016/j.ejmech.2015.08.051
CHEMBL3739862 136104 0 None - 1 Human 8.0 pEC50 = 8.0 Functional
Agonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assayAgonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assay
ChEMBL 384 5 1 5 3.1 CC(C)c1nc(C(=O)NCC2CCN(C3CCOCC3)CC2)c2ccccn12 10.1016/j.ejmech.2015.08.051
44323264 205383 0 None - 1 Rat 8.0 pEC50 = 8.0 Functional
In vitro relaxation of carbachol pre-contracted rat oesophageal TMM.In vitro relaxation of carbachol pre-contracted rat oesophageal TMM.
ChEMBL 322 2 1 5 2.1 Nc1c(Cl)cc(C(=O)O[C@@H]2CN3CCC2CC3)c2c1CCO2 10.1016/0960-894X(96)00002-9
CHEMBL92100 205383 0 None - 1 Rat 8.0 pEC50 = 8.0 Functional
In vitro relaxation of carbachol pre-contracted rat oesophageal TMM.In vitro relaxation of carbachol pre-contracted rat oesophageal TMM.
ChEMBL 322 2 1 5 2.1 Nc1c(Cl)cc(C(=O)O[C@@H]2CN3CCC2CC3)c2c1CCO2 10.1016/0960-894X(96)00002-9
44281492 118367 2 None - 1 Guinea pig 7.0 pEC50 = 7.0 Functional
5-hydroxytryptamine 4 receptor agonist activity as increased response to electrical stimulation in guinea pig ileum5-hydroxytryptamine 4 receptor agonist activity as increased response to electrical stimulation in guinea pig ileum
ChEMBL 298 3 1 5 2.2 COc1cc(N)c(Cl)cc1C(=O)OC1CCN(C)CC1 10.1016/S0960-894X(01)80508-4
CHEMBL34224 118367 2 None - 1 Guinea pig 7.0 pEC50 = 7.0 Functional
5-hydroxytryptamine 4 receptor agonist activity as increased response to electrical stimulation in guinea pig ileum5-hydroxytryptamine 4 receptor agonist activity as increased response to electrical stimulation in guinea pig ileum
ChEMBL 298 3 1 5 2.2 COc1cc(N)c(Cl)cc1C(=O)OC1CCN(C)CC1 10.1016/S0960-894X(01)80508-4
10757374 162542 0 None - 1 Guinea pig 7.0 pEC50 = 7.0 Functional
5-hydroxytryptamine 4 receptor agonist activity as increased response to electrical stimulation in guinea pig ileum5-hydroxytryptamine 4 receptor agonist activity as increased response to electrical stimulation in guinea pig ileum
ChEMBL 310 3 1 5 2.2 COc1cc(N)c(Cl)cc1C(=O)O[C@H]1CN2CCC1CC2 10.1016/S0960-894X(01)80508-4
CHEMBL41769 162542 0 None - 1 Guinea pig 7.0 pEC50 = 7.0 Functional
5-hydroxytryptamine 4 receptor agonist activity as increased response to electrical stimulation in guinea pig ileum5-hydroxytryptamine 4 receptor agonist activity as increased response to electrical stimulation in guinea pig ileum
ChEMBL 310 3 1 5 2.2 COc1cc(N)c(Cl)cc1C(=O)O[C@H]1CN2CCC1CC2 10.1016/S0960-894X(01)80508-4
10757374 162542 0 None - 1 Guinea pig 7.0 pEC50 = 7.0 Functional
5-hydroxytryptamine 4 receptor agonist activity, concentration which gave 50% increase in the response to electrically-stimulated myenteric plexus and longitudinal muscle of the guinea pig ileum5-hydroxytryptamine 4 receptor agonist activity, concentration which gave 50% increase in the response to electrically-stimulated myenteric plexus and longitudinal muscle of the guinea pig ileum
ChEMBL 310 3 1 5 2.2 COc1cc(N)c(Cl)cc1C(=O)O[C@H]1CN2CCC1CC2 10.1021/jm960320m
CHEMBL41769 162542 0 None - 1 Guinea pig 7.0 pEC50 = 7.0 Functional
5-hydroxytryptamine 4 receptor agonist activity, concentration which gave 50% increase in the response to electrically-stimulated myenteric plexus and longitudinal muscle of the guinea pig ileum5-hydroxytryptamine 4 receptor agonist activity, concentration which gave 50% increase in the response to electrically-stimulated myenteric plexus and longitudinal muscle of the guinea pig ileum
ChEMBL 310 3 1 5 2.2 COc1cc(N)c(Cl)cc1C(=O)O[C@H]1CN2CCC1CC2 10.1021/jm960320m
10018558 50479 0 None - 1 Guinea pig 7.0 pEC50 = 7.0 Functional
5-hydroxytryptamine 4 receptor agonist activity, concentration which gave 50% increase in the response to electrically-stimulated myenteric plexus and longitudinal muscle of the guinea pig ileum5-hydroxytryptamine 4 receptor agonist activity, concentration which gave 50% increase in the response to electrically-stimulated myenteric plexus and longitudinal muscle of the guinea pig ileum
ChEMBL 314 5 1 6 1.4 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCOCC1 10.1021/jm960320m
CHEMBL157631 50479 0 None - 1 Guinea pig 7.0 pEC50 = 7.0 Functional
5-hydroxytryptamine 4 receptor agonist activity, concentration which gave 50% increase in the response to electrically-stimulated myenteric plexus and longitudinal muscle of the guinea pig ileum5-hydroxytryptamine 4 receptor agonist activity, concentration which gave 50% increase in the response to electrically-stimulated myenteric plexus and longitudinal muscle of the guinea pig ileum
ChEMBL 314 5 1 6 1.4 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCOCC1 10.1021/jm960320m
5 139 66 None -138 27 Human 7.9 pEC50 = 7.9 Functional
Agonist activity at human 5HT4 isoform E receptor expressed in rat C6 cells assessed as cAMP accumulation by radio-immunoassay relative to 5HTAgonist activity at human 5HT4 isoform E receptor expressed in rat C6 cells assessed as cAMP accumulation by radio-immunoassay relative to 5HT
ChEMBL 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 10.1021/jm801327q
5202 139 66 None -138 27 Human 7.9 pEC50 = 7.9 Functional
Agonist activity at human 5HT4 isoform E receptor expressed in rat C6 cells assessed as cAMP accumulation by radio-immunoassay relative to 5HTAgonist activity at human 5HT4 isoform E receptor expressed in rat C6 cells assessed as cAMP accumulation by radio-immunoassay relative to 5HT
ChEMBL 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 10.1021/jm801327q
CHEMBL39 139 66 None -138 27 Human 7.9 pEC50 = 7.9 Functional
Agonist activity at human 5HT4 isoform E receptor expressed in rat C6 cells assessed as cAMP accumulation by radio-immunoassay relative to 5HTAgonist activity at human 5HT4 isoform E receptor expressed in rat C6 cells assessed as cAMP accumulation by radio-immunoassay relative to 5HT
ChEMBL 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 10.1021/jm801327q
DB08839 139 66 None -138 27 Human 7.9 pEC50 = 7.9 Functional
Agonist activity at human 5HT4 isoform E receptor expressed in rat C6 cells assessed as cAMP accumulation by radio-immunoassay relative to 5HTAgonist activity at human 5HT4 isoform E receptor expressed in rat C6 cells assessed as cAMP accumulation by radio-immunoassay relative to 5HT
ChEMBL 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 10.1021/jm801327q
3037881 99284 1 None - 1 Rat 7.9 pEC50 = 7.9 Functional
5-hydroxytryptamine 4 receptor agonist activity in the rat esophageal muscularis mucosae5-hydroxytryptamine 4 receptor agonist activity in the rat esophageal muscularis mucosae
ChEMBL 355 1 1 4 2.8 Nc1c(Cl)cc2c3c(cccc13)C(=O)N([C@@H]1CN3CCC1CC3)C2=O 10.1016/S0960-894X(00)80352-2
CHEMBL28499 99284 1 None - 1 Rat 7.9 pEC50 = 7.9 Functional
5-hydroxytryptamine 4 receptor agonist activity in the rat esophageal muscularis mucosae5-hydroxytryptamine 4 receptor agonist activity in the rat esophageal muscularis mucosae
ChEMBL 355 1 1 4 2.8 Nc1c(Cl)cc2c3c(cccc13)C(=O)N([C@@H]1CN3CCC1CC3)C2=O 10.1016/S0960-894X(00)80352-2
19081885 203633 0 None - 1 Human 7.9 pEC50 = 7.9 Functional
Agonist activity against 5-HT4 receptor in rat esophageal muscularis mucosaeAgonist activity against 5-HT4 receptor in rat esophageal muscularis mucosae
ChEMBL 338 7 1 4 4.0 CCCN1CCC(CCC(=O)c2cc(Cl)c(N)cc2OC)CC1 10.1016/S0960-894X(01)80413-3
CHEMBL79637 203633 0 None - 1 Human 7.9 pEC50 = 7.9 Functional
Agonist activity against 5-HT4 receptor in rat esophageal muscularis mucosaeAgonist activity against 5-HT4 receptor in rat esophageal muscularis mucosae
ChEMBL 338 7 1 4 4.0 CCCN1CCC(CCC(=O)c2cc(Cl)c(N)cc2OC)CC1 10.1016/S0960-894X(01)80413-3
257 3437 9 None - 1 Human 7.9 pEC50 = 7.9 Functional
Agonist activity at 5HT4 receptor expressed in HEK293/L9 cells by cAMP assayAgonist activity at 5HT4 receptor expressed in HEK293/L9 cells by cAMP assay
ChEMBL 474 6 1 6 3.3 CCCCN1CCC(CC1)COC(=O)c1cc(I)c(c2c1OCCO2)N 10.1021/jm100668r
5311423 3437 9 None - 1 Human 7.9 pEC50 = 7.9 Functional
Agonist activity at 5HT4 receptor expressed in HEK293/L9 cells by cAMP assayAgonist activity at 5HT4 receptor expressed in HEK293/L9 cells by cAMP assay
ChEMBL 474 6 1 6 3.3 CCCCN1CCC(CC1)COC(=O)c1cc(I)c(c2c1OCCO2)N 10.1021/jm100668r
CHEMBL114112 3437 9 None - 1 Human 7.9 pEC50 = 7.9 Functional
Agonist activity at 5HT4 receptor expressed in HEK293/L9 cells by cAMP assayAgonist activity at 5HT4 receptor expressed in HEK293/L9 cells by cAMP assay
ChEMBL 474 6 1 6 3.3 CCCCN1CCC(CC1)COC(=O)c1cc(I)c(c2c1OCCO2)N 10.1021/jm100668r
11842633 3918 17 None -7 2 Guinea pig 7.9 pEC50 = 7.9 Functional
Agonist activity at 5HT4 receptor in guinea pig colonic longitudinal muscle/myenteric plexus assessed as contractionAgonist activity at 5HT4 receptor in guinea pig colonic longitudinal muscle/myenteric plexus assessed as contraction
ChEMBL 504 8 2 7 1.6 O[C@@H](CN(S(=O)(=O)C)C)CN1[C@@H]2CC[C@H]1CC(C2)NC(=O)c1cc2ccccc2n(c1=O)C(C)C 10.1016/j.bmcl.2012.08.051
8425 3918 17 None -7 2 Guinea pig 7.9 pEC50 = 7.9 Functional
Agonist activity at 5HT4 receptor in guinea pig colonic longitudinal muscle/myenteric plexus assessed as contractionAgonist activity at 5HT4 receptor in guinea pig colonic longitudinal muscle/myenteric plexus assessed as contraction
ChEMBL 504 8 2 7 1.6 O[C@@H](CN(S(=O)(=O)C)C)CN1[C@@H]2CC[C@H]1CC(C2)NC(=O)c1cc2ccccc2n(c1=O)C(C)C 10.1016/j.bmcl.2012.08.051
CHEMBL2087337 3918 17 None -7 2 Guinea pig 7.9 pEC50 = 7.9 Functional
Agonist activity at 5HT4 receptor in guinea pig colonic longitudinal muscle/myenteric plexus assessed as contractionAgonist activity at 5HT4 receptor in guinea pig colonic longitudinal muscle/myenteric plexus assessed as contraction
ChEMBL 504 8 2 7 1.6 O[C@@H](CN(S(=O)(=O)C)C)CN1[C@@H]2CC[C@H]1CC(C2)NC(=O)c1cc2ccccc2n(c1=O)C(C)C 10.1016/j.bmcl.2012.08.051
70684288 76067 0 None - 1 Human 7.9 pEC50 = 7.9 Functional
Agonist activity at human 5HT4C receptor expressed at 100 fold physiological-level in HEK293 cells assessed as cAMP accumulationAgonist activity at human 5HT4C receptor expressed at 100 fold physiological-level in HEK293 cells assessed as cAMP accumulation
ChEMBL 558 11 1 7 3.5 CC(C)n1nc(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CCCCCCN2CCN(S(C)(=O)=O)CC2)c2ccccc21 10.1016/j.bmcl.2012.05.034
CHEMBL2059586 76067 0 None - 1 Human 7.9 pEC50 = 7.9 Functional
Agonist activity at human 5HT4C receptor expressed at 100 fold physiological-level in HEK293 cells assessed as cAMP accumulationAgonist activity at human 5HT4C receptor expressed at 100 fold physiological-level in HEK293 cells assessed as cAMP accumulation
ChEMBL 558 11 1 7 3.5 CC(C)n1nc(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CCCCCCN2CCN(S(C)(=O)=O)CC2)c2ccccc21 10.1016/j.bmcl.2012.05.034
44248793 91900478 193950 0 None - 1 Human 7.9 pEC50 = 7.9 Functional
Agonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assayAgonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assay
ChEMBL 339 3 2 4 2.6 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3)cc2ccccc21 10.1021/jm900881j
CHEMBL556235 193950 0 None - 1 Human 7.9 pEC50 = 7.9 Functional
Agonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assayAgonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assay
ChEMBL 339 3 2 4 2.6 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3)cc2ccccc21 10.1021/jm900881j
44248068 194212 0 None - 1 Human 7.9 pEC50 = 7.9 Functional
Agonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assayAgonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assay
ChEMBL 515 10 2 7 1.9 COc1cc(N)c(Cl)cc1C(=O)NC1CCN(CCCCCN2CCN(S(C)(=O)=O)CC2)CC1 10.1021/jm900881j
CHEMBL558924 194212 0 None - 1 Human 7.9 pEC50 = 7.9 Functional
Agonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assayAgonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assay
ChEMBL 515 10 2 7 1.9 COc1cc(N)c(Cl)cc1C(=O)NC1CCN(CCCCCN2CCN(S(C)(=O)=O)CC2)CC1 10.1021/jm900881j
44247817 91900489 194301 0 None - 1 Human 7.9 pEC50 = 7.9 Functional
Agonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assayAgonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assay
ChEMBL 489 9 2 6 3.4 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CCCCCS(=O)(=O)O)cc2ccccc21 10.1021/jm900881j
CHEMBL559746 194301 0 None - 1 Human 7.9 pEC50 = 7.9 Functional
Agonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assayAgonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assay
ChEMBL 489 9 2 6 3.4 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CCCCCS(=O)(=O)O)cc2ccccc21 10.1021/jm900881j
67276147 77146 0 None - 1 Human 7.9 pEC50 = 7.9 Functional
Agonist activity at human recombinant 5HT4c receptor expressed in HEK293 cells at 10-fold physiological level assessed as accumulation of cAMPAgonist activity at human recombinant 5HT4c receptor expressed in HEK293 cells at 10-fold physiological level assessed as accumulation of cAMP
ChEMBL 468 7 2 6 2.1 CC(=O)N(C)CC(O)CN1[C@H]2CC[C@@H]1C[C@H](NC(=O)c1cc3ccccc3n(C(C)C)c1=O)C2 10.1016/j.bmcl.2012.08.051
CHEMBL2087325 77146 0 None - 1 Human 7.9 pEC50 = 7.9 Functional
Agonist activity at human recombinant 5HT4c receptor expressed in HEK293 cells at 10-fold physiological level assessed as accumulation of cAMPAgonist activity at human recombinant 5HT4c receptor expressed in HEK293 cells at 10-fold physiological level assessed as accumulation of cAMP
ChEMBL 468 7 2 6 2.1 CC(=O)N(C)CC(O)CN1[C@H]2CC[C@@H]1C[C@H](NC(=O)c1cc3ccccc3n(C(C)C)c1=O)C2 10.1016/j.bmcl.2012.08.051
70695322 77149 0 None - 1 Human 7.9 pEC50 = 7.9 Functional
Agonist activity at human recombinant 5HT4c receptor expressed in HEK293 cells at 10-fold physiological level assessed as accumulation of cAMPAgonist activity at human recombinant 5HT4c receptor expressed in HEK293 cells at 10-fold physiological level assessed as accumulation of cAMP
ChEMBL 469 7 4 6 1.6 CNC(=O)NCC(O)CN1[C@H]2CC[C@@H]1C[C@H](NC(=O)c1cc3ccccc3n(C(C)C)c1=O)C2 10.1016/j.bmcl.2012.08.051
CHEMBL2087328 77149 0 None - 1 Human 7.9 pEC50 = 7.9 Functional
Agonist activity at human recombinant 5HT4c receptor expressed in HEK293 cells at 10-fold physiological level assessed as accumulation of cAMPAgonist activity at human recombinant 5HT4c receptor expressed in HEK293 cells at 10-fold physiological level assessed as accumulation of cAMP
ChEMBL 469 7 4 6 1.6 CNC(=O)NCC(O)CN1[C@H]2CC[C@@H]1C[C@H](NC(=O)c1cc3ccccc3n(C(C)C)c1=O)C2 10.1016/j.bmcl.2012.08.051
131725 198753 2 None 3 2 Rat 7.9 pEC50 = 7.9 Functional
Tested for its agonist potency against the 5-hydroxytryptamine 4 receptor located in the rat esophageal tunica muscularis mucosaeTested for its agonist potency against the 5-hydroxytryptamine 4 receptor located in the rat esophageal tunica muscularis mucosae
ChEMBL 342 2 1 5 2.6 CC(C)n1c(=O)n(C(=O)NC2CC3CCC(C2)N3C)c2ccccc21 10.1016/S0960-894X(01)81243-9
CHEMBL59834 198753 2 None 3 2 Rat 7.9 pEC50 = 7.9 Functional
Tested for its agonist potency against the 5-hydroxytryptamine 4 receptor located in the rat esophageal tunica muscularis mucosaeTested for its agonist potency against the 5-hydroxytryptamine 4 receptor located in the rat esophageal tunica muscularis mucosae
ChEMBL 342 2 1 5 2.6 CC(C)n1c(=O)n(C(=O)NC2CC3CCC(C2)N3C)c2ccccc21 10.1016/S0960-894X(01)81243-9
44626295 196097 0 None - 1 Human 6.9 pEC50 = 6.9 Functional
Agonist activity at human recombinant 5-HT4 receptorAgonist activity at human recombinant 5-HT4 receptor
ChEMBL 531 8 3 7 3.8 COc1cccc([C@]2(O)CCCC[C@H]2CN2CC[C@@H](NC(=O)c3cc(Cl)c(N)cc3OC)[C@@H](OC)C2)c1 10.1016/j.bmcl.2009.08.016
CHEMBL571799 196097 0 None - 1 Human 6.9 pEC50 = 6.9 Functional
Agonist activity at human recombinant 5-HT4 receptorAgonist activity at human recombinant 5-HT4 receptor
ChEMBL 531 8 3 7 3.8 COc1cccc([C@]2(O)CCCC[C@H]2CN2CC[C@@H](NC(=O)c3cc(Cl)c(N)cc3OC)[C@@H](OC)C2)c1 10.1016/j.bmcl.2009.08.016
44461665 104069 0 None - 1 Human 6.9 pEC50 = 6.9 Functional
Agonist activity against 5-HT4 receptor in rat esophageal muscularis mucosaeAgonist activity against 5-HT4 receptor in rat esophageal muscularis mucosae
ChEMBL 325 6 2 4 2.5 COc1cc(N)c(Cl)cc1C(=O)NCCCN1CCCCC1 10.1016/S0960-894X(01)80413-3
CHEMBL310451 104069 0 None - 1 Human 6.9 pEC50 = 6.9 Functional
Agonist activity against 5-HT4 receptor in rat esophageal muscularis mucosaeAgonist activity against 5-HT4 receptor in rat esophageal muscularis mucosae
ChEMBL 325 6 2 4 2.5 COc1cc(N)c(Cl)cc1C(=O)NCCCN1CCCCC1 10.1016/S0960-894X(01)80413-3
9882676 204046 0 None - 1 Human 6.9 pEC50 = 6.9 Functional
Agonist activity against 5-HT4 receptor in rat esophageal muscularis mucosaeAgonist activity against 5-HT4 receptor in rat esophageal muscularis mucosae
ChEMBL 296 5 2 4 2.9 COc1cc(N)c(Cl)cc1C(=O)CCC1CCNCC1 10.1016/S0960-894X(01)80413-3
CHEMBL82833 204046 0 None - 1 Human 6.9 pEC50 = 6.9 Functional
Agonist activity against 5-HT4 receptor in rat esophageal muscularis mucosaeAgonist activity against 5-HT4 receptor in rat esophageal muscularis mucosae
ChEMBL 296 5 2 4 2.9 COc1cc(N)c(Cl)cc1C(=O)CCC1CCNCC1 10.1016/S0960-894X(01)80413-3
11496400 11703 0 None - 1 Rat 6.9 pEC50 = 6.9 Functional
Agonism at 5HT4 receptor in rat tunica muscularis mucosaAgonism at 5HT4 receptor in rat tunica muscularis mucosa
ChEMBL 338 4 2 3 2.3 COc1cc(N)c(Cl)cc1C(=O)NC[C@@H]1CC[N@@+]2(C)CCC[C@@H]12 10.1021/jm0509501
CHEMBL1181946 11703 0 None - 1 Rat 6.9 pEC50 = 6.9 Functional
Agonism at 5HT4 receptor in rat tunica muscularis mucosaAgonism at 5HT4 receptor in rat tunica muscularis mucosa
ChEMBL 338 4 2 3 2.3 COc1cc(N)c(Cl)cc1C(=O)NC[C@@H]1CC[N@@+]2(C)CCC[C@@H]12 10.1021/jm0509501
CHEMBL199866 11703 0 None - 1 Rat 6.9 pEC50 = 6.9 Functional
Agonism at 5HT4 receptor in rat tunica muscularis mucosaAgonism at 5HT4 receptor in rat tunica muscularis mucosa
ChEMBL 338 4 2 3 2.3 COc1cc(N)c(Cl)cc1C(=O)NC[C@@H]1CC[N@@+]2(C)CCC[C@@H]12 10.1021/jm0509501
10690483 49035 0 None - 1 Guinea pig 7.9 pEC50 = 7.9 Functional
5-hydroxytryptamine 4 receptor agonist activity, concentration which gave 50% increase in the response to electrically-stimulated myenteric plexus and longitudinal muscle of the guinea pig ileum5-hydroxytryptamine 4 receptor agonist activity, concentration which gave 50% increase in the response to electrically-stimulated myenteric plexus and longitudinal muscle of the guinea pig ileum
ChEMBL 369 6 2 6 1.7 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCC(NC(C)=O)CC1 10.1021/jm960320m
CHEMBL156348 49035 0 None - 1 Guinea pig 7.9 pEC50 = 7.9 Functional
5-hydroxytryptamine 4 receptor agonist activity, concentration which gave 50% increase in the response to electrically-stimulated myenteric plexus and longitudinal muscle of the guinea pig ileum5-hydroxytryptamine 4 receptor agonist activity, concentration which gave 50% increase in the response to electrically-stimulated myenteric plexus and longitudinal muscle of the guinea pig ileum
ChEMBL 369 6 2 6 1.7 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCC(NC(C)=O)CC1 10.1021/jm960320m
127039820 136255 0 None - 1 Human 7.9 pEC50 = 7.9 Functional
Agonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assayAgonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assay
ChEMBL 366 6 1 4 3.2 CC(C)c1nc(C(=O)NC[C@H]2[C@@H]3CN(CC4CCC4)C[C@H]23)c2ccccn12 10.1016/j.ejmech.2015.08.051
CHEMBL3741224 136255 0 None - 1 Human 7.9 pEC50 = 7.9 Functional
Agonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assayAgonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assay
ChEMBL 366 6 1 4 3.2 CC(C)c1nc(C(=O)NC[C@H]2[C@@H]3CN(CC4CCC4)C[C@H]23)c2ccccn12 10.1016/j.ejmech.2015.08.051
127039507 136347 0 None - 1 Human 6.9 pEC50 = 6.9 Functional
Agonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assayAgonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assay
ChEMBL 360 5 1 4 3.4 CC(C)c1nc(C(=O)NC2CCN(CC(C)(C)F)CC2)c2ccccn12 10.1016/j.ejmech.2015.08.051
CHEMBL3742086 136347 0 None - 1 Human 6.9 pEC50 = 6.9 Functional
Agonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assayAgonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assay
ChEMBL 360 5 1 4 3.4 CC(C)c1nc(C(=O)NC2CCN(CC(C)(C)F)CC2)c2ccccn12 10.1016/j.ejmech.2015.08.051
127041780 136154 0 None - 1 Human 5.9 pEC50 = 5.9 Functional
Agonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assayAgonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assay
ChEMBL 416 6 1 5 3.4 CC(C)c1nc(C(=O)NCC2(F)CCN(CC3CCOCC3)CC2)c2ccccn12 10.1016/j.ejmech.2015.08.051
CHEMBL3740278 136154 0 None - 1 Human 5.9 pEC50 = 5.9 Functional
Agonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assayAgonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assay
ChEMBL 416 6 1 5 3.4 CC(C)c1nc(C(=O)NCC2(F)CCN(CC3CCOCC3)CC2)c2ccccn12 10.1016/j.ejmech.2015.08.051
44323269 11967 0 None - 1 Rat 5.9 pEC50 = 5.9 Functional
In vitro relaxation of carbachol pre-contracted rat oesophageal TMM.In vitro relaxation of carbachol pre-contracted rat oesophageal TMM.
ChEMBL 378 5 2 3 3.0 CCCC[N+]12CCC(CC1)[C@@H](NC(=O)c1cc(Cl)c(N)c3c1OCC3)C2 10.1016/0960-894X(96)00002-9
CHEMBL1183709 11967 0 None - 1 Rat 5.9 pEC50 = 5.9 Functional
In vitro relaxation of carbachol pre-contracted rat oesophageal TMM.In vitro relaxation of carbachol pre-contracted rat oesophageal TMM.
ChEMBL 378 5 2 3 3.0 CCCC[N+]12CCC(CC1)[C@@H](NC(=O)c1cc(Cl)c(N)c3c1OCC3)C2 10.1016/0960-894X(96)00002-9
CHEMBL314198 11967 0 None - 1 Rat 5.9 pEC50 = 5.9 Functional
In vitro relaxation of carbachol pre-contracted rat oesophageal TMM.In vitro relaxation of carbachol pre-contracted rat oesophageal TMM.
ChEMBL 378 5 2 3 3.0 CCCC[N+]12CCC(CC1)[C@@H](NC(=O)c1cc(Cl)c(N)c3c1OCC3)C2 10.1016/0960-894X(96)00002-9
9905514 119177 0 None - 1 Guinea pig 7.9 pEC50 = 7.9 Functional
5-hydroxytryptamine 4 receptor agonist activity, concentration which gave 50% increase in the response to electrically-stimulated myenteric plexus and longitudinal muscle of the guinea pig ileum5-hydroxytryptamine 4 receptor agonist activity, concentration which gave 50% increase in the response to electrically-stimulated myenteric plexus and longitudinal muscle of the guinea pig ileum
ChEMBL 328 5 2 6 1.5 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCC(O)CC1 10.1021/jm960320m
CHEMBL347235 119177 0 None - 1 Guinea pig 7.9 pEC50 = 7.9 Functional
5-hydroxytryptamine 4 receptor agonist activity, concentration which gave 50% increase in the response to electrically-stimulated myenteric plexus and longitudinal muscle of the guinea pig ileum5-hydroxytryptamine 4 receptor agonist activity, concentration which gave 50% increase in the response to electrically-stimulated myenteric plexus and longitudinal muscle of the guinea pig ileum
ChEMBL 328 5 2 6 1.5 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCC(O)CC1 10.1021/jm960320m
49783209 17427 0 None - 1 Human 7.9 pEC50 = 7.9 Functional
Agonist activity at 5HT4 receptor expressed in HEK293/L9 cells by cAMP assayAgonist activity at 5HT4 receptor expressed in HEK293/L9 cells by cAMP assay
ChEMBL 396 7 1 6 3.8 CCCCN1CCC(COC(=O)c2cc(Cl)c(NC)c3c2OCCO3)CC1 10.1021/jm100668r
CHEMBL1258223 17427 0 None - 1 Human 7.9 pEC50 = 7.9 Functional
Agonist activity at 5HT4 receptor expressed in HEK293/L9 cells by cAMP assayAgonist activity at 5HT4 receptor expressed in HEK293/L9 cells by cAMP assay
ChEMBL 396 7 1 6 3.8 CCCCN1CCC(COC(=O)c2cc(Cl)c(NC)c3c2OCCO3)CC1 10.1021/jm100668r
127042086 136195 0 None - 1 Human 6.8 pEC50 = 6.8 Functional
Agonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assayAgonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assay
ChEMBL 400 5 2 6 2.2 CC(C)c1nc(C(=O)NC2CCN(CC3(O)CCOCC3)CC2)c2ccccn12 10.1016/j.ejmech.2015.08.051
CHEMBL3740708 136195 0 None - 1 Human 6.8 pEC50 = 6.8 Functional
Agonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assayAgonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assay
ChEMBL 400 5 2 6 2.2 CC(C)c1nc(C(=O)NC2CCN(CC3(O)CCOCC3)CC2)c2ccccn12 10.1016/j.ejmech.2015.08.051
127042083 136360 0 None - 1 Human 6.8 pEC50 = 6.8 Functional
Agonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assayAgonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assay
ChEMBL 344 6 1 5 2.3 COCCN1CCC(NC(=O)c2nc(C(C)C)n3ccccc23)CC1 10.1016/j.ejmech.2015.08.051
CHEMBL3742190 136360 0 None - 1 Human 6.8 pEC50 = 6.8 Functional
Agonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assayAgonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assay
ChEMBL 344 6 1 5 2.3 COCCN1CCC(NC(=O)c2nc(C(C)C)n3ccccc23)CC1 10.1016/j.ejmech.2015.08.051
10381762 49038 0 None - 1 Guinea pig 7.8 pEC50 = 7.8 Functional
5-hydroxytryptamine 4 receptor agonist activity, concentration which gave 50% increase in the response to electrically-stimulated myenteric plexus and longitudinal muscle of the guinea pig ileum5-hydroxytryptamine 4 receptor agonist activity, concentration which gave 50% increase in the response to electrically-stimulated myenteric plexus and longitudinal muscle of the guinea pig ileum
ChEMBL 326 5 1 5 2.8 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCCC(C)C1 10.1021/jm960320m
CHEMBL156349 49038 0 None - 1 Guinea pig 7.8 pEC50 = 7.8 Functional
5-hydroxytryptamine 4 receptor agonist activity, concentration which gave 50% increase in the response to electrically-stimulated myenteric plexus and longitudinal muscle of the guinea pig ileum5-hydroxytryptamine 4 receptor agonist activity, concentration which gave 50% increase in the response to electrically-stimulated myenteric plexus and longitudinal muscle of the guinea pig ileum
ChEMBL 326 5 1 5 2.8 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCCC(C)C1 10.1021/jm960320m
127041784 136322 0 None - 1 Human 7.8 pEC50 = 7.8 Functional
Agonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assayAgonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assay
ChEMBL 354 5 1 4 3.5 CC(C)c1nc(C(=O)NC2CCN(CC3CCC3)CC2)c2ccccn12 10.1016/j.ejmech.2015.08.051
CHEMBL3741826 136322 0 None - 1 Human 7.8 pEC50 = 7.8 Functional
Agonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assayAgonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assay
ChEMBL 354 5 1 4 3.5 CC(C)c1nc(C(=O)NC2CCN(CC3CCC3)CC2)c2ccccn12 10.1016/j.ejmech.2015.08.051
19081860 203986 0 None - 1 Human 7.8 pEC50 = 7.8 Functional
Agonist activity against 5-HT4 receptor in rat esophageal muscularis mucosaeAgonist activity against 5-HT4 receptor in rat esophageal muscularis mucosae
ChEMBL 324 6 1 4 3.6 CCN1CCC(CCC(=O)c2cc(Cl)c(N)cc2OC)CC1 10.1016/S0960-894X(01)80413-3
CHEMBL82360 203986 0 None - 1 Human 7.8 pEC50 = 7.8 Functional
Agonist activity against 5-HT4 receptor in rat esophageal muscularis mucosaeAgonist activity against 5-HT4 receptor in rat esophageal muscularis mucosae
ChEMBL 324 6 1 4 3.6 CCN1CCC(CCC(=O)c2cc(Cl)c(N)cc2OC)CC1 10.1016/S0960-894X(01)80413-3
49783212 17494 0 None - 1 Human 7.8 pEC50 = 7.8 Functional
Agonist activity at 5HT4 receptor expressed in HEK293/L9 cells by cAMP assayAgonist activity at 5HT4 receptor expressed in HEK293/L9 cells by cAMP assay
ChEMBL 387 7 1 7 3.0 CCCCN1CCC(COC(=O)c2cc(C#N)c(NC)c3c2OCCO3)CC1 10.1021/jm100668r
CHEMBL1258450 17494 0 None - 1 Human 7.8 pEC50 = 7.8 Functional
Agonist activity at 5HT4 receptor expressed in HEK293/L9 cells by cAMP assayAgonist activity at 5HT4 receptor expressed in HEK293/L9 cells by cAMP assay
ChEMBL 387 7 1 7 3.0 CCCCN1CCC(COC(=O)c2cc(C#N)c(NC)c3c2OCCO3)CC1 10.1021/jm100668r
44249316 91900479 193682 0 None - 1 Human 7.8 pEC50 = 7.8 Functional
Agonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assayAgonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assay
ChEMBL 328 2 2 5 2.2 CC(C)n1c(=O)n(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3)c2ccccc21 10.1021/jm900881j
CHEMBL551820 193682 0 None - 1 Human 7.8 pEC50 = 7.8 Functional
Agonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assayAgonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assay
ChEMBL 328 2 2 5 2.2 CC(C)n1c(=O)n(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3)c2ccccc21 10.1021/jm900881j
44247811 193800 0 None - 1 Human 7.8 pEC50 = 7.8 Functional
Agonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assayAgonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assay
ChEMBL 369 8 3 5 2.3 COc1cc(N)c(Cl)cc1C(=O)NC1CCN(CCCCCO)CC1 10.1021/jm900881j
CHEMBL552693 193800 0 None - 1 Human 7.8 pEC50 = 7.8 Functional
Agonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assayAgonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assay
ChEMBL 369 8 3 5 2.3 COc1cc(N)c(Cl)cc1C(=O)NC1CCN(CCCCCO)CC1 10.1021/jm900881j
44247813 193919 0 None - 1 Human 7.8 pEC50 = 7.8 Functional
Agonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assayAgonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assay
ChEMBL 411 11 3 5 3.5 COc1cc(N)c(Cl)cc1C(=O)NC1CCN(CCCCCCCCO)CC1 10.1021/jm900881j
CHEMBL555447 193919 0 None - 1 Human 7.8 pEC50 = 7.8 Functional
Agonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assayAgonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assay
ChEMBL 411 11 3 5 3.5 COc1cc(N)c(Cl)cc1C(=O)NC1CCN(CCCCCCCCO)CC1 10.1021/jm900881j
44248072 194002 0 None - 1 Human 7.8 pEC50 = 7.8 Functional
Agonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assayAgonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assay
ChEMBL 483 9 3 5 3.8 COc1cc(N)c(Cl)cc1C(=O)NC1CCN(CCN(C)CCc2c[nH]c3ccccc23)CC1 10.1021/jm900881j
CHEMBL556595 194002 0 None - 1 Human 7.8 pEC50 = 7.8 Functional
Agonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assayAgonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assay
ChEMBL 483 9 3 5 3.8 COc1cc(N)c(Cl)cc1C(=O)NC1CCN(CCN(C)CCc2c[nH]c3ccccc23)CC1 10.1021/jm900881j
44249057 91900485 194425 0 None - 1 Human 7.8 pEC50 = 7.8 Functional
Agonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assayAgonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assay
ChEMBL 467 11 2 5 4.6 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CCCCCCCCO)cc2ccccc21 10.1021/jm900881j
CHEMBL560876 194425 0 None - 1 Human 7.8 pEC50 = 7.8 Functional
Agonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assayAgonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assay
ChEMBL 467 11 2 5 4.6 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CCCCCCCCO)cc2ccccc21 10.1021/jm900881j
44249188 194438 1 None - 1 Human 7.8 pEC50 = 7.8 Functional
Agonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assayAgonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assay
ChEMBL 316 3 2 5 1.9 CC(C)n1c(=O)n(C(=O)NCC2CCNCC2)c2ccccc21 10.1021/jm900881j
CHEMBL560940 194438 1 None - 1 Human 7.8 pEC50 = 7.8 Functional
Agonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assayAgonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assay
ChEMBL 316 3 2 5 1.9 CC(C)n1c(=O)n(C(=O)NCC2CCNCC2)c2ccccc21 10.1021/jm900881j
10828800 99726 0 None - 1 Guinea pig 6.8 pEC50 = 6.8 Functional
5-hydroxytryptamine 4 receptor agonist activity as increased response to electrical stimulation in guinea pig ileum5-hydroxytryptamine 4 receptor agonist activity as increased response to electrical stimulation in guinea pig ileum
ChEMBL 310 3 1 5 2.2 COc1cc(N)c(Cl)cc1C(=O)O[C@@H]1CN2CCC1CC2 10.1016/S0960-894X(01)80508-4
CHEMBL288199 99726 0 None - 1 Guinea pig 6.8 pEC50 = 6.8 Functional
5-hydroxytryptamine 4 receptor agonist activity as increased response to electrical stimulation in guinea pig ileum5-hydroxytryptamine 4 receptor agonist activity as increased response to electrical stimulation in guinea pig ileum
ChEMBL 310 3 1 5 2.2 COc1cc(N)c(Cl)cc1C(=O)O[C@@H]1CN2CCC1CC2 10.1016/S0960-894X(01)80508-4
10828800 99726 0 None - 1 Guinea pig 6.8 pEC50 = 6.8 Functional
5-hydroxytryptamine 4 receptor agonist activity, concentration which gave 50% increase in the response to electrically-stimulated myenteric plexus and longitudinal muscle of the guinea pig ileum5-hydroxytryptamine 4 receptor agonist activity, concentration which gave 50% increase in the response to electrically-stimulated myenteric plexus and longitudinal muscle of the guinea pig ileum
ChEMBL 310 3 1 5 2.2 COc1cc(N)c(Cl)cc1C(=O)O[C@@H]1CN2CCC1CC2 10.1021/jm960320m
CHEMBL288199 99726 0 None - 1 Guinea pig 6.8 pEC50 = 6.8 Functional
5-hydroxytryptamine 4 receptor agonist activity, concentration which gave 50% increase in the response to electrically-stimulated myenteric plexus and longitudinal muscle of the guinea pig ileum5-hydroxytryptamine 4 receptor agonist activity, concentration which gave 50% increase in the response to electrically-stimulated myenteric plexus and longitudinal muscle of the guinea pig ileum
ChEMBL 310 3 1 5 2.2 COc1cc(N)c(Cl)cc1C(=O)O[C@@H]1CN2CCC1CC2 10.1021/jm960320m
44249311 193656 0 None - 1 Human 6.8 pEC50 = 6.8 Functional
Agonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assayAgonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assay
ChEMBL 313 3 2 4 2.1 CC(C)n1c(=O)c(C(=O)NC2CCNCC2)cc2ccccc21 10.1021/jm900881j
CHEMBL551614 193656 0 None - 1 Human 6.8 pEC50 = 6.8 Functional
Agonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assayAgonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assay
ChEMBL 313 3 2 4 2.1 CC(C)n1c(=O)c(C(=O)NC2CCNCC2)cc2ccccc21 10.1021/jm900881j
44247945 194396 0 None - 1 Human 5.8 pEC50 = 5.8 Functional
Agonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assayAgonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assay
ChEMBL 391 6 3 6 1.0 COc1cc(N)c(Cl)cc1C(=O)NC1CCN(CCS(=O)(=O)O)CC1 10.1021/jm900881j
CHEMBL560597 194396 0 None - 1 Human 5.8 pEC50 = 5.8 Functional
Agonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assayAgonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assay
ChEMBL 391 6 3 6 1.0 COc1cc(N)c(Cl)cc1C(=O)NC1CCN(CCS(=O)(=O)O)CC1 10.1021/jm900881j
132337 3487 8 None -1 2 Rat 7.8 pEC50 = 7.8 Functional
Agonism at 5HT4 receptor in rat tunica muscularis mucosaAgonism at 5HT4 receptor in rat tunica muscularis mucosa
ChEMBL 323 4 2 4 2.1 COc1cc(N)c(cc1C(=O)NC[C@@H]1CCN2[C@H]1CCC2)Cl 10.1021/jm0509501
238 3487 8 None -1 2 Rat 7.8 pEC50 = 7.8 Functional
Agonism at 5HT4 receptor in rat tunica muscularis mucosaAgonism at 5HT4 receptor in rat tunica muscularis mucosa
ChEMBL 323 4 2 4 2.1 COc1cc(N)c(cc1C(=O)NC[C@@H]1CCN2[C@H]1CCC2)Cl 10.1021/jm0509501
CHEMBL34291 3487 8 None -1 2 Rat 7.8 pEC50 = 7.8 Functional
Agonism at 5HT4 receptor in rat tunica muscularis mucosaAgonism at 5HT4 receptor in rat tunica muscularis mucosa
ChEMBL 323 4 2 4 2.1 COc1cc(N)c(cc1C(=O)NC[C@@H]1CCN2[C@H]1CCC2)Cl 10.1021/jm0509501
44308599 202005 0 None - 1 Rat 5.8 pEC50 = 5.8 Functional
Agonist activity against serotonin 5-HT4 receptor in rat tunica muscularis mucosae assayAgonist activity against serotonin 5-HT4 receptor in rat tunica muscularis mucosae assay
ChEMBL 349 5 2 4 2.4 COc1cc(N)c(Cl)cc1C(=O)NCCC12CC3CN(CC3C1)C2 10.1016/S0960-894X(97)00408-3
CHEMBL67554 202005 0 None - 1 Rat 5.8 pEC50 = 5.8 Functional
Agonist activity against serotonin 5-HT4 receptor in rat tunica muscularis mucosae assayAgonist activity against serotonin 5-HT4 receptor in rat tunica muscularis mucosae assay
ChEMBL 349 5 2 4 2.4 COc1cc(N)c(Cl)cc1C(=O)NCCC12CC3CN(CC3C1)C2 10.1016/S0960-894X(97)00408-3
9819593 98348 2 None 3 2 Guinea pig 6.8 pEC50 = 6.8 Functional
5-hydroxytryptamine 4 receptor agonist activity, concentration which gave 50% increase in the response to electrically-stimulated myenteric plexus and longitudinal muscle of the guinea pig ileum5-hydroxytryptamine 4 receptor agonist activity, concentration which gave 50% increase in the response to electrically-stimulated myenteric plexus and longitudinal muscle of the guinea pig ileum
ChEMBL 309 3 2 4 1.8 COc1cc(N)c(Cl)cc1C(=O)N[C@H]1CN2CCC1CC2 10.1021/jm960320m
CHEMBL27846 98348 2 None 3 2 Guinea pig 6.8 pEC50 = 6.8 Functional
5-hydroxytryptamine 4 receptor agonist activity, concentration which gave 50% increase in the response to electrically-stimulated myenteric plexus and longitudinal muscle of the guinea pig ileum5-hydroxytryptamine 4 receptor agonist activity, concentration which gave 50% increase in the response to electrically-stimulated myenteric plexus and longitudinal muscle of the guinea pig ileum
ChEMBL 309 3 2 4 1.8 COc1cc(N)c(Cl)cc1C(=O)N[C@H]1CN2CCC1CC2 10.1021/jm960320m
10548275 48247 0 None - 1 Guinea pig 7.8 pEC50 = 7.8 Functional
5-hydroxytryptamine 4 receptor agonist activity, concentration which gave 50% increase in the response to electrically-stimulated myenteric plexus and longitudinal muscle of the guinea pig ileum5-hydroxytryptamine 4 receptor agonist activity, concentration which gave 50% increase in the response to electrically-stimulated myenteric plexus and longitudinal muscle of the guinea pig ileum
ChEMBL 307 5 1 4 2.1 COc1cc(N)c(Cl)cc1C(=O)OCC[n+]1ccccc1 10.1021/jm960320m
CHEMBL155631 48247 0 None - 1 Guinea pig 7.8 pEC50 = 7.8 Functional
5-hydroxytryptamine 4 receptor agonist activity, concentration which gave 50% increase in the response to electrically-stimulated myenteric plexus and longitudinal muscle of the guinea pig ileum5-hydroxytryptamine 4 receptor agonist activity, concentration which gave 50% increase in the response to electrically-stimulated myenteric plexus and longitudinal muscle of the guinea pig ileum
ChEMBL 307 5 1 4 2.1 COc1cc(N)c(Cl)cc1C(=O)OCC[n+]1ccccc1 10.1021/jm960320m
54677674 112311 4 None - 1 Human 7.8 pEC50 = 7.8 Functional
Agonist activity at recombinant human 5HT4e receptor expressed in African green monkey COS7 cells assessed as cAMP level after 30 mins by HTRF assayAgonist activity at recombinant human 5HT4e receptor expressed in African green monkey COS7 cells assessed as cAMP level after 30 mins by HTRF assay
ChEMBL 377 6 2 6 3.0 CC(C)n1c(=O)c(C(=O)NCCCN2CCCCC2)c(O)c2ccsc21 10.1016/j.ejmech.2015.08.051
CHEMBL3291085 112311 4 None - 1 Human 7.8 pEC50 = 7.8 Functional
Agonist activity at recombinant human 5HT4e receptor expressed in African green monkey COS7 cells assessed as cAMP level after 30 mins by HTRF assayAgonist activity at recombinant human 5HT4e receptor expressed in African green monkey COS7 cells assessed as cAMP level after 30 mins by HTRF assay
ChEMBL 377 6 2 6 3.0 CC(C)n1c(=O)c(C(=O)NCCCN2CCCCC2)c(O)c2ccsc21 10.1016/j.ejmech.2015.08.051
CHEMBL3306918 112311 4 None - 1 Human 7.8 pEC50 = 7.8 Functional
Agonist activity at recombinant human 5HT4e receptor expressed in African green monkey COS7 cells assessed as cAMP level after 30 mins by HTRF assayAgonist activity at recombinant human 5HT4e receptor expressed in African green monkey COS7 cells assessed as cAMP level after 30 mins by HTRF assay
ChEMBL 377 6 2 6 3.0 CC(C)n1c(=O)c(C(=O)NCCCN2CCCCC2)c(O)c2ccsc21 10.1016/j.ejmech.2015.08.051
5 139 66 None -29 27 Rat 7.8 pEC50 = 7.8 Functional
In vitro relaxation of carbachol pre-contracted rat oesophageal TMM.In vitro relaxation of carbachol pre-contracted rat oesophageal TMM.
ChEMBL 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 10.1016/0960-894X(96)00002-9
5202 139 66 None -29 27 Rat 7.8 pEC50 = 7.8 Functional
In vitro relaxation of carbachol pre-contracted rat oesophageal TMM.In vitro relaxation of carbachol pre-contracted rat oesophageal TMM.
ChEMBL 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 10.1016/0960-894X(96)00002-9
CHEMBL39 139 66 None -29 27 Rat 7.8 pEC50 = 7.8 Functional
In vitro relaxation of carbachol pre-contracted rat oesophageal TMM.In vitro relaxation of carbachol pre-contracted rat oesophageal TMM.
ChEMBL 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 10.1016/0960-894X(96)00002-9
DB08839 139 66 None -29 27 Rat 7.8 pEC50 = 7.8 Functional
In vitro relaxation of carbachol pre-contracted rat oesophageal TMM.In vitro relaxation of carbachol pre-contracted rat oesophageal TMM.
ChEMBL 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 10.1016/0960-894X(96)00002-9
42618248 186445 0 None - 1 Human 7.8 pEC50 = 7.8 Functional
Agonist activity at human 5HT4 isoform E receptor expressed in rat C6 cells assessed as cAMP accumulation by radio-immunoassay relative to 5HTAgonist activity at human 5HT4 isoform E receptor expressed in rat C6 cells assessed as cAMP accumulation by radio-immunoassay relative to 5HT
ChEMBL 479 8 2 6 3.6 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCC(NC(=O)Cc2ccccc2Cl)CC1 10.1021/jm801327q
CHEMBL490852 186445 0 None - 1 Human 7.8 pEC50 = 7.8 Functional
Agonist activity at human 5HT4 isoform E receptor expressed in rat C6 cells assessed as cAMP accumulation by radio-immunoassay relative to 5HTAgonist activity at human 5HT4 isoform E receptor expressed in rat C6 cells assessed as cAMP accumulation by radio-immunoassay relative to 5HT
ChEMBL 479 8 2 6 3.6 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCC(NC(=O)Cc2ccccc2Cl)CC1 10.1021/jm801327q
127039821 136111 0 None - 1 Human 7.8 pEC50 = 7.8 Functional
Agonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assayAgonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assay
ChEMBL 352 5 1 4 2.9 CC(C)c1nc(C(=O)NC[C@H]2[C@@H]3CN(C4CCC4)C[C@H]23)c2ccccn12 10.1016/j.ejmech.2015.08.051
CHEMBL3739931 136111 0 None - 1 Human 7.8 pEC50 = 7.8 Functional
Agonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assayAgonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assay
ChEMBL 352 5 1 4 2.9 CC(C)c1nc(C(=O)NC[C@H]2[C@@H]3CN(C4CCC4)C[C@H]23)c2ccccn12 10.1016/j.ejmech.2015.08.051
127039374 136296 0 None - 1 Human 7.8 pEC50 = 7.8 Functional
Agonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assayAgonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assay
ChEMBL 372 6 1 4 3.1 CC(C)c1nc(C(=O)NC[C@H]2[C@@H]3CN(CC(C)(C)F)C[C@H]23)c2ccccn12 10.1016/j.ejmech.2015.08.051
CHEMBL3741595 136296 0 None - 1 Human 7.8 pEC50 = 7.8 Functional
Agonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assayAgonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assay
ChEMBL 372 6 1 4 3.1 CC(C)c1nc(C(=O)NC[C@H]2[C@@H]3CN(CC(C)(C)F)C[C@H]23)c2ccccn12 10.1016/j.ejmech.2015.08.051
127039822 136210 0 None - 1 Human 7.7 pEC50 = 7.7 Functional
Agonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assayAgonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assay
ChEMBL 340 5 1 4 2.8 CC(C)c1nc(C(=O)NC[C@H]2[C@@H]3CN(C(C)C)C[C@H]23)c2ccccn12 10.1016/j.ejmech.2015.08.051
CHEMBL3740844 136210 0 None - 1 Human 7.7 pEC50 = 7.7 Functional
Agonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assayAgonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assay
ChEMBL 340 5 1 4 2.8 CC(C)c1nc(C(=O)NC[C@H]2[C@@H]3CN(C(C)C)C[C@H]23)c2ccccn12 10.1016/j.ejmech.2015.08.051
9905225 205216 0 None - 1 Rat 7.7 pEC50 = 7.7 Functional
In vitro relaxation of carbachol pre-contracted rat oesophageal TMM.In vitro relaxation of carbachol pre-contracted rat oesophageal TMM.
ChEMBL 321 2 2 4 1.7 Nc1c(Cl)cc(C(=O)N[C@@H]2CN3CCC2CC3)c2c1CCO2 10.1016/0960-894X(96)00002-9
CHEMBL91147 205216 0 None - 1 Rat 7.7 pEC50 = 7.7 Functional
In vitro relaxation of carbachol pre-contracted rat oesophageal TMM.In vitro relaxation of carbachol pre-contracted rat oesophageal TMM.
ChEMBL 321 2 2 4 1.7 Nc1c(Cl)cc(C(=O)N[C@@H]2CN3CCC2CC3)c2c1CCO2 10.1016/0960-894X(96)00002-9
10802184 53873 0 None - 1 Guinea pig 6.8 pEC50 = 6.8 Functional
5-hydroxytryptamine 4 receptor agonist activity, concentration which gave 50% increase in the response to electrically-stimulated myenteric plexus and longitudinal muscle of the guinea pig ileum5-hydroxytryptamine 4 receptor agonist activity, concentration which gave 50% increase in the response to electrically-stimulated myenteric plexus and longitudinal muscle of the guinea pig ileum
ChEMBL 272 5 1 5 1.6 COc1cc(N)c(Cl)cc1C(=O)OCCN(C)C 10.1021/jm960320m
CHEMBL160705 53873 0 None - 1 Guinea pig 6.8 pEC50 = 6.8 Functional
5-hydroxytryptamine 4 receptor agonist activity, concentration which gave 50% increase in the response to electrically-stimulated myenteric plexus and longitudinal muscle of the guinea pig ileum5-hydroxytryptamine 4 receptor agonist activity, concentration which gave 50% increase in the response to electrically-stimulated myenteric plexus and longitudinal muscle of the guinea pig ileum
ChEMBL 272 5 1 5 1.6 COc1cc(N)c(Cl)cc1C(=O)OCCN(C)C 10.1021/jm960320m
10570203 49286 0 None - 1 Guinea pig 7.7 pEC50 = 7.7 Functional
5-hydroxytryptamine 4 receptor agonist activity, concentration which gave 50% increase in the response to electrically-stimulated myenteric plexus and longitudinal muscle of the guinea pig ileum5-hydroxytryptamine 4 receptor agonist activity, concentration which gave 50% increase in the response to electrically-stimulated myenteric plexus and longitudinal muscle of the guinea pig ileum
ChEMBL 355 6 2 6 1.3 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCC(C(N)=O)CC1 10.1021/jm960320m
CHEMBL156554 49286 0 None - 1 Guinea pig 7.7 pEC50 = 7.7 Functional
5-hydroxytryptamine 4 receptor agonist activity, concentration which gave 50% increase in the response to electrically-stimulated myenteric plexus and longitudinal muscle of the guinea pig ileum5-hydroxytryptamine 4 receptor agonist activity, concentration which gave 50% increase in the response to electrically-stimulated myenteric plexus and longitudinal muscle of the guinea pig ileum
ChEMBL 355 6 2 6 1.3 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCC(C(N)=O)CC1 10.1021/jm960320m
9927789 111014 0 None - 1 Rat 7.7 pEC50 = 7.7 Functional
In vitro relaxation of carbachol pre-contracted rat oesophageal TMM.In vitro relaxation of carbachol pre-contracted rat oesophageal TMM.
ChEMBL 337 5 2 4 2.5 Nc1c(Cl)cc(C(=O)NCCCN2CCCCC2)c2c1CCO2 10.1016/0960-894X(96)00002-9
CHEMBL327798 111014 0 None - 1 Rat 7.7 pEC50 = 7.7 Functional
In vitro relaxation of carbachol pre-contracted rat oesophageal TMM.In vitro relaxation of carbachol pre-contracted rat oesophageal TMM.
ChEMBL 337 5 2 4 2.5 Nc1c(Cl)cc(C(=O)NCCCN2CCCCC2)c2c1CCO2 10.1016/0960-894X(96)00002-9
127037820 136329 0 None - 1 Human 7.7 pEC50 = 7.7 Functional
Agonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assayAgonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assay
ChEMBL 398 8 1 5 3.0 COCC(C)(C)CN1C[C@H]2[C@H](CNC(=O)c3nc(C(C)C)n4ccccc34)[C@H]2C1 10.1016/j.ejmech.2015.08.051
CHEMBL3741918 136329 0 None - 1 Human 7.7 pEC50 = 7.7 Functional
Agonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assayAgonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assay
ChEMBL 398 8 1 5 3.0 COCC(C)(C)CN1C[C@H]2[C@H](CNC(=O)c3nc(C(C)C)n4ccccc34)[C@H]2C1 10.1016/j.ejmech.2015.08.051
235 2527 36 None -5 4 Human 7.7 pEC50 = 7.7 Functional
Agonist activity against 5-HT4 receptor in rat esophageal muscularis mucosaeAgonist activity against 5-HT4 receptor in rat esophageal muscularis mucosae
ChEMBL 312 5 1 5 2.6 COc1cc(N)c(cc1C(=O)OCCN1CCCCC1)Cl 10.1016/S0960-894X(01)80413-3
5311299 2527 36 None -5 4 Human 7.7 pEC50 = 7.7 Functional
Agonist activity against 5-HT4 receptor in rat esophageal muscularis mucosaeAgonist activity against 5-HT4 receptor in rat esophageal muscularis mucosae
ChEMBL 312 5 1 5 2.6 COc1cc(N)c(cc1C(=O)OCCN1CCCCC1)Cl 10.1016/S0960-894X(01)80413-3
CHEMBL286136 2527 36 None -5 4 Human 7.7 pEC50 = 7.7 Functional
Agonist activity against 5-HT4 receptor in rat esophageal muscularis mucosaeAgonist activity against 5-HT4 receptor in rat esophageal muscularis mucosae
ChEMBL 312 5 1 5 2.6 COc1cc(N)c(cc1C(=O)OCCN1CCCCC1)Cl 10.1016/S0960-894X(01)80413-3
132337 3487 8 None 1 2 Human 7.7 pEC50 = 7.7 Functional
Agonist activity against 5-HT4 receptor in rat esophageal muscularis mucosaeAgonist activity against 5-HT4 receptor in rat esophageal muscularis mucosae
ChEMBL 323 4 2 4 2.1 COc1cc(N)c(cc1C(=O)NC[C@@H]1CCN2[C@H]1CCC2)Cl 10.1016/S0960-894X(01)80413-3
238 3487 8 None 1 2 Human 7.7 pEC50 = 7.7 Functional
Agonist activity against 5-HT4 receptor in rat esophageal muscularis mucosaeAgonist activity against 5-HT4 receptor in rat esophageal muscularis mucosae
ChEMBL 323 4 2 4 2.1 COc1cc(N)c(cc1C(=O)NC[C@@H]1CCN2[C@H]1CCC2)Cl 10.1016/S0960-894X(01)80413-3
CHEMBL34291 3487 8 None 1 2 Human 7.7 pEC50 = 7.7 Functional
Agonist activity against 5-HT4 receptor in rat esophageal muscularis mucosaeAgonist activity against 5-HT4 receptor in rat esophageal muscularis mucosae
ChEMBL 323 4 2 4 2.1 COc1cc(N)c(cc1C(=O)NC[C@@H]1CCN2[C@H]1CCC2)Cl 10.1016/S0960-894X(01)80413-3
49783211 17458 0 None - 1 Human 7.7 pEC50 = 7.7 Functional
Agonist activity at 5HT4 receptor expressed in HEK293/L9 cells by cAMP assayAgonist activity at 5HT4 receptor expressed in HEK293/L9 cells by cAMP assay
ChEMBL 488 7 1 6 3.8 CCCCN1CCC(COC(=O)c2cc(I)c(NC)c3c2OCCO3)CC1 10.1021/jm100668r
CHEMBL1258339 17458 0 None - 1 Human 7.7 pEC50 = 7.7 Functional
Agonist activity at 5HT4 receptor expressed in HEK293/L9 cells by cAMP assayAgonist activity at 5HT4 receptor expressed in HEK293/L9 cells by cAMP assay
ChEMBL 488 7 1 6 3.8 CCCCN1CCC(COC(=O)c2cc(I)c(NC)c3c2OCCO3)CC1 10.1021/jm100668r
5311047 203055 30 None 1 2 Human 7.7 pEC50 = 7.7 Functional
Agonist activity at human 5HT4C receptor expressed at 100 fold physiological-level in HEK293 cells assessed as cAMP accumulationAgonist activity at human 5HT4C receptor expressed at 100 fold physiological-level in HEK293 cells assessed as cAMP accumulation
ChEMBL 465 9 2 6 3.4 COc1cc(N)c(Cl)cc1C(=O)N[C@H]1CCN(CCCOc2ccc(F)cc2)C[C@H]1OC 10.1016/j.bmcl.2012.05.034
CHEMBL74656 203055 30 None 1 2 Human 7.7 pEC50 = 7.7 Functional
Agonist activity at human 5HT4C receptor expressed at 100 fold physiological-level in HEK293 cells assessed as cAMP accumulationAgonist activity at human 5HT4C receptor expressed at 100 fold physiological-level in HEK293 cells assessed as cAMP accumulation
ChEMBL 465 9 2 6 3.4 COc1cc(N)c(Cl)cc1C(=O)N[C@H]1CCN(CCCOc2ccc(F)cc2)C[C@H]1OC 10.1016/j.bmcl.2012.05.034
44248312 91900490 193460 0 None - 1 Human 7.7 pEC50 = 7.7 Functional
Agonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assayAgonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assay
ChEMBL 531 12 2 6 4.5 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CCCCCCCCS(=O)(=O)O)cc2ccccc21 10.1021/jm900881j
CHEMBL550122 193460 0 None - 1 Human 7.7 pEC50 = 7.7 Functional
Agonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assayAgonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assay
ChEMBL 531 12 2 6 4.5 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CCCCCCCCS(=O)(=O)O)cc2ccccc21 10.1021/jm900881j
44248066 193516 0 None - 1 Human 7.7 pEC50 = 7.7 Functional
Agonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assayAgonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assay
ChEMBL 473 7 2 7 0.7 COc1cc(N)c(Cl)cc1C(=O)NC1CCN(CCN2CCN(S(C)(=O)=O)CC2)CC1 10.1021/jm900881j
CHEMBL550530 193516 0 None - 1 Human 7.7 pEC50 = 7.7 Functional
Agonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assayAgonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assay
ChEMBL 473 7 2 7 0.7 COc1cc(N)c(Cl)cc1C(=O)NC1CCN(CCN2CCN(S(C)(=O)=O)CC2)CC1 10.1021/jm900881j
70691118 77148 0 None - 1 Human 7.7 pEC50 = 7.7 Functional
Agonist activity at human recombinant 5HT4c receptor expressed in HEK293 cells at 10-fold physiological level assessed as accumulation of cAMPAgonist activity at human recombinant 5HT4c receptor expressed in HEK293 cells at 10-fold physiological level assessed as accumulation of cAMP
ChEMBL 469 7 3 6 1.7 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CC(O)CN(C)C(N)=O)cc2ccccc21 10.1016/j.bmcl.2012.08.051
CHEMBL2087327 77148 0 None - 1 Human 7.7 pEC50 = 7.7 Functional
Agonist activity at human recombinant 5HT4c receptor expressed in HEK293 cells at 10-fold physiological level assessed as accumulation of cAMPAgonist activity at human recombinant 5HT4c receptor expressed in HEK293 cells at 10-fold physiological level assessed as accumulation of cAMP
ChEMBL 469 7 3 6 1.7 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CC(O)CN(C)C(N)=O)cc2ccccc21 10.1016/j.bmcl.2012.08.051
70686943 77152 0 None - 1 Human 7.7 pEC50 = 7.7 Functional
Agonist activity at human recombinant 5HT4c receptor expressed in HEK293 cells at 10-fold physiological level assessed as accumulation of cAMPAgonist activity at human recombinant 5HT4c receptor expressed in HEK293 cells at 10-fold physiological level assessed as accumulation of cAMP
ChEMBL 497 7 2 6 2.3 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CC(O)CN(C)C(=O)N(C)C)cc2ccccc21 10.1016/j.bmcl.2012.08.051
CHEMBL2087331 77152 0 None - 1 Human 7.7 pEC50 = 7.7 Functional
Agonist activity at human recombinant 5HT4c receptor expressed in HEK293 cells at 10-fold physiological level assessed as accumulation of cAMPAgonist activity at human recombinant 5HT4c receptor expressed in HEK293 cells at 10-fold physiological level assessed as accumulation of cAMP
ChEMBL 497 7 2 6 2.3 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CC(O)CN(C)C(=O)N(C)C)cc2ccccc21 10.1016/j.bmcl.2012.08.051
1782 2482 81 None -158 12 Rat 5.7 pEC50 = 5.7 Functional
In vitro relaxation of carbachol pre-contracted rat oesophageal TMM.In vitro relaxation of carbachol pre-contracted rat oesophageal TMM.
ChEMBL 299 7 2 4 2.0 CCN(CCNC(=O)c1cc(Cl)c(cc1OC)N)CC 10.1016/0960-894X(96)00002-9
241 2482 81 None -158 12 Rat 5.7 pEC50 = 5.7 Functional
In vitro relaxation of carbachol pre-contracted rat oesophageal TMM.In vitro relaxation of carbachol pre-contracted rat oesophageal TMM.
ChEMBL 299 7 2 4 2.0 CCN(CCNC(=O)c1cc(Cl)c(cc1OC)N)CC 10.1016/0960-894X(96)00002-9
4168 2482 81 None -158 12 Rat 5.7 pEC50 = 5.7 Functional
In vitro relaxation of carbachol pre-contracted rat oesophageal TMM.In vitro relaxation of carbachol pre-contracted rat oesophageal TMM.
ChEMBL 299 7 2 4 2.0 CCN(CCNC(=O)c1cc(Cl)c(cc1OC)N)CC 10.1016/0960-894X(96)00002-9
CHEMBL86 2482 81 None -158 12 Rat 5.7 pEC50 = 5.7 Functional
In vitro relaxation of carbachol pre-contracted rat oesophageal TMM.In vitro relaxation of carbachol pre-contracted rat oesophageal TMM.
ChEMBL 299 7 2 4 2.0 CCN(CCNC(=O)c1cc(Cl)c(cc1OC)N)CC 10.1016/0960-894X(96)00002-9
DB01233 2482 81 None -158 12 Rat 5.7 pEC50 = 5.7 Functional
In vitro relaxation of carbachol pre-contracted rat oesophageal TMM.In vitro relaxation of carbachol pre-contracted rat oesophageal TMM.
ChEMBL 299 7 2 4 2.0 CCN(CCNC(=O)c1cc(Cl)c(cc1OC)N)CC 10.1016/0960-894X(96)00002-9
11493794 72684 0 None 26 2 Rat 6.7 pEC50 = 6.7 Functional
Agonism at 5HT4 receptor in rat tunica muscularis mucosaAgonism at 5HT4 receptor in rat tunica muscularis mucosa
ChEMBL 337 5 2 4 2.5 CCOc1cc(N)c(Cl)cc1C(=O)NC[C@@H]1CCN2CCC[C@@H]12 10.1021/jm0509501
CHEMBL201019 72684 0 None 26 2 Rat 6.7 pEC50 = 6.7 Functional
Agonism at 5HT4 receptor in rat tunica muscularis mucosaAgonism at 5HT4 receptor in rat tunica muscularis mucosa
ChEMBL 337 5 2 4 2.5 CCOc1cc(N)c(Cl)cc1C(=O)NC[C@@H]1CCN2CCC[C@@H]12 10.1021/jm0509501
132164 204922 8 None - 1 Rat 6.7 pEC50 = 6.7 Functional
In vitro relaxation of carbachol pre-contracted rat oesophageal TMM.In vitro relaxation of carbachol pre-contracted rat oesophageal TMM.
ChEMBL 321 2 2 4 1.7 Nc1c(Cl)cc(C(=O)N[C@H]2CN3CCC2CC3)c2c1CCO2 10.1016/0960-894X(96)00002-9
CHEMBL89259 204922 8 None - 1 Rat 6.7 pEC50 = 6.7 Functional
In vitro relaxation of carbachol pre-contracted rat oesophageal TMM.In vitro relaxation of carbachol pre-contracted rat oesophageal TMM.
ChEMBL 321 2 2 4 1.7 Nc1c(Cl)cc(C(=O)N[C@H]2CN3CCC2CC3)c2c1CCO2 10.1016/0960-894X(96)00002-9
127039508 136306 0 None - 1 Human 6.7 pEC50 = 6.7 Functional
Agonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assayAgonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assay
ChEMBL 402 5 1 5 3.2 CC(C)c1nc(C(=O)NC2CCN(CC3(F)CCOCC3)CC2)c2ccccn12 10.1016/j.ejmech.2015.08.051
CHEMBL3741703 136306 0 None - 1 Human 6.7 pEC50 = 6.7 Functional
Agonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assayAgonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assay
ChEMBL 402 5 1 5 3.2 CC(C)c1nc(C(=O)NC2CCN(CC3(F)CCOCC3)CC2)c2ccccn12 10.1016/j.ejmech.2015.08.051
10493462 200800 0 None - 1 Human 6.7 pEC50 = 6.7 Functional
Agonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assayAgonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assay
ChEMBL 286 3 2 4 2.1 CC(C)n1nc(C(=O)NC2CCNCC2)c2ccccc21 10.1021/jm900881j
CHEMBL61130 200800 0 None - 1 Human 6.7 pEC50 = 6.7 Functional
Agonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assayAgonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assay
ChEMBL 286 3 2 4 2.1 CC(C)n1nc(C(=O)NC2CCNCC2)c2ccccc21 10.1021/jm900881j
19081864 104475 0 None - 1 Rat 5.7 pEC50 = 5.7 Functional
Compound was tested against 5-HT4 receptor through agonism of 5-HT mediated relaxation of rat, carbachol contracted esophageal muscularis mucosaeCompound was tested against 5-HT4 receptor through agonism of 5-HT mediated relaxation of rat, carbachol contracted esophageal muscularis mucosae
ChEMBL 352 9 1 4 4.6 CCCOc1cc(N)c(Cl)cc1C(=O)CCCCN1CCCCC1 10.1016/S0960-894X(01)80414-5
CHEMBL311325 104475 0 None - 1 Rat 5.7 pEC50 = 5.7 Functional
Compound was tested against 5-HT4 receptor through agonism of 5-HT mediated relaxation of rat, carbachol contracted esophageal muscularis mucosaeCompound was tested against 5-HT4 receptor through agonism of 5-HT mediated relaxation of rat, carbachol contracted esophageal muscularis mucosae
ChEMBL 352 9 1 4 4.6 CCCOc1cc(N)c(Cl)cc1C(=O)CCCCN1CCCCC1 10.1016/S0960-894X(01)80414-5
183782 3346 15 None 3 3 Human 8.7 pEC50 = 8.7 Functional
Agonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assayAgonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assay
ChEMBL 352 8 1 4 4.4 CCCCN1CCC(CC1)CCC(=O)c1cc(Cl)c(cc1OC)N 10.1016/j.ejmech.2015.08.051
237 3346 15 None 3 3 Human 8.7 pEC50 = 8.7 Functional
Agonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assayAgonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assay
ChEMBL 352 8 1 4 4.4 CCCCN1CCC(CC1)CCC(=O)c1cc(Cl)c(cc1OC)N 10.1016/j.ejmech.2015.08.051
CHEMBL85251 3346 15 None 3 3 Human 8.7 pEC50 = 8.7 Functional
Agonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assayAgonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assay
ChEMBL 352 8 1 4 4.4 CCCCN1CCC(CC1)CCC(=O)c1cc(Cl)c(cc1OC)N 10.1016/j.ejmech.2015.08.051
44213662 204871 0 None - 1 Rat 8.7 pEC50 = 8.7 Functional
In vitro relaxation of carbachol pre-contracted rat oesophageal TMM.In vitro relaxation of carbachol pre-contracted rat oesophageal TMM.
ChEMBL 324 4 1 5 2.5 Nc1c(Cl)cc(C(=O)OCCN2CCCCC2)c2c1CCO2 10.1016/0960-894X(96)00002-9
CHEMBL88973 204871 0 None - 1 Rat 8.7 pEC50 = 8.7 Functional
In vitro relaxation of carbachol pre-contracted rat oesophageal TMM.In vitro relaxation of carbachol pre-contracted rat oesophageal TMM.
ChEMBL 324 4 1 5 2.5 Nc1c(Cl)cc(C(=O)OCCN2CCCCC2)c2c1CCO2 10.1016/0960-894X(96)00002-9
71451950 82263 5 None -1 2 Rat 8.7 pEC50 = 8.7 Functional
Agonist activity at rat 5HT4E receptor expressed in HEK293 cells assessed as increase in cAMP production after 30 mins by HTRF assayAgonist activity at rat 5HT4E receptor expressed in HEK293 cells assessed as increase in cAMP production after 30 mins by HTRF assay
ChEMBL 433 4 2 5 2.4 CC1(C)C(=O)N(C(=O)NCC2CCN(CC3(O)CCOCC3)CC2)c2cc(F)ccc21 10.1021/jm300953p
CHEMBL2179582 82263 5 None -1 2 Rat 8.7 pEC50 = 8.7 Functional
Agonist activity at rat 5HT4E receptor expressed in HEK293 cells assessed as increase in cAMP production after 30 mins by HTRF assayAgonist activity at rat 5HT4E receptor expressed in HEK293 cells assessed as increase in cAMP production after 30 mins by HTRF assay
ChEMBL 433 4 2 5 2.4 CC1(C)C(=O)N(C(=O)NCC2CCN(CC3(O)CCOCC3)CC2)c2cc(F)ccc21 10.1021/jm300953p
235 2527 36 None -5 4 Human 8.6 pEC50 = 8.6 Functional
Agonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assayAgonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assay
ChEMBL 312 5 1 5 2.6 COc1cc(N)c(cc1C(=O)OCCN1CCCCC1)Cl 10.1016/j.ejmech.2015.08.051
5311299 2527 36 None -5 4 Human 8.6 pEC50 = 8.6 Functional
Agonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assayAgonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assay
ChEMBL 312 5 1 5 2.6 COc1cc(N)c(cc1C(=O)OCCN1CCCCC1)Cl 10.1016/j.ejmech.2015.08.051
CHEMBL286136 2527 36 None -5 4 Human 8.6 pEC50 = 8.6 Functional
Agonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assayAgonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assay
ChEMBL 312 5 1 5 2.6 COc1cc(N)c(cc1C(=O)OCCN1CCCCC1)Cl 10.1016/j.ejmech.2015.08.051
133076 3347 4 None -1 2 Human 8.6 pEC50 = 8.6 Functional
Agonist activity against 5-HT4 receptor in rat esophageal muscularis mucosaeAgonist activity against 5-HT4 receptor in rat esophageal muscularis mucosae
ChEMBL 417 9 2 6 2.2 COc1cc(N)c(cc1C(=O)CCC1CCN(CC1)CCNS(=O)(=O)C)Cl 10.1016/S0960-894X(01)80413-3
3230 3347 4 None -1 2 Human 8.6 pEC50 = 8.6 Functional
Agonist activity against 5-HT4 receptor in rat esophageal muscularis mucosaeAgonist activity against 5-HT4 receptor in rat esophageal muscularis mucosae
ChEMBL 417 9 2 6 2.2 COc1cc(N)c(cc1C(=O)CCC1CCN(CC1)CCNS(=O)(=O)C)Cl 10.1016/S0960-894X(01)80413-3
CHEMBL83899 3347 4 None -1 2 Human 8.6 pEC50 = 8.6 Functional
Agonist activity against 5-HT4 receptor in rat esophageal muscularis mucosaeAgonist activity against 5-HT4 receptor in rat esophageal muscularis mucosae
ChEMBL 417 9 2 6 2.2 COc1cc(N)c(cc1C(=O)CCC1CCN(CC1)CCNS(=O)(=O)C)Cl 10.1016/S0960-894X(01)80413-3
70696825 76059 0 None - 1 Human 8.6 pEC50 = 8.6 Functional
Agonist activity at human 5HT4C receptor expressed at 100 fold physiological-level in HEK293 cells assessed as cAMP accumulationAgonist activity at human 5HT4C receptor expressed at 100 fold physiological-level in HEK293 cells assessed as cAMP accumulation
ChEMBL 479 10 1 5 5.4 CC(C)n1nc(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CCCCCCN2CCCCC2)c2ccccc21 10.1016/j.bmcl.2012.05.034
CHEMBL2059578 76059 0 None - 1 Human 8.6 pEC50 = 8.6 Functional
Agonist activity at human 5HT4C receptor expressed at 100 fold physiological-level in HEK293 cells assessed as cAMP accumulationAgonist activity at human 5HT4C receptor expressed at 100 fold physiological-level in HEK293 cells assessed as cAMP accumulation
ChEMBL 479 10 1 5 5.4 CC(C)n1nc(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CCCCCCN2CCCCC2)c2ccccc21 10.1016/j.bmcl.2012.05.034
11677434 76062 0 None - 1 Human 8.6 pEC50 = 8.6 Functional
Agonist activity at human 5HT4C receptor expressed at 100 fold physiological-level in HEK293 cells assessed as cAMP accumulationAgonist activity at human 5HT4C receptor expressed at 100 fold physiological-level in HEK293 cells assessed as cAMP accumulation
ChEMBL 483 9 2 7 2.8 COC[C@@H]1CCCN1CC(O)CN1[C@H]2CC[C@@H]1C[C@H](NC(=O)c1nn(C(C)C)c3ccccc13)C2 10.1016/j.bmcl.2012.05.034
CHEMBL2059581 76062 0 None - 1 Human 8.6 pEC50 = 8.6 Functional
Agonist activity at human 5HT4C receptor expressed at 100 fold physiological-level in HEK293 cells assessed as cAMP accumulationAgonist activity at human 5HT4C receptor expressed at 100 fold physiological-level in HEK293 cells assessed as cAMP accumulation
ChEMBL 483 9 2 7 2.8 COC[C@@H]1CCCN1CC(O)CN1[C@H]2CC[C@@H]1C[C@H](NC(=O)c1nn(C(C)C)c3ccccc13)C2 10.1016/j.bmcl.2012.05.034
11225102 76071 2 None 1 2 Human 8.6 pEC50 = 8.6 Functional
Agonist activity at human 5HT4C receptor expressed at 100 fold physiological-level in HEK293 cells assessed as cAMP accumulationAgonist activity at human 5HT4C receptor expressed at 100 fold physiological-level in HEK293 cells assessed as cAMP accumulation
ChEMBL 466 6 1 6 2.5 CC(=O)N1CCN(CCN2[C@H]3CC[C@@H]2C[C@H](NC(=O)c2nn(C(C)C)c4ccccc24)C3)CC1 10.1016/j.bmcl.2012.05.034
CHEMBL2059590 76071 2 None 1 2 Human 8.6 pEC50 = 8.6 Functional
Agonist activity at human 5HT4C receptor expressed at 100 fold physiological-level in HEK293 cells assessed as cAMP accumulationAgonist activity at human 5HT4C receptor expressed at 100 fold physiological-level in HEK293 cells assessed as cAMP accumulation
ChEMBL 466 6 1 6 2.5 CC(=O)N1CCN(CCN2[C@H]3CC[C@@H]2C[C@H](NC(=O)c2nn(C(C)C)c4ccccc24)C3)CC1 10.1016/j.bmcl.2012.05.034
44248191 193230 0 None - 1 Human 8.6 pEC50 = 8.6 Functional
Agonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assayAgonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assay
ChEMBL 537 8 1 7 3.5 CCOC(=O)N1CCN(CCCN2[C@H]3CC[C@@H]2C[C@H](NC(=O)c2cc4ccccc4n(C(C)C)c2=O)C3)CC1 10.1021/jm900881j
CHEMBL540980 193230 0 None - 1 Human 8.6 pEC50 = 8.6 Functional
Agonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assayAgonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assay
ChEMBL 537 8 1 7 3.5 CCOC(=O)N1CCN(CCCN2[C@H]3CC[C@@H]2C[C@H](NC(=O)c2cc4ccccc4n(C(C)C)c2=O)C3)CC1 10.1021/jm900881j
44248195 193412 0 None - 1 Human 8.6 pEC50 = 8.6 Functional
Agonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assayAgonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assay
ChEMBL 466 7 1 6 3.0 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CCCN2CCOCC2)cc2ccccc21 10.1021/jm900881j
CHEMBL549650 193412 0 None - 1 Human 8.6 pEC50 = 8.6 Functional
Agonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assayAgonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assay
ChEMBL 466 7 1 6 3.0 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CCCN2CCOCC2)cc2ccccc21 10.1021/jm900881j
44248679 193926 0 None - 1 Human 8.6 pEC50 = 8.6 Functional
Agonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assayAgonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assay
ChEMBL 599 12 1 7 3.8 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CCCCCCCN2CCN(S(C)(=O)=O)CC2)cc2ccccc21 10.1021/jm900881j
CHEMBL555693 193926 0 None - 1 Human 8.6 pEC50 = 8.6 Functional
Agonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assayAgonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assay
ChEMBL 599 12 1 7 3.8 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CCCCCCCN2CCN(S(C)(=O)=O)CC2)cc2ccccc21 10.1021/jm900881j
44248315 194247 0 None - 1 Human 8.6 pEC50 = 8.6 Functional
Agonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assayAgonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assay
ChEMBL 522 11 1 6 4.6 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CCCCCCCN2CCOCC2)cc2ccccc21 10.1021/jm900881j
CHEMBL559322 194247 0 None - 1 Human 8.6 pEC50 = 8.6 Functional
Agonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assayAgonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assay
ChEMBL 522 11 1 6 4.6 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CCCCCCCN2CCOCC2)cc2ccccc21 10.1021/jm900881j
135409453 3714 38 None 3 3 Human 8.6 pEC50 = 8.6 Functional
Agonist activity at human recombinant 5HT4 receptor assessed as cAMP accumulationAgonist activity at human recombinant 5HT4 receptor assessed as cAMP accumulation
ChEMBL 301 7 3 3 2.6 CCCCCN=C(N/N=C/c1c[nH]c2c1cc(OC)cc2)N 10.1016/j.bmcl.2013.05.018
226 3714 38 None 3 3 Human 8.6 pEC50 = 8.6 Functional
Agonist activity at human recombinant 5HT4 receptor assessed as cAMP accumulationAgonist activity at human recombinant 5HT4 receptor assessed as cAMP accumulation
ChEMBL 301 7 3 3 2.6 CCCCCN=C(N/N=C/c1c[nH]c2c1cc(OC)cc2)N 10.1016/j.bmcl.2013.05.018
CHEMBL76370 3714 38 None 3 3 Human 8.6 pEC50 = 8.6 Functional
Agonist activity at human recombinant 5HT4 receptor assessed as cAMP accumulationAgonist activity at human recombinant 5HT4 receptor assessed as cAMP accumulation
ChEMBL 301 7 3 3 2.6 CCCCCN=C(N/N=C/c1c[nH]c2c1cc(OC)cc2)N 10.1016/j.bmcl.2013.05.018
135409453 3714 38 None 3 3 Human 8.6 pEC50 = 8.6 Functional
Agonist activity at human recombinant 5HT4c receptor expressed in HEK293 cells at 10-fold physiological level assessed as accumulation of cAMPAgonist activity at human recombinant 5HT4c receptor expressed in HEK293 cells at 10-fold physiological level assessed as accumulation of cAMP
ChEMBL 301 7 3 3 2.6 CCCCCN=C(N/N=C/c1c[nH]c2c1cc(OC)cc2)N 10.1016/j.bmcl.2012.08.051
226 3714 38 None 3 3 Human 8.6 pEC50 = 8.6 Functional
Agonist activity at human recombinant 5HT4c receptor expressed in HEK293 cells at 10-fold physiological level assessed as accumulation of cAMPAgonist activity at human recombinant 5HT4c receptor expressed in HEK293 cells at 10-fold physiological level assessed as accumulation of cAMP
ChEMBL 301 7 3 3 2.6 CCCCCN=C(N/N=C/c1c[nH]c2c1cc(OC)cc2)N 10.1016/j.bmcl.2012.08.051
CHEMBL76370 3714 38 None 3 3 Human 8.6 pEC50 = 8.6 Functional
Agonist activity at human recombinant 5HT4c receptor expressed in HEK293 cells at 10-fold physiological level assessed as accumulation of cAMPAgonist activity at human recombinant 5HT4c receptor expressed in HEK293 cells at 10-fold physiological level assessed as accumulation of cAMP
ChEMBL 301 7 3 3 2.6 CCCCCN=C(N/N=C/c1c[nH]c2c1cc(OC)cc2)N 10.1016/j.bmcl.2012.08.051
155543353 172729 0 None - 1 Human 8.6 pEC50 = 8.6 Functional
Partial agonist activity at human HA-tagged 5HT4 receptor expressed in COS7 cells assessed as induction of cAMP production measured after 10 mins by HTRF assayPartial agonist activity at human HA-tagged 5HT4 receptor expressed in COS7 cells assessed as induction of cAMP production measured after 10 mins by HTRF assay
ChEMBL 418 7 3 6 4.2 COc1cc(N)c(Cl)cc1C(=O)CCC1CCN(Cc2ccc(O)c(O)c2)CC1 10.1016/j.ejmech.2019.111596
CHEMBL4526049 172729 0 None - 1 Human 8.6 pEC50 = 8.6 Functional
Partial agonist activity at human HA-tagged 5HT4 receptor expressed in COS7 cells assessed as induction of cAMP production measured after 10 mins by HTRF assayPartial agonist activity at human HA-tagged 5HT4 receptor expressed in COS7 cells assessed as induction of cAMP production measured after 10 mins by HTRF assay
ChEMBL 418 7 3 6 4.2 COc1cc(N)c(Cl)cc1C(=O)CCC1CCN(Cc2ccc(O)c(O)c2)CC1 10.1016/j.ejmech.2019.111596
127037818 136171 1 None -1 2 Human 7.7 pEC50 = 7.7 Functional
Agonist activity at human 5-HT4A receptor assessed as cAMP level after 4 hrs by luciferase reporter gene assayAgonist activity at human 5-HT4A receptor assessed as cAMP level after 4 hrs by luciferase reporter gene assay
ChEMBL 370 8 1 5 2.4 COCCCN1C[C@H]2[C@H](CNC(=O)c3nc(C(C)C)n4ccccc34)[C@H]2C1 10.1016/j.ejmech.2015.08.051
CHEMBL3740472 136171 1 None -1 2 Human 7.7 pEC50 = 7.7 Functional
Agonist activity at human 5-HT4A receptor assessed as cAMP level after 4 hrs by luciferase reporter gene assayAgonist activity at human 5-HT4A receptor assessed as cAMP level after 4 hrs by luciferase reporter gene assay
ChEMBL 370 8 1 5 2.4 COCCCN1C[C@H]2[C@H](CNC(=O)c3nc(C(C)C)n4ccccc34)[C@H]2C1 10.1016/j.ejmech.2015.08.051
127037818 136171 1 None -1 2 Human 7.7 pEC50 = 7.7 Functional
Agonist activity at human 5-HT4D receptor assessed as cAMP level after 4 hrs by luciferase reporter gene assayAgonist activity at human 5-HT4D receptor assessed as cAMP level after 4 hrs by luciferase reporter gene assay
ChEMBL 370 8 1 5 2.4 COCCCN1C[C@H]2[C@H](CNC(=O)c3nc(C(C)C)n4ccccc34)[C@H]2C1 10.1016/j.ejmech.2015.08.051
CHEMBL3740472 136171 1 None -1 2 Human 7.7 pEC50 = 7.7 Functional
Agonist activity at human 5-HT4D receptor assessed as cAMP level after 4 hrs by luciferase reporter gene assayAgonist activity at human 5-HT4D receptor assessed as cAMP level after 4 hrs by luciferase reporter gene assay
ChEMBL 370 8 1 5 2.4 COCCCN1C[C@H]2[C@H](CNC(=O)c3nc(C(C)C)n4ccccc34)[C@H]2C1 10.1016/j.ejmech.2015.08.051
127037818 136171 1 None 1 2 Rat 7.7 pEC50 = 7.7 Functional
Agonist activity at rat 5-HT4L receptor assessed as cAMP level after 4 hrs by luciferase reporter gene assayAgonist activity at rat 5-HT4L receptor assessed as cAMP level after 4 hrs by luciferase reporter gene assay
ChEMBL 370 8 1 5 2.4 COCCCN1C[C@H]2[C@H](CNC(=O)c3nc(C(C)C)n4ccccc34)[C@H]2C1 10.1016/j.ejmech.2015.08.051
CHEMBL3740472 136171 1 None 1 2 Rat 7.7 pEC50 = 7.7 Functional
Agonist activity at rat 5-HT4L receptor assessed as cAMP level after 4 hrs by luciferase reporter gene assayAgonist activity at rat 5-HT4L receptor assessed as cAMP level after 4 hrs by luciferase reporter gene assay
ChEMBL 370 8 1 5 2.4 COCCCN1C[C@H]2[C@H](CNC(=O)c3nc(C(C)C)n4ccccc34)[C@H]2C1 10.1016/j.ejmech.2015.08.051
127039823 136184 0 None - 1 Human 7.7 pEC50 = 7.7 Functional
Agonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assayAgonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assay
ChEMBL 382 5 1 5 2.5 CC(C)c1nc(C(=O)NC[C@H]2[C@@H]3CN(C4CCOCC4)C[C@H]23)c2ccccn12 10.1016/j.ejmech.2015.08.051
CHEMBL3740612 136184 0 None - 1 Human 7.7 pEC50 = 7.7 Functional
Agonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assayAgonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assay
ChEMBL 382 5 1 5 2.5 CC(C)c1nc(C(=O)NC[C@H]2[C@@H]3CN(C4CCOCC4)C[C@H]23)c2ccccn12 10.1016/j.ejmech.2015.08.051
10567201 183683 0 None - 1 Guinea pig 6.7 pEC50 = 6.7 Functional
concentration which gave a 50% increase in the response to electrical stimulation against 5-hydroxytryptamine 4 receptor in the guinea pig ileum. Activity expressed as percent of the maximum 5-HT response given in brackets.concentration which gave a 50% increase in the response to electrical stimulation against 5-hydroxytryptamine 4 receptor in the guinea pig ileum. Activity expressed as percent of the maximum 5-HT response given in brackets.
ChEMBL 313 5 2 5 2.6 COc1cc(N)c(Cl)cc1NC(=O)OCCN1CCCC1 10.1021/jm960853v
CHEMBL48379 183683 0 None - 1 Guinea pig 6.7 pEC50 = 6.7 Functional
concentration which gave a 50% increase in the response to electrical stimulation against 5-hydroxytryptamine 4 receptor in the guinea pig ileum. Activity expressed as percent of the maximum 5-HT response given in brackets.concentration which gave a 50% increase in the response to electrical stimulation against 5-hydroxytryptamine 4 receptor in the guinea pig ileum. Activity expressed as percent of the maximum 5-HT response given in brackets.
ChEMBL 313 5 2 5 2.6 COc1cc(N)c(Cl)cc1NC(=O)OCCN1CCCC1 10.1021/jm960853v
6604914 99919 2 None -1 2 Rat 6.7 pEC50 = 6.7 Functional
Compound was evaluated for the agonistic activity towards 5-hydroxytryptamine 4 receptor using the rat tunica muscularis mucosae (TMM) esophagus strip assayCompound was evaluated for the agonistic activity towards 5-hydroxytryptamine 4 receptor using the rat tunica muscularis mucosae (TMM) esophagus strip assay
ChEMBL 309 3 2 4 1.8 COc1cc(N)c(Cl)cc1C(=O)N[C@@H]1CN2CCC1CC2 10.1016/S0960-894X(00)80441-2
CHEMBL28992 99919 2 None -1 2 Rat 6.7 pEC50 = 6.7 Functional
Compound was evaluated for the agonistic activity towards 5-hydroxytryptamine 4 receptor using the rat tunica muscularis mucosae (TMM) esophagus strip assayCompound was evaluated for the agonistic activity towards 5-hydroxytryptamine 4 receptor using the rat tunica muscularis mucosae (TMM) esophagus strip assay
ChEMBL 309 3 2 4 1.8 COc1cc(N)c(Cl)cc1C(=O)N[C@@H]1CN2CCC1CC2 10.1016/S0960-894X(00)80441-2
9819119 202006 0 None - 1 Rat 6.7 pEC50 = 6.7 Functional
Agonist activity against serotonin 5-HT4 receptor in rat tunica muscularis mucosae assayAgonist activity against serotonin 5-HT4 receptor in rat tunica muscularis mucosae assay
ChEMBL 335 4 2 4 2.0 COc1cc(N)c(Cl)cc1C(=O)NCC12CC3CN(CC3C1)C2 10.1016/S0960-894X(97)00408-3
CHEMBL67555 202006 0 None - 1 Rat 6.7 pEC50 = 6.7 Functional
Agonist activity against serotonin 5-HT4 receptor in rat tunica muscularis mucosae assayAgonist activity against serotonin 5-HT4 receptor in rat tunica muscularis mucosae assay
ChEMBL 335 4 2 4 2.0 COc1cc(N)c(Cl)cc1C(=O)NCC12CC3CN(CC3C1)C2 10.1016/S0960-894X(97)00408-3
44281102 116215 0 None - 1 Guinea pig 7.7 pEC50 = 7.7 Functional
5-hydroxytryptamine 4 receptor agonist activity as increased response to electrical stimulation in guinea pig ileum5-hydroxytryptamine 4 receptor agonist activity as increased response to electrical stimulation in guinea pig ileum
ChEMBL 312 4 1 5 2.6 CCN1CCC(OC(=O)c2cc(Cl)c(N)cc2OC)CC1 10.1016/S0960-894X(01)80508-4
CHEMBL33732 116215 0 None - 1 Guinea pig 7.7 pEC50 = 7.7 Functional
5-hydroxytryptamine 4 receptor agonist activity as increased response to electrical stimulation in guinea pig ileum5-hydroxytryptamine 4 receptor agonist activity as increased response to electrical stimulation in guinea pig ileum
ChEMBL 312 4 1 5 2.6 CCN1CCC(OC(=O)c2cc(Cl)c(N)cc2OC)CC1 10.1016/S0960-894X(01)80508-4
127037818 136171 1 None -1 2 Human 7.7 pEC50 = 7.7 Functional
Agonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assayAgonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assay
ChEMBL 370 8 1 5 2.4 COCCCN1C[C@H]2[C@H](CNC(=O)c3nc(C(C)C)n4ccccc34)[C@H]2C1 10.1016/j.ejmech.2015.08.051
CHEMBL3740472 136171 1 None -1 2 Human 7.7 pEC50 = 7.7 Functional
Agonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assayAgonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assay
ChEMBL 370 8 1 5 2.4 COCCCN1C[C@H]2[C@H](CNC(=O)c3nc(C(C)C)n4ccccc34)[C@H]2C1 10.1016/j.ejmech.2015.08.051
127039819 136374 0 None - 1 Human 5.7 pEC50 = 5.7 Functional
Agonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assayAgonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assay
ChEMBL 356 5 1 5 2.4 CC(C)c1nc(C(=O)NCC2CN(C3CCC3)CCO2)c2ccccn12 10.1016/j.ejmech.2015.08.051
CHEMBL3742300 136374 0 None - 1 Human 5.7 pEC50 = 5.7 Functional
Agonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assayAgonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assay
ChEMBL 356 5 1 5 2.4 CC(C)c1nc(C(=O)NCC2CN(C3CCC3)CCO2)c2ccccn12 10.1016/j.ejmech.2015.08.051
132337 3487 8 None -1 2 Rat 7.6 pEC50 = 7.6 Functional
Compound was tested for agonist activity at the 5-hydroxytryptamine 4 receptor in the rat tunica muscularis mucosae (TMM) assayCompound was tested for agonist activity at the 5-hydroxytryptamine 4 receptor in the rat tunica muscularis mucosae (TMM) assay
ChEMBL 323 4 2 4 2.1 COc1cc(N)c(cc1C(=O)NC[C@@H]1CCN2[C@H]1CCC2)Cl 10.1016/j.bmcl.2004.04.021
238 3487 8 None -1 2 Rat 7.6 pEC50 = 7.6 Functional
Compound was tested for agonist activity at the 5-hydroxytryptamine 4 receptor in the rat tunica muscularis mucosae (TMM) assayCompound was tested for agonist activity at the 5-hydroxytryptamine 4 receptor in the rat tunica muscularis mucosae (TMM) assay
ChEMBL 323 4 2 4 2.1 COc1cc(N)c(cc1C(=O)NC[C@@H]1CCN2[C@H]1CCC2)Cl 10.1016/j.bmcl.2004.04.021
CHEMBL34291 3487 8 None -1 2 Rat 7.6 pEC50 = 7.6 Functional
Compound was tested for agonist activity at the 5-hydroxytryptamine 4 receptor in the rat tunica muscularis mucosae (TMM) assayCompound was tested for agonist activity at the 5-hydroxytryptamine 4 receptor in the rat tunica muscularis mucosae (TMM) assay
ChEMBL 323 4 2 4 2.1 COc1cc(N)c(cc1C(=O)NC[C@@H]1CCN2[C@H]1CCC2)Cl 10.1016/j.bmcl.2004.04.021
132337 3487 8 None -1 2 Rat 7.6 pEC50 = 7.6 Functional
Efficient 5-hydroxytryptamine 4 agonist in the rat tunica muscularis mucosaeEfficient 5-hydroxytryptamine 4 agonist in the rat tunica muscularis mucosae
ChEMBL 323 4 2 4 2.1 COc1cc(N)c(cc1C(=O)NC[C@@H]1CCN2[C@H]1CCC2)Cl 10.1021/jm020099f
238 3487 8 None -1 2 Rat 7.6 pEC50 = 7.6 Functional
Efficient 5-hydroxytryptamine 4 agonist in the rat tunica muscularis mucosaeEfficient 5-hydroxytryptamine 4 agonist in the rat tunica muscularis mucosae
ChEMBL 323 4 2 4 2.1 COc1cc(N)c(cc1C(=O)NC[C@@H]1CCN2[C@H]1CCC2)Cl 10.1021/jm020099f
CHEMBL34291 3487 8 None -1 2 Rat 7.6 pEC50 = 7.6 Functional
Efficient 5-hydroxytryptamine 4 agonist in the rat tunica muscularis mucosaeEfficient 5-hydroxytryptamine 4 agonist in the rat tunica muscularis mucosae
ChEMBL 323 4 2 4 2.1 COc1cc(N)c(cc1C(=O)NC[C@@H]1CCN2[C@H]1CCC2)Cl 10.1021/jm020099f
127039510 136197 0 None - 1 Human 7.6 pEC50 = 7.6 Functional
Agonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assayAgonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assay
ChEMBL 370 5 1 5 2.7 CC(C)c1nc(C(=O)NC2CCN(CC3CCOC3)CC2)c2ccccn12 10.1016/j.ejmech.2015.08.051
CHEMBL3740732 136197 0 None - 1 Human 7.6 pEC50 = 7.6 Functional
Agonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assayAgonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assay
ChEMBL 370 5 1 5 2.7 CC(C)c1nc(C(=O)NC2CCN(CC3CCOC3)CC2)c2ccccn12 10.1016/j.ejmech.2015.08.051
44248797 194039 0 None - 1 Human 7.6 pEC50 = 7.6 Functional
Agonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assayAgonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assay
ChEMBL 353 7 2 4 3.3 CCCCCN1CCC(NC(=O)c2cc(Cl)c(N)cc2OC)CC1 10.1021/jm900881j
CHEMBL557053 194039 0 None - 1 Human 7.6 pEC50 = 7.6 Functional
Agonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assayAgonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assay
ChEMBL 353 7 2 4 3.3 CCCCCN1CCC(NC(=O)c2cc(Cl)c(N)cc2OC)CC1 10.1021/jm900881j
44248552 91900486 194245 0 None - 1 Human 7.6 pEC50 = 7.6 Functional
Agonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assayAgonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assay
ChEMBL 554 9 1 6 4.8 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CCCCCN2C(=O)c3ccccc3C2=O)cc2ccccc21 10.1021/jm900881j
CHEMBL559317 194245 0 None - 1 Human 7.6 pEC50 = 7.6 Functional
Agonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assayAgonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assay
ChEMBL 554 9 1 6 4.8 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CCCCCN2C(=O)c3ccccc3C2=O)cc2ccccc21 10.1021/jm900881j
10574402 91900484 194798 0 None - 1 Human 7.6 pEC50 = 7.6 Functional
Agonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assayAgonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assay
ChEMBL 425 8 2 5 3.5 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CCCCCO)cc2ccccc21 10.1021/jm900881j
CHEMBL563261 194798 0 None - 1 Human 7.6 pEC50 = 7.6 Functional
Agonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assayAgonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assay
ChEMBL 425 8 2 5 3.5 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CCCCCO)cc2ccccc21 10.1021/jm900881j
70695323 77157 0 None - 1 Human 7.6 pEC50 = 7.6 Functional
Agonist activity at human recombinant 5HT4c receptor expressed in HEK293 cells at 10-fold physiological level assessed as accumulation of cAMPAgonist activity at human recombinant 5HT4c receptor expressed in HEK293 cells at 10-fold physiological level assessed as accumulation of cAMP
ChEMBL 504 8 2 7 1.6 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3C[C@H](O)CN(C)S(C)(=O)=O)cc2ccccc21 10.1016/j.bmcl.2012.08.051
CHEMBL2087336 77157 0 None - 1 Human 7.6 pEC50 = 7.6 Functional
Agonist activity at human recombinant 5HT4c receptor expressed in HEK293 cells at 10-fold physiological level assessed as accumulation of cAMPAgonist activity at human recombinant 5HT4c receptor expressed in HEK293 cells at 10-fold physiological level assessed as accumulation of cAMP
ChEMBL 504 8 2 7 1.6 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3C[C@H](O)CN(C)S(C)(=O)=O)cc2ccccc21 10.1016/j.bmcl.2012.08.051
71450247 82563 0 None - 1 Human 6.6 pEC50 = 6.6 Functional
Inverse agonist activity at human recombinant 5HT4R expressed in HEK293T cells assessed as Gs activationInverse agonist activity at human recombinant 5HT4R expressed in HEK293T cells assessed as Gs activation
ChEMBL 368 5 0 3 5.5 CCCN1CCC(COc2nc3c(Cl)cccc3c3ccccc23)CC1 10.1021/jm300943r
CHEMBL2181188 82563 0 None - 1 Human 6.6 pEC50 = 6.6 Functional
Inverse agonist activity at human recombinant 5HT4R expressed in HEK293T cells assessed as Gs activationInverse agonist activity at human recombinant 5HT4R expressed in HEK293T cells assessed as Gs activation
ChEMBL 368 5 0 3 5.5 CCCN1CCC(COc2nc3c(Cl)cccc3c3ccccc23)CC1 10.1021/jm300943r
203435 163552 2 None - 1 Human 6.6 pEC50 = 6.6 Functional
Agonist activity against 5-HT4 receptor in rat esophageal muscularis mucosaeAgonist activity against 5-HT4 receptor in rat esophageal muscularis mucosae
ChEMBL 311 5 2 4 2.1 COc1cc(N)c(Cl)cc1C(=O)NCCN1CCCCC1 10.1016/S0960-894X(01)80413-3
CHEMBL420969 163552 2 None - 1 Human 6.6 pEC50 = 6.6 Functional
Agonist activity against 5-HT4 receptor in rat esophageal muscularis mucosaeAgonist activity against 5-HT4 receptor in rat esophageal muscularis mucosae
ChEMBL 311 5 2 4 2.1 COc1cc(N)c(Cl)cc1C(=O)NCCN1CCCCC1 10.1016/S0960-894X(01)80413-3
71712612 90947 0 None - 1 Human 6.6 pEC50 = 6.6 Functional
Agonist activity at human recombinant 5HT4 receptor assessed as cAMP accumulationAgonist activity at human recombinant 5HT4 receptor assessed as cAMP accumulation
ChEMBL 490 7 3 7 0.2 CS(=O)(=O)N1CCN(CC(O)CN2[C@H]3CC[C@@H]2C[C@H](NC(=O)c2cccc4[nH]cnc24)C3)CC1 10.1016/j.bmcl.2013.05.018
CHEMBL2402888 90947 0 None - 1 Human 6.6 pEC50 = 6.6 Functional
Agonist activity at human recombinant 5HT4 receptor assessed as cAMP accumulationAgonist activity at human recombinant 5HT4 receptor assessed as cAMP accumulation
ChEMBL 490 7 3 7 0.2 CS(=O)(=O)N1CCN(CC(O)CN2[C@H]3CC[C@@H]2C[C@H](NC(=O)c2cccc4[nH]cnc24)C3)CC1 10.1016/j.bmcl.2013.05.018
44249317 91900480 193671 0 None - 1 Human 5.6 pEC50 = 5.6 Functional
Agonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assayAgonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assay
ChEMBL 299 3 3 3 2.2 COc1ccc2[nH]cc(C(=O)N[C@@H]3C[C@@H]4CC[C@H](C3)N4)c2c1 10.1021/jm900881j
CHEMBL551743 193671 0 None - 1 Human 5.6 pEC50 = 5.6 Functional
Agonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assayAgonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assay
ChEMBL 299 3 3 3 2.2 COc1ccc2[nH]cc(C(=O)N[C@@H]3C[C@@H]4CC[C@H](C3)N4)c2c1 10.1021/jm900881j
243 3153 85 None -1 2 Rat 7.6 pEC50 = 7.6 Functional
Agonist activity at rat 5HT4e receptor expressed in HEK293 cells assessed as cAMP level after 30 mins by HTRF assayAgonist activity at rat 5HT4e receptor expressed in HEK293 cells assessed as cAMP level after 30 mins by HTRF assay
ChEMBL 367 6 2 5 2.1 COCCCN1CCC(CC1)NC(=O)c1cc(Cl)c(c2c1OCC2)N 10.1016/j.ejmech.2015.08.051
3052762 3153 85 None -1 2 Rat 7.6 pEC50 = 7.6 Functional
Agonist activity at rat 5HT4e receptor expressed in HEK293 cells assessed as cAMP level after 30 mins by HTRF assayAgonist activity at rat 5HT4e receptor expressed in HEK293 cells assessed as cAMP level after 30 mins by HTRF assay
ChEMBL 367 6 2 5 2.1 COCCCN1CCC(CC1)NC(=O)c1cc(Cl)c(c2c1OCC2)N 10.1016/j.ejmech.2015.08.051
3502 3153 85 None -1 2 Rat 7.6 pEC50 = 7.6 Functional
Agonist activity at rat 5HT4e receptor expressed in HEK293 cells assessed as cAMP level after 30 mins by HTRF assayAgonist activity at rat 5HT4e receptor expressed in HEK293 cells assessed as cAMP level after 30 mins by HTRF assay
ChEMBL 367 6 2 5 2.1 COCCCN1CCC(CC1)NC(=O)c1cc(Cl)c(c2c1OCC2)N 10.1016/j.ejmech.2015.08.051
CHEMBL117287 3153 85 None -1 2 Rat 7.6 pEC50 = 7.6 Functional
Agonist activity at rat 5HT4e receptor expressed in HEK293 cells assessed as cAMP level after 30 mins by HTRF assayAgonist activity at rat 5HT4e receptor expressed in HEK293 cells assessed as cAMP level after 30 mins by HTRF assay
ChEMBL 367 6 2 5 2.1 COCCCN1CCC(CC1)NC(=O)c1cc(Cl)c(c2c1OCC2)N 10.1016/j.ejmech.2015.08.051
DB06480 3153 85 None -1 2 Rat 7.6 pEC50 = 7.6 Functional
Agonist activity at rat 5HT4e receptor expressed in HEK293 cells assessed as cAMP level after 30 mins by HTRF assayAgonist activity at rat 5HT4e receptor expressed in HEK293 cells assessed as cAMP level after 30 mins by HTRF assay
ChEMBL 367 6 2 5 2.1 COCCCN1CCC(CC1)NC(=O)c1cc(Cl)c(c2c1OCC2)N 10.1016/j.ejmech.2015.08.051
108182 4068 18 None - 1 Guinea pig 6.6 pEC50 = 6.6 Functional
5-hydroxytryptamine 4 receptor agonist activity as increased response to electrical stimulation in guinea pig ileum5-hydroxytryptamine 4 receptor agonist activity as increased response to electrical stimulation in guinea pig ileum
ChEMBL 309 3 2 4 1.8 COc1cc(N)c(cc1C(=O)NC1CN2CCC1CC2)Cl 10.1016/S0960-894X(01)80508-4
245 4068 18 None - 1 Guinea pig 6.6 pEC50 = 6.6 Functional
5-hydroxytryptamine 4 receptor agonist activity as increased response to electrical stimulation in guinea pig ileum5-hydroxytryptamine 4 receptor agonist activity as increased response to electrical stimulation in guinea pig ileum
ChEMBL 309 3 2 4 1.8 COc1cc(N)c(cc1C(=O)NC1CN2CCC1CC2)Cl 10.1016/S0960-894X(01)80508-4
CHEMBL18041 4068 18 None - 1 Guinea pig 6.6 pEC50 = 6.6 Functional
5-hydroxytryptamine 4 receptor agonist activity as increased response to electrical stimulation in guinea pig ileum5-hydroxytryptamine 4 receptor agonist activity as increased response to electrical stimulation in guinea pig ileum
ChEMBL 309 3 2 4 1.8 COc1cc(N)c(cc1C(=O)NC1CN2CCC1CC2)Cl 10.1016/S0960-894X(01)80508-4
44288600 100648 0 None -1 2 Rat 6.6 pEC50 = 6.6 Functional
Compound was evaluated for the agonistic activity towards 5-hydroxytryptamine 4 receptor using the rat tunica muscularis mucosae (TMM) esophagus strip assayCompound was evaluated for the agonistic activity towards 5-hydroxytryptamine 4 receptor using the rat tunica muscularis mucosae (TMM) esophagus strip assay
ChEMBL 335 3 2 4 2.0 COc1cc(N)c(Cl)cc1C(=O)NC1C2CC3CC1CN(C3)C2 10.1016/S0960-894X(00)80441-2
CHEMBL295155 100648 0 None -1 2 Rat 6.6 pEC50 = 6.6 Functional
Compound was evaluated for the agonistic activity towards 5-hydroxytryptamine 4 receptor using the rat tunica muscularis mucosae (TMM) esophagus strip assayCompound was evaluated for the agonistic activity towards 5-hydroxytryptamine 4 receptor using the rat tunica muscularis mucosae (TMM) esophagus strip assay
ChEMBL 335 3 2 4 2.0 COc1cc(N)c(Cl)cc1C(=O)NC1C2CC3CC1CN(C3)C2 10.1016/S0960-894X(00)80441-2
14403199 116110 0 None - 1 Guinea pig 7.6 pEC50 = 7.6 Functional
5-hydroxytryptamine 4 receptor agonist activity as increased response to electrical stimulation in guinea pig ileum5-hydroxytryptamine 4 receptor agonist activity as increased response to electrical stimulation in guinea pig ileum
ChEMBL 324 3 1 5 2.7 COc1cc(N)c(Cl)cc1C(=O)OC1CC2CCC(C1)N2C 10.1016/S0960-894X(01)80508-4
CHEMBL33676 116110 0 None - 1 Guinea pig 7.6 pEC50 = 7.6 Functional
5-hydroxytryptamine 4 receptor agonist activity as increased response to electrical stimulation in guinea pig ileum5-hydroxytryptamine 4 receptor agonist activity as increased response to electrical stimulation in guinea pig ileum
ChEMBL 324 3 1 5 2.7 COc1cc(N)c(Cl)cc1C(=O)OC1CC2CCC(C1)N2C 10.1016/S0960-894X(01)80508-4
14403199 116110 0 None - 1 Guinea pig 7.6 pEC50 = 7.6 Functional
5-hydroxytryptamine 4 receptor agonist activity, concentration which gave 50% increase in the response to electrically-stimulated myenteric plexus and longitudinal muscle of the guinea pig ileum5-hydroxytryptamine 4 receptor agonist activity, concentration which gave 50% increase in the response to electrically-stimulated myenteric plexus and longitudinal muscle of the guinea pig ileum
ChEMBL 324 3 1 5 2.7 COc1cc(N)c(Cl)cc1C(=O)OC1CC2CCC(C1)N2C 10.1021/jm960320m
CHEMBL33676 116110 0 None - 1 Guinea pig 7.6 pEC50 = 7.6 Functional
5-hydroxytryptamine 4 receptor agonist activity, concentration which gave 50% increase in the response to electrically-stimulated myenteric plexus and longitudinal muscle of the guinea pig ileum5-hydroxytryptamine 4 receptor agonist activity, concentration which gave 50% increase in the response to electrically-stimulated myenteric plexus and longitudinal muscle of the guinea pig ileum
ChEMBL 324 3 1 5 2.7 COc1cc(N)c(Cl)cc1C(=O)OC1CC2CCC(C1)N2C 10.1021/jm960320m
10757373 49321 0 None - 1 Guinea pig 7.5 pEC50 = 7.5 Functional
5-hydroxytryptamine 4 receptor agonist activity, concentration which gave 50% increase in the response to electrically-stimulated myenteric plexus and longitudinal muscle of the guinea pig ileum5-hydroxytryptamine 4 receptor agonist activity, concentration which gave 50% increase in the response to electrically-stimulated myenteric plexus and longitudinal muscle of the guinea pig ileum
ChEMBL 310 5 1 5 2.4 COc1cc(N)c(Cl)cc1C(=O)OCCN1CC=CCC1 10.1021/jm960320m
CHEMBL156579 49321 0 None - 1 Guinea pig 7.5 pEC50 = 7.5 Functional
5-hydroxytryptamine 4 receptor agonist activity, concentration which gave 50% increase in the response to electrically-stimulated myenteric plexus and longitudinal muscle of the guinea pig ileum5-hydroxytryptamine 4 receptor agonist activity, concentration which gave 50% increase in the response to electrically-stimulated myenteric plexus and longitudinal muscle of the guinea pig ileum
ChEMBL 310 5 1 5 2.4 COc1cc(N)c(Cl)cc1C(=O)OCCN1CC=CCC1 10.1021/jm960320m
3019427 60063 27 None - 1 Human 6.5 pEC50 = 6.5 Functional
Agonist activity at human recombinant 5-HT4 receptorAgonist activity at human recombinant 5-HT4 receptor
ChEMBL 313 4 3 5 1.0 COc1cc(N)c(Cl)cc1C(=O)NC1CCNCC1OC 10.1016/j.bmcl.2009.08.016
CHEMBL1748 60063 27 None - 1 Human 6.5 pEC50 = 6.5 Functional
Agonist activity at human recombinant 5-HT4 receptorAgonist activity at human recombinant 5-HT4 receptor
ChEMBL 313 4 3 5 1.0 COc1cc(N)c(Cl)cc1C(=O)NC1CCNCC1OC 10.1016/j.bmcl.2009.08.016
9973684 51199 0 None - 1 Guinea pig 8.5 pEC50 = 8.5 Functional
5-hydroxytryptamine 4 receptor agonist activity, concentration which gave 50% increase in the response to electrically-stimulated myenteric plexus and longitudinal muscle of the guinea pig ileum5-hydroxytryptamine 4 receptor agonist activity, concentration which gave 50% increase in the response to electrically-stimulated myenteric plexus and longitudinal muscle of the guinea pig ileum
ChEMBL 326 5 1 5 2.8 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCC(C)CC1 10.1021/jm960320m
CHEMBL158238 51199 0 None - 1 Guinea pig 8.5 pEC50 = 8.5 Functional
5-hydroxytryptamine 4 receptor agonist activity, concentration which gave 50% increase in the response to electrically-stimulated myenteric plexus and longitudinal muscle of the guinea pig ileum5-hydroxytryptamine 4 receptor agonist activity, concentration which gave 50% increase in the response to electrically-stimulated myenteric plexus and longitudinal muscle of the guinea pig ileum
ChEMBL 326 5 1 5 2.8 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCC(C)CC1 10.1021/jm960320m
44248193 193141 0 None - 1 Human 8.5 pEC50 = 8.5 Functional
Agonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assayAgonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assay
ChEMBL 593 12 1 7 5.0 CCOC(=O)N1CCN(CCCCCCCN2[C@H]3CC[C@@H]2C[C@H](NC(=O)c2cc4ccccc4n(C(C)C)c2=O)C3)CC1 10.1021/jm900881j
CHEMBL538956 193141 0 None - 1 Human 8.5 pEC50 = 8.5 Functional
Agonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assayAgonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assay
ChEMBL 593 12 1 7 5.0 CCOC(=O)N1CCN(CCCCCCCN2[C@H]3CC[C@@H]2C[C@H](NC(=O)c2cc4ccccc4n(C(C)C)c2=O)C3)CC1 10.1021/jm900881j
44248434 91900496 193966 0 None - 1 Human 8.5 pEC50 = 8.5 Functional
Agonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assayAgonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assay
ChEMBL 613 13 1 7 4.2 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CCCCCCCCN2CCN(S(C)(=O)=O)CC2)cc2ccccc21 10.1021/jm900881j
CHEMBL556326 193966 0 None - 1 Human 8.5 pEC50 = 8.5 Functional
Agonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assayAgonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assay
ChEMBL 613 13 1 7 4.2 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CCCCCCCCN2CCN(S(C)(=O)=O)CC2)cc2ccccc21 10.1021/jm900881j
44247943 194274 0 None - 1 Human 8.5 pEC50 = 8.5 Functional
Agonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assayAgonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assay
ChEMBL 540 12 2 6 4.8 COc1cc(N)c(Cl)cc1C(=O)NC1CCN(CCCCCCCCN2C(=O)c3ccccc3C2=O)CC1 10.1021/jm900881j
CHEMBL559548 194274 0 None - 1 Human 8.5 pEC50 = 8.5 Functional
Agonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assayAgonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assay
ChEMBL 540 12 2 6 4.8 COc1cc(N)c(Cl)cc1C(=O)NC1CCN(CCCCCCCCN2C(=O)c3ccccc3C2=O)CC1 10.1021/jm900881j
44249183 194706 0 None - 1 Human 8.5 pEC50 = 8.5 Functional
Agonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assayAgonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assay
ChEMBL 478 12 2 5 5.0 COc1cc(N)c(Cl)cc1C(=O)NC1CCN(CCCCCCCCN2CCCCC2)CC1 10.1021/jm900881j
CHEMBL562636 194706 0 None - 1 Human 8.5 pEC50 = 8.5 Functional
Agonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assayAgonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assay
ChEMBL 478 12 2 5 5.0 COc1cc(N)c(Cl)cc1C(=O)NC1CCN(CCCCCCCCN2CCCCC2)CC1 10.1021/jm900881j
71714543 90952 0 None - 1 Human 8.5 pEC50 = 8.5 Functional
Agonist activity at human recombinant 5HT4 receptor assessed as cAMP accumulationAgonist activity at human recombinant 5HT4 receptor assessed as cAMP accumulation
ChEMBL 534 8 3 7 1.2 CC(C)(C)c1nc2c(C(=O)NCC3CCN(CC(O)CN4CCN(S(C)(=O)=O)CC4)CC3)cccc2[nH]1 10.1016/j.bmcl.2013.05.018
CHEMBL2402893 90952 0 None - 1 Human 8.5 pEC50 = 8.5 Functional
Agonist activity at human recombinant 5HT4 receptor assessed as cAMP accumulationAgonist activity at human recombinant 5HT4 receptor assessed as cAMP accumulation
ChEMBL 534 8 3 7 1.2 CC(C)(C)c1nc2c(C(=O)NCC3CCN(CC(O)CN4CCN(S(C)(=O)=O)CC4)CC3)cccc2[nH]1 10.1016/j.bmcl.2013.05.018
71712329 90958 0 None - 1 Human 8.5 pEC50 = 8.5 Functional
Agonist activity at human recombinant 5HT4 receptor assessed as cAMP accumulationAgonist activity at human recombinant 5HT4 receptor assessed as cAMP accumulation
ChEMBL 454 7 2 5 2.3 CC(=O)N1CCN(CCN2CCC(CNC(=O)c3cccc4[nH]c(C(C)C)nc34)CC2)CC1 10.1016/j.bmcl.2013.05.018
CHEMBL2402899 90958 0 None - 1 Human 8.5 pEC50 = 8.5 Functional
Agonist activity at human recombinant 5HT4 receptor assessed as cAMP accumulationAgonist activity at human recombinant 5HT4 receptor assessed as cAMP accumulation
ChEMBL 454 7 2 5 2.3 CC(=O)N1CCN(CCN2CCC(CNC(=O)c3cccc4[nH]c(C(C)C)nc34)CC2)CC1 10.1016/j.bmcl.2013.05.018
127041783 136065 0 None - 1 Human 8.5 pEC50 = 8.5 Functional
Agonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assayAgonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assay
ChEMBL 328 4 1 4 3.1 CC(C)c1nc(C(=O)NC2CCN(C(C)C)CC2)c2ccccn12 10.1016/j.ejmech.2015.08.051
CHEMBL3739521 136065 0 None - 1 Human 8.5 pEC50 = 8.5 Functional
Agonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assayAgonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assay
ChEMBL 328 4 1 4 3.1 CC(C)c1nc(C(=O)NC2CCN(C(C)C)CC2)c2ccccn12 10.1016/j.ejmech.2015.08.051
127039509 136218 0 None - 1 Human 8.4 pEC50 = 8.4 Functional
Agonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assayAgonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assay
ChEMBL 332 5 1 4 2.6 CC(C)c1nc(C(=O)NC2CCN(CCF)CC2)c2ccccn12 10.1016/j.ejmech.2015.08.051
CHEMBL3740908 136218 0 None - 1 Human 8.4 pEC50 = 8.4 Functional
Agonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assayAgonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assay
ChEMBL 332 5 1 4 2.6 CC(C)c1nc(C(=O)NC2CCN(CCF)CC2)c2ccccn12 10.1016/j.ejmech.2015.08.051
183782 3346 15 None 3 3 Human 8.4 pEC50 = 8.4 Functional
Agonist activity against 5-HT4 receptor in rat esophageal muscularis mucosaeAgonist activity against 5-HT4 receptor in rat esophageal muscularis mucosae
ChEMBL 352 8 1 4 4.4 CCCCN1CCC(CC1)CCC(=O)c1cc(Cl)c(cc1OC)N 10.1016/S0960-894X(01)80413-3
237 3346 15 None 3 3 Human 8.4 pEC50 = 8.4 Functional
Agonist activity against 5-HT4 receptor in rat esophageal muscularis mucosaeAgonist activity against 5-HT4 receptor in rat esophageal muscularis mucosae
ChEMBL 352 8 1 4 4.4 CCCCN1CCC(CC1)CCC(=O)c1cc(Cl)c(cc1OC)N 10.1016/S0960-894X(01)80413-3
CHEMBL85251 3346 15 None 3 3 Human 8.4 pEC50 = 8.4 Functional
Agonist activity against 5-HT4 receptor in rat esophageal muscularis mucosaeAgonist activity against 5-HT4 receptor in rat esophageal muscularis mucosae
ChEMBL 352 8 1 4 4.4 CCCCN1CCC(CC1)CCC(=O)c1cc(Cl)c(cc1OC)N 10.1016/S0960-894X(01)80413-3
11168006 76070 0 None - 1 Human 8.4 pEC50 = 8.4 Functional
Agonist activity at human 5HT4C receptor expressed at 100 fold physiological-level in HEK293 cells assessed as cAMP accumulationAgonist activity at human 5HT4C receptor expressed at 100 fold physiological-level in HEK293 cells assessed as cAMP accumulation
ChEMBL 502 7 1 7 1.9 CC(C)n1nc(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CCN2CCN(S(C)(=O)=O)CC2)c2ccccc21 10.1016/j.bmcl.2012.05.034
CHEMBL2059589 76070 0 None - 1 Human 8.4 pEC50 = 8.4 Functional
Agonist activity at human 5HT4C receptor expressed at 100 fold physiological-level in HEK293 cells assessed as cAMP accumulationAgonist activity at human 5HT4C receptor expressed at 100 fold physiological-level in HEK293 cells assessed as cAMP accumulation
ChEMBL 502 7 1 7 1.9 CC(C)n1nc(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CCN2CCN(S(C)(=O)=O)CC2)c2ccccc21 10.1016/j.bmcl.2012.05.034
44248080 91900498 194203 0 None - 1 Human 8.4 pEC50 = 8.4 Functional
Agonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assayAgonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assay
ChEMBL 493 8 2 6 2.6 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CCCN2CCC[C@@H]2C(N)=O)cc2ccccc21 10.1021/jm900881j
CHEMBL558855 194203 0 None - 1 Human 8.4 pEC50 = 8.4 Functional
Agonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assayAgonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assay
ChEMBL 493 8 2 6 2.6 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CCCN2CCC[C@@H]2C(N)=O)cc2ccccc21 10.1021/jm900881j
182593 3343 4 None 1 2 Guinea pig 7.5 pEC50 = 7.5 Functional
5-hydroxytryptamine 4 receptor agonist activity, concentration which gave 50% increase in the response to electrically-stimulated myenteric plexus and longitudinal muscle of the guinea pig ileum5-hydroxytryptamine 4 receptor agonist activity, concentration which gave 50% increase in the response to electrically-stimulated myenteric plexus and longitudinal muscle of the guinea pig ileum
ChEMBL 326 6 1 5 3.0 COc1cc(N)c(cc1C(=O)OCCCN1CCCCC1)Cl 10.1021/jm960320m
254 3343 4 None 1 2 Guinea pig 7.5 pEC50 = 7.5 Functional
5-hydroxytryptamine 4 receptor agonist activity, concentration which gave 50% increase in the response to electrically-stimulated myenteric plexus and longitudinal muscle of the guinea pig ileum5-hydroxytryptamine 4 receptor agonist activity, concentration which gave 50% increase in the response to electrically-stimulated myenteric plexus and longitudinal muscle of the guinea pig ileum
ChEMBL 326 6 1 5 3.0 COc1cc(N)c(cc1C(=O)OCCCN1CCCCC1)Cl 10.1021/jm960320m
CHEMBL83954 3343 4 None 1 2 Guinea pig 7.5 pEC50 = 7.5 Functional
5-hydroxytryptamine 4 receptor agonist activity, concentration which gave 50% increase in the response to electrically-stimulated myenteric plexus and longitudinal muscle of the guinea pig ileum5-hydroxytryptamine 4 receptor agonist activity, concentration which gave 50% increase in the response to electrically-stimulated myenteric plexus and longitudinal muscle of the guinea pig ileum
ChEMBL 326 6 1 5 3.0 COc1cc(N)c(cc1C(=O)OCCCN1CCCCC1)Cl 10.1021/jm960320m
10615288 186426 0 None - 1 Guinea pig 6.5 pEC50 = 6.5 Functional
concentration which gave a 50% increase in the response to electrical stimulation against 5-hydroxytryptamine 4 receptor in the guinea pig ileum. Activity expressed as percent of the maximum 5-HT response given in brackets.concentration which gave a 50% increase in the response to electrical stimulation against 5-hydroxytryptamine 4 receptor in the guinea pig ileum. Activity expressed as percent of the maximum 5-HT response given in brackets.
ChEMBL 315 7 2 5 2.8 CCN(CC)CCOC(=O)Nc1cc(Cl)c(N)cc1OC 10.1021/jm960853v
CHEMBL49072 186426 0 None - 1 Guinea pig 6.5 pEC50 = 6.5 Functional
concentration which gave a 50% increase in the response to electrical stimulation against 5-hydroxytryptamine 4 receptor in the guinea pig ileum. Activity expressed as percent of the maximum 5-HT response given in brackets.concentration which gave a 50% increase in the response to electrical stimulation against 5-hydroxytryptamine 4 receptor in the guinea pig ileum. Activity expressed as percent of the maximum 5-HT response given in brackets.
ChEMBL 315 7 2 5 2.8 CCN(CC)CCOC(=O)Nc1cc(Cl)c(N)cc1OC 10.1021/jm960853v
127039824 136078 0 None - 1 Human 7.5 pEC50 = 7.5 Functional
Agonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assayAgonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assay
ChEMBL 396 6 1 5 2.8 CC(C)c1nc(C(=O)NC[C@H]2[C@@H]3CN(CC4CCOCC4)C[C@H]23)c2ccccn12 10.1016/j.ejmech.2015.08.051
CHEMBL3739647 136078 0 None - 1 Human 7.5 pEC50 = 7.5 Functional
Agonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assayAgonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assay
ChEMBL 396 6 1 5 2.8 CC(C)c1nc(C(=O)NC[C@H]2[C@@H]3CN(CC4CCOCC4)C[C@H]23)c2ccccn12 10.1016/j.ejmech.2015.08.051
10315431 98493 0 None - 1 Rat 7.5 pEC50 = 7.5 Functional
5-hydroxytryptamine 4 receptor agonist activity in the rat esophageal muscularis mucosae5-hydroxytryptamine 4 receptor agonist activity in the rat esophageal muscularis mucosae
ChEMBL 343 1 1 4 2.8 CN1CCC(N2C(=O)c3cccc4c(N)c(Cl)cc(c34)C2=O)CC1 10.1016/S0960-894X(00)80352-2
CHEMBL27966 98493 0 None - 1 Rat 7.5 pEC50 = 7.5 Functional
5-hydroxytryptamine 4 receptor agonist activity in the rat esophageal muscularis mucosae5-hydroxytryptamine 4 receptor agonist activity in the rat esophageal muscularis mucosae
ChEMBL 343 1 1 4 2.8 CN1CCC(N2C(=O)c3cccc4c(N)c(Cl)cc(c34)C2=O)CC1 10.1016/S0960-894X(00)80352-2
44249055 91900481 193748 0 None - 1 Human 7.5 pEC50 = 7.5 Functional
Agonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assayAgonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assay
ChEMBL 367 4 1 4 3.3 CCN1[C@H]2CC[C@@H]1C[C@H](NC(=O)c1cc3ccccc3n(C(C)C)c1=O)C2 10.1021/jm900881j
CHEMBL552218 193748 0 None - 1 Human 7.5 pEC50 = 7.5 Functional
Agonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assayAgonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assay
ChEMBL 367 4 1 4 3.3 CCN1[C@H]2CC[C@@H]1C[C@H](NC(=O)c1cc3ccccc3n(C(C)C)c1=O)C2 10.1021/jm900881j
10643698 193781 0 None - 1 Human 7.5 pEC50 = 7.5 Functional
Agonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assayAgonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assay
ChEMBL 383 5 2 5 2.3 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CCO)cc2ccccc21 10.1021/jm900881j
CHEMBL552420 193781 0 None - 1 Human 7.5 pEC50 = 7.5 Functional
Agonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assayAgonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assay
ChEMBL 383 5 2 5 2.3 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CCO)cc2ccccc21 10.1021/jm900881j
70682705 77150 0 None - 1 Human 7.5 pEC50 = 7.5 Functional
Agonist activity at human recombinant 5HT4c receptor expressed in HEK293 cells at 10-fold physiological level assessed as accumulation of cAMPAgonist activity at human recombinant 5HT4c receptor expressed in HEK293 cells at 10-fold physiological level assessed as accumulation of cAMP
ChEMBL 483 7 3 6 1.9 CNC(=O)N(C)CC(O)CN1[C@H]2CC[C@@H]1C[C@H](NC(=O)c1cc3ccccc3n(C(C)C)c1=O)C2 10.1016/j.bmcl.2012.08.051
CHEMBL2087329 77150 0 None - 1 Human 7.5 pEC50 = 7.5 Functional
Agonist activity at human recombinant 5HT4c receptor expressed in HEK293 cells at 10-fold physiological level assessed as accumulation of cAMPAgonist activity at human recombinant 5HT4c receptor expressed in HEK293 cells at 10-fold physiological level assessed as accumulation of cAMP
ChEMBL 483 7 3 6 1.9 CNC(=O)N(C)CC(O)CN1[C@H]2CC[C@@H]1C[C@H](NC(=O)c1cc3ccccc3n(C(C)C)c1=O)C2 10.1016/j.bmcl.2012.08.051
127041781 136126 0 None - 1 Human 6.5 pEC50 = 6.5 Functional
Agonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assayAgonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assay
ChEMBL 388 8 2 6 2.1 COCCCN1CCC(O)(CNC(=O)c2nc(C(C)C)n3ccccc23)CC1 10.1016/j.ejmech.2015.08.051
CHEMBL3740030 136126 0 None - 1 Human 6.5 pEC50 = 6.5 Functional
Agonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assayAgonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assay
ChEMBL 388 8 2 6 2.1 COCCCN1CCC(O)(CNC(=O)c2nc(C(C)C)n3ccccc23)CC1 10.1016/j.ejmech.2015.08.051
10828801 103692 0 None - 1 Human 6.5 pEC50 = 6.5 Functional
Agonist activity against 5-HT4 receptor in rat esophageal muscularis mucosaeAgonist activity against 5-HT4 receptor in rat esophageal muscularis mucosae
ChEMBL 310 6 1 4 3.4 COc1cc(N)c(Cl)cc1C(=O)CCCN1CCCCC1 10.1016/S0960-894X(01)80413-3
CHEMBL309655 103692 0 None - 1 Human 6.5 pEC50 = 6.5 Functional
Agonist activity against 5-HT4 receptor in rat esophageal muscularis mucosaeAgonist activity against 5-HT4 receptor in rat esophageal muscularis mucosae
ChEMBL 310 6 1 4 3.4 COc1cc(N)c(Cl)cc1C(=O)CCCN1CCCCC1 10.1016/S0960-894X(01)80413-3
44248794 193840 0 None - 1 Human 6.5 pEC50 = 6.5 Functional
Agonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assayAgonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assay
ChEMBL 302 2 2 5 1.7 CC(C)n1c(=O)n(C(=O)NC2CCNCC2)c2ccccc21 10.1021/jm900881j
CHEMBL553658 193840 0 None - 1 Human 6.5 pEC50 = 6.5 Functional
Agonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assayAgonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assay
ChEMBL 302 2 2 5 1.7 CC(C)n1c(=O)n(C(=O)NC2CCNCC2)c2ccccc21 10.1021/jm900881j
15095973 135745 0 None 12 2 Rat 6.5 pEC50 = 6.5 Functional
Agonism at 5HT4 receptor in rat tunica muscularis mucosaAgonism at 5HT4 receptor in rat tunica muscularis mucosa
ChEMBL 323 4 2 4 2.1 COc1cc(N)c(Cl)cc1C(=O)NC[C@H]1CCN2CCC[C@H]12 10.1021/jm0509501
CHEMBL37333 135745 0 None 12 2 Rat 6.5 pEC50 = 6.5 Functional
Agonism at 5HT4 receptor in rat tunica muscularis mucosaAgonism at 5HT4 receptor in rat tunica muscularis mucosa
ChEMBL 323 4 2 4 2.1 COc1cc(N)c(Cl)cc1C(=O)NC[C@H]1CCN2CCC[C@H]12 10.1021/jm0509501
22400452 101914 0 None - 1 Rat 5.5 pEC50 = 5.5 Functional
Agonist activity against serotonin 5-HT4 receptor in rat tunica muscularis mucosae assayAgonist activity against serotonin 5-HT4 receptor in rat tunica muscularis mucosae assay
ChEMBL 363 4 2 4 2.1 COc1cc(NC(C)=O)c(Cl)cc1C(=O)NC1C2CC3CC1CN3C2 10.1016/S0960-894X(97)00408-3
CHEMBL303877 101914 0 None - 1 Rat 5.5 pEC50 = 5.5 Functional
Agonist activity against serotonin 5-HT4 receptor in rat tunica muscularis mucosae assayAgonist activity against serotonin 5-HT4 receptor in rat tunica muscularis mucosae assay
ChEMBL 363 4 2 4 2.1 COc1cc(NC(C)=O)c(Cl)cc1C(=O)NC1C2CC3CC1CN3C2 10.1016/S0960-894X(97)00408-3
127037821 136273 0 None - 1 Human 7.5 pEC50 = 7.5 Functional
Agonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assayAgonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assay
ChEMBL 370 6 2 5 2.1 CC(C)c1nc(C(=O)NC[C@H]2[C@@H]3CN(CC(C)(C)O)C[C@H]23)c2ccccn12 10.1016/j.ejmech.2015.08.051
CHEMBL3741377 136273 0 None - 1 Human 7.5 pEC50 = 7.5 Functional
Agonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assayAgonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assay
ChEMBL 370 6 2 5 2.1 CC(C)c1nc(C(=O)NC[C@H]2[C@@H]3CN(CC(C)(C)O)C[C@H]23)c2ccccn12 10.1016/j.ejmech.2015.08.051
44213663 204855 0 None - 1 Rat 7.5 pEC50 = 7.5 Functional
In vitro relaxation of carbachol pre-contracted rat oesophageal TMM.In vitro relaxation of carbachol pre-contracted rat oesophageal TMM.
ChEMBL 323 4 2 4 2.1 Nc1c(Cl)cc(C(=O)NCCN2CCCCC2)c2c1CCO2 10.1016/0960-894X(96)00002-9
CHEMBL88867 204855 0 None - 1 Rat 7.5 pEC50 = 7.5 Functional
In vitro relaxation of carbachol pre-contracted rat oesophageal TMM.In vitro relaxation of carbachol pre-contracted rat oesophageal TMM.
ChEMBL 323 4 2 4 2.1 Nc1c(Cl)cc(C(=O)NCCN2CCCCC2)c2c1CCO2 10.1016/0960-894X(96)00002-9
11596009 73027 0 None - 1 Rat 6.4 pEC50 = 6.4 Functional
Agonism at 5HT4 receptor in rat tunica muscularis mucosaAgonism at 5HT4 receptor in rat tunica muscularis mucosa
ChEMBL 342 3 1 5 2.4 CC(C)n1c(=O)n(C(=O)NC[C@@H]2CCN3CCC[C@@H]23)c2ccccc21 10.1021/jm0509501
CHEMBL201414 73027 0 None - 1 Rat 6.4 pEC50 = 6.4 Functional
Agonism at 5HT4 receptor in rat tunica muscularis mucosaAgonism at 5HT4 receptor in rat tunica muscularis mucosa
ChEMBL 342 3 1 5 2.4 CC(C)n1c(=O)n(C(=O)NC[C@@H]2CCN3CCC[C@@H]23)c2ccccc21 10.1021/jm0509501
9861932 201882 0 None - 1 Rat 6.4 pEC50 = 6.4 Functional
Agonist activity against serotonin 5-HT4 receptor in rat tunica muscularis mucosae assayAgonist activity against serotonin 5-HT4 receptor in rat tunica muscularis mucosae assay
ChEMBL 321 3 2 4 1.8 COc1cc(N)c(Cl)cc1C(=O)NC1C2CC3CC1CN3C2 10.1016/S0960-894X(97)00408-3
CHEMBL66768 201882 0 None - 1 Rat 6.4 pEC50 = 6.4 Functional
Agonist activity against serotonin 5-HT4 receptor in rat tunica muscularis mucosae assayAgonist activity against serotonin 5-HT4 receptor in rat tunica muscularis mucosae assay
ChEMBL 321 3 2 4 1.8 COc1cc(N)c(Cl)cc1C(=O)NC1C2CC3CC1CN3C2 10.1016/S0960-894X(97)00408-3
44323245 106541 0 None - 1 Rat 6.4 pEC50 = 6.4 Functional
In vitro relaxation of carbachol pre-contracted rat oesophageal TMM.In vitro relaxation of carbachol pre-contracted rat oesophageal TMM.
ChEMBL 322 2 1 5 2.1 Nc1c(Cl)cc(C(=O)O[C@H]2CN3CCC2CC3)c2c1CCO2 10.1016/0960-894X(96)00002-9
CHEMBL315443 106541 0 None - 1 Rat 6.4 pEC50 = 6.4 Functional
In vitro relaxation of carbachol pre-contracted rat oesophageal TMM.In vitro relaxation of carbachol pre-contracted rat oesophageal TMM.
ChEMBL 322 2 1 5 2.1 Nc1c(Cl)cc(C(=O)O[C@H]2CN3CCC2CC3)c2c1CCO2 10.1016/0960-894X(96)00002-9
73352662 92808 0 None - 1 Rat 5.4 pEC50 = 5.4 Functional
Compound was evaluated for the agonistic activity towards 5-hydroxytryptamine 4 receptor using the rat tunica muscularis mucosae (TMM) esophagus strip assayCompound was evaluated for the agonistic activity towards 5-hydroxytryptamine 4 receptor using the rat tunica muscularis mucosae (TMM) esophagus strip assay
ChEMBL 321 3 2 4 1.6 COc1cc(N)c(Cl)cc1C(=O)N[C@H]1C2CC3CN(C2)CC31 10.1016/S0960-894X(00)80441-2
CHEMBL2448137 92808 0 None - 1 Rat 5.4 pEC50 = 5.4 Functional
Compound was evaluated for the agonistic activity towards 5-hydroxytryptamine 4 receptor using the rat tunica muscularis mucosae (TMM) esophagus strip assayCompound was evaluated for the agonistic activity towards 5-hydroxytryptamine 4 receptor using the rat tunica muscularis mucosae (TMM) esophagus strip assay
ChEMBL 321 3 2 4 1.6 COc1cc(N)c(Cl)cc1C(=O)N[C@H]1C2CC3CN(C2)CC31 10.1016/S0960-894X(00)80441-2
127042089 136101 0 None - 1 Human 7.4 pEC50 = 7.4 Functional
Agonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assayAgonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assay
ChEMBL 384 5 2 5 3.0 CC(C)c1nc(C(=O)NC2CC3CCC(C2)N3CC(C)(C)O)c2ccccn12 10.1016/j.ejmech.2015.08.051
CHEMBL3739826 136101 0 None - 1 Human 7.4 pEC50 = 7.4 Functional
Agonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assayAgonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assay
ChEMBL 384 5 2 5 3.0 CC(C)c1nc(C(=O)NC2CC3CCC(C2)N3CC(C)(C)O)c2ccccn12 10.1016/j.ejmech.2015.08.051
19081862 203683 0 None - 1 Human 7.4 pEC50 = 7.4 Functional
Agonist activity against 5-HT4 receptor in rat esophageal muscularis mucosaeAgonist activity against 5-HT4 receptor in rat esophageal muscularis mucosae
ChEMBL 310 5 1 4 3.2 COc1cc(N)c(Cl)cc1C(=O)CCC1CCN(C)CC1 10.1016/S0960-894X(01)80413-3
CHEMBL80015 203683 0 None - 1 Human 7.4 pEC50 = 7.4 Functional
Agonist activity against 5-HT4 receptor in rat esophageal muscularis mucosaeAgonist activity against 5-HT4 receptor in rat esophageal muscularis mucosae
ChEMBL 310 5 1 4 3.2 COc1cc(N)c(Cl)cc1C(=O)CCC1CCN(C)CC1 10.1016/S0960-894X(01)80413-3
9799010 204165 0 None 1 2 Human 7.4 pEC50 = 7.4 Functional
Agonist activity against 5-HT4 receptor in rat esophageal muscularis mucosaeAgonist activity against 5-HT4 receptor in rat esophageal muscularis mucosae
ChEMBL 324 7 1 4 3.8 COc1cc(N)c(Cl)cc1C(=O)CCCCN1CCCCC1 10.1016/S0960-894X(01)80413-3
CHEMBL83841 204165 0 None 1 2 Human 7.4 pEC50 = 7.4 Functional
Agonist activity against 5-HT4 receptor in rat esophageal muscularis mucosaeAgonist activity against 5-HT4 receptor in rat esophageal muscularis mucosae
ChEMBL 324 7 1 4 3.8 COc1cc(N)c(Cl)cc1C(=O)CCCCN1CCCCC1 10.1016/S0960-894X(01)80413-3
10757502 91929739 193455 0 None - 1 Human 7.4 pEC50 = 7.4 Functional
Agonist activity at human 5HT4C receptor expressed at 100 fold physiological-level in HEK293 cells assessed as cAMP accumulationAgonist activity at human 5HT4C receptor expressed at 100 fold physiological-level in HEK293 cells assessed as cAMP accumulation
ChEMBL 312 3 2 4 2.6 CC(C)n1nc(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3)c2ccccc21 10.1016/j.bmcl.2012.05.034
CHEMBL550064 193455 0 None - 1 Human 7.4 pEC50 = 7.4 Functional
Agonist activity at human 5HT4C receptor expressed at 100 fold physiological-level in HEK293 cells assessed as cAMP accumulationAgonist activity at human 5HT4C receptor expressed at 100 fold physiological-level in HEK293 cells assessed as cAMP accumulation
ChEMBL 312 3 2 4 2.6 CC(C)n1nc(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3)c2ccccc21 10.1016/j.bmcl.2012.05.034
10757502 91929739 193455 0 None - 1 Human 7.4 pEC50 = 7.4 Functional
Agonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assayAgonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assay
ChEMBL 312 3 2 4 2.6 CC(C)n1nc(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3)c2ccccc21 10.1021/jm900881j
CHEMBL550064 193455 0 None - 1 Human 7.4 pEC50 = 7.4 Functional
Agonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assayAgonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assay
ChEMBL 312 3 2 4 2.6 CC(C)n1nc(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3)c2ccccc21 10.1021/jm900881j
44247808 193709 0 None - 1 Human 7.4 pEC50 = 7.4 Functional
Agonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assayAgonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assay
ChEMBL 395 10 2 4 4.5 CCCCCCCCN1CCC(NC(=O)c2cc(Cl)c(N)cc2OC)CC1 10.1021/jm900881j
CHEMBL551940 193709 0 None - 1 Human 7.4 pEC50 = 7.4 Functional
Agonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assayAgonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assay
ChEMBL 395 10 2 4 4.5 CCCCCCCCN1CCC(NC(=O)c2cc(Cl)c(N)cc2OC)CC1 10.1021/jm900881j
44248187 91900482 193710 0 None - 1 Human 7.4 pEC50 = 7.4 Functional
Agonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assayAgonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assay
ChEMBL 409 7 1 4 4.5 CCCCCN1[C@H]2CC[C@@H]1C[C@H](NC(=O)c1cc3ccccc3n(C(C)C)c1=O)C2 10.1021/jm900881j
CHEMBL551941 193710 0 None - 1 Human 7.4 pEC50 = 7.4 Functional
Agonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assayAgonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assay
ChEMBL 409 7 1 4 4.5 CCCCCN1[C@H]2CC[C@@H]1C[C@H](NC(=O)c1cc3ccccc3n(C(C)C)c1=O)C2 10.1021/jm900881j
44248070 194151 0 None - 1 Human 7.4 pEC50 = 7.4 Functional
Agonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assayAgonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assay
ChEMBL 557 13 2 7 3.0 COc1cc(N)c(Cl)cc1C(=O)NC1CCN(CCCCCCCCN2CCN(S(C)(=O)=O)CC2)CC1 10.1021/jm900881j
CHEMBL558261 194151 0 None - 1 Human 7.4 pEC50 = 7.4 Functional
Agonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assayAgonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assay
ChEMBL 557 13 2 7 3.0 COc1cc(N)c(Cl)cc1C(=O)NC1CCN(CCCCCCCCN2CCN(S(C)(=O)=O)CC2)CC1 10.1021/jm900881j
44249056 91900483 194663 0 None - 1 Human 7.4 pEC50 = 7.4 Functional
Agonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assayAgonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assay
ChEMBL 451 10 1 4 5.7 CCCCCCCCN1[C@H]2CC[C@@H]1C[C@H](NC(=O)c1cc3ccccc3n(C(C)C)c1=O)C2 10.1021/jm900881j
CHEMBL562400 194663 0 None - 1 Human 7.4 pEC50 = 7.4 Functional
Agonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assayAgonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assay
ChEMBL 451 10 1 4 5.7 CCCCCCCCN1[C@H]2CC[C@@H]1C[C@H](NC(=O)c1cc3ccccc3n(C(C)C)c1=O)C2 10.1021/jm900881j
9799010 204165 0 None -1 2 Rat 7.4 pEC50 = 7.4 Functional
Compound was tested against 5-HT4 receptor through agonism of 5-HT mediated relaxation of rat, carbachol contracted esophageal muscularis mucosaeCompound was tested against 5-HT4 receptor through agonism of 5-HT mediated relaxation of rat, carbachol contracted esophageal muscularis mucosae
ChEMBL 324 7 1 4 3.8 COc1cc(N)c(Cl)cc1C(=O)CCCCN1CCCCC1 10.1016/S0960-894X(01)80414-5
CHEMBL83841 204165 0 None -1 2 Rat 7.4 pEC50 = 7.4 Functional
Compound was tested against 5-HT4 receptor through agonism of 5-HT mediated relaxation of rat, carbachol contracted esophageal muscularis mucosaeCompound was tested against 5-HT4 receptor through agonism of 5-HT mediated relaxation of rat, carbachol contracted esophageal muscularis mucosae
ChEMBL 324 7 1 4 3.8 COc1cc(N)c(Cl)cc1C(=O)CCCCN1CCCCC1 10.1016/S0960-894X(01)80414-5
9817713 193169 53 None - 1 Human 6.4 pEC50 = 6.4 Functional
Agonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assayAgonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assay
ChEMBL 297 4 3 4 1.7 COc1cc(N)c(Cl)cc1C(=O)NCC1CCNCC1 10.1021/jm900881j
CHEMBL539652 193169 53 None - 1 Human 6.4 pEC50 = 6.4 Functional
Agonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assayAgonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assay
ChEMBL 297 4 3 4 1.7 COc1cc(N)c(Cl)cc1C(=O)NCC1CCNCC1 10.1021/jm900881j
42499 193268 20 None - 1 Human 6.4 pEC50 = 6.4 Functional
Agonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assayAgonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assay
ChEMBL 283 3 3 4 1.4 COc1cc(N)c(Cl)cc1C(=O)NC1CCNCC1 10.1021/jm900881j
CHEMBL541969 193268 20 None - 1 Human 6.4 pEC50 = 6.4 Functional
Agonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assayAgonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assay
ChEMBL 283 3 3 4 1.4 COc1cc(N)c(Cl)cc1C(=O)NC1CCNCC1 10.1021/jm900881j
44247947 193663 0 None - 1 Human 6.4 pEC50 = 6.4 Functional
Agonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assayAgonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assay
ChEMBL 433 9 3 6 2.2 COc1cc(N)c(Cl)cc1C(=O)NC1CCN(CCCCCS(=O)(=O)O)CC1 10.1021/jm900881j
CHEMBL551678 193663 0 None - 1 Human 6.4 pEC50 = 6.4 Functional
Agonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assayAgonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assay
ChEMBL 433 9 3 6 2.2 COc1cc(N)c(Cl)cc1C(=O)NC1CCN(CCCCCS(=O)(=O)O)CC1 10.1021/jm900881j
235 2527 36 None -1 4 Guinea pig 8.4 pEC50 = 8.4 Functional
5-hydroxytryptamine 4 receptor agonist activity as increased response to electrical stimulation in guinea pig ileum5-hydroxytryptamine 4 receptor agonist activity as increased response to electrical stimulation in guinea pig ileum
ChEMBL 312 5 1 5 2.6 COc1cc(N)c(cc1C(=O)OCCN1CCCCC1)Cl 10.1016/S0960-894X(01)80508-4
5311299 2527 36 None -1 4 Guinea pig 8.4 pEC50 = 8.4 Functional
5-hydroxytryptamine 4 receptor agonist activity as increased response to electrical stimulation in guinea pig ileum5-hydroxytryptamine 4 receptor agonist activity as increased response to electrical stimulation in guinea pig ileum
ChEMBL 312 5 1 5 2.6 COc1cc(N)c(cc1C(=O)OCCN1CCCCC1)Cl 10.1016/S0960-894X(01)80508-4
CHEMBL286136 2527 36 None -1 4 Guinea pig 8.4 pEC50 = 8.4 Functional
5-hydroxytryptamine 4 receptor agonist activity as increased response to electrical stimulation in guinea pig ileum5-hydroxytryptamine 4 receptor agonist activity as increased response to electrical stimulation in guinea pig ileum
ChEMBL 312 5 1 5 2.6 COc1cc(N)c(cc1C(=O)OCCN1CCCCC1)Cl 10.1016/S0960-894X(01)80508-4
235 2527 36 None -1 4 Guinea pig 8.4 pEC50 = 8.4 Functional
5-hydroxytryptamine 4 receptor agonist activity, concentration which gave 50% increase in the response to electrically-stimulated myenteric plexus and longitudinal muscle of the guinea pig ileum5-hydroxytryptamine 4 receptor agonist activity, concentration which gave 50% increase in the response to electrically-stimulated myenteric plexus and longitudinal muscle of the guinea pig ileum
ChEMBL 312 5 1 5 2.6 COc1cc(N)c(cc1C(=O)OCCN1CCCCC1)Cl 10.1021/jm960320m
5311299 2527 36 None -1 4 Guinea pig 8.4 pEC50 = 8.4 Functional
5-hydroxytryptamine 4 receptor agonist activity, concentration which gave 50% increase in the response to electrically-stimulated myenteric plexus and longitudinal muscle of the guinea pig ileum5-hydroxytryptamine 4 receptor agonist activity, concentration which gave 50% increase in the response to electrically-stimulated myenteric plexus and longitudinal muscle of the guinea pig ileum
ChEMBL 312 5 1 5 2.6 COc1cc(N)c(cc1C(=O)OCCN1CCCCC1)Cl 10.1021/jm960320m
CHEMBL286136 2527 36 None -1 4 Guinea pig 8.4 pEC50 = 8.4 Functional
5-hydroxytryptamine 4 receptor agonist activity, concentration which gave 50% increase in the response to electrically-stimulated myenteric plexus and longitudinal muscle of the guinea pig ileum5-hydroxytryptamine 4 receptor agonist activity, concentration which gave 50% increase in the response to electrically-stimulated myenteric plexus and longitudinal muscle of the guinea pig ileum
ChEMBL 312 5 1 5 2.6 COc1cc(N)c(cc1C(=O)OCCN1CCCCC1)Cl 10.1021/jm960320m
15295138 50789 0 None - 1 Guinea pig 8.4 pEC50 = 8.4 Functional
5-hydroxytryptamine 4 receptor agonist activity, concentration which gave 50% increase in the response to electrically-stimulated myenteric plexus and longitudinal muscle of the guinea pig ileum5-hydroxytryptamine 4 receptor agonist activity, concentration which gave 50% increase in the response to electrically-stimulated myenteric plexus and longitudinal muscle of the guinea pig ileum
ChEMBL 328 5 2 6 1.5 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCCC(O)C1 10.1021/jm960320m
CHEMBL157880 50789 0 None - 1 Guinea pig 8.4 pEC50 = 8.4 Functional
5-hydroxytryptamine 4 receptor agonist activity, concentration which gave 50% increase in the response to electrically-stimulated myenteric plexus and longitudinal muscle of the guinea pig ileum5-hydroxytryptamine 4 receptor agonist activity, concentration which gave 50% increase in the response to electrically-stimulated myenteric plexus and longitudinal muscle of the guinea pig ileum
ChEMBL 328 5 2 6 1.5 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCCC(O)C1 10.1021/jm960320m
44582815 172657 0 None - 1 Human 8.4 pEC50 = 8.4 Functional
Agonist activity at human 5HT4 isoform E receptor expressed in rat C6 cells assessed as cAMP accumulation by radio-immunoassay relative to 5HTAgonist activity at human 5HT4 isoform E receptor expressed in rat C6 cells assessed as cAMP accumulation by radio-immunoassay relative to 5HT
ChEMBL 621 11 3 9 3.9 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCC(NC(=O)CCCCN2C(=O)c3cccc4c(N)ccc(c34)C2=O)CC1 10.1021/jm801327q
CHEMBL452353 172657 0 None - 1 Human 8.4 pEC50 = 8.4 Functional
Agonist activity at human 5HT4 isoform E receptor expressed in rat C6 cells assessed as cAMP accumulation by radio-immunoassay relative to 5HTAgonist activity at human 5HT4 isoform E receptor expressed in rat C6 cells assessed as cAMP accumulation by radio-immunoassay relative to 5HT
ChEMBL 621 11 3 9 3.9 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCC(NC(=O)CCCCN2C(=O)c3cccc4c(N)ccc(c34)C2=O)CC1 10.1021/jm801327q
9973683 119302 0 None - 1 Guinea pig 8.4 pEC50 = 8.4 Functional
5-hydroxytryptamine 4 receptor agonist activity, concentration which gave 50% increase in the response to electrically-stimulated myenteric plexus and longitudinal muscle of the guinea pig ileum5-hydroxytryptamine 4 receptor agonist activity, concentration which gave 50% increase in the response to electrically-stimulated myenteric plexus and longitudinal muscle of the guinea pig ileum
ChEMBL 326 5 1 5 3.0 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCCCCC1 10.1021/jm960320m
CHEMBL348311 119302 0 None - 1 Guinea pig 8.4 pEC50 = 8.4 Functional
5-hydroxytryptamine 4 receptor agonist activity, concentration which gave 50% increase in the response to electrically-stimulated myenteric plexus and longitudinal muscle of the guinea pig ileum5-hydroxytryptamine 4 receptor agonist activity, concentration which gave 50% increase in the response to electrically-stimulated myenteric plexus and longitudinal muscle of the guinea pig ileum
ChEMBL 326 5 1 5 3.0 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCCCCC1 10.1021/jm960320m
22708808 205334 0 None - 1 Rat 8.4 pEC50 = 8.4 Functional
In vitro relaxation of carbachol pre-contracted rat oesophageal TMM.In vitro relaxation of carbachol pre-contracted rat oesophageal TMM.
ChEMBL 365 6 2 4 3.1 CCCCN1CCC(CNC(=O)c2cc(Cl)c(N)c3c2OCC3)CC1 10.1016/0960-894X(96)00002-9
CHEMBL91771 205334 0 None - 1 Rat 8.4 pEC50 = 8.4 Functional
In vitro relaxation of carbachol pre-contracted rat oesophageal TMM.In vitro relaxation of carbachol pre-contracted rat oesophageal TMM.
ChEMBL 365 6 2 4 3.1 CCCCN1CCC(CNC(=O)c2cc(Cl)c(N)c3c2OCC3)CC1 10.1016/0960-894X(96)00002-9
155525723 170519 0 None - 1 Human 8.4 pEC50 = 8.4 Functional
Partial agonist activity at human HA-tagged 5HT4 receptor expressed in COS7 cells assessed as induction of cAMP production measured after 10 mins by HTRF assayPartial agonist activity at human HA-tagged 5HT4 receptor expressed in COS7 cells assessed as induction of cAMP production measured after 10 mins by HTRF assay
ChEMBL 515 11 3 7 4.2 COc1cc(/C=C/C(=O)NCCN2CCC(CCC(=O)c3cc(Cl)c(N)cc3OC)CC2)ccc1O 10.1016/j.ejmech.2019.111596
CHEMBL4457426 170519 0 None - 1 Human 8.4 pEC50 = 8.4 Functional
Partial agonist activity at human HA-tagged 5HT4 receptor expressed in COS7 cells assessed as induction of cAMP production measured after 10 mins by HTRF assayPartial agonist activity at human HA-tagged 5HT4 receptor expressed in COS7 cells assessed as induction of cAMP production measured after 10 mins by HTRF assay
ChEMBL 515 11 3 7 4.2 COc1cc(/C=C/C(=O)NCCN2CCC(CCC(=O)c3cc(Cl)c(N)cc3OC)CC2)ccc1O 10.1016/j.ejmech.2019.111596
127041479 136321 0 None - 1 Human 8.3 pEC50 = 8.3 Functional
Agonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assayAgonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assay
ChEMBL 372 8 1 5 2.9 COCCCN1CCC(CNC(=O)c2nc(C(C)C)n3ccccc23)CC1 10.1016/j.ejmech.2015.08.051
CHEMBL3741821 136321 0 None - 1 Human 8.3 pEC50 = 8.3 Functional
Agonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assayAgonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assay
ChEMBL 372 8 1 5 2.9 COCCCN1CCC(CNC(=O)c2nc(C(C)C)n3ccccc23)CC1 10.1016/j.ejmech.2015.08.051
44371317 49793 0 None - 1 Guinea pig 7.4 pEC50 = 7.4 Functional
5-hydroxytryptamine 4 receptor agonist activity, concentration which gave 50% increase in the response to electrically-stimulated myenteric plexus and longitudinal muscle of the guinea pig ileum5-hydroxytryptamine 4 receptor agonist activity, concentration which gave 50% increase in the response to electrically-stimulated myenteric plexus and longitudinal muscle of the guinea pig ileum
ChEMBL 338 5 1 5 3.1 COc1cc(N)c(Cl)cc1C(=O)OCCN1C2CCCC1CC2 10.1021/jm960320m
CHEMBL156965 49793 0 None - 1 Guinea pig 7.4 pEC50 = 7.4 Functional
5-hydroxytryptamine 4 receptor agonist activity, concentration which gave 50% increase in the response to electrically-stimulated myenteric plexus and longitudinal muscle of the guinea pig ileum5-hydroxytryptamine 4 receptor agonist activity, concentration which gave 50% increase in the response to electrically-stimulated myenteric plexus and longitudinal muscle of the guinea pig ileum
ChEMBL 338 5 1 5 3.1 COc1cc(N)c(Cl)cc1C(=O)OCCN1C2CCCC1CC2 10.1021/jm960320m
10447437 49796 0 None - 1 Guinea pig 7.4 pEC50 = 7.4 Functional
5-hydroxytryptamine 4 receptor agonist activity, concentration which gave 50% increase in the response to electrically-stimulated myenteric plexus and longitudinal muscle of the guinea pig ileum5-hydroxytryptamine 4 receptor agonist activity, concentration which gave 50% increase in the response to electrically-stimulated myenteric plexus and longitudinal muscle of the guinea pig ileum
ChEMBL 298 5 1 5 2.2 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCCC1 10.1021/jm960320m
CHEMBL156970 49796 0 None - 1 Guinea pig 7.4 pEC50 = 7.4 Functional
5-hydroxytryptamine 4 receptor agonist activity, concentration which gave 50% increase in the response to electrically-stimulated myenteric plexus and longitudinal muscle of the guinea pig ileum5-hydroxytryptamine 4 receptor agonist activity, concentration which gave 50% increase in the response to electrically-stimulated myenteric plexus and longitudinal muscle of the guinea pig ileum
ChEMBL 298 5 1 5 2.2 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCCC1 10.1021/jm960320m
127038726 136074 0 None - 1 Human 7.4 pEC50 = 7.4 Functional
Agonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assayAgonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assay
ChEMBL 358 5 2 5 2.4 CC(C)c1nc(C(=O)NC2CCN(CC(C)(C)O)CC2)c2ccccn12 10.1016/j.ejmech.2015.08.051
CHEMBL3739611 136074 0 None - 1 Human 7.4 pEC50 = 7.4 Functional
Agonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assayAgonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assay
ChEMBL 358 5 2 5 2.4 CC(C)c1nc(C(=O)NC2CCN(CC(C)(C)O)CC2)c2ccccn12 10.1016/j.ejmech.2015.08.051
127042084 136316 0 None - 1 Human 7.4 pEC50 = 7.4 Functional
Agonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assayAgonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assay
ChEMBL 358 7 1 5 2.7 COCCCN1CCC(NC(=O)c2nc(C(C)C)n3ccccc23)CC1 10.1016/j.ejmech.2015.08.051
CHEMBL3741776 136316 0 None - 1 Human 7.4 pEC50 = 7.4 Functional
Agonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assayAgonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assay
ChEMBL 358 7 1 5 2.7 COCCCN1CCC(NC(=O)c2nc(C(C)C)n3ccccc23)CC1 10.1016/j.ejmech.2015.08.051
44343153 109858 0 None 1 2 Rat 7.4 pEC50 = 7.4 Functional
Efficient 5-hydroxytryptamine 4 agonist in the rat tunica muscularis mucosaeEfficient 5-hydroxytryptamine 4 agonist in the rat tunica muscularis mucosae
ChEMBL 356 2 1 5 3.0 CC(C)n1c(=O)n(C(=O)NC2CC3CCCC(C2)N3C)c2ccccc21 10.1021/jm020099f
CHEMBL324057 109858 0 None 1 2 Rat 7.4 pEC50 = 7.4 Functional
Efficient 5-hydroxytryptamine 4 agonist in the rat tunica muscularis mucosaeEfficient 5-hydroxytryptamine 4 agonist in the rat tunica muscularis mucosae
ChEMBL 356 2 1 5 3.0 CC(C)n1c(=O)n(C(=O)NC2CC3CCCC(C2)N3C)c2ccccc21 10.1021/jm020099f
22400445 202395 0 None - 1 Rat 6.4 pEC50 = 6.4 Functional
Agonist activity against serotonin 5-HT4 receptor in rat tunica muscularis mucosae assayAgonist activity against serotonin 5-HT4 receptor in rat tunica muscularis mucosae assay
ChEMBL 335 4 2 4 2.0 COc1cc(N)c(Cl)cc1C(=O)NCC1C2CC3CC1CN3C2 10.1016/S0960-894X(97)00408-3
CHEMBL70205 202395 0 None - 1 Rat 6.4 pEC50 = 6.4 Functional
Agonist activity against serotonin 5-HT4 receptor in rat tunica muscularis mucosae assayAgonist activity against serotonin 5-HT4 receptor in rat tunica muscularis mucosae assay
ChEMBL 335 4 2 4 2.0 COc1cc(N)c(Cl)cc1C(=O)NCC1C2CC3CC1CN3C2 10.1016/S0960-894X(97)00408-3
131725 198753 2 None -3 2 Guinea pig 7.4 pEC50 = 7.4 Functional
5-hydroxytryptamine 4 receptor agonist activity, concentration which gave 50% increase in the response to electrically-stimulated myenteric plexus and longitudinal muscle of the guinea pig ileum5-hydroxytryptamine 4 receptor agonist activity, concentration which gave 50% increase in the response to electrically-stimulated myenteric plexus and longitudinal muscle of the guinea pig ileum
ChEMBL 342 2 1 5 2.6 CC(C)n1c(=O)n(C(=O)NC2CC3CCC(C2)N3C)c2ccccc21 10.1021/jm960320m
CHEMBL59834 198753 2 None -3 2 Guinea pig 7.4 pEC50 = 7.4 Functional
5-hydroxytryptamine 4 receptor agonist activity, concentration which gave 50% increase in the response to electrically-stimulated myenteric plexus and longitudinal muscle of the guinea pig ileum5-hydroxytryptamine 4 receptor agonist activity, concentration which gave 50% increase in the response to electrically-stimulated myenteric plexus and longitudinal muscle of the guinea pig ileum
ChEMBL 342 2 1 5 2.6 CC(C)n1c(=O)n(C(=O)NC2CC3CCC(C2)N3C)c2ccccc21 10.1021/jm960320m
44281491 111982 0 None - 1 Guinea pig 7.4 pEC50 = 7.4 Functional
5-hydroxytryptamine 4 receptor agonist activity as increased response to electrical stimulation in guinea pig ileum5-hydroxytryptamine 4 receptor agonist activity as increased response to electrical stimulation in guinea pig ileum
ChEMBL 312 4 1 5 2.6 CCN1CCCC(OC(=O)c2cc(Cl)c(N)cc2OC)C1 10.1016/S0960-894X(01)80508-4
CHEMBL32986 111982 0 None - 1 Guinea pig 7.4 pEC50 = 7.4 Functional
5-hydroxytryptamine 4 receptor agonist activity as increased response to electrical stimulation in guinea pig ileum5-hydroxytryptamine 4 receptor agonist activity as increased response to electrical stimulation in guinea pig ileum
ChEMBL 312 4 1 5 2.6 CCN1CCCC(OC(=O)c2cc(Cl)c(N)cc2OC)C1 10.1016/S0960-894X(01)80508-4
10065690 106943 0 None - 1 Rat 6.4 pEC50 = 6.4 Functional
Compound was tested for agonist activity at the 5-hydroxytryptamine 4 receptor in the rat tunica muscularis mucosae (TMM) assayCompound was tested for agonist activity at the 5-hydroxytryptamine 4 receptor in the rat tunica muscularis mucosae (TMM) assay
ChEMBL 337 4 2 4 2.5 COc1cc(N)c(Cl)cc1C(=O)NC[C@@H]1CCN2CCC[C@@]12C 10.1016/j.bmcl.2004.04.021
CHEMBL318154 106943 0 None - 1 Rat 6.4 pEC50 = 6.4 Functional
Compound was tested for agonist activity at the 5-hydroxytryptamine 4 receptor in the rat tunica muscularis mucosae (TMM) assayCompound was tested for agonist activity at the 5-hydroxytryptamine 4 receptor in the rat tunica muscularis mucosae (TMM) assay
ChEMBL 337 4 2 4 2.5 COc1cc(N)c(Cl)cc1C(=O)NC[C@@H]1CCN2CCC[C@@]12C 10.1016/j.bmcl.2004.04.021
127042087 136285 0 None - 1 Human 6.3 pEC50 = 6.3 Functional
Agonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assayAgonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assay
ChEMBL 386 5 1 6 2.1 CC(C)c1nc(C(=O)NCC2CN(C3CCOCC3)CCO2)c2ccccn12 10.1016/j.ejmech.2015.08.051
CHEMBL3741508 136285 0 None - 1 Human 6.3 pEC50 = 6.3 Functional
Agonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assayAgonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assay
ChEMBL 386 5 1 6 2.1 CC(C)c1nc(C(=O)NCC2CN(C3CCOCC3)CCO2)c2ccccn12 10.1016/j.ejmech.2015.08.051
127038354 136112 0 None - 1 Human 7.3 pEC50 = 7.3 Functional
Agonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assayAgonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assay
ChEMBL 386 7 1 5 3.3 COCC(C)(C)CN1CCC(NC(=O)c2nc(C(C)C)n3ccccc23)CC1 10.1016/j.ejmech.2015.08.051
CHEMBL3739933 136112 0 None - 1 Human 7.3 pEC50 = 7.3 Functional
Agonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assayAgonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assay
ChEMBL 386 7 1 5 3.3 COCC(C)(C)CN1CCC(NC(=O)c2nc(C(C)C)n3ccccc23)CC1 10.1016/j.ejmech.2015.08.051
127041786 136058 0 None - 1 Human 7.3 pEC50 = 7.3 Functional
Agonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assayAgonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assay
ChEMBL 340 5 1 4 3.1 CC(C)c1nc(C(=O)NC2CCN(CC3CC3)CC2)c2ccccn12 10.1016/j.ejmech.2015.08.051
CHEMBL3739470 136058 0 None - 1 Human 7.3 pEC50 = 7.3 Functional
Agonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assayAgonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assay
ChEMBL 340 5 1 4 3.1 CC(C)c1nc(C(=O)NC2CCN(CC3CC3)CC2)c2ccccn12 10.1016/j.ejmech.2015.08.051
127042085 136264 0 None - 1 Human 7.3 pEC50 = 7.3 Functional
Agonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assayAgonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assay
ChEMBL 370 4 1 5 2.8 CC(C)c1nc(C(=O)NC2CCN(C3CCOCC3)CC2)c2ccccn12 10.1016/j.ejmech.2015.08.051
CHEMBL3741322 136264 0 None - 1 Human 7.3 pEC50 = 7.3 Functional
Agonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assayAgonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assay
ChEMBL 370 4 1 5 2.8 CC(C)c1nc(C(=O)NC2CCN(C3CCOCC3)CC2)c2ccccn12 10.1016/j.ejmech.2015.08.051
5 139 66 None -13 27 Guinea pig 8.3 pEC50 = 8.3 Functional
5-hydroxytryptamine 4 receptor agonist activity as increased response to electrical stimulation in guinea pig ileum5-hydroxytryptamine 4 receptor agonist activity as increased response to electrical stimulation in guinea pig ileum
ChEMBL 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 10.1016/S0960-894X(01)80508-4
5202 139 66 None -13 27 Guinea pig 8.3 pEC50 = 8.3 Functional
5-hydroxytryptamine 4 receptor agonist activity as increased response to electrical stimulation in guinea pig ileum5-hydroxytryptamine 4 receptor agonist activity as increased response to electrical stimulation in guinea pig ileum
ChEMBL 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 10.1016/S0960-894X(01)80508-4
CHEMBL39 139 66 None -13 27 Guinea pig 8.3 pEC50 = 8.3 Functional
5-hydroxytryptamine 4 receptor agonist activity as increased response to electrical stimulation in guinea pig ileum5-hydroxytryptamine 4 receptor agonist activity as increased response to electrical stimulation in guinea pig ileum
ChEMBL 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 10.1016/S0960-894X(01)80508-4
DB08839 139 66 None -13 27 Guinea pig 8.3 pEC50 = 8.3 Functional
5-hydroxytryptamine 4 receptor agonist activity as increased response to electrical stimulation in guinea pig ileum5-hydroxytryptamine 4 receptor agonist activity as increased response to electrical stimulation in guinea pig ileum
ChEMBL 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 10.1016/S0960-894X(01)80508-4
5 139 66 None -13 27 Guinea pig 8.3 pEC50 = 8.3 Functional
5-hydroxytryptamine 4 receptor agonist activity, concentration which gave 50% increase in the response to electrically-stimulated myenteric plexus and longitudinal muscle of the guinea pig ileum5-hydroxytryptamine 4 receptor agonist activity, concentration which gave 50% increase in the response to electrically-stimulated myenteric plexus and longitudinal muscle of the guinea pig ileum
ChEMBL 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 10.1021/jm960320m
5202 139 66 None -13 27 Guinea pig 8.3 pEC50 = 8.3 Functional
5-hydroxytryptamine 4 receptor agonist activity, concentration which gave 50% increase in the response to electrically-stimulated myenteric plexus and longitudinal muscle of the guinea pig ileum5-hydroxytryptamine 4 receptor agonist activity, concentration which gave 50% increase in the response to electrically-stimulated myenteric plexus and longitudinal muscle of the guinea pig ileum
ChEMBL 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 10.1021/jm960320m
CHEMBL39 139 66 None -13 27 Guinea pig 8.3 pEC50 = 8.3 Functional
5-hydroxytryptamine 4 receptor agonist activity, concentration which gave 50% increase in the response to electrically-stimulated myenteric plexus and longitudinal muscle of the guinea pig ileum5-hydroxytryptamine 4 receptor agonist activity, concentration which gave 50% increase in the response to electrically-stimulated myenteric plexus and longitudinal muscle of the guinea pig ileum
ChEMBL 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 10.1021/jm960320m
DB08839 139 66 None -13 27 Guinea pig 8.3 pEC50 = 8.3 Functional
5-hydroxytryptamine 4 receptor agonist activity, concentration which gave 50% increase in the response to electrically-stimulated myenteric plexus and longitudinal muscle of the guinea pig ileum5-hydroxytryptamine 4 receptor agonist activity, concentration which gave 50% increase in the response to electrically-stimulated myenteric plexus and longitudinal muscle of the guinea pig ileum
ChEMBL 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 10.1021/jm960320m
15295138 50789 0 None - 1 Guinea pig 8.3 pEC50 = 8.3 Functional
5-hydroxytryptamine 4 receptor agonist activity, concentration which gave 50% increase in the response to electrically-stimulated myenteric plexus and longitudinal muscle of the guinea pig ileum5-hydroxytryptamine 4 receptor agonist activity, concentration which gave 50% increase in the response to electrically-stimulated myenteric plexus and longitudinal muscle of the guinea pig ileum
ChEMBL 328 5 2 6 1.5 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCCC(O)C1 10.1021/jm960320m
CHEMBL157880 50789 0 None - 1 Guinea pig 8.3 pEC50 = 8.3 Functional
5-hydroxytryptamine 4 receptor agonist activity, concentration which gave 50% increase in the response to electrically-stimulated myenteric plexus and longitudinal muscle of the guinea pig ileum5-hydroxytryptamine 4 receptor agonist activity, concentration which gave 50% increase in the response to electrically-stimulated myenteric plexus and longitudinal muscle of the guinea pig ileum
ChEMBL 328 5 2 6 1.5 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCCC(O)C1 10.1021/jm960320m
70688534 76060 0 None - 1 Human 8.3 pEC50 = 8.3 Functional
Agonist activity at human 5HT4C receptor expressed at 100 fold physiological-level in HEK293 cells assessed as cAMP accumulationAgonist activity at human 5HT4C receptor expressed at 100 fold physiological-level in HEK293 cells assessed as cAMP accumulation
ChEMBL 441 8 2 6 3.0 CC(C)N(C)CC(O)CN1[C@H]2CC[C@@H]1C[C@H](NC(=O)c1nn(C(C)C)c3ccccc13)C2 10.1016/j.bmcl.2012.05.034
CHEMBL2059579 76060 0 None - 1 Human 8.3 pEC50 = 8.3 Functional
Agonist activity at human 5HT4C receptor expressed at 100 fold physiological-level in HEK293 cells assessed as cAMP accumulationAgonist activity at human 5HT4C receptor expressed at 100 fold physiological-level in HEK293 cells assessed as cAMP accumulation
ChEMBL 441 8 2 6 3.0 CC(C)N(C)CC(O)CN1[C@H]2CC[C@@H]1C[C@H](NC(=O)c1nn(C(C)C)c3ccccc13)C2 10.1016/j.bmcl.2012.05.034
70696826 76061 0 None - 1 Human 8.3 pEC50 = 8.3 Functional
Agonist activity at human 5HT4C receptor expressed at 100 fold physiological-level in HEK293 cells assessed as cAMP accumulationAgonist activity at human 5HT4C receptor expressed at 100 fold physiological-level in HEK293 cells assessed as cAMP accumulation
ChEMBL 467 11 1 5 5.2 CC(C)N(C)CCCCCCN1[C@H]2CC[C@@H]1C[C@H](NC(=O)c1nn(C(C)C)c3ccccc13)C2 10.1016/j.bmcl.2012.05.034
CHEMBL2059580 76061 0 None - 1 Human 8.3 pEC50 = 8.3 Functional
Agonist activity at human 5HT4C receptor expressed at 100 fold physiological-level in HEK293 cells assessed as cAMP accumulationAgonist activity at human 5HT4C receptor expressed at 100 fold physiological-level in HEK293 cells assessed as cAMP accumulation
ChEMBL 467 11 1 5 5.2 CC(C)N(C)CCCCCCN1[C@H]2CC[C@@H]1C[C@H](NC(=O)c1nn(C(C)C)c3ccccc13)C2 10.1016/j.bmcl.2012.05.034
44247941 194115 0 None - 1 Human 8.3 pEC50 = 8.3 Functional
Agonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assayAgonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assay
ChEMBL 498 9 2 6 3.6 COc1cc(N)c(Cl)cc1C(=O)NC1CCN(CCCCCN2C(=O)c3ccccc3C2=O)CC1 10.1021/jm900881j
CHEMBL557867 194115 0 None - 1 Human 8.3 pEC50 = 8.3 Functional
Agonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assayAgonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assay
ChEMBL 498 9 2 6 3.6 COc1cc(N)c(Cl)cc1C(=O)NC1CCN(CCCCCN2C(=O)c3ccccc3C2=O)CC1 10.1021/jm900881j
44248925 194746 0 None - 1 Human 8.3 pEC50 = 8.3 Functional
Agonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assayAgonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assay
ChEMBL 436 9 2 5 3.8 COc1cc(N)c(Cl)cc1C(=O)NC1CCN(CCCCCN2CCCCC2)CC1 10.1021/jm900881j
CHEMBL562902 194746 0 None - 1 Human 8.3 pEC50 = 8.3 Functional
Agonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assayAgonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assay
ChEMBL 436 9 2 5 3.8 COc1cc(N)c(Cl)cc1C(=O)NC1CCN(CCCCCN2CCCCC2)CC1 10.1021/jm900881j
11842633 3918 17 None 7 2 Human 8.3 pEC50 = 8.3 Functional
Agonist activity at human recombinant 5HT4c receptor expressed in HEK293 cells at 10-fold physiological level assessed as accumulation of cAMPAgonist activity at human recombinant 5HT4c receptor expressed in HEK293 cells at 10-fold physiological level assessed as accumulation of cAMP
ChEMBL 504 8 2 7 1.6 O[C@@H](CN(S(=O)(=O)C)C)CN1[C@@H]2CC[C@H]1CC(C2)NC(=O)c1cc2ccccc2n(c1=O)C(C)C 10.1016/j.bmcl.2012.08.051
8425 3918 17 None 7 2 Human 8.3 pEC50 = 8.3 Functional
Agonist activity at human recombinant 5HT4c receptor expressed in HEK293 cells at 10-fold physiological level assessed as accumulation of cAMPAgonist activity at human recombinant 5HT4c receptor expressed in HEK293 cells at 10-fold physiological level assessed as accumulation of cAMP
ChEMBL 504 8 2 7 1.6 O[C@@H](CN(S(=O)(=O)C)C)CN1[C@@H]2CC[C@H]1CC(C2)NC(=O)c1cc2ccccc2n(c1=O)C(C)C 10.1016/j.bmcl.2012.08.051
CHEMBL2087337 3918 17 None 7 2 Human 8.3 pEC50 = 8.3 Functional
Agonist activity at human recombinant 5HT4c receptor expressed in HEK293 cells at 10-fold physiological level assessed as accumulation of cAMPAgonist activity at human recombinant 5HT4c receptor expressed in HEK293 cells at 10-fold physiological level assessed as accumulation of cAMP
ChEMBL 504 8 2 7 1.6 O[C@@H](CN(S(=O)(=O)C)C)CN1[C@@H]2CC[C@H]1CC(C2)NC(=O)c1cc2ccccc2n(c1=O)C(C)C 10.1016/j.bmcl.2012.08.051
70695321 77147 0 None - 1 Human 8.3 pEC50 = 8.3 Functional
Agonist activity at human recombinant 5HT4c receptor expressed in HEK293 cells at 10-fold physiological level assessed as accumulation of cAMPAgonist activity at human recombinant 5HT4c receptor expressed in HEK293 cells at 10-fold physiological level assessed as accumulation of cAMP
ChEMBL 455 7 4 6 1.3 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CC(O)CNC(N)=O)cc2ccccc21 10.1016/j.bmcl.2012.08.051
CHEMBL2087326 77147 0 None - 1 Human 8.3 pEC50 = 8.3 Functional
Agonist activity at human recombinant 5HT4c receptor expressed in HEK293 cells at 10-fold physiological level assessed as accumulation of cAMPAgonist activity at human recombinant 5HT4c receptor expressed in HEK293 cells at 10-fold physiological level assessed as accumulation of cAMP
ChEMBL 455 7 4 6 1.3 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CC(O)CNC(N)=O)cc2ccccc21 10.1016/j.bmcl.2012.08.051
243 3153 85 None 1 2 Human 8.3 pEC50 = 8.3 Functional
Agonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assayAgonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assay
ChEMBL 367 6 2 5 2.1 COCCCN1CCC(CC1)NC(=O)c1cc(Cl)c(c2c1OCC2)N 10.1016/j.ejmech.2015.08.051
3052762 3153 85 None 1 2 Human 8.3 pEC50 = 8.3 Functional
Agonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assayAgonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assay
ChEMBL 367 6 2 5 2.1 COCCCN1CCC(CC1)NC(=O)c1cc(Cl)c(c2c1OCC2)N 10.1016/j.ejmech.2015.08.051
3502 3153 85 None 1 2 Human 8.3 pEC50 = 8.3 Functional
Agonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assayAgonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assay
ChEMBL 367 6 2 5 2.1 COCCCN1CCC(CC1)NC(=O)c1cc(Cl)c(c2c1OCC2)N 10.1016/j.ejmech.2015.08.051
CHEMBL117287 3153 85 None 1 2 Human 8.3 pEC50 = 8.3 Functional
Agonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assayAgonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assay
ChEMBL 367 6 2 5 2.1 COCCCN1CCC(CC1)NC(=O)c1cc(Cl)c(c2c1OCC2)N 10.1016/j.ejmech.2015.08.051
DB06480 3153 85 None 1 2 Human 8.3 pEC50 = 8.3 Functional
Agonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assayAgonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assay
ChEMBL 367 6 2 5 2.1 COCCCN1CCC(CC1)NC(=O)c1cc(Cl)c(c2c1OCC2)N 10.1016/j.ejmech.2015.08.051
10764565 48748 0 None - 1 Guinea pig 8.3 pEC50 = 8.3 Functional
5-hydroxytryptamine 4 receptor agonist activity, concentration which gave 50% increase in the response to electrically-stimulated myenteric plexus and longitudinal muscle of the guinea pig ileum5-hydroxytryptamine 4 receptor agonist activity, concentration which gave 50% increase in the response to electrically-stimulated myenteric plexus and longitudinal muscle of the guinea pig ileum
ChEMBL 339 5 1 4 2.7 COc1cc(N)c(Cl)cc1C(=O)OCC[N+]12CCC(CC1)CC2 10.1021/jm960320m
CHEMBL156088 48748 0 None - 1 Guinea pig 8.3 pEC50 = 8.3 Functional
5-hydroxytryptamine 4 receptor agonist activity, concentration which gave 50% increase in the response to electrically-stimulated myenteric plexus and longitudinal muscle of the guinea pig ileum5-hydroxytryptamine 4 receptor agonist activity, concentration which gave 50% increase in the response to electrically-stimulated myenteric plexus and longitudinal muscle of the guinea pig ileum
ChEMBL 339 5 1 4 2.7 COc1cc(N)c(Cl)cc1C(=O)OCC[N+]12CCC(CC1)CC2 10.1021/jm960320m
1782 2482 81 None -3 12 Guinea pig 8.2 pEC50 = 8.2 Functional
5-hydroxytryptamine 4 receptor agonist activity, concentration which gave 50% increase in the response to electrically-stimulated myenteric plexus and longitudinal muscle of the guinea pig ileum5-hydroxytryptamine 4 receptor agonist activity, concentration which gave 50% increase in the response to electrically-stimulated myenteric plexus and longitudinal muscle of the guinea pig ileum
ChEMBL 299 7 2 4 2.0 CCN(CCNC(=O)c1cc(Cl)c(cc1OC)N)CC 10.1021/jm960320m
241 2482 81 None -3 12 Guinea pig 8.2 pEC50 = 8.2 Functional
5-hydroxytryptamine 4 receptor agonist activity, concentration which gave 50% increase in the response to electrically-stimulated myenteric plexus and longitudinal muscle of the guinea pig ileum5-hydroxytryptamine 4 receptor agonist activity, concentration which gave 50% increase in the response to electrically-stimulated myenteric plexus and longitudinal muscle of the guinea pig ileum
ChEMBL 299 7 2 4 2.0 CCN(CCNC(=O)c1cc(Cl)c(cc1OC)N)CC 10.1021/jm960320m
4168 2482 81 None -3 12 Guinea pig 8.2 pEC50 = 8.2 Functional
5-hydroxytryptamine 4 receptor agonist activity, concentration which gave 50% increase in the response to electrically-stimulated myenteric plexus and longitudinal muscle of the guinea pig ileum5-hydroxytryptamine 4 receptor agonist activity, concentration which gave 50% increase in the response to electrically-stimulated myenteric plexus and longitudinal muscle of the guinea pig ileum
ChEMBL 299 7 2 4 2.0 CCN(CCNC(=O)c1cc(Cl)c(cc1OC)N)CC 10.1021/jm960320m
CHEMBL86 2482 81 None -3 12 Guinea pig 8.2 pEC50 = 8.2 Functional
5-hydroxytryptamine 4 receptor agonist activity, concentration which gave 50% increase in the response to electrically-stimulated myenteric plexus and longitudinal muscle of the guinea pig ileum5-hydroxytryptamine 4 receptor agonist activity, concentration which gave 50% increase in the response to electrically-stimulated myenteric plexus and longitudinal muscle of the guinea pig ileum
ChEMBL 299 7 2 4 2.0 CCN(CCNC(=O)c1cc(Cl)c(cc1OC)N)CC 10.1021/jm960320m
DB01233 2482 81 None -3 12 Guinea pig 8.2 pEC50 = 8.2 Functional
5-hydroxytryptamine 4 receptor agonist activity, concentration which gave 50% increase in the response to electrically-stimulated myenteric plexus and longitudinal muscle of the guinea pig ileum5-hydroxytryptamine 4 receptor agonist activity, concentration which gave 50% increase in the response to electrically-stimulated myenteric plexus and longitudinal muscle of the guinea pig ileum
ChEMBL 299 7 2 4 2.0 CCN(CCNC(=O)c1cc(Cl)c(cc1OC)N)CC 10.1021/jm960320m
127042670 136289 0 None - 1 Human 8.2 pEC50 = 8.2 Functional
Agonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assayAgonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assay
ChEMBL 384 7 2 5 2.4 CC(C)c1nc(C(=O)NC[C@H]2[C@@H]3CN(CC(C)(C)CO)C[C@H]23)c2ccccn12 10.1016/j.ejmech.2015.08.051
CHEMBL3741548 136289 0 None - 1 Human 8.2 pEC50 = 8.2 Functional
Agonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assayAgonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assay
ChEMBL 384 7 2 5 2.4 CC(C)c1nc(C(=O)NC[C@H]2[C@@H]3CN(CC(C)(C)CO)C[C@H]23)c2ccccn12 10.1016/j.ejmech.2015.08.051
49783419 17567 0 None - 1 Human 8.2 pEC50 = 8.2 Functional
Agonist activity at 5HT4 receptor expressed in HEK293/L9 cells by cAMP assayAgonist activity at 5HT4 receptor expressed in HEK293/L9 cells by cAMP assay
ChEMBL 366 6 1 6 2.8 CCCCN1CCC(COC(=O)c2cc(F)c(N)c3c2OCCO3)CC1 10.1021/jm100668r
CHEMBL1258671 17567 0 None - 1 Human 8.2 pEC50 = 8.2 Functional
Agonist activity at 5HT4 receptor expressed in HEK293/L9 cells by cAMP assayAgonist activity at 5HT4 receptor expressed in HEK293/L9 cells by cAMP assay
ChEMBL 366 6 1 6 2.8 CCCCN1CCC(COC(=O)c2cc(F)c(N)c3c2OCCO3)CC1 10.1021/jm100668r
127041785 136167 0 None - 1 Human 7.3 pEC50 = 7.3 Functional
Agonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assayAgonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assay
ChEMBL 314 4 1 4 2.7 CCN1CCC(NC(=O)c2nc(C(C)C)n3ccccc23)CC1 10.1016/j.ejmech.2015.08.051
CHEMBL3740400 136167 0 None - 1 Human 7.3 pEC50 = 7.3 Functional
Agonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assayAgonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assay
ChEMBL 314 4 1 4 2.7 CCN1CCC(NC(=O)c2nc(C(C)C)n3ccccc23)CC1 10.1016/j.ejmech.2015.08.051
44248311 91900487 193957 0 None - 1 Human 7.3 pEC50 = 7.3 Functional
Agonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assayAgonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assay
ChEMBL 596 12 1 6 5.9 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CCCCCCCCN2C(=O)c3ccccc3C2=O)cc2ccccc21 10.1021/jm900881j
CHEMBL556279 193957 0 None - 1 Human 7.3 pEC50 = 7.3 Functional
Agonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assayAgonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assay
ChEMBL 596 12 1 6 5.9 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CCCCCCCCN2C(=O)c3ccccc3C2=O)cc2ccccc21 10.1021/jm900881j
127039505 136160 0 None - 1 Human 6.3 pEC50 = 6.3 Functional
Agonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assayAgonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assay
ChEMBL 353 4 0 6 4.1 CC(C)c1nc(-c2nnc(C3CCN(C(C)C)CC3)o2)c2ccccn12 10.1016/j.ejmech.2015.08.051
CHEMBL3740313 136160 0 None - 1 Human 6.3 pEC50 = 6.3 Functional
Agonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assayAgonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assay
ChEMBL 353 4 0 6 4.1 CC(C)c1nc(-c2nnc(C3CCN(C(C)C)CC3)o2)c2ccccn12 10.1016/j.ejmech.2015.08.051
9819593 98348 2 None -3 2 Rat 6.3 pEC50 = 6.3 Functional
5-hydroxytryptamine 4 receptor agonist activity in the rat esophageal muscularis mucosae5-hydroxytryptamine 4 receptor agonist activity in the rat esophageal muscularis mucosae
ChEMBL 309 3 2 4 1.8 COc1cc(N)c(Cl)cc1C(=O)N[C@H]1CN2CCC1CC2 10.1016/S0960-894X(00)80352-2
CHEMBL27846 98348 2 None -3 2 Rat 6.3 pEC50 = 6.3 Functional
5-hydroxytryptamine 4 receptor agonist activity in the rat esophageal muscularis mucosae5-hydroxytryptamine 4 receptor agonist activity in the rat esophageal muscularis mucosae
ChEMBL 309 3 2 4 1.8 COc1cc(N)c(Cl)cc1C(=O)N[C@H]1CN2CCC1CC2 10.1016/S0960-894X(00)80352-2
44249179 193155 1 None - 1 Human 6.3 pEC50 = 6.3 Functional
Agonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assayAgonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assay
ChEMBL 312 5 3 5 0.6 COc1cc(N)c(Cl)cc1C(=O)NCCN1CCNCC1 10.1021/jm900881j
CHEMBL539212 193155 1 None - 1 Human 6.3 pEC50 = 6.3 Functional
Agonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assayAgonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assay
ChEMBL 312 5 3 5 0.6 COc1cc(N)c(Cl)cc1C(=O)NCCN1CCNCC1 10.1021/jm900881j
9906777 92812 0 None - 1 Rat 7.3 pEC50 = 7.3 Functional
Agonism at 5HT4 receptor in rat tunica muscularis mucosaAgonism at 5HT4 receptor in rat tunica muscularis mucosa
ChEMBL 321 3 2 4 1.6 COc1cc(N)c(Cl)cc1C(=O)N[C@@H]1C2CC3CN(C2)CC31 10.1021/jm0509501
CHEMBL2448165 92812 0 None - 1 Rat 7.3 pEC50 = 7.3 Functional
Agonism at 5HT4 receptor in rat tunica muscularis mucosaAgonism at 5HT4 receptor in rat tunica muscularis mucosa
ChEMBL 321 3 2 4 1.6 COc1cc(N)c(Cl)cc1C(=O)N[C@@H]1C2CC3CN(C2)CC31 10.1021/jm0509501
9885123 107729 1 None - 1 Rat 7.3 pEC50 = 7.3 Functional
Agonist activity against serotonin 5-HT4 receptor in rat tunica muscularis mucosae assayAgonist activity against serotonin 5-HT4 receptor in rat tunica muscularis mucosae assay
ChEMBL 321 3 2 4 1.6 COc1cc(N)c(Cl)cc1C(=O)NC1C2CC3CN(C2)CC31 10.1016/S0960-894X(97)00408-3
CHEMBL319673 107729 1 None - 1 Rat 7.3 pEC50 = 7.3 Functional
Agonist activity against serotonin 5-HT4 receptor in rat tunica muscularis mucosae assayAgonist activity against serotonin 5-HT4 receptor in rat tunica muscularis mucosae assay
ChEMBL 321 3 2 4 1.6 COc1cc(N)c(Cl)cc1C(=O)NC1C2CC3CN(C2)CC31 10.1016/S0960-894X(97)00408-3
CHEMBL558226 107729 1 None - 1 Rat 7.3 pEC50 = 7.3 Functional
Agonist activity against serotonin 5-HT4 receptor in rat tunica muscularis mucosae assayAgonist activity against serotonin 5-HT4 receptor in rat tunica muscularis mucosae assay
ChEMBL 321 3 2 4 1.6 COc1cc(N)c(Cl)cc1C(=O)NC1C2CC3CN(C2)CC31 10.1016/S0960-894X(97)00408-3
235 2527 36 None -5 4 Human 7.3 pEC50 = 7.3 Functional
Agonist activity at human 5HT4 isoform E receptor expressed in rat C6 cells assessed as cAMP accumulation by radio-immunoassay relative to 5HTAgonist activity at human 5HT4 isoform E receptor expressed in rat C6 cells assessed as cAMP accumulation by radio-immunoassay relative to 5HT
ChEMBL 312 5 1 5 2.6 COc1cc(N)c(cc1C(=O)OCCN1CCCCC1)Cl 10.1021/jm801327q
5311299 2527 36 None -5 4 Human 7.3 pEC50 = 7.3 Functional
Agonist activity at human 5HT4 isoform E receptor expressed in rat C6 cells assessed as cAMP accumulation by radio-immunoassay relative to 5HTAgonist activity at human 5HT4 isoform E receptor expressed in rat C6 cells assessed as cAMP accumulation by radio-immunoassay relative to 5HT
ChEMBL 312 5 1 5 2.6 COc1cc(N)c(cc1C(=O)OCCN1CCCCC1)Cl 10.1021/jm801327q
CHEMBL286136 2527 36 None -5 4 Human 7.3 pEC50 = 7.3 Functional
Agonist activity at human 5HT4 isoform E receptor expressed in rat C6 cells assessed as cAMP accumulation by radio-immunoassay relative to 5HTAgonist activity at human 5HT4 isoform E receptor expressed in rat C6 cells assessed as cAMP accumulation by radio-immunoassay relative to 5HT
ChEMBL 312 5 1 5 2.6 COc1cc(N)c(cc1C(=O)OCCN1CCCCC1)Cl 10.1021/jm801327q
9906777 92812 0 None - 1 Rat 7.3 pEC50 = 7.3 Functional
Compound was evaluated for the agonistic activity towards 5-hydroxytryptamine 4 receptor using the rat tunica muscularis mucosae (TMM) esophagus strip assayCompound was evaluated for the agonistic activity towards 5-hydroxytryptamine 4 receptor using the rat tunica muscularis mucosae (TMM) esophagus strip assay
ChEMBL 321 3 2 4 1.6 COc1cc(N)c(Cl)cc1C(=O)N[C@@H]1C2CC3CN(C2)CC31 10.1016/S0960-894X(00)80441-2
CHEMBL2448165 92812 0 None - 1 Rat 7.3 pEC50 = 7.3 Functional
Compound was evaluated for the agonistic activity towards 5-hydroxytryptamine 4 receptor using the rat tunica muscularis mucosae (TMM) esophagus strip assayCompound was evaluated for the agonistic activity towards 5-hydroxytryptamine 4 receptor using the rat tunica muscularis mucosae (TMM) esophagus strip assay
ChEMBL 321 3 2 4 1.6 COc1cc(N)c(Cl)cc1C(=O)N[C@@H]1C2CC3CN(C2)CC31 10.1016/S0960-894X(00)80441-2
127039503 136055 0 None - 1 Human 6.3 pEC50 = 6.3 Functional
Agonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assayAgonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assay
ChEMBL 379 5 0 6 4.5 CC(C)c1nc(-c2nnc(C3CCN(CC4CCC4)CC3)o2)c2ccccn12 10.1016/j.ejmech.2015.08.051
CHEMBL3739455 136055 0 None - 1 Human 6.3 pEC50 = 6.3 Functional
Agonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assayAgonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assay
ChEMBL 379 5 0 6 4.5 CC(C)c1nc(-c2nnc(C3CCN(CC4CCC4)CC3)o2)c2ccccn12 10.1016/j.ejmech.2015.08.051
127039169 136237 0 None - 1 Human 7.3 pEC50 = 7.3 Functional
Agonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assayAgonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assay
ChEMBL 412 6 1 5 3.7 CC(C)c1nc(C(=O)NCC2(C)CCN(CC3CCOCC3)CC2)c2ccccn12 10.1016/j.ejmech.2015.08.051
CHEMBL3741062 136237 0 None - 1 Human 7.3 pEC50 = 7.3 Functional
Agonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assayAgonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assay
ChEMBL 412 6 1 5 3.7 CC(C)c1nc(C(=O)NCC2(C)CCN(CC3CCOCC3)CC2)c2ccccn12 10.1016/j.ejmech.2015.08.051
44288600 100648 0 None -1 2 Rat 6.3 pEC50 = 6.3 Functional
Compound was evaluated for the agonistic activity towards 5-hydroxytryptamine 4 receptor using the rat tunica muscularis mucosae (TMM) esophagus strip assayCompound was evaluated for the agonistic activity towards 5-hydroxytryptamine 4 receptor using the rat tunica muscularis mucosae (TMM) esophagus strip assay
ChEMBL 335 3 2 4 2.0 COc1cc(N)c(Cl)cc1C(=O)NC1C2CC3CC1CN(C3)C2 10.1016/S0960-894X(00)80441-2
CHEMBL295155 100648 0 None -1 2 Rat 6.3 pEC50 = 6.3 Functional
Compound was evaluated for the agonistic activity towards 5-hydroxytryptamine 4 receptor using the rat tunica muscularis mucosae (TMM) esophagus strip assayCompound was evaluated for the agonistic activity towards 5-hydroxytryptamine 4 receptor using the rat tunica muscularis mucosae (TMM) esophagus strip assay
ChEMBL 335 3 2 4 2.0 COc1cc(N)c(Cl)cc1C(=O)NC1C2CC3CC1CN(C3)C2 10.1016/S0960-894X(00)80441-2
240 931 39 None -14 18 Rat 7.3 pEC50 = 7.3 Functional
Agonism at 5HT4 receptor in rat tunica muscularis mucosaAgonism at 5HT4 receptor in rat tunica muscularis mucosa
ChEMBL 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N 10.1021/jm0509501
2769 931 39 None -14 18 Rat 7.3 pEC50 = 7.3 Functional
Agonism at 5HT4 receptor in rat tunica muscularis mucosaAgonism at 5HT4 receptor in rat tunica muscularis mucosa
ChEMBL 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N 10.1021/jm0509501
44279790 931 39 None -14 18 Rat 7.3 pEC50 = 7.3 Functional
Agonism at 5HT4 receptor in rat tunica muscularis mucosaAgonism at 5HT4 receptor in rat tunica muscularis mucosa
ChEMBL 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N 10.1021/jm0509501
660 931 39 None -14 18 Rat 7.3 pEC50 = 7.3 Functional
Agonism at 5HT4 receptor in rat tunica muscularis mucosaAgonism at 5HT4 receptor in rat tunica muscularis mucosa
ChEMBL 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N 10.1021/jm0509501
CHEMBL1729 931 39 None -14 18 Rat 7.3 pEC50 = 7.3 Functional
Agonism at 5HT4 receptor in rat tunica muscularis mucosaAgonism at 5HT4 receptor in rat tunica muscularis mucosa
ChEMBL 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N 10.1021/jm0509501
CHEMBL560739 931 39 None -14 18 Rat 7.3 pEC50 = 7.3 Functional
Agonism at 5HT4 receptor in rat tunica muscularis mucosaAgonism at 5HT4 receptor in rat tunica muscularis mucosa
ChEMBL 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N 10.1021/jm0509501
DB00604 931 39 None -14 18 Rat 7.3 pEC50 = 7.3 Functional
Agonism at 5HT4 receptor in rat tunica muscularis mucosaAgonism at 5HT4 receptor in rat tunica muscularis mucosa
ChEMBL 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N 10.1021/jm0509501
240 931 39 None -14 18 Rat 7.3 pEC50 = 7.3 Functional
Compound was evaluated for the agonistic activity towards 5-hydroxytryptamine 4 receptor using the rat tunica muscularis mucosae (TMM) esophagus strip assayCompound was evaluated for the agonistic activity towards 5-hydroxytryptamine 4 receptor using the rat tunica muscularis mucosae (TMM) esophagus strip assay
ChEMBL 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N 10.1016/S0960-894X(00)80441-2
2769 931 39 None -14 18 Rat 7.3 pEC50 = 7.3 Functional
Compound was evaluated for the agonistic activity towards 5-hydroxytryptamine 4 receptor using the rat tunica muscularis mucosae (TMM) esophagus strip assayCompound was evaluated for the agonistic activity towards 5-hydroxytryptamine 4 receptor using the rat tunica muscularis mucosae (TMM) esophagus strip assay
ChEMBL 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N 10.1016/S0960-894X(00)80441-2
44279790 931 39 None -14 18 Rat 7.3 pEC50 = 7.3 Functional
Compound was evaluated for the agonistic activity towards 5-hydroxytryptamine 4 receptor using the rat tunica muscularis mucosae (TMM) esophagus strip assayCompound was evaluated for the agonistic activity towards 5-hydroxytryptamine 4 receptor using the rat tunica muscularis mucosae (TMM) esophagus strip assay
ChEMBL 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N 10.1016/S0960-894X(00)80441-2
660 931 39 None -14 18 Rat 7.3 pEC50 = 7.3 Functional
Compound was evaluated for the agonistic activity towards 5-hydroxytryptamine 4 receptor using the rat tunica muscularis mucosae (TMM) esophagus strip assayCompound was evaluated for the agonistic activity towards 5-hydroxytryptamine 4 receptor using the rat tunica muscularis mucosae (TMM) esophagus strip assay
ChEMBL 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N 10.1016/S0960-894X(00)80441-2
CHEMBL1729 931 39 None -14 18 Rat 7.3 pEC50 = 7.3 Functional
Compound was evaluated for the agonistic activity towards 5-hydroxytryptamine 4 receptor using the rat tunica muscularis mucosae (TMM) esophagus strip assayCompound was evaluated for the agonistic activity towards 5-hydroxytryptamine 4 receptor using the rat tunica muscularis mucosae (TMM) esophagus strip assay
ChEMBL 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N 10.1016/S0960-894X(00)80441-2
CHEMBL560739 931 39 None -14 18 Rat 7.3 pEC50 = 7.3 Functional
Compound was evaluated for the agonistic activity towards 5-hydroxytryptamine 4 receptor using the rat tunica muscularis mucosae (TMM) esophagus strip assayCompound was evaluated for the agonistic activity towards 5-hydroxytryptamine 4 receptor using the rat tunica muscularis mucosae (TMM) esophagus strip assay
ChEMBL 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N 10.1016/S0960-894X(00)80441-2
DB00604 931 39 None -14 18 Rat 7.3 pEC50 = 7.3 Functional
Compound was evaluated for the agonistic activity towards 5-hydroxytryptamine 4 receptor using the rat tunica muscularis mucosae (TMM) esophagus strip assayCompound was evaluated for the agonistic activity towards 5-hydroxytryptamine 4 receptor using the rat tunica muscularis mucosae (TMM) esophagus strip assay
ChEMBL 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N 10.1016/S0960-894X(00)80441-2
6604914 99919 2 None -1 2 Rat 7.3 pEC50 = 7.3 Functional
In vitro relaxation of carbachol pre-contracted rat oesophageal TMM.In vitro relaxation of carbachol pre-contracted rat oesophageal TMM.
ChEMBL 309 3 2 4 1.8 COc1cc(N)c(Cl)cc1C(=O)N[C@@H]1CN2CCC1CC2 10.1016/0960-894X(96)00002-9
CHEMBL28992 99919 2 None -1 2 Rat 7.3 pEC50 = 7.3 Functional
In vitro relaxation of carbachol pre-contracted rat oesophageal TMM.In vitro relaxation of carbachol pre-contracted rat oesophageal TMM.
ChEMBL 309 3 2 4 1.8 COc1cc(N)c(Cl)cc1C(=O)N[C@@H]1CN2CCC1CC2 10.1016/0960-894X(96)00002-9
127041782 136056 0 None - 1 Human 7.3 pEC50 = 7.3 Functional
Agonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assayAgonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assay
ChEMBL 414 6 2 6 2.4 CC(C)c1nc(C(=O)NCC2(O)CCN(CC3CCOCC3)CC2)c2ccccn12 10.1016/j.ejmech.2015.08.051
CHEMBL3739459 136056 0 None - 1 Human 7.3 pEC50 = 7.3 Functional
Agonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assayAgonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assay
ChEMBL 414 6 2 6 2.4 CC(C)c1nc(C(=O)NCC2(O)CCN(CC3CCOCC3)CC2)c2ccccn12 10.1016/j.ejmech.2015.08.051
54677674 112311 4 None - 1 Human 7.2 pEC50 = 7.2 Functional
Agonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assayAgonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assay
ChEMBL 377 6 2 6 3.0 CC(C)n1c(=O)c(C(=O)NCCCN2CCCCC2)c(O)c2ccsc21 10.1016/j.ejmech.2015.08.051
CHEMBL3291085 112311 4 None - 1 Human 7.2 pEC50 = 7.2 Functional
Agonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assayAgonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assay
ChEMBL 377 6 2 6 3.0 CC(C)n1c(=O)c(C(=O)NCCCN2CCCCC2)c(O)c2ccsc21 10.1016/j.ejmech.2015.08.051
CHEMBL3306918 112311 4 None - 1 Human 7.2 pEC50 = 7.2 Functional
Agonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assayAgonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assay
ChEMBL 377 6 2 6 3.0 CC(C)n1c(=O)c(C(=O)NCCCN2CCCCC2)c(O)c2ccsc21 10.1016/j.ejmech.2015.08.051
10449091 119460 0 None - 1 Guinea pig 8.2 pEC50 = 8.2 Functional
5-hydroxytryptamine 4 receptor agonist activity, concentration which gave 50% increase in the response to electrically-stimulated myenteric plexus and longitudinal muscle of the guinea pig ileum5-hydroxytryptamine 4 receptor agonist activity, concentration which gave 50% increase in the response to electrically-stimulated myenteric plexus and longitudinal muscle of the guinea pig ileum
ChEMBL 326 5 1 5 3.0 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCCCC1C 10.1021/jm960320m
CHEMBL349809 119460 0 None - 1 Guinea pig 8.2 pEC50 = 8.2 Functional
5-hydroxytryptamine 4 receptor agonist activity, concentration which gave 50% increase in the response to electrically-stimulated myenteric plexus and longitudinal muscle of the guinea pig ileum5-hydroxytryptamine 4 receptor agonist activity, concentration which gave 50% increase in the response to electrically-stimulated myenteric plexus and longitudinal muscle of the guinea pig ileum
ChEMBL 326 5 1 5 3.0 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCCCC1C 10.1021/jm960320m
71460941 82269 0 None - 1 Human 8.2 pEC50 = 8.2 Functional
Agonist activity at human 5HT4D receptor expressed in HEK293 cells assessed as cAMP production after 30 mins by HTRF assayAgonist activity at human 5HT4D receptor expressed in HEK293 cells assessed as cAMP production after 30 mins by HTRF assay
ChEMBL 374 8 0 5 5.1 CCCCN1CCC(COc2noc3cccc(OCC(C)(C)C)c23)CC1 10.1021/jm300953p
CHEMBL2179588 82269 0 None - 1 Human 8.2 pEC50 = 8.2 Functional
Agonist activity at human 5HT4D receptor expressed in HEK293 cells assessed as cAMP production after 30 mins by HTRF assayAgonist activity at human 5HT4D receptor expressed in HEK293 cells assessed as cAMP production after 30 mins by HTRF assay
ChEMBL 374 8 0 5 5.1 CCCCN1CCC(COc2noc3cccc(OCC(C)(C)C)c23)CC1 10.1021/jm300953p
5 139 66 None -29 27 Rat 8.2 pEC50 = 8.2 Functional
5-hydroxytryptamine 4 receptor agonist activity in the rat esophageal muscularis mucosae5-hydroxytryptamine 4 receptor agonist activity in the rat esophageal muscularis mucosae
ChEMBL 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 10.1016/S0960-894X(00)80352-2
5202 139 66 None -29 27 Rat 8.2 pEC50 = 8.2 Functional
5-hydroxytryptamine 4 receptor agonist activity in the rat esophageal muscularis mucosae5-hydroxytryptamine 4 receptor agonist activity in the rat esophageal muscularis mucosae
ChEMBL 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 10.1016/S0960-894X(00)80352-2
CHEMBL39 139 66 None -29 27 Rat 8.2 pEC50 = 8.2 Functional
5-hydroxytryptamine 4 receptor agonist activity in the rat esophageal muscularis mucosae5-hydroxytryptamine 4 receptor agonist activity in the rat esophageal muscularis mucosae
ChEMBL 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 10.1016/S0960-894X(00)80352-2
DB08839 139 66 None -29 27 Rat 8.2 pEC50 = 8.2 Functional
5-hydroxytryptamine 4 receptor agonist activity in the rat esophageal muscularis mucosae5-hydroxytryptamine 4 receptor agonist activity in the rat esophageal muscularis mucosae
ChEMBL 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 10.1016/S0960-894X(00)80352-2
135409453 3714 38 None -3 3 Guinea pig 8.2 pEC50 = 8.2 Functional
Agonist activity at 5HT4 receptor in guinea pig colon assessed as longitudinal muscle plexus contractionAgonist activity at 5HT4 receptor in guinea pig colon assessed as longitudinal muscle plexus contraction
ChEMBL 301 7 3 3 2.6 CCCCCN=C(N/N=C/c1c[nH]c2c1cc(OC)cc2)N 10.1016/j.bmcl.2012.05.034
226 3714 38 None -3 3 Guinea pig 8.2 pEC50 = 8.2 Functional
Agonist activity at 5HT4 receptor in guinea pig colon assessed as longitudinal muscle plexus contractionAgonist activity at 5HT4 receptor in guinea pig colon assessed as longitudinal muscle plexus contraction
ChEMBL 301 7 3 3 2.6 CCCCCN=C(N/N=C/c1c[nH]c2c1cc(OC)cc2)N 10.1016/j.bmcl.2012.05.034
CHEMBL76370 3714 38 None -3 3 Guinea pig 8.2 pEC50 = 8.2 Functional
Agonist activity at 5HT4 receptor in guinea pig colon assessed as longitudinal muscle plexus contractionAgonist activity at 5HT4 receptor in guinea pig colon assessed as longitudinal muscle plexus contraction
ChEMBL 301 7 3 3 2.6 CCCCCN=C(N/N=C/c1c[nH]c2c1cc(OC)cc2)N 10.1016/j.bmcl.2012.05.034
135409453 3714 38 None -3 3 Guinea pig 8.2 pEC50 = 8.2 Functional
Agonist activity at 5HT4 receptor in guinea pig colonic longitudinal muscle/myenteric plexus assessed as contractionAgonist activity at 5HT4 receptor in guinea pig colonic longitudinal muscle/myenteric plexus assessed as contraction
ChEMBL 301 7 3 3 2.6 CCCCCN=C(N/N=C/c1c[nH]c2c1cc(OC)cc2)N 10.1016/j.bmcl.2012.08.051
226 3714 38 None -3 3 Guinea pig 8.2 pEC50 = 8.2 Functional
Agonist activity at 5HT4 receptor in guinea pig colonic longitudinal muscle/myenteric plexus assessed as contractionAgonist activity at 5HT4 receptor in guinea pig colonic longitudinal muscle/myenteric plexus assessed as contraction
ChEMBL 301 7 3 3 2.6 CCCCCN=C(N/N=C/c1c[nH]c2c1cc(OC)cc2)N 10.1016/j.bmcl.2012.08.051
CHEMBL76370 3714 38 None -3 3 Guinea pig 8.2 pEC50 = 8.2 Functional
Agonist activity at 5HT4 receptor in guinea pig colonic longitudinal muscle/myenteric plexus assessed as contractionAgonist activity at 5HT4 receptor in guinea pig colonic longitudinal muscle/myenteric plexus assessed as contraction
ChEMBL 301 7 3 3 2.6 CCCCCN=C(N/N=C/c1c[nH]c2c1cc(OC)cc2)N 10.1016/j.bmcl.2012.08.051
44249189 91900488 193731 0 None - 1 Human 8.2 pEC50 = 8.2 Functional
Agonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assayAgonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assay
ChEMBL 447 6 2 6 2.2 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CCS(=O)(=O)O)cc2ccccc21 10.1021/jm900881j
CHEMBL552075 193731 0 None - 1 Human 8.2 pEC50 = 8.2 Functional
Agonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assayAgonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assay
ChEMBL 447 6 2 6 2.2 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CCS(=O)(=O)O)cc2ccccc21 10.1021/jm900881j
44248433 91900494 195066 0 None - 1 Human 8.2 pEC50 = 8.2 Functional
Agonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assayAgonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assay
ChEMBL 529 7 1 7 1.9 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CCN2CCN(S(C)(=O)=O)CC2)cc2ccccc21 10.1021/jm900881j
CHEMBL565146 195066 0 None - 1 Human 8.2 pEC50 = 8.2 Functional
Agonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assayAgonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assay
ChEMBL 529 7 1 7 1.9 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CCN2CCN(S(C)(=O)=O)CC2)cc2ccccc21 10.1021/jm900881j
67276466 77145 0 None - 1 Human 8.2 pEC50 = 8.2 Functional
Agonist activity at human recombinant 5HT4c receptor expressed in HEK293 cells at 10-fold physiological level assessed as accumulation of cAMPAgonist activity at human recombinant 5HT4c receptor expressed in HEK293 cells at 10-fold physiological level assessed as accumulation of cAMP
ChEMBL 454 7 3 6 1.8 CC(=O)NCC(O)CN1[C@H]2CC[C@@H]1C[C@H](NC(=O)c1cc3ccccc3n(C(C)C)c1=O)C2 10.1016/j.bmcl.2012.08.051
CHEMBL2087324 77145 0 None - 1 Human 8.2 pEC50 = 8.2 Functional
Agonist activity at human recombinant 5HT4c receptor expressed in HEK293 cells at 10-fold physiological level assessed as accumulation of cAMPAgonist activity at human recombinant 5HT4c receptor expressed in HEK293 cells at 10-fold physiological level assessed as accumulation of cAMP
ChEMBL 454 7 3 6 1.8 CC(=O)NCC(O)CN1[C@H]2CC[C@@H]1C[C@H](NC(=O)c1cc3ccccc3n(C(C)C)c1=O)C2 10.1016/j.bmcl.2012.08.051
10569278 186667 0 None - 1 Guinea pig 7.2 pEC50 = 7.2 Functional
concentration which gave a 50% increase in the response to electrical stimulation against 5-hydroxytryptamine 4 receptor in the guinea pig ileum. Activity expressed as percent of the maximum 5-HT response given in brackets.concentration which gave a 50% increase in the response to electrical stimulation against 5-hydroxytryptamine 4 receptor in the guinea pig ileum. Activity expressed as percent of the maximum 5-HT response given in brackets.
ChEMBL 341 5 2 5 3.2 COc1cc(N)c(Cl)cc1NC(=O)OCCN1CCC(C)CC1 10.1021/jm960853v
CHEMBL49266 186667 0 None - 1 Guinea pig 7.2 pEC50 = 7.2 Functional
concentration which gave a 50% increase in the response to electrical stimulation against 5-hydroxytryptamine 4 receptor in the guinea pig ileum. Activity expressed as percent of the maximum 5-HT response given in brackets.concentration which gave a 50% increase in the response to electrical stimulation against 5-hydroxytryptamine 4 receptor in the guinea pig ileum. Activity expressed as percent of the maximum 5-HT response given in brackets.
ChEMBL 341 5 2 5 3.2 COc1cc(N)c(Cl)cc1NC(=O)OCCN1CCC(C)CC1 10.1021/jm960853v
6604914 99919 2 None -1 2 Rat 7.2 pEC50 = 7.2 Functional
5-hydroxytryptamine 4 receptor agonist activity in the rat esophageal muscularis mucosae5-hydroxytryptamine 4 receptor agonist activity in the rat esophageal muscularis mucosae
ChEMBL 309 3 2 4 1.8 COc1cc(N)c(Cl)cc1C(=O)N[C@@H]1CN2CCC1CC2 10.1016/S0960-894X(00)80352-2
CHEMBL28992 99919 2 None -1 2 Rat 7.2 pEC50 = 7.2 Functional
5-hydroxytryptamine 4 receptor agonist activity in the rat esophageal muscularis mucosae5-hydroxytryptamine 4 receptor agonist activity in the rat esophageal muscularis mucosae
ChEMBL 309 3 2 4 1.8 COc1cc(N)c(Cl)cc1C(=O)N[C@@H]1CN2CCC1CC2 10.1016/S0960-894X(00)80352-2
19081962 106376 0 None - 1 Human 7.2 pEC50 = 7.2 Functional
Agonist activity against 5-HT4 receptor in rat esophageal muscularis mucosaeAgonist activity against 5-HT4 receptor in rat esophageal muscularis mucosae
ChEMBL 380 10 1 4 5.2 CCCCCCN1CCC(CCC(=O)c2cc(Cl)c(N)cc2OC)CC1 10.1016/S0960-894X(01)80413-3
CHEMBL314489 106376 0 None - 1 Human 7.2 pEC50 = 7.2 Functional
Agonist activity against 5-HT4 receptor in rat esophageal muscularis mucosaeAgonist activity against 5-HT4 receptor in rat esophageal muscularis mucosae
ChEMBL 380 10 1 4 5.2 CCCCCCN1CCC(CCC(=O)c2cc(Cl)c(N)cc2OC)CC1 10.1016/S0960-894X(01)80413-3
20030109 194677 0 None - 1 Human 7.2 pEC50 = 7.2 Functional
Agonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assayAgonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assay
ChEMBL 327 5 3 5 1.1 COc1cc(N)c(Cl)cc1C(=O)NC1CCN(CCO)CC1 10.1021/jm900881j
CHEMBL562477 194677 0 None - 1 Human 7.2 pEC50 = 7.2 Functional
Agonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assayAgonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assay
ChEMBL 327 5 3 5 1.1 COc1cc(N)c(Cl)cc1C(=O)NC1CCN(CCO)CC1 10.1021/jm900881j
71461050 82564 0 None - 1 Human 7.2 pEC50 = 7.2 Functional
Inverse agonist activity at human recombinant 5HT4R expressed in HEK293T cells assessed as Gs activationInverse agonist activity at human recombinant 5HT4R expressed in HEK293T cells assessed as Gs activation
ChEMBL 352 5 0 3 5.0 CCCN1CCC(COc2nc3c(F)cccc3c3ccccc23)CC1 10.1021/jm300943r
CHEMBL2181189 82564 0 None - 1 Human 7.2 pEC50 = 7.2 Functional
Inverse agonist activity at human recombinant 5HT4R expressed in HEK293T cells assessed as Gs activationInverse agonist activity at human recombinant 5HT4R expressed in HEK293T cells assessed as Gs activation
ChEMBL 352 5 0 3 5.0 CCCN1CCC(COc2nc3c(F)cccc3c3ccccc23)CC1 10.1021/jm300943r
44374544 52873 0 None - 1 Rat 7.2 pEC50 = 7.2 Functional
Tested for its agonist potency against the 5-hydroxytryptamine 4 receptor located in the rat esophageal tunica muscularis mucosaeTested for its agonist potency against the 5-hydroxytryptamine 4 receptor located in the rat esophageal tunica muscularis mucosae
ChEMBL 309 3 2 4 1.8 COc1cc(N)c(Cl)cc1C(=O)NC1CCN2CCC1C2 10.1016/S0960-894X(01)81243-9
CHEMBL159825 52873 0 None - 1 Rat 7.2 pEC50 = 7.2 Functional
Tested for its agonist potency against the 5-hydroxytryptamine 4 receptor located in the rat esophageal tunica muscularis mucosaeTested for its agonist potency against the 5-hydroxytryptamine 4 receptor located in the rat esophageal tunica muscularis mucosae
ChEMBL 309 3 2 4 1.8 COc1cc(N)c(Cl)cc1C(=O)NC1CCN2CCC1C2 10.1016/S0960-894X(01)81243-9
44247815 194801 0 None - 1 Human 6.2 pEC50 = 6.2 Functional
Agonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assayAgonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assay
ChEMBL 456 6 2 6 2.4 COc1cc(N)c(Cl)cc1C(=O)NC1CCN(CCN2C(=O)c3ccccc3C2=O)CC1 10.1021/jm900881j
CHEMBL563276 194801 0 None - 1 Human 6.2 pEC50 = 6.2 Functional
Agonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assayAgonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assay
ChEMBL 456 6 2 6 2.4 COc1cc(N)c(Cl)cc1C(=O)NC1CCN(CCN2C(=O)c3ccccc3C2=O)CC1 10.1021/jm900881j
71712613 90948 0 None - 1 Human 6.2 pEC50 = 6.2 Functional
Agonist activity at human recombinant 5HT4 receptor assessed as cAMP accumulationAgonist activity at human recombinant 5HT4 receptor assessed as cAMP accumulation
ChEMBL 464 7 3 7 -0.3 CS(=O)(=O)N1CCN(CC(O)CN2CCC(NC(=O)c3cccc4[nH]cnc34)CC2)CC1 10.1016/j.bmcl.2013.05.018
CHEMBL2402889 90948 0 None - 1 Human 6.2 pEC50 = 6.2 Functional
Agonist activity at human recombinant 5HT4 receptor assessed as cAMP accumulationAgonist activity at human recombinant 5HT4 receptor assessed as cAMP accumulation
ChEMBL 464 7 3 7 -0.3 CS(=O)(=O)N1CCN(CC(O)CN2CCC(NC(=O)c3cccc4[nH]cnc34)CC2)CC1 10.1016/j.bmcl.2013.05.018
44248795 195954 0 None - 1 Human 5.2 pEC50 = 5.2 Functional
Agonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assayAgonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assay
ChEMBL 287 4 3 3 1.9 COc1ccc2[nH]cc(C(=O)NCC3CCNCC3)c2c1 10.1021/jm900881j
CHEMBL570780 195954 0 None - 1 Human 5.2 pEC50 = 5.2 Functional
Agonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assayAgonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assay
ChEMBL 287 4 3 3 1.9 COc1ccc2[nH]cc(C(=O)NCC3CCNCC3)c2c1 10.1021/jm900881j
127041779 136214 0 None - 1 Human 6.2 pEC50 = 6.2 Functional
Agonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assayAgonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assay
ChEMBL 390 8 1 5 3.0 COCCCN1CCC(F)(CNC(=O)c2nc(C(C)C)n3ccccc23)CC1 10.1016/j.ejmech.2015.08.051
CHEMBL3740864 136214 0 None - 1 Human 6.2 pEC50 = 6.2 Functional
Agonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assayAgonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assay
ChEMBL 390 8 1 5 3.0 COCCCN1CCC(F)(CNC(=O)c2nc(C(C)C)n3ccccc23)CC1 10.1016/j.ejmech.2015.08.051
132337 3487 8 None -1 2 Rat 7.2 pEC50 = 7.2 Functional
Tested for agonist activity at the 5-hydroxytryptamine 4 receptor in the rat tunica muscularis mucosae (TMM) assay of racemate mixtureTested for agonist activity at the 5-hydroxytryptamine 4 receptor in the rat tunica muscularis mucosae (TMM) assay of racemate mixture
ChEMBL 323 4 2 4 2.1 COc1cc(N)c(cc1C(=O)NC[C@@H]1CCN2[C@H]1CCC2)Cl 10.1016/j.bmcl.2004.04.021
238 3487 8 None -1 2 Rat 7.2 pEC50 = 7.2 Functional
Tested for agonist activity at the 5-hydroxytryptamine 4 receptor in the rat tunica muscularis mucosae (TMM) assay of racemate mixtureTested for agonist activity at the 5-hydroxytryptamine 4 receptor in the rat tunica muscularis mucosae (TMM) assay of racemate mixture
ChEMBL 323 4 2 4 2.1 COc1cc(N)c(cc1C(=O)NC[C@@H]1CCN2[C@H]1CCC2)Cl 10.1016/j.bmcl.2004.04.021
CHEMBL34291 3487 8 None -1 2 Rat 7.2 pEC50 = 7.2 Functional
Tested for agonist activity at the 5-hydroxytryptamine 4 receptor in the rat tunica muscularis mucosae (TMM) assay of racemate mixtureTested for agonist activity at the 5-hydroxytryptamine 4 receptor in the rat tunica muscularis mucosae (TMM) assay of racemate mixture
ChEMBL 323 4 2 4 2.1 COc1cc(N)c(cc1C(=O)NC[C@@H]1CCN2[C@H]1CCC2)Cl 10.1016/j.bmcl.2004.04.021
22400445 202395 0 None - 1 Rat 6.2 pEC50 = 6.2 Functional
Agonist activity against serotonin 5-HT4 receptor in rat tunica muscularis mucosae assayAgonist activity against serotonin 5-HT4 receptor in rat tunica muscularis mucosae assay
ChEMBL 335 4 2 4 2.0 COc1cc(N)c(Cl)cc1C(=O)NCC1C2CC3CC1CN3C2 10.1016/S0960-894X(97)00408-3
CHEMBL70205 202395 0 None - 1 Rat 6.2 pEC50 = 6.2 Functional
Agonist activity against serotonin 5-HT4 receptor in rat tunica muscularis mucosae assayAgonist activity against serotonin 5-HT4 receptor in rat tunica muscularis mucosae assay
ChEMBL 335 4 2 4 2.0 COc1cc(N)c(Cl)cc1C(=O)NCC1C2CC3CC1CN3C2 10.1016/S0960-894X(97)00408-3
42618252 186098 0 None - 1 Human 7.2 pEC50 = 7.2 Functional
Agonist activity at human 5HT4 isoform E receptor expressed in rat C6 cells assessed as cAMP accumulation by radio-immunoassay relative to 5HTAgonist activity at human 5HT4 isoform E receptor expressed in rat C6 cells assessed as cAMP accumulation by radio-immunoassay relative to 5HT
ChEMBL 580 13 3 8 3.0 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCC(CNC(=O)CCCNS(=O)(=O)c2ccc(C)cc2)CC1 10.1021/jm801327q
CHEMBL488325 186098 0 None - 1 Human 7.2 pEC50 = 7.2 Functional
Agonist activity at human 5HT4 isoform E receptor expressed in rat C6 cells assessed as cAMP accumulation by radio-immunoassay relative to 5HTAgonist activity at human 5HT4 isoform E receptor expressed in rat C6 cells assessed as cAMP accumulation by radio-immunoassay relative to 5HT
ChEMBL 580 13 3 8 3.0 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCC(CNC(=O)CCCNS(=O)(=O)c2ccc(C)cc2)CC1 10.1021/jm801327q
44213661 205348 0 None - 1 Rat 8.1 pEC50 = 8.1 Functional
In vitro relaxation of carbachol pre-contracted rat oesophageal TMM.In vitro relaxation of carbachol pre-contracted rat oesophageal TMM.
ChEMBL 338 5 1 5 2.9 Nc1c(Cl)cc(C(=O)OCCCN2CCCCC2)c2c1CCO2 10.1016/0960-894X(96)00002-9
CHEMBL91842 205348 0 None - 1 Rat 8.1 pEC50 = 8.1 Functional
In vitro relaxation of carbachol pre-contracted rat oesophageal TMM.In vitro relaxation of carbachol pre-contracted rat oesophageal TMM.
ChEMBL 338 5 1 5 2.9 Nc1c(Cl)cc(C(=O)OCCCN2CCCCC2)c2c1CCO2 10.1016/0960-894X(96)00002-9
10498232 51091 0 None - 1 Guinea pig 8.1 pEC50 = 8.1 Functional
5-hydroxytryptamine 4 receptor agonist activity, concentration which gave 50% increase in the response to electrically-stimulated myenteric plexus and longitudinal muscle of the guinea pig ileum5-hydroxytryptamine 4 receptor agonist activity, concentration which gave 50% increase in the response to electrically-stimulated myenteric plexus and longitudinal muscle of the guinea pig ileum
ChEMBL 352 5 1 5 3.2 COc1cc(N)c(Cl)cc1C(=O)OCCN1CC2CCC(CC2)C1 10.1021/jm960320m
CHEMBL158147 51091 0 None - 1 Guinea pig 8.1 pEC50 = 8.1 Functional
5-hydroxytryptamine 4 receptor agonist activity, concentration which gave 50% increase in the response to electrically-stimulated myenteric plexus and longitudinal muscle of the guinea pig ileum5-hydroxytryptamine 4 receptor agonist activity, concentration which gave 50% increase in the response to electrically-stimulated myenteric plexus and longitudinal muscle of the guinea pig ileum
ChEMBL 352 5 1 5 3.2 COc1cc(N)c(Cl)cc1C(=O)OCCN1CC2CCC(CC2)C1 10.1021/jm960320m
44248437 193168 0 None - 1 Human 8.1 pEC50 = 8.1 Functional
Agonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assayAgonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assay
ChEMBL 597 12 1 6 6.1 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CCCCCCCN2CCN(c3ccccc3)CC2)cc2ccccc21 10.1021/jm900881j
CHEMBL539651 193168 0 None - 1 Human 8.1 pEC50 = 8.1 Functional
Agonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assayAgonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assay
ChEMBL 597 12 1 6 6.1 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CCCCCCCN2CCN(c3ccccc3)CC2)cc2ccccc21 10.1021/jm900881j
44249315 193505 0 None - 1 Human 8.1 pEC50 = 8.1 Functional
Agonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assayAgonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assay
ChEMBL 331 4 2 6 0.8 CC(C)n1c(=O)n(C(=O)NCCN2CCNCC2)c2ccccc21 10.1021/jm900881j
CHEMBL550459 193505 0 None - 1 Human 8.1 pEC50 = 8.1 Functional
Agonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assayAgonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assay
ChEMBL 331 4 2 6 0.8 CC(C)n1c(=O)n(C(=O)NCCN2CCNCC2)c2ccccc21 10.1021/jm900881j
67276168 77155 0 None - 1 Human 8.1 pEC50 = 8.1 Functional
Agonist activity at human recombinant 5HT4c receptor expressed in HEK293 cells at 10-fold physiological level assessed as accumulation of cAMPAgonist activity at human recombinant 5HT4c receptor expressed in HEK293 cells at 10-fold physiological level assessed as accumulation of cAMP
ChEMBL 490 8 3 7 1.2 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CC(O)CNS(C)(=O)=O)cc2ccccc21 10.1016/j.bmcl.2012.08.051
CHEMBL2087334 77155 0 None - 1 Human 8.1 pEC50 = 8.1 Functional
Agonist activity at human recombinant 5HT4c receptor expressed in HEK293 cells at 10-fold physiological level assessed as accumulation of cAMPAgonist activity at human recombinant 5HT4c receptor expressed in HEK293 cells at 10-fold physiological level assessed as accumulation of cAMP
ChEMBL 490 8 3 7 1.2 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CC(O)CNS(C)(=O)=O)cc2ccccc21 10.1016/j.bmcl.2012.08.051
9861932 201882 0 None - 1 Rat 6.2 pEC50 = 6.2 Functional
Agonist activity against serotonin 5-HT4 receptor in rat tunica muscularis mucosae assayAgonist activity against serotonin 5-HT4 receptor in rat tunica muscularis mucosae assay
ChEMBL 321 3 2 4 1.8 COc1cc(N)c(Cl)cc1C(=O)NC1C2CC3CC1CN3C2 10.1016/S0960-894X(97)00408-3
CHEMBL66768 201882 0 None - 1 Rat 6.2 pEC50 = 6.2 Functional
Agonist activity against serotonin 5-HT4 receptor in rat tunica muscularis mucosae assayAgonist activity against serotonin 5-HT4 receptor in rat tunica muscularis mucosae assay
ChEMBL 321 3 2 4 1.8 COc1cc(N)c(Cl)cc1C(=O)NC1C2CC3CC1CN3C2 10.1016/S0960-894X(97)00408-3
127039168 136357 0 None - 1 Human 7.1 pEC50 = 7.1 Functional
Agonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assayAgonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assay
ChEMBL 388 6 3 6 1.8 CC(C)c1nc(C(=O)NCC2(O)CCN(CC(C)(C)O)CC2)c2ccccn12 10.1016/j.ejmech.2015.08.051
CHEMBL3742145 136357 0 None - 1 Human 7.1 pEC50 = 7.1 Functional
Agonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assayAgonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assay
ChEMBL 388 6 3 6 1.8 CC(C)c1nc(C(=O)NCC2(O)CCN(CC(C)(C)O)CC2)c2ccccn12 10.1016/j.ejmech.2015.08.051
127039506 136057 0 None - 1 Human 6.1 pEC50 = 6.1 Functional
Agonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assayAgonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assay
ChEMBL 383 7 0 7 3.7 COCCCN1CCC(c2nnc(-c3nc(C(C)C)n4ccccc34)o2)CC1 10.1016/j.ejmech.2015.08.051
CHEMBL3739467 136057 0 None - 1 Human 6.1 pEC50 = 6.1 Functional
Agonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assayAgonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assay
ChEMBL 383 7 0 7 3.7 COCCCN1CCC(c2nnc(-c3nc(C(C)C)n4ccccc34)o2)CC1 10.1016/j.ejmech.2015.08.051
6604914 99919 2 None 1 2 Guinea pig 7.1 pEC50 = 7.1 Functional
5-hydroxytryptamine 4 receptor agonist activity, concentration which gave 50% increase in the response to electrically-stimulated myenteric plexus and longitudinal muscle of the guinea pig ileum5-hydroxytryptamine 4 receptor agonist activity, concentration which gave 50% increase in the response to electrically-stimulated myenteric plexus and longitudinal muscle of the guinea pig ileum
ChEMBL 309 3 2 4 1.8 COc1cc(N)c(Cl)cc1C(=O)N[C@@H]1CN2CCC1CC2 10.1021/jm960320m
CHEMBL28992 99919 2 None 1 2 Guinea pig 7.1 pEC50 = 7.1 Functional
5-hydroxytryptamine 4 receptor agonist activity, concentration which gave 50% increase in the response to electrically-stimulated myenteric plexus and longitudinal muscle of the guinea pig ileum5-hydroxytryptamine 4 receptor agonist activity, concentration which gave 50% increase in the response to electrically-stimulated myenteric plexus and longitudinal muscle of the guinea pig ileum
ChEMBL 309 3 2 4 1.8 COc1cc(N)c(Cl)cc1C(=O)N[C@@H]1CN2CCC1CC2 10.1021/jm960320m
71461049 82562 0 None - 1 Human 7.1 pEC50 = 7.1 Functional
Inverse agonist activity at human recombinant 5HT4R expressed in HEK293T cells assessed as Gs activationInverse agonist activity at human recombinant 5HT4R expressed in HEK293T cells assessed as Gs activation
ChEMBL 364 6 0 4 4.9 CCCN1CCC(COc2nc3c(OC)cccc3c3ccccc23)CC1 10.1021/jm300943r
CHEMBL2181187 82562 0 None - 1 Human 7.1 pEC50 = 7.1 Functional
Inverse agonist activity at human recombinant 5HT4R expressed in HEK293T cells assessed as Gs activationInverse agonist activity at human recombinant 5HT4R expressed in HEK293T cells assessed as Gs activation
ChEMBL 364 6 0 4 4.9 CCCN1CCC(COc2nc3c(OC)cccc3c3ccccc23)CC1 10.1021/jm300943r
44248310 194881 0 None - 1 Human 7.1 pEC50 = 7.1 Functional
Agonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assayAgonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assay
ChEMBL 512 6 1 6 3.6 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CCN2C(=O)c3ccccc3C2=O)cc2ccccc21 10.1021/jm900881j
CHEMBL563799 194881 0 None - 1 Human 7.1 pEC50 = 7.1 Functional
Agonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assayAgonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assay
ChEMBL 512 6 1 6 3.6 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CCN2C(=O)c3ccccc3C2=O)cc2ccccc21 10.1021/jm900881j
44575 195839 1 None - 1 Human 7.1 pEC50 = 7.1 Functional
Agonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assayAgonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assay
ChEMBL 311 4 2 4 2.1 CCN1CCC(NC(=O)c2cc(Cl)c(N)cc2OC)CC1 10.1021/jm900881j
CHEMBL570074 195839 1 None - 1 Human 7.1 pEC50 = 7.1 Functional
Agonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assayAgonist activity at human 5HT4C receptor expressed in HEK293 cells assessed as accumulation of cAMP by flash plate adenylyl cyclase activation assay
ChEMBL 311 4 2 4 2.1 CCN1CCC(NC(=O)c2cc(Cl)c(N)cc2OC)CC1 10.1021/jm900881j
240 931 39 None -1 18 Human 7.1 pEC50 = 7.1 Functional
Agonist activity at human recombinant 5HT4 receptor assessed as cAMP accumulationAgonist activity at human recombinant 5HT4 receptor assessed as cAMP accumulation
ChEMBL 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N 10.1016/j.bmcl.2013.05.018
2769 931 39 None -1 18 Human 7.1 pEC50 = 7.1 Functional
Agonist activity at human recombinant 5HT4 receptor assessed as cAMP accumulationAgonist activity at human recombinant 5HT4 receptor assessed as cAMP accumulation
ChEMBL 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N 10.1016/j.bmcl.2013.05.018
44279790 931 39 None -1 18 Human 7.1 pEC50 = 7.1 Functional
Agonist activity at human recombinant 5HT4 receptor assessed as cAMP accumulationAgonist activity at human recombinant 5HT4 receptor assessed as cAMP accumulation
ChEMBL 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N 10.1016/j.bmcl.2013.05.018
660 931 39 None -1 18 Human 7.1 pEC50 = 7.1 Functional
Agonist activity at human recombinant 5HT4 receptor assessed as cAMP accumulationAgonist activity at human recombinant 5HT4 receptor assessed as cAMP accumulation
ChEMBL 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N 10.1016/j.bmcl.2013.05.018
CHEMBL1729 931 39 None -1 18 Human 7.1 pEC50 = 7.1 Functional
Agonist activity at human recombinant 5HT4 receptor assessed as cAMP accumulationAgonist activity at human recombinant 5HT4 receptor assessed as cAMP accumulation
ChEMBL 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N 10.1016/j.bmcl.2013.05.018
CHEMBL560739 931 39 None -1 18 Human 7.1 pEC50 = 7.1 Functional
Agonist activity at human recombinant 5HT4 receptor assessed as cAMP accumulationAgonist activity at human recombinant 5HT4 receptor assessed as cAMP accumulation
ChEMBL 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N 10.1016/j.bmcl.2013.05.018
DB00604 931 39 None -1 18 Human 7.1 pEC50 = 7.1 Functional
Agonist activity at human recombinant 5HT4 receptor assessed as cAMP accumulationAgonist activity at human recombinant 5HT4 receptor assessed as cAMP accumulation
ChEMBL 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N 10.1016/j.bmcl.2013.05.018
5311047 203055 30 None 1 2 Human 7.1 pEC50 = 7.1 Functional
Agonist activity at human recombinant 5HT4c receptor expressed in HEK293 cells at 10-fold physiological level assessed as accumulation of cAMPAgonist activity at human recombinant 5HT4c receptor expressed in HEK293 cells at 10-fold physiological level assessed as accumulation of cAMP
ChEMBL 465 9 2 6 3.4 COc1cc(N)c(Cl)cc1C(=O)N[C@H]1CCN(CCCOc2ccc(F)cc2)C[C@H]1OC 10.1016/j.bmcl.2012.08.051
CHEMBL74656 203055 30 None 1 2 Human 7.1 pEC50 = 7.1 Functional
Agonist activity at human recombinant 5HT4c receptor expressed in HEK293 cells at 10-fold physiological level assessed as accumulation of cAMPAgonist activity at human recombinant 5HT4c receptor expressed in HEK293 cells at 10-fold physiological level assessed as accumulation of cAMP
ChEMBL 465 9 2 6 3.4 COc1cc(N)c(Cl)cc1C(=O)N[C@H]1CCN(CCCOc2ccc(F)cc2)C[C@H]1OC 10.1016/j.bmcl.2012.08.051
1782 2482 81 None -3 12 Human 6.1 pEC50 = 6.1 Functional
Agonist activity against 5-HT4 receptor in rat esophageal muscularis mucosaeAgonist activity against 5-HT4 receptor in rat esophageal muscularis mucosae
ChEMBL 299 7 2 4 2.0 CCN(CCNC(=O)c1cc(Cl)c(cc1OC)N)CC 10.1016/S0960-894X(01)80413-3
241 2482 81 None -3 12 Human 6.1 pEC50 = 6.1 Functional
Agonist activity against 5-HT4 receptor in rat esophageal muscularis mucosaeAgonist activity against 5-HT4 receptor in rat esophageal muscularis mucosae
ChEMBL 299 7 2 4 2.0 CCN(CCNC(=O)c1cc(Cl)c(cc1OC)N)CC 10.1016/S0960-894X(01)80413-3
4168 2482 81 None -3 12 Human 6.1 pEC50 = 6.1 Functional
Agonist activity against 5-HT4 receptor in rat esophageal muscularis mucosaeAgonist activity against 5-HT4 receptor in rat esophageal muscularis mucosae
ChEMBL 299 7 2 4 2.0 CCN(CCNC(=O)c1cc(Cl)c(cc1OC)N)CC 10.1016/S0960-894X(01)80413-3
CHEMBL86 2482 81 None -3 12 Human 6.1 pEC50 = 6.1 Functional
Agonist activity against 5-HT4 receptor in rat esophageal muscularis mucosaeAgonist activity against 5-HT4 receptor in rat esophageal muscularis mucosae
ChEMBL 299 7 2 4 2.0 CCN(CCNC(=O)c1cc(Cl)c(cc1OC)N)CC 10.1016/S0960-894X(01)80413-3
DB01233 2482 81 None -3 12 Human 6.1 pEC50 = 6.1 Functional
Agonist activity against 5-HT4 receptor in rat esophageal muscularis mucosaeAgonist activity against 5-HT4 receptor in rat esophageal muscularis mucosae
ChEMBL 299 7 2 4 2.0 CCN(CCNC(=O)c1cc(Cl)c(cc1OC)N)CC 10.1016/S0960-894X(01)80413-3
1782 2482 81 None -158 12 Rat 6.1 pEC50 = 6.1 Functional
Tested for its agonist potency against the 5-hydroxytryptamine 4 receptor located in the rat esophageal tunica muscularis mucosaeTested for its agonist potency against the 5-hydroxytryptamine 4 receptor located in the rat esophageal tunica muscularis mucosae
ChEMBL 299 7 2 4 2.0 CCN(CCNC(=O)c1cc(Cl)c(cc1OC)N)CC 10.1016/S0960-894X(01)81243-9
241 2482 81 None -158 12 Rat 6.1 pEC50 = 6.1 Functional
Tested for its agonist potency against the 5-hydroxytryptamine 4 receptor located in the rat esophageal tunica muscularis mucosaeTested for its agonist potency against the 5-hydroxytryptamine 4 receptor located in the rat esophageal tunica muscularis mucosae
ChEMBL 299 7 2 4 2.0 CCN(CCNC(=O)c1cc(Cl)c(cc1OC)N)CC 10.1016/S0960-894X(01)81243-9
4168 2482 81 None -158 12 Rat 6.1 pEC50 = 6.1 Functional
Tested for its agonist potency against the 5-hydroxytryptamine 4 receptor located in the rat esophageal tunica muscularis mucosaeTested for its agonist potency against the 5-hydroxytryptamine 4 receptor located in the rat esophageal tunica muscularis mucosae
ChEMBL 299 7 2 4 2.0 CCN(CCNC(=O)c1cc(Cl)c(cc1OC)N)CC 10.1016/S0960-894X(01)81243-9
CHEMBL86 2482 81 None -158 12 Rat 6.1 pEC50 = 6.1 Functional
Tested for its agonist potency against the 5-hydroxytryptamine 4 receptor located in the rat esophageal tunica muscularis mucosaeTested for its agonist potency against the 5-hydroxytryptamine 4 receptor located in the rat esophageal tunica muscularis mucosae
ChEMBL 299 7 2 4 2.0 CCN(CCNC(=O)c1cc(Cl)c(cc1OC)N)CC 10.1016/S0960-894X(01)81243-9
DB01233 2482 81 None -158 12 Rat 6.1 pEC50 = 6.1 Functional
Tested for its agonist potency against the 5-hydroxytryptamine 4 receptor located in the rat esophageal tunica muscularis mucosaeTested for its agonist potency against the 5-hydroxytryptamine 4 receptor located in the rat esophageal tunica muscularis mucosae
ChEMBL 299 7 2 4 2.0 CCN(CCNC(=O)c1cc(Cl)c(cc1OC)N)CC 10.1016/S0960-894X(01)81243-9
44323244 12279 0 None - 1 Rat 8.1 pEC50 = 8.1 Functional
In vitro relaxation of carbachol pre-contracted rat oesophageal TMM.In vitro relaxation of carbachol pre-contracted rat oesophageal TMM.
ChEMBL 378 5 2 3 3.0 CCCC[N+]12CCC(CC1)[C@H](NC(=O)c1cc(Cl)c(N)c3c1OCC3)C2 10.1016/0960-894X(96)00002-9
CHEMBL1185621 12279 0 None - 1 Rat 8.1 pEC50 = 8.1 Functional
In vitro relaxation of carbachol pre-contracted rat oesophageal TMM.In vitro relaxation of carbachol pre-contracted rat oesophageal TMM.
ChEMBL 378 5 2 3 3.0 CCCC[N+]12CCC(CC1)[C@H](NC(=O)c1cc(Cl)c(N)c3c1OCC3)C2 10.1016/0960-894X(96)00002-9
CHEMBL423504 12279 0 None - 1 Rat 8.1 pEC50 = 8.1 Functional
In vitro relaxation of carbachol pre-contracted rat oesophageal TMM.In vitro relaxation of carbachol pre-contracted rat oesophageal TMM.
ChEMBL 378 5 2 3 3.0 CCCC[N+]12CCC(CC1)[C@H](NC(=O)c1cc(Cl)c(N)c3c1OCC3)C2 10.1016/0960-894X(96)00002-9
127037819 136190 0 None - 1 Human 8.1 pEC50 = 8.1 Functional
Agonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assayAgonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assay
ChEMBL 453 6 1 6 2.8 COC(=O)N1CCC(CN2C[C@H]3[C@H](CNC(=O)c4nc(C(C)C)n5ccccc45)[C@H]3C2)CC1 10.1016/j.ejmech.2015.08.051
CHEMBL3740669 136190 0 None - 1 Human 8.1 pEC50 = 8.1 Functional
Agonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assayAgonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assay
ChEMBL 453 6 1 6 2.8 COC(=O)N1CCC(CN2C[C@H]3[C@H](CNC(=O)c4nc(C(C)C)n5ccccc45)[C@H]3C2)CC1 10.1016/j.ejmech.2015.08.051
49783207 17396 0 None - 1 Human 8.1 pEC50 = 8.1 Functional
Agonist activity at 5HT4 receptor expressed in HEK293/L9 cells by cAMP assayAgonist activity at 5HT4 receptor expressed in HEK293/L9 cells by cAMP assay
ChEMBL 362 7 1 6 3.2 CCCCN1CCC(COC(=O)c2ccc(NC)c3c2OCCO3)CC1 10.1021/jm100668r
CHEMBL1258109 17396 0 None - 1 Human 8.1 pEC50 = 8.1 Functional
Agonist activity at 5HT4 receptor expressed in HEK293/L9 cells by cAMP assayAgonist activity at 5HT4 receptor expressed in HEK293/L9 cells by cAMP assay
ChEMBL 362 7 1 6 3.2 CCCCN1CCC(COC(=O)c2ccc(NC)c3c2OCCO3)CC1 10.1021/jm100668r
127039170 136250 0 None - 1 Human 6.1 pEC50 = 6.1 Functional
Agonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assayAgonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assay
ChEMBL 365 4 0 6 4.2 CC(C)c1nc(-c2nnc(C3CCN(C4CCC4)CC3)o2)c2ccccn12 10.1016/j.ejmech.2015.08.051
CHEMBL3741199 136250 0 None - 1 Human 6.1 pEC50 = 6.1 Functional
Agonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assayAgonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assay
ChEMBL 365 4 0 6 4.2 CC(C)c1nc(-c2nnc(C3CCN(C4CCC4)CC3)o2)c2ccccn12 10.1016/j.ejmech.2015.08.051
127039504 136122 0 None - 1 Human 6.1 pEC50 = 6.1 Functional
Agonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assayAgonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assay
ChEMBL 365 5 0 6 4.1 CC(C)c1nc(-c2nnc(C3CCN(CC4CC4)CC3)o2)c2ccccn12 10.1016/j.ejmech.2015.08.051
CHEMBL3740000 136122 0 None - 1 Human 6.1 pEC50 = 6.1 Functional
Agonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assayAgonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assay
ChEMBL 365 5 0 6 4.1 CC(C)c1nc(-c2nnc(C3CCN(CC4CC4)CC3)o2)c2ccccn12 10.1016/j.ejmech.2015.08.051
127042088 136346 0 None - 1 Human 7.1 pEC50 = 7.1 Functional
Agonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assayAgonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assay
ChEMBL 426 5 2 6 2.7 CC(C)c1nc(C(=O)NC2CC3CCC(C2)N3CC2(O)CCOCC2)c2ccccn12 10.1016/j.ejmech.2015.08.051
CHEMBL3742080 136346 0 None - 1 Human 7.1 pEC50 = 7.1 Functional
Agonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assayAgonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assay
ChEMBL 426 5 2 6 2.7 CC(C)c1nc(C(=O)NC2CC3CCC(C2)N3CC2(O)CCOCC2)c2ccccn12 10.1016/j.ejmech.2015.08.051
42618250 168894 0 None - 1 Human 8.1 pEC50 = 8.1 Functional
Agonist activity at human 5HT4 isoform E receptor expressed in rat C6 cells assessed as cAMP accumulation by radio-immunoassay relative to 5HTAgonist activity at human 5HT4 isoform E receptor expressed in rat C6 cells assessed as cAMP accumulation by radio-immunoassay relative to 5HT
ChEMBL 982 28 6 14 5.7 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCC(NC(=O)CCCNCCCc2ccc(CCCNCCCC(=O)NC3CCN(CCOC(=O)c4cc(Cl)c(N)cc4OC)CC3)cc2)CC1 10.1021/jm801327q
CHEMBL442869 168894 0 None - 1 Human 8.1 pEC50 = 8.1 Functional
Agonist activity at human 5HT4 isoform E receptor expressed in rat C6 cells assessed as cAMP accumulation by radio-immunoassay relative to 5HTAgonist activity at human 5HT4 isoform E receptor expressed in rat C6 cells assessed as cAMP accumulation by radio-immunoassay relative to 5HT
ChEMBL 982 28 6 14 5.7 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCC(NC(=O)CCCNCCCc2ccc(CCCNCCCC(=O)NC3CCN(CCOC(=O)c4cc(Cl)c(N)cc4OC)CC3)cc2)CC1 10.1021/jm801327q
44372468 11570 0 None - 1 Rat 8.0 pEC50 = 8.0 Functional
Tested for its agonist potency against the 5-hydroxytryptamine 4 receptor located in the rat esophageal tunica muscularis mucosaeTested for its agonist potency against the 5-hydroxytryptamine 4 receptor located in the rat esophageal tunica muscularis mucosae
ChEMBL 380 6 2 3 3.5 CCCC[N+]12CCCC(C1)C(NC(=O)c1cc(Cl)c(N)cc1OC)CC2 10.1016/S0960-894X(01)81243-9
CHEMBL1181147 11570 0 None - 1 Rat 8.0 pEC50 = 8.0 Functional
Tested for its agonist potency against the 5-hydroxytryptamine 4 receptor located in the rat esophageal tunica muscularis mucosaeTested for its agonist potency against the 5-hydroxytryptamine 4 receptor located in the rat esophageal tunica muscularis mucosae
ChEMBL 380 6 2 3 3.5 CCCC[N+]12CCCC(C1)C(NC(=O)c1cc(Cl)c(N)cc1OC)CC2 10.1016/S0960-894X(01)81243-9
CHEMBL156977 11570 0 None - 1 Rat 8.0 pEC50 = 8.0 Functional
Tested for its agonist potency against the 5-hydroxytryptamine 4 receptor located in the rat esophageal tunica muscularis mucosaeTested for its agonist potency against the 5-hydroxytryptamine 4 receptor located in the rat esophageal tunica muscularis mucosae
ChEMBL 380 6 2 3 3.5 CCCC[N+]12CCCC(C1)C(NC(=O)c1cc(Cl)c(N)cc1OC)CC2 10.1016/S0960-894X(01)81243-9
127039825 136318 0 None - 1 Human 8.0 pEC50 = 8.0 Functional
Agonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assayAgonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assay
ChEMBL 439 5 1 6 2.6 COC(=O)N1CCC(N2C[C@H]3[C@H](CNC(=O)c4nc(C(C)C)n5ccccc45)[C@H]3C2)CC1 10.1016/j.ejmech.2015.08.051
CHEMBL3741787 136318 0 None - 1 Human 8.0 pEC50 = 8.0 Functional
Agonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assayAgonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assay
ChEMBL 439 5 1 6 2.6 COC(=O)N1CCC(N2C[C@H]3[C@H](CNC(=O)c4nc(C(C)C)n5ccccc45)[C@H]3C2)CC1 10.1016/j.ejmech.2015.08.051
439280 119514 104 None -13 7 Rat 8.0 pEC50 = 8.0 Functional
Tested for its agonist potency against the 5-hydroxytryptamine 4 receptor located in the rat esophageal tunica muscularis mucosaeTested for its agonist potency against the 5-hydroxytryptamine 4 receptor located in the rat esophageal tunica muscularis mucosae
ChEMBL 220 3 4 3 0.8 N[C@@H](Cc1c[nH]c2ccc(O)cc12)C(=O)O 10.1016/S0960-894X(01)81243-9
6971044 119514 104 None -13 7 Rat 8.0 pEC50 = 8.0 Functional
Tested for its agonist potency against the 5-hydroxytryptamine 4 receptor located in the rat esophageal tunica muscularis mucosaeTested for its agonist potency against the 5-hydroxytryptamine 4 receptor located in the rat esophageal tunica muscularis mucosae
ChEMBL 220 3 4 3 0.8 N[C@@H](Cc1c[nH]c2ccc(O)cc12)C(=O)O 10.1016/S0960-894X(01)81243-9
CHEMBL350221 119514 104 None -13 7 Rat 8.0 pEC50 = 8.0 Functional
Tested for its agonist potency against the 5-hydroxytryptamine 4 receptor located in the rat esophageal tunica muscularis mucosaeTested for its agonist potency against the 5-hydroxytryptamine 4 receptor located in the rat esophageal tunica muscularis mucosae
ChEMBL 220 3 4 3 0.8 N[C@@H](Cc1c[nH]c2ccc(O)cc12)C(=O)O 10.1016/S0960-894X(01)81243-9
127041481 136310 0 None - 1 Human 8.0 pEC50 = 8.0 Functional
Agonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assayAgonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assay
ChEMBL 354 5 1 4 3.5 CC(C)c1nc(C(=O)NCC2CCN(C3CCC3)CC2)c2ccccn12 10.1016/j.ejmech.2015.08.051
CHEMBL3741733 136310 0 None - 1 Human 8.0 pEC50 = 8.0 Functional
Agonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assayAgonist activity at human 5HT4e receptor expressed in CHO cells assessed as cAMP level after 4 hrs by luciferase reporter gene assay
ChEMBL 354 5 1 4 3.5 CC(C)c1nc(C(=O)NCC2CCN(C3CCC3)CC2)c2ccccn12 10.1016/j.ejmech.2015.08.051
44626294 197321 0 None -2 2 Human 7.1 pEC50 = 7.1 Functional
Agonist activity at human recombinant 5-HT4 receptorAgonist activity at human recombinant 5-HT4 receptor
ChEMBL 517 7 4 7 3.5 COc1cc(N)c(Cl)cc1C(=O)N[C@H]1CCN(C[C@@H]2CCCC[C@@]2(O)c2cccc(O)c2)C[C@H]1OC 10.1016/j.bmcl.2009.08.016
CHEMBL585567 197321 0 None -2 2 Human 7.1 pEC50 = 7.1 Functional
Agonist activity at human recombinant 5-HT4 receptorAgonist activity at human recombinant 5-HT4 receptor
ChEMBL 517 7 4 7 3.5 COc1cc(N)c(Cl)cc1C(=O)N[C@H]1CCN(C[C@@H]2CCCC[C@@]2(O)c2cccc(O)c2)C[C@H]1OC 10.1016/j.bmcl.2009.08.016
6917985 92821 6 None 64 2 Rat 7.0 pEC50 = 7.0 Functional
Agonism at 5HT4 receptor in rat tunica muscularis mucosaAgonism at 5HT4 receptor in rat tunica muscularis mucosa
ChEMBL 323 3 2 4 2.1 COc1cc(N)c(Cl)cc1C(=O)N[C@H]1CCN2CCC[C@@H]1C2 10.1021/jm0509501
CHEMBL2448558 92821 6 None 64 2 Rat 7.0 pEC50 = 7.0 Functional
Agonism at 5HT4 receptor in rat tunica muscularis mucosaAgonism at 5HT4 receptor in rat tunica muscularis mucosa
ChEMBL 323 3 2 4 2.1 COc1cc(N)c(Cl)cc1C(=O)N[C@H]1CCN2CCC[C@@H]1C2 10.1021/jm0509501
44374544 52873 0 None - 1 Rat 7.0 pEC50 = 7.0 Functional
Compound was evaluated for the agonistic activity towards 5-hydroxytryptamine 4 receptor using the rat tunica muscularis mucosae (TMM) esophagus strip assayCompound was evaluated for the agonistic activity towards 5-hydroxytryptamine 4 receptor using the rat tunica muscularis mucosae (TMM) esophagus strip assay
ChEMBL 309 3 2 4 1.8 COc1cc(N)c(Cl)cc1C(=O)NC1CCN2CCC1C2 10.1016/S0960-894X(00)80441-2
CHEMBL159825 52873 0 None - 1 Rat 7.0 pEC50 = 7.0 Functional
Compound was evaluated for the agonistic activity towards 5-hydroxytryptamine 4 receptor using the rat tunica muscularis mucosae (TMM) esophagus strip assayCompound was evaluated for the agonistic activity towards 5-hydroxytryptamine 4 receptor using the rat tunica muscularis mucosae (TMM) esophagus strip assay
ChEMBL 309 3 2 4 1.8 COc1cc(N)c(Cl)cc1C(=O)NC1CCN2CCC1C2 10.1016/S0960-894X(00)80441-2
121881 3434 21 None 281 3 Guinea pig 10.0 pIC50 = 10 Functional
Inhibition of 5-HT-evoked 5-HT4 receptor-mediated contractions in the guinea pig distal colon longitudinal muscle myenteric plexus (LMMP)Inhibition of 5-HT-evoked 5-HT4 receptor-mediated contractions in the guinea pig distal colon longitudinal muscle myenteric plexus (LMMP)
ChEMBL 382 6 1 6 3.4 CCCCN1CCC(CC1)COC(=O)c1cc(Cl)c(c2c1OCCO2)N 10.1021/jm00077a018
256 3434 21 None 281 3 Guinea pig 10.0 pIC50 = 10 Functional
Inhibition of 5-HT-evoked 5-HT4 receptor-mediated contractions in the guinea pig distal colon longitudinal muscle myenteric plexus (LMMP)Inhibition of 5-HT-evoked 5-HT4 receptor-mediated contractions in the guinea pig distal colon longitudinal muscle myenteric plexus (LMMP)
ChEMBL 382 6 1 6 3.4 CCCCN1CCC(CC1)COC(=O)c1cc(Cl)c(c2c1OCCO2)N 10.1021/jm00077a018
CHEMBL68131 3434 21 None 281 3 Guinea pig 10.0 pIC50 = 10 Functional
Inhibition of 5-HT-evoked 5-HT4 receptor-mediated contractions in the guinea pig distal colon longitudinal muscle myenteric plexus (LMMP)Inhibition of 5-HT-evoked 5-HT4 receptor-mediated contractions in the guinea pig distal colon longitudinal muscle myenteric plexus (LMMP)
ChEMBL 382 6 1 6 3.4 CCCCN1CCC(CC1)COC(=O)c1cc(Cl)c(c2c1OCCO2)N 10.1021/jm00077a018
119376 1811 41 None 61 4 Human 9.7 pIC50 = 9.7 Functional
Antagonist activity at human 5HT4ER expressed in CHO cells assessed as reduction in cAMP levelsAntagonist activity at human 5HT4ER expressed in CHO cells assessed as reduction in cAMP levels
ChEMBL 393 7 1 6 1.6 O=C(c1cn(c2c1cccc2)C)OCC1CCN(CC1)CCNS(=O)(=O)C 10.1021/jm300573d
247 1811 41 None 61 4 Human 9.7 pIC50 = 9.7 Functional
Antagonist activity at human 5HT4ER expressed in CHO cells assessed as reduction in cAMP levelsAntagonist activity at human 5HT4ER expressed in CHO cells assessed as reduction in cAMP levels
ChEMBL 393 7 1 6 1.6 O=C(c1cn(c2c1cccc2)C)OCC1CCN(CC1)CCNS(=O)(=O)C 10.1021/jm300573d
CHEMBL33884 1811 41 None 61 4 Human 9.7 pIC50 = 9.7 Functional
Antagonist activity at human 5HT4ER expressed in CHO cells assessed as reduction in cAMP levelsAntagonist activity at human 5HT4ER expressed in CHO cells assessed as reduction in cAMP levels
ChEMBL 393 7 1 6 1.6 O=C(c1cn(c2c1cccc2)C)OCC1CCN(CC1)CCNS(=O)(=O)C 10.1021/jm300573d
10066755 114761 1 None - 1 Guinea pig 9.0 pIC50 = 9 Functional
Inhibition of 5-HT-evoked 5-HT4 receptor-mediated contractions in the guinea pig distal colon longitudinal muscle myenteric plexus (LMMP)Inhibition of 5-HT-evoked 5-HT4 receptor-mediated contractions in the guinea pig distal colon longitudinal muscle myenteric plexus (LMMP)
ChEMBL 354 7 1 5 3.6 CCCCN1CCC(COC(=O)c2cc(Cl)c(N)cc2OC)CC1 10.1021/jm00077a018
CHEMBL334818 114761 1 None - 1 Guinea pig 9.0 pIC50 = 9 Functional
Inhibition of 5-HT-evoked 5-HT4 receptor-mediated contractions in the guinea pig distal colon longitudinal muscle myenteric plexus (LMMP)Inhibition of 5-HT-evoked 5-HT4 receptor-mediated contractions in the guinea pig distal colon longitudinal muscle myenteric plexus (LMMP)
ChEMBL 354 7 1 5 3.6 CCCCN1CCC(COC(=O)c2cc(Cl)c(N)cc2OC)CC1 10.1021/jm00077a018
9998229 20395 0 None - 1 Guinea pig 8.0 pIC50 = 8 Functional
Inhibition of 5-HT-evoked 5-HT4 receptor-mediated contractions in the guinea pig distal colon longitudinal muscle myenteric plexus (LMMP)Inhibition of 5-HT-evoked 5-HT4 receptor-mediated contractions in the guinea pig distal colon longitudinal muscle myenteric plexus (LMMP)
ChEMBL 353 7 2 4 3.2 CCCCN1CCC(CNC(=O)c2cc(Cl)c(N)cc2OC)CC1 10.1021/jm00077a018
CHEMBL130809 20395 0 None - 1 Guinea pig 8.0 pIC50 = 8 Functional
Inhibition of 5-HT-evoked 5-HT4 receptor-mediated contractions in the guinea pig distal colon longitudinal muscle myenteric plexus (LMMP)Inhibition of 5-HT-evoked 5-HT4 receptor-mediated contractions in the guinea pig distal colon longitudinal muscle myenteric plexus (LMMP)
ChEMBL 353 7 2 4 3.2 CCCCN1CCC(CNC(=O)c2cc(Cl)c(N)cc2OC)CC1 10.1021/jm00077a018
10408029 16283 0 None - 1 Guinea pig 7.0 pIC50 = 7 Functional
5-hydroxytryptamine 4 receptor antagonist activity, concentration which gave 50% reduction of the 5-HT-induced contractions in the guinea pig ileum5-hydroxytryptamine 4 receptor antagonist activity, concentration which gave 50% reduction of the 5-HT-induced contractions in the guinea pig ileum
ChEMBL 389 6 1 6 2.9 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCN(c2ccccc2)CC1 10.1021/jm960320m
CHEMBL123377 16283 0 None - 1 Guinea pig 7.0 pIC50 = 7 Functional
5-hydroxytryptamine 4 receptor antagonist activity, concentration which gave 50% reduction of the 5-HT-induced contractions in the guinea pig ileum5-hydroxytryptamine 4 receptor antagonist activity, concentration which gave 50% reduction of the 5-HT-induced contractions in the guinea pig ileum
ChEMBL 389 6 1 6 2.9 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCN(c2ccccc2)CC1 10.1021/jm960320m
10788092 53306 0 None - 1 Guinea pig 7.0 pIC50 = 7 Functional
5-hydroxytryptamine 4 receptor antagonist activity, concentration which gave 50% reduction of the 5-HT-induced contractions in the guinea pig ileum5-hydroxytryptamine 4 receptor antagonist activity, concentration which gave 50% reduction of the 5-HT-induced contractions in the guinea pig ileum
ChEMBL 416 7 1 6 3.7 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCC(C(=O)c2ccccc2)CC1 10.1021/jm960320m
CHEMBL160237 53306 0 None - 1 Guinea pig 7.0 pIC50 = 7 Functional
5-hydroxytryptamine 4 receptor antagonist activity, concentration which gave 50% reduction of the 5-HT-induced contractions in the guinea pig ileum5-hydroxytryptamine 4 receptor antagonist activity, concentration which gave 50% reduction of the 5-HT-induced contractions in the guinea pig ileum
ChEMBL 416 7 1 6 3.7 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCC(C(=O)c2ccccc2)CC1 10.1021/jm960320m
10615288 186426 0 None - 1 Guinea pig 6.0 pIC50 = 6 Functional
The antagonist activity was calculated as the concentration which produced a 50% reduction against 5-hydroxytryptamine 4 receptor in guinea pig ileum.The antagonist activity was calculated as the concentration which produced a 50% reduction against 5-hydroxytryptamine 4 receptor in guinea pig ileum.
ChEMBL 315 7 2 5 2.8 CCN(CC)CCOC(=O)Nc1cc(Cl)c(N)cc1OC 10.1021/jm960853v
CHEMBL49072 186426 0 None - 1 Guinea pig 6.0 pIC50 = 6 Functional
The antagonist activity was calculated as the concentration which produced a 50% reduction against 5-hydroxytryptamine 4 receptor in guinea pig ileum.The antagonist activity was calculated as the concentration which produced a 50% reduction against 5-hydroxytryptamine 4 receptor in guinea pig ileum.
ChEMBL 315 7 2 5 2.8 CCN(CC)CCOC(=O)Nc1cc(Cl)c(N)cc1OC 10.1021/jm960853v
249 2528 3 None - 1 Guinea pig 8.0 pIC50 = 8.0 Functional
5-hydroxytryptamine 4 receptor antagonist activity, concentration which gave 50% reduction of the 5-HT-induced contractions in the guinea pig ileum5-hydroxytryptamine 4 receptor antagonist activity, concentration which gave 50% reduction of the 5-HT-induced contractions in the guinea pig ileum
ChEMBL 340 5 1 5 3.1 COc1cc(N)c(cc1C(=O)OCCN1CC(C)CC(C1)C)Cl 10.1021/jm960320m
9905972 2528 3 None - 1 Guinea pig 8.0 pIC50 = 8.0 Functional
5-hydroxytryptamine 4 receptor antagonist activity, concentration which gave 50% reduction of the 5-HT-induced contractions in the guinea pig ileum5-hydroxytryptamine 4 receptor antagonist activity, concentration which gave 50% reduction of the 5-HT-induced contractions in the guinea pig ileum
ChEMBL 340 5 1 5 3.1 COc1cc(N)c(cc1C(=O)OCCN1CC(C)CC(C1)C)Cl 10.1021/jm960320m
CHEMBL155917 2528 3 None - 1 Guinea pig 8.0 pIC50 = 8.0 Functional
5-hydroxytryptamine 4 receptor antagonist activity, concentration which gave 50% reduction of the 5-HT-induced contractions in the guinea pig ileum5-hydroxytryptamine 4 receptor antagonist activity, concentration which gave 50% reduction of the 5-HT-induced contractions in the guinea pig ileum
ChEMBL 340 5 1 5 3.1 COc1cc(N)c(cc1C(=O)OCCN1CC(C)CC(C1)C)Cl 10.1021/jm960320m
119376 1811 41 None -61 4 Guinea pig 7.9 pIC50 = 7.9 Functional
5-hydroxytryptamine 4 receptor antagonist activity, concentration which gave 50% reduction of the 5-HT-induced contractions in the guinea pig ileum5-hydroxytryptamine 4 receptor antagonist activity, concentration which gave 50% reduction of the 5-HT-induced contractions in the guinea pig ileum
ChEMBL 393 7 1 6 1.6 O=C(c1cn(c2c1cccc2)C)OCC1CCN(CC1)CCNS(=O)(=O)C 10.1021/jm960320m
247 1811 41 None -61 4 Guinea pig 7.9 pIC50 = 7.9 Functional
5-hydroxytryptamine 4 receptor antagonist activity, concentration which gave 50% reduction of the 5-HT-induced contractions in the guinea pig ileum5-hydroxytryptamine 4 receptor antagonist activity, concentration which gave 50% reduction of the 5-HT-induced contractions in the guinea pig ileum
ChEMBL 393 7 1 6 1.6 O=C(c1cn(c2c1cccc2)C)OCC1CCN(CC1)CCNS(=O)(=O)C 10.1021/jm960320m
CHEMBL33884 1811 41 None -61 4 Guinea pig 7.9 pIC50 = 7.9 Functional
5-hydroxytryptamine 4 receptor antagonist activity, concentration which gave 50% reduction of the 5-HT-induced contractions in the guinea pig ileum5-hydroxytryptamine 4 receptor antagonist activity, concentration which gave 50% reduction of the 5-HT-induced contractions in the guinea pig ileum
ChEMBL 393 7 1 6 1.6 O=C(c1cn(c2c1cccc2)C)OCC1CCN(CC1)CCNS(=O)(=O)C 10.1021/jm960320m
249 2528 3 None - 1 Guinea pig 7.9 pIC50 = 7.9 Functional
5-hydroxytryptamine 4 receptor antagonist activity, concentration which gave 50% reduction of the 5-HT-induced contractions in the guinea pig ileum5-hydroxytryptamine 4 receptor antagonist activity, concentration which gave 50% reduction of the 5-HT-induced contractions in the guinea pig ileum
ChEMBL 340 5 1 5 3.1 COc1cc(N)c(cc1C(=O)OCCN1CC(C)CC(C1)C)Cl 10.1021/jm960320m
9905972 2528 3 None - 1 Guinea pig 7.9 pIC50 = 7.9 Functional
5-hydroxytryptamine 4 receptor antagonist activity, concentration which gave 50% reduction of the 5-HT-induced contractions in the guinea pig ileum5-hydroxytryptamine 4 receptor antagonist activity, concentration which gave 50% reduction of the 5-HT-induced contractions in the guinea pig ileum
ChEMBL 340 5 1 5 3.1 COc1cc(N)c(cc1C(=O)OCCN1CC(C)CC(C1)C)Cl 10.1021/jm960320m
CHEMBL155917 2528 3 None - 1 Guinea pig 7.9 pIC50 = 7.9 Functional
5-hydroxytryptamine 4 receptor antagonist activity, concentration which gave 50% reduction of the 5-HT-induced contractions in the guinea pig ileum5-hydroxytryptamine 4 receptor antagonist activity, concentration which gave 50% reduction of the 5-HT-induced contractions in the guinea pig ileum
ChEMBL 340 5 1 5 3.1 COc1cc(N)c(cc1C(=O)OCCN1CC(C)CC(C1)C)Cl 10.1021/jm960320m
10854687 48292 0 None - 1 Guinea pig 6.8 pIC50 = 6.8 Functional
5-hydroxytryptamine 4 receptor antagonist activity, concentration which gave 50% reduction of the 5-HT-induced contractions in the guinea pig ileum5-hydroxytryptamine 4 receptor antagonist activity, concentration which gave 50% reduction of the 5-HT-induced contractions in the guinea pig ileum
ChEMBL 340 5 1 5 3.2 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCCC(C)(C)C1 10.1021/jm960320m
CHEMBL155682 48292 0 None - 1 Guinea pig 6.8 pIC50 = 6.8 Functional
5-hydroxytryptamine 4 receptor antagonist activity, concentration which gave 50% reduction of the 5-HT-induced contractions in the guinea pig ileum5-hydroxytryptamine 4 receptor antagonist activity, concentration which gave 50% reduction of the 5-HT-induced contractions in the guinea pig ileum
ChEMBL 340 5 1 5 3.2 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCCC(C)(C)C1 10.1021/jm960320m
10522209 101226 0 None - 1 Guinea pig 6.8 pIC50 = 6.8 Functional
The antagonist activity was calculated as the concentration which produced a 50% reduction against 5-hydroxytryptamine 4 receptor in guinea pig ileum.The antagonist activity was calculated as the concentration which produced a 50% reduction against 5-hydroxytryptamine 4 receptor in guinea pig ileum.
ChEMBL 355 5 2 5 3.5 COc1cc(N)c(Cl)cc1NC(=O)OCCN1CC(C)CC(C)C1 10.1021/jm960853v
CHEMBL299408 101226 0 None - 1 Guinea pig 6.8 pIC50 = 6.8 Functional
The antagonist activity was calculated as the concentration which produced a 50% reduction against 5-hydroxytryptamine 4 receptor in guinea pig ileum.The antagonist activity was calculated as the concentration which produced a 50% reduction against 5-hydroxytryptamine 4 receptor in guinea pig ileum.
ChEMBL 355 5 2 5 3.5 COc1cc(N)c(Cl)cc1NC(=O)OCCN1CC(C)CC(C)C1 10.1021/jm960853v
235 2527 36 None 1 4 Rat 8.6 pIC50 = 8.6 Functional
5-hydroxytryptamine 4 receptor agonist activity was determined by the relaxation of the carbachol-contracted rat esophageal tunica muscularis mucosae5-hydroxytryptamine 4 receptor agonist activity was determined by the relaxation of the carbachol-contracted rat esophageal tunica muscularis mucosae
ChEMBL 312 5 1 5 2.6 COc1cc(N)c(cc1C(=O)OCCN1CCCCC1)Cl 10.1016/S0960-894X(01)80508-4
5311299 2527 36 None 1 4 Rat 8.6 pIC50 = 8.6 Functional
5-hydroxytryptamine 4 receptor agonist activity was determined by the relaxation of the carbachol-contracted rat esophageal tunica muscularis mucosae5-hydroxytryptamine 4 receptor agonist activity was determined by the relaxation of the carbachol-contracted rat esophageal tunica muscularis mucosae
ChEMBL 312 5 1 5 2.6 COc1cc(N)c(cc1C(=O)OCCN1CCCCC1)Cl 10.1016/S0960-894X(01)80508-4
CHEMBL286136 2527 36 None 1 4 Rat 8.6 pIC50 = 8.6 Functional
5-hydroxytryptamine 4 receptor agonist activity was determined by the relaxation of the carbachol-contracted rat esophageal tunica muscularis mucosae5-hydroxytryptamine 4 receptor agonist activity was determined by the relaxation of the carbachol-contracted rat esophageal tunica muscularis mucosae
ChEMBL 312 5 1 5 2.6 COc1cc(N)c(cc1C(=O)OCCN1CCCCC1)Cl 10.1016/S0960-894X(01)80508-4
44628198 82311 0 None - 1 Human 8.6 pIC50 = 8.6 Functional
Antagonist activity at human 5HT4ER expressed in CHO cells assessed as reduction in cAMP levelsAntagonist activity at human 5HT4ER expressed in CHO cells assessed as reduction in cAMP levels
ChEMBL 443 7 1 5 4.8 Cn1cc2c(OCC3CCN(CCc4ccc(C(=O)O)cc4)CC3)nc3ccccc3c2c1 10.1021/jm300573d
CHEMBL2179674 82311 0 None - 1 Human 8.6 pIC50 = 8.6 Functional
Antagonist activity at human 5HT4ER expressed in CHO cells assessed as reduction in cAMP levelsAntagonist activity at human 5HT4ER expressed in CHO cells assessed as reduction in cAMP levels
ChEMBL 443 7 1 5 4.8 Cn1cc2c(OCC3CCN(CCc4ccc(C(=O)O)cc4)CC3)nc3ccccc3c2c1 10.1021/jm300573d
10447437 49796 0 None - 1 Guinea pig 6.7 pIC50 = 6.7 Functional
5-hydroxytryptamine 4 receptor antagonist activity, concentration which gave 50% reduction of the 5-HT-induced contractions in the guinea pig ileum5-hydroxytryptamine 4 receptor antagonist activity, concentration which gave 50% reduction of the 5-HT-induced contractions in the guinea pig ileum
ChEMBL 298 5 1 5 2.2 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCCC1 10.1021/jm960320m
CHEMBL156970 49796 0 None - 1 Guinea pig 6.7 pIC50 = 6.7 Functional
5-hydroxytryptamine 4 receptor antagonist activity, concentration which gave 50% reduction of the 5-HT-induced contractions in the guinea pig ileum5-hydroxytryptamine 4 receptor antagonist activity, concentration which gave 50% reduction of the 5-HT-induced contractions in the guinea pig ileum
ChEMBL 298 5 1 5 2.2 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCCC1 10.1021/jm960320m
10569278 186667 0 None - 1 Guinea pig 6.7 pIC50 = 6.7 Functional
The antagonist activity was calculated as the concentration which produced a 50% reduction against 5-hydroxytryptamine 4 receptor in guinea pig ileum.The antagonist activity was calculated as the concentration which produced a 50% reduction against 5-hydroxytryptamine 4 receptor in guinea pig ileum.
ChEMBL 341 5 2 5 3.2 COc1cc(N)c(Cl)cc1NC(=O)OCCN1CCC(C)CC1 10.1021/jm960853v
CHEMBL49266 186667 0 None - 1 Guinea pig 6.7 pIC50 = 6.7 Functional
The antagonist activity was calculated as the concentration which produced a 50% reduction against 5-hydroxytryptamine 4 receptor in guinea pig ileum.The antagonist activity was calculated as the concentration which produced a 50% reduction against 5-hydroxytryptamine 4 receptor in guinea pig ileum.
ChEMBL 341 5 2 5 3.2 COc1cc(N)c(Cl)cc1NC(=O)OCCN1CCC(C)CC1 10.1021/jm960853v
10545215 188395 0 None - 1 Guinea pig 6.7 pIC50 = 6.7 Functional
The antagonist activity was calculated as the concentration which produced a 50% reduction against 5-hydroxytryptamine 4 receptor in guinea pig ileum. 95% confidence limits are in brackets.The antagonist activity was calculated as the concentration which produced a 50% reduction against 5-hydroxytryptamine 4 receptor in guinea pig ileum. 95% confidence limits are in brackets.
ChEMBL 341 5 2 5 3.4 COc1cc(N)c(Cl)cc1NC(=O)OCCN1CCCCCC1 10.1021/jm960853v
CHEMBL50852 188395 0 None - 1 Guinea pig 6.7 pIC50 = 6.7 Functional
The antagonist activity was calculated as the concentration which produced a 50% reduction against 5-hydroxytryptamine 4 receptor in guinea pig ileum. 95% confidence limits are in brackets.The antagonist activity was calculated as the concentration which produced a 50% reduction against 5-hydroxytryptamine 4 receptor in guinea pig ileum. 95% confidence limits are in brackets.
ChEMBL 341 5 2 5 3.4 COc1cc(N)c(Cl)cc1NC(=O)OCCN1CCCCCC1 10.1021/jm960853v
258 3511 25 None 2 3 Guinea pig 6.6 pIC50 = 6.6 Functional
Inhibition of 5-HT-evoked 5-HT4 receptor-mediated contractions in the guinea pig distal colon longitudinal muscle myenteric plexus (LMMP)Inhibition of 5-HT-evoked 5-HT4 receptor-mediated contractions in the guinea pig distal colon longitudinal muscle myenteric plexus (LMMP)
ChEMBL 300 7 1 5 2.4 CCN(CCOC(=O)c1cc(Cl)c(cc1OC)N)CC 10.1021/jm00077a018
5191 3511 25 None 2 3 Guinea pig 6.6 pIC50 = 6.6 Functional
Inhibition of 5-HT-evoked 5-HT4 receptor-mediated contractions in the guinea pig distal colon longitudinal muscle myenteric plexus (LMMP)Inhibition of 5-HT-evoked 5-HT4 receptor-mediated contractions in the guinea pig distal colon longitudinal muscle myenteric plexus (LMMP)
ChEMBL 300 7 1 5 2.4 CCN(CCOC(=O)c1cc(Cl)c(cc1OC)N)CC 10.1021/jm00077a018
CHEMBL287045 3511 25 None 2 3 Guinea pig 6.6 pIC50 = 6.6 Functional
Inhibition of 5-HT-evoked 5-HT4 receptor-mediated contractions in the guinea pig distal colon longitudinal muscle myenteric plexus (LMMP)Inhibition of 5-HT-evoked 5-HT4 receptor-mediated contractions in the guinea pig distal colon longitudinal muscle myenteric plexus (LMMP)
ChEMBL 300 7 1 5 2.4 CCN(CCOC(=O)c1cc(Cl)c(cc1OC)N)CC 10.1021/jm00077a018
5 139 66 None -29 27 Rat 8.4 pIC50 = 8.4 Functional
5-hydroxytryptamine 4 receptor agonist activity was determined by the relaxation of the carbachol-contracted rat esophageal tunica muscularis mucosae5-hydroxytryptamine 4 receptor agonist activity was determined by the relaxation of the carbachol-contracted rat esophageal tunica muscularis mucosae
ChEMBL 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 10.1016/S0960-894X(01)80508-4
5202 139 66 None -29 27 Rat 8.4 pIC50 = 8.4 Functional
5-hydroxytryptamine 4 receptor agonist activity was determined by the relaxation of the carbachol-contracted rat esophageal tunica muscularis mucosae5-hydroxytryptamine 4 receptor agonist activity was determined by the relaxation of the carbachol-contracted rat esophageal tunica muscularis mucosae
ChEMBL 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 10.1016/S0960-894X(01)80508-4
CHEMBL39 139 66 None -29 27 Rat 8.4 pIC50 = 8.4 Functional
5-hydroxytryptamine 4 receptor agonist activity was determined by the relaxation of the carbachol-contracted rat esophageal tunica muscularis mucosae5-hydroxytryptamine 4 receptor agonist activity was determined by the relaxation of the carbachol-contracted rat esophageal tunica muscularis mucosae
ChEMBL 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 10.1016/S0960-894X(01)80508-4
DB08839 139 66 None -29 27 Rat 8.4 pIC50 = 8.4 Functional
5-hydroxytryptamine 4 receptor agonist activity was determined by the relaxation of the carbachol-contracted rat esophageal tunica muscularis mucosae5-hydroxytryptamine 4 receptor agonist activity was determined by the relaxation of the carbachol-contracted rat esophageal tunica muscularis mucosae
ChEMBL 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 10.1016/S0960-894X(01)80508-4
10757374 162542 0 None - 1 Guinea pig 7.5 pIC50 = 7.5 Functional
5-hydroxytryptamine 4 receptor antagonist activity expressed as the concentration which produced a 50% reduction of 5-HT induced contraction in guinea pig ileum5-hydroxytryptamine 4 receptor antagonist activity expressed as the concentration which produced a 50% reduction of 5-HT induced contraction in guinea pig ileum
ChEMBL 310 3 1 5 2.2 COc1cc(N)c(Cl)cc1C(=O)O[C@H]1CN2CCC1CC2 10.1016/S0960-894X(01)80508-4
CHEMBL41769 162542 0 None - 1 Guinea pig 7.5 pIC50 = 7.5 Functional
5-hydroxytryptamine 4 receptor antagonist activity expressed as the concentration which produced a 50% reduction of 5-HT induced contraction in guinea pig ileum5-hydroxytryptamine 4 receptor antagonist activity expressed as the concentration which produced a 50% reduction of 5-HT induced contraction in guinea pig ileum
ChEMBL 310 3 1 5 2.2 COc1cc(N)c(Cl)cc1C(=O)O[C@H]1CN2CCC1CC2 10.1016/S0960-894X(01)80508-4
10757374 162542 0 None - 1 Guinea pig 7.5 pIC50 = 7.5 Functional
5-hydroxytryptamine 4 receptor antagonist activity, concentration which gave 50% reduction of the 5-HT-induced contractions in the guinea pig ileum5-hydroxytryptamine 4 receptor antagonist activity, concentration which gave 50% reduction of the 5-HT-induced contractions in the guinea pig ileum
ChEMBL 310 3 1 5 2.2 COc1cc(N)c(Cl)cc1C(=O)O[C@H]1CN2CCC1CC2 10.1021/jm960320m
CHEMBL41769 162542 0 None - 1 Guinea pig 7.5 pIC50 = 7.5 Functional
5-hydroxytryptamine 4 receptor antagonist activity, concentration which gave 50% reduction of the 5-HT-induced contractions in the guinea pig ileum5-hydroxytryptamine 4 receptor antagonist activity, concentration which gave 50% reduction of the 5-HT-induced contractions in the guinea pig ileum
ChEMBL 310 3 1 5 2.2 COc1cc(N)c(Cl)cc1C(=O)O[C@H]1CN2CCC1CC2 10.1021/jm960320m
44371350 119663 0 None - 1 Guinea pig 6.5 pIC50 = 6.5 Functional
5-hydroxytryptamine 4 receptor antagonist activity, concentration which gave 50% reduction of the 5-HT-induced contractions in the guinea pig ileum5-hydroxytryptamine 4 receptor antagonist activity, concentration which gave 50% reduction of the 5-HT-induced contractions in the guinea pig ileum
ChEMBL 342 5 1 6 2.2 COc1cc(N)c(Cl)cc1C(=O)OCCN1CC(C)OC(C)C1 10.1021/jm960320m
CHEMBL351570 119663 0 None - 1 Guinea pig 6.5 pIC50 = 6.5 Functional
5-hydroxytryptamine 4 receptor antagonist activity, concentration which gave 50% reduction of the 5-HT-induced contractions in the guinea pig ileum5-hydroxytryptamine 4 receptor antagonist activity, concentration which gave 50% reduction of the 5-HT-induced contractions in the guinea pig ileum
ChEMBL 342 5 1 6 2.2 COc1cc(N)c(Cl)cc1C(=O)OCCN1CC(C)OC(C)C1 10.1021/jm960320m
260 3808 49 None 3 3 Guinea pig 5.5 pIC50 = 5.5 Functional
Inhibition of 5-HT-evoked 5-HT4 receptor-mediated contractions in the guinea pig distal colon longitudinal muscle myenteric plexus (LMMP)Inhibition of 5-HT-evoked 5-HT4 receptor-mediated contractions in the guinea pig distal colon longitudinal muscle myenteric plexus (LMMP)
ChEMBL 284 2 1 3 3.0 CN1[C@@H]2CC[C@H]1C[C@H](C2)OC(=O)c1c[nH]c2c1cccc2 10.1021/jm00077a018
2775 3808 49 None 3 3 Guinea pig 5.5 pIC50 = 5.5 Functional
Inhibition of 5-HT-evoked 5-HT4 receptor-mediated contractions in the guinea pig distal colon longitudinal muscle myenteric plexus (LMMP)Inhibition of 5-HT-evoked 5-HT4 receptor-mediated contractions in the guinea pig distal colon longitudinal muscle myenteric plexus (LMMP)
ChEMBL 284 2 1 3 3.0 CN1[C@@H]2CC[C@H]1C[C@H](C2)OC(=O)c1c[nH]c2c1cccc2 10.1021/jm00077a018
656665 3808 49 None 3 3 Guinea pig 5.5 pIC50 = 5.5 Functional
Inhibition of 5-HT-evoked 5-HT4 receptor-mediated contractions in the guinea pig distal colon longitudinal muscle myenteric plexus (LMMP)Inhibition of 5-HT-evoked 5-HT4 receptor-mediated contractions in the guinea pig distal colon longitudinal muscle myenteric plexus (LMMP)
ChEMBL 284 2 1 3 3.0 CN1[C@@H]2CC[C@H]1C[C@H](C2)OC(=O)c1c[nH]c2c1cccc2 10.1021/jm00077a018
CHEMBL56564 3808 49 None 3 3 Guinea pig 5.5 pIC50 = 5.5 Functional
Inhibition of 5-HT-evoked 5-HT4 receptor-mediated contractions in the guinea pig distal colon longitudinal muscle myenteric plexus (LMMP)Inhibition of 5-HT-evoked 5-HT4 receptor-mediated contractions in the guinea pig distal colon longitudinal muscle myenteric plexus (LMMP)
ChEMBL 284 2 1 3 3.0 CN1[C@@H]2CC[C@H]1C[C@H](C2)OC(=O)c1c[nH]c2c1cccc2 10.1021/jm00077a018
DB11699 3808 49 None 3 3 Guinea pig 5.5 pIC50 = 5.5 Functional
Inhibition of 5-HT-evoked 5-HT4 receptor-mediated contractions in the guinea pig distal colon longitudinal muscle myenteric plexus (LMMP)Inhibition of 5-HT-evoked 5-HT4 receptor-mediated contractions in the guinea pig distal colon longitudinal muscle myenteric plexus (LMMP)
ChEMBL 284 2 1 3 3.0 CN1[C@@H]2CC[C@H]1C[C@H](C2)OC(=O)c1c[nH]c2c1cccc2 10.1021/jm00077a018
10828800 99726 0 None - 1 Guinea pig 6.4 pIC50 = 6.4 Functional
5-hydroxytryptamine 4 receptor antagonist activity expressed as the concentration which produced a 50% reduction of 5-HT induced contraction in guinea pig ileum5-hydroxytryptamine 4 receptor antagonist activity expressed as the concentration which produced a 50% reduction of 5-HT induced contraction in guinea pig ileum
ChEMBL 310 3 1 5 2.2 COc1cc(N)c(Cl)cc1C(=O)O[C@@H]1CN2CCC1CC2 10.1016/S0960-894X(01)80508-4
CHEMBL288199 99726 0 None - 1 Guinea pig 6.4 pIC50 = 6.4 Functional
5-hydroxytryptamine 4 receptor antagonist activity expressed as the concentration which produced a 50% reduction of 5-HT induced contraction in guinea pig ileum5-hydroxytryptamine 4 receptor antagonist activity expressed as the concentration which produced a 50% reduction of 5-HT induced contraction in guinea pig ileum
ChEMBL 310 3 1 5 2.2 COc1cc(N)c(Cl)cc1C(=O)O[C@@H]1CN2CCC1CC2 10.1016/S0960-894X(01)80508-4
10828800 99726 0 None - 1 Guinea pig 6.4 pIC50 = 6.4 Functional
5-hydroxytryptamine 4 receptor antagonist activity, concentration which gave 50% reduction of the 5-HT-induced contractions in the guinea pig ileum5-hydroxytryptamine 4 receptor antagonist activity, concentration which gave 50% reduction of the 5-HT-induced contractions in the guinea pig ileum
ChEMBL 310 3 1 5 2.2 COc1cc(N)c(Cl)cc1C(=O)O[C@@H]1CN2CCC1CC2 10.1021/jm960320m
CHEMBL288199 99726 0 None - 1 Guinea pig 6.4 pIC50 = 6.4 Functional
5-hydroxytryptamine 4 receptor antagonist activity, concentration which gave 50% reduction of the 5-HT-induced contractions in the guinea pig ileum5-hydroxytryptamine 4 receptor antagonist activity, concentration which gave 50% reduction of the 5-HT-induced contractions in the guinea pig ileum
ChEMBL 310 3 1 5 2.2 COc1cc(N)c(Cl)cc1C(=O)O[C@@H]1CN2CCC1CC2 10.1021/jm960320m
10020607 19538 0 None - 1 Guinea pig 7.3 pIC50 = 7.3 Functional
Inhibition of 5-HT-evoked 5-HT4 receptor-mediated contractions in the guinea pig distal colon longitudinal muscle myenteric plexus (LMMP)Inhibition of 5-HT-evoked 5-HT4 receptor-mediated contractions in the guinea pig distal colon longitudinal muscle myenteric plexus (LMMP)
ChEMBL 347 6 0 5 3.5 CCCCN1CCC(COC(=O)c2cccc3c2OCCCO3)CC1 10.1021/jm00077a018
CHEMBL130118 19538 0 None - 1 Guinea pig 7.3 pIC50 = 7.3 Functional
Inhibition of 5-HT-evoked 5-HT4 receptor-mediated contractions in the guinea pig distal colon longitudinal muscle myenteric plexus (LMMP)Inhibition of 5-HT-evoked 5-HT4 receptor-mediated contractions in the guinea pig distal colon longitudinal muscle myenteric plexus (LMMP)
ChEMBL 347 6 0 5 3.5 CCCCN1CCC(COC(=O)c2cccc3c2OCCCO3)CC1 10.1021/jm00077a018
10404587 3338 3 None - 1 Guinea pig 8.2 pIC50 = 8.2 Functional
Inhibition of 5-HT-evoked 5-HT4 receptor-mediated contractions in the guinea pig distal colon longitudinal muscle myenteric plexus (LMMP)Inhibition of 5-HT-evoked 5-HT4 receptor-mediated contractions in the guinea pig distal colon longitudinal muscle myenteric plexus (LMMP)
ChEMBL 333 6 0 5 3.1 CCCCN1CCC(CC1)COC(=O)c1cccc2c1OCCO2 10.1021/jm00077a018
251 3338 3 None - 1 Guinea pig 8.2 pIC50 = 8.2 Functional
Inhibition of 5-HT-evoked 5-HT4 receptor-mediated contractions in the guinea pig distal colon longitudinal muscle myenteric plexus (LMMP)Inhibition of 5-HT-evoked 5-HT4 receptor-mediated contractions in the guinea pig distal colon longitudinal muscle myenteric plexus (LMMP)
ChEMBL 333 6 0 5 3.1 CCCCN1CCC(CC1)COC(=O)c1cccc2c1OCCO2 10.1021/jm00077a018
CHEMBL130040 3338 3 None - 1 Guinea pig 8.2 pIC50 = 8.2 Functional
Inhibition of 5-HT-evoked 5-HT4 receptor-mediated contractions in the guinea pig distal colon longitudinal muscle myenteric plexus (LMMP)Inhibition of 5-HT-evoked 5-HT4 receptor-mediated contractions in the guinea pig distal colon longitudinal muscle myenteric plexus (LMMP)
ChEMBL 333 6 0 5 3.1 CCCCN1CCC(CC1)COC(=O)c1cccc2c1OCCO2 10.1021/jm00077a018
44281492 118367 2 None - 1 Guinea pig 7.2 pIC50 = 7.2 Functional
5-hydroxytryptamine 4 receptor antagonist activity expressed as the concentration which produced a 50% reduction of 5-HT induced contraction in guinea pig ileum5-hydroxytryptamine 4 receptor antagonist activity expressed as the concentration which produced a 50% reduction of 5-HT induced contraction in guinea pig ileum
ChEMBL 298 3 1 5 2.2 COc1cc(N)c(Cl)cc1C(=O)OC1CCN(C)CC1 10.1016/S0960-894X(01)80508-4
CHEMBL34224 118367 2 None - 1 Guinea pig 7.2 pIC50 = 7.2 Functional
5-hydroxytryptamine 4 receptor antagonist activity expressed as the concentration which produced a 50% reduction of 5-HT induced contraction in guinea pig ileum5-hydroxytryptamine 4 receptor antagonist activity expressed as the concentration which produced a 50% reduction of 5-HT induced contraction in guinea pig ileum
ChEMBL 298 3 1 5 2.2 COc1cc(N)c(Cl)cc1C(=O)OC1CCN(C)CC1 10.1016/S0960-894X(01)80508-4
10802184 53873 0 None - 1 Guinea pig 6.2 pIC50 = 6.2 Functional
5-hydroxytryptamine 4 receptor antagonist activity, concentration which gave 50% reduction of the 5-HT-induced contractions in the guinea pig ileum5-hydroxytryptamine 4 receptor antagonist activity, concentration which gave 50% reduction of the 5-HT-induced contractions in the guinea pig ileum
ChEMBL 272 5 1 5 1.6 COc1cc(N)c(Cl)cc1C(=O)OCCN(C)C 10.1021/jm960320m
CHEMBL160705 53873 0 None - 1 Guinea pig 6.2 pIC50 = 6.2 Functional
5-hydroxytryptamine 4 receptor antagonist activity, concentration which gave 50% reduction of the 5-HT-induced contractions in the guinea pig ileum5-hydroxytryptamine 4 receptor antagonist activity, concentration which gave 50% reduction of the 5-HT-induced contractions in the guinea pig ileum
ChEMBL 272 5 1 5 1.6 COc1cc(N)c(Cl)cc1C(=O)OCCN(C)C 10.1021/jm960320m
10041634 22626 1 None - 1 Guinea pig 7.2 pIC50 = 7.2 Functional
Inhibition of 5-HT-evoked 5-HT4 receptor-mediated contractions in the guinea pig distal colon longitudinal muscle myenteric plexus (LMMP)Inhibition of 5-HT-evoked 5-HT4 receptor-mediated contractions in the guinea pig distal colon longitudinal muscle myenteric plexus (LMMP)
ChEMBL 319 6 0 5 3.1 CCCCN1CCC(COC(=O)c2cccc3c2OCO3)CC1 10.1021/jm00077a018
CHEMBL132826 22626 1 None - 1 Guinea pig 7.2 pIC50 = 7.2 Functional
Inhibition of 5-HT-evoked 5-HT4 receptor-mediated contractions in the guinea pig distal colon longitudinal muscle myenteric plexus (LMMP)Inhibition of 5-HT-evoked 5-HT4 receptor-mediated contractions in the guinea pig distal colon longitudinal muscle myenteric plexus (LMMP)
ChEMBL 319 6 0 5 3.1 CCCCN1CCC(COC(=O)c2cccc3c2OCO3)CC1 10.1021/jm00077a018
258 3511 25 None 2 3 Guinea pig 7.1 pIC50 = 7.1 Functional
5-hydroxytryptamine 4 receptor antagonist activity expressed as the concentration which produced a 50% reduction of 5-HT induced contraction in guinea pig ileum; Not evaluable5-hydroxytryptamine 4 receptor antagonist activity expressed as the concentration which produced a 50% reduction of 5-HT induced contraction in guinea pig ileum; Not evaluable
ChEMBL 300 7 1 5 2.4 CCN(CCOC(=O)c1cc(Cl)c(cc1OC)N)CC 10.1016/S0960-894X(01)80508-4
5191 3511 25 None 2 3 Guinea pig 7.1 pIC50 = 7.1 Functional
5-hydroxytryptamine 4 receptor antagonist activity expressed as the concentration which produced a 50% reduction of 5-HT induced contraction in guinea pig ileum; Not evaluable5-hydroxytryptamine 4 receptor antagonist activity expressed as the concentration which produced a 50% reduction of 5-HT induced contraction in guinea pig ileum; Not evaluable
ChEMBL 300 7 1 5 2.4 CCN(CCOC(=O)c1cc(Cl)c(cc1OC)N)CC 10.1016/S0960-894X(01)80508-4
CHEMBL287045 3511 25 None 2 3 Guinea pig 7.1 pIC50 = 7.1 Functional
5-hydroxytryptamine 4 receptor antagonist activity expressed as the concentration which produced a 50% reduction of 5-HT induced contraction in guinea pig ileum; Not evaluable5-hydroxytryptamine 4 receptor antagonist activity expressed as the concentration which produced a 50% reduction of 5-HT induced contraction in guinea pig ileum; Not evaluable
ChEMBL 300 7 1 5 2.4 CCN(CCOC(=O)c1cc(Cl)c(cc1OC)N)CC 10.1016/S0960-894X(01)80508-4
258 3511 25 None 2 3 Guinea pig 7.1 pIC50 = 7.1 Functional
5-hydroxytryptamine 4 receptor antagonist activity, concentration which gave 50% reduction of the 5-HT-induced contractions in the guinea pig ileum5-hydroxytryptamine 4 receptor antagonist activity, concentration which gave 50% reduction of the 5-HT-induced contractions in the guinea pig ileum
ChEMBL 300 7 1 5 2.4 CCN(CCOC(=O)c1cc(Cl)c(cc1OC)N)CC 10.1021/jm960320m
5191 3511 25 None 2 3 Guinea pig 7.1 pIC50 = 7.1 Functional
5-hydroxytryptamine 4 receptor antagonist activity, concentration which gave 50% reduction of the 5-HT-induced contractions in the guinea pig ileum5-hydroxytryptamine 4 receptor antagonist activity, concentration which gave 50% reduction of the 5-HT-induced contractions in the guinea pig ileum
ChEMBL 300 7 1 5 2.4 CCN(CCOC(=O)c1cc(Cl)c(cc1OC)N)CC 10.1021/jm960320m
CHEMBL287045 3511 25 None 2 3 Guinea pig 7.1 pIC50 = 7.1 Functional
5-hydroxytryptamine 4 receptor antagonist activity, concentration which gave 50% reduction of the 5-HT-induced contractions in the guinea pig ileum5-hydroxytryptamine 4 receptor antagonist activity, concentration which gave 50% reduction of the 5-HT-induced contractions in the guinea pig ileum
ChEMBL 300 7 1 5 2.4 CCN(CCOC(=O)c1cc(Cl)c(cc1OC)N)CC 10.1021/jm960320m
19956256 114799 0 None -1 5 Human 6.1 pIC50 = 6.1 Functional
Compound was tested for agonistic activity against 5-hydroxytryptamine 4 receptor on guinea colon at a concentration 0.1 uMCompound was tested for agonistic activity against 5-hydroxytryptamine 4 receptor on guinea colon at a concentration 0.1 uM
ChEMBL 275 4 0 5 2.5 Cc1csc2c1-n1cccc1/C2=N/OCCN(C)C 10.1016/s0960-894x(00)00691-0
CHEMBL334923 114799 0 None -1 5 Human 6.1 pIC50 = 6.1 Functional
Compound was tested for agonistic activity against 5-hydroxytryptamine 4 receptor on guinea colon at a concentration 0.1 uMCompound was tested for agonistic activity against 5-hydroxytryptamine 4 receptor on guinea colon at a concentration 0.1 uM
ChEMBL 275 4 0 5 2.5 Cc1csc2c1-n1cccc1/C2=N/OCCN(C)C 10.1016/s0960-894x(00)00691-0
68490431 82316 0 None - 1 Human 8.0 pIC50 = 8.0 Functional
Antagonist activity at human 5HT4ER expressed in CHO cells assessed as reduction in cAMP levelsAntagonist activity at human 5HT4ER expressed in CHO cells assessed as reduction in cAMP levels
ChEMBL 448 8 2 5 4.0 CC(C)n1nc(C(=O)NCC2CCN(CCc3ccc(C(=O)O)cc3)CC2)c2ccccc21 10.1021/jm300573d
CHEMBL2179707 82316 0 None - 1 Human 8.0 pIC50 = 8.0 Functional
Antagonist activity at human 5HT4ER expressed in CHO cells assessed as reduction in cAMP levelsAntagonist activity at human 5HT4ER expressed in CHO cells assessed as reduction in cAMP levels
ChEMBL 448 8 2 5 4.0 CC(C)n1nc(C(=O)NCC2CCN(CCc3ccc(C(=O)O)cc3)CC2)c2ccccc21 10.1021/jm300573d
9800656 15375 0 None - 1 Human 9.2 pKd = 9.2 Functional
,Antagonism of stimulation of 5-hydroxytryptamine receptor on the L-type calcium current (I Ca) in isolated human atrial myocytes,Antagonism of stimulation of 5-hydroxytryptamine receptor on the L-type calcium current (I Ca) in isolated human atrial myocytes
ChEMBL 391 6 1 8 1.7 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCN(c2ncccn2)CC1 10.1021/jm0009538
CHEMBL121913 15375 0 None - 1 Human 9.2 pKd = 9.2 Functional
,Antagonism of stimulation of 5-hydroxytryptamine receptor on the L-type calcium current (I Ca) in isolated human atrial myocytes,Antagonism of stimulation of 5-hydroxytryptamine receptor on the L-type calcium current (I Ca) in isolated human atrial myocytes
ChEMBL 391 6 1 8 1.7 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCN(c2ncccn2)CC1 10.1021/jm0009538
44407083 73562 0 None - 0 Rat 8.9 pKd = 8.9 Functional
Antagonism at 5HT4 receptor in rat tunica muscularis mucosaAntagonism at 5HT4 receptor in rat tunica muscularis mucosa
ChEMBL 284 3 1 3 2.8 O=C(OC[C@@H]1CCN2CCC[C@@H]12)c1c[nH]c2ccccc12 10.1021/jm0509501
CHEMBL201946 73562 0 None - 0 Rat 8.9 pKd = 8.9 Functional
Antagonism at 5HT4 receptor in rat tunica muscularis mucosaAntagonism at 5HT4 receptor in rat tunica muscularis mucosa
ChEMBL 284 3 1 3 2.8 O=C(OC[C@@H]1CCN2CCC[C@@H]12)c1c[nH]c2ccccc12 10.1021/jm0509501
11537858 134306 0 None - 0 Rat 7.0 pKd = 7 Functional
Antagonism at 5HT4 receptor in rat tunica muscularis mucosaAntagonism at 5HT4 receptor in rat tunica muscularis mucosa
ChEMBL 327 2 1 3 2.5 CC1(C)C(=O)N(C(=O)NC[C@@H]2CCN3CCC[C@@H]23)c2ccccc21 10.1021/jm0509501
CHEMBL371883 134306 0 None - 0 Rat 7.0 pKd = 7 Functional
Antagonism at 5HT4 receptor in rat tunica muscularis mucosaAntagonism at 5HT4 receptor in rat tunica muscularis mucosa
ChEMBL 327 2 1 3 2.5 CC1(C)C(=O)N(C(=O)NC[C@@H]2CCN3CCC[C@@H]23)c2ccccc21 10.1021/jm0509501
11515258 74051 0 None - 0 Rat 6.8 pKd = 6.8 Functional
Antagonism at 5HT4 receptor in rat tunica muscularis mucosaAntagonism at 5HT4 receptor in rat tunica muscularis mucosa
ChEMBL 319 3 0 5 2.6 O=C(OC[C@@H]1CCN2CCC[C@@H]12)c1cc(Cl)cn2ccnc12 10.1021/jm0509501
CHEMBL202481 74051 0 None - 0 Rat 6.8 pKd = 6.8 Functional
Antagonism at 5HT4 receptor in rat tunica muscularis mucosaAntagonism at 5HT4 receptor in rat tunica muscularis mucosa
ChEMBL 319 3 0 5 2.6 O=C(OC[C@@H]1CCN2CCC[C@@H]12)c1cc(Cl)cn2ccnc12 10.1021/jm0509501
11529314 140809 0 None - 0 Rat 6.8 pKd = 6.8 Functional
Antagonism at 5HT4 receptor in rat tunica muscularis mucosaAntagonism at 5HT4 receptor in rat tunica muscularis mucosa
ChEMBL 284 3 1 4 1.5 O=C(NC[C@@H]1CCN2CCC[C@@H]12)c1cccn2ccnc12 10.1021/jm0509501
CHEMBL383554 140809 0 None - 0 Rat 6.8 pKd = 6.8 Functional
Antagonism at 5HT4 receptor in rat tunica muscularis mucosaAntagonism at 5HT4 receptor in rat tunica muscularis mucosa
ChEMBL 284 3 1 4 1.5 O=C(NC[C@@H]1CCN2CCC[C@@H]12)c1cccn2ccnc12 10.1021/jm0509501
260 3808 49 None 3 3 Guinea pig 5.7 pKd = 5.7 Functional
Evaluated for the antagonistic activity against Serotonin 5-hydroxytryptamine 4 receptor in non-electrically stimulated guinea-pig ileum.Evaluated for the antagonistic activity against Serotonin 5-hydroxytryptamine 4 receptor in non-electrically stimulated guinea-pig ileum.
ChEMBL 284 2 1 3 3.0 CN1[C@@H]2CC[C@H]1C[C@H](C2)OC(=O)c1c[nH]c2c1cccc2 10.1016/S0960-894X(00)80170-5
2775 3808 49 None 3 3 Guinea pig 5.7 pKd = 5.7 Functional
Evaluated for the antagonistic activity against Serotonin 5-hydroxytryptamine 4 receptor in non-electrically stimulated guinea-pig ileum.Evaluated for the antagonistic activity against Serotonin 5-hydroxytryptamine 4 receptor in non-electrically stimulated guinea-pig ileum.
ChEMBL 284 2 1 3 3.0 CN1[C@@H]2CC[C@H]1C[C@H](C2)OC(=O)c1c[nH]c2c1cccc2 10.1016/S0960-894X(00)80170-5
656665 3808 49 None 3 3 Guinea pig 5.7 pKd = 5.7 Functional
Evaluated for the antagonistic activity against Serotonin 5-hydroxytryptamine 4 receptor in non-electrically stimulated guinea-pig ileum.Evaluated for the antagonistic activity against Serotonin 5-hydroxytryptamine 4 receptor in non-electrically stimulated guinea-pig ileum.
ChEMBL 284 2 1 3 3.0 CN1[C@@H]2CC[C@H]1C[C@H](C2)OC(=O)c1c[nH]c2c1cccc2 10.1016/S0960-894X(00)80170-5
CHEMBL56564 3808 49 None 3 3 Guinea pig 5.7 pKd = 5.7 Functional
Evaluated for the antagonistic activity against Serotonin 5-hydroxytryptamine 4 receptor in non-electrically stimulated guinea-pig ileum.Evaluated for the antagonistic activity against Serotonin 5-hydroxytryptamine 4 receptor in non-electrically stimulated guinea-pig ileum.
ChEMBL 284 2 1 3 3.0 CN1[C@@H]2CC[C@H]1C[C@H](C2)OC(=O)c1c[nH]c2c1cccc2 10.1016/S0960-894X(00)80170-5
DB11699 3808 49 None 3 3 Guinea pig 5.7 pKd = 5.7 Functional
Evaluated for the antagonistic activity against Serotonin 5-hydroxytryptamine 4 receptor in non-electrically stimulated guinea-pig ileum.Evaluated for the antagonistic activity against Serotonin 5-hydroxytryptamine 4 receptor in non-electrically stimulated guinea-pig ileum.
ChEMBL 284 2 1 3 3.0 CN1[C@@H]2CC[C@H]1C[C@H](C2)OC(=O)c1c[nH]c2c1cccc2 10.1016/S0960-894X(00)80170-5
11522273 140814 0 None - 0 Rat 8.6 pKd = 8.6 Functional
Antagonism at 5HT4 receptor in rat tunica muscularis mucosaAntagonism at 5HT4 receptor in rat tunica muscularis mucosa
ChEMBL 299 3 0 5 2.2 Cn1nc(C(=O)OC[C@@H]2CCN3CCC[C@@H]23)c2ccccc21 10.1021/jm0509501
CHEMBL383577 140814 0 None - 0 Rat 8.6 pKd = 8.6 Functional
Antagonism at 5HT4 receptor in rat tunica muscularis mucosaAntagonism at 5HT4 receptor in rat tunica muscularis mucosa
ChEMBL 299 3 0 5 2.2 Cn1nc(C(=O)OC[C@@H]2CCN3CCC[C@@H]23)c2ccccc21 10.1021/jm0509501
11580445 73616 0 None - 0 Rat 6.6 pKd = 6.6 Functional
Antagonism at 5HT4 receptor in rat tunica muscularis mucosaAntagonism at 5HT4 receptor in rat tunica muscularis mucosa
ChEMBL 312 4 1 4 2.1 CCc1nc(C(=O)NC[C@@H]2CCN3CCC[C@@H]23)c2ccccn12 10.1021/jm0509501
CHEMBL202149 73616 0 None - 0 Rat 6.6 pKd = 6.6 Functional
Antagonism at 5HT4 receptor in rat tunica muscularis mucosaAntagonism at 5HT4 receptor in rat tunica muscularis mucosa
ChEMBL 312 4 1 4 2.1 CCc1nc(C(=O)NC[C@@H]2CCN3CCC[C@@H]23)c2ccccn12 10.1021/jm0509501
11580890 73598 0 None - 0 Rat 8.5 pKd = 8.5 Functional
Antagonism at 5HT4 receptor in rat tunica muscularis mucosaAntagonism at 5HT4 receptor in rat tunica muscularis mucosa
ChEMBL 302 3 1 3 2.9 O=C(OC[C@@H]1CCN2CCC[C@@H]12)c1c[nH]c2ccc(F)cc12 10.1021/jm0509501
CHEMBL202122 73598 0 None - 0 Rat 8.5 pKd = 8.5 Functional
Antagonism at 5HT4 receptor in rat tunica muscularis mucosaAntagonism at 5HT4 receptor in rat tunica muscularis mucosa
ChEMBL 302 3 1 3 2.9 O=C(OC[C@@H]1CCN2CCC[C@@H]12)c1c[nH]c2ccc(F)cc12 10.1021/jm0509501
11508052 73489 0 None - 0 Rat 8.5 pKd = 8.5 Functional
Antagonism at 5HT4 receptor in rat tunica muscularis mucosaAntagonism at 5HT4 receptor in rat tunica muscularis mucosa
ChEMBL 285 3 1 4 2.2 O=C(OC[C@@H]1CCN2CCC[C@@H]12)c1[nH]nc2ccccc12 10.1021/jm0509501
CHEMBL201878 73489 0 None - 0 Rat 8.5 pKd = 8.5 Functional
Antagonism at 5HT4 receptor in rat tunica muscularis mucosaAntagonism at 5HT4 receptor in rat tunica muscularis mucosa
ChEMBL 285 3 1 4 2.2 O=C(OC[C@@H]1CCN2CCC[C@@H]12)c1[nH]nc2ccccc12 10.1021/jm0509501
14403147 34668 2 None - 0 Guinea pig 6.3 pKd = 6.3 Functional
Evaluated for the antagonistic activity against Serotonin 5-hydroxytryptamine 4 receptor in non-electrically stimulated guinea-pig ileum.Evaluated for the antagonistic activity against Serotonin 5-hydroxytryptamine 4 receptor in non-electrically stimulated guinea-pig ileum.
ChEMBL 298 2 1 4 1.9 CN1C2CC(OC(=O)c3c[nH]c4ccccc34)CC1C1OC12 10.1016/S0960-894X(00)80170-5
CHEMBL143197 34668 2 None - 0 Guinea pig 6.3 pKd = 6.3 Functional
Evaluated for the antagonistic activity against Serotonin 5-hydroxytryptamine 4 receptor in non-electrically stimulated guinea-pig ileum.Evaluated for the antagonistic activity against Serotonin 5-hydroxytryptamine 4 receptor in non-electrically stimulated guinea-pig ileum.
ChEMBL 298 2 1 4 1.9 CN1C2CC(OC(=O)c3c[nH]c4ccccc34)CC1C1OC12 10.1016/S0960-894X(00)80170-5
133999 73966 6 None - 0 Rat 8.1 pKd = 8.1 Functional
Antagonism at 5HT4 receptor in rat tunica muscularis mucosaAntagonism at 5HT4 receptor in rat tunica muscularis mucosa
ChEMBL 318 3 1 4 2.2 O=C(NC[C@@H]1CCN2CCC[C@@H]12)c1cc(Cl)cn2ccnc12 10.1021/jm0509501
CHEMBL202434 73966 6 None - 0 Rat 8.1 pKd = 8.1 Functional
Antagonism at 5HT4 receptor in rat tunica muscularis mucosaAntagonism at 5HT4 receptor in rat tunica muscularis mucosa
ChEMBL 318 3 1 4 2.2 O=C(NC[C@@H]1CCN2CCC[C@@H]12)c1cc(Cl)cn2ccnc12 10.1021/jm0509501
11508567 165416 0 None - 0 Rat 7.2 pKd = 7.2 Functional
Antagonism at 5HT4 receptor in rat tunica muscularis mucosaAntagonism at 5HT4 receptor in rat tunica muscularis mucosa
ChEMBL 314 4 1 4 2.8 COc1ccc2[nH]cc(C(=O)OC[C@@H]3CCN4CCC[C@@H]34)c2c1 10.1021/jm0509501
CHEMBL425222 165416 0 None - 0 Rat 7.2 pKd = 7.2 Functional
Antagonism at 5HT4 receptor in rat tunica muscularis mucosaAntagonism at 5HT4 receptor in rat tunica muscularis mucosa
ChEMBL 314 4 1 4 2.8 COc1ccc2[nH]cc(C(=O)OC[C@@H]3CCN4CCC[C@@H]34)c2c1 10.1021/jm0509501
11500906 134834 0 None - 0 Rat 7.1 pKd = 7.1 Functional
Antagonism at 5HT4 receptor in rat tunica muscularis mucosaAntagonism at 5HT4 receptor in rat tunica muscularis mucosa
ChEMBL 332 3 1 4 2.5 Cc1cnc2c(C(=O)NC[C@@H]3CCN4CCC[C@@H]34)cc(Cl)cn12 10.1021/jm0509501
CHEMBL372776 134834 0 None - 0 Rat 7.1 pKd = 7.1 Functional
Antagonism at 5HT4 receptor in rat tunica muscularis mucosaAntagonism at 5HT4 receptor in rat tunica muscularis mucosa
ChEMBL 332 3 1 4 2.5 Cc1cnc2c(C(=O)NC[C@@H]3CCN4CCC[C@@H]34)cc(Cl)cn12 10.1021/jm0509501
119376 1811 41 None 61 4 Human 10.1 pKi = 10.1 Functional
Antagonistic activity at human 5HT4 receptor expressed in HEK293 cellsAntagonistic activity at human 5HT4 receptor expressed in HEK293 cells
ChEMBL 393 7 1 6 1.6 O=C(c1cn(c2c1cccc2)C)OCC1CCN(CC1)CCNS(=O)(=O)C 10.1016/j.bmc.2010.10.011
247 1811 41 None 61 4 Human 10.1 pKi = 10.1 Functional
Antagonistic activity at human 5HT4 receptor expressed in HEK293 cellsAntagonistic activity at human 5HT4 receptor expressed in HEK293 cells
ChEMBL 393 7 1 6 1.6 O=C(c1cn(c2c1cccc2)C)OCC1CCN(CC1)CCNS(=O)(=O)C 10.1016/j.bmc.2010.10.011
CHEMBL33884 1811 41 None 61 4 Human 10.1 pKi = 10.1 Functional
Antagonistic activity at human 5HT4 receptor expressed in HEK293 cellsAntagonistic activity at human 5HT4 receptor expressed in HEK293 cells
ChEMBL 393 7 1 6 1.6 O=C(c1cn(c2c1cccc2)C)OCC1CCN(CC1)CCNS(=O)(=O)C 10.1016/j.bmc.2010.10.011
119376 1811 41 None 61 4 Human 9.3 pKi = 9.3 Functional
Displacement of [3H]GR-113808 from human 5HT4e receptor expressed in C6 cellsDisplacement of [3H]GR-113808 from human 5HT4e receptor expressed in C6 cells
ChEMBL 393 7 1 6 1.6 O=C(c1cn(c2c1cccc2)C)OCC1CCN(CC1)CCNS(=O)(=O)C 10.1021/jm070552t
247 1811 41 None 61 4 Human 9.3 pKi = 9.3 Functional
Displacement of [3H]GR-113808 from human 5HT4e receptor expressed in C6 cellsDisplacement of [3H]GR-113808 from human 5HT4e receptor expressed in C6 cells
ChEMBL 393 7 1 6 1.6 O=C(c1cn(c2c1cccc2)C)OCC1CCN(CC1)CCNS(=O)(=O)C 10.1021/jm070552t
CHEMBL33884 1811 41 None 61 4 Human 9.3 pKi = 9.3 Functional
Displacement of [3H]GR-113808 from human 5HT4e receptor expressed in C6 cellsDisplacement of [3H]GR-113808 from human 5HT4e receptor expressed in C6 cells
ChEMBL 393 7 1 6 1.6 O=C(c1cn(c2c1cccc2)C)OCC1CCN(CC1)CCNS(=O)(=O)C 10.1021/jm070552t
53318069 56142 0 None - 0 Human 9.1 pKi = 9.1 Functional
Antagonistic activity at human 5HT4 receptor expressed in HEK293 cellsAntagonistic activity at human 5HT4 receptor expressed in HEK293 cells
ChEMBL 344 7 2 4 2.9 O=C(O)CCCN1CCC(COC(=O)c2c[nH]c3ccccc23)CC1 10.1016/j.bmc.2010.10.011
CHEMBL1632154 56142 0 None - 0 Human 9.1 pKi = 9.1 Functional
Antagonistic activity at human 5HT4 receptor expressed in HEK293 cellsAntagonistic activity at human 5HT4 receptor expressed in HEK293 cells
ChEMBL 344 7 2 4 2.9 O=C(O)CCCN1CCC(COC(=O)c2c[nH]c3ccccc23)CC1 10.1016/j.bmc.2010.10.011
53318070 56143 0 None - 0 Human 7.0 pKi = 7.0 Functional
Antagonistic activity at human 5HT4 receptor expressed in HEK293 cellsAntagonistic activity at human 5HT4 receptor expressed in HEK293 cells
ChEMBL 371 8 2 4 3.0 CCOC(=O)CCCN1CCC(CNC(=O)c2c[nH]c3ccccc23)CC1 10.1016/j.bmc.2010.10.011
CHEMBL1632155 56143 0 None - 0 Human 7.0 pKi = 7.0 Functional
Antagonistic activity at human 5HT4 receptor expressed in HEK293 cellsAntagonistic activity at human 5HT4 receptor expressed in HEK293 cells
ChEMBL 371 8 2 4 3.0 CCOC(=O)CCCN1CCC(CNC(=O)c2c[nH]c3ccccc23)CC1 10.1016/j.bmc.2010.10.011
11557207 78645 0 None - 0 Human 7.0 pKi = 7.0 Functional
Displacement of [3H]GR-113808 from human 5HT4e receptor expressed in C6 cellsDisplacement of [3H]GR-113808 from human 5HT4e receptor expressed in C6 cells
ChEMBL 1203 39 7 18 10.7 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCC(NC(=O)CCCCCCCCCCNc2nc(NCCCCCCCCCCC(=O)NC3CCN(CCOC(=O)c4cc(Cl)c(N)cc4OC)CC3)nc(NCc3ccccc3)n2)CC1 10.1021/jm070552t
CHEMBL2113160 78645 0 None - 0 Human 7.0 pKi = 7.0 Functional
Displacement of [3H]GR-113808 from human 5HT4e receptor expressed in C6 cellsDisplacement of [3H]GR-113808 from human 5HT4e receptor expressed in C6 cells
ChEMBL 1203 39 7 18 10.7 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCC(NC(=O)CCCCCCCCCCNc2nc(NCCCCCCCCCCC(=O)NC3CCN(CCOC(=O)c4cc(Cl)c(N)cc4OC)CC3)nc(NCc3ccccc3)n2)CC1 10.1021/jm070552t
17755141 78715 0 None - 0 Human 7.9 pKi = 7.9 Functional
Displacement of [3H]GR-113808 from human 5HT4e receptor expressed in C6 cellsDisplacement of [3H]GR-113808 from human 5HT4e receptor expressed in C6 cells
ChEMBL 1183 28 4 16 9.0 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCC(NC(=O)CCCN(CCCc2ccc(CCCN(CCCC(=O)NC3CCN(CCOC(=O)c4cc(Cl)c(N)cc4OC)CC3)C(=O)OC(C)(C)C)cc2)C(=O)OC(C)(C)C)CC1 10.1021/jm070552t
CHEMBL2113289 78715 0 None - 0 Human 7.9 pKi = 7.9 Functional
Displacement of [3H]GR-113808 from human 5HT4e receptor expressed in C6 cellsDisplacement of [3H]GR-113808 from human 5HT4e receptor expressed in C6 cells
ChEMBL 1183 28 4 16 9.0 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCC(NC(=O)CCCN(CCCc2ccc(CCCN(CCCC(=O)NC3CCN(CCOC(=O)c4cc(Cl)c(N)cc4OC)CC3)C(=O)OC(C)(C)C)cc2)C(=O)OC(C)(C)C)CC1 10.1021/jm070552t
46905984 10316 0 None - 0 Human 7.8 pKi = 7.8 Functional
Displacement of [3H]GR-113808 from human 5HT4e receptor expressed in C6 cellsDisplacement of [3H]GR-113808 from human 5HT4e receptor expressed in C6 cells
ChEMBL 1179 30 4 14 8.7 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCC(CNC(=O)CCCN(CCCc2ccc(CCCN(CCCC(=O)NCC3CCN(CCOC(=O)c4cc(Cl)c(N)cc4OC)CC3)C(=O)C(C)(C)C)cc2)C(=O)C(C)(C)C)CC1 10.1021/jm070552t
CHEMBL1162955 10316 0 None - 0 Human 7.8 pKi = 7.8 Functional
Displacement of [3H]GR-113808 from human 5HT4e receptor expressed in C6 cellsDisplacement of [3H]GR-113808 from human 5HT4e receptor expressed in C6 cells
ChEMBL 1179 30 4 14 8.7 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCC(CNC(=O)CCCN(CCCc2ccc(CCCN(CCCC(=O)NCC3CCN(CCOC(=O)c4cc(Cl)c(N)cc4OC)CC3)C(=O)C(C)(C)C)cc2)C(=O)C(C)(C)C)CC1 10.1021/jm070552t
44427806 143381 0 None - 0 Human 7.8 pKi = 7.8 Functional
Displacement of [3H]GR-113808 from human 5HT4e receptor expressed in C6 cellsDisplacement of [3H]GR-113808 from human 5HT4e receptor expressed in C6 cells
ChEMBL 1151 28 4 14 8.2 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCC(NC(=O)CCCN(CCCc2cccc(CCCN(CCCC(=O)NC3CCN(CCOC(=O)c4cc(Cl)c(N)cc4OC)CC3)C(=O)C(C)(C)C)c2)C(=O)C(C)(C)C)CC1 10.1021/jm070552t
CHEMBL390202 143381 0 None - 0 Human 7.8 pKi = 7.8 Functional
Displacement of [3H]GR-113808 from human 5HT4e receptor expressed in C6 cellsDisplacement of [3H]GR-113808 from human 5HT4e receptor expressed in C6 cells
ChEMBL 1151 28 4 14 8.2 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCC(NC(=O)CCCN(CCCc2cccc(CCCN(CCCC(=O)NC3CCN(CCOC(=O)c4cc(Cl)c(N)cc4OC)CC3)C(=O)C(C)(C)C)c2)C(=O)C(C)(C)C)CC1 10.1021/jm070552t
10666935 206211 0 None - 0 Human 7.8 pKi = 7.8 Functional
Tested for 5-hydroxytryptamine 4 receptor antagonist activityTested for 5-hydroxytryptamine 4 receptor antagonist activity
ChEMBL 371 5 1 6 1.7 CC(C)N1CCN(CCNC(=O)n2c(=O)n(C3CC3)c3ccccc32)CC1 10.1021/jm020099f
CHEMBL97019 206211 0 None - 0 Human 7.8 pKi = 7.8 Functional
Tested for 5-hydroxytryptamine 4 receptor antagonist activityTested for 5-hydroxytryptamine 4 receptor antagonist activity
ChEMBL 371 5 1 6 1.7 CC(C)N1CCN(CCNC(=O)n2c(=O)n(C3CC3)c3ccccc32)CC1 10.1021/jm020099f
17755040 78711 0 None - 0 Human 7.8 pKi = 7.8 Functional
Displacement of [3H]GR-113808 from human 5HT4e receptor expressed in C6 cellsDisplacement of [3H]GR-113808 from human 5HT4e receptor expressed in C6 cells
ChEMBL 1175 22 4 16 7.8 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCC(NC(=O)CCCN(CC#Cc2ccc(C#CCN(CCCC(=O)NC3CCN(CCOC(=O)c4cc(Cl)c(N)cc4OC)CC3)C(=O)OC(C)(C)C)cc2)C(=O)OC(C)(C)C)CC1 10.1021/jm070552t
CHEMBL2113285 78711 0 None - 0 Human 7.8 pKi = 7.8 Functional
Displacement of [3H]GR-113808 from human 5HT4e receptor expressed in C6 cellsDisplacement of [3H]GR-113808 from human 5HT4e receptor expressed in C6 cells
ChEMBL 1175 22 4 16 7.8 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCC(NC(=O)CCCN(CC#Cc2ccc(C#CCN(CCCC(=O)NC3CCN(CCOC(=O)c4cc(Cl)c(N)cc4OC)CC3)C(=O)OC(C)(C)C)cc2)C(=O)OC(C)(C)C)CC1 10.1021/jm070552t
17755140 78714 0 None - 0 Human 7.7 pKi = 7.7 Functional
Displacement of [3H]GR-113808 from human 5HT4e receptor expressed in C6 cellsDisplacement of [3H]GR-113808 from human 5HT4e receptor expressed in C6 cells
ChEMBL 1155 26 4 16 7.9 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCC(CNC(=O)CN(CCCc2ccc(CCCN(CC(=O)NCC3CCN(CCOC(=O)c4cc(Cl)c(N)cc4OC)CC3)C(=O)OC(C)(C)C)cc2)C(=O)OC(C)(C)C)CC1 10.1021/jm070552t
CHEMBL2113288 78714 0 None - 0 Human 7.7 pKi = 7.7 Functional
Displacement of [3H]GR-113808 from human 5HT4e receptor expressed in C6 cellsDisplacement of [3H]GR-113808 from human 5HT4e receptor expressed in C6 cells
ChEMBL 1155 26 4 16 7.9 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCC(CNC(=O)CN(CCCc2ccc(CCCN(CC(=O)NCC3CCN(CCOC(=O)c4cc(Cl)c(N)cc4OC)CC3)C(=O)OC(C)(C)C)cc2)C(=O)OC(C)(C)C)CC1 10.1021/jm070552t
11622025 143214 0 None - 0 Human 7.7 pKi = 7.7 Functional
Displacement of [3H]GR-113808 from human 5HT4e receptor expressed in C6 cellsDisplacement of [3H]GR-113808 from human 5HT4e receptor expressed in C6 cells
ChEMBL 848 23 4 12 6.1 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCC(NC(=O)CCCCCCCCCCNC(=O)C2CCN(CCOC(=O)c3cc(Cl)c(N)cc3OC)CC2)CC1 10.1021/jm070552t
CHEMBL390075 143214 0 None - 0 Human 7.7 pKi = 7.7 Functional
Displacement of [3H]GR-113808 from human 5HT4e receptor expressed in C6 cellsDisplacement of [3H]GR-113808 from human 5HT4e receptor expressed in C6 cells
ChEMBL 848 23 4 12 6.1 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCC(NC(=O)CCCCCCCCCCNC(=O)C2CCN(CCOC(=O)c3cc(Cl)c(N)cc3OC)CC2)CC1 10.1021/jm070552t
17756519 78716 0 None - 0 Human 7.6 pKi = 7.6 Functional
Displacement of [3H]GR-113808 from human 5HT4e receptor expressed in C6 cellsDisplacement of [3H]GR-113808 from human 5HT4e receptor expressed in C6 cells
ChEMBL 1211 30 4 16 9.4 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCC(CNC(=O)CCCN(CCCc2cccc(CCCN(CCCC(=O)NCC3CCN(CCOC(=O)c4cc(Cl)c(N)cc4OC)CC3)C(=O)OC(C)(C)C)c2)C(=O)OC(C)(C)C)CC1 10.1021/jm070552t
CHEMBL2113290 78716 0 None - 0 Human 7.6 pKi = 7.6 Functional
Displacement of [3H]GR-113808 from human 5HT4e receptor expressed in C6 cellsDisplacement of [3H]GR-113808 from human 5HT4e receptor expressed in C6 cells
ChEMBL 1211 30 4 16 9.4 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCC(CNC(=O)CCCN(CCCc2cccc(CCCN(CCCC(=O)NCC3CCN(CCOC(=O)c4cc(Cl)c(N)cc4OC)CC3)C(=O)OC(C)(C)C)c2)C(=O)OC(C)(C)C)CC1 10.1021/jm070552t
17756415 78713 0 None - 0 Human 7.6 pKi = 7.6 Functional
Displacement of [3H]GR-113808 from human 5HT4e receptor expressed in C6 cellsDisplacement of [3H]GR-113808 from human 5HT4e receptor expressed in C6 cells
ChEMBL 1203 24 4 16 8.3 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCC(CNC(=O)CCCN(CC#Cc2ccc(C#CCN(CCCC(=O)NCC3CCN(CCOC(=O)c4cc(Cl)c(N)cc4OC)CC3)C(=O)OC(C)(C)C)cc2)C(=O)OC(C)(C)C)CC1 10.1021/jm070552t
CHEMBL2113287 78713 0 None - 0 Human 7.6 pKi = 7.6 Functional
Displacement of [3H]GR-113808 from human 5HT4e receptor expressed in C6 cellsDisplacement of [3H]GR-113808 from human 5HT4e receptor expressed in C6 cells
ChEMBL 1203 24 4 16 8.3 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCC(CNC(=O)CCCN(CC#Cc2ccc(C#CCN(CCCC(=O)NCC3CCN(CCOC(=O)c4cc(Cl)c(N)cc4OC)CC3)C(=O)OC(C)(C)C)cc2)C(=O)OC(C)(C)C)CC1 10.1021/jm070552t
11724799 10432 0 None - 0 Rat 7.5 pKi = 7.5 Functional
Tested for potency against 5-hydroxytryptamine 4 receptor agonist in rat brainTested for potency against 5-hydroxytryptamine 4 receptor agonist in rat brain
ChEMBL 339 0 2 5 1.5 Nc1cc2c(cc1Cl)C(=O)NC1CCN(CCOCCO2)CC1 10.1021/jm020099f
CHEMBL116913 10432 0 None - 0 Rat 7.5 pKi = 7.5 Functional
Tested for potency against 5-hydroxytryptamine 4 receptor agonist in rat brainTested for potency against 5-hydroxytryptamine 4 receptor agonist in rat brain
ChEMBL 339 0 2 5 1.5 Nc1cc2c(cc1Cl)C(=O)NC1CCN(CCOCCO2)CC1 10.1021/jm020099f
17754944 78717 0 None - 0 Human 7.5 pKi = 7.5 Functional
Displacement of [3H]GR-113808 from human 5HT4e receptor expressed in C6 cellsDisplacement of [3H]GR-113808 from human 5HT4e receptor expressed in C6 cells
ChEMBL 955 23 3 11 8.7 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCC(NC(=O)CCCN(CCCc2ccc(CCCN(CCCC(=O)NC3CCCCC3)C(=O)OC(C)(C)C)cc2)C(=O)OC(C)(C)C)CC1 10.1021/jm070552t
CHEMBL2113291 78717 0 None - 0 Human 7.5 pKi = 7.5 Functional
Displacement of [3H]GR-113808 from human 5HT4e receptor expressed in C6 cellsDisplacement of [3H]GR-113808 from human 5HT4e receptor expressed in C6 cells
ChEMBL 955 23 3 11 8.7 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCC(NC(=O)CCCN(CCCc2ccc(CCCN(CCCC(=O)NC3CCCCC3)C(=O)OC(C)(C)C)cc2)C(=O)OC(C)(C)C)CC1 10.1021/jm070552t
53325991 56144 3 None - 0 Human 5.4 pKi = 5.4 Functional
Antagonistic activity at human 5HT4 receptor expressed in HEK293 cellsAntagonistic activity at human 5HT4 receptor expressed in HEK293 cells
ChEMBL 343 7 3 3 2.5 O=C(O)CCCN1CCC(CNC(=O)c2c[nH]c3ccccc23)CC1 10.1016/j.bmc.2010.10.011
CHEMBL1632156 56144 3 None - 0 Human 5.4 pKi = 5.4 Functional
Antagonistic activity at human 5HT4 receptor expressed in HEK293 cellsAntagonistic activity at human 5HT4 receptor expressed in HEK293 cells
ChEMBL 343 7 3 3 2.5 O=C(O)CCCN1CCC(CNC(=O)c2c[nH]c3ccccc23)CC1 10.1016/j.bmc.2010.10.011
17756414 78712 0 None - 0 Human 7.4 pKi = 7.4 Functional
Displacement of [3H]GR-113808 from human 5HT4e receptor expressed in C6 cellsDisplacement of [3H]GR-113808 from human 5HT4e receptor expressed in C6 cells
ChEMBL 1203 24 4 16 8.3 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCC(CNC(=O)CCCN(CC#Cc2cccc(C#CCN(CCCC(=O)NCC3CCN(CCOC(=O)c4cc(Cl)c(N)cc4OC)CC3)C(=O)OC(C)(C)C)c2)C(=O)OC(C)(C)C)CC1 10.1021/jm070552t
CHEMBL2113286 78712 0 None - 0 Human 7.4 pKi = 7.4 Functional
Displacement of [3H]GR-113808 from human 5HT4e receptor expressed in C6 cellsDisplacement of [3H]GR-113808 from human 5HT4e receptor expressed in C6 cells
ChEMBL 1203 24 4 16 8.3 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCC(CNC(=O)CCCN(CC#Cc2cccc(C#CCN(CCCC(=O)NCC3CCN(CCOC(=O)c4cc(Cl)c(N)cc4OC)CC3)C(=O)OC(C)(C)C)c2)C(=O)OC(C)(C)C)CC1 10.1021/jm070552t
17755039 78709 0 None - 0 Human 7.4 pKi = 7.4 Functional
Displacement of [3H]GR-113808 from human 5HT4e receptor expressed in C6 cellsDisplacement of [3H]GR-113808 from human 5HT4e receptor expressed in C6 cells
ChEMBL 1146 20 4 16 6.7 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCC(CNC(=O)CN(CC#Cc2ccc(C#CCN(CC(=O)NCC3CCN(CCOC(=O)c4cc(Cl)c(N)cc4OC)CC3)C(=O)OC(C)(C)C)cc2)C(=O)OC(C)(C)C)CC1 10.1021/jm070552t
CHEMBL2113283 78709 0 None - 0 Human 7.4 pKi = 7.4 Functional
Displacement of [3H]GR-113808 from human 5HT4e receptor expressed in C6 cellsDisplacement of [3H]GR-113808 from human 5HT4e receptor expressed in C6 cells
ChEMBL 1146 20 4 16 6.7 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCC(CNC(=O)CN(CC#Cc2ccc(C#CCN(CC(=O)NCC3CCN(CCOC(=O)c4cc(Cl)c(N)cc4OC)CC3)C(=O)OC(C)(C)C)cc2)C(=O)OC(C)(C)C)CC1 10.1021/jm070552t
235 2527 36 None -5 4 Human 8.3 pKi = 8.3 Functional
Displacement of [3H]GR-113808 from human 5HT4e receptor expressed in C6 cellsDisplacement of [3H]GR-113808 from human 5HT4e receptor expressed in C6 cells
ChEMBL 312 5 1 5 2.6 COc1cc(N)c(cc1C(=O)OCCN1CCCCC1)Cl 10.1021/jm070552t
5311299 2527 36 None -5 4 Human 8.3 pKi = 8.3 Functional
Displacement of [3H]GR-113808 from human 5HT4e receptor expressed in C6 cellsDisplacement of [3H]GR-113808 from human 5HT4e receptor expressed in C6 cells
ChEMBL 312 5 1 5 2.6 COc1cc(N)c(cc1C(=O)OCCN1CCCCC1)Cl 10.1021/jm070552t
CHEMBL286136 2527 36 None -5 4 Human 8.3 pKi = 8.3 Functional
Displacement of [3H]GR-113808 from human 5HT4e receptor expressed in C6 cellsDisplacement of [3H]GR-113808 from human 5HT4e receptor expressed in C6 cells
ChEMBL 312 5 1 5 2.6 COc1cc(N)c(cc1C(=O)OCCN1CCCCC1)Cl 10.1021/jm070552t
11643822 157317 0 None - 0 Human 7.3 pKi = 7.3 Functional
Displacement of [3H]GR-113808 from human 5HT4e receptor expressed in C6 cellsDisplacement of [3H]GR-113808 from human 5HT4e receptor expressed in C6 cells
ChEMBL 1158 38 6 15 8.8 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCC(NC(=O)CCCCCCCCCCN(CCCCCCCCCCC(=O)NC2CCN(CCOC(=O)c3cc(Cl)c(N)cc3OC)CC2)CC(=O)NCC2CCNCC2)CC1 10.1021/jm070552t
CHEMBL408379 157317 0 None - 0 Human 7.3 pKi = 7.3 Functional
Displacement of [3H]GR-113808 from human 5HT4e receptor expressed in C6 cellsDisplacement of [3H]GR-113808 from human 5HT4e receptor expressed in C6 cells
ChEMBL 1158 38 6 15 8.8 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCC(NC(=O)CCCCCCCCCCN(CCCCCCCCCCC(=O)NC2CCN(CCOC(=O)c3cc(Cl)c(N)cc3OC)CC2)CC(=O)NCC2CCNCC2)CC1 10.1021/jm070552t
10666935 206211 0 None - 0 Human 8.2 pKi = 8.2 Functional
Tested for 5-hydroxytryptamine 4 receptor antagonist activityTested for 5-hydroxytryptamine 4 receptor antagonist activity
ChEMBL 371 5 1 6 1.7 CC(C)N1CCN(CCNC(=O)n2c(=O)n(C3CC3)c3ccccc32)CC1 10.1021/jm020099f
CHEMBL97019 206211 0 None - 0 Human 8.2 pKi = 8.2 Functional
Tested for 5-hydroxytryptamine 4 receptor antagonist activityTested for 5-hydroxytryptamine 4 receptor antagonist activity
ChEMBL 371 5 1 6 1.7 CC(C)N1CCN(CCNC(=O)n2c(=O)n(C3CC3)c3ccccc32)CC1 10.1021/jm020099f
11513350 143384 0 None - 0 Human 8.2 pKi = 8.2 Functional
Displacement of [3H]GR-113808 from human 5HT4e receptor expressed in C6 cellsDisplacement of [3H]GR-113808 from human 5HT4e receptor expressed in C6 cells
ChEMBL 778 18 4 12 4.2 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCC(NC(=O)CCCCCNC(=O)C2CCN(CCOC(=O)c3cc(Cl)c(N)cc3OC)CC2)CC1 10.1021/jm070552t
CHEMBL390205 143384 0 None - 0 Human 8.2 pKi = 8.2 Functional
Displacement of [3H]GR-113808 from human 5HT4e receptor expressed in C6 cellsDisplacement of [3H]GR-113808 from human 5HT4e receptor expressed in C6 cells
ChEMBL 778 18 4 12 4.2 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCC(NC(=O)CCCCCNC(=O)C2CCN(CCOC(=O)c3cc(Cl)c(N)cc3OC)CC2)CC1 10.1021/jm070552t
243 3153 85 None 1 2 Human 8.1 pKi = 8.1 Functional
Tested for agonist activity against 5-hydroxytryptamine 4 receptorTested for agonist activity against 5-hydroxytryptamine 4 receptor
ChEMBL 367 6 2 5 2.1 COCCCN1CCC(CC1)NC(=O)c1cc(Cl)c(c2c1OCC2)N 10.1021/jm020099f
3052762 3153 85 None 1 2 Human 8.1 pKi = 8.1 Functional
Tested for agonist activity against 5-hydroxytryptamine 4 receptorTested for agonist activity against 5-hydroxytryptamine 4 receptor
ChEMBL 367 6 2 5 2.1 COCCCN1CCC(CC1)NC(=O)c1cc(Cl)c(c2c1OCC2)N 10.1021/jm020099f
3502 3153 85 None 1 2 Human 8.1 pKi = 8.1 Functional
Tested for agonist activity against 5-hydroxytryptamine 4 receptorTested for agonist activity against 5-hydroxytryptamine 4 receptor
ChEMBL 367 6 2 5 2.1 COCCCN1CCC(CC1)NC(=O)c1cc(Cl)c(c2c1OCC2)N 10.1021/jm020099f
CHEMBL117287 3153 85 None 1 2 Human 8.1 pKi = 8.1 Functional
Tested for agonist activity against 5-hydroxytryptamine 4 receptorTested for agonist activity against 5-hydroxytryptamine 4 receptor
ChEMBL 367 6 2 5 2.1 COCCCN1CCC(CC1)NC(=O)c1cc(Cl)c(c2c1OCC2)N 10.1021/jm020099f
DB06480 3153 85 None 1 2 Human 8.1 pKi = 8.1 Functional
Tested for agonist activity against 5-hydroxytryptamine 4 receptorTested for agonist activity against 5-hydroxytryptamine 4 receptor
ChEMBL 367 6 2 5 2.1 COCCCN1CCC(CC1)NC(=O)c1cc(Cl)c(c2c1OCC2)N 10.1021/jm020099f
17756314 78710 0 None - 0 Human 8.1 pKi = 8.1 Functional
Displacement of [3H]GR-113808 from human 5HT4e receptor expressed in C6 cellsDisplacement of [3H]GR-113808 from human 5HT4e receptor expressed in C6 cells
ChEMBL 1175 22 4 16 7.8 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCC(NC(=O)CCCN(CC#Cc2cccc(C#CCN(CCCC(=O)NC3CCN(CCOC(=O)c4cc(Cl)c(N)cc4OC)CC3)C(=O)OC(C)(C)C)c2)C(=O)OC(C)(C)C)CC1 10.1021/jm070552t
CHEMBL2113284 78710 0 None - 0 Human 8.1 pKi = 8.1 Functional
Displacement of [3H]GR-113808 from human 5HT4e receptor expressed in C6 cellsDisplacement of [3H]GR-113808 from human 5HT4e receptor expressed in C6 cells
ChEMBL 1175 22 4 16 7.8 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCC(NC(=O)CCCN(CC#Cc2cccc(C#CCN(CCCC(=O)NC3CCN(CCOC(=O)c4cc(Cl)c(N)cc4OC)CC3)C(=O)OC(C)(C)C)c2)C(=O)OC(C)(C)C)CC1 10.1021/jm070552t
11714901 133809 0 None - 0 Human 8.1 pKi = 8.1 Functional
Displacement of [3H]GR-113808 from human 5HT4e receptor expressed in C6 cellsDisplacement of [3H]GR-113808 from human 5HT4e receptor expressed in C6 cells
ChEMBL 904 27 4 12 7.5 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCC(CCNC(=O)CCCCCCCCCCC(=O)NCCC2CCN(CCOC(=O)c3cc(Cl)c(N)cc3OC)CC2)CC1 10.1021/jm070552t
CHEMBL371718 133809 0 None - 0 Human 8.1 pKi = 8.1 Functional
Displacement of [3H]GR-113808 from human 5HT4e receptor expressed in C6 cellsDisplacement of [3H]GR-113808 from human 5HT4e receptor expressed in C6 cells
ChEMBL 904 27 4 12 7.5 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCC(CCNC(=O)CCCCCCCCCCC(=O)NCCC2CCN(CCOC(=O)c3cc(Cl)c(N)cc3OC)CC2)CC1 10.1021/jm070552t
10688893 206646 0 None - 0 Human 7.0 pKi = 7.0 Functional
Tested for 5-hydroxytryptamine 4 receptor antagonist activityTested for 5-hydroxytryptamine 4 receptor antagonist activity
ChEMBL 345 4 1 6 1.2 CC(C)n1c(=O)n(C(=O)NCCN2CCN(C)CC2)c2ccccc21 10.1021/jm020099f
CHEMBL99591 206646 0 None - 0 Human 7.0 pKi = 7.0 Functional
Tested for 5-hydroxytryptamine 4 receptor antagonist activityTested for 5-hydroxytryptamine 4 receptor antagonist activity
ChEMBL 345 4 1 6 1.2 CC(C)n1c(=O)n(C(=O)NCCN2CCN(C)CC2)c2ccccc21 10.1021/jm020099f
1782 2482 81 None -3 12 Human 8.2 pEC50 = 8.2 Functional
NoneNone
Drug Central 299 7 2 4 2.0 CCN(CCNC(=O)c1cc(Cl)c(cc1OC)N)CC None
241 2482 81 None -3 12 Human 8.2 pEC50 = 8.2 Functional
NoneNone
Drug Central 299 7 2 4 2.0 CCN(CCNC(=O)c1cc(Cl)c(cc1OC)N)CC None
4168 2482 81 None -3 12 Human 8.2 pEC50 = 8.2 Functional
NoneNone
Drug Central 299 7 2 4 2.0 CCN(CCNC(=O)c1cc(Cl)c(cc1OC)N)CC None
CHEMBL86 2482 81 None -3 12 Human 8.2 pEC50 = 8.2 Functional
NoneNone
Drug Central 299 7 2 4 2.0 CCN(CCNC(=O)c1cc(Cl)c(cc1OC)N)CC None
DB01233 2482 81 None -3 12 Human 8.2 pEC50 = 8.2 Functional
NoneNone
Drug Central 299 7 2 4 2.0 CCN(CCNC(=O)c1cc(Cl)c(cc1OC)N)CC None
243 3153 85 None -1 2 Rat 8.1 pEC50 = 8.1 Functional
Agonist activity at rat 5HT4e receptor expressed in HEK293 cells assessed as cAMP level after 30 mins by HTRF assayAgonist activity at rat 5HT4e receptor expressed in HEK293 cells assessed as cAMP level after 30 mins by HTRF assay
Drug Central 367 6 2 5 2.1 COCCCN1CCC(CC1)NC(=O)c1cc(Cl)c(c2c1OCC2)N None
3052762 3153 85 None -1 2 Rat 8.1 pEC50 = 8.1 Functional
Agonist activity at rat 5HT4e receptor expressed in HEK293 cells assessed as cAMP level after 30 mins by HTRF assayAgonist activity at rat 5HT4e receptor expressed in HEK293 cells assessed as cAMP level after 30 mins by HTRF assay
Drug Central 367 6 2 5 2.1 COCCCN1CCC(CC1)NC(=O)c1cc(Cl)c(c2c1OCC2)N None
3502 3153 85 None -1 2 Rat 8.1 pEC50 = 8.1 Functional
Agonist activity at rat 5HT4e receptor expressed in HEK293 cells assessed as cAMP level after 30 mins by HTRF assayAgonist activity at rat 5HT4e receptor expressed in HEK293 cells assessed as cAMP level after 30 mins by HTRF assay
Drug Central 367 6 2 5 2.1 COCCCN1CCC(CC1)NC(=O)c1cc(Cl)c(c2c1OCC2)N None
CHEMBL117287 3153 85 None -1 2 Rat 8.1 pEC50 = 8.1 Functional
Agonist activity at rat 5HT4e receptor expressed in HEK293 cells assessed as cAMP level after 30 mins by HTRF assayAgonist activity at rat 5HT4e receptor expressed in HEK293 cells assessed as cAMP level after 30 mins by HTRF assay
Drug Central 367 6 2 5 2.1 COCCCN1CCC(CC1)NC(=O)c1cc(Cl)c(c2c1OCC2)N None
DB06480 3153 85 None -1 2 Rat 8.1 pEC50 = 8.1 Functional
Agonist activity at rat 5HT4e receptor expressed in HEK293 cells assessed as cAMP level after 30 mins by HTRF assayAgonist activity at rat 5HT4e receptor expressed in HEK293 cells assessed as cAMP level after 30 mins by HTRF assay
Drug Central 367 6 2 5 2.1 COCCCN1CCC(CC1)NC(=O)c1cc(Cl)c(c2c1OCC2)N None
135526515 216000 0 None - 1 Guinea pig 8.1 pEC50 = 8.1 Functional
Induction of 5-HT4 receptor-mediated contraction in guinea pig longitudinal muscle myenteric plexusInduction of 5-HT4 receptor-mediated contraction in guinea pig longitudinal muscle myenteric plexus
Drug Central 301 7 4 3 2.8 CCCCCNC(=N)NN=CC1=CNC2=C1C=C(OC)C=C2 None
133076 3347 4 None 1 2 Rat 8.8 pEC50 = 8.8 Functional
UnclassifiedUnclassified
Guide to Pharmacology 417 9 2 6 2.2 COc1cc(N)c(cc1C(=O)CCC1CCN(CC1)CCNS(=O)(=O)C)Cl 8903510
3230 3347 4 None 1 2 Rat 8.8 pEC50 = 8.8 Functional
UnclassifiedUnclassified
Guide to Pharmacology 417 9 2 6 2.2 COc1cc(N)c(cc1C(=O)CCC1CCN(CC1)CCNS(=O)(=O)C)Cl 8903510
CHEMBL83899 3347 4 None 1 2 Rat 8.8 pEC50 = 8.8 Functional
UnclassifiedUnclassified
Guide to Pharmacology 417 9 2 6 2.2 COc1cc(N)c(cc1C(=O)CCC1CCN(CC1)CCNS(=O)(=O)C)Cl 8903510
4223 3929 88 None -177 15 Rat 8.2 pIC50 = 8.2 Functional
Inhibition of rat hydroxytryptamine 4 receptorInhibition of rat hydroxytryptamine 4 receptor
Drug Central 441 7 2 5 4.0 N#Cc1ccc2c(c1)c(CCCCN1CCN(CC1)c1ccc3c(c1)cc(o3)C(=O)N)c[nH]2 None
6918314 3929 88 None -177 15 Rat 8.2 pIC50 = 8.2 Functional
Inhibition of rat hydroxytryptamine 4 receptorInhibition of rat hydroxytryptamine 4 receptor
Drug Central 441 7 2 5 4.0 N#Cc1ccc2c(c1)c(CCCCN1CCN(CC1)c1ccc3c(c1)cc(o3)C(=O)N)c[nH]2 None
7427 3929 88 None -177 15 Rat 8.2 pIC50 = 8.2 Functional
Inhibition of rat hydroxytryptamine 4 receptorInhibition of rat hydroxytryptamine 4 receptor
Drug Central 441 7 2 5 4.0 N#Cc1ccc2c(c1)c(CCCCN1CCN(CC1)c1ccc3c(c1)cc(o3)C(=O)N)c[nH]2 None
CHEMBL439849 3929 88 None -177 15 Rat 8.2 pIC50 = 8.2 Functional
Inhibition of rat hydroxytryptamine 4 receptorInhibition of rat hydroxytryptamine 4 receptor
Drug Central 441 7 2 5 4.0 N#Cc1ccc2c(c1)c(CCCCN1CCN(CC1)c1ccc3c(c1)cc(o3)C(=O)N)c[nH]2 None
DB06684 3929 88 None -177 15 Rat 8.2 pIC50 = 8.2 Functional
Inhibition of rat hydroxytryptamine 4 receptorInhibition of rat hydroxytryptamine 4 receptor
Drug Central 441 7 2 5 4.0 N#Cc1ccc2c(c1)c(CCCCN1CCN(CC1)c1ccc3c(c1)cc(o3)C(=O)N)c[nH]2 None
4223 3929 88 None -177 15 Human 8.2 pIC50 = 8.2 Functional
NoneNone
Drug Central 441 7 2 5 4.0 N#Cc1ccc2c(c1)c(CCCCN1CCN(CC1)c1ccc3c(c1)cc(o3)C(=O)N)c[nH]2 None
6918314 3929 88 None -177 15 Human 8.2 pIC50 = 8.2 Functional
NoneNone
Drug Central 441 7 2 5 4.0 N#Cc1ccc2c(c1)c(CCCCN1CCN(CC1)c1ccc3c(c1)cc(o3)C(=O)N)c[nH]2 None
7427 3929 88 None -177 15 Human 8.2 pIC50 = 8.2 Functional
NoneNone
Drug Central 441 7 2 5 4.0 N#Cc1ccc2c(c1)c(CCCCN1CCN(CC1)c1ccc3c(c1)cc(o3)C(=O)N)c[nH]2 None
CHEMBL439849 3929 88 None -177 15 Human 8.2 pIC50 = 8.2 Functional
NoneNone
Drug Central 441 7 2 5 4.0 N#Cc1ccc2c(c1)c(CCCCN1CCN(CC1)c1ccc3c(c1)cc(o3)C(=O)N)c[nH]2 None
DB06684 3929 88 None -177 15 Human 8.2 pIC50 = 8.2 Functional
NoneNone
Drug Central 441 7 2 5 4.0 N#Cc1ccc2c(c1)c(CCCCN1CCN(CC1)c1ccc3c(c1)cc(o3)C(=O)N)c[nH]2 None
4223 3929 88 None -177 15 Human 6.6 pIC50 = 6.6 Functional
UnclassifiedUnclassified
Guide to Pharmacology 441 7 2 5 4.0 N#Cc1ccc2c(c1)c(CCCCN1CCN(CC1)c1ccc3c(c1)cc(o3)C(=O)N)c[nH]2 15341484
6918314 3929 88 None -177 15 Human 6.6 pIC50 = 6.6 Functional
UnclassifiedUnclassified
Guide to Pharmacology 441 7 2 5 4.0 N#Cc1ccc2c(c1)c(CCCCN1CCN(CC1)c1ccc3c(c1)cc(o3)C(=O)N)c[nH]2 15341484
7427 3929 88 None -177 15 Human 6.6 pIC50 = 6.6 Functional
UnclassifiedUnclassified
Guide to Pharmacology 441 7 2 5 4.0 N#Cc1ccc2c(c1)c(CCCCN1CCN(CC1)c1ccc3c(c1)cc(o3)C(=O)N)c[nH]2 15341484
CHEMBL439849 3929 88 None -177 15 Human 6.6 pIC50 = 6.6 Functional
UnclassifiedUnclassified
Guide to Pharmacology 441 7 2 5 4.0 N#Cc1ccc2c(c1)c(CCCCN1CCN(CC1)c1ccc3c(c1)cc(o3)C(=O)N)c[nH]2 15341484
DB06684 3929 88 None -177 15 Human 6.6 pIC50 = 6.6 Functional
UnclassifiedUnclassified
Guide to Pharmacology 441 7 2 5 4.0 N#Cc1ccc2c(c1)c(CCCCN1CCN(CC1)c1ccc3c(c1)cc(o3)C(=O)N)c[nH]2 15341484




Ligands Receptor Assay information Chemical information
Sel. page Common
name
GPCRdb ID #Vendors Reference
ligand
Fold selectivity
(Affinity)
# tested GPCRs
(Affinity)
Species p-value
(-log)
Type Activity
Relation
Activity
Value
Assay Type Assay Description Source Mol
weight
Rot
Bonds
H don H acc LogP Smiles DOI
145973928 164017 0 None - 0 Human 10.0 pEC50 = 10 Binding
Agonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assayAgonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assay
ChEMBL 398 6 1 5 3.3 CC(C)c1cc2cccc(C(=O)NCC3CCN(CC4CCOCC4)CC3)n2n1 10.1021/acs.jmedchem.8b00457
CHEMBL4215329 164017 0 None - 0 Human 10.0 pEC50 = 10 Binding
Agonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assayAgonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assay
ChEMBL 398 6 1 5 3.3 CC(C)c1cc2cccc(C(=O)NCC3CCN(CC4CCOCC4)CC3)n2n1 10.1021/acs.jmedchem.8b00457
53354764 3015 30 None 1 2 Human 9.6 pEC50 = 9.6 Binding
Agonist activity at 5-HT4E receptor (unknown origin)Agonist activity at 5-HT4E receptor (unknown origin)
ChEMBL 432 7 1 8 2.6 OC1(CCOCC1)CN1CCC(CC1)COc1noc2c1c(ccc2)O[C@H]1COCC1 10.1021/acs.jmedchem.8b00457
9059 3015 30 None 1 2 Human 9.6 pEC50 = 9.6 Binding
Agonist activity at 5-HT4E receptor (unknown origin)Agonist activity at 5-HT4E receptor (unknown origin)
ChEMBL 432 7 1 8 2.6 OC1(CCOCC1)CN1CCC(CC1)COc1noc2c1c(ccc2)O[C@H]1COCC1 10.1021/acs.jmedchem.8b00457
CHEMBL2152922 3015 30 None 1 2 Human 9.6 pEC50 = 9.6 Binding
Agonist activity at 5-HT4E receptor (unknown origin)Agonist activity at 5-HT4E receptor (unknown origin)
ChEMBL 432 7 1 8 2.6 OC1(CCOCC1)CN1CCC(CC1)COc1noc2c1c(ccc2)O[C@H]1COCC1 10.1021/acs.jmedchem.8b00457
DB12675 3015 30 None 1 2 Human 9.6 pEC50 = 9.6 Binding
Agonist activity at 5-HT4E receptor (unknown origin)Agonist activity at 5-HT4E receptor (unknown origin)
ChEMBL 432 7 1 8 2.6 OC1(CCOCC1)CN1CCC(CC1)COc1noc2c1c(ccc2)O[C@H]1COCC1 10.1021/acs.jmedchem.8b00457
145975193 163319 0 None - 0 Human 9.5 pEC50 = 9.5 Binding
Agonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assayAgonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assay
ChEMBL 372 8 1 5 2.9 COCCCN1CCC(CNC(=O)c2cccc3cc(C(C)C)nn23)CC1 10.1021/acs.jmedchem.8b00457
CHEMBL4206847 163319 0 None - 0 Human 9.5 pEC50 = 9.5 Binding
Agonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assayAgonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assay
ChEMBL 372 8 1 5 2.9 COCCCN1CCC(CNC(=O)c2cccc3cc(C(C)C)nn23)CC1 10.1021/acs.jmedchem.8b00457
145973097 164166 0 None - 0 Human 9.5 pEC50 = 9.5 Binding
Agonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assayAgonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assay
ChEMBL 412 6 2 5 3.6 CC(C)c1cn2cccc(C(=O)NCC3CCN(CC4(O)CCCCC4)CC3)c2n1 10.1021/acs.jmedchem.8b00457
CHEMBL4217381 164166 0 None - 0 Human 9.5 pEC50 = 9.5 Binding
Agonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assayAgonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assay
ChEMBL 412 6 2 5 3.6 CC(C)c1cn2cccc(C(=O)NCC3CCN(CC4(O)CCCCC4)CC3)c2n1 10.1021/acs.jmedchem.8b00457
145965246 163669 0 None - 0 Human 9.4 pEC50 = 9.4 Binding
Agonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assayAgonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assay
ChEMBL 414 6 2 6 2.4 CC(C)c1cn2cccc(C(=O)NCC3CCN(CC4(O)CCOCC4)CC3)c2n1 10.1021/acs.jmedchem.8b00457
CHEMBL4211044 163669 0 None - 0 Human 9.4 pEC50 = 9.4 Binding
Agonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assayAgonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assay
ChEMBL 414 6 2 6 2.4 CC(C)c1cn2cccc(C(=O)NCC3CCN(CC4(O)CCOCC4)CC3)c2n1 10.1021/acs.jmedchem.8b00457
77105903 163448 0 None - 0 Human 9.2 pEC50 = 9.2 Binding
Agonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assayAgonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assay
ChEMBL 398 6 1 5 3.3 CC(C)c1cn2cccc(C(=O)NCC3CCN(CC4CCOCC4)CC3)c2n1 10.1021/acs.jmedchem.8b00457
CHEMBL4208302 163448 0 None - 0 Human 9.2 pEC50 = 9.2 Binding
Agonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assayAgonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assay
ChEMBL 398 6 1 5 3.3 CC(C)c1cn2cccc(C(=O)NCC3CCN(CC4CCOCC4)CC3)c2n1 10.1021/acs.jmedchem.8b00457
145967487 163848 0 None - 0 Human 9.2 pEC50 = 9.2 Binding
Agonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assayAgonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assay
ChEMBL 455 6 1 6 3.4 COC(=O)N1CCC(CN2CCC(CNC(=O)c3cccn4cc(C(C)C)nc34)CC2)CC1 10.1021/acs.jmedchem.8b00457
CHEMBL4213334 163848 0 None - 0 Human 9.2 pEC50 = 9.2 Binding
Agonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assayAgonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assay
ChEMBL 455 6 1 6 3.4 COC(=O)N1CCC(CN2CCC(CNC(=O)c3cccn4cc(C(C)C)nc34)CC2)CC1 10.1021/acs.jmedchem.8b00457
145972577 164065 0 None - 0 Human 9.2 pEC50 = 9.2 Binding
Agonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assayAgonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assay
ChEMBL 372 6 2 5 2.7 CC(C)c1cn2cccc(C(=O)NCC3CCN(CC(C)(C)O)CC3)c2n1 10.1021/acs.jmedchem.8b00457
CHEMBL4216003 164065 0 None - 0 Human 9.2 pEC50 = 9.2 Binding
Agonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assayAgonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assay
ChEMBL 372 6 2 5 2.7 CC(C)c1cn2cccc(C(=O)NCC3CCN(CC(C)(C)O)CC3)c2n1 10.1021/acs.jmedchem.8b00457
11350913 136272 1 None - 0 Human 8.9 pEC50 = 8.9 Binding
Agonist activity at 5-HT4D receptor (unknown origin)Agonist activity at 5-HT4D receptor (unknown origin)
ChEMBL 430 5 2 7 2.2 CC(C)n1c(=O)n(C(=O)NCC2CCN(CC3(O)CCOCC3)CC2)c2ccccc21 10.1016/j.ejmech.2015.08.051
CHEMBL3741376 136272 1 None - 0 Human 8.9 pEC50 = 8.9 Binding
Agonist activity at 5-HT4D receptor (unknown origin)Agonist activity at 5-HT4D receptor (unknown origin)
ChEMBL 430 5 2 7 2.2 CC(C)n1c(=O)n(C(=O)NCC2CCN(CC3(O)CCOCC3)CC2)c2ccccc21 10.1016/j.ejmech.2015.08.051
53354764 3015 30 None 1 2 Human 8.8 pEC50 = 8.8 Binding
Agonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assayAgonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assay
ChEMBL 432 7 1 8 2.6 OC1(CCOCC1)CN1CCC(CC1)COc1noc2c1c(ccc2)O[C@H]1COCC1 10.1021/acs.jmedchem.8b00457
9059 3015 30 None 1 2 Human 8.8 pEC50 = 8.8 Binding
Agonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assayAgonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assay
ChEMBL 432 7 1 8 2.6 OC1(CCOCC1)CN1CCC(CC1)COc1noc2c1c(ccc2)O[C@H]1COCC1 10.1021/acs.jmedchem.8b00457
CHEMBL2152922 3015 30 None 1 2 Human 8.8 pEC50 = 8.8 Binding
Agonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assayAgonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assay
ChEMBL 432 7 1 8 2.6 OC1(CCOCC1)CN1CCC(CC1)COc1noc2c1c(ccc2)O[C@H]1COCC1 10.1021/acs.jmedchem.8b00457
DB12675 3015 30 None 1 2 Human 8.8 pEC50 = 8.8 Binding
Agonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assayAgonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assay
ChEMBL 432 7 1 8 2.6 OC1(CCOCC1)CN1CCC(CC1)COc1noc2c1c(ccc2)O[C@H]1COCC1 10.1021/acs.jmedchem.8b00457
145975035 162979 0 None - 0 Human 8.8 pEC50 = 8.8 Binding
Agonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assayAgonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assay
ChEMBL 372 8 1 5 2.9 COCCCN1CCC(CNC(=O)c2cccn3cc(C(C)C)nc23)CC1 10.1021/acs.jmedchem.8b00457
CHEMBL4202791 162979 0 None - 0 Human 8.8 pEC50 = 8.8 Binding
Agonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assayAgonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assay
ChEMBL 372 8 1 5 2.9 COCCCN1CCC(CNC(=O)c2cccn3cc(C(C)C)nc23)CC1 10.1021/acs.jmedchem.8b00457
145966407 163663 0 None - 0 Human 8.0 pEC50 = 8.0 Binding
Agonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assayAgonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assay
ChEMBL 382 5 1 5 2.5 CC(C)c1nc(C(=O)NCC2C3CN(C4CCOCC4)CC23)n2ccccc12 10.1021/acs.jmedchem.8b00457
CHEMBL4210983 163663 0 None - 0 Human 8.0 pEC50 = 8.0 Binding
Agonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assayAgonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assay
ChEMBL 382 5 1 5 2.5 CC(C)c1nc(C(=O)NCC2C3CN(C4CCOCC4)CC23)n2ccccc12 10.1021/acs.jmedchem.8b00457
68592173 137316 0 None - 0 Rat 7.0 pEC50 = 7 Binding
Agonist activity at 5-HT4 receptor in rat esophageal thoracic muscularis mucosae assessed as carbachol-induced contractionAgonist activity at 5-HT4 receptor in rat esophageal thoracic muscularis mucosae assessed as carbachol-induced contraction
ChEMBL 494 6 2 6 3.0 COc1cc(N)c(Cl)cc1C(=O)N[C@H]1CCN(CC2CCN(C(=O)C(C)(C)C)CC2)C[C@H]1OC 10.1016/j.ejmech.2015.12.006
CHEMBL3759944 137316 0 None - 0 Rat 7.0 pEC50 = 7 Binding
Agonist activity at 5-HT4 receptor in rat esophageal thoracic muscularis mucosae assessed as carbachol-induced contractionAgonist activity at 5-HT4 receptor in rat esophageal thoracic muscularis mucosae assessed as carbachol-induced contraction
ChEMBL 494 6 2 6 3.0 COc1cc(N)c(Cl)cc1C(=O)N[C@H]1CCN(CC2CCN(C(=O)C(C)(C)C)CC2)C[C@H]1OC 10.1016/j.ejmech.2015.12.006
240 931 39 None -4 25 Guinea pig 7.0 pEC50 = 7 Binding
Induction of 5-HT4 receptor-mediated contraction in guinea pig longitudinal muscle myenteric plexusInduction of 5-HT4 receptor-mediated contraction in guinea pig longitudinal muscle myenteric plexus
ChEMBL 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N 10.1016/j.bmcl.2013.05.018
2769 931 39 None -4 25 Guinea pig 7.0 pEC50 = 7 Binding
Induction of 5-HT4 receptor-mediated contraction in guinea pig longitudinal muscle myenteric plexusInduction of 5-HT4 receptor-mediated contraction in guinea pig longitudinal muscle myenteric plexus
ChEMBL 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N 10.1016/j.bmcl.2013.05.018
44279790 931 39 None -4 25 Guinea pig 7.0 pEC50 = 7 Binding
Induction of 5-HT4 receptor-mediated contraction in guinea pig longitudinal muscle myenteric plexusInduction of 5-HT4 receptor-mediated contraction in guinea pig longitudinal muscle myenteric plexus
ChEMBL 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N 10.1016/j.bmcl.2013.05.018
660 931 39 None -4 25 Guinea pig 7.0 pEC50 = 7 Binding
Induction of 5-HT4 receptor-mediated contraction in guinea pig longitudinal muscle myenteric plexusInduction of 5-HT4 receptor-mediated contraction in guinea pig longitudinal muscle myenteric plexus
ChEMBL 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N 10.1016/j.bmcl.2013.05.018
CHEMBL1729 931 39 None -4 25 Guinea pig 7.0 pEC50 = 7 Binding
Induction of 5-HT4 receptor-mediated contraction in guinea pig longitudinal muscle myenteric plexusInduction of 5-HT4 receptor-mediated contraction in guinea pig longitudinal muscle myenteric plexus
ChEMBL 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N 10.1016/j.bmcl.2013.05.018
CHEMBL560739 931 39 None -4 25 Guinea pig 7.0 pEC50 = 7 Binding
Induction of 5-HT4 receptor-mediated contraction in guinea pig longitudinal muscle myenteric plexusInduction of 5-HT4 receptor-mediated contraction in guinea pig longitudinal muscle myenteric plexus
ChEMBL 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N 10.1016/j.bmcl.2013.05.018
DB00604 931 39 None -4 25 Guinea pig 7.0 pEC50 = 7 Binding
Induction of 5-HT4 receptor-mediated contraction in guinea pig longitudinal muscle myenteric plexusInduction of 5-HT4 receptor-mediated contraction in guinea pig longitudinal muscle myenteric plexus
ChEMBL 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N 10.1016/j.bmcl.2013.05.018
5311047 203055 30 None - 2 Rat 7.0 pEC50 = 7.0 Binding
Agonist activity at 5-HT4 receptor in rat esophageal thoracic muscularis mucosae assessed as carbachol-induced contractionAgonist activity at 5-HT4 receptor in rat esophageal thoracic muscularis mucosae assessed as carbachol-induced contraction
ChEMBL 465 9 2 6 3.4 COc1cc(N)c(Cl)cc1C(=O)N[C@H]1CCN(CCCOc2ccc(F)cc2)C[C@H]1OC 10.1016/j.ejmech.2015.12.006
CHEMBL74656 203055 30 None - 2 Rat 7.0 pEC50 = 7.0 Binding
Agonist activity at 5-HT4 receptor in rat esophageal thoracic muscularis mucosae assessed as carbachol-induced contractionAgonist activity at 5-HT4 receptor in rat esophageal thoracic muscularis mucosae assessed as carbachol-induced contraction
ChEMBL 465 9 2 6 3.4 COc1cc(N)c(Cl)cc1C(=O)N[C@H]1CCN(CCCOc2ccc(F)cc2)C[C@H]1OC 10.1016/j.ejmech.2015.12.006
67922794 137195 0 None - 0 Rat 6.0 pEC50 = 6.0 Binding
Agonist activity at 5-HT4 receptor in rat esophageal thoracic muscularis mucosae assessed as carbachol-induced contractionAgonist activity at 5-HT4 receptor in rat esophageal thoracic muscularis mucosae assessed as carbachol-induced contraction
ChEMBL 452 7 2 6 2.2 COc1cc(N)c(Cl)cc1C(=O)N[C@H]1CCN(CCC(=O)N2CCCCC2)C[C@H]1OC 10.1016/j.ejmech.2015.12.006
CHEMBL3758945 137195 0 None - 0 Rat 6.0 pEC50 = 6.0 Binding
Agonist activity at 5-HT4 receptor in rat esophageal thoracic muscularis mucosae assessed as carbachol-induced contractionAgonist activity at 5-HT4 receptor in rat esophageal thoracic muscularis mucosae assessed as carbachol-induced contraction
ChEMBL 452 7 2 6 2.2 COc1cc(N)c(Cl)cc1C(=O)N[C@H]1CCN(CCC(=O)N2CCCCC2)C[C@H]1OC 10.1016/j.ejmech.2015.12.006
145977971 163456 0 None - 0 Human 6.0 pEC50 = 6.0 Binding
Agonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assayAgonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assay
ChEMBL 406 8 1 5 3.6 COCCCN1CCC(CNC(=O)c2cccn3c(Cl)c(C(C)C)nc23)CC1 10.1021/acs.jmedchem.8b00457
CHEMBL4208394 163456 0 None - 0 Human 6.0 pEC50 = 6.0 Binding
Agonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assayAgonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assay
ChEMBL 406 8 1 5 3.6 COCCCN1CCC(CNC(=O)c2cccn3c(Cl)c(C(C)C)nc23)CC1 10.1021/acs.jmedchem.8b00457
10584 1435 0 None -1 2 Human 8.0 pEC50 = 8.0 Binding
Activity at 5-HT4R (unknown origin) expressed in COS7 cells assessed as increase in sAPPalpha releaseActivity at 5-HT4R (unknown origin) expressed in COS7 cells assessed as increase in sAPPalpha release
ChEMBL 392 7 1 4 5.2 COc1cc(N)c(cc1C(=O)CCC1CCN(CC1)CC1CCCCC1)Cl 10.1021/acs.jmedchem.5b00115
86582973 1435 0 None -1 2 Human 8.0 pEC50 = 8.0 Binding
Activity at 5-HT4R (unknown origin) expressed in COS7 cells assessed as increase in sAPPalpha releaseActivity at 5-HT4R (unknown origin) expressed in COS7 cells assessed as increase in sAPPalpha release
ChEMBL 392 7 1 4 5.2 COc1cc(N)c(cc1C(=O)CCC1CCN(CC1)CC1CCCCC1)Cl 10.1021/acs.jmedchem.5b00115
CHEMBL3417009 1435 0 None -1 2 Human 8.0 pEC50 = 8.0 Binding
Activity at 5-HT4R (unknown origin) expressed in COS7 cells assessed as increase in sAPPalpha releaseActivity at 5-HT4R (unknown origin) expressed in COS7 cells assessed as increase in sAPPalpha release
ChEMBL 392 7 1 4 5.2 COc1cc(N)c(cc1C(=O)CCC1CCN(CC1)CC1CCCCC1)Cl 10.1021/acs.jmedchem.5b00115
9975257 48490 1 None - 0 Human 6.0 pEC50 = 6.0 Binding
Tested for 5-hydroxytryptamine 4 binding affinity against zacoprideTested for 5-hydroxytryptamine 4 binding affinity against zacopride
ChEMBL 351 3 2 4 3.1 COc1cc(N)c(Cl)cc1C(=O)NC1CCN2C(C)CCCC2C1 10.1021/jm020099f
CHEMBL15585 48490 1 None - 0 Human 6.0 pEC50 = 6.0 Binding
Tested for 5-hydroxytryptamine 4 binding affinity against zacoprideTested for 5-hydroxytryptamine 4 binding affinity against zacopride
ChEMBL 351 3 2 4 3.1 COc1cc(N)c(Cl)cc1C(=O)NC1CCN2C(C)CCCC2C1 10.1021/jm020099f
9797313 101459 1 None - 3 Human 6.0 pEC50 = 6.0 Binding
Tested for 5-hydroxytryptamine 4 binding affinity against zacoprideTested for 5-hydroxytryptamine 4 binding affinity against zacopride
ChEMBL 323 3 2 4 2.3 COc1cc(N)c(Cl)cc1C(=O)NC1CC2CCC(C1)N2C 10.1021/jm020099f
CHEMBL301039 101459 1 None - 3 Human 6.0 pEC50 = 6.0 Binding
Tested for 5-hydroxytryptamine 4 binding affinity against zacoprideTested for 5-hydroxytryptamine 4 binding affinity against zacopride
ChEMBL 323 3 2 4 2.3 COc1cc(N)c(Cl)cc1C(=O)NC1CC2CCC(C1)N2C 10.1021/jm020099f
145975740 163435 0 None - 0 Human 6.9 pEC50 = 6.9 Binding
Agonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assayAgonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assay
ChEMBL 396 6 1 5 2.8 CC(C)c1cn2cccc(C(=O)NCC3C4CN(CC5CCOCC5)CC34)c2n1 10.1021/acs.jmedchem.8b00457
CHEMBL4208144 163435 0 None - 0 Human 6.9 pEC50 = 6.9 Binding
Agonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assayAgonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assay
ChEMBL 396 6 1 5 2.8 CC(C)c1cn2cccc(C(=O)NCC3C4CN(CC5CCOCC5)CC34)c2n1 10.1021/acs.jmedchem.8b00457
135409453 3714 38 None - 2 Guinea pig 7.9 pEC50 = 7.9 Binding
Induction of 5-HT4 receptor-mediated contraction in guinea pig longitudinal muscle myenteric plexusInduction of 5-HT4 receptor-mediated contraction in guinea pig longitudinal muscle myenteric plexus
ChEMBL 301 7 3 3 2.6 CCCCCN=C(N/N=C/c1c[nH]c2c1cc(OC)cc2)N 10.1016/j.bmcl.2013.05.018
226 3714 38 None - 2 Guinea pig 7.9 pEC50 = 7.9 Binding
Induction of 5-HT4 receptor-mediated contraction in guinea pig longitudinal muscle myenteric plexusInduction of 5-HT4 receptor-mediated contraction in guinea pig longitudinal muscle myenteric plexus
ChEMBL 301 7 3 3 2.6 CCCCCN=C(N/N=C/c1c[nH]c2c1cc(OC)cc2)N 10.1016/j.bmcl.2013.05.018
CHEMBL76370 3714 38 None - 2 Guinea pig 7.9 pEC50 = 7.9 Binding
Induction of 5-HT4 receptor-mediated contraction in guinea pig longitudinal muscle myenteric plexusInduction of 5-HT4 receptor-mediated contraction in guinea pig longitudinal muscle myenteric plexus
ChEMBL 301 7 3 3 2.6 CCCCCN=C(N/N=C/c1c[nH]c2c1cc(OC)cc2)N 10.1016/j.bmcl.2013.05.018
9975257 48490 1 None - 0 Human 6.9 pEC50 = 6.9 Binding
Tested for 5-hydroxytryptamine 4 binding affinity against renzaprideTested for 5-hydroxytryptamine 4 binding affinity against renzapride
ChEMBL 351 3 2 4 3.1 COc1cc(N)c(Cl)cc1C(=O)NC1CCN2C(C)CCCC2C1 10.1021/jm020099f
CHEMBL15585 48490 1 None - 0 Human 6.9 pEC50 = 6.9 Binding
Tested for 5-hydroxytryptamine 4 binding affinity against renzaprideTested for 5-hydroxytryptamine 4 binding affinity against renzapride
ChEMBL 351 3 2 4 3.1 COc1cc(N)c(Cl)cc1C(=O)NC1CCN2C(C)CCCC2C1 10.1021/jm020099f
9797313 101459 1 None - 3 Human 6.9 pEC50 = 6.9 Binding
Tested for 5-hydroxytryptamine 4 binding affinity against renzaprideTested for 5-hydroxytryptamine 4 binding affinity against renzapride
ChEMBL 323 3 2 4 2.3 COc1cc(N)c(Cl)cc1C(=O)NC1CC2CCC(C1)N2C 10.1021/jm020099f
CHEMBL301039 101459 1 None - 3 Human 6.9 pEC50 = 6.9 Binding
Tested for 5-hydroxytryptamine 4 binding affinity against renzaprideTested for 5-hydroxytryptamine 4 binding affinity against renzapride
ChEMBL 323 3 2 4 2.3 COc1cc(N)c(Cl)cc1C(=O)NC1CC2CCC(C1)N2C 10.1021/jm020099f
145973946 164059 0 None - 0 Human 7.9 pEC50 = 7.9 Binding
Agonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assayAgonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assay
ChEMBL 370 8 1 5 2.4 COCCCN1CC2C(CNC(=O)c3nc(C(C)C)c4ccccn34)C2C1 10.1021/acs.jmedchem.8b00457
CHEMBL4215943 164059 0 None - 0 Human 7.9 pEC50 = 7.9 Binding
Agonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assayAgonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assay
ChEMBL 370 8 1 5 2.4 COCCCN1CC2C(CNC(=O)c3nc(C(C)C)c4ccccn34)C2C1 10.1021/acs.jmedchem.8b00457
145978459 163025 0 None - 0 Human 7.9 pEC50 = 7.9 Binding
Agonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assayAgonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assay
ChEMBL 370 8 1 5 2.4 COCCCN1CC2C(CNC(=O)c3cccn4cc(C(C)C)nc34)C2C1 10.1021/acs.jmedchem.8b00457
CHEMBL4203277 163025 0 None - 0 Human 7.9 pEC50 = 7.9 Binding
Agonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assayAgonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assay
ChEMBL 370 8 1 5 2.4 COCCCN1CC2C(CNC(=O)c3cccn4cc(C(C)C)nc34)C2C1 10.1021/acs.jmedchem.8b00457
10521792 110102 0 None - 0 Human 7.9 pEC50 = 7.9 Binding
Compound was tested for 5-hydroxytryptamine 4 binding affinityCompound was tested for 5-hydroxytryptamine 4 binding affinity
ChEMBL 349 4 2 4 2.6 Nc1c(Cl)cc(C(=O)NCCC23CCCN2CCC3)c2c1CCO2 10.1021/jm020099f
CHEMBL325494 110102 0 None - 0 Human 7.9 pEC50 = 7.9 Binding
Compound was tested for 5-hydroxytryptamine 4 binding affinityCompound was tested for 5-hydroxytryptamine 4 binding affinity
ChEMBL 349 4 2 4 2.6 Nc1c(Cl)cc(C(=O)NCCC23CCCN2CCC3)c2c1CCO2 10.1021/jm020099f
135409453 3714 38 None -2 2 Human 7.8 pEC50 = 7.8 Binding
5-HT4C receptor-mediated exchange of GDP for europium labeled GTP (pEC50)5-HT4C receptor-mediated exchange of GDP for europium labeled GTP (pEC50)
ChEMBL 301 7 3 3 2.6 CCCCCN=C(N/N=C/c1c[nH]c2c1cc(OC)cc2)N 10.1016/j.bmcl.2012.05.034
226 3714 38 None -2 2 Human 7.8 pEC50 = 7.8 Binding
5-HT4C receptor-mediated exchange of GDP for europium labeled GTP (pEC50)5-HT4C receptor-mediated exchange of GDP for europium labeled GTP (pEC50)
ChEMBL 301 7 3 3 2.6 CCCCCN=C(N/N=C/c1c[nH]c2c1cc(OC)cc2)N 10.1016/j.bmcl.2012.05.034
CHEMBL76370 3714 38 None -2 2 Human 7.8 pEC50 = 7.8 Binding
5-HT4C receptor-mediated exchange of GDP for europium labeled GTP (pEC50)5-HT4C receptor-mediated exchange of GDP for europium labeled GTP (pEC50)
ChEMBL 301 7 3 3 2.6 CCCCCN=C(N/N=C/c1c[nH]c2c1cc(OC)cc2)N 10.1016/j.bmcl.2012.05.034
68593871 137239 0 None - 0 Rat 5.8 pEC50 = 5.8 Binding
Agonist activity at 5-HT4 receptor in rat esophageal thoracic muscularis mucosae assessed as carbachol-induced contractionAgonist activity at 5-HT4 receptor in rat esophageal thoracic muscularis mucosae assessed as carbachol-induced contraction
ChEMBL 466 7 2 6 2.4 CCC(=O)N1CCCC(CN2CC[C@H](NC(=O)c3cc(Cl)c(N)cc3OC)[C@H](OC)C2)C1 10.1016/j.ejmech.2015.12.006
CHEMBL3759348 137239 0 None - 0 Rat 5.8 pEC50 = 5.8 Binding
Agonist activity at 5-HT4 receptor in rat esophageal thoracic muscularis mucosae assessed as carbachol-induced contractionAgonist activity at 5-HT4 receptor in rat esophageal thoracic muscularis mucosae assessed as carbachol-induced contraction
ChEMBL 466 7 2 6 2.4 CCC(=O)N1CCCC(CN2CC[C@H](NC(=O)c3cc(Cl)c(N)cc3OC)[C@H](OC)C2)C1 10.1016/j.ejmech.2015.12.006
54677674 112311 4 None - 1 Human 7.8 pEC50 = 7.8 Binding
Agonist activity at 5-HT4E receptor (unknown origin)Agonist activity at 5-HT4E receptor (unknown origin)
ChEMBL 377 6 2 6 3.0 CC(C)n1c(=O)c(C(=O)NCCCN2CCCCC2)c(O)c2ccsc21 10.1021/acs.jmedchem.8b00457
CHEMBL3291085 112311 4 None - 1 Human 7.8 pEC50 = 7.8 Binding
Agonist activity at 5-HT4E receptor (unknown origin)Agonist activity at 5-HT4E receptor (unknown origin)
ChEMBL 377 6 2 6 3.0 CC(C)n1c(=O)c(C(=O)NCCCN2CCCCC2)c(O)c2ccsc21 10.1021/acs.jmedchem.8b00457
CHEMBL3306918 112311 4 None - 1 Human 7.8 pEC50 = 7.8 Binding
Agonist activity at 5-HT4E receptor (unknown origin)Agonist activity at 5-HT4E receptor (unknown origin)
ChEMBL 377 6 2 6 3.0 CC(C)n1c(=O)c(C(=O)NCCCN2CCCCC2)c(O)c2ccsc21 10.1021/acs.jmedchem.8b00457
145964870 163858 0 None - 0 Human 7.8 pEC50 = 7.8 Binding
Agonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assayAgonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assay
ChEMBL 370 6 2 5 2.1 CC(C)c1cn2cccc(C(=O)NCC3C4CN(CC(C)(C)O)CC34)c2n1 10.1021/acs.jmedchem.8b00457
CHEMBL4213441 163858 0 None - 0 Human 7.8 pEC50 = 7.8 Binding
Agonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assayAgonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assay
ChEMBL 370 6 2 5 2.1 CC(C)c1cn2cccc(C(=O)NCC3C4CN(CC(C)(C)O)CC34)c2n1 10.1021/acs.jmedchem.8b00457
145976249 162993 0 None - 0 Human 5.7 pEC50 = 5.7 Binding
Agonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assayAgonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assay
ChEMBL 373 8 1 6 2.3 COCCCN1CCC(CNC(=O)c2cccn3nc(C(C)C)nc23)CC1 10.1021/acs.jmedchem.8b00457
CHEMBL4202922 162993 0 None - 0 Human 5.7 pEC50 = 5.7 Binding
Agonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assayAgonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assay
ChEMBL 373 8 1 6 2.3 COCCCN1CCC(CNC(=O)c2cccn3nc(C(C)C)nc23)CC1 10.1021/acs.jmedchem.8b00457
145977126 163246 0 None - 0 Human 5.7 pEC50 = 5.7 Binding
Agonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assayAgonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assay
ChEMBL 373 8 1 6 2.3 COCCCN1CCC(CNC(=O)c2cccc3nc(C(C)C)nn23)CC1 10.1021/acs.jmedchem.8b00457
CHEMBL4206020 163246 0 None - 0 Human 5.7 pEC50 = 5.7 Binding
Agonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assayAgonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assay
ChEMBL 373 8 1 6 2.3 COCCCN1CCC(CNC(=O)c2cccc3nc(C(C)C)nn23)CC1 10.1021/acs.jmedchem.8b00457
11961293 3710 13 None - 1 Guinea pig 8.6 pEC50 = 8.6 Binding
Induction of 5-HT4 receptor-mediated contraction in guinea pig longitudinal muscle myenteric plexusInduction of 5-HT4 receptor-mediated contraction in guinea pig longitudinal muscle myenteric plexus
ChEMBL 455 6 2 5 3.6 COC(=O)N1CCC(CC1)CN1CCC(CC1)CNC(=O)c1cccc2c1nc([nH]2)C(C)C 10.1016/j.bmcl.2013.05.018
8426 3710 13 None - 1 Guinea pig 8.6 pEC50 = 8.6 Binding
Induction of 5-HT4 receptor-mediated contraction in guinea pig longitudinal muscle myenteric plexusInduction of 5-HT4 receptor-mediated contraction in guinea pig longitudinal muscle myenteric plexus
ChEMBL 455 6 2 5 3.6 COC(=O)N1CCC(CC1)CN1CCC(CC1)CNC(=O)c1cccc2c1nc([nH]2)C(C)C 10.1016/j.bmcl.2013.05.018
CHEMBL2402904 3710 13 None - 1 Guinea pig 8.6 pEC50 = 8.6 Binding
Induction of 5-HT4 receptor-mediated contraction in guinea pig longitudinal muscle myenteric plexusInduction of 5-HT4 receptor-mediated contraction in guinea pig longitudinal muscle myenteric plexus
ChEMBL 455 6 2 5 3.6 COC(=O)N1CCC(CC1)CN1CCC(CC1)CNC(=O)c1cccc2c1nc([nH]2)C(C)C 10.1016/j.bmcl.2013.05.018
DB12725 3710 13 None - 1 Guinea pig 8.6 pEC50 = 8.6 Binding
Induction of 5-HT4 receptor-mediated contraction in guinea pig longitudinal muscle myenteric plexusInduction of 5-HT4 receptor-mediated contraction in guinea pig longitudinal muscle myenteric plexus
ChEMBL 455 6 2 5 3.6 COC(=O)N1CCC(CC1)CN1CCC(CC1)CNC(=O)c1cccc2c1nc([nH]2)C(C)C 10.1016/j.bmcl.2013.05.018
138376515 163236 3 None - 0 Human 7.7 pEC50 = 7.7 Binding
Agonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assayAgonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assay
ChEMBL 409 5 0 7 4.1 CC(C)c1cc2cccc(-c3nnc(C4CCN(CC5CCOCC5)CC4)o3)n2n1 10.1021/acs.jmedchem.8b00457
CHEMBL4205936 163236 3 None - 0 Human 7.7 pEC50 = 7.7 Binding
Agonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assayAgonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assay
ChEMBL 409 5 0 7 4.1 CC(C)c1cc2cccc(-c3nnc(C4CCN(CC5CCOCC5)CC4)o3)n2n1 10.1021/acs.jmedchem.8b00457
127037818 136171 1 None - 0 Human 7.7 pEC50 = 7.7 Binding
Inhibition of 5-HT4 receptor (unknown origin)Inhibition of 5-HT4 receptor (unknown origin)
ChEMBL 370 8 1 5 2.4 COCCCN1C[C@H]2[C@H](CNC(=O)c3nc(C(C)C)n4ccccc34)[C@H]2C1 10.1016/j.ejmech.2019.111569
CHEMBL3740472 136171 1 None - 0 Human 7.7 pEC50 = 7.7 Binding
Inhibition of 5-HT4 receptor (unknown origin)Inhibition of 5-HT4 receptor (unknown origin)
ChEMBL 370 8 1 5 2.4 COCCCN1C[C@H]2[C@H](CNC(=O)c3nc(C(C)C)n4ccccc34)[C@H]2C1 10.1016/j.ejmech.2019.111569
127027397 137105 0 None - 0 Rat 6.6 pEC50 = 6.6 Binding
Agonist activity at 5-HT4 receptor in rat esophageal thoracic muscularis mucosae assessed as carbachol-induced contractionAgonist activity at 5-HT4 receptor in rat esophageal thoracic muscularis mucosae assessed as carbachol-induced contraction
ChEMBL 421 8 2 7 2.0 COc1cc(N)c(Cl)cc1C(=O)N[C@H]1CCN(CCCn2ccnc2)C[C@H]1OC 10.1016/j.ejmech.2015.12.006
CHEMBL3758199 137105 0 None - 0 Rat 6.6 pEC50 = 6.6 Binding
Agonist activity at 5-HT4 receptor in rat esophageal thoracic muscularis mucosae assessed as carbachol-induced contractionAgonist activity at 5-HT4 receptor in rat esophageal thoracic muscularis mucosae assessed as carbachol-induced contraction
ChEMBL 421 8 2 7 2.0 COc1cc(N)c(Cl)cc1C(=O)N[C@H]1CCN(CCCn2ccnc2)C[C@H]1OC 10.1016/j.ejmech.2015.12.006
243 3153 85 None 12 34 Human 7.6 pEC50 = 7.6 Binding
Agonist activity at 5-HT4E receptor (unknown origin)Agonist activity at 5-HT4E receptor (unknown origin)
ChEMBL 367 6 2 5 2.1 COCCCN1CCC(CC1)NC(=O)c1cc(Cl)c(c2c1OCC2)N 10.1021/acs.jmedchem.8b00457
3052762 3153 85 None 12 34 Human 7.6 pEC50 = 7.6 Binding
Agonist activity at 5-HT4E receptor (unknown origin)Agonist activity at 5-HT4E receptor (unknown origin)
ChEMBL 367 6 2 5 2.1 COCCCN1CCC(CC1)NC(=O)c1cc(Cl)c(c2c1OCC2)N 10.1021/acs.jmedchem.8b00457
3502 3153 85 None 12 34 Human 7.6 pEC50 = 7.6 Binding
Agonist activity at 5-HT4E receptor (unknown origin)Agonist activity at 5-HT4E receptor (unknown origin)
ChEMBL 367 6 2 5 2.1 COCCCN1CCC(CC1)NC(=O)c1cc(Cl)c(c2c1OCC2)N 10.1021/acs.jmedchem.8b00457
CHEMBL117287 3153 85 None 12 34 Human 7.6 pEC50 = 7.6 Binding
Agonist activity at 5-HT4E receptor (unknown origin)Agonist activity at 5-HT4E receptor (unknown origin)
ChEMBL 367 6 2 5 2.1 COCCCN1CCC(CC1)NC(=O)c1cc(Cl)c(c2c1OCC2)N 10.1021/acs.jmedchem.8b00457
DB06480 3153 85 None 12 34 Human 7.6 pEC50 = 7.6 Binding
Agonist activity at 5-HT4E receptor (unknown origin)Agonist activity at 5-HT4E receptor (unknown origin)
ChEMBL 367 6 2 5 2.1 COCCCN1CCC(CC1)NC(=O)c1cc(Cl)c(c2c1OCC2)N 10.1021/acs.jmedchem.8b00457
44288600 100648 0 None - 1 Guinea pig 6.6 pEC50 = 6.6 Binding
Effective concentration required towards 5-hydroxytryptamine 4 receptor in guinea pig striatum using [3H]GR-113808 as the radioligandEffective concentration required towards 5-hydroxytryptamine 4 receptor in guinea pig striatum using [3H]GR-113808 as the radioligand
ChEMBL 335 3 2 4 2.0 COc1cc(N)c(Cl)cc1C(=O)NC1C2CC3CC1CN(C3)C2 10.1016/j.bmcl.2004.09.005
CHEMBL295155 100648 0 None - 1 Guinea pig 6.6 pEC50 = 6.6 Binding
Effective concentration required towards 5-hydroxytryptamine 4 receptor in guinea pig striatum using [3H]GR-113808 as the radioligandEffective concentration required towards 5-hydroxytryptamine 4 receptor in guinea pig striatum using [3H]GR-113808 as the radioligand
ChEMBL 335 3 2 4 2.0 COc1cc(N)c(Cl)cc1C(=O)NC1C2CC3CC1CN(C3)C2 10.1016/j.bmcl.2004.09.005
145974756 164205 0 None - 0 Human 6.5 pEC50 = 6.5 Binding
Agonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assayAgonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assay
ChEMBL 416 5 1 5 3.2 CC(C)c1nn2c(C(=O)NCC3C4CN(C5CCOCC5)CC34)cccc2c1Cl 10.1021/acs.jmedchem.8b00457
CHEMBL4217842 164205 0 None - 0 Human 6.5 pEC50 = 6.5 Binding
Agonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assayAgonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assay
ChEMBL 416 5 1 5 3.2 CC(C)c1nn2c(C(=O)NCC3C4CN(C5CCOCC5)CC34)cccc2c1Cl 10.1021/acs.jmedchem.8b00457
44224237 193122 7 None - 1 Human 8.4 pEC50 = 8.4 Binding
5-HT4C receptor-mediated exchange of GDP for europium labeled GTP (pEC50)5-HT4C receptor-mediated exchange of GDP for europium labeled GTP (pEC50)
ChEMBL 559 8 2 8 1.2 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3C[C@@H](O)CN2CCN(S(C)(=O)=O)CC2)cc2ccccc21 10.1016/j.bmcl.2012.05.034
CHEMBL538635 193122 7 None - 1 Human 8.4 pEC50 = 8.4 Binding
5-HT4C receptor-mediated exchange of GDP for europium labeled GTP (pEC50)5-HT4C receptor-mediated exchange of GDP for europium labeled GTP (pEC50)
ChEMBL 559 8 2 8 1.2 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3C[C@@H](O)CN2CCN(S(C)(=O)=O)CC2)cc2ccccc21 10.1016/j.bmcl.2012.05.034
145975076 163070 0 None - 0 Human 7.5 pEC50 = 7.5 Binding
Agonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assayAgonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assay
ChEMBL 340 5 1 4 2.8 CC(C)c1cn2cccc(C(=O)NCC3C4CN(C(C)C)CC34)c2n1 10.1021/acs.jmedchem.8b00457
CHEMBL4203778 163070 0 None - 0 Human 7.5 pEC50 = 7.5 Binding
Agonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assayAgonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assay
ChEMBL 340 5 1 4 2.8 CC(C)c1cn2cccc(C(=O)NCC3C4CN(C(C)C)CC34)c2n1 10.1021/acs.jmedchem.8b00457
145972323 164039 0 None - 0 Human 7.4 pEC50 = 7.4 Binding
Agonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assayAgonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assay
ChEMBL 382 5 1 5 2.5 CC(C)c1cn2cccc(C(=O)NCC3C4CN(C5CCOCC5)CC34)c2n1 10.1021/acs.jmedchem.8b00457
CHEMBL4215651 164039 0 None - 0 Human 7.4 pEC50 = 7.4 Binding
Agonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assayAgonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assay
ChEMBL 382 5 1 5 2.5 CC(C)c1cn2cccc(C(=O)NCC3C4CN(C5CCOCC5)CC34)c2n1 10.1021/acs.jmedchem.8b00457
155554403 174060 0 None - 0 Human 6.4 pEC50 = 6.4 Binding
Inhibition of 5-HT4 receptor (unknown origin)Inhibition of 5-HT4 receptor (unknown origin)
ChEMBL 330 2 1 3 1.9 CCN1C(=O)N(C(=O)NC2CC3CCC(C2)N3C)C2C=CC=CC21 10.1016/j.ejmech.2019.111569
CHEMBL4557961 174060 0 None - 0 Human 6.4 pEC50 = 6.4 Binding
Inhibition of 5-HT4 receptor (unknown origin)Inhibition of 5-HT4 receptor (unknown origin)
ChEMBL 330 2 1 3 1.9 CCN1C(=O)N(C(=O)NC2CC3CCC(C2)N3C)C2C=CC=CC21 10.1016/j.ejmech.2019.111569
19426720 110117 0 None - 0 Mouse 6.4 pEC50 = 6.4 Binding
Tested for ability to stimulate production of cAMP mediated by 5-hydroxytryptamine 4 receptor in mouse Coliculi neuronsTested for ability to stimulate production of cAMP mediated by 5-hydroxytryptamine 4 receptor in mouse Coliculi neurons
ChEMBL 342 2 1 5 2.4 CCn1c(=O)n(C(=O)NC2CC3CCCC(C2)N3C)c2ccccc21 10.1021/jm020099f
CHEMBL325603 110117 0 None - 0 Mouse 6.4 pEC50 = 6.4 Binding
Tested for ability to stimulate production of cAMP mediated by 5-hydroxytryptamine 4 receptor in mouse Coliculi neuronsTested for ability to stimulate production of cAMP mediated by 5-hydroxytryptamine 4 receptor in mouse Coliculi neurons
ChEMBL 342 2 1 5 2.4 CCn1c(=O)n(C(=O)NC2CC3CCCC(C2)N3C)c2ccccc21 10.1021/jm020099f
68592299 137229 0 None - 0 Rat 6.4 pEC50 = 6.4 Binding
Agonist activity at 5-HT4 receptor in rat esophageal thoracic muscularis mucosae assessed as carbachol-induced contractionAgonist activity at 5-HT4 receptor in rat esophageal thoracic muscularis mucosae assessed as carbachol-induced contraction
ChEMBL 466 7 2 6 2.4 CCC(=O)N1CCC(CN2CC[C@H](NC(=O)c3cc(Cl)c(N)cc3OC)[C@H](OC)C2)CC1 10.1016/j.ejmech.2015.12.006
CHEMBL3759259 137229 0 None - 0 Rat 6.4 pEC50 = 6.4 Binding
Agonist activity at 5-HT4 receptor in rat esophageal thoracic muscularis mucosae assessed as carbachol-induced contractionAgonist activity at 5-HT4 receptor in rat esophageal thoracic muscularis mucosae assessed as carbachol-induced contraction
ChEMBL 466 7 2 6 2.4 CCC(=O)N1CCC(CN2CC[C@H](NC(=O)c3cc(Cl)c(N)cc3OC)[C@H](OC)C2)CC1 10.1016/j.ejmech.2015.12.006
235 2527 36 None -5 3 Guinea pig 8.4 pEC50 = 8.4 Binding
Agonist activity at 5-HT4 receptor in guinea pig ileum assessed as increase in response to electrical stimulationAgonist activity at 5-HT4 receptor in guinea pig ileum assessed as increase in response to electrical stimulation
ChEMBL 312 5 1 5 2.6 COc1cc(N)c(cc1C(=O)OCCN1CCCCC1)Cl 10.1016/j.ejmech.2015.08.051
5311299 2527 36 None -5 3 Guinea pig 8.4 pEC50 = 8.4 Binding
Agonist activity at 5-HT4 receptor in guinea pig ileum assessed as increase in response to electrical stimulationAgonist activity at 5-HT4 receptor in guinea pig ileum assessed as increase in response to electrical stimulation
ChEMBL 312 5 1 5 2.6 COc1cc(N)c(cc1C(=O)OCCN1CCCCC1)Cl 10.1016/j.ejmech.2015.08.051
CHEMBL286136 2527 36 None -5 3 Guinea pig 8.4 pEC50 = 8.4 Binding
Agonist activity at 5-HT4 receptor in guinea pig ileum assessed as increase in response to electrical stimulationAgonist activity at 5-HT4 receptor in guinea pig ileum assessed as increase in response to electrical stimulation
ChEMBL 312 5 1 5 2.6 COc1cc(N)c(cc1C(=O)OCCN1CCCCC1)Cl 10.1016/j.ejmech.2015.08.051
9800656 15375 0 None - 1 Human 8.4 pEC50 = 8.4 Binding
Concentration required to produce half-maximal response against 5-hydroxytryptamine receptor on the L-type calcium current (I Ca) in isolated human atrial myocytesConcentration required to produce half-maximal response against 5-hydroxytryptamine receptor on the L-type calcium current (I Ca) in isolated human atrial myocytes
ChEMBL 391 6 1 8 1.7 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCN(c2ncccn2)CC1 10.1021/jm0009538
CHEMBL121913 15375 0 None - 1 Human 8.4 pEC50 = 8.4 Binding
Concentration required to produce half-maximal response against 5-hydroxytryptamine receptor on the L-type calcium current (I Ca) in isolated human atrial myocytesConcentration required to produce half-maximal response against 5-hydroxytryptamine receptor on the L-type calcium current (I Ca) in isolated human atrial myocytes
ChEMBL 391 6 1 8 1.7 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCN(c2ncccn2)CC1 10.1021/jm0009538
145975067 163040 0 None - 0 Human 8.3 pEC50 = 8.3 Binding
Agonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assayAgonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assay
ChEMBL 455 6 1 6 3.4 COC(=O)N1CCC(CN2CCC(CNC(=O)c3nc(C(C)C)c4ccccn34)CC2)CC1 10.1021/acs.jmedchem.8b00457
CHEMBL4203491 163040 0 None - 0 Human 8.3 pEC50 = 8.3 Binding
Agonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assayAgonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assay
ChEMBL 455 6 1 6 3.4 COC(=O)N1CCC(CN2CCC(CNC(=O)c3nc(C(C)C)c4ccccn34)CC2)CC1 10.1021/acs.jmedchem.8b00457
145964080 163612 0 None - 0 Human 7.4 pEC50 = 7.4 Binding
Agonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assayAgonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assay
ChEMBL 384 5 1 5 3.1 CC(C)c1nc(C(=O)NCC2CCN(C3CCOCC3)CC2)n2ccccc12 10.1021/acs.jmedchem.8b00457
CHEMBL4210381 163612 0 None - 0 Human 7.4 pEC50 = 7.4 Binding
Agonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assayAgonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assay
ChEMBL 384 5 1 5 3.1 CC(C)c1nc(C(=O)NCC2CCN(C3CCOCC3)CC2)n2ccccc12 10.1021/acs.jmedchem.8b00457
25016328 137300 0 None - 0 Rat 7.3 pEC50 = 7.3 Binding
Agonist activity at 5-HT4 receptor in rat esophageal thoracic muscularis mucosae assessed as carbachol-induced contractionAgonist activity at 5-HT4 receptor in rat esophageal thoracic muscularis mucosae assessed as carbachol-induced contraction
ChEMBL 480 7 2 6 2.6 COc1cc(N)c(Cl)cc1C(=O)N[C@H]1CCN(CC2CCN(C(=O)C(C)C)CC2)C[C@H]1OC 10.1016/j.ejmech.2015.12.006
CHEMBL3759860 137300 0 None - 0 Rat 7.3 pEC50 = 7.3 Binding
Agonist activity at 5-HT4 receptor in rat esophageal thoracic muscularis mucosae assessed as carbachol-induced contractionAgonist activity at 5-HT4 receptor in rat esophageal thoracic muscularis mucosae assessed as carbachol-induced contraction
ChEMBL 480 7 2 6 2.6 COc1cc(N)c(Cl)cc1C(=O)N[C@H]1CCN(CC2CCN(C(=O)C(C)C)CC2)C[C@H]1OC 10.1016/j.ejmech.2015.12.006
145977443 163385 0 None - 0 Human 7.3 pEC50 = 7.3 Binding
Agonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assayAgonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assay
ChEMBL 342 5 1 4 3.3 CC(C)c1nc(C(=O)NCC2CCN(C(C)C)CC2)n2ccccc12 10.1021/acs.jmedchem.8b00457
CHEMBL4207586 163385 0 None - 0 Human 7.3 pEC50 = 7.3 Binding
Agonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assayAgonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assay
ChEMBL 342 5 1 4 3.3 CC(C)c1nc(C(=O)NCC2CCN(C(C)C)CC2)n2ccccc12 10.1021/acs.jmedchem.8b00457
145978825 163346 0 None - 0 Human 6.3 pEC50 = 6.3 Binding
Agonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assayAgonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assay
ChEMBL 409 5 0 7 4.1 CC(C)c1nc(-c2nnc(C3CCN(CC4CCOCC4)CC3)o2)n2ccccc12 10.1021/acs.jmedchem.8b00457
CHEMBL4207136 163346 0 None - 0 Human 6.3 pEC50 = 6.3 Binding
Agonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assayAgonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assay
ChEMBL 409 5 0 7 4.1 CC(C)c1nc(-c2nnc(C3CCN(CC4CCOCC4)CC3)o2)n2ccccc12 10.1021/acs.jmedchem.8b00457
243 3153 85 None 12 34 Human 8.3 pEC50 = 8.3 Binding
Agonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assayAgonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assay
ChEMBL 367 6 2 5 2.1 COCCCN1CCC(CC1)NC(=O)c1cc(Cl)c(c2c1OCC2)N 10.1021/acs.jmedchem.8b00457
3052762 3153 85 None 12 34 Human 8.3 pEC50 = 8.3 Binding
Agonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assayAgonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assay
ChEMBL 367 6 2 5 2.1 COCCCN1CCC(CC1)NC(=O)c1cc(Cl)c(c2c1OCC2)N 10.1021/acs.jmedchem.8b00457
3502 3153 85 None 12 34 Human 8.3 pEC50 = 8.3 Binding
Agonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assayAgonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assay
ChEMBL 367 6 2 5 2.1 COCCCN1CCC(CC1)NC(=O)c1cc(Cl)c(c2c1OCC2)N 10.1021/acs.jmedchem.8b00457
CHEMBL117287 3153 85 None 12 34 Human 8.3 pEC50 = 8.3 Binding
Agonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assayAgonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assay
ChEMBL 367 6 2 5 2.1 COCCCN1CCC(CC1)NC(=O)c1cc(Cl)c(c2c1OCC2)N 10.1021/acs.jmedchem.8b00457
DB06480 3153 85 None 12 34 Human 8.3 pEC50 = 8.3 Binding
Agonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assayAgonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assay
ChEMBL 367 6 2 5 2.1 COCCCN1CCC(CC1)NC(=O)c1cc(Cl)c(c2c1OCC2)N 10.1021/acs.jmedchem.8b00457
44288600 100648 0 None - 1 Guinea pig 6.3 pEC50 = 6.3 Binding
Effective concentration required towards 5-hydroxytryptamine 4 receptor in guinea pig striatum using [3H]GR-113808 as the radioligandEffective concentration required towards 5-hydroxytryptamine 4 receptor in guinea pig striatum using [3H]GR-113808 as the radioligand
ChEMBL 335 3 2 4 2.0 COc1cc(N)c(Cl)cc1C(=O)NC1C2CC3CC1CN(C3)C2 10.1016/j.bmcl.2004.09.005
CHEMBL295155 100648 0 None - 1 Guinea pig 6.3 pEC50 = 6.3 Binding
Effective concentration required towards 5-hydroxytryptamine 4 receptor in guinea pig striatum using [3H]GR-113808 as the radioligandEffective concentration required towards 5-hydroxytryptamine 4 receptor in guinea pig striatum using [3H]GR-113808 as the radioligand
ChEMBL 335 3 2 4 2.0 COc1cc(N)c(Cl)cc1C(=O)NC1C2CC3CC1CN(C3)C2 10.1016/j.bmcl.2004.09.005
145975297 163041 0 None - 0 Human 7.3 pEC50 = 7.3 Binding
Agonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assayAgonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assay
ChEMBL 353 4 0 6 4.1 CC(C)c1cc2cccc(-c3nnc(C4CCN(C(C)C)CC4)o3)n2n1 10.1021/acs.jmedchem.8b00457
CHEMBL4203494 163041 0 None - 0 Human 7.3 pEC50 = 7.3 Binding
Agonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assayAgonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assay
ChEMBL 353 4 0 6 4.1 CC(C)c1cc2cccc(-c3nnc(C4CCN(C(C)C)CC4)o3)n2n1 10.1021/acs.jmedchem.8b00457
9928343 102995 0 None - 1 Guinea pig 6.3 pEC50 = 6.3 Binding
Effective concentration required towards 5-hydroxytryptamine 4 receptor in guinea pig striatum using [3H]GR-113808 as the radioligandEffective concentration required towards 5-hydroxytryptamine 4 receptor in guinea pig striatum using [3H]GR-113808 as the radioligand
ChEMBL 349 4 2 4 2.2 COc1cc(N)c(Cl)cc1C(=O)NCC1C2CC3CC1CN(C3)C2 10.1016/j.bmcl.2004.09.005
CHEMBL3085015 102995 0 None - 1 Guinea pig 6.3 pEC50 = 6.3 Binding
Effective concentration required towards 5-hydroxytryptamine 4 receptor in guinea pig striatum using [3H]GR-113808 as the radioligandEffective concentration required towards 5-hydroxytryptamine 4 receptor in guinea pig striatum using [3H]GR-113808 as the radioligand
ChEMBL 349 4 2 4 2.2 COc1cc(N)c(Cl)cc1C(=O)NCC1C2CC3CC1CN(C3)C2 10.1016/j.bmcl.2004.09.005
54677674 112311 4 None - 1 Human 7.2 pEC50 = 7.2 Binding
Agonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assayAgonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assay
ChEMBL 377 6 2 6 3.0 CC(C)n1c(=O)c(C(=O)NCCCN2CCCCC2)c(O)c2ccsc21 10.1021/acs.jmedchem.8b00457
CHEMBL3291085 112311 4 None - 1 Human 7.2 pEC50 = 7.2 Binding
Agonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assayAgonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assay
ChEMBL 377 6 2 6 3.0 CC(C)n1c(=O)c(C(=O)NCCCN2CCCCC2)c(O)c2ccsc21 10.1021/acs.jmedchem.8b00457
CHEMBL3306918 112311 4 None - 1 Human 7.2 pEC50 = 7.2 Binding
Agonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assayAgonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assay
ChEMBL 377 6 2 6 3.0 CC(C)n1c(=O)c(C(=O)NCCCN2CCCCC2)c(O)c2ccsc21 10.1021/acs.jmedchem.8b00457
145966243 163808 0 None - 0 Human 6.2 pEC50 = 6.2 Binding
Agonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assayAgonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assay
ChEMBL 409 5 0 7 4.1 CC(C)c1cn2cccc(-c3nnc(C4CCN(CC5CCOCC5)CC4)o3)c2n1 10.1021/acs.jmedchem.8b00457
CHEMBL4212757 163808 0 None - 0 Human 6.2 pEC50 = 6.2 Binding
Agonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assayAgonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assay
ChEMBL 409 5 0 7 4.1 CC(C)c1cn2cccc(-c3nnc(C4CCN(CC5CCOCC5)CC4)o3)c2n1 10.1021/acs.jmedchem.8b00457
138376515 163236 3 None - 0 Human 8.2 pEC50 = 8.2 Binding
Agonist activity at recombinant human 5-HT4D receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assayAgonist activity at recombinant human 5-HT4D receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assay
ChEMBL 409 5 0 7 4.1 CC(C)c1cc2cccc(-c3nnc(C4CCN(CC5CCOCC5)CC4)o3)n2n1 10.1021/acs.jmedchem.8b00457
CHEMBL4205936 163236 3 None - 0 Human 8.2 pEC50 = 8.2 Binding
Agonist activity at recombinant human 5-HT4D receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assayAgonist activity at recombinant human 5-HT4D receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assay
ChEMBL 409 5 0 7 4.1 CC(C)c1cc2cccc(-c3nnc(C4CCN(CC5CCOCC5)CC4)o3)n2n1 10.1021/acs.jmedchem.8b00457
145972573 164057 0 None - 0 Human 8.2 pEC50 = 8.2 Binding
Agonist activity at recombinant human 5-HT4D receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assayAgonist activity at recombinant human 5-HT4D receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assay
ChEMBL 383 7 0 7 3.7 COCCCN1CCC(c2nnc(-c3cccc4cc(C(C)C)nn34)o2)CC1 10.1021/acs.jmedchem.8b00457
CHEMBL4215911 164057 0 None - 0 Human 8.2 pEC50 = 8.2 Binding
Agonist activity at recombinant human 5-HT4D receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assayAgonist activity at recombinant human 5-HT4D receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assay
ChEMBL 383 7 0 7 3.7 COCCCN1CCC(c2nnc(-c3cccc4cc(C(C)C)nn34)o2)CC1 10.1021/acs.jmedchem.8b00457
138376515 163236 3 None - 0 Rat 8.2 pEC50 = 8.2 Binding
Agonist activity at recombinant rat 5-HT4L receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assayAgonist activity at recombinant rat 5-HT4L receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assay
ChEMBL 409 5 0 7 4.1 CC(C)c1cc2cccc(-c3nnc(C4CCN(CC5CCOCC5)CC4)o3)n2n1 10.1021/acs.jmedchem.8b00457
CHEMBL4205936 163236 3 None - 0 Rat 8.2 pEC50 = 8.2 Binding
Agonist activity at recombinant rat 5-HT4L receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assayAgonist activity at recombinant rat 5-HT4L receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assay
ChEMBL 409 5 0 7 4.1 CC(C)c1cc2cccc(-c3nnc(C4CCN(CC5CCOCC5)CC4)o3)n2n1 10.1021/acs.jmedchem.8b00457
145972573 164057 0 None - 0 Rat 8.2 pEC50 = 8.2 Binding
Agonist activity at recombinant rat 5-HT4L receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assayAgonist activity at recombinant rat 5-HT4L receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assay
ChEMBL 383 7 0 7 3.7 COCCCN1CCC(c2nnc(-c3cccc4cc(C(C)C)nn34)o2)CC1 10.1021/acs.jmedchem.8b00457
CHEMBL4215911 164057 0 None - 0 Rat 8.2 pEC50 = 8.2 Binding
Agonist activity at recombinant rat 5-HT4L receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assayAgonist activity at recombinant rat 5-HT4L receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assay
ChEMBL 383 7 0 7 3.7 COCCCN1CCC(c2nnc(-c3cccc4cc(C(C)C)nn34)o2)CC1 10.1021/acs.jmedchem.8b00457
11225102 76071 2 None - 1 Human 8.2 pEC50 = 8.2 Binding
5-HT4C receptor-mediated exchange of GDP for europium labeled GTP (pEC50)5-HT4C receptor-mediated exchange of GDP for europium labeled GTP (pEC50)
ChEMBL 466 6 1 6 2.5 CC(=O)N1CCN(CCN2[C@H]3CC[C@@H]2C[C@H](NC(=O)c2nn(C(C)C)c4ccccc24)C3)CC1 10.1016/j.bmcl.2012.05.034
CHEMBL2059590 76071 2 None - 1 Human 8.2 pEC50 = 8.2 Binding
5-HT4C receptor-mediated exchange of GDP for europium labeled GTP (pEC50)5-HT4C receptor-mediated exchange of GDP for europium labeled GTP (pEC50)
ChEMBL 466 6 1 6 2.5 CC(=O)N1CCN(CCN2[C@H]3CC[C@@H]2C[C@H](NC(=O)c2nn(C(C)C)c4ccccc24)C3)CC1 10.1016/j.bmcl.2012.05.034
127027375 137315 0 None - 0 Rat 5.2 pEC50 = 5.2 Binding
Agonist activity at 5-HT4 receptor in rat esophageal thoracic muscularis mucosae assessed as carbachol-induced contractionAgonist activity at 5-HT4 receptor in rat esophageal thoracic muscularis mucosae assessed as carbachol-induced contraction
ChEMBL 542 9 2 6 3.6 COc1cc(N)c(Cl)cc1C(=O)N[C@H]1CCN(CCC(=O)N2CCC(Cc3ccccc3)CC2)C[C@H]1OC 10.1016/j.ejmech.2015.12.006
CHEMBL3759928 137315 0 None - 0 Rat 5.2 pEC50 = 5.2 Binding
Agonist activity at 5-HT4 receptor in rat esophageal thoracic muscularis mucosae assessed as carbachol-induced contractionAgonist activity at 5-HT4 receptor in rat esophageal thoracic muscularis mucosae assessed as carbachol-induced contraction
ChEMBL 542 9 2 6 3.6 COc1cc(N)c(Cl)cc1C(=O)N[C@H]1CCN(CCC(=O)N2CCC(Cc3ccccc3)CC2)C[C@H]1OC 10.1016/j.ejmech.2015.12.006
145972573 164057 0 None - 0 Human 7.2 pEC50 = 7.2 Binding
Agonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assayAgonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assay
ChEMBL 383 7 0 7 3.7 COCCCN1CCC(c2nnc(-c3cccc4cc(C(C)C)nn34)o2)CC1 10.1021/acs.jmedchem.8b00457
CHEMBL4215911 164057 0 None - 0 Human 7.2 pEC50 = 7.2 Binding
Agonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assayAgonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assay
ChEMBL 383 7 0 7 3.7 COCCCN1CCC(c2nnc(-c3cccc4cc(C(C)C)nn34)o2)CC1 10.1021/acs.jmedchem.8b00457
145978541 163193 0 None - 0 Human 7.2 pEC50 = 7.2 Binding
Agonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assayAgonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assay
ChEMBL 372 8 1 5 2.9 COCCCN1CCC(CNC(=O)c2nc(C(C)C)c3ccccn23)CC1 10.1021/acs.jmedchem.8b00457
CHEMBL4205387 163193 0 None - 0 Human 7.2 pEC50 = 7.2 Binding
Agonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assayAgonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assay
ChEMBL 372 8 1 5 2.9 COCCCN1CCC(CNC(=O)c2nc(C(C)C)c3ccccn23)CC1 10.1021/acs.jmedchem.8b00457
9800656 15375 0 None - 1 Human 7.2 pEC50 = 7.2 Binding
Concentration required to produce half-maximal response against 5-hydroxytryptamine receptor in the presence of 10 nM compound in isolated human atrial myocytesConcentration required to produce half-maximal response against 5-hydroxytryptamine receptor in the presence of 10 nM compound in isolated human atrial myocytes
ChEMBL 391 6 1 8 1.7 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCN(c2ncccn2)CC1 10.1021/jm0009538
CHEMBL121913 15375 0 None - 1 Human 7.2 pEC50 = 7.2 Binding
Concentration required to produce half-maximal response against 5-hydroxytryptamine receptor in the presence of 10 nM compound in isolated human atrial myocytesConcentration required to produce half-maximal response against 5-hydroxytryptamine receptor in the presence of 10 nM compound in isolated human atrial myocytes
ChEMBL 391 6 1 8 1.7 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCN(c2ncccn2)CC1 10.1021/jm0009538
68592484 137193 0 None - 0 Rat 6.2 pEC50 = 6.2 Binding
Agonist activity at 5-HT4 receptor in rat esophageal thoracic muscularis mucosae assessed as carbachol-induced contractionAgonist activity at 5-HT4 receptor in rat esophageal thoracic muscularis mucosae assessed as carbachol-induced contraction
ChEMBL 420 8 2 6 2.6 COc1cc(N)c(Cl)cc1C(=O)N[C@H]1CCN(CCCn2cccc2)C[C@H]1OC 10.1016/j.ejmech.2015.12.006
CHEMBL3758932 137193 0 None - 0 Rat 6.2 pEC50 = 6.2 Binding
Agonist activity at 5-HT4 receptor in rat esophageal thoracic muscularis mucosae assessed as carbachol-induced contractionAgonist activity at 5-HT4 receptor in rat esophageal thoracic muscularis mucosae assessed as carbachol-induced contraction
ChEMBL 420 8 2 6 2.6 COc1cc(N)c(Cl)cc1C(=O)N[C@H]1CCN(CCCn2cccc2)C[C@H]1OC 10.1016/j.ejmech.2015.12.006
145968234 164230 0 None - 0 Human 6.2 pEC50 = 6.2 Binding
Agonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assayAgonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assay
ChEMBL 383 7 0 7 3.7 COCCCN1CCC(c2nnc(-c3cccn4cc(C(C)C)nc34)o2)CC1 10.1021/acs.jmedchem.8b00457
CHEMBL4218152 164230 0 None - 0 Human 6.2 pEC50 = 6.2 Binding
Agonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assayAgonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assay
ChEMBL 383 7 0 7 3.7 COCCCN1CCC(c2nnc(-c3cccn4cc(C(C)C)nc34)o2)CC1 10.1021/acs.jmedchem.8b00457
145966863 163593 0 None - 0 Human 8.1 pEC50 = 8.1 Binding
Agonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assayAgonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assay
ChEMBL 370 8 1 5 2.4 COCCCN1CC2C(CNC(=O)c3cccc4cc(C(C)C)nn34)C2C1 10.1021/acs.jmedchem.8b00457
CHEMBL4210176 163593 0 None - 0 Human 8.1 pEC50 = 8.1 Binding
Agonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assayAgonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assay
ChEMBL 370 8 1 5 2.4 COCCCN1CC2C(CNC(=O)c3cccc4cc(C(C)C)nn34)C2C1 10.1021/acs.jmedchem.8b00457
68593479 137274 0 None - 0 Rat 6.2 pEC50 = 6.2 Binding
Agonist activity at 5-HT4 receptor in rat esophageal thoracic muscularis mucosae assessed as carbachol-induced contractionAgonist activity at 5-HT4 receptor in rat esophageal thoracic muscularis mucosae assessed as carbachol-induced contraction
ChEMBL 422 8 2 8 1.4 COc1cc(N)c(Cl)cc1C(=O)N[C@H]1CCN(CCCn2cncn2)C[C@H]1OC 10.1016/j.ejmech.2015.12.006
CHEMBL3759601 137274 0 None - 0 Rat 6.2 pEC50 = 6.2 Binding
Agonist activity at 5-HT4 receptor in rat esophageal thoracic muscularis mucosae assessed as carbachol-induced contractionAgonist activity at 5-HT4 receptor in rat esophageal thoracic muscularis mucosae assessed as carbachol-induced contraction
ChEMBL 422 8 2 8 1.4 COc1cc(N)c(Cl)cc1C(=O)N[C@H]1CCN(CCCn2cncn2)C[C@H]1OC 10.1016/j.ejmech.2015.12.006
155558212 174154 0 None - 0 Human 7.1 pEC50 = 7.1 Binding
Inhibition of 5-HT4 receptor (unknown origin)Inhibition of 5-HT4 receptor (unknown origin)
ChEMBL 344 2 1 3 2.3 CC(C)N1C(=O)N(C(=O)NC2CC3CCC(C2)N3C)C2C=CC=CC21 10.1016/j.ejmech.2019.111569
CHEMBL4560185 174154 0 None - 0 Human 7.1 pEC50 = 7.1 Binding
Inhibition of 5-HT4 receptor (unknown origin)Inhibition of 5-HT4 receptor (unknown origin)
ChEMBL 344 2 1 3 2.3 CC(C)N1C(=O)N(C(=O)NC2CC3CCC(C2)N3C)C2C=CC=CC21 10.1016/j.ejmech.2019.111569
44343153 109858 0 None - 0 Mouse 7.1 pEC50 = 7.1 Binding
Tested for ability to stimulate production of cAMP mediated by 5-hydroxytryptamine 4 receptor in mouse Coliculi neuronsTested for ability to stimulate production of cAMP mediated by 5-hydroxytryptamine 4 receptor in mouse Coliculi neurons
ChEMBL 356 2 1 5 3.0 CC(C)n1c(=O)n(C(=O)NC2CC3CCCC(C2)N3C)c2ccccc21 10.1021/jm020099f
CHEMBL324057 109858 0 None - 0 Mouse 7.1 pEC50 = 7.1 Binding
Tested for ability to stimulate production of cAMP mediated by 5-hydroxytryptamine 4 receptor in mouse Coliculi neuronsTested for ability to stimulate production of cAMP mediated by 5-hydroxytryptamine 4 receptor in mouse Coliculi neurons
ChEMBL 356 2 1 5 3.0 CC(C)n1c(=O)n(C(=O)NC2CC3CCCC(C2)N3C)c2ccccc21 10.1021/jm020099f
9975257 48490 1 None - 0 Human 7.1 pEC50 = 7.1 Binding
Tested for 5-hydroxytryptamine 4 binding affinity against cisaprideTested for 5-hydroxytryptamine 4 binding affinity against cisapride
ChEMBL 351 3 2 4 3.1 COc1cc(N)c(Cl)cc1C(=O)NC1CCN2C(C)CCCC2C1 10.1021/jm020099f
CHEMBL15585 48490 1 None - 0 Human 7.1 pEC50 = 7.1 Binding
Tested for 5-hydroxytryptamine 4 binding affinity against cisaprideTested for 5-hydroxytryptamine 4 binding affinity against cisapride
ChEMBL 351 3 2 4 3.1 COc1cc(N)c(Cl)cc1C(=O)NC1CCN2C(C)CCCC2C1 10.1021/jm020099f
9797313 101459 1 None - 3 Human 7.1 pEC50 = 7.1 Binding
Tested for 5-hydroxytryptamine 4 binding affinity against cisaprideTested for 5-hydroxytryptamine 4 binding affinity against cisapride
ChEMBL 323 3 2 4 2.3 COc1cc(N)c(Cl)cc1C(=O)NC1CC2CCC(C1)N2C 10.1021/jm020099f
CHEMBL301039 101459 1 None - 3 Human 7.1 pEC50 = 7.1 Binding
Tested for 5-hydroxytryptamine 4 binding affinity against cisaprideTested for 5-hydroxytryptamine 4 binding affinity against cisapride
ChEMBL 323 3 2 4 2.3 COc1cc(N)c(Cl)cc1C(=O)NC1CC2CCC(C1)N2C 10.1021/jm020099f
9928343 102995 0 None - 1 Guinea pig 7.1 pEC50 = 7.1 Binding
Effective concentration required towards 5-hydroxytryptamine 4 receptor in guinea pig striatum using [3H]GR-113808 as the radioligandEffective concentration required towards 5-hydroxytryptamine 4 receptor in guinea pig striatum using [3H]GR-113808 as the radioligand
ChEMBL 349 4 2 4 2.2 COc1cc(N)c(Cl)cc1C(=O)NCC1C2CC3CC1CN(C3)C2 10.1016/j.bmcl.2004.09.005
CHEMBL3085015 102995 0 None - 1 Guinea pig 7.1 pEC50 = 7.1 Binding
Effective concentration required towards 5-hydroxytryptamine 4 receptor in guinea pig striatum using [3H]GR-113808 as the radioligandEffective concentration required towards 5-hydroxytryptamine 4 receptor in guinea pig striatum using [3H]GR-113808 as the radioligand
ChEMBL 349 4 2 4 2.2 COc1cc(N)c(Cl)cc1C(=O)NCC1C2CC3CC1CN(C3)C2 10.1016/j.bmcl.2004.09.005
145978151 163375 0 None - 0 Human 6.1 pEC50 = 6.1 Binding
Agonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assayAgonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assay
ChEMBL 353 4 0 6 4.1 CC(C)c1nc(-c2nnc(C3CCN(C(C)C)CC3)o2)n2ccccc12 10.1021/acs.jmedchem.8b00457
CHEMBL4207406 163375 0 None - 0 Human 6.1 pEC50 = 6.1 Binding
Agonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assayAgonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assay
ChEMBL 353 4 0 6 4.1 CC(C)c1nc(-c2nnc(C3CCN(C(C)C)CC3)o2)n2ccccc12 10.1021/acs.jmedchem.8b00457
145964746 163598 0 None - 0 Human 7.1 pEC50 = 7.1 Binding
Agonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assayAgonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assay
ChEMBL 399 6 1 6 2.7 CC(C)c1nc2c(C(=O)NCC3CCN(CC4CCOCC4)CC3)cccn2n1 10.1021/acs.jmedchem.8b00457
CHEMBL4210213 163598 0 None - 0 Human 7.1 pEC50 = 7.1 Binding
Agonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assayAgonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assay
ChEMBL 399 6 1 6 2.7 CC(C)c1nc2c(C(=O)NCC3CCN(CC4CCOCC4)CC3)cccn2n1 10.1021/acs.jmedchem.8b00457
145977409 163304 0 None - 0 Human 6.1 pEC50 = 6.1 Binding
Agonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assayAgonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assay
ChEMBL 383 7 0 7 3.7 COCCCN1CCC(c2nnc(-c3nc(C(C)C)c4ccccn34)o2)CC1 10.1021/acs.jmedchem.8b00457
CHEMBL4206608 163304 0 None - 0 Human 6.1 pEC50 = 6.1 Binding
Agonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assayAgonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assay
ChEMBL 383 7 0 7 3.7 COCCCN1CCC(c2nnc(-c3nc(C(C)C)c4ccccn34)o2)CC1 10.1021/acs.jmedchem.8b00457
145978067 163183 0 None - 0 Human 8.1 pEC50 = 8.1 Binding
Agonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assayAgonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assay
ChEMBL 453 6 1 6 2.8 COC(=O)N1CCC(CN2CC3C(CNC(=O)c4cccc5cc(C(C)C)nn45)C3C2)CC1 10.1021/acs.jmedchem.8b00457
CHEMBL4205273 163183 0 None - 0 Human 8.1 pEC50 = 8.1 Binding
Agonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assayAgonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assay
ChEMBL 453 6 1 6 2.8 COC(=O)N1CCC(CN2CC3C(CNC(=O)c4cccc5cc(C(C)C)nn45)C3C2)CC1 10.1021/acs.jmedchem.8b00457
145965914 163583 0 None - 0 Human 8.1 pEC50 = 8.1 Binding
Agonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assayAgonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assay
ChEMBL 441 5 1 6 3.1 COC(=O)N1CCC(N2CCC(CNC(=O)c3cccn4cc(C(C)C)nc34)CC2)CC1 10.1021/acs.jmedchem.8b00457
CHEMBL4210063 163583 0 None - 0 Human 8.1 pEC50 = 8.1 Binding
Agonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assayAgonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assay
ChEMBL 441 5 1 6 3.1 COC(=O)N1CCC(N2CCC(CNC(=O)c3cccn4cc(C(C)C)nc34)CC2)CC1 10.1021/acs.jmedchem.8b00457
11961293 3710 13 None - 1 Guinea pig 8.1 pEC50 = 8.1 Binding
Agonist activity at 5-HT4 receptor in guinea pig colonAgonist activity at 5-HT4 receptor in guinea pig colon
ChEMBL 455 6 2 5 3.6 COC(=O)N1CCC(CC1)CN1CCC(CC1)CNC(=O)c1cccc2c1nc([nH]2)C(C)C 10.1016/j.ejmech.2015.08.051
8426 3710 13 None - 1 Guinea pig 8.1 pEC50 = 8.1 Binding
Agonist activity at 5-HT4 receptor in guinea pig colonAgonist activity at 5-HT4 receptor in guinea pig colon
ChEMBL 455 6 2 5 3.6 COC(=O)N1CCC(CC1)CN1CCC(CC1)CNC(=O)c1cccc2c1nc([nH]2)C(C)C 10.1016/j.ejmech.2015.08.051
CHEMBL2402904 3710 13 None - 1 Guinea pig 8.1 pEC50 = 8.1 Binding
Agonist activity at 5-HT4 receptor in guinea pig colonAgonist activity at 5-HT4 receptor in guinea pig colon
ChEMBL 455 6 2 5 3.6 COC(=O)N1CCC(CC1)CN1CCC(CC1)CNC(=O)c1cccc2c1nc([nH]2)C(C)C 10.1016/j.ejmech.2015.08.051
DB12725 3710 13 None - 1 Guinea pig 8.1 pEC50 = 8.1 Binding
Agonist activity at 5-HT4 receptor in guinea pig colonAgonist activity at 5-HT4 receptor in guinea pig colon
ChEMBL 455 6 2 5 3.6 COC(=O)N1CCC(CC1)CN1CCC(CC1)CNC(=O)c1cccc2c1nc([nH]2)C(C)C 10.1016/j.ejmech.2015.08.051
183782 3346 15 None - 14 Rat 8.1 pEC50 = 8.1 Binding
Agonist activity at 5-HT4 receptor in Sprague-Dawley rat oesophagus assessed as relaxation of carbachol precontracted oesophagusAgonist activity at 5-HT4 receptor in Sprague-Dawley rat oesophagus assessed as relaxation of carbachol precontracted oesophagus
ChEMBL 352 8 1 4 4.4 CCCCN1CCC(CC1)CCC(=O)c1cc(Cl)c(cc1OC)N 10.1016/j.ejmech.2015.08.051
237 3346 15 None - 14 Rat 8.1 pEC50 = 8.1 Binding
Agonist activity at 5-HT4 receptor in Sprague-Dawley rat oesophagus assessed as relaxation of carbachol precontracted oesophagusAgonist activity at 5-HT4 receptor in Sprague-Dawley rat oesophagus assessed as relaxation of carbachol precontracted oesophagus
ChEMBL 352 8 1 4 4.4 CCCCN1CCC(CC1)CCC(=O)c1cc(Cl)c(cc1OC)N 10.1016/j.ejmech.2015.08.051
CHEMBL85251 3346 15 None - 14 Rat 8.1 pEC50 = 8.1 Binding
Agonist activity at 5-HT4 receptor in Sprague-Dawley rat oesophagus assessed as relaxation of carbachol precontracted oesophagusAgonist activity at 5-HT4 receptor in Sprague-Dawley rat oesophagus assessed as relaxation of carbachol precontracted oesophagus
ChEMBL 352 8 1 4 4.4 CCCCN1CCC(CC1)CCC(=O)c1cc(Cl)c(cc1OC)N 10.1016/j.ejmech.2015.08.051
145964157 163776 0 None - 0 Human 8.1 pEC50 = 8.1 Binding
Agonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assayAgonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assay
ChEMBL 396 6 1 5 2.8 CC(C)c1cc2cccc(C(=O)NCC3C4CN(CC5CCOCC5)CC34)n2n1 10.1021/acs.jmedchem.8b00457
CHEMBL4212433 163776 0 None - 0 Human 8.1 pEC50 = 8.1 Binding
Agonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assayAgonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assay
ChEMBL 396 6 1 5 2.8 CC(C)c1cc2cccc(C(=O)NCC3C4CN(CC5CCOCC5)CC34)n2n1 10.1021/acs.jmedchem.8b00457
145977034 163064 0 None - 0 Human 8.1 pEC50 = 8.1 Binding
Agonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assayAgonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assay
ChEMBL 398 6 1 5 3.3 CC(C)c1nc(C(=O)NCC2CCN(CC3CCOCC3)CC2)n2ccccc12 10.1021/acs.jmedchem.8b00457
CHEMBL4203734 163064 0 None - 0 Human 8.1 pEC50 = 8.1 Binding
Agonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assayAgonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assay
ChEMBL 398 6 1 5 3.3 CC(C)c1nc(C(=O)NCC2CCN(CC3CCOCC3)CC2)n2ccccc12 10.1021/acs.jmedchem.8b00457
145968730 164288 0 None - 0 Human 8.1 pEC50 = 8.1 Binding
Agonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assayAgonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assay
ChEMBL 342 5 1 4 3.3 CC(C)c1cn2cccc(C(=O)NCC3CCN(C(C)C)CC3)c2n1 10.1021/acs.jmedchem.8b00457
CHEMBL4218868 164288 0 None - 0 Human 8.1 pEC50 = 8.1 Binding
Agonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assayAgonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assay
ChEMBL 342 5 1 4 3.3 CC(C)c1cn2cccc(C(=O)NCC3CCN(C(C)C)CC3)c2n1 10.1021/acs.jmedchem.8b00457
145974160 164028 0 None - 0 Human 7.0 pEC50 = 7.0 Binding
Agonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assayAgonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assay
ChEMBL 342 5 1 4 3.3 CC(C)c1cc2cccc(C(=O)NCC3CCN(C(C)C)CC3)n2n1 10.1021/acs.jmedchem.8b00457
CHEMBL4215511 164028 0 None - 0 Human 7.0 pEC50 = 7.0 Binding
Agonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assayAgonist activity at recombinant human 5-HT4E receptor expressed in CHO cells assessed as induction of c-AMP accumulation after 4 hrs by luciferase reporter assay
ChEMBL 342 5 1 4 3.3 CC(C)c1cc2cccc(C(=O)NCC3CCN(C(C)C)CC3)n2n1 10.1021/acs.jmedchem.8b00457
15166837 121873 0 None - 1 Rat 5.9 pED50 = 5.9 Binding
Relaxation of carbachol induced contractions of rat tunica muscularis mucosaeRelaxation of carbachol induced contractions of rat tunica muscularis mucosae
ChEMBL 337 5 2 4 2.5 CCOc1cc(N)c(Cl)cc1C(=O)NCC1CCN2CCCC12 10.1021/jm00086a019
CHEMBL36005 121873 0 None - 1 Rat 5.9 pED50 = 5.9 Binding
Relaxation of carbachol induced contractions of rat tunica muscularis mucosaeRelaxation of carbachol induced contractions of rat tunica muscularis mucosae
ChEMBL 337 5 2 4 2.5 CCOc1cc(N)c(Cl)cc1C(=O)NCC1CCN2CCCC12 10.1021/jm00086a019
5 139 66 None -117 54 Rat 7.8 pED50 = 7.8 Binding
Relaxation of carbachol induced contractions of rat tunica muscularis mucosaeRelaxation of carbachol induced contractions of rat tunica muscularis mucosae
ChEMBL 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 10.1021/jm00086a019
5202 139 66 None -117 54 Rat 7.8 pED50 = 7.8 Binding
Relaxation of carbachol induced contractions of rat tunica muscularis mucosaeRelaxation of carbachol induced contractions of rat tunica muscularis mucosae
ChEMBL 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 10.1021/jm00086a019
CHEMBL39 139 66 None -117 54 Rat 7.8 pED50 = 7.8 Binding
Relaxation of carbachol induced contractions of rat tunica muscularis mucosaeRelaxation of carbachol induced contractions of rat tunica muscularis mucosae
ChEMBL 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 10.1021/jm00086a019
DB08839 139 66 None -117 54 Rat 7.8 pED50 = 7.8 Binding
Relaxation of carbachol induced contractions of rat tunica muscularis mucosaeRelaxation of carbachol induced contractions of rat tunica muscularis mucosae
ChEMBL 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 10.1021/jm00086a019
57391435 67389 0 None - 0 Rat 6.8 pED50 = 6.8 Binding
Relaxation of carbachol induced contractions of rat tunica muscularis mucosaeRelaxation of carbachol induced contractions of rat tunica muscularis mucosae
ChEMBL 307 3 2 4 1.4 COc1cc(N)c(Cl)cc1C(=O)N[C@]12CN3CCC1C2C3 10.1021/jm00086a019
CHEMBL1907770 67389 0 None - 0 Rat 6.8 pED50 = 6.8 Binding
Relaxation of carbachol induced contractions of rat tunica muscularis mucosaeRelaxation of carbachol induced contractions of rat tunica muscularis mucosae
ChEMBL 307 3 2 4 1.4 COc1cc(N)c(Cl)cc1C(=O)N[C@]12CN3CCC1C2C3 10.1021/jm00086a019
15166838 41450 0 None - 0 Rat 6.7 pED50 = 6.7 Binding
Relaxation of carbachol induced contractions of rat tunica muscularis mucosaeRelaxation of carbachol induced contractions of rat tunica muscularis mucosae
ChEMBL 309 3 2 4 1.9 COc1cc(N)c(Cl)cc1C(=O)NC1CCN2CCCC12 10.1021/jm00086a019
CHEMBL14923 41450 0 None - 0 Rat 6.7 pED50 = 6.7 Binding
Relaxation of carbachol induced contractions of rat tunica muscularis mucosaeRelaxation of carbachol induced contractions of rat tunica muscularis mucosae
ChEMBL 309 3 2 4 1.9 COc1cc(N)c(Cl)cc1C(=O)NC1CCN2CCCC12 10.1021/jm00086a019
10358856 119683 0 None - 1 Rat 5.6 pED50 = 5.6 Binding
Relaxation of carbachol induced contractions of rat tunica muscularis mucosaeRelaxation of carbachol induced contractions of rat tunica muscularis mucosae
ChEMBL 323 4 2 4 2.3 CCOc1cc(N)c(Cl)cc1C(=O)NC1CCN2CCCC12 10.1021/jm00086a019
CHEMBL35180 119683 0 None - 1 Rat 5.6 pED50 = 5.6 Binding
Relaxation of carbachol induced contractions of rat tunica muscularis mucosaeRelaxation of carbachol induced contractions of rat tunica muscularis mucosae
ChEMBL 323 4 2 4 2.3 CCOc1cc(N)c(Cl)cc1C(=O)NC1CCN2CCCC12 10.1021/jm00086a019
132337 3487 8 None - 2 Rat 7.6 pED50 = 7.6 Binding
Relaxation of carbachol induced contractions of rat tunica muscularis mucosaeRelaxation of carbachol induced contractions of rat tunica muscularis mucosae
ChEMBL 323 4 2 4 2.1 COc1cc(N)c(cc1C(=O)NC[C@@H]1CCN2[C@H]1CCC2)Cl 10.1021/jm00086a019
238 3487 8 None - 2 Rat 7.6 pED50 = 7.6 Binding
Relaxation of carbachol induced contractions of rat tunica muscularis mucosaeRelaxation of carbachol induced contractions of rat tunica muscularis mucosae
ChEMBL 323 4 2 4 2.1 COc1cc(N)c(cc1C(=O)NC[C@@H]1CCN2[C@H]1CCC2)Cl 10.1021/jm00086a019
CHEMBL34291 3487 8 None - 2 Rat 7.6 pED50 = 7.6 Binding
Relaxation of carbachol induced contractions of rat tunica muscularis mucosaeRelaxation of carbachol induced contractions of rat tunica muscularis mucosae
ChEMBL 323 4 2 4 2.1 COc1cc(N)c(cc1C(=O)NC[C@@H]1CCN2[C@H]1CCC2)Cl 10.1021/jm00086a019
1782 2482 81 None -11 22 Rat 4.6 pED50 = 4.6 Binding
Relaxation of carbachol induced contractions of rat tunica muscularis mucosaeRelaxation of carbachol induced contractions of rat tunica muscularis mucosae
ChEMBL 299 7 2 4 2.0 CCN(CCNC(=O)c1cc(Cl)c(cc1OC)N)CC 10.1021/jm00086a019
241 2482 81 None -11 22 Rat 4.6 pED50 = 4.6 Binding
Relaxation of carbachol induced contractions of rat tunica muscularis mucosaeRelaxation of carbachol induced contractions of rat tunica muscularis mucosae
ChEMBL 299 7 2 4 2.0 CCN(CCNC(=O)c1cc(Cl)c(cc1OC)N)CC 10.1021/jm00086a019
4168 2482 81 None -11 22 Rat 4.6 pED50 = 4.6 Binding
Relaxation of carbachol induced contractions of rat tunica muscularis mucosaeRelaxation of carbachol induced contractions of rat tunica muscularis mucosae
ChEMBL 299 7 2 4 2.0 CCN(CCNC(=O)c1cc(Cl)c(cc1OC)N)CC 10.1021/jm00086a019
CHEMBL86 2482 81 None -11 22 Rat 4.6 pED50 = 4.6 Binding
Relaxation of carbachol induced contractions of rat tunica muscularis mucosaeRelaxation of carbachol induced contractions of rat tunica muscularis mucosae
ChEMBL 299 7 2 4 2.0 CCN(CCNC(=O)c1cc(Cl)c(cc1OC)N)CC 10.1021/jm00086a019
DB01233 2482 81 None -11 22 Rat 4.6 pED50 = 4.6 Binding
Relaxation of carbachol induced contractions of rat tunica muscularis mucosaeRelaxation of carbachol induced contractions of rat tunica muscularis mucosae
ChEMBL 299 7 2 4 2.0 CCN(CCNC(=O)c1cc(Cl)c(cc1OC)N)CC 10.1021/jm00086a019
15095972 137020 0 None - 0 Rat 6.6 pED50 = 6.6 Binding
Relaxation of carbachol induced contractions of rat tunica muscularis mucosaeRelaxation of carbachol induced contractions of rat tunica muscularis mucosae
ChEMBL 323 4 2 4 2.1 COc1cc(N)c(Cl)cc1C(=O)NCC1CCN2CCCC12 10.1021/jm00086a019
CHEMBL37544 137020 0 None - 0 Rat 6.6 pED50 = 6.6 Binding
Relaxation of carbachol induced contractions of rat tunica muscularis mucosaeRelaxation of carbachol induced contractions of rat tunica muscularis mucosae
ChEMBL 323 4 2 4 2.1 COc1cc(N)c(Cl)cc1C(=O)NCC1CCN2CCCC12 10.1021/jm00086a019
15095973 135745 0 None - 0 Rat 6.5 pED50 = 6.5 Binding
Relaxation of carbachol induced contractions of rat tunica muscularis mucosaeRelaxation of carbachol induced contractions of rat tunica muscularis mucosae
ChEMBL 323 4 2 4 2.1 COc1cc(N)c(Cl)cc1C(=O)NC[C@H]1CCN2CCC[C@H]12 10.1021/jm00086a019
CHEMBL37333 135745 0 None - 0 Rat 6.5 pED50 = 6.5 Binding
Relaxation of carbachol induced contractions of rat tunica muscularis mucosaeRelaxation of carbachol induced contractions of rat tunica muscularis mucosae
ChEMBL 323 4 2 4 2.1 COc1cc(N)c(Cl)cc1C(=O)NC[C@H]1CCN2CCC[C@H]12 10.1021/jm00086a019
15166838 41450 0 None - 0 Rat 5.5 pED50 = 5.5 Binding
Relaxation of carbachol induced contractions of rat tunica muscularis mucosaeRelaxation of carbachol induced contractions of rat tunica muscularis mucosae
ChEMBL 309 3 2 4 1.9 COc1cc(N)c(Cl)cc1C(=O)NC1CCN2CCCC12 10.1021/jm00086a019
CHEMBL14923 41450 0 None - 0 Rat 5.5 pED50 = 5.5 Binding
Relaxation of carbachol induced contractions of rat tunica muscularis mucosaeRelaxation of carbachol induced contractions of rat tunica muscularis mucosae
ChEMBL 309 3 2 4 1.9 COc1cc(N)c(Cl)cc1C(=O)NC1CCN2CCCC12 10.1021/jm00086a019
44283512 139650 0 None - 0 Rat 7.4 pED50 = 7.4 Binding
Relaxation of carbachol induced contractions of rat tunica muscularis mucosaeRelaxation of carbachol induced contractions of rat tunica muscularis mucosae
ChEMBL 341 3 0 5 3.3 CC(C)n1c(=O)n(C(=O)CC2CC3CCC(C2)N3C)c2ccccc21 10.1021/jm00086a019
CHEMBL38041 139650 0 None - 0 Rat 7.4 pED50 = 7.4 Binding
Relaxation of carbachol induced contractions of rat tunica muscularis mucosaeRelaxation of carbachol induced contractions of rat tunica muscularis mucosae
ChEMBL 341 3 0 5 3.3 CC(C)n1c(=O)n(C(=O)CC2CC3CCC(C2)N3C)c2ccccc21 10.1021/jm00086a019
44374544 52873 0 None - 1 Rat 7.4 pED50 = 7.4 Binding
Relaxation of carbachol induced contractions of rat tunica muscularis mucosaeRelaxation of carbachol induced contractions of rat tunica muscularis mucosae
ChEMBL 309 3 2 4 1.8 COc1cc(N)c(Cl)cc1C(=O)NC1CCN2CCC1C2 10.1021/jm00086a019
CHEMBL159825 52873 0 None - 1 Rat 7.4 pED50 = 7.4 Binding
Relaxation of carbachol induced contractions of rat tunica muscularis mucosaeRelaxation of carbachol induced contractions of rat tunica muscularis mucosae
ChEMBL 309 3 2 4 1.8 COc1cc(N)c(Cl)cc1C(=O)NC1CCN2CCC1C2 10.1021/jm00086a019
9819593 98348 2 None 1 2 Rat 6.3 pED50 = 6.3 Binding
Relaxation of carbachol induced contractions of rat tunica muscularis mucosaeRelaxation of carbachol induced contractions of rat tunica muscularis mucosae
ChEMBL 309 3 2 4 1.8 COc1cc(N)c(Cl)cc1C(=O)N[C@H]1CN2CCC1CC2 10.1021/jm00086a019
CHEMBL27846 98348 2 None 1 2 Rat 6.3 pED50 = 6.3 Binding
Relaxation of carbachol induced contractions of rat tunica muscularis mucosaeRelaxation of carbachol induced contractions of rat tunica muscularis mucosae
ChEMBL 309 3 2 4 1.8 COc1cc(N)c(Cl)cc1C(=O)N[C@H]1CN2CCC1CC2 10.1021/jm00086a019
240 931 39 None -8 25 Rat 7.3 pED50 = 7.3 Binding
Relaxation of carbachol induced contractions of rat tunica muscularis mucosaeRelaxation of carbachol induced contractions of rat tunica muscularis mucosae
ChEMBL 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N 10.1021/jm00086a019
2769 931 39 None -8 25 Rat 7.3 pED50 = 7.3 Binding
Relaxation of carbachol induced contractions of rat tunica muscularis mucosaeRelaxation of carbachol induced contractions of rat tunica muscularis mucosae
ChEMBL 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N 10.1021/jm00086a019
44279790 931 39 None -8 25 Rat 7.3 pED50 = 7.3 Binding
Relaxation of carbachol induced contractions of rat tunica muscularis mucosaeRelaxation of carbachol induced contractions of rat tunica muscularis mucosae
ChEMBL 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N 10.1021/jm00086a019
660 931 39 None -8 25 Rat 7.3 pED50 = 7.3 Binding
Relaxation of carbachol induced contractions of rat tunica muscularis mucosaeRelaxation of carbachol induced contractions of rat tunica muscularis mucosae
ChEMBL 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N 10.1021/jm00086a019
CHEMBL1729 931 39 None -8 25 Rat 7.3 pED50 = 7.3 Binding
Relaxation of carbachol induced contractions of rat tunica muscularis mucosaeRelaxation of carbachol induced contractions of rat tunica muscularis mucosae
ChEMBL 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N 10.1021/jm00086a019
CHEMBL560739 931 39 None -8 25 Rat 7.3 pED50 = 7.3 Binding
Relaxation of carbachol induced contractions of rat tunica muscularis mucosaeRelaxation of carbachol induced contractions of rat tunica muscularis mucosae
ChEMBL 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N 10.1021/jm00086a019
DB00604 931 39 None -8 25 Rat 7.3 pED50 = 7.3 Binding
Relaxation of carbachol induced contractions of rat tunica muscularis mucosaeRelaxation of carbachol induced contractions of rat tunica muscularis mucosae
ChEMBL 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N 10.1021/jm00086a019
15095972 137020 0 None - 0 Rat 7.2 pED50 = 7.2 Binding
Relaxation of carbachol induced contractions of rat tunica muscularis mucosaeRelaxation of carbachol induced contractions of rat tunica muscularis mucosae
ChEMBL 323 4 2 4 2.1 COc1cc(N)c(Cl)cc1C(=O)NCC1CCN2CCCC12 10.1021/jm00086a019
CHEMBL37544 137020 0 None - 0 Rat 7.2 pED50 = 7.2 Binding
Relaxation of carbachol induced contractions of rat tunica muscularis mucosaeRelaxation of carbachol induced contractions of rat tunica muscularis mucosae
ChEMBL 323 4 2 4 2.1 COc1cc(N)c(Cl)cc1C(=O)NCC1CCN2CCCC12 10.1021/jm00086a019
9864179 120840 0 None - 0 Guinea pig 10.6 pIC50 = 10.6 Binding
Ability to antagonize 5-HT-evoked contractions mediated through 5-hydroxytryptamine 4 receptor activation in the guinea pig distal colon LMMPAbility to antagonize 5-HT-evoked contractions mediated through 5-hydroxytryptamine 4 receptor activation in the guinea pig distal colon LMMP
ChEMBL 370 6 0 5 4.1 CCCCN1CCC(COC(=O)c2c3n(c4ccccc24)CCCO3)CC1 10.1021/jm00024a002
CHEMBL358119 120840 0 None - 0 Guinea pig 10.6 pIC50 = 10.6 Binding
Ability to antagonize 5-HT-evoked contractions mediated through 5-hydroxytryptamine 4 receptor activation in the guinea pig distal colon LMMPAbility to antagonize 5-HT-evoked contractions mediated through 5-hydroxytryptamine 4 receptor activation in the guinea pig distal colon LMMP
ChEMBL 370 6 0 5 4.1 CCCCN1CCC(COC(=O)c2c3n(c4ccccc24)CCCO3)CC1 10.1021/jm00024a002
9864179 120840 0 None - 0 Guinea pig 10.6 pIC50 = 10.6 Binding
Ability to block 5-HT4 receptor mediated effect of 5-HT was assessed in the guinea-pig distal colon longitudinal muscle myenteric plexus preparation (LMMP)Ability to block 5-HT4 receptor mediated effect of 5-HT was assessed in the guinea-pig distal colon longitudinal muscle myenteric plexus preparation (LMMP)
ChEMBL 370 6 0 5 4.1 CCCCN1CCC(COC(=O)c2c3n(c4ccccc24)CCCO3)CC1 10.1016/S0960-894X(01)80176-1
CHEMBL358119 120840 0 None - 0 Guinea pig 10.6 pIC50 = 10.6 Binding
Ability to block 5-HT4 receptor mediated effect of 5-HT was assessed in the guinea-pig distal colon longitudinal muscle myenteric plexus preparation (LMMP)Ability to block 5-HT4 receptor mediated effect of 5-HT was assessed in the guinea-pig distal colon longitudinal muscle myenteric plexus preparation (LMMP)
ChEMBL 370 6 0 5 4.1 CCCCN1CCC(COC(=O)c2c3n(c4ccccc24)CCCO3)CC1 10.1016/S0960-894X(01)80176-1
54575167 151500 0 None - 0 Human 10.4 pIC50 = 10.4 Binding
Binding Assay: The binding affinity of the compounds for a human 5-HT4 receptor was assayed according to the method as disclosed in the literature [Wyngaert et al., Journal of Neurochemistry, (1997) 69, 1810-1819]. For this purpose, COS-7 cells expressing the human 5-HT4 receptor were constructed and homogenized to obtain membrane homogenates which were then used in binding assay experiments. For the binding assay, the membrane homogenates were respectively mixed and incubated with different concentrations of test materials and [H3]-GR113808 (Amersham Biosciences). The concentrations of the individual test materials were set to 4 uM, 1 uM, 0.25 uM, and 0.0625 uM, respectively, and the concentration of [H3]-GR113808 was set to 0.595 nM. After the incubation was completed, the reaction products were collected in GF/B glass fiber filters using a Packard cell harvester, and the bound radioactivity was then determined using a liquid cell scintillation counter (Packard TopCount NXT).Binding Assay: The binding affinity of the compounds for a human 5-HT4 receptor was assayed according to the method as disclosed in the literature [Wyngaert et al., Journal of Neurochemistry, (1997) 69, 1810-1819]. For this purpose, COS-7 cells expressing the human 5-HT4 receptor were constructed and homogenized to obtain membrane homogenates which were then used in binding assay experiments. For the binding assay, the membrane homogenates were respectively mixed and incubated with different concentrations of test materials and [H3]-GR113808 (Amersham Biosciences). The concentrations of the individual test materials were set to 4 uM, 1 uM, 0.25 uM, and 0.0625 uM, respectively, and the concentration of [H3]-GR113808 was set to 0.595 nM. After the incubation was completed, the reaction products were collected in GF/B glass fiber filters using a Packard cell harvester, and the bound radioactivity was then determined using a liquid cell scintillation counter (Packard TopCount NXT).
ChEMBL 454 8 2 5 4.4 COc1cc(N)c(Cl)cc1C(=O)NCC1CCN(CCCn2ccc3ccccc32)CC1 nan
CHEMBL3967117 151500 0 None - 0 Human 10.4 pIC50 = 10.4 Binding
Binding Assay: The binding affinity of the compounds for a human 5-HT4 receptor was assayed according to the method as disclosed in the literature [Wyngaert et al., Journal of Neurochemistry, (1997) 69, 1810-1819]. For this purpose, COS-7 cells expressing the human 5-HT4 receptor were constructed and homogenized to obtain membrane homogenates which were then used in binding assay experiments. For the binding assay, the membrane homogenates were respectively mixed and incubated with different concentrations of test materials and [H3]-GR113808 (Amersham Biosciences). The concentrations of the individual test materials were set to 4 uM, 1 uM, 0.25 uM, and 0.0625 uM, respectively, and the concentration of [H3]-GR113808 was set to 0.595 nM. After the incubation was completed, the reaction products were collected in GF/B glass fiber filters using a Packard cell harvester, and the bound radioactivity was then determined using a liquid cell scintillation counter (Packard TopCount NXT).Binding Assay: The binding affinity of the compounds for a human 5-HT4 receptor was assayed according to the method as disclosed in the literature [Wyngaert et al., Journal of Neurochemistry, (1997) 69, 1810-1819]. For this purpose, COS-7 cells expressing the human 5-HT4 receptor were constructed and homogenized to obtain membrane homogenates which were then used in binding assay experiments. For the binding assay, the membrane homogenates were respectively mixed and incubated with different concentrations of test materials and [H3]-GR113808 (Amersham Biosciences). The concentrations of the individual test materials were set to 4 uM, 1 uM, 0.25 uM, and 0.0625 uM, respectively, and the concentration of [H3]-GR113808 was set to 0.595 nM. After the incubation was completed, the reaction products were collected in GF/B glass fiber filters using a Packard cell harvester, and the bound radioactivity was then determined using a liquid cell scintillation counter (Packard TopCount NXT).
ChEMBL 454 8 2 5 4.4 COc1cc(N)c(Cl)cc1C(=O)NCC1CCN(CCCn2ccc3ccccc32)CC1 nan
54575171 149532 1 None - 0 Human 10.2 pIC50 = 10.2 Binding
Binding Assay: The binding affinity of the compounds for a human 5-HT4 receptor was assayed according to the method as disclosed in the literature [Wyngaert et al., Journal of Neurochemistry, (1997) 69, 1810-1819]. For this purpose, COS-7 cells expressing the human 5-HT4 receptor were constructed and homogenized to obtain membrane homogenates which were then used in binding assay experiments. For the binding assay, the membrane homogenates were respectively mixed and incubated with different concentrations of test materials and [H3]-GR113808 (Amersham Biosciences). The concentrations of the individual test materials were set to 4 uM, 1 uM, 0.25 uM, and 0.0625 uM, respectively, and the concentration of [H3]-GR113808 was set to 0.595 nM. After the incubation was completed, the reaction products were collected in GF/B glass fiber filters using a Packard cell harvester, and the bound radioactivity was then determined using a liquid cell scintillation counter (Packard TopCount NXT).Binding Assay: The binding affinity of the compounds for a human 5-HT4 receptor was assayed according to the method as disclosed in the literature [Wyngaert et al., Journal of Neurochemistry, (1997) 69, 1810-1819]. For this purpose, COS-7 cells expressing the human 5-HT4 receptor were constructed and homogenized to obtain membrane homogenates which were then used in binding assay experiments. For the binding assay, the membrane homogenates were respectively mixed and incubated with different concentrations of test materials and [H3]-GR113808 (Amersham Biosciences). The concentrations of the individual test materials were set to 4 uM, 1 uM, 0.25 uM, and 0.0625 uM, respectively, and the concentration of [H3]-GR113808 was set to 0.595 nM. After the incubation was completed, the reaction products were collected in GF/B glass fiber filters using a Packard cell harvester, and the bound radioactivity was then determined using a liquid cell scintillation counter (Packard TopCount NXT).
ChEMBL 406 8 2 7 2.1 COc1cc(N)c(Cl)cc1C(=O)NCC1CCN(CCCn2ccnn2)CC1 nan
CHEMBL3950712 149532 1 None - 0 Human 10.2 pIC50 = 10.2 Binding
Binding Assay: The binding affinity of the compounds for a human 5-HT4 receptor was assayed according to the method as disclosed in the literature [Wyngaert et al., Journal of Neurochemistry, (1997) 69, 1810-1819]. For this purpose, COS-7 cells expressing the human 5-HT4 receptor were constructed and homogenized to obtain membrane homogenates which were then used in binding assay experiments. For the binding assay, the membrane homogenates were respectively mixed and incubated with different concentrations of test materials and [H3]-GR113808 (Amersham Biosciences). The concentrations of the individual test materials were set to 4 uM, 1 uM, 0.25 uM, and 0.0625 uM, respectively, and the concentration of [H3]-GR113808 was set to 0.595 nM. After the incubation was completed, the reaction products were collected in GF/B glass fiber filters using a Packard cell harvester, and the bound radioactivity was then determined using a liquid cell scintillation counter (Packard TopCount NXT).Binding Assay: The binding affinity of the compounds for a human 5-HT4 receptor was assayed according to the method as disclosed in the literature [Wyngaert et al., Journal of Neurochemistry, (1997) 69, 1810-1819]. For this purpose, COS-7 cells expressing the human 5-HT4 receptor were constructed and homogenized to obtain membrane homogenates which were then used in binding assay experiments. For the binding assay, the membrane homogenates were respectively mixed and incubated with different concentrations of test materials and [H3]-GR113808 (Amersham Biosciences). The concentrations of the individual test materials were set to 4 uM, 1 uM, 0.25 uM, and 0.0625 uM, respectively, and the concentration of [H3]-GR113808 was set to 0.595 nM. After the incubation was completed, the reaction products were collected in GF/B glass fiber filters using a Packard cell harvester, and the bound radioactivity was then determined using a liquid cell scintillation counter (Packard TopCount NXT).
ChEMBL 406 8 2 7 2.1 COc1cc(N)c(Cl)cc1C(=O)NCC1CCN(CCCn2ccnn2)CC1 nan
54575225 147478 0 None - 0 Human 10.1 pIC50 = 10.1 Binding
Binding Assay: The binding affinity of the compounds for a human 5-HT4 receptor was assayed according to the method as disclosed in the literature [Wyngaert et al., Journal of Neurochemistry, (1997) 69, 1810-1819]. For this purpose, COS-7 cells expressing the human 5-HT4 receptor were constructed and homogenized to obtain membrane homogenates which were then used in binding assay experiments. For the binding assay, the membrane homogenates were respectively mixed and incubated with different concentrations of test materials and [H3]-GR113808 (Amersham Biosciences). The concentrations of the individual test materials were set to 4 uM, 1 uM, 0.25 uM, and 0.0625 uM, respectively, and the concentration of [H3]-GR113808 was set to 0.595 nM. After the incubation was completed, the reaction products were collected in GF/B glass fiber filters using a Packard cell harvester, and the bound radioactivity was then determined using a liquid cell scintillation counter (Packard TopCount NXT).Binding Assay: The binding affinity of the compounds for a human 5-HT4 receptor was assayed according to the method as disclosed in the literature [Wyngaert et al., Journal of Neurochemistry, (1997) 69, 1810-1819]. For this purpose, COS-7 cells expressing the human 5-HT4 receptor were constructed and homogenized to obtain membrane homogenates which were then used in binding assay experiments. For the binding assay, the membrane homogenates were respectively mixed and incubated with different concentrations of test materials and [H3]-GR113808 (Amersham Biosciences). The concentrations of the individual test materials were set to 4 uM, 1 uM, 0.25 uM, and 0.0625 uM, respectively, and the concentration of [H3]-GR113808 was set to 0.595 nM. After the incubation was completed, the reaction products were collected in GF/B glass fiber filters using a Packard cell harvester, and the bound radioactivity was then determined using a liquid cell scintillation counter (Packard TopCount NXT).
ChEMBL 440 6 2 5 4.1 COc1cc(N)c(Cl)cc1C(=O)NCC1CCN(Cc2cn(C)c3ccccc23)CC1 nan
CHEMBL3934371 147478 0 None - 0 Human 10.1 pIC50 = 10.1 Binding
Binding Assay: The binding affinity of the compounds for a human 5-HT4 receptor was assayed according to the method as disclosed in the literature [Wyngaert et al., Journal of Neurochemistry, (1997) 69, 1810-1819]. For this purpose, COS-7 cells expressing the human 5-HT4 receptor were constructed and homogenized to obtain membrane homogenates which were then used in binding assay experiments. For the binding assay, the membrane homogenates were respectively mixed and incubated with different concentrations of test materials and [H3]-GR113808 (Amersham Biosciences). The concentrations of the individual test materials were set to 4 uM, 1 uM, 0.25 uM, and 0.0625 uM, respectively, and the concentration of [H3]-GR113808 was set to 0.595 nM. After the incubation was completed, the reaction products were collected in GF/B glass fiber filters using a Packard cell harvester, and the bound radioactivity was then determined using a liquid cell scintillation counter (Packard TopCount NXT).Binding Assay: The binding affinity of the compounds for a human 5-HT4 receptor was assayed according to the method as disclosed in the literature [Wyngaert et al., Journal of Neurochemistry, (1997) 69, 1810-1819]. For this purpose, COS-7 cells expressing the human 5-HT4 receptor were constructed and homogenized to obtain membrane homogenates which were then used in binding assay experiments. For the binding assay, the membrane homogenates were respectively mixed and incubated with different concentrations of test materials and [H3]-GR113808 (Amersham Biosciences). The concentrations of the individual test materials were set to 4 uM, 1 uM, 0.25 uM, and 0.0625 uM, respectively, and the concentration of [H3]-GR113808 was set to 0.595 nM. After the incubation was completed, the reaction products were collected in GF/B glass fiber filters using a Packard cell harvester, and the bound radioactivity was then determined using a liquid cell scintillation counter (Packard TopCount NXT).
ChEMBL 440 6 2 5 4.1 COc1cc(N)c(Cl)cc1C(=O)NCC1CCN(Cc2cn(C)c3ccccc23)CC1 nan
121881 3434 21 None 2 15 Guinea pig 10.1 pIC50 = 10.1 Binding
Ability to antagonize 5-HT-evoked contractions mediated through 5-hydroxytryptamine 4 receptor activation in the guinea pig distal colon LMMPAbility to antagonize 5-HT-evoked contractions mediated through 5-hydroxytryptamine 4 receptor activation in the guinea pig distal colon LMMP
ChEMBL 382 6 1 6 3.4 CCCCN1CCC(CC1)COC(=O)c1cc(Cl)c(c2c1OCCO2)N 10.1021/jm00024a002
256 3434 21 None 2 15 Guinea pig 10.1 pIC50 = 10.1 Binding
Ability to antagonize 5-HT-evoked contractions mediated through 5-hydroxytryptamine 4 receptor activation in the guinea pig distal colon LMMPAbility to antagonize 5-HT-evoked contractions mediated through 5-hydroxytryptamine 4 receptor activation in the guinea pig distal colon LMMP
ChEMBL 382 6 1 6 3.4 CCCCN1CCC(CC1)COC(=O)c1cc(Cl)c(c2c1OCCO2)N 10.1021/jm00024a002
CHEMBL68131 3434 21 None 2 15 Guinea pig 10.1 pIC50 = 10.1 Binding
Ability to antagonize 5-HT-evoked contractions mediated through 5-hydroxytryptamine 4 receptor activation in the guinea pig distal colon LMMPAbility to antagonize 5-HT-evoked contractions mediated through 5-hydroxytryptamine 4 receptor activation in the guinea pig distal colon LMMP
ChEMBL 382 6 1 6 3.4 CCCCN1CCC(CC1)COC(=O)c1cc(Cl)c(c2c1OCCO2)N 10.1021/jm00024a002
121881 3434 21 None 2 15 Guinea pig 10.1 pIC50 = 10.1 Binding
Ability to block 5-HT4 receptor mediated effect of 5-HT was assessed in the guinea-pig distal colon longitudinal muscle myenteric plexus preparation (LMMP)Ability to block 5-HT4 receptor mediated effect of 5-HT was assessed in the guinea-pig distal colon longitudinal muscle myenteric plexus preparation (LMMP)
ChEMBL 382 6 1 6 3.4 CCCCN1CCC(CC1)COC(=O)c1cc(Cl)c(c2c1OCCO2)N 10.1016/S0960-894X(01)80176-1
256 3434 21 None 2 15 Guinea pig 10.1 pIC50 = 10.1 Binding
Ability to block 5-HT4 receptor mediated effect of 5-HT was assessed in the guinea-pig distal colon longitudinal muscle myenteric plexus preparation (LMMP)Ability to block 5-HT4 receptor mediated effect of 5-HT was assessed in the guinea-pig distal colon longitudinal muscle myenteric plexus preparation (LMMP)
ChEMBL 382 6 1 6 3.4 CCCCN1CCC(CC1)COC(=O)c1cc(Cl)c(c2c1OCCO2)N 10.1016/S0960-894X(01)80176-1
CHEMBL68131 3434 21 None 2 15 Guinea pig 10.1 pIC50 = 10.1 Binding
Ability to block 5-HT4 receptor mediated effect of 5-HT was assessed in the guinea-pig distal colon longitudinal muscle myenteric plexus preparation (LMMP)Ability to block 5-HT4 receptor mediated effect of 5-HT was assessed in the guinea-pig distal colon longitudinal muscle myenteric plexus preparation (LMMP)
ChEMBL 382 6 1 6 3.4 CCCCN1CCC(CC1)COC(=O)c1cc(Cl)c(c2c1OCCO2)N 10.1016/S0960-894X(01)80176-1
10617443 33825 0 None - 0 Guinea pig 10.0 pIC50 = 10 Binding
Ability to antagonize 5-HT-evoked contractions mediated through 5-hydroxytryptamine 4 receptor activation in the guinea pig distal colon LMMPAbility to antagonize 5-HT-evoked contractions mediated through 5-hydroxytryptamine 4 receptor activation in the guinea pig distal colon LMMP
ChEMBL 344 7 1 4 3.8 CCCCN1CCC(COC(=O)c2c(OC)[nH]c3ccccc23)CC1 10.1021/jm00024a002
CHEMBL142490 33825 0 None - 0 Guinea pig 10.0 pIC50 = 10 Binding
Ability to antagonize 5-HT-evoked contractions mediated through 5-hydroxytryptamine 4 receptor activation in the guinea pig distal colon LMMPAbility to antagonize 5-HT-evoked contractions mediated through 5-hydroxytryptamine 4 receptor activation in the guinea pig distal colon LMMP
ChEMBL 344 7 1 4 3.8 CCCCN1CCC(COC(=O)c2c(OC)[nH]c3ccccc23)CC1 10.1021/jm00024a002
10736989 36653 0 None - 0 Guinea pig 10.0 pIC50 = 10 Binding
Ability to antagonize 5-HT-evoked contractions mediated through 5-hydroxytryptamine 4 receptor activation in the guinea pig distal colon LMMPAbility to antagonize 5-HT-evoked contractions mediated through 5-hydroxytryptamine 4 receptor activation in the guinea pig distal colon LMMP
ChEMBL 356 6 0 5 3.7 CCCCN1CCC(COC(=O)c2c3n(c4ccccc24)CCO3)CC1 10.1021/jm00024a002
CHEMBL145075 36653 0 None - 0 Guinea pig 10.0 pIC50 = 10 Binding
Ability to antagonize 5-HT-evoked contractions mediated through 5-hydroxytryptamine 4 receptor activation in the guinea pig distal colon LMMPAbility to antagonize 5-HT-evoked contractions mediated through 5-hydroxytryptamine 4 receptor activation in the guinea pig distal colon LMMP
ChEMBL 356 6 0 5 3.7 CCCCN1CCC(COC(=O)c2c3n(c4ccccc24)CCO3)CC1 10.1021/jm00024a002
10736989 36653 0 None - 0 Guinea pig 10.0 pIC50 = 10 Binding
Ability to block 5-HT4 receptor mediated effect of 5-HT was assessed in the guinea-pig distal colon longitudinal muscle myenteric plexus preparation (LMMP)Ability to block 5-HT4 receptor mediated effect of 5-HT was assessed in the guinea-pig distal colon longitudinal muscle myenteric plexus preparation (LMMP)
ChEMBL 356 6 0 5 3.7 CCCCN1CCC(COC(=O)c2c3n(c4ccccc24)CCO3)CC1 10.1016/S0960-894X(01)80176-1
CHEMBL145075 36653 0 None - 0 Guinea pig 10.0 pIC50 = 10 Binding
Ability to block 5-HT4 receptor mediated effect of 5-HT was assessed in the guinea-pig distal colon longitudinal muscle myenteric plexus preparation (LMMP)Ability to block 5-HT4 receptor mediated effect of 5-HT was assessed in the guinea-pig distal colon longitudinal muscle myenteric plexus preparation (LMMP)
ChEMBL 356 6 0 5 3.7 CCCCN1CCC(COC(=O)c2c3n(c4ccccc24)CCO3)CC1 10.1016/S0960-894X(01)80176-1
54575170 146455 0 None - 0 Human 10.0 pIC50 = 10.0 Binding
Binding Assay: The binding affinity of the compounds for a human 5-HT4 receptor was assayed according to the method as disclosed in the literature [Wyngaert et al., Journal of Neurochemistry, (1997) 69, 1810-1819]. For this purpose, COS-7 cells expressing the human 5-HT4 receptor were constructed and homogenized to obtain membrane homogenates which were then used in binding assay experiments. For the binding assay, the membrane homogenates were respectively mixed and incubated with different concentrations of test materials and [H3]-GR113808 (Amersham Biosciences). The concentrations of the individual test materials were set to 4 uM, 1 uM, 0.25 uM, and 0.0625 uM, respectively, and the concentration of [H3]-GR113808 was set to 0.595 nM. After the incubation was completed, the reaction products were collected in GF/B glass fiber filters using a Packard cell harvester, and the bound radioactivity was then determined using a liquid cell scintillation counter (Packard TopCount NXT).Binding Assay: The binding affinity of the compounds for a human 5-HT4 receptor was assayed according to the method as disclosed in the literature [Wyngaert et al., Journal of Neurochemistry, (1997) 69, 1810-1819]. For this purpose, COS-7 cells expressing the human 5-HT4 receptor were constructed and homogenized to obtain membrane homogenates which were then used in binding assay experiments. For the binding assay, the membrane homogenates were respectively mixed and incubated with different concentrations of test materials and [H3]-GR113808 (Amersham Biosciences). The concentrations of the individual test materials were set to 4 uM, 1 uM, 0.25 uM, and 0.0625 uM, respectively, and the concentration of [H3]-GR113808 was set to 0.595 nM. After the incubation was completed, the reaction products were collected in GF/B glass fiber filters using a Packard cell harvester, and the bound radioactivity was then determined using a liquid cell scintillation counter (Packard TopCount NXT).
ChEMBL 434 10 2 7 2.8 COc1cc(N)c(Cl)cc1C(=O)NCC1CCN(CCCCCn2ccnn2)CC1 nan
CHEMBL3926377 146455 0 None - 0 Human 10.0 pIC50 = 10.0 Binding
Binding Assay: The binding affinity of the compounds for a human 5-HT4 receptor was assayed according to the method as disclosed in the literature [Wyngaert et al., Journal of Neurochemistry, (1997) 69, 1810-1819]. For this purpose, COS-7 cells expressing the human 5-HT4 receptor were constructed and homogenized to obtain membrane homogenates which were then used in binding assay experiments. For the binding assay, the membrane homogenates were respectively mixed and incubated with different concentrations of test materials and [H3]-GR113808 (Amersham Biosciences). The concentrations of the individual test materials were set to 4 uM, 1 uM, 0.25 uM, and 0.0625 uM, respectively, and the concentration of [H3]-GR113808 was set to 0.595 nM. After the incubation was completed, the reaction products were collected in GF/B glass fiber filters using a Packard cell harvester, and the bound radioactivity was then determined using a liquid cell scintillation counter (Packard TopCount NXT).Binding Assay: The binding affinity of the compounds for a human 5-HT4 receptor was assayed according to the method as disclosed in the literature [Wyngaert et al., Journal of Neurochemistry, (1997) 69, 1810-1819]. For this purpose, COS-7 cells expressing the human 5-HT4 receptor were constructed and homogenized to obtain membrane homogenates which were then used in binding assay experiments. For the binding assay, the membrane homogenates were respectively mixed and incubated with different concentrations of test materials and [H3]-GR113808 (Amersham Biosciences). The concentrations of the individual test materials were set to 4 uM, 1 uM, 0.25 uM, and 0.0625 uM, respectively, and the concentration of [H3]-GR113808 was set to 0.595 nM. After the incubation was completed, the reaction products were collected in GF/B glass fiber filters using a Packard cell harvester, and the bound radioactivity was then determined using a liquid cell scintillation counter (Packard TopCount NXT).
ChEMBL 434 10 2 7 2.8 COc1cc(N)c(Cl)cc1C(=O)NCC1CCN(CCCCCn2ccnn2)CC1 nan
54575227 141997 0 None - 0 Human 9.9 pIC50 = 9.9 Binding
Binding Assay: The binding affinity of the compounds for a human 5-HT4 receptor was assayed according to the method as disclosed in the literature [Wyngaert et al., Journal of Neurochemistry, (1997) 69, 1810-1819]. For this purpose, COS-7 cells expressing the human 5-HT4 receptor were constructed and homogenized to obtain membrane homogenates which were then used in binding assay experiments. For the binding assay, the membrane homogenates were respectively mixed and incubated with different concentrations of test materials and [H3]-GR113808 (Amersham Biosciences). The concentrations of the individual test materials were set to 4 uM, 1 uM, 0.25 uM, and 0.0625 uM, respectively, and the concentration of [H3]-GR113808 was set to 0.595 nM. After the incubation was completed, the reaction products were collected in GF/B glass fiber filters using a Packard cell harvester, and the bound radioactivity was then determined using a liquid cell scintillation counter (Packard TopCount NXT).Binding Assay: The binding affinity of the compounds for a human 5-HT4 receptor was assayed according to the method as disclosed in the literature [Wyngaert et al., Journal of Neurochemistry, (1997) 69, 1810-1819]. For this purpose, COS-7 cells expressing the human 5-HT4 receptor were constructed and homogenized to obtain membrane homogenates which were then used in binding assay experiments. For the binding assay, the membrane homogenates were respectively mixed and incubated with different concentrations of test materials and [H3]-GR113808 (Amersham Biosciences). The concentrations of the individual test materials were set to 4 uM, 1 uM, 0.25 uM, and 0.0625 uM, respectively, and the concentration of [H3]-GR113808 was set to 0.595 nM. After the incubation was completed, the reaction products were collected in GF/B glass fiber filters using a Packard cell harvester, and the bound radioactivity was then determined using a liquid cell scintillation counter (Packard TopCount NXT).
ChEMBL 405 6 2 4 3.7 COc1cc(N)c(Cl)cc1C(=O)NCC1CCN(Cc2ccc(F)cc2)CC1 nan
CHEMBL3890747 141997 0 None - 0 Human 9.9 pIC50 = 9.9 Binding
Binding Assay: The binding affinity of the compounds for a human 5-HT4 receptor was assayed according to the method as disclosed in the literature [Wyngaert et al., Journal of Neurochemistry, (1997) 69, 1810-1819]. For this purpose, COS-7 cells expressing the human 5-HT4 receptor were constructed and homogenized to obtain membrane homogenates which were then used in binding assay experiments. For the binding assay, the membrane homogenates were respectively mixed and incubated with different concentrations of test materials and [H3]-GR113808 (Amersham Biosciences). The concentrations of the individual test materials were set to 4 uM, 1 uM, 0.25 uM, and 0.0625 uM, respectively, and the concentration of [H3]-GR113808 was set to 0.595 nM. After the incubation was completed, the reaction products were collected in GF/B glass fiber filters using a Packard cell harvester, and the bound radioactivity was then determined using a liquid cell scintillation counter (Packard TopCount NXT).Binding Assay: The binding affinity of the compounds for a human 5-HT4 receptor was assayed according to the method as disclosed in the literature [Wyngaert et al., Journal of Neurochemistry, (1997) 69, 1810-1819]. For this purpose, COS-7 cells expressing the human 5-HT4 receptor were constructed and homogenized to obtain membrane homogenates which were then used in binding assay experiments. For the binding assay, the membrane homogenates were respectively mixed and incubated with different concentrations of test materials and [H3]-GR113808 (Amersham Biosciences). The concentrations of the individual test materials were set to 4 uM, 1 uM, 0.25 uM, and 0.0625 uM, respectively, and the concentration of [H3]-GR113808 was set to 0.595 nM. After the incubation was completed, the reaction products were collected in GF/B glass fiber filters using a Packard cell harvester, and the bound radioactivity was then determined using a liquid cell scintillation counter (Packard TopCount NXT).
ChEMBL 405 6 2 4 3.7 COc1cc(N)c(Cl)cc1C(=O)NCC1CCN(Cc2ccc(F)cc2)CC1 nan
10691444 35272 0 None - 0 Guinea pig 9.8 pIC50 = 9.8 Binding
Ability to antagonize 5-HT-evoked contractions mediated through 5-hydroxytryptamine 4 receptor activation in the guinea pig distal colon LMMPAbility to antagonize 5-HT-evoked contractions mediated through 5-hydroxytryptamine 4 receptor activation in the guinea pig distal colon LMMP
ChEMBL 384 6 0 5 4.5 CCCCN1CCC(COC(=O)c2c3n(c4ccccc24)CCCCO3)CC1 10.1021/jm00024a002
CHEMBL143862 35272 0 None - 0 Guinea pig 9.8 pIC50 = 9.8 Binding
Ability to antagonize 5-HT-evoked contractions mediated through 5-hydroxytryptamine 4 receptor activation in the guinea pig distal colon LMMPAbility to antagonize 5-HT-evoked contractions mediated through 5-hydroxytryptamine 4 receptor activation in the guinea pig distal colon LMMP
ChEMBL 384 6 0 5 4.5 CCCCN1CCC(COC(=O)c2c3n(c4ccccc24)CCCCO3)CC1 10.1021/jm00024a002
10691444 35272 0 None - 0 Guinea pig 9.8 pIC50 = 9.8 Binding
Ability to block 5-HT4 receptor mediated effect of 5-HT was assessed in the guinea-pig distal colon longitudinal muscle myenteric plexus preparation (LMMP)Ability to block 5-HT4 receptor mediated effect of 5-HT was assessed in the guinea-pig distal colon longitudinal muscle myenteric plexus preparation (LMMP)
ChEMBL 384 6 0 5 4.5 CCCCN1CCC(COC(=O)c2c3n(c4ccccc24)CCCCO3)CC1 10.1016/S0960-894X(01)80176-1
CHEMBL143862 35272 0 None - 0 Guinea pig 9.8 pIC50 = 9.8 Binding
Ability to block 5-HT4 receptor mediated effect of 5-HT was assessed in the guinea-pig distal colon longitudinal muscle myenteric plexus preparation (LMMP)Ability to block 5-HT4 receptor mediated effect of 5-HT was assessed in the guinea-pig distal colon longitudinal muscle myenteric plexus preparation (LMMP)
ChEMBL 384 6 0 5 4.5 CCCCN1CCC(COC(=O)c2c3n(c4ccccc24)CCCCO3)CC1 10.1016/S0960-894X(01)80176-1
54575166 153807 0 None - 0 Human 9.8 pIC50 = 9.8 Binding
Binding Assay: The binding affinity of the compounds for a human 5-HT4 receptor was assayed according to the method as disclosed in the literature [Wyngaert et al., Journal of Neurochemistry, (1997) 69, 1810-1819]. For this purpose, COS-7 cells expressing the human 5-HT4 receptor were constructed and homogenized to obtain membrane homogenates which were then used in binding assay experiments. For the binding assay, the membrane homogenates were respectively mixed and incubated with different concentrations of test materials and [H3]-GR113808 (Amersham Biosciences). The concentrations of the individual test materials were set to 4 uM, 1 uM, 0.25 uM, and 0.0625 uM, respectively, and the concentration of [H3]-GR113808 was set to 0.595 nM. After the incubation was completed, the reaction products were collected in GF/B glass fiber filters using a Packard cell harvester, and the bound radioactivity was then determined using a liquid cell scintillation counter (Packard TopCount NXT).Binding Assay: The binding affinity of the compounds for a human 5-HT4 receptor was assayed according to the method as disclosed in the literature [Wyngaert et al., Journal of Neurochemistry, (1997) 69, 1810-1819]. For this purpose, COS-7 cells expressing the human 5-HT4 receptor were constructed and homogenized to obtain membrane homogenates which were then used in binding assay experiments. For the binding assay, the membrane homogenates were respectively mixed and incubated with different concentrations of test materials and [H3]-GR113808 (Amersham Biosciences). The concentrations of the individual test materials were set to 4 uM, 1 uM, 0.25 uM, and 0.0625 uM, respectively, and the concentration of [H3]-GR113808 was set to 0.595 nM. After the incubation was completed, the reaction products were collected in GF/B glass fiber filters using a Packard cell harvester, and the bound radioactivity was then determined using a liquid cell scintillation counter (Packard TopCount NXT).
ChEMBL 407 8 2 8 1.4 COc1cc(N)c(Cl)cc1C(=O)NCC1CCN(CCCn2cnnn2)CC1 nan
CHEMBL3986866 153807 0 None - 0 Human 9.8 pIC50 = 9.8 Binding
Binding Assay: The binding affinity of the compounds for a human 5-HT4 receptor was assayed according to the method as disclosed in the literature [Wyngaert et al., Journal of Neurochemistry, (1997) 69, 1810-1819]. For this purpose, COS-7 cells expressing the human 5-HT4 receptor were constructed and homogenized to obtain membrane homogenates which were then used in binding assay experiments. For the binding assay, the membrane homogenates were respectively mixed and incubated with different concentrations of test materials and [H3]-GR113808 (Amersham Biosciences). The concentrations of the individual test materials were set to 4 uM, 1 uM, 0.25 uM, and 0.0625 uM, respectively, and the concentration of [H3]-GR113808 was set to 0.595 nM. After the incubation was completed, the reaction products were collected in GF/B glass fiber filters using a Packard cell harvester, and the bound radioactivity was then determined using a liquid cell scintillation counter (Packard TopCount NXT).Binding Assay: The binding affinity of the compounds for a human 5-HT4 receptor was assayed according to the method as disclosed in the literature [Wyngaert et al., Journal of Neurochemistry, (1997) 69, 1810-1819]. For this purpose, COS-7 cells expressing the human 5-HT4 receptor were constructed and homogenized to obtain membrane homogenates which were then used in binding assay experiments. For the binding assay, the membrane homogenates were respectively mixed and incubated with different concentrations of test materials and [H3]-GR113808 (Amersham Biosciences). The concentrations of the individual test materials were set to 4 uM, 1 uM, 0.25 uM, and 0.0625 uM, respectively, and the concentration of [H3]-GR113808 was set to 0.595 nM. After the incubation was completed, the reaction products were collected in GF/B glass fiber filters using a Packard cell harvester, and the bound radioactivity was then determined using a liquid cell scintillation counter (Packard TopCount NXT).
ChEMBL 407 8 2 8 1.4 COc1cc(N)c(Cl)cc1C(=O)NCC1CCN(CCCn2cnnn2)CC1 nan
54575223 150321 0 None - 0 Human 9.7 pIC50 = 9.7 Binding
Binding Assay: The binding affinity of the compounds for a human 5-HT4 receptor was assayed according to the method as disclosed in the literature [Wyngaert et al., Journal of Neurochemistry, (1997) 69, 1810-1819]. For this purpose, COS-7 cells expressing the human 5-HT4 receptor were constructed and homogenized to obtain membrane homogenates which were then used in binding assay experiments. For the binding assay, the membrane homogenates were respectively mixed and incubated with different concentrations of test materials and [H3]-GR113808 (Amersham Biosciences). The concentrations of the individual test materials were set to 4 uM, 1 uM, 0.25 uM, and 0.0625 uM, respectively, and the concentration of [H3]-GR113808 was set to 0.595 nM. After the incubation was completed, the reaction products were collected in GF/B glass fiber filters using a Packard cell harvester, and the bound radioactivity was then determined using a liquid cell scintillation counter (Packard TopCount NXT).Binding Assay: The binding affinity of the compounds for a human 5-HT4 receptor was assayed according to the method as disclosed in the literature [Wyngaert et al., Journal of Neurochemistry, (1997) 69, 1810-1819]. For this purpose, COS-7 cells expressing the human 5-HT4 receptor were constructed and homogenized to obtain membrane homogenates which were then used in binding assay experiments. For the binding assay, the membrane homogenates were respectively mixed and incubated with different concentrations of test materials and [H3]-GR113808 (Amersham Biosciences). The concentrations of the individual test materials were set to 4 uM, 1 uM, 0.25 uM, and 0.0625 uM, respectively, and the concentration of [H3]-GR113808 was set to 0.595 nM. After the incubation was completed, the reaction products were collected in GF/B glass fiber filters using a Packard cell harvester, and the bound radioactivity was then determined using a liquid cell scintillation counter (Packard TopCount NXT).
ChEMBL 406 8 2 7 2.1 COc1cc(N)c(Cl)cc1C(=O)NCC1CCN(CCCn2nccn2)CC1 nan
CHEMBL3957180 150321 0 None - 0 Human 9.7 pIC50 = 9.7 Binding
Binding Assay: The binding affinity of the compounds for a human 5-HT4 receptor was assayed according to the method as disclosed in the literature [Wyngaert et al., Journal of Neurochemistry, (1997) 69, 1810-1819]. For this purpose, COS-7 cells expressing the human 5-HT4 receptor were constructed and homogenized to obtain membrane homogenates which were then used in binding assay experiments. For the binding assay, the membrane homogenates were respectively mixed and incubated with different concentrations of test materials and [H3]-GR113808 (Amersham Biosciences). The concentrations of the individual test materials were set to 4 uM, 1 uM, 0.25 uM, and 0.0625 uM, respectively, and the concentration of [H3]-GR113808 was set to 0.595 nM. After the incubation was completed, the reaction products were collected in GF/B glass fiber filters using a Packard cell harvester, and the bound radioactivity was then determined using a liquid cell scintillation counter (Packard TopCount NXT).Binding Assay: The binding affinity of the compounds for a human 5-HT4 receptor was assayed according to the method as disclosed in the literature [Wyngaert et al., Journal of Neurochemistry, (1997) 69, 1810-1819]. For this purpose, COS-7 cells expressing the human 5-HT4 receptor were constructed and homogenized to obtain membrane homogenates which were then used in binding assay experiments. For the binding assay, the membrane homogenates were respectively mixed and incubated with different concentrations of test materials and [H3]-GR113808 (Amersham Biosciences). The concentrations of the individual test materials were set to 4 uM, 1 uM, 0.25 uM, and 0.0625 uM, respectively, and the concentration of [H3]-GR113808 was set to 0.595 nM. After the incubation was completed, the reaction products were collected in GF/B glass fiber filters using a Packard cell harvester, and the bound radioactivity was then determined using a liquid cell scintillation counter (Packard TopCount NXT).
ChEMBL 406 8 2 7 2.1 COc1cc(N)c(Cl)cc1C(=O)NCC1CCN(CCCn2nccn2)CC1 nan
66780300 148936 0 None - 0 Human 9.7 pIC50 = 9.7 Binding
Binding Assay: The binding affinity of the compounds for a human 5-HT4 receptor was assayed according to the method as disclosed in the literature [Wyngaert et al., Journal of Neurochemistry, (1997) 69, 1810-1819]. For this purpose, COS-7 cells expressing the human 5-HT4 receptor were constructed and homogenized to obtain membrane homogenates which were then used in binding assay experiments. For the binding assay, the membrane homogenates were respectively mixed and incubated with different concentrations of test materials and [H3]-GR113808 (Amersham Biosciences). The concentrations of the individual test materials were set to 4 uM, 1 uM, 0.25 uM, and 0.0625 uM, respectively, and the concentration of [H3]-GR113808 was set to 0.595 nM. After the incubation was completed, the reaction products were collected in GF/B glass fiber filters using a Packard cell harvester, and the bound radioactivity was then determined using a liquid cell scintillation counter (Packard TopCount NXT).Binding Assay: The binding affinity of the compounds for a human 5-HT4 receptor was assayed according to the method as disclosed in the literature [Wyngaert et al., Journal of Neurochemistry, (1997) 69, 1810-1819]. For this purpose, COS-7 cells expressing the human 5-HT4 receptor were constructed and homogenized to obtain membrane homogenates which were then used in binding assay experiments. For the binding assay, the membrane homogenates were respectively mixed and incubated with different concentrations of test materials and [H3]-GR113808 (Amersham Biosciences). The concentrations of the individual test materials were set to 4 uM, 1 uM, 0.25 uM, and 0.0625 uM, respectively, and the concentration of [H3]-GR113808 was set to 0.595 nM. After the incubation was completed, the reaction products were collected in GF/B glass fiber filters using a Packard cell harvester, and the bound radioactivity was then determined using a liquid cell scintillation counter (Packard TopCount NXT).
ChEMBL 406 8 2 7 2.1 COc1cc(N)c(Cl)cc1C(=O)NCC1CCN(CCCn2cncn2)CC1 nan
CHEMBL3946162 148936 0 None - 0 Human 9.7 pIC50 = 9.7 Binding
Binding Assay: The binding affinity of the compounds for a human 5-HT4 receptor was assayed according to the method as disclosed in the literature [Wyngaert et al., Journal of Neurochemistry, (1997) 69, 1810-1819]. For this purpose, COS-7 cells expressing the human 5-HT4 receptor were constructed and homogenized to obtain membrane homogenates which were then used in binding assay experiments. For the binding assay, the membrane homogenates were respectively mixed and incubated with different concentrations of test materials and [H3]-GR113808 (Amersham Biosciences). The concentrations of the individual test materials were set to 4 uM, 1 uM, 0.25 uM, and 0.0625 uM, respectively, and the concentration of [H3]-GR113808 was set to 0.595 nM. After the incubation was completed, the reaction products were collected in GF/B glass fiber filters using a Packard cell harvester, and the bound radioactivity was then determined using a liquid cell scintillation counter (Packard TopCount NXT).Binding Assay: The binding affinity of the compounds for a human 5-HT4 receptor was assayed according to the method as disclosed in the literature [Wyngaert et al., Journal of Neurochemistry, (1997) 69, 1810-1819]. For this purpose, COS-7 cells expressing the human 5-HT4 receptor were constructed and homogenized to obtain membrane homogenates which were then used in binding assay experiments. For the binding assay, the membrane homogenates were respectively mixed and incubated with different concentrations of test materials and [H3]-GR113808 (Amersham Biosciences). The concentrations of the individual test materials were set to 4 uM, 1 uM, 0.25 uM, and 0.0625 uM, respectively, and the concentration of [H3]-GR113808 was set to 0.595 nM. After the incubation was completed, the reaction products were collected in GF/B glass fiber filters using a Packard cell harvester, and the bound radioactivity was then determined using a liquid cell scintillation counter (Packard TopCount NXT).
ChEMBL 406 8 2 7 2.1 COc1cc(N)c(Cl)cc1C(=O)NCC1CCN(CCCn2cncn2)CC1 nan
54575168 146661 0 None - 0 Human 9.6 pIC50 = 9.6 Binding
Binding Assay: The binding affinity of the compounds for a human 5-HT4 receptor was assayed according to the method as disclosed in the literature [Wyngaert et al., Journal of Neurochemistry, (1997) 69, 1810-1819]. For this purpose, COS-7 cells expressing the human 5-HT4 receptor were constructed and homogenized to obtain membrane homogenates which were then used in binding assay experiments. For the binding assay, the membrane homogenates were respectively mixed and incubated with different concentrations of test materials and [H3]-GR113808 (Amersham Biosciences). The concentrations of the individual test materials were set to 4 uM, 1 uM, 0.25 uM, and 0.0625 uM, respectively, and the concentration of [H3]-GR113808 was set to 0.595 nM. After the incubation was completed, the reaction products were collected in GF/B glass fiber filters using a Packard cell harvester, and the bound radioactivity was then determined using a liquid cell scintillation counter (Packard TopCount NXT).Binding Assay: The binding affinity of the compounds for a human 5-HT4 receptor was assayed according to the method as disclosed in the literature [Wyngaert et al., Journal of Neurochemistry, (1997) 69, 1810-1819]. For this purpose, COS-7 cells expressing the human 5-HT4 receptor were constructed and homogenized to obtain membrane homogenates which were then used in binding assay experiments. For the binding assay, the membrane homogenates were respectively mixed and incubated with different concentrations of test materials and [H3]-GR113808 (Amersham Biosciences). The concentrations of the individual test materials were set to 4 uM, 1 uM, 0.25 uM, and 0.0625 uM, respectively, and the concentration of [H3]-GR113808 was set to 0.595 nM. After the incubation was completed, the reaction products were collected in GF/B glass fiber filters using a Packard cell harvester, and the bound radioactivity was then determined using a liquid cell scintillation counter (Packard TopCount NXT).
ChEMBL 419 8 2 6 3.0 COc1cc(N)c(Cl)cc1C(=O)NCC1CCN(CCCn2ccnc2C)CC1 nan
CHEMBL3928124 146661 0 None - 0 Human 9.6 pIC50 = 9.6 Binding
Binding Assay: The binding affinity of the compounds for a human 5-HT4 receptor was assayed according to the method as disclosed in the literature [Wyngaert et al., Journal of Neurochemistry, (1997) 69, 1810-1819]. For this purpose, COS-7 cells expressing the human 5-HT4 receptor were constructed and homogenized to obtain membrane homogenates which were then used in binding assay experiments. For the binding assay, the membrane homogenates were respectively mixed and incubated with different concentrations of test materials and [H3]-GR113808 (Amersham Biosciences). The concentrations of the individual test materials were set to 4 uM, 1 uM, 0.25 uM, and 0.0625 uM, respectively, and the concentration of [H3]-GR113808 was set to 0.595 nM. After the incubation was completed, the reaction products were collected in GF/B glass fiber filters using a Packard cell harvester, and the bound radioactivity was then determined using a liquid cell scintillation counter (Packard TopCount NXT).Binding Assay: The binding affinity of the compounds for a human 5-HT4 receptor was assayed according to the method as disclosed in the literature [Wyngaert et al., Journal of Neurochemistry, (1997) 69, 1810-1819]. For this purpose, COS-7 cells expressing the human 5-HT4 receptor were constructed and homogenized to obtain membrane homogenates which were then used in binding assay experiments. For the binding assay, the membrane homogenates were respectively mixed and incubated with different concentrations of test materials and [H3]-GR113808 (Amersham Biosciences). The concentrations of the individual test materials were set to 4 uM, 1 uM, 0.25 uM, and 0.0625 uM, respectively, and the concentration of [H3]-GR113808 was set to 0.595 nM. After the incubation was completed, the reaction products were collected in GF/B glass fiber filters using a Packard cell harvester, and the bound radioactivity was then determined using a liquid cell scintillation counter (Packard TopCount NXT).
ChEMBL 419 8 2 6 3.0 COc1cc(N)c(Cl)cc1C(=O)NCC1CCN(CCCn2ccnc2C)CC1 nan
54575224 153288 0 None - 0 Human 9.6 pIC50 = 9.6 Binding
Binding Assay: The binding affinity of the compounds for a human 5-HT4 receptor was assayed according to the method as disclosed in the literature [Wyngaert et al., Journal of Neurochemistry, (1997) 69, 1810-1819]. For this purpose, COS-7 cells expressing the human 5-HT4 receptor were constructed and homogenized to obtain membrane homogenates which were then used in binding assay experiments. For the binding assay, the membrane homogenates were respectively mixed and incubated with different concentrations of test materials and [H3]-GR113808 (Amersham Biosciences). The concentrations of the individual test materials were set to 4 uM, 1 uM, 0.25 uM, and 0.0625 uM, respectively, and the concentration of [H3]-GR113808 was set to 0.595 nM. After the incubation was completed, the reaction products were collected in GF/B glass fiber filters using a Packard cell harvester, and the bound radioactivity was then determined using a liquid cell scintillation counter (Packard TopCount NXT).Binding Assay: The binding affinity of the compounds for a human 5-HT4 receptor was assayed according to the method as disclosed in the literature [Wyngaert et al., Journal of Neurochemistry, (1997) 69, 1810-1819]. For this purpose, COS-7 cells expressing the human 5-HT4 receptor were constructed and homogenized to obtain membrane homogenates which were then used in binding assay experiments. For the binding assay, the membrane homogenates were respectively mixed and incubated with different concentrations of test materials and [H3]-GR113808 (Amersham Biosciences). The concentrations of the individual test materials were set to 4 uM, 1 uM, 0.25 uM, and 0.0625 uM, respectively, and the concentration of [H3]-GR113808 was set to 0.595 nM. After the incubation was completed, the reaction products were collected in GF/B glass fiber filters using a Packard cell harvester, and the bound radioactivity was then determined using a liquid cell scintillation counter (Packard TopCount NXT).
ChEMBL 388 6 2 5 3.0 COc1cc(N)c(Cl)cc1C(=O)NCC1CCN(Cc2cccnc2)CC1 nan
CHEMBL3982522 153288 0 None - 0 Human 9.6 pIC50 = 9.6 Binding
Binding Assay: The binding affinity of the compounds for a human 5-HT4 receptor was assayed according to the method as disclosed in the literature [Wyngaert et al., Journal of Neurochemistry, (1997) 69, 1810-1819]. For this purpose, COS-7 cells expressing the human 5-HT4 receptor were constructed and homogenized to obtain membrane homogenates which were then used in binding assay experiments. For the binding assay, the membrane homogenates were respectively mixed and incubated with different concentrations of test materials and [H3]-GR113808 (Amersham Biosciences). The concentrations of the individual test materials were set to 4 uM, 1 uM, 0.25 uM, and 0.0625 uM, respectively, and the concentration of [H3]-GR113808 was set to 0.595 nM. After the incubation was completed, the reaction products were collected in GF/B glass fiber filters using a Packard cell harvester, and the bound radioactivity was then determined using a liquid cell scintillation counter (Packard TopCount NXT).Binding Assay: The binding affinity of the compounds for a human 5-HT4 receptor was assayed according to the method as disclosed in the literature [Wyngaert et al., Journal of Neurochemistry, (1997) 69, 1810-1819]. For this purpose, COS-7 cells expressing the human 5-HT4 receptor were constructed and homogenized to obtain membrane homogenates which were then used in binding assay experiments. For the binding assay, the membrane homogenates were respectively mixed and incubated with different concentrations of test materials and [H3]-GR113808 (Amersham Biosciences). The concentrations of the individual test materials were set to 4 uM, 1 uM, 0.25 uM, and 0.0625 uM, respectively, and the concentration of [H3]-GR113808 was set to 0.595 nM. After the incubation was completed, the reaction products were collected in GF/B glass fiber filters using a Packard cell harvester, and the bound radioactivity was then determined using a liquid cell scintillation counter (Packard TopCount NXT).
ChEMBL 388 6 2 5 3.0 COc1cc(N)c(Cl)cc1C(=O)NCC1CCN(Cc2cccnc2)CC1 nan
240 931 39 None -11 25 Human 9.4 pIC50 = 9.4 Binding
Binding Assay: The binding affinity of the compounds for a human 5-HT4 receptor was assayed according to the method as disclosed in the literature [Wyngaert et al., Journal of Neurochemistry, (1997) 69, 1810-1819]. For this purpose, COS-7 cells expressing the human 5-HT4 receptor were constructed and homogenized to obtain membrane homogenates which were then used in binding assay experiments. For the binding assay, the membrane homogenates were respectively mixed and incubated with different concentrations of test materials and [H3]-GR113808 (Amersham Biosciences). The concentrations of the individual test materials were set to 4 uM, 1 uM, 0.25 uM, and 0.0625 uM, respectively, and the concentration of [H3]-GR113808 was set to 0.595 nM. After the incubation was completed, the reaction products were collected in GF/B glass fiber filters using a Packard cell harvester, and the bound radioactivity was then determined using a liquid cell scintillation counter (Packard TopCount NXT).Binding Assay: The binding affinity of the compounds for a human 5-HT4 receptor was assayed according to the method as disclosed in the literature [Wyngaert et al., Journal of Neurochemistry, (1997) 69, 1810-1819]. For this purpose, COS-7 cells expressing the human 5-HT4 receptor were constructed and homogenized to obtain membrane homogenates which were then used in binding assay experiments. For the binding assay, the membrane homogenates were respectively mixed and incubated with different concentrations of test materials and [H3]-GR113808 (Amersham Biosciences). The concentrations of the individual test materials were set to 4 uM, 1 uM, 0.25 uM, and 0.0625 uM, respectively, and the concentration of [H3]-GR113808 was set to 0.595 nM. After the incubation was completed, the reaction products were collected in GF/B glass fiber filters using a Packard cell harvester, and the bound radioactivity was then determined using a liquid cell scintillation counter (Packard TopCount NXT).
ChEMBL 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N nan
2769 931 39 None -11 25 Human 9.4 pIC50 = 9.4 Binding
Binding Assay: The binding affinity of the compounds for a human 5-HT4 receptor was assayed according to the method as disclosed in the literature [Wyngaert et al., Journal of Neurochemistry, (1997) 69, 1810-1819]. For this purpose, COS-7 cells expressing the human 5-HT4 receptor were constructed and homogenized to obtain membrane homogenates which were then used in binding assay experiments. For the binding assay, the membrane homogenates were respectively mixed and incubated with different concentrations of test materials and [H3]-GR113808 (Amersham Biosciences). The concentrations of the individual test materials were set to 4 uM, 1 uM, 0.25 uM, and 0.0625 uM, respectively, and the concentration of [H3]-GR113808 was set to 0.595 nM. After the incubation was completed, the reaction products were collected in GF/B glass fiber filters using a Packard cell harvester, and the bound radioactivity was then determined using a liquid cell scintillation counter (Packard TopCount NXT).Binding Assay: The binding affinity of the compounds for a human 5-HT4 receptor was assayed according to the method as disclosed in the literature [Wyngaert et al., Journal of Neurochemistry, (1997) 69, 1810-1819]. For this purpose, COS-7 cells expressing the human 5-HT4 receptor were constructed and homogenized to obtain membrane homogenates which were then used in binding assay experiments. For the binding assay, the membrane homogenates were respectively mixed and incubated with different concentrations of test materials and [H3]-GR113808 (Amersham Biosciences). The concentrations of the individual test materials were set to 4 uM, 1 uM, 0.25 uM, and 0.0625 uM, respectively, and the concentration of [H3]-GR113808 was set to 0.595 nM. After the incubation was completed, the reaction products were collected in GF/B glass fiber filters using a Packard cell harvester, and the bound radioactivity was then determined using a liquid cell scintillation counter (Packard TopCount NXT).
ChEMBL 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N nan
44279790 931 39 None -11 25 Human 9.4 pIC50 = 9.4 Binding
Binding Assay: The binding affinity of the compounds for a human 5-HT4 receptor was assayed according to the method as disclosed in the literature [Wyngaert et al., Journal of Neurochemistry, (1997) 69, 1810-1819]. For this purpose, COS-7 cells expressing the human 5-HT4 receptor were constructed and homogenized to obtain membrane homogenates which were then used in binding assay experiments. For the binding assay, the membrane homogenates were respectively mixed and incubated with different concentrations of test materials and [H3]-GR113808 (Amersham Biosciences). The concentrations of the individual test materials were set to 4 uM, 1 uM, 0.25 uM, and 0.0625 uM, respectively, and the concentration of [H3]-GR113808 was set to 0.595 nM. After the incubation was completed, the reaction products were collected in GF/B glass fiber filters using a Packard cell harvester, and the bound radioactivity was then determined using a liquid cell scintillation counter (Packard TopCount NXT).Binding Assay: The binding affinity of the compounds for a human 5-HT4 receptor was assayed according to the method as disclosed in the literature [Wyngaert et al., Journal of Neurochemistry, (1997) 69, 1810-1819]. For this purpose, COS-7 cells expressing the human 5-HT4 receptor were constructed and homogenized to obtain membrane homogenates which were then used in binding assay experiments. For the binding assay, the membrane homogenates were respectively mixed and incubated with different concentrations of test materials and [H3]-GR113808 (Amersham Biosciences). The concentrations of the individual test materials were set to 4 uM, 1 uM, 0.25 uM, and 0.0625 uM, respectively, and the concentration of [H3]-GR113808 was set to 0.595 nM. After the incubation was completed, the reaction products were collected in GF/B glass fiber filters using a Packard cell harvester, and the bound radioactivity was then determined using a liquid cell scintillation counter (Packard TopCount NXT).
ChEMBL 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N nan
660 931 39 None -11 25 Human 9.4 pIC50 = 9.4 Binding
Binding Assay: The binding affinity of the compounds for a human 5-HT4 receptor was assayed according to the method as disclosed in the literature [Wyngaert et al., Journal of Neurochemistry, (1997) 69, 1810-1819]. For this purpose, COS-7 cells expressing the human 5-HT4 receptor were constructed and homogenized to obtain membrane homogenates which were then used in binding assay experiments. For the binding assay, the membrane homogenates were respectively mixed and incubated with different concentrations of test materials and [H3]-GR113808 (Amersham Biosciences). The concentrations of the individual test materials were set to 4 uM, 1 uM, 0.25 uM, and 0.0625 uM, respectively, and the concentration of [H3]-GR113808 was set to 0.595 nM. After the incubation was completed, the reaction products were collected in GF/B glass fiber filters using a Packard cell harvester, and the bound radioactivity was then determined using a liquid cell scintillation counter (Packard TopCount NXT).Binding Assay: The binding affinity of the compounds for a human 5-HT4 receptor was assayed according to the method as disclosed in the literature [Wyngaert et al., Journal of Neurochemistry, (1997) 69, 1810-1819]. For this purpose, COS-7 cells expressing the human 5-HT4 receptor were constructed and homogenized to obtain membrane homogenates which were then used in binding assay experiments. For the binding assay, the membrane homogenates were respectively mixed and incubated with different concentrations of test materials and [H3]-GR113808 (Amersham Biosciences). The concentrations of the individual test materials were set to 4 uM, 1 uM, 0.25 uM, and 0.0625 uM, respectively, and the concentration of [H3]-GR113808 was set to 0.595 nM. After the incubation was completed, the reaction products were collected in GF/B glass fiber filters using a Packard cell harvester, and the bound radioactivity was then determined using a liquid cell scintillation counter (Packard TopCount NXT).
ChEMBL 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N nan
CHEMBL1729 931 39 None -11 25 Human 9.4 pIC50 = 9.4 Binding
Binding Assay: The binding affinity of the compounds for a human 5-HT4 receptor was assayed according to the method as disclosed in the literature [Wyngaert et al., Journal of Neurochemistry, (1997) 69, 1810-1819]. For this purpose, COS-7 cells expressing the human 5-HT4 receptor were constructed and homogenized to obtain membrane homogenates which were then used in binding assay experiments. For the binding assay, the membrane homogenates were respectively mixed and incubated with different concentrations of test materials and [H3]-GR113808 (Amersham Biosciences). The concentrations of the individual test materials were set to 4 uM, 1 uM, 0.25 uM, and 0.0625 uM, respectively, and the concentration of [H3]-GR113808 was set to 0.595 nM. After the incubation was completed, the reaction products were collected in GF/B glass fiber filters using a Packard cell harvester, and the bound radioactivity was then determined using a liquid cell scintillation counter (Packard TopCount NXT).Binding Assay: The binding affinity of the compounds for a human 5-HT4 receptor was assayed according to the method as disclosed in the literature [Wyngaert et al., Journal of Neurochemistry, (1997) 69, 1810-1819]. For this purpose, COS-7 cells expressing the human 5-HT4 receptor were constructed and homogenized to obtain membrane homogenates which were then used in binding assay experiments. For the binding assay, the membrane homogenates were respectively mixed and incubated with different concentrations of test materials and [H3]-GR113808 (Amersham Biosciences). The concentrations of the individual test materials were set to 4 uM, 1 uM, 0.25 uM, and 0.0625 uM, respectively, and the concentration of [H3]-GR113808 was set to 0.595 nM. After the incubation was completed, the reaction products were collected in GF/B glass fiber filters using a Packard cell harvester, and the bound radioactivity was then determined using a liquid cell scintillation counter (Packard TopCount NXT).
ChEMBL 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N nan
CHEMBL560739 931 39 None -11 25 Human 9.4 pIC50 = 9.4 Binding
Binding Assay: The binding affinity of the compounds for a human 5-HT4 receptor was assayed according to the method as disclosed in the literature [Wyngaert et al., Journal of Neurochemistry, (1997) 69, 1810-1819]. For this purpose, COS-7 cells expressing the human 5-HT4 receptor were constructed and homogenized to obtain membrane homogenates which were then used in binding assay experiments. For the binding assay, the membrane homogenates were respectively mixed and incubated with different concentrations of test materials and [H3]-GR113808 (Amersham Biosciences). The concentrations of the individual test materials were set to 4 uM, 1 uM, 0.25 uM, and 0.0625 uM, respectively, and the concentration of [H3]-GR113808 was set to 0.595 nM. After the incubation was completed, the reaction products were collected in GF/B glass fiber filters using a Packard cell harvester, and the bound radioactivity was then determined using a liquid cell scintillation counter (Packard TopCount NXT).Binding Assay: The binding affinity of the compounds for a human 5-HT4 receptor was assayed according to the method as disclosed in the literature [Wyngaert et al., Journal of Neurochemistry, (1997) 69, 1810-1819]. For this purpose, COS-7 cells expressing the human 5-HT4 receptor were constructed and homogenized to obtain membrane homogenates which were then used in binding assay experiments. For the binding assay, the membrane homogenates were respectively mixed and incubated with different concentrations of test materials and [H3]-GR113808 (Amersham Biosciences). The concentrations of the individual test materials were set to 4 uM, 1 uM, 0.25 uM, and 0.0625 uM, respectively, and the concentration of [H3]-GR113808 was set to 0.595 nM. After the incubation was completed, the reaction products were collected in GF/B glass fiber filters using a Packard cell harvester, and the bound radioactivity was then determined using a liquid cell scintillation counter (Packard TopCount NXT).
ChEMBL 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N nan
DB00604 931 39 None -11 25 Human 9.4 pIC50 = 9.4 Binding
Binding Assay: The binding affinity of the compounds for a human 5-HT4 receptor was assayed according to the method as disclosed in the literature [Wyngaert et al., Journal of Neurochemistry, (1997) 69, 1810-1819]. For this purpose, COS-7 cells expressing the human 5-HT4 receptor were constructed and homogenized to obtain membrane homogenates which were then used in binding assay experiments. For the binding assay, the membrane homogenates were respectively mixed and incubated with different concentrations of test materials and [H3]-GR113808 (Amersham Biosciences). The concentrations of the individual test materials were set to 4 uM, 1 uM, 0.25 uM, and 0.0625 uM, respectively, and the concentration of [H3]-GR113808 was set to 0.595 nM. After the incubation was completed, the reaction products were collected in GF/B glass fiber filters using a Packard cell harvester, and the bound radioactivity was then determined using a liquid cell scintillation counter (Packard TopCount NXT).Binding Assay: The binding affinity of the compounds for a human 5-HT4 receptor was assayed according to the method as disclosed in the literature [Wyngaert et al., Journal of Neurochemistry, (1997) 69, 1810-1819]. For this purpose, COS-7 cells expressing the human 5-HT4 receptor were constructed and homogenized to obtain membrane homogenates which were then used in binding assay experiments. For the binding assay, the membrane homogenates were respectively mixed and incubated with different concentrations of test materials and [H3]-GR113808 (Amersham Biosciences). The concentrations of the individual test materials were set to 4 uM, 1 uM, 0.25 uM, and 0.0625 uM, respectively, and the concentration of [H3]-GR113808 was set to 0.595 nM. After the incubation was completed, the reaction products were collected in GF/B glass fiber filters using a Packard cell harvester, and the bound radioactivity was then determined using a liquid cell scintillation counter (Packard TopCount NXT).
ChEMBL 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N nan
54575228 145654 0 None - 0 Human 9.4 pIC50 = 9.4 Binding
Binding Assay: The binding affinity of the compounds for a human 5-HT4 receptor was assayed according to the method as disclosed in the literature [Wyngaert et al., Journal of Neurochemistry, (1997) 69, 1810-1819]. For this purpose, COS-7 cells expressing the human 5-HT4 receptor were constructed and homogenized to obtain membrane homogenates which were then used in binding assay experiments. For the binding assay, the membrane homogenates were respectively mixed and incubated with different concentrations of test materials and [H3]-GR113808 (Amersham Biosciences). The concentrations of the individual test materials were set to 4 uM, 1 uM, 0.25 uM, and 0.0625 uM, respectively, and the concentration of [H3]-GR113808 was set to 0.595 nM. After the incubation was completed, the reaction products were collected in GF/B glass fiber filters using a Packard cell harvester, and the bound radioactivity was then determined using a liquid cell scintillation counter (Packard TopCount NXT).Binding Assay: The binding affinity of the compounds for a human 5-HT4 receptor was assayed according to the method as disclosed in the literature [Wyngaert et al., Journal of Neurochemistry, (1997) 69, 1810-1819]. For this purpose, COS-7 cells expressing the human 5-HT4 receptor were constructed and homogenized to obtain membrane homogenates which were then used in binding assay experiments. For the binding assay, the membrane homogenates were respectively mixed and incubated with different concentrations of test materials and [H3]-GR113808 (Amersham Biosciences). The concentrations of the individual test materials were set to 4 uM, 1 uM, 0.25 uM, and 0.0625 uM, respectively, and the concentration of [H3]-GR113808 was set to 0.595 nM. After the incubation was completed, the reaction products were collected in GF/B glass fiber filters using a Packard cell harvester, and the bound radioactivity was then determined using a liquid cell scintillation counter (Packard TopCount NXT).
ChEMBL 403 6 3 5 3.3 COc1cc(N)c(Cl)cc1C(=O)NCC1CCN(Cc2ccc(O)cc2)CC1 nan
CHEMBL3920018 145654 0 None - 0 Human 9.4 pIC50 = 9.4 Binding
Binding Assay: The binding affinity of the compounds for a human 5-HT4 receptor was assayed according to the method as disclosed in the literature [Wyngaert et al., Journal of Neurochemistry, (1997) 69, 1810-1819]. For this purpose, COS-7 cells expressing the human 5-HT4 receptor were constructed and homogenized to obtain membrane homogenates which were then used in binding assay experiments. For the binding assay, the membrane homogenates were respectively mixed and incubated with different concentrations of test materials and [H3]-GR113808 (Amersham Biosciences). The concentrations of the individual test materials were set to 4 uM, 1 uM, 0.25 uM, and 0.0625 uM, respectively, and the concentration of [H3]-GR113808 was set to 0.595 nM. After the incubation was completed, the reaction products were collected in GF/B glass fiber filters using a Packard cell harvester, and the bound radioactivity was then determined using a liquid cell scintillation counter (Packard TopCount NXT).Binding Assay: The binding affinity of the compounds for a human 5-HT4 receptor was assayed according to the method as disclosed in the literature [Wyngaert et al., Journal of Neurochemistry, (1997) 69, 1810-1819]. For this purpose, COS-7 cells expressing the human 5-HT4 receptor were constructed and homogenized to obtain membrane homogenates which were then used in binding assay experiments. For the binding assay, the membrane homogenates were respectively mixed and incubated with different concentrations of test materials and [H3]-GR113808 (Amersham Biosciences). The concentrations of the individual test materials were set to 4 uM, 1 uM, 0.25 uM, and 0.0625 uM, respectively, and the concentration of [H3]-GR113808 was set to 0.595 nM. After the incubation was completed, the reaction products were collected in GF/B glass fiber filters using a Packard cell harvester, and the bound radioactivity was then determined using a liquid cell scintillation counter (Packard TopCount NXT).
ChEMBL 403 6 3 5 3.3 COc1cc(N)c(Cl)cc1C(=O)NCC1CCN(Cc2ccc(O)cc2)CC1 nan
53472864 145036 0 None - 0 Human 9.4 pIC50 = 9.4 Binding
Binding Assay: The binding affinity of the compounds for a human 5-HT4 receptor was assayed according to the method as disclosed in the literature [Wyngaert et al., Journal of Neurochemistry, (1997) 69, 1810-1819]. For this purpose, COS-7 cells expressing the human 5-HT4 receptor were constructed and homogenized to obtain membrane homogenates which were then used in binding assay experiments. For the binding assay, the membrane homogenates were respectively mixed and incubated with different concentrations of test materials and [H3]-GR113808 (Amersham Biosciences). The concentrations of the individual test materials were set to 4 uM, 1 uM, 0.25 uM, and 0.0625 uM, respectively, and the concentration of [H3]-GR113808 was set to 0.595 nM. After the incubation was completed, the reaction products were collected in GF/B glass fiber filters using a Packard cell harvester, and the bound radioactivity was then determined using a liquid cell scintillation counter (Packard TopCount NXT).Binding Assay: The binding affinity of the compounds for a human 5-HT4 receptor was assayed according to the method as disclosed in the literature [Wyngaert et al., Journal of Neurochemistry, (1997) 69, 1810-1819]. For this purpose, COS-7 cells expressing the human 5-HT4 receptor were constructed and homogenized to obtain membrane homogenates which were then used in binding assay experiments. For the binding assay, the membrane homogenates were respectively mixed and incubated with different concentrations of test materials and [H3]-GR113808 (Amersham Biosciences). The concentrations of the individual test materials were set to 4 uM, 1 uM, 0.25 uM, and 0.0625 uM, respectively, and the concentration of [H3]-GR113808 was set to 0.595 nM. After the incubation was completed, the reaction products were collected in GF/B glass fiber filters using a Packard cell harvester, and the bound radioactivity was then determined using a liquid cell scintillation counter (Packard TopCount NXT).
ChEMBL 390 6 2 5 2.9 COc1cc(N)c(Cl)cc1C(=O)NCC1CCN(Cc2cccn2C)CC1 nan
CHEMBL3915236 145036 0 None - 0 Human 9.4 pIC50 = 9.4 Binding
Binding Assay: The binding affinity of the compounds for a human 5-HT4 receptor was assayed according to the method as disclosed in the literature [Wyngaert et al., Journal of Neurochemistry, (1997) 69, 1810-1819]. For this purpose, COS-7 cells expressing the human 5-HT4 receptor were constructed and homogenized to obtain membrane homogenates which were then used in binding assay experiments. For the binding assay, the membrane homogenates were respectively mixed and incubated with different concentrations of test materials and [H3]-GR113808 (Amersham Biosciences). The concentrations of the individual test materials were set to 4 uM, 1 uM, 0.25 uM, and 0.0625 uM, respectively, and the concentration of [H3]-GR113808 was set to 0.595 nM. After the incubation was completed, the reaction products were collected in GF/B glass fiber filters using a Packard cell harvester, and the bound radioactivity was then determined using a liquid cell scintillation counter (Packard TopCount NXT).Binding Assay: The binding affinity of the compounds for a human 5-HT4 receptor was assayed according to the method as disclosed in the literature [Wyngaert et al., Journal of Neurochemistry, (1997) 69, 1810-1819]. For this purpose, COS-7 cells expressing the human 5-HT4 receptor were constructed and homogenized to obtain membrane homogenates which were then used in binding assay experiments. For the binding assay, the membrane homogenates were respectively mixed and incubated with different concentrations of test materials and [H3]-GR113808 (Amersham Biosciences). The concentrations of the individual test materials were set to 4 uM, 1 uM, 0.25 uM, and 0.0625 uM, respectively, and the concentration of [H3]-GR113808 was set to 0.595 nM. After the incubation was completed, the reaction products were collected in GF/B glass fiber filters using a Packard cell harvester, and the bound radioactivity was then determined using a liquid cell scintillation counter (Packard TopCount NXT).
ChEMBL 390 6 2 5 2.9 COc1cc(N)c(Cl)cc1C(=O)NCC1CCN(Cc2cccn2C)CC1 nan
54575226 144456 0 None - 0 Human 9.3 pIC50 = 9.3 Binding
Binding Assay: The binding affinity of the compounds for a human 5-HT4 receptor was assayed according to the method as disclosed in the literature [Wyngaert et al., Journal of Neurochemistry, (1997) 69, 1810-1819]. For this purpose, COS-7 cells expressing the human 5-HT4 receptor were constructed and homogenized to obtain membrane homogenates which were then used in binding assay experiments. For the binding assay, the membrane homogenates were respectively mixed and incubated with different concentrations of test materials and [H3]-GR113808 (Amersham Biosciences). The concentrations of the individual test materials were set to 4 uM, 1 uM, 0.25 uM, and 0.0625 uM, respectively, and the concentration of [H3]-GR113808 was set to 0.595 nM. After the incubation was completed, the reaction products were collected in GF/B glass fiber filters using a Packard cell harvester, and the bound radioactivity was then determined using a liquid cell scintillation counter (Packard TopCount NXT).Binding Assay: The binding affinity of the compounds for a human 5-HT4 receptor was assayed according to the method as disclosed in the literature [Wyngaert et al., Journal of Neurochemistry, (1997) 69, 1810-1819]. For this purpose, COS-7 cells expressing the human 5-HT4 receptor were constructed and homogenized to obtain membrane homogenates which were then used in binding assay experiments. For the binding assay, the membrane homogenates were respectively mixed and incubated with different concentrations of test materials and [H3]-GR113808 (Amersham Biosciences). The concentrations of the individual test materials were set to 4 uM, 1 uM, 0.25 uM, and 0.0625 uM, respectively, and the concentration of [H3]-GR113808 was set to 0.595 nM. After the incubation was completed, the reaction products were collected in GF/B glass fiber filters using a Packard cell harvester, and the bound radioactivity was then determined using a liquid cell scintillation counter (Packard TopCount NXT).
ChEMBL 377 6 3 5 2.3 COc1cc(N)c(Cl)cc1C(=O)NCC1CCN(Cc2ncc[nH]2)CC1 nan
CHEMBL3910849 144456 0 None - 0 Human 9.3 pIC50 = 9.3 Binding
Binding Assay: The binding affinity of the compounds for a human 5-HT4 receptor was assayed according to the method as disclosed in the literature [Wyngaert et al., Journal of Neurochemistry, (1997) 69, 1810-1819]. For this purpose, COS-7 cells expressing the human 5-HT4 receptor were constructed and homogenized to obtain membrane homogenates which were then used in binding assay experiments. For the binding assay, the membrane homogenates were respectively mixed and incubated with different concentrations of test materials and [H3]-GR113808 (Amersham Biosciences). The concentrations of the individual test materials were set to 4 uM, 1 uM, 0.25 uM, and 0.0625 uM, respectively, and the concentration of [H3]-GR113808 was set to 0.595 nM. After the incubation was completed, the reaction products were collected in GF/B glass fiber filters using a Packard cell harvester, and the bound radioactivity was then determined using a liquid cell scintillation counter (Packard TopCount NXT).Binding Assay: The binding affinity of the compounds for a human 5-HT4 receptor was assayed according to the method as disclosed in the literature [Wyngaert et al., Journal of Neurochemistry, (1997) 69, 1810-1819]. For this purpose, COS-7 cells expressing the human 5-HT4 receptor were constructed and homogenized to obtain membrane homogenates which were then used in binding assay experiments. For the binding assay, the membrane homogenates were respectively mixed and incubated with different concentrations of test materials and [H3]-GR113808 (Amersham Biosciences). The concentrations of the individual test materials were set to 4 uM, 1 uM, 0.25 uM, and 0.0625 uM, respectively, and the concentration of [H3]-GR113808 was set to 0.595 nM. After the incubation was completed, the reaction products were collected in GF/B glass fiber filters using a Packard cell harvester, and the bound radioactivity was then determined using a liquid cell scintillation counter (Packard TopCount NXT).
ChEMBL 377 6 3 5 2.3 COc1cc(N)c(Cl)cc1C(=O)NCC1CCN(Cc2ncc[nH]2)CC1 nan
10852772 34901 1 None - 0 Guinea pig 9.3 pIC50 = 9.3 Binding
Ability to antagonize 5-HT-evoked contractions mediated through 5-hydroxytryptamine 4 receptor activation in the guinea pig distal colon LMMPAbility to antagonize 5-HT-evoked contractions mediated through 5-hydroxytryptamine 4 receptor activation in the guinea pig distal colon LMMP
ChEMBL 314 6 1 3 3.8 CCCCN1CCC(COC(=O)c2c[nH]c3ccccc23)CC1 10.1021/jm00024a002
CHEMBL143426 34901 1 None - 0 Guinea pig 9.3 pIC50 = 9.3 Binding
Ability to antagonize 5-HT-evoked contractions mediated through 5-hydroxytryptamine 4 receptor activation in the guinea pig distal colon LMMPAbility to antagonize 5-HT-evoked contractions mediated through 5-hydroxytryptamine 4 receptor activation in the guinea pig distal colon LMMP
ChEMBL 314 6 1 3 3.8 CCCCN1CCC(COC(=O)c2c[nH]c3ccccc23)CC1 10.1021/jm00024a002
10852772 34901 1 None - 0 Guinea pig 9.3 pIC50 = 9.3 Binding
Ability to block 5-HT4 receptor mediated effect of 5-HT was assessed in the guinea-pig distal colon longitudinal muscle myenteric plexus preparation (LMMP)Ability to block 5-HT4 receptor mediated effect of 5-HT was assessed in the guinea-pig distal colon longitudinal muscle myenteric plexus preparation (LMMP)
ChEMBL 314 6 1 3 3.8 CCCCN1CCC(COC(=O)c2c[nH]c3ccccc23)CC1 10.1016/S0960-894X(01)80176-1
CHEMBL143426 34901 1 None - 0 Guinea pig 9.3 pIC50 = 9.3 Binding
Ability to block 5-HT4 receptor mediated effect of 5-HT was assessed in the guinea-pig distal colon longitudinal muscle myenteric plexus preparation (LMMP)Ability to block 5-HT4 receptor mediated effect of 5-HT was assessed in the guinea-pig distal colon longitudinal muscle myenteric plexus preparation (LMMP)
ChEMBL 314 6 1 3 3.8 CCCCN1CCC(COC(=O)c2c[nH]c3ccccc23)CC1 10.1016/S0960-894X(01)80176-1
9881053 119740 0 None - 1 Mouse 9.3 pIC50 = 9.3 Binding
Ability to displace [3H]GR-113808 from mouse 5-hydroxytryptamine 4 receptor in COS7 cellsAbility to displace [3H]GR-113808 from mouse 5-hydroxytryptamine 4 receptor in COS7 cells
ChEMBL 339 5 1 4 4.1 CCCN1CCC(COc2nc3ccccc3c3c2CCCN3)CC1 10.1021/jm020954v
CHEMBL35226 119740 0 None - 1 Mouse 9.3 pIC50 = 9.3 Binding
Ability to displace [3H]GR-113808 from mouse 5-hydroxytryptamine 4 receptor in COS7 cellsAbility to displace [3H]GR-113808 from mouse 5-hydroxytryptamine 4 receptor in COS7 cells
ChEMBL 339 5 1 4 4.1 CCCN1CCC(COc2nc3ccccc3c3c2CCCN3)CC1 10.1021/jm020954v
177336 3071 45 None 6 3 Human 9.2 pIC50 = 9.2 Binding
Binding affinity was determined against 5-hydroxytryptamine 3 receptorBinding affinity was determined against 5-hydroxytryptamine 3 receptor
ChEMBL 369 6 1 4 3.7 CCCCN1CCC(CC1)CNC(=O)c1c2OCCCn2c2c1cccc2 10.1021/jm00024a002
225 3071 45 None 6 3 Human 9.2 pIC50 = 9.2 Binding
Binding affinity was determined against 5-hydroxytryptamine 3 receptorBinding affinity was determined against 5-hydroxytryptamine 3 receptor
ChEMBL 369 6 1 4 3.7 CCCCN1CCC(CC1)CNC(=O)c1c2OCCCn2c2c1cccc2 10.1021/jm00024a002
CHEMBL356359 3071 45 None 6 3 Human 9.2 pIC50 = 9.2 Binding
Binding affinity was determined against 5-hydroxytryptamine 3 receptorBinding affinity was determined against 5-hydroxytryptamine 3 receptor
ChEMBL 369 6 1 4 3.7 CCCCN1CCC(CC1)CNC(=O)c1c2OCCCn2c2c1cccc2 10.1021/jm00024a002
DB04873 3071 45 None 6 3 Human 9.2 pIC50 = 9.2 Binding
Binding affinity was determined against 5-hydroxytryptamine 3 receptorBinding affinity was determined against 5-hydroxytryptamine 3 receptor
ChEMBL 369 6 1 4 3.7 CCCCN1CCC(CC1)CNC(=O)c1c2OCCCn2c2c1cccc2 10.1021/jm00024a002
90666907 108963 0 None - 0 Human 8.9 pIC50 = 8.9 Binding
Antagonist activity at 5TH4 receptor (unknown origin)Antagonist activity at 5TH4 receptor (unknown origin)
ChEMBL 467 7 1 8 3.4 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCN(c2ccccc2-c2cnccn2)CC1 10.1039/C1MD00213A
CHEMBL3220223 108963 0 None - 0 Human 8.9 pIC50 = 8.9 Binding
Antagonist activity at 5TH4 receptor (unknown origin)Antagonist activity at 5TH4 receptor (unknown origin)
ChEMBL 467 7 1 8 3.4 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCN(c2ccccc2-c2cnccn2)CC1 10.1039/C1MD00213A
44300153 195810 0 None - 1 Guinea pig 6.0 pIC50 = 6 Binding
Binding affinity towards 5-HT4 receptor in striatum membranes of guinea-pig brain was evaluatedBinding affinity towards 5-HT4 receptor in striatum membranes of guinea-pig brain was evaluated
ChEMBL 323 3 2 4 2.1 COc1cc(N)c(Cl)cc1C(=O)NC1CC2CCC1CN2C 10.1016/s0960-894x(01)00693-x
CHEMBL56994 195810 0 None - 1 Guinea pig 6.0 pIC50 = 6 Binding
Binding affinity towards 5-HT4 receptor in striatum membranes of guinea-pig brain was evaluatedBinding affinity towards 5-HT4 receptor in striatum membranes of guinea-pig brain was evaluated
ChEMBL 323 3 2 4 2.1 COc1cc(N)c(Cl)cc1C(=O)NC1CC2CCC1CN2C 10.1016/s0960-894x(01)00693-x
44300154 196721 0 None - 0 Guinea pig 6.0 pIC50 = 6 Binding
Binding affinity towards 5-hydroxytryptamine 4 receptor in striatum membranes of guinea-pig brain was evaluatedBinding affinity towards 5-hydroxytryptamine 4 receptor in striatum membranes of guinea-pig brain was evaluated
ChEMBL 323 3 2 4 2.1 COc1cc(N)c(Cl)cc1C(=O)NC1CC2CCC1N(C)C2 10.1016/s0960-894x(01)00693-x
CHEMBL57686 196721 0 None - 0 Guinea pig 6.0 pIC50 = 6 Binding
Binding affinity towards 5-hydroxytryptamine 4 receptor in striatum membranes of guinea-pig brain was evaluatedBinding affinity towards 5-hydroxytryptamine 4 receptor in striatum membranes of guinea-pig brain was evaluated
ChEMBL 323 3 2 4 2.1 COc1cc(N)c(Cl)cc1C(=O)NC1CC2CCC1N(C)C2 10.1016/s0960-894x(01)00693-x
3245407 47841 23 None - 0 Guinea pig 6.0 pIC50 = 6 Binding
Displacement of [3H]-GR113808 from guinea pig 5HT4 receptorDisplacement of [3H]-GR113808 from guinea pig 5HT4 receptor
ChEMBL 212 1 2 1 2.9 Cc1[nH]c2ccccc2c1C1=CCNCC1 10.1016/j.ejmech.2013.03.006
CHEMBL1550957 47841 23 None - 0 Guinea pig 6.0 pIC50 = 6 Binding
Displacement of [3H]-GR113808 from guinea pig 5HT4 receptorDisplacement of [3H]-GR113808 from guinea pig 5HT4 receptor
ChEMBL 212 1 2 1 2.9 Cc1[nH]c2ccccc2c1C1=CCNCC1 10.1016/j.ejmech.2013.03.006
10590554 206640 0 None - 0 Guinea pig 6.0 pIC50 = 6 Binding
Displacement of [3H]GR-113808 from 5-hydroxytryptamine 4 receptor in guinea pig striatumDisplacement of [3H]GR-113808 from 5-hydroxytryptamine 4 receptor in guinea pig striatum
ChEMBL 303 3 2 5 0.1 CN1CCN(CCNC(=O)n2c(=O)[nH]c3ccccc32)CC1 10.1021/jm981098j
CHEMBL99577 206640 0 None - 0 Guinea pig 6.0 pIC50 = 6 Binding
Displacement of [3H]GR-113808 from 5-hydroxytryptamine 4 receptor in guinea pig striatumDisplacement of [3H]GR-113808 from 5-hydroxytryptamine 4 receptor in guinea pig striatum
ChEMBL 303 3 2 5 0.1 CN1CCN(CCNC(=O)n2c(=O)[nH]c3ccccc32)CC1 10.1021/jm981098j
155525723 170519 0 None - 1 Human 7.0 pIC50 = 7 Binding
Displacement of [3H]-GR 113808 from recombinant human brain 5HT4 receptor measured after 60 mins by radio ligand binding assayDisplacement of [3H]-GR 113808 from recombinant human brain 5HT4 receptor measured after 60 mins by radio ligand binding assay
ChEMBL 515 11 3 7 4.2 COc1cc(/C=C/C(=O)NCCN2CCC(CCC(=O)c3cc(Cl)c(N)cc3OC)CC2)ccc1O 10.1016/j.ejmech.2019.111596
CHEMBL4457426 170519 0 None - 1 Human 7.0 pIC50 = 7 Binding
Displacement of [3H]-GR 113808 from recombinant human brain 5HT4 receptor measured after 60 mins by radio ligand binding assayDisplacement of [3H]-GR 113808 from recombinant human brain 5HT4 receptor measured after 60 mins by radio ligand binding assay
ChEMBL 515 11 3 7 4.2 COc1cc(/C=C/C(=O)NCCN2CCC(CCC(=O)c3cc(Cl)c(N)cc3OC)CC2)ccc1O 10.1016/j.ejmech.2019.111596
176155 4101 0 None -1 4 Guinea pig 5.0 pIC50 = 5.0 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
ChEMBL 377 4 1 3 4.7 C[S+]([O-])c1ccc(-c2nc(-c3ccc(F)cc3)c(-c3ccncc3)[nH]2)cc1 nan
CHEMBL10 4101 0 None -1 4 Guinea pig 5.0 pIC50 = 5.0 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
ChEMBL 377 4 1 3 4.7 C[S+]([O-])c1ccc(-c2nc(-c3ccc(F)cc3)c(-c3ccncc3)[nH]2)cc1 nan
2585 790 100 None -57 22 Guinea pig 6.0 pIC50 = 6.0 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
ChEMBL 406 10 3 5 3.7 COc1ccccc1OCCNCC(COc1cccc2c1c1ccccc1[nH]2)O nan
522 790 100 None -57 22 Guinea pig 6.0 pIC50 = 6.0 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
ChEMBL 406 10 3 5 3.7 COc1ccccc1OCCNCC(COc1cccc2c1c1ccccc1[nH]2)O nan
551 790 100 None -57 22 Guinea pig 6.0 pIC50 = 6.0 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
ChEMBL 406 10 3 5 3.7 COc1ccccc1OCCNCC(COc1cccc2c1c1ccccc1[nH]2)O nan
CHEMBL723 790 100 None -57 22 Guinea pig 6.0 pIC50 = 6.0 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
ChEMBL 406 10 3 5 3.7 COc1ccccc1OCCNCC(COc1cccc2c1c1ccccc1[nH]2)O nan
DB01136 790 100 None -57 22 Guinea pig 6.0 pIC50 = 6.0 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
ChEMBL 406 10 3 5 3.7 COc1ccccc1OCCNCC(COc1cccc2c1c1ccccc1[nH]2)O nan
44385634 61779 0 None - 0 Guinea pig 8.0 pIC50 = 8.0 Binding
Inhibitory activity against 5-hydroxytryptamine 4 receptor of guinea pig striatum using [3H]GR-113808 as radioligandInhibitory activity against 5-hydroxytryptamine 4 receptor of guinea pig striatum using [3H]GR-113808 as radioligand
ChEMBL 465 10 3 6 3.0 COc1cc(N)c(Cl)cc1C(=O)NC1CCN(CC2CCN(CCCCCN)CC2)CC1 10.1016/s0960-894x(02)00060-4
CHEMBL177573 61779 0 None - 0 Guinea pig 8.0 pIC50 = 8.0 Binding
Inhibitory activity against 5-hydroxytryptamine 4 receptor of guinea pig striatum using [3H]GR-113808 as radioligandInhibitory activity against 5-hydroxytryptamine 4 receptor of guinea pig striatum using [3H]GR-113808 as radioligand
ChEMBL 465 10 3 6 3.0 COc1cc(N)c(Cl)cc1C(=O)NC1CCN(CC2CCN(CCCCCN)CC2)CC1 10.1016/s0960-894x(02)00060-4
90644473 111788 0 None - 1 Human 7.0 pIC50 = 7.0 Binding
Antagonist activity at Rluc-tagged human 5HT4R expressed in human SH-SY5Y cells assessed as inhibition of serotonin-induced receptor/Gbeta1 coupling by BRET assayAntagonist activity at Rluc-tagged human 5HT4R expressed in human SH-SY5Y cells assessed as inhibition of serotonin-induced receptor/Gbeta1 coupling by BRET assay
ChEMBL 353 5 0 5 2.7 COc1cc2c3c(cccc3n1)C(=O)N(CCCN1CCCCC1)C2=O 10.1016/j.ejmech.2014.05.015
CHEMBL3291078 111788 0 None - 1 Human 7.0 pIC50 = 7.0 Binding
Antagonist activity at Rluc-tagged human 5HT4R expressed in human SH-SY5Y cells assessed as inhibition of serotonin-induced receptor/Gbeta1 coupling by BRET assayAntagonist activity at Rluc-tagged human 5HT4R expressed in human SH-SY5Y cells assessed as inhibition of serotonin-induced receptor/Gbeta1 coupling by BRET assay
ChEMBL 353 5 0 5 2.7 COc1cc2c3c(cccc3n1)C(=O)N(CCCN1CCCCC1)C2=O 10.1016/j.ejmech.2014.05.015
127027374 137142 0 None - 0 Human 6.0 pIC50 = 6.0 Binding
Displacement of [3H]-GR113808 from human 5-HT4 receptor expressed in African green monkey COS7 cell membranes after 30 mins by liquid scintillation counting analysisDisplacement of [3H]-GR113808 from human 5-HT4 receptor expressed in African green monkey COS7 cell membranes after 30 mins by liquid scintillation counting analysis
ChEMBL 423 8 2 9 0.8 COc1cc(N)c(Cl)cc1C(=O)N[C@H]1CCN(CCCn2ncnn2)C[C@H]1OC 10.1016/j.ejmech.2015.12.006
CHEMBL3758523 137142 0 None - 0 Human 6.0 pIC50 = 6.0 Binding
Displacement of [3H]-GR113808 from human 5-HT4 receptor expressed in African green monkey COS7 cell membranes after 30 mins by liquid scintillation counting analysisDisplacement of [3H]-GR113808 from human 5-HT4 receptor expressed in African green monkey COS7 cell membranes after 30 mins by liquid scintillation counting analysis
ChEMBL 423 8 2 9 0.8 COc1cc(N)c(Cl)cc1C(=O)N[C@H]1CCN(CCCn2ncnn2)C[C@H]1OC 10.1016/j.ejmech.2015.12.006
119584 2557 99 None -1 6 Guinea pig 7.0 pIC50 = 7.0 Binding
Inhibitory activity against 5-hydroxytryptamine 4 receptor of guinea pig striatum using [3H]GR-113808 as radioligandInhibitory activity against 5-hydroxytryptamine 4 receptor of guinea pig striatum using [3H]GR-113808 as radioligand
ChEMBL 421 7 2 5 3.1 CCOc1cc(N)c(cc1C(=O)NCC1OCCN(C1)Cc1ccc(cc1)F)Cl 10.1016/s0960-894x(02)00060-4
1848 2557 99 None -1 6 Guinea pig 7.0 pIC50 = 7.0 Binding
Inhibitory activity against 5-hydroxytryptamine 4 receptor of guinea pig striatum using [3H]GR-113808 as radioligandInhibitory activity against 5-hydroxytryptamine 4 receptor of guinea pig striatum using [3H]GR-113808 as radioligand
ChEMBL 421 7 2 5 3.1 CCOc1cc(N)c(cc1C(=O)NCC1OCCN(C1)Cc1ccc(cc1)F)Cl 10.1016/s0960-894x(02)00060-4
242 2557 99 None -1 6 Guinea pig 7.0 pIC50 = 7.0 Binding
Inhibitory activity against 5-hydroxytryptamine 4 receptor of guinea pig striatum using [3H]GR-113808 as radioligandInhibitory activity against 5-hydroxytryptamine 4 receptor of guinea pig striatum using [3H]GR-113808 as radioligand
ChEMBL 421 7 2 5 3.1 CCOc1cc(N)c(cc1C(=O)NCC1OCCN(C1)Cc1ccc(cc1)F)Cl 10.1016/s0960-894x(02)00060-4
CHEMBL60889 2557 99 None -1 6 Guinea pig 7.0 pIC50 = 7.0 Binding
Inhibitory activity against 5-hydroxytryptamine 4 receptor of guinea pig striatum using [3H]GR-113808 as radioligandInhibitory activity against 5-hydroxytryptamine 4 receptor of guinea pig striatum using [3H]GR-113808 as radioligand
ChEMBL 421 7 2 5 3.1 CCOc1cc(N)c(cc1C(=O)NCC1OCCN(C1)Cc1ccc(cc1)F)Cl 10.1016/s0960-894x(02)00060-4
DB11675 2557 99 None -1 6 Guinea pig 7.0 pIC50 = 7.0 Binding
Inhibitory activity against 5-hydroxytryptamine 4 receptor of guinea pig striatum using [3H]GR-113808 as radioligandInhibitory activity against 5-hydroxytryptamine 4 receptor of guinea pig striatum using [3H]GR-113808 as radioligand
ChEMBL 421 7 2 5 3.1 CCOc1cc(N)c(cc1C(=O)NCC1OCCN(C1)Cc1ccc(cc1)F)Cl 10.1016/s0960-894x(02)00060-4
2274 3124 53 None -17 32 Guinea pig 5.9 pIC50 = 5.9 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
ChEMBL 373 4 0 4 4.6 CN1CCN(CC1)CCCN1c2ccccc2Sc2c1cc(Cl)cc2 nan
4917 3124 53 None -17 32 Guinea pig 5.9 pIC50 = 5.9 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
ChEMBL 373 4 0 4 4.6 CN1CCN(CC1)CCCN1c2ccccc2Sc2c1cc(Cl)cc2 nan
7279 3124 53 None -17 32 Guinea pig 5.9 pIC50 = 5.9 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
ChEMBL 373 4 0 4 4.6 CN1CCN(CC1)CCCN1c2ccccc2Sc2c1cc(Cl)cc2 nan
CHEMBL728 3124 53 None -17 32 Guinea pig 5.9 pIC50 = 5.9 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
ChEMBL 373 4 0 4 4.6 CN1CCN(CC1)CCCN1c2ccccc2Sc2c1cc(Cl)cc2 nan
DB00433 3124 53 None -17 32 Guinea pig 5.9 pIC50 = 5.9 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
ChEMBL 373 4 0 4 4.6 CN1CCN(CC1)CCCN1c2ccccc2Sc2c1cc(Cl)cc2 nan
127027397 137105 0 None - 0 Human 5.9 pIC50 = 5.9 Binding
Displacement of [3H]-GR113808 from human 5-HT4 receptor expressed in African green monkey COS7 cell membranes after 30 mins by liquid scintillation counting analysisDisplacement of [3H]-GR113808 from human 5-HT4 receptor expressed in African green monkey COS7 cell membranes after 30 mins by liquid scintillation counting analysis
ChEMBL 421 8 2 7 2.0 COc1cc(N)c(Cl)cc1C(=O)N[C@H]1CCN(CCCn2ccnc2)C[C@H]1OC 10.1016/j.ejmech.2015.12.006
CHEMBL3758199 137105 0 None - 0 Human 5.9 pIC50 = 5.9 Binding
Displacement of [3H]-GR113808 from human 5-HT4 receptor expressed in African green monkey COS7 cell membranes after 30 mins by liquid scintillation counting analysisDisplacement of [3H]-GR113808 from human 5-HT4 receptor expressed in African green monkey COS7 cell membranes after 30 mins by liquid scintillation counting analysis
ChEMBL 421 8 2 7 2.0 COc1cc(N)c(Cl)cc1C(=O)N[C@H]1CCN(CCCn2ccnc2)C[C@H]1OC 10.1016/j.ejmech.2015.12.006
68592173 137316 0 None - 0 Human 6.9 pIC50 = 6.9 Binding
Displacement of [3H]-GR113808 from human 5-HT4 receptor expressed in African green monkey COS7 cell membranes after 30 mins by liquid scintillation counting analysisDisplacement of [3H]-GR113808 from human 5-HT4 receptor expressed in African green monkey COS7 cell membranes after 30 mins by liquid scintillation counting analysis
ChEMBL 494 6 2 6 3.0 COc1cc(N)c(Cl)cc1C(=O)N[C@H]1CCN(CC2CCN(C(=O)C(C)(C)C)CC2)C[C@H]1OC 10.1016/j.ejmech.2015.12.006
CHEMBL3759944 137316 0 None - 0 Human 6.9 pIC50 = 6.9 Binding
Displacement of [3H]-GR113808 from human 5-HT4 receptor expressed in African green monkey COS7 cell membranes after 30 mins by liquid scintillation counting analysisDisplacement of [3H]-GR113808 from human 5-HT4 receptor expressed in African green monkey COS7 cell membranes after 30 mins by liquid scintillation counting analysis
ChEMBL 494 6 2 6 3.0 COc1cc(N)c(Cl)cc1C(=O)N[C@H]1CCN(CC2CCN(C(=O)C(C)(C)C)CC2)C[C@H]1OC 10.1016/j.ejmech.2015.12.006
31703 193050 59 None 1 3 Guinea pig 4.9 pIC50 = 4.9 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
ChEMBL 543 5 6 12 0.0 COc1cccc2c1C(=O)c1c(O)c3c(c(O)c1C2=O)C[C@@](O)(C(=O)CO)C[C@@H]3O[C@H]1C[C@H](N)[C@H](O)[C@H](C)O1 nan
CHEMBL359744 193050 59 None 1 3 Guinea pig 4.9 pIC50 = 4.9 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
ChEMBL 543 5 6 12 0.0 COc1cccc2c1C(=O)c1c(O)c3c(c(O)c1C2=O)C[C@@](O)(C(=O)CO)C[C@@H]3O[C@H]1C[C@H](N)[C@H](O)[C@H](C)O1 nan
CHEMBL53463 193050 59 None 1 3 Guinea pig 4.9 pIC50 = 4.9 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
ChEMBL 543 5 6 12 0.0 COc1cccc2c1C(=O)c1c(O)c3c(c(O)c1C2=O)C[C@@](O)(C(=O)CO)C[C@@H]3O[C@H]1C[C@H](N)[C@H](O)[C@H](C)O1 nan
68593479 137274 0 None - 0 Human 5.9 pIC50 = 5.9 Binding
Displacement of [3H]-GR113808 from human 5-HT4 receptor expressed in African green monkey COS7 cell membranes after 30 mins by liquid scintillation counting analysisDisplacement of [3H]-GR113808 from human 5-HT4 receptor expressed in African green monkey COS7 cell membranes after 30 mins by liquid scintillation counting analysis
ChEMBL 422 8 2 8 1.4 COc1cc(N)c(Cl)cc1C(=O)N[C@H]1CCN(CCCn2cncn2)C[C@H]1OC 10.1016/j.ejmech.2015.12.006
CHEMBL3759601 137274 0 None - 0 Human 5.9 pIC50 = 5.9 Binding
Displacement of [3H]-GR113808 from human 5-HT4 receptor expressed in African green monkey COS7 cell membranes after 30 mins by liquid scintillation counting analysisDisplacement of [3H]-GR113808 from human 5-HT4 receptor expressed in African green monkey COS7 cell membranes after 30 mins by liquid scintillation counting analysis
ChEMBL 422 8 2 8 1.4 COc1cc(N)c(Cl)cc1C(=O)N[C@H]1CCN(CCCn2cncn2)C[C@H]1OC 10.1016/j.ejmech.2015.12.006
44214754 60080 0 None - 0 Guinea pig 7.9 pIC50 = 7.9 Binding
Inhibitory activity against 5-hydroxytryptamine 4 receptor of guinea pig striatum using [3H]GR-113808 as radioligandInhibitory activity against 5-hydroxytryptamine 4 receptor of guinea pig striatum using [3H]GR-113808 as radioligand
ChEMBL 437 8 3 6 2.2 COc1cc(N)c(Cl)cc1C(=O)NC1CCN(CC2CCN(CCCN)CC2)CC1 10.1016/s0960-894x(02)00060-4
CHEMBL174935 60080 0 None - 0 Guinea pig 7.9 pIC50 = 7.9 Binding
Inhibitory activity against 5-hydroxytryptamine 4 receptor of guinea pig striatum using [3H]GR-113808 as radioligandInhibitory activity against 5-hydroxytryptamine 4 receptor of guinea pig striatum using [3H]GR-113808 as radioligand
ChEMBL 437 8 3 6 2.2 COc1cc(N)c(Cl)cc1C(=O)NC1CCN(CC2CCN(CCCN)CC2)CC1 10.1016/s0960-894x(02)00060-4
68592826 137156 0 None - 0 Human 6.9 pIC50 = 6.9 Binding
Displacement of [3H]-GR113808 from human 5-HT4 receptor expressed in African green monkey COS7 cell membranes after 30 mins by liquid scintillation counting analysisDisplacement of [3H]-GR113808 from human 5-HT4 receptor expressed in African green monkey COS7 cell membranes after 30 mins by liquid scintillation counting analysis
ChEMBL 496 8 2 7 3.0 CCCOC(=O)N1CCC(CN2CC[C@H](NC(=O)c3cc(Cl)c(N)cc3OC)[C@H](OC)C2)CC1 10.1016/j.ejmech.2015.12.006
CHEMBL3758641 137156 0 None - 0 Human 6.9 pIC50 = 6.9 Binding
Displacement of [3H]-GR113808 from human 5-HT4 receptor expressed in African green monkey COS7 cell membranes after 30 mins by liquid scintillation counting analysisDisplacement of [3H]-GR113808 from human 5-HT4 receptor expressed in African green monkey COS7 cell membranes after 30 mins by liquid scintillation counting analysis
ChEMBL 496 8 2 7 3.0 CCCOC(=O)N1CCC(CN2CC[C@H](NC(=O)c3cc(Cl)c(N)cc3OC)[C@H](OC)C2)CC1 10.1016/j.ejmech.2015.12.006
25016328 137300 0 None - 0 Human 6.9 pIC50 = 6.9 Binding
Displacement of [3H]-GR113808 from human 5-HT4 receptor expressed in African green monkey COS7 cell membranes after 30 mins by liquid scintillation counting analysisDisplacement of [3H]-GR113808 from human 5-HT4 receptor expressed in African green monkey COS7 cell membranes after 30 mins by liquid scintillation counting analysis
ChEMBL 480 7 2 6 2.6 COc1cc(N)c(Cl)cc1C(=O)N[C@H]1CCN(CC2CCN(C(=O)C(C)C)CC2)C[C@H]1OC 10.1016/j.ejmech.2015.12.006
CHEMBL3759860 137300 0 None - 0 Human 6.9 pIC50 = 6.9 Binding
Displacement of [3H]-GR113808 from human 5-HT4 receptor expressed in African green monkey COS7 cell membranes after 30 mins by liquid scintillation counting analysisDisplacement of [3H]-GR113808 from human 5-HT4 receptor expressed in African green monkey COS7 cell membranes after 30 mins by liquid scintillation counting analysis
ChEMBL 480 7 2 6 2.6 COc1cc(N)c(Cl)cc1C(=O)N[C@H]1CCN(CC2CCN(C(=O)C(C)C)CC2)C[C@H]1OC 10.1016/j.ejmech.2015.12.006
3397 203777 104 None 1 2 Guinea pig 4.9 pIC50 = 4.9 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
ChEMBL 276 3 1 3 3.2 CC(C)C(=O)Nc1ccc([N+](=O)[O-])c(C(F)(F)F)c1 nan
CHEMBL806 203777 104 None 1 2 Guinea pig 4.9 pIC50 = 4.9 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
ChEMBL 276 3 1 3 3.2 CC(C)C(=O)Nc1ccc([N+](=O)[O-])c(C(F)(F)F)c1 nan
44384769 130841 0 None - 0 Guinea pig 7.8 pIC50 = 7.8 Binding
Inhibitory activity against 5-hydroxytryptamine 4 receptor of guinea pig striatum using [3H]GR-113808 as radioligandInhibitory activity against 5-hydroxytryptamine 4 receptor of guinea pig striatum using [3H]GR-113808 as radioligand
ChEMBL 451 8 3 6 2.4 COc1cc(N)c(Cl)cc1C(=O)NC1CCN(CC2CCN(CC(C)CN)CC2)CC1 10.1016/s0960-894x(02)00060-4
CHEMBL368844 130841 0 None - 0 Guinea pig 7.8 pIC50 = 7.8 Binding
Inhibitory activity against 5-hydroxytryptamine 4 receptor of guinea pig striatum using [3H]GR-113808 as radioligandInhibitory activity against 5-hydroxytryptamine 4 receptor of guinea pig striatum using [3H]GR-113808 as radioligand
ChEMBL 451 8 3 6 2.4 COc1cc(N)c(Cl)cc1C(=O)NC1CCN(CC2CCN(CC(C)CN)CC2)CC1 10.1016/s0960-894x(02)00060-4
44386218 165594 0 None - 0 Guinea pig 7.8 pIC50 = 7.8 Binding
Inhibitory activity against 5-hydroxytryptamine 4 receptor of guinea pig striatum using [3H]GR-113808 as radioligandInhibitory activity against 5-hydroxytryptamine 4 receptor of guinea pig striatum using [3H]GR-113808 as radioligand
ChEMBL 423 7 3 6 1.8 COc1cc(N)c(Cl)cc1C(=O)NC1CCN(CC2CCN(CCN)CC2)CC1 10.1016/s0960-894x(02)00060-4
CHEMBL426216 165594 0 None - 0 Guinea pig 7.8 pIC50 = 7.8 Binding
Inhibitory activity against 5-hydroxytryptamine 4 receptor of guinea pig striatum using [3H]GR-113808 as radioligandInhibitory activity against 5-hydroxytryptamine 4 receptor of guinea pig striatum using [3H]GR-113808 as radioligand
ChEMBL 423 7 3 6 1.8 COc1cc(N)c(Cl)cc1C(=O)NC1CCN(CC2CCN(CCN)CC2)CC1 10.1016/s0960-894x(02)00060-4
44386168 167719 0 None - 0 Guinea pig 7.8 pIC50 = 7.8 Binding
Inhibitory activity against 5-hydroxytryptamine 4 receptor of guinea pig striatum using [3H]GR-113808 as radioligandInhibitory activity against 5-hydroxytryptamine 4 receptor of guinea pig striatum using [3H]GR-113808 as radioligand
ChEMBL 453 8 4 7 1.2 COc1cc(N)c(Cl)cc1C(=O)NC1CCN(CC2CCN(CC(O)CN)CC2)CC1 10.1016/s0960-894x(02)00060-4
CHEMBL433984 167719 0 None - 0 Guinea pig 7.8 pIC50 = 7.8 Binding
Inhibitory activity against 5-hydroxytryptamine 4 receptor of guinea pig striatum using [3H]GR-113808 as radioligandInhibitory activity against 5-hydroxytryptamine 4 receptor of guinea pig striatum using [3H]GR-113808 as radioligand
ChEMBL 453 8 4 7 1.2 COc1cc(N)c(Cl)cc1C(=O)NC1CCN(CC2CCN(CC(O)CN)CC2)CC1 10.1016/s0960-894x(02)00060-4
155565664 175030 0 None - 1 Human 7.8 pIC50 = 7.8 Binding
Displacement of [3H]-GR 113808 from recombinant human brain 5HT4 receptor measured after 60 mins by radio ligand binding assayDisplacement of [3H]-GR 113808 from recombinant human brain 5HT4 receptor measured after 60 mins by radio ligand binding assay
ChEMBL 432 8 2 6 4.5 COc1ccc(CN2CCC(CCC(=O)c3cc(Cl)c(N)cc3OC)CC2)cc1O 10.1016/j.ejmech.2019.111596
CHEMBL4580044 175030 0 None - 1 Human 7.8 pIC50 = 7.8 Binding
Displacement of [3H]-GR 113808 from recombinant human brain 5HT4 receptor measured after 60 mins by radio ligand binding assayDisplacement of [3H]-GR 113808 from recombinant human brain 5HT4 receptor measured after 60 mins by radio ligand binding assay
ChEMBL 432 8 2 6 4.5 COc1ccc(CN2CCC(CCC(=O)c3cc(Cl)c(N)cc3OC)CC2)cc1O 10.1016/j.ejmech.2019.111596
16005860 186823 6 None - 0 Human 5.9 pIC50 = 5.9 Binding
Inhibition of 5HT4 receptorInhibition of 5HT4 receptor
ChEMBL 388 5 1 2 4.8 CC(C)(C)CCN1CC[C@H](CNC(=O)c2cc(Cl)cc(Cl)c2)[C@H](F)C1 10.1021/jm800830n
CHEMBL493677 186823 6 None - 0 Human 5.9 pIC50 = 5.9 Binding
Inhibition of 5HT4 receptorInhibition of 5HT4 receptor
ChEMBL 388 5 1 2 4.8 CC(C)(C)CCN1CC[C@H](CNC(=O)c2cc(Cl)cc(Cl)c2)[C@H](F)C1 10.1021/jm800830n
5 139 66 None -117 54 Rat 6.8 pIC50 = 6.8 Binding
Inhibition of radiolabeled [3H]GR-113808 ligand binding to 5-hydroxytryptamine 4 receptorInhibition of radiolabeled [3H]GR-113808 ligand binding to 5-hydroxytryptamine 4 receptor
ChEMBL 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 10.1021/jm970376w
5202 139 66 None -117 54 Rat 6.8 pIC50 = 6.8 Binding
Inhibition of radiolabeled [3H]GR-113808 ligand binding to 5-hydroxytryptamine 4 receptorInhibition of radiolabeled [3H]GR-113808 ligand binding to 5-hydroxytryptamine 4 receptor
ChEMBL 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 10.1021/jm970376w
CHEMBL39 139 66 None -117 54 Rat 6.8 pIC50 = 6.8 Binding
Inhibition of radiolabeled [3H]GR-113808 ligand binding to 5-hydroxytryptamine 4 receptorInhibition of radiolabeled [3H]GR-113808 ligand binding to 5-hydroxytryptamine 4 receptor
ChEMBL 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 10.1021/jm970376w
DB08839 139 66 None -117 54 Rat 6.8 pIC50 = 6.8 Binding
Inhibition of radiolabeled [3H]GR-113808 ligand binding to 5-hydroxytryptamine 4 receptorInhibition of radiolabeled [3H]GR-113808 ligand binding to 5-hydroxytryptamine 4 receptor
ChEMBL 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 10.1021/jm970376w
441383 20133 54 None -5 17 Guinea pig 4.8 pIC50 = 4.8 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
ChEMBL 531 8 0 8 4.5 CC(C)N1CCN(c2ccc(OC[C@H]3CO[C@](Cn4cncn4)(c4ccc(Cl)cc4Cl)O3)cc2)CC1 nan
CHEMBL1306 20133 54 None -5 17 Guinea pig 4.8 pIC50 = 4.8 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
ChEMBL 531 8 0 8 4.5 CC(C)N1CCN(c2ccc(OC[C@H]3CO[C@](Cn4cncn4)(c4ccc(Cl)cc4Cl)O3)cc2)CC1 nan
10784420 120505 0 None - 0 Guinea pig 7.8 pIC50 = 7.8 Binding
Ability to antagonize 5-HT-evoked contractions mediated through 5-hydroxytryptamine 4 receptor activation in the guinea pig distal colon LMMPAbility to antagonize 5-HT-evoked contractions mediated through 5-hydroxytryptamine 4 receptor activation in the guinea pig distal colon LMMP
ChEMBL 355 6 1 4 3.3 CCCCN1CCC(CNC(=O)c2c3n(c4ccccc24)CCO3)CC1 10.1021/jm00024a002
CHEMBL356546 120505 0 None - 0 Guinea pig 7.8 pIC50 = 7.8 Binding
Ability to antagonize 5-HT-evoked contractions mediated through 5-hydroxytryptamine 4 receptor activation in the guinea pig distal colon LMMPAbility to antagonize 5-HT-evoked contractions mediated through 5-hydroxytryptamine 4 receptor activation in the guinea pig distal colon LMMP
ChEMBL 355 6 1 4 3.3 CCCCN1CCC(CNC(=O)c2c3n(c4ccccc24)CCO3)CC1 10.1021/jm00024a002
87509467 137158 0 None - 0 Human 6.8 pIC50 = 6.8 Binding
Displacement of [3H]-GR113808 from human 5-HT4 receptor expressed in African green monkey COS7 cell membranes after 30 mins by liquid scintillation counting analysisDisplacement of [3H]-GR113808 from human 5-HT4 receptor expressed in African green monkey COS7 cell membranes after 30 mins by liquid scintillation counting analysis
ChEMBL 496 7 2 6 3.4 COc1cc(N)c(Cl)cc1C(=O)N[C@H]1CCN(CC2CCN(C(=S)C(C)C)CC2)C[C@H]1OC 10.1016/j.ejmech.2015.12.006
CHEMBL3758674 137158 0 None - 0 Human 6.8 pIC50 = 6.8 Binding
Displacement of [3H]-GR113808 from human 5-HT4 receptor expressed in African green monkey COS7 cell membranes after 30 mins by liquid scintillation counting analysisDisplacement of [3H]-GR113808 from human 5-HT4 receptor expressed in African green monkey COS7 cell membranes after 30 mins by liquid scintillation counting analysis
ChEMBL 496 7 2 6 3.4 COc1cc(N)c(Cl)cc1C(=O)N[C@H]1CCN(CC2CCN(C(=S)C(C)C)CC2)C[C@H]1OC 10.1016/j.ejmech.2015.12.006
1043 1552 13 None -2884 28 Guinea pig 5.8 pIC50 = 5.8 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
ChEMBL 581 4 3 6 2.0 O=C([C@H]1CN(C)[C@H]2C(=C1)c1cccc3c1c(C2)c[nH]3)N[C@]1(C)O[C@@]2(N(C1=O)[C@@H](Cc1ccccc1)C(=O)N1[C@H]2CCC1)O nan
149 1552 13 None -2884 28 Guinea pig 5.8 pIC50 = 5.8 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
ChEMBL 581 4 3 6 2.0 O=C([C@H]1CN(C)[C@H]2C(=C1)c1cccc3c1c(C2)c[nH]3)N[C@]1(C)O[C@@]2(N(C1=O)[C@@H](Cc1ccccc1)C(=O)N1[C@H]2CCC1)O nan
8223 1552 13 None -2884 28 Guinea pig 5.8 pIC50 = 5.8 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
ChEMBL 581 4 3 6 2.0 O=C([C@H]1CN(C)[C@H]2C(=C1)c1cccc3c1c(C2)c[nH]3)N[C@]1(C)O[C@@]2(N(C1=O)[C@@H](Cc1ccccc1)C(=O)N1[C@H]2CCC1)O nan
CHEMBL442 1552 13 None -2884 28 Guinea pig 5.8 pIC50 = 5.8 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
ChEMBL 581 4 3 6 2.0 O=C([C@H]1CN(C)[C@H]2C(=C1)c1cccc3c1c(C2)c[nH]3)N[C@]1(C)O[C@@]2(N(C1=O)[C@@H](Cc1ccccc1)C(=O)N1[C@H]2CCC1)O nan
DB00696 1552 13 None -2884 28 Guinea pig 5.8 pIC50 = 5.8 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
ChEMBL 581 4 3 6 2.0 O=C([C@H]1CN(C)[C@H]2C(=C1)c1cccc3c1c(C2)c[nH]3)N[C@]1(C)O[C@@]2(N(C1=O)[C@@H](Cc1ccccc1)C(=O)N1[C@H]2CCC1)O nan
10645984 18629 0 None - 1 Human 6.8 pIC50 = 6.8 Binding
Antagonist activity at 5TH4 receptor (unknown origin)Antagonist activity at 5TH4 receptor (unknown origin)
ChEMBL 423 6 1 6 3.6 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCN(c2cccc(Cl)c2)CC1 10.1039/C1MD00213A
CHEMBL127876 18629 0 None - 1 Human 6.8 pIC50 = 6.8 Binding
Antagonist activity at 5TH4 receptor (unknown origin)Antagonist activity at 5TH4 receptor (unknown origin)
ChEMBL 423 6 1 6 3.6 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCN(c2cccc(Cl)c2)CC1 10.1039/C1MD00213A
133 2460 48 None -79 42 Guinea pig 5.8 pIC50 = 5.8 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
ChEMBL 403 4 1 4 4.1 O=C(OCc1ccccc1)NC[C@H]1CN(C)[C@H]2[C@H](C1)c1cccc3c1c(C2)cn3C nan
1723 2460 48 None -79 42 Guinea pig 5.8 pIC50 = 5.8 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
ChEMBL 403 4 1 4 4.1 O=C(OCc1ccccc1)NC[C@H]1CN(C)[C@H]2[C@H](C1)c1cccc3c1c(C2)cn3C nan
28693 2460 48 None -79 42 Guinea pig 5.8 pIC50 = 5.8 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
ChEMBL 403 4 1 4 4.1 O=C(OCc1ccccc1)NC[C@H]1CN(C)[C@H]2[C@H](C1)c1cccc3c1c(C2)cn3C nan
CHEMBL19215 2460 48 None -79 42 Guinea pig 5.8 pIC50 = 5.8 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
ChEMBL 403 4 1 4 4.1 O=C(OCc1ccccc1)NC[C@H]1CN(C)[C@H]2[C@H](C1)c1cccc3c1c(C2)cn3C nan
DB13520 2460 48 None -79 42 Guinea pig 5.8 pIC50 = 5.8 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
ChEMBL 403 4 1 4 4.1 O=C(OCc1ccccc1)NC[C@H]1CN(C)[C@H]2[C@H](C1)c1cccc3c1c(C2)cn3C nan
10645103 163789 0 None - 1 Human 7.8 pIC50 = 7.8 Binding
Antagonist activity at 5TH4 receptor (unknown origin)Antagonist activity at 5TH4 receptor (unknown origin)
ChEMBL 407 6 1 6 3.0 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCN(c2ccccc2F)CC1 10.1039/C1MD00213A
CHEMBL421256 163789 0 None - 1 Human 7.8 pIC50 = 7.8 Binding
Antagonist activity at 5TH4 receptor (unknown origin)Antagonist activity at 5TH4 receptor (unknown origin)
ChEMBL 407 6 1 6 3.0 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCN(c2ccccc2F)CC1 10.1039/C1MD00213A
68593295 137262 0 None - 0 Human 6.8 pIC50 = 6.8 Binding
Displacement of [3H]-GR113808 from human 5-HT4 receptor expressed in African green monkey COS7 cell membranes after 30 mins by liquid scintillation counting analysisDisplacement of [3H]-GR113808 from human 5-HT4 receptor expressed in African green monkey COS7 cell membranes after 30 mins by liquid scintillation counting analysis
ChEMBL 480 8 2 6 2.8 CCCC(=O)N1CCC(CN2CC[C@H](NC(=O)c3cc(Cl)c(N)cc3OC)[C@H](OC)C2)CC1 10.1016/j.ejmech.2015.12.006
CHEMBL3759546 137262 0 None - 0 Human 6.8 pIC50 = 6.8 Binding
Displacement of [3H]-GR113808 from human 5-HT4 receptor expressed in African green monkey COS7 cell membranes after 30 mins by liquid scintillation counting analysisDisplacement of [3H]-GR113808 from human 5-HT4 receptor expressed in African green monkey COS7 cell membranes after 30 mins by liquid scintillation counting analysis
ChEMBL 480 8 2 6 2.8 CCCC(=O)N1CCC(CN2CC[C@H](NC(=O)c3cc(Cl)c(N)cc3OC)[C@H](OC)C2)CC1 10.1016/j.ejmech.2015.12.006
10669778 116972 0 None - 1 Human 7.8 pIC50 = 7.8 Binding
Antagonist activity at 5TH4 receptor (unknown origin)Antagonist activity at 5TH4 receptor (unknown origin)
ChEMBL 419 7 1 7 2.9 COc1ccc(N2CCN(CCOC(=O)c3cc(Cl)c(N)cc3OC)CC2)cc1 10.1039/C1MD00213A
CHEMBL339936 116972 0 None - 1 Human 7.8 pIC50 = 7.8 Binding
Antagonist activity at 5TH4 receptor (unknown origin)Antagonist activity at 5TH4 receptor (unknown origin)
ChEMBL 419 7 1 7 2.9 COc1ccc(N2CCN(CCOC(=O)c3cc(Cl)c(N)cc3OC)CC2)cc1 10.1039/C1MD00213A
3019427 60063 27 None - 0 Human 7.7 pIC50 = 7.7 Binding
Displacement of [3H]GR-113808 from human recombinant 5-HT4 receptorDisplacement of [3H]GR-113808 from human recombinant 5-HT4 receptor
ChEMBL 313 4 3 5 1.0 COc1cc(N)c(Cl)cc1C(=O)NC1CCNCC1OC 10.1016/j.bmcl.2009.08.016
CHEMBL1748 60063 27 None - 0 Human 7.7 pIC50 = 7.7 Binding
Displacement of [3H]GR-113808 from human recombinant 5-HT4 receptorDisplacement of [3H]GR-113808 from human recombinant 5-HT4 receptor
ChEMBL 313 4 3 5 1.0 COc1cc(N)c(Cl)cc1C(=O)NC1CCNCC1OC 10.1016/j.bmcl.2009.08.016
68593458 137318 0 None - 0 Human 6.7 pIC50 = 6.7 Binding
Displacement of [3H]-GR113808 from human 5-HT4 receptor expressed in African green monkey COS7 cell membranes after 30 mins by liquid scintillation counting analysisDisplacement of [3H]-GR113808 from human 5-HT4 receptor expressed in African green monkey COS7 cell membranes after 30 mins by liquid scintillation counting analysis
ChEMBL 468 6 2 7 2.2 COC(=O)N1CCC(CN2CC[C@H](NC(=O)c3cc(Cl)c(N)cc3OC)[C@H](OC)C2)CC1 10.1016/j.ejmech.2015.12.006
CHEMBL3759969 137318 0 None - 0 Human 6.7 pIC50 = 6.7 Binding
Displacement of [3H]-GR113808 from human 5-HT4 receptor expressed in African green monkey COS7 cell membranes after 30 mins by liquid scintillation counting analysisDisplacement of [3H]-GR113808 from human 5-HT4 receptor expressed in African green monkey COS7 cell membranes after 30 mins by liquid scintillation counting analysis
ChEMBL 468 6 2 7 2.2 COC(=O)N1CCC(CN2CC[C@H](NC(=O)c3cc(Cl)c(N)cc3OC)[C@H](OC)C2)CC1 10.1016/j.ejmech.2015.12.006
90644474 111789 0 None - 1 Human 6.7 pIC50 = 6.7 Binding
Partial agonist activity at Rluc-tagged human 5HT4R expressed in human SH-SY5Y cells assessed as effect on serotonin-induced receptor/Gbeta1 coupling by BRET assayPartial agonist activity at Rluc-tagged human 5HT4R expressed in human SH-SY5Y cells assessed as effect on serotonin-induced receptor/Gbeta1 coupling by BRET assay
ChEMBL 343 4 0 3 3.7 O=C1c2cc(Cl)nc3cccc(c23)CN1CCCN1CCCCC1 10.1016/j.ejmech.2014.05.015
CHEMBL3291079 111789 0 None - 1 Human 6.7 pIC50 = 6.7 Binding
Partial agonist activity at Rluc-tagged human 5HT4R expressed in human SH-SY5Y cells assessed as effect on serotonin-induced receptor/Gbeta1 coupling by BRET assayPartial agonist activity at Rluc-tagged human 5HT4R expressed in human SH-SY5Y cells assessed as effect on serotonin-induced receptor/Gbeta1 coupling by BRET assay
ChEMBL 343 4 0 3 3.7 O=C1c2cc(Cl)nc3cccc(c23)CN1CCCN1CCCCC1 10.1016/j.ejmech.2014.05.015
10591304 38205 2 None - 0 Guinea pig 6.7 pIC50 = 6.7 Binding
Ability to antagonize 5-HT-evoked contractions mediated through 5-hydroxytryptamine 4 receptor activation in the guinea pig distal colon LMMPAbility to antagonize 5-HT-evoked contractions mediated through 5-hydroxytryptamine 4 receptor activation in the guinea pig distal colon LMMP
ChEMBL 313 6 2 2 3.4 CCCCN1CCC(CNC(=O)c2c[nH]c3ccccc23)CC1 10.1021/jm00024a002
CHEMBL146386 38205 2 None - 0 Guinea pig 6.7 pIC50 = 6.7 Binding
Ability to antagonize 5-HT-evoked contractions mediated through 5-hydroxytryptamine 4 receptor activation in the guinea pig distal colon LMMPAbility to antagonize 5-HT-evoked contractions mediated through 5-hydroxytryptamine 4 receptor activation in the guinea pig distal colon LMMP
ChEMBL 313 6 2 2 3.4 CCCCN1CCC(CNC(=O)c2c[nH]c3ccccc23)CC1 10.1021/jm00024a002
44384896 59974 0 None - 0 Guinea pig 8.6 pIC50 = 8.6 Binding
Inhibitory activity against 5-hydroxytryptamine 4 receptor of guinea pig striatum using [3H]GR-113808 as radioligandInhibitory activity against 5-hydroxytryptamine 4 receptor of guinea pig striatum using [3H]GR-113808 as radioligand
ChEMBL 479 7 3 6 2.3 COc1cc(N)c(Cl)cc1C(=O)NC1CCN(CC2CCN(C(=O)C(N)C(C)C)CC2)CC1 10.1016/s0960-894x(02)00060-4
CHEMBL174284 59974 0 None - 0 Guinea pig 8.6 pIC50 = 8.6 Binding
Inhibitory activity against 5-hydroxytryptamine 4 receptor of guinea pig striatum using [3H]GR-113808 as radioligandInhibitory activity against 5-hydroxytryptamine 4 receptor of guinea pig striatum using [3H]GR-113808 as radioligand
ChEMBL 479 7 3 6 2.3 COc1cc(N)c(Cl)cc1C(=O)NC1CCN(CC2CCN(C(=O)C(N)C(C)C)CC2)CC1 10.1016/s0960-894x(02)00060-4
44384728 59514 0 None - 0 Guinea pig 8.6 pIC50 = 8.6 Binding
Inhibitory activity against 5-hydroxytryptamine 4 receptor of guinea pig striatum using [3H]GR-113808 as radioligandInhibitory activity against 5-hydroxytryptamine 4 receptor of guinea pig striatum using [3H]GR-113808 as radioligand
ChEMBL 479 8 3 6 2.5 CCCC(N)C(=O)N1CCC(CN2CCC(NC(=O)c3cc(Cl)c(N)cc3OC)CC2)CC1 10.1016/s0960-894x(02)00060-4
CHEMBL172802 59514 0 None - 0 Guinea pig 8.6 pIC50 = 8.6 Binding
Inhibitory activity against 5-hydroxytryptamine 4 receptor of guinea pig striatum using [3H]GR-113808 as radioligandInhibitory activity against 5-hydroxytryptamine 4 receptor of guinea pig striatum using [3H]GR-113808 as radioligand
ChEMBL 479 8 3 6 2.5 CCCC(N)C(=O)N1CCC(CN2CCC(NC(=O)c3cc(Cl)c(N)cc3OC)CC2)CC1 10.1016/s0960-894x(02)00060-4
44384721 130143 0 None - 0 Guinea pig 8.6 pIC50 = 8.6 Binding
Inhibitory activity against 5-hydroxytryptamine 4 receptor of guinea pig striatum using [3H]GR-113808 as radioligandInhibitory activity against 5-hydroxytryptamine 4 receptor of guinea pig striatum using [3H]GR-113808 as radioligand
ChEMBL 465 6 3 6 2.1 COc1cc(N)c(Cl)cc1C(=O)NC1CCN(CC2CCN(C(=O)C(C)(C)N)CC2)CC1 10.1016/s0960-894x(02)00060-4
CHEMBL368213 130143 0 None - 0 Guinea pig 8.6 pIC50 = 8.6 Binding
Inhibitory activity against 5-hydroxytryptamine 4 receptor of guinea pig striatum using [3H]GR-113808 as radioligandInhibitory activity against 5-hydroxytryptamine 4 receptor of guinea pig striatum using [3H]GR-113808 as radioligand
ChEMBL 465 6 3 6 2.1 COc1cc(N)c(Cl)cc1C(=O)NC1CCN(CC2CCN(C(=O)C(C)(C)N)CC2)CC1 10.1016/s0960-894x(02)00060-4
90644470 111786 0 None - 1 Human 6.7 pIC50 = 6.7 Binding
Antagonist activity at Rluc-tagged human 5HT4R expressed in human SH-SY5Y cells assessed as inhibition of serotonin-induced receptor/Gbeta1 coupling by BRET assayAntagonist activity at Rluc-tagged human 5HT4R expressed in human SH-SY5Y cells assessed as inhibition of serotonin-induced receptor/Gbeta1 coupling by BRET assay
ChEMBL 328 6 0 5 3.3 COc1cc(C(=O)OCCCN2CCCCC2)c2ccccc2n1 10.1016/j.ejmech.2014.05.015
CHEMBL3291075 111786 0 None - 1 Human 6.7 pIC50 = 6.7 Binding
Antagonist activity at Rluc-tagged human 5HT4R expressed in human SH-SY5Y cells assessed as inhibition of serotonin-induced receptor/Gbeta1 coupling by BRET assayAntagonist activity at Rluc-tagged human 5HT4R expressed in human SH-SY5Y cells assessed as inhibition of serotonin-induced receptor/Gbeta1 coupling by BRET assay
ChEMBL 328 6 0 5 3.3 COc1cc(C(=O)OCCCN2CCCCC2)c2ccccc2n1 10.1016/j.ejmech.2014.05.015
44385584 129663 0 None - 0 Guinea pig 7.7 pIC50 = 7.7 Binding
Inhibitory activity against 5-hydroxytryptamine 4 receptor of guinea pig striatum using [3H]GR-113808 as radioligandInhibitory activity against 5-hydroxytryptamine 4 receptor of guinea pig striatum using [3H]GR-113808 as radioligand
ChEMBL 515 10 3 7 1.8 COc1cc(N)c(Cl)cc1C(=O)NC1CCN(CC2CCN(CCCNS(C)(=O)=O)CC2)CC1 10.1016/s0960-894x(02)00060-4
CHEMBL367877 129663 0 None - 0 Guinea pig 7.7 pIC50 = 7.7 Binding
Inhibitory activity against 5-hydroxytryptamine 4 receptor of guinea pig striatum using [3H]GR-113808 as radioligandInhibitory activity against 5-hydroxytryptamine 4 receptor of guinea pig striatum using [3H]GR-113808 as radioligand
ChEMBL 515 10 3 7 1.8 COc1cc(N)c(Cl)cc1C(=O)NC1CCN(CC2CCN(CCCNS(C)(=O)=O)CC2)CC1 10.1016/s0960-894x(02)00060-4
2353 100643 75 None -1 5 Guinea pig 5.7 pIC50 = 5.7 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
ChEMBL 336 2 0 4 3.1 COc1ccc2cc3[n+](cc2c1OC)CCc1cc2c(cc1-3)OCO2 nan
CHEMBL12089 100643 75 None -1 5 Guinea pig 5.7 pIC50 = 5.7 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
ChEMBL 336 2 0 4 3.1 COc1ccc2cc3[n+](cc2c1OC)CCc1cc2c(cc1-3)OCO2 nan
CHEMBL295124 100643 75 None -1 5 Guinea pig 5.7 pIC50 = 5.7 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
ChEMBL 336 2 0 4 3.1 COc1ccc2cc3[n+](cc2c1OC)CCc1cc2c(cc1-3)OCO2 nan
4223 3929 88 None - 3 Rat 6.6 pIC50 = 6.6 Binding
Inhibition of rat hydroxytryptamine 4 receptorInhibition of rat hydroxytryptamine 4 receptor
ChEMBL 441 7 2 5 4.0 N#Cc1ccc2c(c1)c(CCCCN1CCN(CC1)c1ccc3c(c1)cc(o3)C(=O)N)c[nH]2 10.1021/jm040793q
6918314 3929 88 None - 3 Rat 6.6 pIC50 = 6.6 Binding
Inhibition of rat hydroxytryptamine 4 receptorInhibition of rat hydroxytryptamine 4 receptor
ChEMBL 441 7 2 5 4.0 N#Cc1ccc2c(c1)c(CCCCN1CCN(CC1)c1ccc3c(c1)cc(o3)C(=O)N)c[nH]2 10.1021/jm040793q
7427 3929 88 None - 3 Rat 6.6 pIC50 = 6.6 Binding
Inhibition of rat hydroxytryptamine 4 receptorInhibition of rat hydroxytryptamine 4 receptor
ChEMBL 441 7 2 5 4.0 N#Cc1ccc2c(c1)c(CCCCN1CCN(CC1)c1ccc3c(c1)cc(o3)C(=O)N)c[nH]2 10.1021/jm040793q
CHEMBL439849 3929 88 None - 3 Rat 6.6 pIC50 = 6.6 Binding
Inhibition of rat hydroxytryptamine 4 receptorInhibition of rat hydroxytryptamine 4 receptor
ChEMBL 441 7 2 5 4.0 N#Cc1ccc2c(c1)c(CCCCN1CCN(CC1)c1ccc3c(c1)cc(o3)C(=O)N)c[nH]2 10.1021/jm040793q
DB06684 3929 88 None - 3 Rat 6.6 pIC50 = 6.6 Binding
Inhibition of rat hydroxytryptamine 4 receptorInhibition of rat hydroxytryptamine 4 receptor
ChEMBL 441 7 2 5 4.0 N#Cc1ccc2c(c1)c(CCCCN1CCN(CC1)c1ccc3c(c1)cc(o3)C(=O)N)c[nH]2 10.1021/jm040793q
240 931 39 None -4 25 Guinea pig 6.6 pIC50 = 6.6 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
ChEMBL 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N nan
2769 931 39 None -4 25 Guinea pig 6.6 pIC50 = 6.6 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
ChEMBL 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N nan
44279790 931 39 None -4 25 Guinea pig 6.6 pIC50 = 6.6 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
ChEMBL 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N nan
660 931 39 None -4 25 Guinea pig 6.6 pIC50 = 6.6 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
ChEMBL 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N nan
CHEMBL1729 931 39 None -4 25 Guinea pig 6.6 pIC50 = 6.6 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
ChEMBL 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N nan
CHEMBL560739 931 39 None -4 25 Guinea pig 6.6 pIC50 = 6.6 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
ChEMBL 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N nan
DB00604 931 39 None -4 25 Guinea pig 6.6 pIC50 = 6.6 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
ChEMBL 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N nan
10550242 17075 0 None - 1 Human 6.5 pIC50 = 6.5 Binding
Antagonist activity at 5TH4 receptor (unknown origin)Antagonist activity at 5TH4 receptor (unknown origin)
ChEMBL 423 6 1 6 3.6 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCN(c2ccccc2Cl)CC1 10.1039/C1MD00213A
CHEMBL125670 17075 0 None - 1 Human 6.5 pIC50 = 6.5 Binding
Antagonist activity at 5TH4 receptor (unknown origin)Antagonist activity at 5TH4 receptor (unknown origin)
ChEMBL 423 6 1 6 3.6 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCN(c2ccccc2Cl)CC1 10.1039/C1MD00213A
11796362 114603 0 None - 1 Human 8.5 pIC50 = 8.5 Binding
Antagonist activity at 5TH4 receptor (unknown origin)Antagonist activity at 5TH4 receptor (unknown origin)
ChEMBL 419 7 1 7 2.9 COc1cccc(N2CCN(CCOC(=O)c3cc(Cl)c(N)cc3OC)CC2)c1 10.1039/C1MD00213A
CHEMBL334325 114603 0 None - 1 Human 8.5 pIC50 = 8.5 Binding
Antagonist activity at 5TH4 receptor (unknown origin)Antagonist activity at 5TH4 receptor (unknown origin)
ChEMBL 419 7 1 7 2.9 COc1cccc(N2CCN(CCOC(=O)c3cc(Cl)c(N)cc3OC)CC2)c1 10.1039/C1MD00213A
44384735 59594 0 None - 0 Guinea pig 8.4 pIC50 = 8.4 Binding
Inhibitory activity against 5-hydroxytryptamine 4 receptor of guinea pig striatum using [3H]GR-113808 as radioligandInhibitory activity against 5-hydroxytryptamine 4 receptor of guinea pig striatum using [3H]GR-113808 as radioligand
ChEMBL 479 9 3 6 2.5 COc1cc(N)c(Cl)cc1C(=O)NC1CCN(CC2CCN(C(=O)CCCCN)CC2)CC1 10.1016/s0960-894x(02)00060-4
CHEMBL173089 59594 0 None - 0 Guinea pig 8.4 pIC50 = 8.4 Binding
Inhibitory activity against 5-hydroxytryptamine 4 receptor of guinea pig striatum using [3H]GR-113808 as radioligandInhibitory activity against 5-hydroxytryptamine 4 receptor of guinea pig striatum using [3H]GR-113808 as radioligand
ChEMBL 479 9 3 6 2.5 COc1cc(N)c(Cl)cc1C(=O)NC1CCN(CC2CCN(C(=O)CCCCN)CC2)CC1 10.1016/s0960-894x(02)00060-4
44384689 59323 0 None - 0 Guinea pig 8.4 pIC50 = 8.4 Binding
Inhibitory activity against 5-hydroxytryptamine 4 receptor of guinea pig striatum using [3H]GR-113808 as radioligandInhibitory activity against 5-hydroxytryptamine 4 receptor of guinea pig striatum using [3H]GR-113808 as radioligand
ChEMBL 465 8 3 6 2.1 COc1cc(N)c(Cl)cc1C(=O)NC1CCN(CC2CCN(C(=O)CCCN)CC2)CC1 10.1016/s0960-894x(02)00060-4
CHEMBL172074 59323 0 None - 0 Guinea pig 8.4 pIC50 = 8.4 Binding
Inhibitory activity against 5-hydroxytryptamine 4 receptor of guinea pig striatum using [3H]GR-113808 as radioligandInhibitory activity against 5-hydroxytryptamine 4 receptor of guinea pig striatum using [3H]GR-113808 as radioligand
ChEMBL 465 8 3 6 2.1 COc1cc(N)c(Cl)cc1C(=O)NC1CCN(CC2CCN(C(=O)CCCN)CC2)CC1 10.1016/s0960-894x(02)00060-4
5 139 66 None -288 54 Human 6.5 pIC50 = 6.5 Binding
Displacement of [3H]-GR 113808 from recombinant human brain 5HT4 receptor measured after 60 mins by radio ligand binding assayDisplacement of [3H]-GR 113808 from recombinant human brain 5HT4 receptor measured after 60 mins by radio ligand binding assay
ChEMBL 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 10.1016/j.ejmech.2019.111596
5202 139 66 None -288 54 Human 6.5 pIC50 = 6.5 Binding
Displacement of [3H]-GR 113808 from recombinant human brain 5HT4 receptor measured after 60 mins by radio ligand binding assayDisplacement of [3H]-GR 113808 from recombinant human brain 5HT4 receptor measured after 60 mins by radio ligand binding assay
ChEMBL 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 10.1016/j.ejmech.2019.111596
CHEMBL39 139 66 None -288 54 Human 6.5 pIC50 = 6.5 Binding
Displacement of [3H]-GR 113808 from recombinant human brain 5HT4 receptor measured after 60 mins by radio ligand binding assayDisplacement of [3H]-GR 113808 from recombinant human brain 5HT4 receptor measured after 60 mins by radio ligand binding assay
ChEMBL 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 10.1016/j.ejmech.2019.111596
DB08839 139 66 None -288 54 Human 6.5 pIC50 = 6.5 Binding
Displacement of [3H]-GR 113808 from recombinant human brain 5HT4 receptor measured after 60 mins by radio ligand binding assayDisplacement of [3H]-GR 113808 from recombinant human brain 5HT4 receptor measured after 60 mins by radio ligand binding assay
ChEMBL 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 10.1016/j.ejmech.2019.111596
260 3808 49 None -45 6 Guinea pig 6.5 pIC50 = 6.5 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
ChEMBL 284 2 1 3 3.0 CN1[C@@H]2CC[C@H]1C[C@H](C2)OC(=O)c1c[nH]c2c1cccc2 nan
2775 3808 49 None -45 6 Guinea pig 6.5 pIC50 = 6.5 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
ChEMBL 284 2 1 3 3.0 CN1[C@@H]2CC[C@H]1C[C@H](C2)OC(=O)c1c[nH]c2c1cccc2 nan
656665 3808 49 None -45 6 Guinea pig 6.5 pIC50 = 6.5 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
ChEMBL 284 2 1 3 3.0 CN1[C@@H]2CC[C@H]1C[C@H](C2)OC(=O)c1c[nH]c2c1cccc2 nan
CHEMBL56564 3808 49 None -45 6 Guinea pig 6.5 pIC50 = 6.5 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
ChEMBL 284 2 1 3 3.0 CN1[C@@H]2CC[C@H]1C[C@H](C2)OC(=O)c1c[nH]c2c1cccc2 nan
DB11699 3808 49 None -45 6 Guinea pig 6.5 pIC50 = 6.5 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
ChEMBL 284 2 1 3 3.0 CN1[C@@H]2CC[C@H]1C[C@H](C2)OC(=O)c1c[nH]c2c1cccc2 nan
68592299 137229 0 None - 0 Human 6.5 pIC50 = 6.5 Binding
Displacement of [3H]-GR113808 from human 5-HT4 receptor expressed in African green monkey COS7 cell membranes after 30 mins by liquid scintillation counting analysisDisplacement of [3H]-GR113808 from human 5-HT4 receptor expressed in African green monkey COS7 cell membranes after 30 mins by liquid scintillation counting analysis
ChEMBL 466 7 2 6 2.4 CCC(=O)N1CCC(CN2CC[C@H](NC(=O)c3cc(Cl)c(N)cc3OC)[C@H](OC)C2)CC1 10.1016/j.ejmech.2015.12.006
CHEMBL3759259 137229 0 None - 0 Human 6.5 pIC50 = 6.5 Binding
Displacement of [3H]-GR113808 from human 5-HT4 receptor expressed in African green monkey COS7 cell membranes after 30 mins by liquid scintillation counting analysisDisplacement of [3H]-GR113808 from human 5-HT4 receptor expressed in African green monkey COS7 cell membranes after 30 mins by liquid scintillation counting analysis
ChEMBL 466 7 2 6 2.4 CCC(=O)N1CCC(CN2CC[C@H](NC(=O)c3cc(Cl)c(N)cc3OC)[C@H](OC)C2)CC1 10.1016/j.ejmech.2015.12.006
68593622 137128 0 None - 0 Human 6.4 pIC50 = 6.4 Binding
Displacement of [3H]-GR113808 from human 5-HT4 receptor expressed in African green monkey COS7 cell membranes after 30 mins by liquid scintillation counting analysisDisplacement of [3H]-GR113808 from human 5-HT4 receptor expressed in African green monkey COS7 cell membranes after 30 mins by liquid scintillation counting analysis
ChEMBL 482 7 2 7 2.6 CCOC(=O)N1CCC(CN2CC[C@H](NC(=O)c3cc(Cl)c(N)cc3OC)[C@H](OC)C2)CC1 10.1016/j.ejmech.2015.12.006
CHEMBL3758398 137128 0 None - 0 Human 6.4 pIC50 = 6.4 Binding
Displacement of [3H]-GR113808 from human 5-HT4 receptor expressed in African green monkey COS7 cell membranes after 30 mins by liquid scintillation counting analysisDisplacement of [3H]-GR113808 from human 5-HT4 receptor expressed in African green monkey COS7 cell membranes after 30 mins by liquid scintillation counting analysis
ChEMBL 482 7 2 7 2.6 CCOC(=O)N1CCC(CN2CC[C@H](NC(=O)c3cc(Cl)c(N)cc3OC)[C@H](OC)C2)CC1 10.1016/j.ejmech.2015.12.006
3168 9172 84 None -93 21 Guinea pig 5.4 pIC50 = 5.4 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
ChEMBL 379 6 1 4 3.7 O=C(CCCN1CC=C(n2c(=O)[nH]c3ccccc32)CC1)c1ccc(F)cc1 nan
CHEMBL1108 9172 84 None -93 21 Guinea pig 5.4 pIC50 = 5.4 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
ChEMBL 379 6 1 4 3.7 O=C(CCCN1CC=C(n2c(=O)[nH]c3ccccc32)CC1)c1ccc(F)cc1 nan
44626295 196097 0 None - 0 Human 5.4 pIC50 = 5.4 Binding
Displacement of [3H]GR-113808 from human recombinant 5-HT4 receptorDisplacement of [3H]GR-113808 from human recombinant 5-HT4 receptor
ChEMBL 531 8 3 7 3.8 COc1cccc([C@]2(O)CCCC[C@H]2CN2CC[C@@H](NC(=O)c3cc(Cl)c(N)cc3OC)[C@@H](OC)C2)c1 10.1016/j.bmcl.2009.08.016
CHEMBL571799 196097 0 None - 0 Human 5.4 pIC50 = 5.4 Binding
Displacement of [3H]GR-113808 from human recombinant 5-HT4 receptorDisplacement of [3H]GR-113808 from human recombinant 5-HT4 receptor
ChEMBL 531 8 3 7 3.8 COc1cccc([C@]2(O)CCCC[C@H]2CN2CC[C@@H](NC(=O)c3cc(Cl)c(N)cc3OC)[C@@H](OC)C2)c1 10.1016/j.bmcl.2009.08.016
44385532 60955 0 None - 0 Guinea pig 7.4 pIC50 = 7.4 Binding
Inhibitory activity against 5-hydroxytryptamine 4 receptor of guinea pig striatum using [3H]GR-113808 as radioligandInhibitory activity against 5-hydroxytryptamine 4 receptor of guinea pig striatum using [3H]GR-113808 as radioligand
ChEMBL 453 8 4 7 1.2 COc1cc(N)c(Cl)cc1C(=O)NCC(O)CN1CCC(CN2CCC(N)CC2)CC1 10.1016/s0960-894x(02)00060-4
CHEMBL176672 60955 0 None - 0 Guinea pig 7.4 pIC50 = 7.4 Binding
Inhibitory activity against 5-hydroxytryptamine 4 receptor of guinea pig striatum using [3H]GR-113808 as radioligandInhibitory activity against 5-hydroxytryptamine 4 receptor of guinea pig striatum using [3H]GR-113808 as radioligand
ChEMBL 453 8 4 7 1.2 COc1cc(N)c(Cl)cc1C(=O)NCC(O)CN1CCC(CN2CCC(N)CC2)CC1 10.1016/s0960-894x(02)00060-4
44384630 128496 0 None - 0 Guinea pig 6.4 pIC50 = 6.4 Binding
Inhibitory activity against 5-hydroxytryptamine 4 receptor of guinea pig striatum using [3H]GR-113808 as radioligandInhibitory activity against 5-hydroxytryptamine 4 receptor of guinea pig striatum using [3H]GR-113808 as radioligand
ChEMBL 479 7 3 6 1.6 COc1cc(N)c(Cl)cc1C(=O)NC1CCN(C(=O)C2CCN(C(=O)CCCN)CC2)CC1 10.1016/s0960-894x(02)00060-4
CHEMBL366986 128496 0 None - 0 Guinea pig 6.4 pIC50 = 6.4 Binding
Inhibitory activity against 5-hydroxytryptamine 4 receptor of guinea pig striatum using [3H]GR-113808 as radioligandInhibitory activity against 5-hydroxytryptamine 4 receptor of guinea pig striatum using [3H]GR-113808 as radioligand
ChEMBL 479 7 3 6 1.6 COc1cc(N)c(Cl)cc1C(=O)NC1CCN(C(=O)C2CCN(C(=O)CCCN)CC2)CC1 10.1016/s0960-894x(02)00060-4
12 1524 14 None - 7 Guinea pig 7.4 pIC50 = 7.4 Binding
Inhibitory activity against 5-hydroxytryptamine 4 receptor in guinea pigInhibitory activity against 5-hydroxytryptamine 4 receptor in guinea pig
ChEMBL 246 5 1 2 2.8 CCc1[nH]c2c(c1CCN(C)C)cc(cc2)OC 10.1016/j.bmcl.2005.06.067
6918513 1524 14 None - 7 Guinea pig 7.4 pIC50 = 7.4 Binding
Inhibitory activity against 5-hydroxytryptamine 4 receptor in guinea pigInhibitory activity against 5-hydroxytryptamine 4 receptor in guinea pig
ChEMBL 246 5 1 2 2.8 CCc1[nH]c2c(c1CCN(C)C)cc(cc2)OC 10.1016/j.bmcl.2005.06.067
CHEMBL267615 1524 14 None - 7 Guinea pig 7.4 pIC50 = 7.4 Binding
Inhibitory activity against 5-hydroxytryptamine 4 receptor in guinea pigInhibitory activity against 5-hydroxytryptamine 4 receptor in guinea pig
ChEMBL 246 5 1 2 2.8 CCc1[nH]c2c(c1CCN(C)C)cc(cc2)OC 10.1016/j.bmcl.2005.06.067
90644475 111790 0 None - 1 Human 6.3 pIC50 = 6.3 Binding
Antagonist activity at Rluc-tagged human 5HT4R expressed in human SH-SY5Y cells assessed as inhibition of serotonin-induced receptor/Gbeta1 coupling by BRET assayAntagonist activity at Rluc-tagged human 5HT4R expressed in human SH-SY5Y cells assessed as inhibition of serotonin-induced receptor/Gbeta1 coupling by BRET assay
ChEMBL 357 4 0 4 3.4 O=C1c2cccc3nc(Cl)cc(c23)C(=O)N1CCCN1CCCCC1 10.1016/j.ejmech.2014.05.015
CHEMBL3291080 111790 0 None - 1 Human 6.3 pIC50 = 6.3 Binding
Antagonist activity at Rluc-tagged human 5HT4R expressed in human SH-SY5Y cells assessed as inhibition of serotonin-induced receptor/Gbeta1 coupling by BRET assayAntagonist activity at Rluc-tagged human 5HT4R expressed in human SH-SY5Y cells assessed as inhibition of serotonin-induced receptor/Gbeta1 coupling by BRET assay
ChEMBL 357 4 0 4 3.4 O=C1c2cccc3nc(Cl)cc(c23)C(=O)N1CCCN1CCCCC1 10.1016/j.ejmech.2014.05.015
45485653 195907 0 None - 0 Human 5.3 pIC50 = 5.3 Binding
Displacement of [3H]GR-113808 from human recombinant 5-HT4 receptorDisplacement of [3H]GR-113808 from human recombinant 5-HT4 receptor
ChEMBL 531 8 3 7 3.8 COc1cccc([C@]2(O)CCCC[C@H]2CN2CC[C@H](NC(=O)c3cc(Cl)c(N)cc3OC)[C@H](OC)C2)c1 10.1016/j.bmcl.2009.08.016
CHEMBL570487 195907 0 None - 0 Human 5.3 pIC50 = 5.3 Binding
Displacement of [3H]GR-113808 from human recombinant 5-HT4 receptorDisplacement of [3H]GR-113808 from human recombinant 5-HT4 receptor
ChEMBL 531 8 3 7 3.8 COc1cccc([C@]2(O)CCCC[C@H]2CN2CC[C@H](NC(=O)c3cc(Cl)c(N)cc3OC)[C@H](OC)C2)c1 10.1016/j.bmcl.2009.08.016
5311047 203055 30 None -5 2 Human 6.3 pIC50 = 6.3 Binding
Displacement of [3H]-GR113808 from human 5-HT4 receptor expressed in African green monkey COS7 cell membranes after 30 mins by liquid scintillation counting analysisDisplacement of [3H]-GR113808 from human 5-HT4 receptor expressed in African green monkey COS7 cell membranes after 30 mins by liquid scintillation counting analysis
ChEMBL 465 9 2 6 3.4 COc1cc(N)c(Cl)cc1C(=O)N[C@H]1CCN(CCCOc2ccc(F)cc2)C[C@H]1OC 10.1016/j.ejmech.2015.12.006
CHEMBL74656 203055 30 None -5 2 Human 6.3 pIC50 = 6.3 Binding
Displacement of [3H]-GR113808 from human 5-HT4 receptor expressed in African green monkey COS7 cell membranes after 30 mins by liquid scintillation counting analysisDisplacement of [3H]-GR113808 from human 5-HT4 receptor expressed in African green monkey COS7 cell membranes after 30 mins by liquid scintillation counting analysis
ChEMBL 465 9 2 6 3.4 COc1cc(N)c(Cl)cc1C(=O)N[C@H]1CCN(CCCOc2ccc(F)cc2)C[C@H]1OC 10.1016/j.ejmech.2015.12.006
182593 3343 4 None 1 3 Human 7.3 pIC50 = 7.3 Binding
Partial agonist activity at Rluc-tagged human 5HT4R expressed in human SH-SY5Y cells assessed as effect on serotonin-induced receptor/Gbeta1 coupling by BRET assayPartial agonist activity at Rluc-tagged human 5HT4R expressed in human SH-SY5Y cells assessed as effect on serotonin-induced receptor/Gbeta1 coupling by BRET assay
ChEMBL 326 6 1 5 3.0 COc1cc(N)c(cc1C(=O)OCCCN1CCCCC1)Cl 10.1016/j.ejmech.2014.05.015
254 3343 4 None 1 3 Human 7.3 pIC50 = 7.3 Binding
Partial agonist activity at Rluc-tagged human 5HT4R expressed in human SH-SY5Y cells assessed as effect on serotonin-induced receptor/Gbeta1 coupling by BRET assayPartial agonist activity at Rluc-tagged human 5HT4R expressed in human SH-SY5Y cells assessed as effect on serotonin-induced receptor/Gbeta1 coupling by BRET assay
ChEMBL 326 6 1 5 3.0 COc1cc(N)c(cc1C(=O)OCCCN1CCCCC1)Cl 10.1016/j.ejmech.2014.05.015
CHEMBL83954 3343 4 None 1 3 Human 7.3 pIC50 = 7.3 Binding
Partial agonist activity at Rluc-tagged human 5HT4R expressed in human SH-SY5Y cells assessed as effect on serotonin-induced receptor/Gbeta1 coupling by BRET assayPartial agonist activity at Rluc-tagged human 5HT4R expressed in human SH-SY5Y cells assessed as effect on serotonin-induced receptor/Gbeta1 coupling by BRET assay
ChEMBL 326 6 1 5 3.0 COc1cc(N)c(cc1C(=O)OCCCN1CCCCC1)Cl 10.1016/j.ejmech.2014.05.015
107715 199260 18 None -165 20 Guinea pig 5.3 pIC50 = 5.3 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
ChEMBL 611 5 3 6 2.7 CC(C)[C@@]1(NC(=O)[C@@H]2C[C@@H]3c4cccc5[nH]cc(c45)C[C@H]3N(C)C2)O[C@@]2(O)[C@@H]3CCCN3C(=O)[C@H](Cc3ccccc3)N2C1=O nan
CHEMBL1255837 199260 18 None -165 20 Guinea pig 5.3 pIC50 = 5.3 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
ChEMBL 611 5 3 6 2.7 CC(C)[C@@]1(NC(=O)[C@@H]2C[C@@H]3c4cccc5[nH]cc(c45)C[C@H]3N(C)C2)O[C@@]2(O)[C@@H]3CCCN3C(=O)[C@H](Cc3ccccc3)N2C1=O nan
CHEMBL601773 199260 18 None -165 20 Guinea pig 5.3 pIC50 = 5.3 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
ChEMBL 611 5 3 6 2.7 CC(C)[C@@]1(NC(=O)[C@@H]2C[C@@H]3c4cccc5[nH]cc(c45)C[C@H]3N(C)C2)O[C@@]2(O)[C@@H]3CCCN3C(=O)[C@H](Cc3ccccc3)N2C1=O nan
68593871 137239 0 None - 0 Human 6.3 pIC50 = 6.3 Binding
Displacement of [3H]-GR113808 from human 5-HT4 receptor expressed in African green monkey COS7 cell membranes after 30 mins by liquid scintillation counting analysisDisplacement of [3H]-GR113808 from human 5-HT4 receptor expressed in African green monkey COS7 cell membranes after 30 mins by liquid scintillation counting analysis
ChEMBL 466 7 2 6 2.4 CCC(=O)N1CCCC(CN2CC[C@H](NC(=O)c3cc(Cl)c(N)cc3OC)[C@H](OC)C2)C1 10.1016/j.ejmech.2015.12.006
CHEMBL3759348 137239 0 None - 0 Human 6.3 pIC50 = 6.3 Binding
Displacement of [3H]-GR113808 from human 5-HT4 receptor expressed in African green monkey COS7 cell membranes after 30 mins by liquid scintillation counting analysisDisplacement of [3H]-GR113808 from human 5-HT4 receptor expressed in African green monkey COS7 cell membranes after 30 mins by liquid scintillation counting analysis
ChEMBL 466 7 2 6 2.4 CCC(=O)N1CCCC(CN2CC[C@H](NC(=O)c3cc(Cl)c(N)cc3OC)[C@H](OC)C2)C1 10.1016/j.ejmech.2015.12.006
44384684 59542 0 None - 0 Guinea pig 8.3 pIC50 = 8.3 Binding
Inhibitory activity against 5-hydroxytryptamine 4 receptor of guinea pig striatum using [3H]GR-113808 as radioligandInhibitory activity against 5-hydroxytryptamine 4 receptor of guinea pig striatum using [3H]GR-113808 as radioligand
ChEMBL 451 6 3 6 1.7 COc1cc(N)c(Cl)cc1C(=O)NC1CCN(CC2CCN(C(=O)C(C)N)CC2)CC1 10.1016/s0960-894x(02)00060-4
CHEMBL172899 59542 0 None - 0 Guinea pig 8.3 pIC50 = 8.3 Binding
Inhibitory activity against 5-hydroxytryptamine 4 receptor of guinea pig striatum using [3H]GR-113808 as radioligandInhibitory activity against 5-hydroxytryptamine 4 receptor of guinea pig striatum using [3H]GR-113808 as radioligand
ChEMBL 451 6 3 6 1.7 COc1cc(N)c(Cl)cc1C(=O)NC1CCN(CC2CCN(C(=O)C(C)N)CC2)CC1 10.1016/s0960-894x(02)00060-4
44384624 165434 0 None - 0 Guinea pig 8.3 pIC50 = 8.3 Binding
Inhibitory activity against 5-hydroxytryptamine 4 receptor of guinea pig striatum using [3H]GR-113808 as radioligandInhibitory activity against 5-hydroxytryptamine 4 receptor of guinea pig striatum using [3H]GR-113808 as radioligand
ChEMBL 465 7 3 6 2.0 COc1cc(N)c(Cl)cc1C(=O)NC1CCN(CC2CCN(C(=O)C(C)CN)CC2)CC1 10.1016/s0960-894x(02)00060-4
CHEMBL425329 165434 0 None - 0 Guinea pig 8.3 pIC50 = 8.3 Binding
Inhibitory activity against 5-hydroxytryptamine 4 receptor of guinea pig striatum using [3H]GR-113808 as radioligandInhibitory activity against 5-hydroxytryptamine 4 receptor of guinea pig striatum using [3H]GR-113808 as radioligand
ChEMBL 465 7 3 6 2.0 COc1cc(N)c(Cl)cc1C(=O)NC1CCN(CC2CCN(C(=O)C(C)CN)CC2)CC1 10.1016/s0960-894x(02)00060-4
45485563 196123 0 None - 0 Human 5.3 pIC50 = 5.3 Binding
Displacement of [3H]GR-113808 from human recombinant 5-HT4 receptorDisplacement of [3H]GR-113808 from human recombinant 5-HT4 receptor
ChEMBL 475 9 3 6 3.7 COc1cccc([C@@]2(O)CCCC[C@@H]2CN(C)CCNC(=O)c2cc(Cl)c(N)cc2OC)c1 10.1016/j.bmcl.2009.08.016
CHEMBL572038 196123 0 None - 0 Human 5.3 pIC50 = 5.3 Binding
Displacement of [3H]GR-113808 from human recombinant 5-HT4 receptorDisplacement of [3H]GR-113808 from human recombinant 5-HT4 receptor
ChEMBL 475 9 3 6 3.7 COc1cccc([C@@]2(O)CCCC[C@@H]2CN(C)CCNC(=O)c2cc(Cl)c(N)cc2OC)c1 10.1016/j.bmcl.2009.08.016
68592632 137290 0 None - 0 Human 7.3 pIC50 = 7.3 Binding
Displacement of [3H]-GR113808 from human 5-HT4 receptor expressed in African green monkey COS7 cell membranes after 30 mins by liquid scintillation counting analysisDisplacement of [3H]-GR113808 from human 5-HT4 receptor expressed in African green monkey COS7 cell membranes after 30 mins by liquid scintillation counting analysis
ChEMBL 481 6 2 6 2.1 COc1cc(N)c(Cl)cc1C(=O)N[C@H]1CCN(CC2CCN(C(=O)N(C)C)CC2)C[C@H]1OC 10.1016/j.ejmech.2015.12.006
CHEMBL3759759 137290 0 None - 0 Human 7.3 pIC50 = 7.3 Binding
Displacement of [3H]-GR113808 from human 5-HT4 receptor expressed in African green monkey COS7 cell membranes after 30 mins by liquid scintillation counting analysisDisplacement of [3H]-GR113808 from human 5-HT4 receptor expressed in African green monkey COS7 cell membranes after 30 mins by liquid scintillation counting analysis
ChEMBL 481 6 2 6 2.1 COc1cc(N)c(Cl)cc1C(=O)N[C@H]1CCN(CC2CCN(C(=O)N(C)C)CC2)C[C@H]1OC 10.1016/j.ejmech.2015.12.006
67922794 137195 0 None - 0 Human 6.3 pIC50 = 6.3 Binding
Displacement of [3H]-GR113808 from human 5-HT4 receptor expressed in African green monkey COS7 cell membranes after 30 mins by liquid scintillation counting analysisDisplacement of [3H]-GR113808 from human 5-HT4 receptor expressed in African green monkey COS7 cell membranes after 30 mins by liquid scintillation counting analysis
ChEMBL 452 7 2 6 2.2 COc1cc(N)c(Cl)cc1C(=O)N[C@H]1CCN(CCC(=O)N2CCCCC2)C[C@H]1OC 10.1016/j.ejmech.2015.12.006
CHEMBL3758945 137195 0 None - 0 Human 6.3 pIC50 = 6.3 Binding
Displacement of [3H]-GR113808 from human 5-HT4 receptor expressed in African green monkey COS7 cell membranes after 30 mins by liquid scintillation counting analysisDisplacement of [3H]-GR113808 from human 5-HT4 receptor expressed in African green monkey COS7 cell membranes after 30 mins by liquid scintillation counting analysis
ChEMBL 452 7 2 6 2.2 COc1cc(N)c(Cl)cc1C(=O)N[C@H]1CCN(CCC(=O)N2CCCCC2)C[C@H]1OC 10.1016/j.ejmech.2015.12.006
68593774 137168 0 None - 0 Human 5.2 pIC50 = 5.2 Binding
Displacement of [3H]-GR113808 from human 5-HT4 receptor expressed in African green monkey COS7 cell membranes after 30 mins by liquid scintillation counting analysisDisplacement of [3H]-GR113808 from human 5-HT4 receptor expressed in African green monkey COS7 cell membranes after 30 mins by liquid scintillation counting analysis
ChEMBL 406 7 2 6 2.3 COc1cc(N)c(Cl)cc1C(=O)N[C@H]1CCN(CCn2cccc2)C[C@H]1OC 10.1016/j.ejmech.2015.12.006
CHEMBL3758721 137168 0 None - 0 Human 5.2 pIC50 = 5.2 Binding
Displacement of [3H]-GR113808 from human 5-HT4 receptor expressed in African green monkey COS7 cell membranes after 30 mins by liquid scintillation counting analysisDisplacement of [3H]-GR113808 from human 5-HT4 receptor expressed in African green monkey COS7 cell membranes after 30 mins by liquid scintillation counting analysis
ChEMBL 406 7 2 6 2.3 COc1cc(N)c(Cl)cc1C(=O)N[C@H]1CCN(CCn2cccc2)C[C@H]1OC 10.1016/j.ejmech.2015.12.006
68591735 137241 0 None - 0 Human 6.2 pIC50 = 6.2 Binding
Displacement of [3H]-GR113808 from human 5-HT4 receptor expressed in African green monkey COS7 cell membranes after 30 mins by liquid scintillation counting analysisDisplacement of [3H]-GR113808 from human 5-HT4 receptor expressed in African green monkey COS7 cell membranes after 30 mins by liquid scintillation counting analysis
ChEMBL 452 6 2 6 2.0 COc1cc(N)c(Cl)cc1C(=O)N[C@H]1CCN(CC2CCN(C(C)=O)CC2)C[C@H]1OC 10.1016/j.ejmech.2015.12.006
CHEMBL3759362 137241 0 None - 0 Human 6.2 pIC50 = 6.2 Binding
Displacement of [3H]-GR113808 from human 5-HT4 receptor expressed in African green monkey COS7 cell membranes after 30 mins by liquid scintillation counting analysisDisplacement of [3H]-GR113808 from human 5-HT4 receptor expressed in African green monkey COS7 cell membranes after 30 mins by liquid scintillation counting analysis
ChEMBL 452 6 2 6 2.0 COc1cc(N)c(Cl)cc1C(=O)N[C@H]1CCN(CC2CCN(C(C)=O)CC2)C[C@H]1OC 10.1016/j.ejmech.2015.12.006
87509988 137127 0 None - 0 Human 6.2 pIC50 = 6.2 Binding
Displacement of [3H]-GR113808 from human 5-HT4 receptor expressed in African green monkey COS7 cell membranes after 30 mins by liquid scintillation counting analysisDisplacement of [3H]-GR113808 from human 5-HT4 receptor expressed in African green monkey COS7 cell membranes after 30 mins by liquid scintillation counting analysis
ChEMBL 482 7 2 6 3.2 CCC(=S)N1CCC(CN2CC[C@H](NC(=O)c3cc(Cl)c(N)cc3OC)[C@H](OC)C2)CC1 10.1016/j.ejmech.2015.12.006
CHEMBL3758397 137127 0 None - 0 Human 6.2 pIC50 = 6.2 Binding
Displacement of [3H]-GR113808 from human 5-HT4 receptor expressed in African green monkey COS7 cell membranes after 30 mins by liquid scintillation counting analysisDisplacement of [3H]-GR113808 from human 5-HT4 receptor expressed in African green monkey COS7 cell membranes after 30 mins by liquid scintillation counting analysis
ChEMBL 482 7 2 6 3.2 CCC(=S)N1CCC(CN2CC[C@H](NC(=O)c3cc(Cl)c(N)cc3OC)[C@H](OC)C2)CC1 10.1016/j.ejmech.2015.12.006
9911674 130913 0 None - 0 Guinea pig 8.2 pIC50 = 8.2 Binding
Inhibitory activity against 5-hydroxytryptamine 4 receptor of guinea pig striatum using [3H]GR-113808 as radioligandInhibitory activity against 5-hydroxytryptamine 4 receptor of guinea pig striatum using [3H]GR-113808 as radioligand
ChEMBL 451 9 3 6 2.6 COc1cc(N)c(Cl)cc1C(=O)NC1CCN(CC2CCN(CCCCN)CC2)CC1 10.1016/s0960-894x(02)00060-4
CHEMBL369037 130913 0 None - 0 Guinea pig 8.2 pIC50 = 8.2 Binding
Inhibitory activity against 5-hydroxytryptamine 4 receptor of guinea pig striatum using [3H]GR-113808 as radioligandInhibitory activity against 5-hydroxytryptamine 4 receptor of guinea pig striatum using [3H]GR-113808 as radioligand
ChEMBL 451 9 3 6 2.6 COc1cc(N)c(Cl)cc1C(=O)NC1CCN(CC2CCN(CCCCN)CC2)CC1 10.1016/s0960-894x(02)00060-4
45485620 195744 0 None - 0 Human 5.2 pIC50 = 5.2 Binding
Displacement of [3H]GR-113808 from human recombinant 5-HT4 receptorDisplacement of [3H]GR-113808 from human recombinant 5-HT4 receptor
ChEMBL 531 8 3 7 3.8 COc1cccc([C@@]2(O)CCCC[C@@H]2CN2CC[C@H](NC(=O)c3cc(Cl)c(N)cc3OC)[C@H](OC)C2)c1 10.1016/j.bmcl.2009.08.016
CHEMBL569585 195744 0 None - 0 Human 5.2 pIC50 = 5.2 Binding
Displacement of [3H]GR-113808 from human recombinant 5-HT4 receptorDisplacement of [3H]GR-113808 from human recombinant 5-HT4 receptor
ChEMBL 531 8 3 7 3.8 COc1cccc([C@@]2(O)CCCC[C@@H]2CN2CC[C@H](NC(=O)c3cc(Cl)c(N)cc3OC)[C@H](OC)C2)c1 10.1016/j.bmcl.2009.08.016
10131112 1523 21 None - 0 Guinea pig 6.2 pIC50 = 6.2 Binding
Inhibitory activity against 5-hydroxytryptamine 4 receptor in guinea pigInhibitory activity against 5-hydroxytryptamine 4 receptor in guinea pig
ChEMBL 246 1 2 1 3.5 Clc1ccc2c(c1)c(C1=CCNCC1)c([nH]2)C 10.1016/j.bmcl.2005.06.067
8428 1523 21 None - 0 Guinea pig 6.2 pIC50 = 6.2 Binding
Inhibitory activity against 5-hydroxytryptamine 4 receptor in guinea pigInhibitory activity against 5-hydroxytryptamine 4 receptor in guinea pig
ChEMBL 246 1 2 1 3.5 Clc1ccc2c(c1)c(C1=CCNCC1)c([nH]2)C 10.1016/j.bmcl.2005.06.067
CHEMBL364005 1523 21 None - 0 Guinea pig 6.2 pIC50 = 6.2 Binding
Inhibitory activity against 5-hydroxytryptamine 4 receptor in guinea pigInhibitory activity against 5-hydroxytryptamine 4 receptor in guinea pig
ChEMBL 246 1 2 1 3.5 Clc1ccc2c(c1)c(C1=CCNCC1)c([nH]2)C 10.1016/j.bmcl.2005.06.067
10812045 15346 0 None - 1 Human 7.2 pIC50 = 7.2 Binding
Antagonist activity at 5TH4 receptor (unknown origin)Antagonist activity at 5TH4 receptor (unknown origin)
ChEMBL 419 7 1 7 2.9 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCN(c2ccccc2OC)CC1 10.1039/C1MD00213A
CHEMBL121766 15346 0 None - 1 Human 7.2 pIC50 = 7.2 Binding
Antagonist activity at 5TH4 receptor (unknown origin)Antagonist activity at 5TH4 receptor (unknown origin)
ChEMBL 419 7 1 7 2.9 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCN(c2ccccc2OC)CC1 10.1039/C1MD00213A
68592484 137193 0 None - 0 Human 6.2 pIC50 = 6.2 Binding
Displacement of [3H]-GR113808 from human 5-HT4 receptor expressed in African green monkey COS7 cell membranes after 30 mins by liquid scintillation counting analysisDisplacement of [3H]-GR113808 from human 5-HT4 receptor expressed in African green monkey COS7 cell membranes after 30 mins by liquid scintillation counting analysis
ChEMBL 420 8 2 6 2.6 COc1cc(N)c(Cl)cc1C(=O)N[C@H]1CCN(CCCn2cccc2)C[C@H]1OC 10.1016/j.ejmech.2015.12.006
CHEMBL3758932 137193 0 None - 0 Human 6.2 pIC50 = 6.2 Binding
Displacement of [3H]-GR113808 from human 5-HT4 receptor expressed in African green monkey COS7 cell membranes after 30 mins by liquid scintillation counting analysisDisplacement of [3H]-GR113808 from human 5-HT4 receptor expressed in African green monkey COS7 cell membranes after 30 mins by liquid scintillation counting analysis
ChEMBL 420 8 2 6 2.6 COc1cc(N)c(Cl)cc1C(=O)N[C@H]1CCN(CCCn2cccc2)C[C@H]1OC 10.1016/j.ejmech.2015.12.006
127027375 137315 0 None - 0 Human 7.2 pIC50 = 7.2 Binding
Displacement of [3H]-GR113808 from human 5-HT4 receptor expressed in African green monkey COS7 cell membranes after 30 mins by liquid scintillation counting analysisDisplacement of [3H]-GR113808 from human 5-HT4 receptor expressed in African green monkey COS7 cell membranes after 30 mins by liquid scintillation counting analysis
ChEMBL 542 9 2 6 3.6 COc1cc(N)c(Cl)cc1C(=O)N[C@H]1CCN(CCC(=O)N2CCC(Cc3ccccc3)CC2)C[C@H]1OC 10.1016/j.ejmech.2015.12.006
CHEMBL3759928 137315 0 None - 0 Human 7.2 pIC50 = 7.2 Binding
Displacement of [3H]-GR113808 from human 5-HT4 receptor expressed in African green monkey COS7 cell membranes after 30 mins by liquid scintillation counting analysisDisplacement of [3H]-GR113808 from human 5-HT4 receptor expressed in African green monkey COS7 cell membranes after 30 mins by liquid scintillation counting analysis
ChEMBL 542 9 2 6 3.6 COc1cc(N)c(Cl)cc1C(=O)N[C@H]1CCN(CCC(=O)N2CCC(Cc3ccccc3)CC2)C[C@H]1OC 10.1016/j.ejmech.2015.12.006
25016330 137118 0 None - 0 Human 7.2 pIC50 = 7.2 Binding
Displacement of [3H]-GR113808 from human 5-HT4 receptor expressed in African green monkey COS7 cell membranes after 30 mins by liquid scintillation counting analysisDisplacement of [3H]-GR113808 from human 5-HT4 receptor expressed in African green monkey COS7 cell membranes after 30 mins by liquid scintillation counting analysis
ChEMBL 480 7 2 6 2.6 COc1cc(N)c(Cl)cc1C(=O)N[C@@H]1CCN(CC2CCN(C(=O)C(C)C)CC2)C[C@@H]1OC 10.1016/j.ejmech.2015.12.006
CHEMBL3758309 137118 0 None - 0 Human 7.2 pIC50 = 7.2 Binding
Displacement of [3H]-GR113808 from human 5-HT4 receptor expressed in African green monkey COS7 cell membranes after 30 mins by liquid scintillation counting analysisDisplacement of [3H]-GR113808 from human 5-HT4 receptor expressed in African green monkey COS7 cell membranes after 30 mins by liquid scintillation counting analysis
ChEMBL 480 7 2 6 2.6 COc1cc(N)c(Cl)cc1C(=O)N[C@@H]1CCN(CC2CCN(C(=O)C(C)C)CC2)C[C@@H]1OC 10.1016/j.ejmech.2015.12.006
155543353 172729 0 None - 1 Human 8.1 pIC50 = 8.1 Binding
Displacement of [3H]-GR 113808 from recombinant human brain 5HT4 receptor measured after 60 mins by radio ligand binding assayDisplacement of [3H]-GR 113808 from recombinant human brain 5HT4 receptor measured after 60 mins by radio ligand binding assay
ChEMBL 418 7 3 6 4.2 COc1cc(N)c(Cl)cc1C(=O)CCC1CCN(Cc2ccc(O)c(O)c2)CC1 10.1016/j.ejmech.2019.111596
CHEMBL4526049 172729 0 None - 1 Human 8.1 pIC50 = 8.1 Binding
Displacement of [3H]-GR 113808 from recombinant human brain 5HT4 receptor measured after 60 mins by radio ligand binding assayDisplacement of [3H]-GR 113808 from recombinant human brain 5HT4 receptor measured after 60 mins by radio ligand binding assay
ChEMBL 418 7 3 6 4.2 COc1cc(N)c(Cl)cc1C(=O)CCC1CCN(Cc2ccc(O)c(O)c2)CC1 10.1016/j.ejmech.2019.111596
10620001 33978 0 None - 0 Guinea pig 8.1 pIC50 = 8.1 Binding
Ability to antagonize 5-HT-evoked contractions mediated through 5-hydroxytryptamine 4 receptor activation in the guinea pig distal colon LMMPAbility to antagonize 5-HT-evoked contractions mediated through 5-hydroxytryptamine 4 receptor activation in the guinea pig distal colon LMMP
ChEMBL 383 6 1 4 4.1 CCCCN1CCC(CNC(=O)c2c3n(c4ccccc24)CCCCO3)CC1 10.1021/jm00024a002
CHEMBL142621 33978 0 None - 0 Guinea pig 8.1 pIC50 = 8.1 Binding
Ability to antagonize 5-HT-evoked contractions mediated through 5-hydroxytryptamine 4 receptor activation in the guinea pig distal colon LMMPAbility to antagonize 5-HT-evoked contractions mediated through 5-hydroxytryptamine 4 receptor activation in the guinea pig distal colon LMMP
ChEMBL 383 6 1 4 4.1 CCCCN1CCC(CNC(=O)c2c3n(c4ccccc24)CCCCO3)CC1 10.1021/jm00024a002
10717193 16603 0 None - 1 Human 6.2 pIC50 = 6.2 Binding
Antagonist activity at 5TH4 receptor (unknown origin)Antagonist activity at 5TH4 receptor (unknown origin)
ChEMBL 423 6 1 6 3.6 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCN(c2ccc(Cl)cc2)CC1 10.1039/C1MD00213A
CHEMBL124485 16603 0 None - 1 Human 6.2 pIC50 = 6.2 Binding
Antagonist activity at 5TH4 receptor (unknown origin)Antagonist activity at 5TH4 receptor (unknown origin)
ChEMBL 423 6 1 6 3.6 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCN(c2ccc(Cl)cc2)CC1 10.1039/C1MD00213A
68592631 137199 0 None - 0 Human 7.1 pIC50 = 7.1 Binding
Displacement of [3H]-GR113808 from human 5-HT4 receptor expressed in African green monkey COS7 cell membranes after 30 mins by liquid scintillation counting analysisDisplacement of [3H]-GR113808 from human 5-HT4 receptor expressed in African green monkey COS7 cell membranes after 30 mins by liquid scintillation counting analysis
ChEMBL 495 7 3 6 2.6 COc1cc(N)c(Cl)cc1C(=O)N[C@H]1CCN(CC2CCN(C(=O)NC(C)C)CC2)C[C@H]1OC 10.1016/j.ejmech.2015.12.006
CHEMBL3758976 137199 0 None - 0 Human 7.1 pIC50 = 7.1 Binding
Displacement of [3H]-GR113808 from human 5-HT4 receptor expressed in African green monkey COS7 cell membranes after 30 mins by liquid scintillation counting analysisDisplacement of [3H]-GR113808 from human 5-HT4 receptor expressed in African green monkey COS7 cell membranes after 30 mins by liquid scintillation counting analysis
ChEMBL 495 7 3 6 2.6 COc1cc(N)c(Cl)cc1C(=O)N[C@H]1CCN(CC2CCN(C(=O)NC(C)C)CC2)C[C@H]1OC 10.1016/j.ejmech.2015.12.006
3157 1442 69 None -27 12 Guinea pig 6.1 pIC50 = 6.1 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
ChEMBL 451 4 2 8 1.5 COc1cc2nc([nH]c(=N)c2cc1OC)N1CCN(CC1)C(=O)C1COc2c(O1)cccc2 nan
7170 1442 69 None -27 12 Guinea pig 6.1 pIC50 = 6.1 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
ChEMBL 451 4 2 8 1.5 COc1cc2nc([nH]c(=N)c2cc1OC)N1CCN(CC1)C(=O)C1COc2c(O1)cccc2 nan
954 1442 69 None -27 12 Guinea pig 6.1 pIC50 = 6.1 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
ChEMBL 451 4 2 8 1.5 COc1cc2nc([nH]c(=N)c2cc1OC)N1CCN(CC1)C(=O)C1COc2c(O1)cccc2 nan
CHEMBL707 1442 69 None -27 12 Guinea pig 6.1 pIC50 = 6.1 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
ChEMBL 451 4 2 8 1.5 COc1cc2nc([nH]c(=N)c2cc1OC)N1CCN(CC1)C(=O)C1COc2c(O1)cccc2 nan
DB00590 1442 69 None -27 12 Guinea pig 6.1 pIC50 = 6.1 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
ChEMBL 451 4 2 8 1.5 COc1cc2nc([nH]c(=N)c2cc1OC)N1CCN(CC1)C(=O)C1COc2c(O1)cccc2 nan
68593153 137134 0 None - 0 Human 7.1 pIC50 = 7.1 Binding
Displacement of [3H]-GR113808 from human 5-HT4 receptor expressed in African green monkey COS7 cell membranes after 30 mins by liquid scintillation counting analysisDisplacement of [3H]-GR113808 from human 5-HT4 receptor expressed in African green monkey COS7 cell membranes after 30 mins by liquid scintillation counting analysis
ChEMBL 494 8 2 6 3.0 COc1cc(N)c(Cl)cc1C(=O)N[C@H]1CCN(CC2CCN(C(=O)CC(C)C)CC2)C[C@H]1OC 10.1016/j.ejmech.2015.12.006
CHEMBL3758433 137134 0 None - 0 Human 7.1 pIC50 = 7.1 Binding
Displacement of [3H]-GR113808 from human 5-HT4 receptor expressed in African green monkey COS7 cell membranes after 30 mins by liquid scintillation counting analysisDisplacement of [3H]-GR113808 from human 5-HT4 receptor expressed in African green monkey COS7 cell membranes after 30 mins by liquid scintillation counting analysis
ChEMBL 494 8 2 6 3.0 COc1cc(N)c(Cl)cc1C(=O)N[C@H]1CCN(CC2CCN(C(=O)CC(C)C)CC2)C[C@H]1OC 10.1016/j.ejmech.2015.12.006
10545343 164334 0 None - 0 Guinea pig 7.1 pIC50 = 7.1 Binding
Ability to antagonize 5-HT-evoked contractions mediated through 5-hydroxytryptamine 4 receptor activation in the guinea pig distal colon LMMPAbility to antagonize 5-HT-evoked contractions mediated through 5-hydroxytryptamine 4 receptor activation in the guinea pig distal colon LMMP
ChEMBL 343 7 2 3 3.4 CCCCN1CCC(CNC(=O)c2c(OC)[nH]c3ccccc23)CC1 10.1021/jm00024a002
CHEMBL422116 164334 0 None - 0 Guinea pig 7.1 pIC50 = 7.1 Binding
Ability to antagonize 5-HT-evoked contractions mediated through 5-hydroxytryptamine 4 receptor activation in the guinea pig distal colon LMMPAbility to antagonize 5-HT-evoked contractions mediated through 5-hydroxytryptamine 4 receptor activation in the guinea pig distal colon LMMP
ChEMBL 343 7 2 3 3.4 CCCCN1CCC(CNC(=O)c2c(OC)[nH]c3ccccc23)CC1 10.1021/jm00024a002
151537 162114 43 None - 1 Guinea pig 5.1 pIC50 = 5.1 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
ChEMBL 543 5 6 12 0.0 COc1cccc2c1C(=O)c1c(O)c3c(c(O)c1C2=O)C[C@@](O)(C(=O)CO)C[C@@H]3O[C@H]1C[C@H](N)[C@@H](O)[C@H](C)O1 nan
41867 162114 43 None - 1 Guinea pig 5.1 pIC50 = 5.1 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
ChEMBL 543 5 6 12 0.0 COc1cccc2c1C(=O)c1c(O)c3c(c(O)c1C2=O)C[C@@](O)(C(=O)CO)C[C@@H]3O[C@H]1C[C@H](N)[C@@H](O)[C@H](C)O1 nan
CHEMBL417 162114 43 None - 1 Guinea pig 5.1 pIC50 = 5.1 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
ChEMBL 543 5 6 12 0.0 COc1cccc2c1C(=O)c1c(O)c3c(c(O)c1C2=O)C[C@@](O)(C(=O)CO)C[C@@H]3O[C@H]1C[C@H](N)[C@@H](O)[C@H](C)O1 nan
5991 202221 68 None 2 5 Guinea pig 5.1 pIC50 = 5.1 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
ChEMBL 296 0 2 2 3.6 C#C[C@]1(O)CC[C@H]2[C@@H]3CCc4cc(O)ccc4[C@H]3CC[C@@]21C nan
CHEMBL691 202221 68 None 2 5 Guinea pig 5.1 pIC50 = 5.1 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
ChEMBL 296 0 2 2 3.6 C#C[C@]1(O)CC[C@H]2[C@@H]3CCc4cc(O)ccc4[C@H]3CC[C@@]21C nan
68593732 137298 0 None - 0 Human 6.1 pIC50 = 6.1 Binding
Displacement of [3H]-GR113808 from human 5-HT4 receptor expressed in African green monkey COS7 cell membranes after 30 mins by liquid scintillation counting analysisDisplacement of [3H]-GR113808 from human 5-HT4 receptor expressed in African green monkey COS7 cell membranes after 30 mins by liquid scintillation counting analysis
ChEMBL 480 8 2 6 2.8 CCC(=O)N1CCC(CCN2CC[C@H](NC(=O)c3cc(Cl)c(N)cc3OC)[C@H](OC)C2)CC1 10.1016/j.ejmech.2015.12.006
CHEMBL3759824 137298 0 None - 0 Human 6.1 pIC50 = 6.1 Binding
Displacement of [3H]-GR113808 from human 5-HT4 receptor expressed in African green monkey COS7 cell membranes after 30 mins by liquid scintillation counting analysisDisplacement of [3H]-GR113808 from human 5-HT4 receptor expressed in African green monkey COS7 cell membranes after 30 mins by liquid scintillation counting analysis
ChEMBL 480 8 2 6 2.8 CCC(=O)N1CCC(CCN2CC[C@H](NC(=O)c3cc(Cl)c(N)cc3OC)[C@H](OC)C2)CC1 10.1016/j.ejmech.2015.12.006
119584 2557 99 None -1 6 Guinea pig 6.1 pIC50 = 6.1 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
ChEMBL 421 7 2 5 3.1 CCOc1cc(N)c(cc1C(=O)NCC1OCCN(C1)Cc1ccc(cc1)F)Cl nan
1848 2557 99 None -1 6 Guinea pig 6.1 pIC50 = 6.1 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
ChEMBL 421 7 2 5 3.1 CCOc1cc(N)c(cc1C(=O)NCC1OCCN(C1)Cc1ccc(cc1)F)Cl nan
242 2557 99 None -1 6 Guinea pig 6.1 pIC50 = 6.1 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
ChEMBL 421 7 2 5 3.1 CCOc1cc(N)c(cc1C(=O)NCC1OCCN(C1)Cc1ccc(cc1)F)Cl nan
CHEMBL60889 2557 99 None -1 6 Guinea pig 6.1 pIC50 = 6.1 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
ChEMBL 421 7 2 5 3.1 CCOc1cc(N)c(cc1C(=O)NCC1OCCN(C1)Cc1ccc(cc1)F)Cl nan
DB11675 2557 99 None -1 6 Guinea pig 6.1 pIC50 = 6.1 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
ChEMBL 421 7 2 5 3.1 CCOc1cc(N)c(cc1C(=O)NCC1OCCN(C1)Cc1ccc(cc1)F)Cl nan
44384672 59390 0 None - 0 Guinea pig 8.0 pIC50 = 8.0 Binding
Inhibitory activity against 5-hydroxytryptamine 4 receptor of guinea pig striatum using [3H]GR-113808 as radioligandInhibitory activity against 5-hydroxytryptamine 4 receptor of guinea pig striatum using [3H]GR-113808 as radioligand
ChEMBL 437 6 3 6 1.3 COc1cc(N)c(Cl)cc1C(=O)NC1CCN(CC2CCN(C(=O)CN)CC2)CC1 10.1016/s0960-894x(02)00060-4
CHEMBL172314 59390 0 None - 0 Guinea pig 8.0 pIC50 = 8.0 Binding
Inhibitory activity against 5-hydroxytryptamine 4 receptor of guinea pig striatum using [3H]GR-113808 as radioligandInhibitory activity against 5-hydroxytryptamine 4 receptor of guinea pig striatum using [3H]GR-113808 as radioligand
ChEMBL 437 6 3 6 1.3 COc1cc(N)c(Cl)cc1C(=O)NC1CCN(CC2CCN(C(=O)CN)CC2)CC1 10.1016/s0960-894x(02)00060-4
44384738 60027 0 None - 0 Guinea pig 8.0 pIC50 = 8.0 Binding
Inhibitory activity against 5-hydroxytryptamine 4 receptor of guinea pig striatum using [3H]GR-113808 as radioligandInhibitory activity against 5-hydroxytryptamine 4 receptor of guinea pig striatum using [3H]GR-113808 as radioligand
ChEMBL 451 7 3 6 1.7 COc1cc(N)c(Cl)cc1C(=O)NC1CCN(CC2CCN(C(=O)CCN)CC2)CC1 10.1016/s0960-894x(02)00060-4
CHEMBL174524 60027 0 None - 0 Guinea pig 8.0 pIC50 = 8.0 Binding
Inhibitory activity against 5-hydroxytryptamine 4 receptor of guinea pig striatum using [3H]GR-113808 as radioligandInhibitory activity against 5-hydroxytryptamine 4 receptor of guinea pig striatum using [3H]GR-113808 as radioligand
ChEMBL 451 7 3 6 1.7 COc1cc(N)c(Cl)cc1C(=O)NC1CCN(CC2CCN(C(=O)CCN)CC2)CC1 10.1016/s0960-894x(02)00060-4
1782 2482 81 None -12 22 Guinea pig 6.0 pIC50 = 6.0 Binding
Concentration of compound required to inhibit the binding of radioligand [3H]GR-113808 to serotonin 5-hydroxytryptamine 4 receptor in guinea-pig striatumConcentration of compound required to inhibit the binding of radioligand [3H]GR-113808 to serotonin 5-hydroxytryptamine 4 receptor in guinea-pig striatum
ChEMBL 299 7 2 4 2.0 CCN(CCNC(=O)c1cc(Cl)c(cc1OC)N)CC 10.1021/jm020270n
241 2482 81 None -12 22 Guinea pig 6.0 pIC50 = 6.0 Binding
Concentration of compound required to inhibit the binding of radioligand [3H]GR-113808 to serotonin 5-hydroxytryptamine 4 receptor in guinea-pig striatumConcentration of compound required to inhibit the binding of radioligand [3H]GR-113808 to serotonin 5-hydroxytryptamine 4 receptor in guinea-pig striatum
ChEMBL 299 7 2 4 2.0 CCN(CCNC(=O)c1cc(Cl)c(cc1OC)N)CC 10.1021/jm020270n
4168 2482 81 None -12 22 Guinea pig 6.0 pIC50 = 6.0 Binding
Concentration of compound required to inhibit the binding of radioligand [3H]GR-113808 to serotonin 5-hydroxytryptamine 4 receptor in guinea-pig striatumConcentration of compound required to inhibit the binding of radioligand [3H]GR-113808 to serotonin 5-hydroxytryptamine 4 receptor in guinea-pig striatum
ChEMBL 299 7 2 4 2.0 CCN(CCNC(=O)c1cc(Cl)c(cc1OC)N)CC 10.1021/jm020270n
CHEMBL86 2482 81 None -12 22 Guinea pig 6.0 pIC50 = 6.0 Binding
Concentration of compound required to inhibit the binding of radioligand [3H]GR-113808 to serotonin 5-hydroxytryptamine 4 receptor in guinea-pig striatumConcentration of compound required to inhibit the binding of radioligand [3H]GR-113808 to serotonin 5-hydroxytryptamine 4 receptor in guinea-pig striatum
ChEMBL 299 7 2 4 2.0 CCN(CCNC(=O)c1cc(Cl)c(cc1OC)N)CC 10.1021/jm020270n
DB01233 2482 81 None -12 22 Guinea pig 6.0 pIC50 = 6.0 Binding
Concentration of compound required to inhibit the binding of radioligand [3H]GR-113808 to serotonin 5-hydroxytryptamine 4 receptor in guinea-pig striatumConcentration of compound required to inhibit the binding of radioligand [3H]GR-113808 to serotonin 5-hydroxytryptamine 4 receptor in guinea-pig striatum
ChEMBL 299 7 2 4 2.0 CCN(CCNC(=O)c1cc(Cl)c(cc1OC)N)CC 10.1021/jm020270n
90644472 111787 0 None - 1 Human 6.0 pIC50 = 6.0 Binding
Antagonist activity at Rluc-tagged human 5HT4R expressed in human SH-SY5Y cells assessed as inhibition of serotonin-induced receptor/Gbeta1 coupling by BRET assayAntagonist activity at Rluc-tagged human 5HT4R expressed in human SH-SY5Y cells assessed as inhibition of serotonin-induced receptor/Gbeta1 coupling by BRET assay
ChEMBL 339 5 0 4 3.1 COc1cc2c3c(cccc3n1)CN(CCCN1CCCCC1)C2=O 10.1016/j.ejmech.2014.05.015
CHEMBL3291077 111787 0 None - 1 Human 6.0 pIC50 = 6.0 Binding
Antagonist activity at Rluc-tagged human 5HT4R expressed in human SH-SY5Y cells assessed as inhibition of serotonin-induced receptor/Gbeta1 coupling by BRET assayAntagonist activity at Rluc-tagged human 5HT4R expressed in human SH-SY5Y cells assessed as inhibition of serotonin-induced receptor/Gbeta1 coupling by BRET assay
ChEMBL 339 5 0 4 3.1 COc1cc2c3c(cccc3n1)CN(CCCN1CCCCC1)C2=O 10.1016/j.ejmech.2014.05.015
127028946 137149 0 None - 0 Human 6.0 pIC50 = 6.0 Binding
Displacement of [3H]-GR113808 from human 5-HT4 receptor expressed in African green monkey COS7 cell membranes after 30 mins by liquid scintillation counting analysisDisplacement of [3H]-GR113808 from human 5-HT4 receptor expressed in African green monkey COS7 cell membranes after 30 mins by liquid scintillation counting analysis
ChEMBL 438 7 2 6 1.8 COc1cc(N)c(Cl)cc1C(=O)N[C@H]1CCN(CCC(=O)N2CCCC2)C[C@H]1OC 10.1016/j.ejmech.2015.12.006
CHEMBL3758578 137149 0 None - 0 Human 6.0 pIC50 = 6.0 Binding
Displacement of [3H]-GR113808 from human 5-HT4 receptor expressed in African green monkey COS7 cell membranes after 30 mins by liquid scintillation counting analysisDisplacement of [3H]-GR113808 from human 5-HT4 receptor expressed in African green monkey COS7 cell membranes after 30 mins by liquid scintillation counting analysis
ChEMBL 438 7 2 6 1.8 COc1cc(N)c(Cl)cc1C(=O)N[C@H]1CCN(CCC(=O)N2CCCC2)C[C@H]1OC 10.1016/j.ejmech.2015.12.006
10531 1392 18 None -87 24 Guinea pig 6.0 pIC50 = 6.0 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
ChEMBL 583 4 3 6 2.1 CN1C[C@@H](C[C@H]2[C@H]1Cc1c[nH]c3c1c2ccc3)C(=O)N[C@]1(C)O[C@@]2(N(C1=O)[C@@H](Cc1ccccc1)C(=O)N1[C@H]2CCC1)O nan
121 1392 18 None -87 24 Guinea pig 6.0 pIC50 = 6.0 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
ChEMBL 583 4 3 6 2.1 CN1C[C@@H](C[C@H]2[C@H]1Cc1c[nH]c3c1c2ccc3)C(=O)N[C@]1(C)O[C@@]2(N(C1=O)[C@@H](Cc1ccccc1)C(=O)N1[C@H]2CCC1)O nan
888 1392 18 None -87 24 Guinea pig 6.0 pIC50 = 6.0 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
ChEMBL 583 4 3 6 2.1 CN1C[C@@H](C[C@H]2[C@H]1Cc1c[nH]c3c1c2ccc3)C(=O)N[C@]1(C)O[C@@]2(N(C1=O)[C@@H](Cc1ccccc1)C(=O)N1[C@H]2CCC1)O nan
CHEMBL1732 1392 18 None -87 24 Guinea pig 6.0 pIC50 = 6.0 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
ChEMBL 583 4 3 6 2.1 CN1C[C@@H](C[C@H]2[C@H]1Cc1c[nH]c3c1c2ccc3)C(=O)N[C@]1(C)O[C@@]2(N(C1=O)[C@@H](Cc1ccccc1)C(=O)N1[C@H]2CCC1)O nan
DB00320 1392 18 None -87 24 Guinea pig 6.0 pIC50 = 6.0 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
ChEMBL 583 4 3 6 2.1 CN1C[C@@H](C[C@H]2[C@H]1Cc1c[nH]c3c1c2ccc3)C(=O)N[C@]1(C)O[C@@]2(N(C1=O)[C@@H](Cc1ccccc1)C(=O)N1[C@H]2CCC1)O nan
127027702 137131 0 None - 0 Human 6.0 pIC50 = 6.0 Binding
Displacement of [3H]-GR113808 from human 5-HT4 receptor expressed in African green monkey COS7 cell membranes after 30 mins by liquid scintillation counting analysisDisplacement of [3H]-GR113808 from human 5-HT4 receptor expressed in African green monkey COS7 cell membranes after 30 mins by liquid scintillation counting analysis
ChEMBL 454 7 2 7 1.0 COc1cc(N)c(Cl)cc1C(=O)N[C@H]1CCN(CCC(=O)N2CCOCC2)C[C@H]1OC 10.1016/j.ejmech.2015.12.006
CHEMBL3758410 137131 0 None - 0 Human 6.0 pIC50 = 6.0 Binding
Displacement of [3H]-GR113808 from human 5-HT4 receptor expressed in African green monkey COS7 cell membranes after 30 mins by liquid scintillation counting analysisDisplacement of [3H]-GR113808 from human 5-HT4 receptor expressed in African green monkey COS7 cell membranes after 30 mins by liquid scintillation counting analysis
ChEMBL 454 7 2 7 1.0 COc1cc(N)c(Cl)cc1C(=O)N[C@H]1CCN(CCC(=O)N2CCOCC2)C[C@H]1OC 10.1016/j.ejmech.2015.12.006
3066250 69943 2 None - 0 Guinea pig 5.0 pIC50 = 5.0 Binding
Inhibitory activity against 5-hydroxytryptamine 4 receptor in guinea pigInhibitory activity against 5-hydroxytryptamine 4 receptor in guinea pig
ChEMBL 242 2 2 2 2.9 COc1ccc2[nH]c(C)c(C3=CCNCC3)c2c1 10.1016/j.bmcl.2005.06.067
CHEMBL194305 69943 2 None - 0 Guinea pig 5.0 pIC50 = 5.0 Binding
Inhibitory activity against 5-hydroxytryptamine 4 receptor in guinea pigInhibitory activity against 5-hydroxytryptamine 4 receptor in guinea pig
ChEMBL 242 2 2 2 2.9 COc1ccc2[nH]c(C)c(C3=CCNCC3)c2c1 10.1016/j.bmcl.2005.06.067
44626294 197321 0 None - 0 Human 5.0 pIC50 = 5 Binding
Displacement of [3H]GR-113808 from human recombinant 5-HT4 receptorDisplacement of [3H]GR-113808 from human recombinant 5-HT4 receptor
ChEMBL 517 7 4 7 3.5 COc1cc(N)c(Cl)cc1C(=O)N[C@H]1CCN(C[C@@H]2CCCC[C@@]2(O)c2cccc(O)c2)C[C@H]1OC 10.1016/j.bmcl.2009.08.016
CHEMBL585567 197321 0 None - 0 Human 5.0 pIC50 = 5 Binding
Displacement of [3H]GR-113808 from human recombinant 5-HT4 receptorDisplacement of [3H]GR-113808 from human recombinant 5-HT4 receptor
ChEMBL 517 7 4 7 3.5 COc1cc(N)c(Cl)cc1C(=O)N[C@H]1CCN(C[C@@H]2CCCC[C@@]2(O)c2cccc(O)c2)C[C@H]1OC 10.1016/j.bmcl.2009.08.016
121881 3434 21 None 2 15 Guinea pig 10.7 pKd = 10.7 Binding
Binding affinity to 5HT4 receptor in guinea pig distal colonBinding affinity to 5HT4 receptor in guinea pig distal colon
ChEMBL 382 6 1 6 3.4 CCCCN1CCC(CC1)COC(=O)c1cc(Cl)c(c2c1OCCO2)N 10.1016/j.bmcl.2013.09.097
256 3434 21 None 2 15 Guinea pig 10.7 pKd = 10.7 Binding
Binding affinity to 5HT4 receptor in guinea pig distal colonBinding affinity to 5HT4 receptor in guinea pig distal colon
ChEMBL 382 6 1 6 3.4 CCCCN1CCC(CC1)COC(=O)c1cc(Cl)c(c2c1OCCO2)N 10.1016/j.bmcl.2013.09.097
CHEMBL68131 3434 21 None 2 15 Guinea pig 10.7 pKd = 10.7 Binding
Binding affinity to 5HT4 receptor in guinea pig distal colonBinding affinity to 5HT4 receptor in guinea pig distal colon
ChEMBL 382 6 1 6 3.4 CCCCN1CCC(CC1)COC(=O)c1cc(Cl)c(c2c1OCCO2)N 10.1016/j.bmcl.2013.09.097
257 3437 9 None -1 4 Rat 9.5 pKd = 9.5 Binding
Binding affinity to 5HT4 receptor in rat striatal membranesBinding affinity to 5HT4 receptor in rat striatal membranes
ChEMBL 474 6 1 6 3.3 CCCCN1CCC(CC1)COC(=O)c1cc(I)c(c2c1OCCO2)N 10.1016/j.bmcl.2013.09.097
5311423 3437 9 None -1 4 Rat 9.5 pKd = 9.5 Binding
Binding affinity to 5HT4 receptor in rat striatal membranesBinding affinity to 5HT4 receptor in rat striatal membranes
ChEMBL 474 6 1 6 3.3 CCCCN1CCC(CC1)COC(=O)c1cc(I)c(c2c1OCCO2)N 10.1016/j.bmcl.2013.09.097
CHEMBL114112 3437 9 None -1 4 Rat 9.5 pKd = 9.5 Binding
Binding affinity to 5HT4 receptor in rat striatal membranesBinding affinity to 5HT4 receptor in rat striatal membranes
ChEMBL 474 6 1 6 3.3 CCCCN1CCC(CC1)COC(=O)c1cc(I)c(c2c1OCCO2)N 10.1016/j.bmcl.2013.09.097
76310958 105247 1 None -1 2 Rat 9.5 pKd = 9.5 Binding
Binding affinity to 5HT4 receptor in rat striatal membranesBinding affinity to 5HT4 receptor in rat striatal membranes
ChEMBL 340 3 1 6 2.2 CN1CCC(COC(=O)c2cc(Cl)c(N)c3c2OCCO3)CC1 10.1016/j.bmcl.2013.09.097
CHEMBL3126112 105247 1 None -1 2 Rat 9.5 pKd = 9.5 Binding
Binding affinity to 5HT4 receptor in rat striatal membranesBinding affinity to 5HT4 receptor in rat striatal membranes
ChEMBL 340 3 1 6 2.2 CN1CCC(COC(=O)c2cc(Cl)c(N)c3c2OCCO3)CC1 10.1016/j.bmcl.2013.09.097
CHEMBL5182119 105247 1 None -1 2 Rat 9.5 pKd = 9.5 Binding
Binding affinity to 5HT4 receptor in rat striatal membranesBinding affinity to 5HT4 receptor in rat striatal membranes
ChEMBL 340 3 1 6 2.2 CN1CCC(COC(=O)c2cc(Cl)c(N)c3c2OCCO3)CC1 10.1016/j.bmcl.2013.09.097
119376 1811 41 None -1 26 Human 7.8 pKd = 7.8 Binding
Binding affinity to human 5HT4 receptor expressed in HEK293 cells by saturation binding methodBinding affinity to human 5HT4 receptor expressed in HEK293 cells by saturation binding method
ChEMBL 393 7 1 6 1.6 O=C(c1cn(c2c1cccc2)C)OCC1CCN(CC1)CCNS(=O)(=O)C 10.1021/np0601760
247 1811 41 None -1 26 Human 7.8 pKd = 7.8 Binding
Binding affinity to human 5HT4 receptor expressed in HEK293 cells by saturation binding methodBinding affinity to human 5HT4 receptor expressed in HEK293 cells by saturation binding method
ChEMBL 393 7 1 6 1.6 O=C(c1cn(c2c1cccc2)C)OCC1CCN(CC1)CCNS(=O)(=O)C 10.1021/np0601760
CHEMBL33884 1811 41 None -1 26 Human 7.8 pKd = 7.8 Binding
Binding affinity to human 5HT4 receptor expressed in HEK293 cells by saturation binding methodBinding affinity to human 5HT4 receptor expressed in HEK293 cells by saturation binding method
ChEMBL 393 7 1 6 1.6 O=C(c1cn(c2c1cccc2)C)OCC1CCN(CC1)CCNS(=O)(=O)C 10.1021/np0601760
243 3153 85 None 12 34 Human 8.7 pKd = 8.7 Binding
Binding affinity to 5-HT4 receptor (unknown origin) assessed as dissociation constantBinding affinity to 5-HT4 receptor (unknown origin) assessed as dissociation constant
ChEMBL 367 6 2 5 2.1 COCCCN1CCC(CC1)NC(=O)c1cc(Cl)c(c2c1OCC2)N 10.1021/acs.jmedchem.2c00633
3052762 3153 85 None 12 34 Human 8.7 pKd = 8.7 Binding
Binding affinity to 5-HT4 receptor (unknown origin) assessed as dissociation constantBinding affinity to 5-HT4 receptor (unknown origin) assessed as dissociation constant
ChEMBL 367 6 2 5 2.1 COCCCN1CCC(CC1)NC(=O)c1cc(Cl)c(c2c1OCC2)N 10.1021/acs.jmedchem.2c00633
3502 3153 85 None 12 34 Human 8.7 pKd = 8.7 Binding
Binding affinity to 5-HT4 receptor (unknown origin) assessed as dissociation constantBinding affinity to 5-HT4 receptor (unknown origin) assessed as dissociation constant
ChEMBL 367 6 2 5 2.1 COCCCN1CCC(CC1)NC(=O)c1cc(Cl)c(c2c1OCC2)N 10.1021/acs.jmedchem.2c00633
CHEMBL117287 3153 85 None 12 34 Human 8.7 pKd = 8.7 Binding
Binding affinity to 5-HT4 receptor (unknown origin) assessed as dissociation constantBinding affinity to 5-HT4 receptor (unknown origin) assessed as dissociation constant
ChEMBL 367 6 2 5 2.1 COCCCN1CCC(CC1)NC(=O)c1cc(Cl)c(c2c1OCC2)N 10.1021/acs.jmedchem.2c00633
DB06480 3153 85 None 12 34 Human 8.7 pKd = 8.7 Binding
Binding affinity to 5-HT4 receptor (unknown origin) assessed as dissociation constantBinding affinity to 5-HT4 receptor (unknown origin) assessed as dissociation constant
ChEMBL 367 6 2 5 2.1 COCCCN1CCC(CC1)NC(=O)c1cc(Cl)c(c2c1OCC2)N 10.1021/acs.jmedchem.2c00633
121881 3434 21 None 2 15 Guinea pig 10.9 pKi = 10.9 Binding
Compound was tested for binding affinity against 5-HT4 receptor in guinea pig striata using [3H]GR-113808 as radioligandCompound was tested for binding affinity against 5-HT4 receptor in guinea pig striata using [3H]GR-113808 as radioligand
ChEMBL 382 6 1 6 3.4 CCCCN1CCC(CC1)COC(=O)c1cc(Cl)c(c2c1OCCO2)N 10.1016/S0960-894X(01)80414-5
256 3434 21 None 2 15 Guinea pig 10.9 pKi = 10.9 Binding
Compound was tested for binding affinity against 5-HT4 receptor in guinea pig striata using [3H]GR-113808 as radioligandCompound was tested for binding affinity against 5-HT4 receptor in guinea pig striata using [3H]GR-113808 as radioligand
ChEMBL 382 6 1 6 3.4 CCCCN1CCC(CC1)COC(=O)c1cc(Cl)c(c2c1OCCO2)N 10.1016/S0960-894X(01)80414-5
CHEMBL68131 3434 21 None 2 15 Guinea pig 10.9 pKi = 10.9 Binding
Compound was tested for binding affinity against 5-HT4 receptor in guinea pig striata using [3H]GR-113808 as radioligandCompound was tested for binding affinity against 5-HT4 receptor in guinea pig striata using [3H]GR-113808 as radioligand
ChEMBL 382 6 1 6 3.4 CCCCN1CCC(CC1)COC(=O)c1cc(Cl)c(c2c1OCCO2)N 10.1016/S0960-894X(01)80414-5
121881 3434 21 None -2 15 Human 10.8 pKi = 10.8 Binding
Binding affinity at 5HT4 receptorBinding affinity at 5HT4 receptor
ChEMBL 382 6 1 6 3.4 CCCCN1CCC(CC1)COC(=O)c1cc(Cl)c(c2c1OCCO2)N 10.1016/j.bmc.2008.11.045
256 3434 21 None -2 15 Human 10.8 pKi = 10.8 Binding
Binding affinity at 5HT4 receptorBinding affinity at 5HT4 receptor
ChEMBL 382 6 1 6 3.4 CCCCN1CCC(CC1)COC(=O)c1cc(Cl)c(c2c1OCCO2)N 10.1016/j.bmc.2008.11.045
CHEMBL68131 3434 21 None -2 15 Human 10.8 pKi = 10.8 Binding
Binding affinity at 5HT4 receptorBinding affinity at 5HT4 receptor
ChEMBL 382 6 1 6 3.4 CCCCN1CCC(CC1)COC(=O)c1cc(Cl)c(c2c1OCCO2)N 10.1016/j.bmc.2008.11.045
9936969 63803 0 None - 1 Human 10.8 pKi = 10.8 Binding
Inhibitory constant for human cloned 5-HT4 receptorInhibitory constant for human cloned 5-HT4 receptor
ChEMBL 534 9 1 7 2.2 O=C(NCC1CCN(CCCS(=O)(=O)N2CCN(C3CCCC3)CC2)CC1)c1cccc2c1OCCO2 10.1016/j.bmcl.2005.01.039
CHEMBL180835 63803 0 None - 1 Human 10.8 pKi = 10.8 Binding
Inhibitory constant for human cloned 5-HT4 receptorInhibitory constant for human cloned 5-HT4 receptor
ChEMBL 534 9 1 7 2.2 O=C(NCC1CCN(CCCS(=O)(=O)N2CCN(C3CCCC3)CC2)CC1)c1cccc2c1OCCO2 10.1016/j.bmcl.2005.01.039
44390256 64008 0 None - 1 Human 10.6 pKi = 10.6 Binding
Inhibitory constant for human cloned 5-HT4 receptorInhibitory constant for human cloned 5-HT4 receptor
ChEMBL 522 10 1 7 2.0 CCC(C)N1CCN(S(=O)(=O)CCCN2CCC(CNC(=O)c3cccc4c3OCCO4)CC2)CC1 10.1016/j.bmcl.2005.01.039
CHEMBL181202 64008 0 None - 1 Human 10.6 pKi = 10.6 Binding
Inhibitory constant for human cloned 5-HT4 receptorInhibitory constant for human cloned 5-HT4 receptor
ChEMBL 522 10 1 7 2.0 CCC(C)N1CCN(S(=O)(=O)CCCN2CCC(CNC(=O)c3cccc4c3OCCO4)CC2)CC1 10.1016/j.bmcl.2005.01.039
9914629 122599 0 None - 1 Human 10.6 pKi = 10.6 Binding
Inhibitory constant for human cloned 5-HT4 receptorInhibitory constant for human cloned 5-HT4 receptor
ChEMBL 519 8 1 6 3.3 O=C(NCC1CCN(CCCS(=O)(=O)N2CCC3(CCCC3)CC2)CC1)c1cccc2c1OCCO2 10.1016/j.bmcl.2005.01.039
CHEMBL361118 122599 0 None - 1 Human 10.6 pKi = 10.6 Binding
Inhibitory constant for human cloned 5-HT4 receptorInhibitory constant for human cloned 5-HT4 receptor
ChEMBL 519 8 1 6 3.3 O=C(NCC1CCN(CCCS(=O)(=O)N2CCC3(CCCC3)CC2)CC1)c1cccc2c1OCCO2 10.1016/j.bmcl.2005.01.039
9870916 63991 0 None - 1 Human 10.5 pKi = 10.5 Binding
Inhibitory constant for human cloned 5-HT4 receptorInhibitory constant for human cloned 5-HT4 receptor
ChEMBL 508 10 1 7 1.6 CCCN1CCN(S(=O)(=O)CCCN2CCC(CNC(=O)c3cccc4c3OCCO4)CC2)CC1 10.1016/j.bmcl.2005.01.039
CHEMBL181126 63991 0 None - 1 Human 10.5 pKi = 10.5 Binding
Inhibitory constant for human cloned 5-HT4 receptorInhibitory constant for human cloned 5-HT4 receptor
ChEMBL 508 10 1 7 1.6 CCCN1CCN(S(=O)(=O)CCCN2CCC(CNC(=O)c3cccc4c3OCCO4)CC2)CC1 10.1016/j.bmcl.2005.01.039
9892494 65137 0 None - 1 Human 10.5 pKi = 10.5 Binding
Inhibitory constant for human cloned 5-HT4 receptorInhibitory constant for human cloned 5-HT4 receptor
ChEMBL 508 9 1 7 1.6 CC(C)N1CCN(S(=O)(=O)CCCN2CCC(CNC(=O)c3cccc4c3OCCO4)CC2)CC1 10.1016/j.bmcl.2005.01.039
CHEMBL182999 65137 0 None - 1 Human 10.5 pKi = 10.5 Binding
Inhibitory constant for human cloned 5-HT4 receptorInhibitory constant for human cloned 5-HT4 receptor
ChEMBL 508 9 1 7 1.6 CC(C)N1CCN(S(=O)(=O)CCCN2CCC(CNC(=O)c3cccc4c3OCCO4)CC2)CC1 10.1016/j.bmcl.2005.01.039
9873926 129134 0 None - 1 Human 10.5 pKi = 10.5 Binding
Inhibitory constant for human cloned 5-HT4 receptorInhibitory constant for human cloned 5-HT4 receptor
ChEMBL 624 10 1 8 1.8 O=C(NCC1CCN(CCCS(=O)(=O)N2CCN(S(=O)(=O)c3ccc(F)cc3)CC2)CC1)c1cccc2c1OCCO2 10.1016/j.bmcl.2005.01.039
CHEMBL367354 129134 0 None - 1 Human 10.5 pKi = 10.5 Binding
Inhibitory constant for human cloned 5-HT4 receptorInhibitory constant for human cloned 5-HT4 receptor
ChEMBL 624 10 1 8 1.8 O=C(NCC1CCN(CCCS(=O)(=O)N2CCN(S(=O)(=O)c3ccc(F)cc3)CC2)CC1)c1cccc2c1OCCO2 10.1016/j.bmcl.2005.01.039
119376 1811 41 None -1 26 Human 10.4 pKi = 10.4 Binding
Displacement of [3H]GR113808 from human 5-HT4B receptor expressed in HEK293 cells after 1 hr by liquid scintillation counting analysisDisplacement of [3H]GR113808 from human 5-HT4B receptor expressed in HEK293 cells after 1 hr by liquid scintillation counting analysis
ChEMBL 393 7 1 6 1.6 O=C(c1cn(c2c1cccc2)C)OCC1CCN(CC1)CCNS(=O)(=O)C 10.1016/j.ejmech.2013.03.060
247 1811 41 None -1 26 Human 10.4 pKi = 10.4 Binding
Displacement of [3H]GR113808 from human 5-HT4B receptor expressed in HEK293 cells after 1 hr by liquid scintillation counting analysisDisplacement of [3H]GR113808 from human 5-HT4B receptor expressed in HEK293 cells after 1 hr by liquid scintillation counting analysis
ChEMBL 393 7 1 6 1.6 O=C(c1cn(c2c1cccc2)C)OCC1CCN(CC1)CCNS(=O)(=O)C 10.1016/j.ejmech.2013.03.060
CHEMBL33884 1811 41 None -1 26 Human 10.4 pKi = 10.4 Binding
Displacement of [3H]GR113808 from human 5-HT4B receptor expressed in HEK293 cells after 1 hr by liquid scintillation counting analysisDisplacement of [3H]GR113808 from human 5-HT4B receptor expressed in HEK293 cells after 1 hr by liquid scintillation counting analysis
ChEMBL 393 7 1 6 1.6 O=C(c1cn(c2c1cccc2)C)OCC1CCN(CC1)CCNS(=O)(=O)C 10.1016/j.ejmech.2013.03.060
119376 1811 41 None -1 26 Human 10.4 pKi = 10.4 Binding
Displacement of [3H]GR113808 from human 5HT4B receptor expressed in HEK293 cellsDisplacement of [3H]GR113808 from human 5HT4B receptor expressed in HEK293 cells
ChEMBL 393 7 1 6 1.6 O=C(c1cn(c2c1cccc2)C)OCC1CCN(CC1)CCNS(=O)(=O)C 10.1016/j.bmc.2013.09.004
247 1811 41 None -1 26 Human 10.4 pKi = 10.4 Binding
Displacement of [3H]GR113808 from human 5HT4B receptor expressed in HEK293 cellsDisplacement of [3H]GR113808 from human 5HT4B receptor expressed in HEK293 cells
ChEMBL 393 7 1 6 1.6 O=C(c1cn(c2c1cccc2)C)OCC1CCN(CC1)CCNS(=O)(=O)C 10.1016/j.bmc.2013.09.004
CHEMBL33884 1811 41 None -1 26 Human 10.4 pKi = 10.4 Binding
Displacement of [3H]GR113808 from human 5HT4B receptor expressed in HEK293 cellsDisplacement of [3H]GR113808 from human 5HT4B receptor expressed in HEK293 cells
ChEMBL 393 7 1 6 1.6 O=C(c1cn(c2c1cccc2)C)OCC1CCN(CC1)CCNS(=O)(=O)C 10.1016/j.bmc.2013.09.004
71455625 82551 0 None 54 6 Human 10.4 pKi = 10.4 Binding
Displacement of radioligand from human 5HT4R by Cerep protocol based assayDisplacement of radioligand from human 5HT4R by Cerep protocol based assay
ChEMBL 353 5 0 4 4.4 CCCN1CCC(COc2nc3c(F)cccc3c3ncccc23)CC1 10.1021/jm300943r
CHEMBL2181170 82551 0 None 54 6 Human 10.4 pKi = 10.4 Binding
Displacement of radioligand from human 5HT4R by Cerep protocol based assayDisplacement of radioligand from human 5HT4R by Cerep protocol based assay
ChEMBL 353 5 0 4 4.4 CCCN1CCC(COc2nc3c(F)cccc3c3ncccc23)CC1 10.1021/jm300943r
71455625 82551 0 None 54 6 Human 10.4 pKi = 10.4 Binding
Binding affinity to human 5HT4RBinding affinity to human 5HT4R
ChEMBL 353 5 0 4 4.4 CCCN1CCC(COc2nc3c(F)cccc3c3ncccc23)CC1 10.1016/j.bmc.2013.08.061
CHEMBL2181170 82551 0 None 54 6 Human 10.4 pKi = 10.4 Binding
Binding affinity to human 5HT4RBinding affinity to human 5HT4R
ChEMBL 353 5 0 4 4.4 CCCN1CCC(COc2nc3c(F)cccc3c3ncccc23)CC1 10.1016/j.bmc.2013.08.061
71455625 82551 0 None 54 6 Human 10.4 pKi = 10.4 Binding
Displacement of radioligand from human 5HT4R by Cerep protocol based assayDisplacement of radioligand from human 5HT4R by Cerep protocol based assay
ChEMBL 353 5 0 4 4.4 CCCN1CCC(COc2nc3c(F)cccc3c3ncccc23)CC1 10.1021/jm300943r
CHEMBL2181170 82551 0 None 54 6 Human 10.4 pKi = 10.4 Binding
Displacement of radioligand from human 5HT4R by Cerep protocol based assayDisplacement of radioligand from human 5HT4R by Cerep protocol based assay
ChEMBL 353 5 0 4 4.4 CCCN1CCC(COc2nc3c(F)cccc3c3ncccc23)CC1 10.1021/jm300943r
53325605 56153 0 None - 1 Human 10.4 pKi = 10.4 Binding
Displacement of [3H]GR113808 from human 5HT4 receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [3H]GR113808 from human 5HT4 receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 489 9 1 6 4.4 O=C(CCCN1CCC(CNC(=O)c2c3n(c4ccccc24)CCCO3)CC1)OCc1ccccc1 10.1016/j.bmc.2010.10.011
CHEMBL1632165 56153 0 None - 1 Human 10.4 pKi = 10.4 Binding
Displacement of [3H]GR113808 from human 5HT4 receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [3H]GR113808 from human 5HT4 receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 489 9 1 6 4.4 O=C(CCCN1CCC(CNC(=O)c2c3n(c4ccccc24)CCCO3)CC1)OCc1ccccc1 10.1016/j.bmc.2010.10.011
46935636 102099 0 None 31622 2 Human 10.3 pKi = 10.3 Binding
Displacement of [3H]GR113808 from human 5HT4B receptor expressed in HEK293 cellsDisplacement of [3H]GR113808 from human 5HT4B receptor expressed in HEK293 cells
ChEMBL 524 7 1 6 5.9 O=C(O)c1ccccc1-c1ccc(CN2CCC(COC(=O)c3c4n(c5ccccc35)CCCO4)CC2)cc1 10.1016/j.bmc.2013.09.004
CHEMBL2440460 102099 0 None 31622 2 Human 10.3 pKi = 10.3 Binding
Displacement of [3H]GR113808 from human 5HT4B receptor expressed in HEK293 cellsDisplacement of [3H]GR113808 from human 5HT4B receptor expressed in HEK293 cells
ChEMBL 524 7 1 6 5.9 O=C(O)c1ccccc1-c1ccc(CN2CCC(COC(=O)c3c4n(c5ccccc35)CCCO4)CC2)cc1 10.1016/j.bmc.2013.09.004
CHEMBL3040772 102099 0 None 31622 2 Human 10.3 pKi = 10.3 Binding
Displacement of [3H]GR113808 from human 5HT4B receptor expressed in HEK293 cellsDisplacement of [3H]GR113808 from human 5HT4B receptor expressed in HEK293 cells
ChEMBL 524 7 1 6 5.9 O=C(O)c1ccccc1-c1ccc(CN2CCC(COC(=O)c3c4n(c5ccccc35)CCCO4)CC2)cc1 10.1016/j.bmc.2013.09.004
118712571 113734 0 None - 1 Human 10.3 pKi = 10.3 Binding
Displacement of [3H]GR113808 from human 5HT4b receptor expressed in HEK293 cell membranesDisplacement of [3H]GR113808 from human 5HT4b receptor expressed in HEK293 cell membranes
ChEMBL 538 9 2 6 4.5 CC(C)CS(=O)(=O)Nc1ccc(CN2CCC(CNC(=O)c3c4n(c5ccccc35)CCCO4)CC2)cc1 10.1016/j.bmcl.2014.06.083
CHEMBL3329805 113734 0 None - 1 Human 10.3 pKi = 10.3 Binding
Displacement of [3H]GR113808 from human 5HT4b receptor expressed in HEK293 cell membranesDisplacement of [3H]GR113808 from human 5HT4b receptor expressed in HEK293 cell membranes
ChEMBL 538 9 2 6 4.5 CC(C)CS(=O)(=O)Nc1ccc(CN2CCC(CNC(=O)c3c4n(c5ccccc35)CCCO4)CC2)cc1 10.1016/j.bmcl.2014.06.083
9807895 63619 0 None - 1 Human 10.3 pKi = 10.3 Binding
Inhibitory constant for human cloned 5-HT4 receptorInhibitory constant for human cloned 5-HT4 receptor
ChEMBL 560 9 1 7 2.6 O=C(NCC1CCN(CCCS(=O)(=O)N2CCN(c3ccc(F)cc3)CC2)CC1)c1cccc2c1OCCO2 10.1016/j.bmcl.2005.01.039
CHEMBL180680 63619 0 None - 1 Human 10.3 pKi = 10.3 Binding
Inhibitory constant for human cloned 5-HT4 receptorInhibitory constant for human cloned 5-HT4 receptor
ChEMBL 560 9 1 7 2.6 O=C(NCC1CCN(CCCS(=O)(=O)N2CCN(c3ccc(F)cc3)CC2)CC1)c1cccc2c1OCCO2 10.1016/j.bmcl.2005.01.039
9870390 165239 0 None - 1 Human 10.3 pKi = 10.3 Binding
Inhibitory constant for human cloned 5-HT4 receptorInhibitory constant for human cloned 5-HT4 receptor
ChEMBL 494 9 1 7 1.3 CCN1CCN(S(=O)(=O)CCCN2CCC(CNC(=O)c3cccc4c3OCCO4)CC2)CC1 10.1016/j.bmcl.2005.01.039
CHEMBL424790 165239 0 None - 1 Human 10.3 pKi = 10.3 Binding
Inhibitory constant for human cloned 5-HT4 receptorInhibitory constant for human cloned 5-HT4 receptor
ChEMBL 494 9 1 7 1.3 CCN1CCN(S(=O)(=O)CCCN2CCC(CNC(=O)c3cccc4c3OCCO4)CC2)CC1 10.1016/j.bmcl.2005.01.039
177336 3071 45 None 6 3 Human 10.3 pKi = 10.3 Binding
Displacement of [3H]GR113808 from human 5HT4 receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [3H]GR113808 from human 5HT4 receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 369 6 1 4 3.7 CCCCN1CCC(CC1)CNC(=O)c1c2OCCCn2c2c1cccc2 10.1016/j.bmc.2010.10.011
225 3071 45 None 6 3 Human 10.3 pKi = 10.3 Binding
Displacement of [3H]GR113808 from human 5HT4 receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [3H]GR113808 from human 5HT4 receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 369 6 1 4 3.7 CCCCN1CCC(CC1)CNC(=O)c1c2OCCCn2c2c1cccc2 10.1016/j.bmc.2010.10.011
CHEMBL356359 3071 45 None 6 3 Human 10.3 pKi = 10.3 Binding
Displacement of [3H]GR113808 from human 5HT4 receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [3H]GR113808 from human 5HT4 receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 369 6 1 4 3.7 CCCCN1CCC(CC1)CNC(=O)c1c2OCCCn2c2c1cccc2 10.1016/j.bmc.2010.10.011
DB04873 3071 45 None 6 3 Human 10.3 pKi = 10.3 Binding
Displacement of [3H]GR113808 from human 5HT4 receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [3H]GR113808 from human 5HT4 receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 369 6 1 4 3.7 CCCCN1CCC(CC1)CNC(=O)c1c2OCCCn2c2c1cccc2 10.1016/j.bmc.2010.10.011
50898776 56151 0 None - 1 Human 10.3 pKi = 10.3 Binding
Displacement of [3H]GR113808 from human 5HT4 receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [3H]GR113808 from human 5HT4 receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 483 9 1 6 4.8 CC(C)(C)OC(=O)CCCCCN1CCC(CNC(=O)c2c3n(c4ccccc24)CCCO3)CC1 10.1016/j.bmc.2010.10.011
CHEMBL1632163 56151 0 None - 1 Human 10.3 pKi = 10.3 Binding
Displacement of [3H]GR113808 from human 5HT4 receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [3H]GR113808 from human 5HT4 receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 483 9 1 6 4.8 CC(C)(C)OC(=O)CCCCCN1CCC(CNC(=O)c2c3n(c4ccccc24)CCCO3)CC1 10.1016/j.bmc.2010.10.011
46935596 92444 0 None - 1 Human 10.2 pKi = 10.2 Binding
Displacement of [3H]GR113808 from human 5HT4B receptor expressed in HEK293 cellsDisplacement of [3H]GR113808 from human 5HT4B receptor expressed in HEK293 cells
ChEMBL 537 7 1 6 5.5 COC(=O)c1ccccc1-c1ccc(CN2CCC(CNC(=O)c3c4n(c5ccccc35)CCCO4)CC2)cc1 10.1016/j.bmc.2013.09.004
CHEMBL2440457 92444 0 None - 1 Human 10.2 pKi = 10.2 Binding
Displacement of [3H]GR113808 from human 5HT4B receptor expressed in HEK293 cellsDisplacement of [3H]GR113808 from human 5HT4B receptor expressed in HEK293 cells
ChEMBL 537 7 1 6 5.5 COC(=O)c1ccccc1-c1ccc(CN2CCC(CNC(=O)c3c4n(c5ccccc35)CCCO4)CC2)cc1 10.1016/j.bmc.2013.09.004
9892465 63458 0 None - 1 Human 10.2 pKi = 10.2 Binding
Inhibitory constant for human cloned 5-HT4 receptorInhibitory constant for human cloned 5-HT4 receptor
ChEMBL 507 10 1 6 3.1 CCCC1CCN(S(=O)(=O)CCCN2CCC(CNC(=O)c3cccc4c3OCCO4)CC2)CC1 10.1016/j.bmcl.2005.01.039
CHEMBL180201 63458 0 None - 1 Human 10.2 pKi = 10.2 Binding
Inhibitory constant for human cloned 5-HT4 receptorInhibitory constant for human cloned 5-HT4 receptor
ChEMBL 507 10 1 6 3.1 CCCC1CCN(S(=O)(=O)CCCN2CCC(CNC(=O)c3cccc4c3OCCO4)CC2)CC1 10.1016/j.bmcl.2005.01.039
50898699 56156 0 None - 1 Human 10.2 pKi = 10.2 Binding
Displacement of [3H]GR113808 from human 5HT4 receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [3H]GR113808 from human 5HT4 receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 541 11 1 8 4.5 CC(C)(C)C(=O)OCOC(=O)CCCCCN1CCC(CNC(=O)c2c3n(c4ccccc24)CCCO3)CC1 10.1016/j.bmc.2010.10.011
CHEMBL1632169 56156 0 None - 1 Human 10.2 pKi = 10.2 Binding
Displacement of [3H]GR113808 from human 5HT4 receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [3H]GR113808 from human 5HT4 receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 541 11 1 8 4.5 CC(C)(C)C(=O)OCOC(=O)CCCCCN1CCC(CNC(=O)c2c3n(c4ccccc24)CCCO3)CC1 10.1016/j.bmc.2010.10.011
72545050 105245 0 None - 1 Rat 10.2 pKi = 10.2 Binding
Displacement of [3H]GR113808 from 5HT4 receptor in Sprague-Dawley rat striatal membranes after 1 hr by gamma countingDisplacement of [3H]GR113808 from 5HT4 receptor in Sprague-Dawley rat striatal membranes after 1 hr by gamma counting
ChEMBL 386 6 1 6 2.9 Nc1c(Cl)cc(C(=O)OCC2CCN(CCCF)CC2)c2c1OCCO2 10.1016/j.bmcl.2013.09.097
CHEMBL3126108 105245 0 None - 1 Rat 10.2 pKi = 10.2 Binding
Displacement of [3H]GR113808 from 5HT4 receptor in Sprague-Dawley rat striatal membranes after 1 hr by gamma countingDisplacement of [3H]GR113808 from 5HT4 receptor in Sprague-Dawley rat striatal membranes after 1 hr by gamma counting
ChEMBL 386 6 1 6 2.9 Nc1c(Cl)cc(C(=O)OCC2CCN(CCCF)CC2)c2c1OCCO2 10.1016/j.bmcl.2013.09.097
119376 1811 41 None -1 26 Human 10.1 pKi = 10.1 Binding
Binding affinity was determined against cloned 5-hydroxytryptamine 4D receptor isoform expressed in COS-7 cellsBinding affinity was determined against cloned 5-hydroxytryptamine 4D receptor isoform expressed in COS-7 cells
ChEMBL 393 7 1 6 1.6 O=C(c1cn(c2c1cccc2)C)OCC1CCN(CC1)CCNS(=O)(=O)C 10.1021/jm0009538
247 1811 41 None -1 26 Human 10.1 pKi = 10.1 Binding
Binding affinity was determined against cloned 5-hydroxytryptamine 4D receptor isoform expressed in COS-7 cellsBinding affinity was determined against cloned 5-hydroxytryptamine 4D receptor isoform expressed in COS-7 cells
ChEMBL 393 7 1 6 1.6 O=C(c1cn(c2c1cccc2)C)OCC1CCN(CC1)CCNS(=O)(=O)C 10.1021/jm0009538
CHEMBL33884 1811 41 None -1 26 Human 10.1 pKi = 10.1 Binding
Binding affinity was determined against cloned 5-hydroxytryptamine 4D receptor isoform expressed in COS-7 cellsBinding affinity was determined against cloned 5-hydroxytryptamine 4D receptor isoform expressed in COS-7 cells
ChEMBL 393 7 1 6 1.6 O=C(c1cn(c2c1cccc2)C)OCC1CCN(CC1)CCNS(=O)(=O)C 10.1021/jm0009538
9954930 84162 0 None 398 2 Human 10.1 pKi = 10.1 Binding
Displacement of [3H](1-(2-(methylsulfonamido)ethyl)piperidin-4-yl)methyl 1-methyl-1H-indole-3-carboxylate from human 5HT4R expressed in HEK293 cellsDisplacement of [3H](1-(2-(methylsulfonamido)ethyl)piperidin-4-yl)methyl 1-methyl-1H-indole-3-carboxylate from human 5HT4R expressed in HEK293 cells
ChEMBL 404 7 1 4 4.3 CC(C)n1nc(C(=O)NCC2CCN(CCc3ccccc3)CC2)c2ccccc21 10.1021/jm300573d
CHEMBL2177130 84162 0 None 398 2 Human 10.1 pKi = 10.1 Binding
Displacement of [3H](1-(2-(methylsulfonamido)ethyl)piperidin-4-yl)methyl 1-methyl-1H-indole-3-carboxylate from human 5HT4R expressed in HEK293 cellsDisplacement of [3H](1-(2-(methylsulfonamido)ethyl)piperidin-4-yl)methyl 1-methyl-1H-indole-3-carboxylate from human 5HT4R expressed in HEK293 cells
ChEMBL 404 7 1 4 4.3 CC(C)n1nc(C(=O)NCC2CCN(CCc3ccccc3)CC2)c2ccccc21 10.1021/jm300573d
CHEMBL2220969 84162 0 None 398 2 Human 10.1 pKi = 10.1 Binding
Displacement of [3H](1-(2-(methylsulfonamido)ethyl)piperidin-4-yl)methyl 1-methyl-1H-indole-3-carboxylate from human 5HT4R expressed in HEK293 cellsDisplacement of [3H](1-(2-(methylsulfonamido)ethyl)piperidin-4-yl)methyl 1-methyl-1H-indole-3-carboxylate from human 5HT4R expressed in HEK293 cells
ChEMBL 404 7 1 4 4.3 CC(C)n1nc(C(=O)NCC2CCN(CCc3ccccc3)CC2)c2ccccc21 10.1021/jm300573d
91754444 113743 0 None - 1 Human 10.1 pKi = 10.1 Binding
Displacement of [3H]GR113808 from human 5HT4b receptor expressed in HEK293 cell membranesDisplacement of [3H]GR113808 from human 5HT4b receptor expressed in HEK293 cell membranes
ChEMBL 388 6 2 7 1.6 O=C(OCC1CCN(CC(O)CO)CC1)c1c2n(c3ccccc13)CCCO2 10.1016/j.bmcl.2014.06.083
CHEMBL3329814 113743 0 None - 1 Human 10.1 pKi = 10.1 Binding
Displacement of [3H]GR113808 from human 5HT4b receptor expressed in HEK293 cell membranesDisplacement of [3H]GR113808 from human 5HT4b receptor expressed in HEK293 cell membranes
ChEMBL 388 6 2 7 1.6 O=C(OCC1CCN(CC(O)CO)CC1)c1c2n(c3ccccc13)CCCO2 10.1016/j.bmcl.2014.06.083
21268036 122219 0 None - 1 Human 10.1 pKi = 10.1 Binding
Inhibitory constant for human cloned 5-HT4 receptorInhibitory constant for human cloned 5-HT4 receptor
ChEMBL 599 10 1 8 0.6 O=C(NCC1CCN(CCCS(=O)(=O)N2CCN(S(=O)(=O)N3CCCC3)CC2)CC1)c1cccc2c1OCCO2 10.1016/j.bmcl.2005.01.039
CHEMBL360449 122219 0 None - 1 Human 10.1 pKi = 10.1 Binding
Inhibitory constant for human cloned 5-HT4 receptorInhibitory constant for human cloned 5-HT4 receptor
ChEMBL 599 10 1 8 0.6 O=C(NCC1CCN(CCCS(=O)(=O)N2CCN(S(=O)(=O)N3CCCC3)CC2)CC1)c1cccc2c1OCCO2 10.1016/j.bmcl.2005.01.039
90667897 109042 0 None - 1 Rat 10.1 pKi = 10.1 Binding
Displacement of [3H]GR113808 from 5-HT4 receptor in rat striatal membranes after 30 mins by liquid scintillation spectrometric analysisDisplacement of [3H]GR113808 from 5-HT4 receptor in rat striatal membranes after 30 mins by liquid scintillation spectrometric analysis
ChEMBL 364 6 2 3 4.0 CCCCN1CCC(CNC(=S)c2cc(Cl)cc3[nH]cnc23)CC1 10.1039/C0MD00258E
CHEMBL3221572 109042 0 None - 1 Rat 10.1 pKi = 10.1 Binding
Displacement of [3H]GR113808 from 5-HT4 receptor in rat striatal membranes after 30 mins by liquid scintillation spectrometric analysisDisplacement of [3H]GR113808 from 5-HT4 receptor in rat striatal membranes after 30 mins by liquid scintillation spectrometric analysis
ChEMBL 364 6 2 3 4.0 CCCCN1CCC(CNC(=S)c2cc(Cl)cc3[nH]cnc23)CC1 10.1039/C0MD00258E
119376 1811 41 None -1 26 Human 10.0 pKi = 10 Binding
Binding affinity was determined against cloned 5-hydroxytryptamine 4E receptor isoform expressed in C6 glial cells incubated with 0.2 nM [3H]GR-113808Binding affinity was determined against cloned 5-hydroxytryptamine 4E receptor isoform expressed in C6 glial cells incubated with 0.2 nM [3H]GR-113808
ChEMBL 393 7 1 6 1.6 O=C(c1cn(c2c1cccc2)C)OCC1CCN(CC1)CCNS(=O)(=O)C 10.1021/jm0009538
247 1811 41 None -1 26 Human 10.0 pKi = 10 Binding
Binding affinity was determined against cloned 5-hydroxytryptamine 4E receptor isoform expressed in C6 glial cells incubated with 0.2 nM [3H]GR-113808Binding affinity was determined against cloned 5-hydroxytryptamine 4E receptor isoform expressed in C6 glial cells incubated with 0.2 nM [3H]GR-113808
ChEMBL 393 7 1 6 1.6 O=C(c1cn(c2c1cccc2)C)OCC1CCN(CC1)CCNS(=O)(=O)C 10.1021/jm0009538
CHEMBL33884 1811 41 None -1 26 Human 10.0 pKi = 10 Binding
Binding affinity was determined against cloned 5-hydroxytryptamine 4E receptor isoform expressed in C6 glial cells incubated with 0.2 nM [3H]GR-113808Binding affinity was determined against cloned 5-hydroxytryptamine 4E receptor isoform expressed in C6 glial cells incubated with 0.2 nM [3H]GR-113808
ChEMBL 393 7 1 6 1.6 O=C(c1cn(c2c1cccc2)C)OCC1CCN(CC1)CCNS(=O)(=O)C 10.1021/jm0009538
250 3334 5 None -2 13 Guinea pig 10.0 pKi = 10 Binding
Compound was evaluated for binding affinity against 5-hydroxytryptamine 4 receptor using radioligand binding assay using [3H]GR as radioligandCompound was evaluated for binding affinity against 5-hydroxytryptamine 4 receptor using radioligand binding assay using [3H]GR as radioligand
ChEMBL 502 10 1 7 5.0 COc1cc(CCCN2CCC(CC2)CCC(=O)c2cc(Cl)c(c3c2OCCO3)N)ccc1OC 10.1016/0960-894X(95)00358-Z
5311416 3334 5 None -2 13 Guinea pig 10.0 pKi = 10 Binding
Compound was evaluated for binding affinity against 5-hydroxytryptamine 4 receptor using radioligand binding assay using [3H]GR as radioligandCompound was evaluated for binding affinity against 5-hydroxytryptamine 4 receptor using radioligand binding assay using [3H]GR as radioligand
ChEMBL 502 10 1 7 5.0 COc1cc(CCCN2CCC(CC2)CCC(=O)c2cc(Cl)c(c3c2OCCO3)N)ccc1OC 10.1016/0960-894X(95)00358-Z
CHEMBL69733 3334 5 None -2 13 Guinea pig 10.0 pKi = 10 Binding
Compound was evaluated for binding affinity against 5-hydroxytryptamine 4 receptor using radioligand binding assay using [3H]GR as radioligandCompound was evaluated for binding affinity against 5-hydroxytryptamine 4 receptor using radioligand binding assay using [3H]GR as radioligand
ChEMBL 502 10 1 7 5.0 COc1cc(CCCN2CCC(CC2)CCC(=O)c2cc(Cl)c(c3c2OCCO3)N)ccc1OC 10.1016/0960-894X(95)00358-Z
11153975 84143 4 None 1000 2 Human 10.0 pKi = 10 Binding
Displacement of [3H](1-(2-(methylsulfonamido)ethyl)piperidin-4-yl)methyl 1-methyl-1H-indole-3-carboxylate from human 5HT4R expressed in HEK293 cellsDisplacement of [3H](1-(2-(methylsulfonamido)ethyl)piperidin-4-yl)methyl 1-methyl-1H-indole-3-carboxylate from human 5HT4R expressed in HEK293 cells
ChEMBL 405 7 1 5 3.7 CC(C)n1nc(C(=O)NCC2CCN(CCc3ccccn3)CC2)c2ccccc21 10.1021/jm300573d
CHEMBL2179697 84143 4 None 1000 2 Human 10.0 pKi = 10 Binding
Displacement of [3H](1-(2-(methylsulfonamido)ethyl)piperidin-4-yl)methyl 1-methyl-1H-indole-3-carboxylate from human 5HT4R expressed in HEK293 cellsDisplacement of [3H](1-(2-(methylsulfonamido)ethyl)piperidin-4-yl)methyl 1-methyl-1H-indole-3-carboxylate from human 5HT4R expressed in HEK293 cells
ChEMBL 405 7 1 5 3.7 CC(C)n1nc(C(=O)NCC2CCN(CCc3ccccn3)CC2)c2ccccc21 10.1021/jm300573d
CHEMBL2220892 84143 4 None 1000 2 Human 10.0 pKi = 10 Binding
Displacement of [3H](1-(2-(methylsulfonamido)ethyl)piperidin-4-yl)methyl 1-methyl-1H-indole-3-carboxylate from human 5HT4R expressed in HEK293 cellsDisplacement of [3H](1-(2-(methylsulfonamido)ethyl)piperidin-4-yl)methyl 1-methyl-1H-indole-3-carboxylate from human 5HT4R expressed in HEK293 cells
ChEMBL 405 7 1 5 3.7 CC(C)n1nc(C(=O)NCC2CCN(CCc3ccccn3)CC2)c2ccccc21 10.1021/jm300573d
177336 3071 45 None 6 3 Human 10.0 pKi = 10 Binding
Displacement of [3H]GR113808 from human 5-HT4B receptor expressed in HEK293 cells after 1 hr by liquid scintillation counting analysisDisplacement of [3H]GR113808 from human 5-HT4B receptor expressed in HEK293 cells after 1 hr by liquid scintillation counting analysis
ChEMBL 369 6 1 4 3.7 CCCCN1CCC(CC1)CNC(=O)c1c2OCCCn2c2c1cccc2 10.1016/j.ejmech.2013.03.060
225 3071 45 None 6 3 Human 10.0 pKi = 10 Binding
Displacement of [3H]GR113808 from human 5-HT4B receptor expressed in HEK293 cells after 1 hr by liquid scintillation counting analysisDisplacement of [3H]GR113808 from human 5-HT4B receptor expressed in HEK293 cells after 1 hr by liquid scintillation counting analysis
ChEMBL 369 6 1 4 3.7 CCCCN1CCC(CC1)CNC(=O)c1c2OCCCn2c2c1cccc2 10.1016/j.ejmech.2013.03.060
CHEMBL356359 3071 45 None 6 3 Human 10.0 pKi = 10 Binding
Displacement of [3H]GR113808 from human 5-HT4B receptor expressed in HEK293 cells after 1 hr by liquid scintillation counting analysisDisplacement of [3H]GR113808 from human 5-HT4B receptor expressed in HEK293 cells after 1 hr by liquid scintillation counting analysis
ChEMBL 369 6 1 4 3.7 CCCCN1CCC(CC1)CNC(=O)c1c2OCCCn2c2c1cccc2 10.1016/j.ejmech.2013.03.060
DB04873 3071 45 None 6 3 Human 10.0 pKi = 10 Binding
Displacement of [3H]GR113808 from human 5-HT4B receptor expressed in HEK293 cells after 1 hr by liquid scintillation counting analysisDisplacement of [3H]GR113808 from human 5-HT4B receptor expressed in HEK293 cells after 1 hr by liquid scintillation counting analysis
ChEMBL 369 6 1 4 3.7 CCCCN1CCC(CC1)CNC(=O)c1c2OCCCn2c2c1cccc2 10.1016/j.ejmech.2013.03.060
177336 3071 45 None 6 3 Human 10.0 pKi = 10 Binding
Displacement of [3H]GR113808 from human 5HT4B receptor expressed in HEK293 cellsDisplacement of [3H]GR113808 from human 5HT4B receptor expressed in HEK293 cells
ChEMBL 369 6 1 4 3.7 CCCCN1CCC(CC1)CNC(=O)c1c2OCCCn2c2c1cccc2 10.1016/j.bmc.2013.09.004
225 3071 45 None 6 3 Human 10.0 pKi = 10 Binding
Displacement of [3H]GR113808 from human 5HT4B receptor expressed in HEK293 cellsDisplacement of [3H]GR113808 from human 5HT4B receptor expressed in HEK293 cells
ChEMBL 369 6 1 4 3.7 CCCCN1CCC(CC1)CNC(=O)c1c2OCCCn2c2c1cccc2 10.1016/j.bmc.2013.09.004
CHEMBL356359 3071 45 None 6 3 Human 10.0 pKi = 10 Binding
Displacement of [3H]GR113808 from human 5HT4B receptor expressed in HEK293 cellsDisplacement of [3H]GR113808 from human 5HT4B receptor expressed in HEK293 cells
ChEMBL 369 6 1 4 3.7 CCCCN1CCC(CC1)CNC(=O)c1c2OCCCn2c2c1cccc2 10.1016/j.bmc.2013.09.004
DB04873 3071 45 None 6 3 Human 10.0 pKi = 10 Binding
Displacement of [3H]GR113808 from human 5HT4B receptor expressed in HEK293 cellsDisplacement of [3H]GR113808 from human 5HT4B receptor expressed in HEK293 cells
ChEMBL 369 6 1 4 3.7 CCCCN1CCC(CC1)CNC(=O)c1c2OCCCn2c2c1cccc2 10.1016/j.bmc.2013.09.004
21268033 63797 0 None - 1 Human 10.0 pKi = 10 Binding
Inhibitory constant for human cloned 5-HT4 receptorInhibitory constant for human cloned 5-HT4 receptor
ChEMBL 560 9 1 8 1.7 O=C(NCC1CCN(CCCS(=O)(=O)N2CCN(C(=O)c3ccco3)CC2)CC1)c1cccc2c1OCCO2 10.1016/j.bmcl.2005.01.039
CHEMBL180830 63797 0 None - 1 Human 10.0 pKi = 10 Binding
Inhibitory constant for human cloned 5-HT4 receptorInhibitory constant for human cloned 5-HT4 receptor
ChEMBL 560 9 1 8 1.7 O=C(NCC1CCN(CCCS(=O)(=O)N2CCN(C(=O)c3ccco3)CC2)CC1)c1cccc2c1OCCO2 10.1016/j.bmcl.2005.01.039
15485936 122092 0 None - 1 Human 10.0 pKi = 10 Binding
Inhibitory constant for human cloned 5-HT4 receptorInhibitory constant for human cloned 5-HT4 receptor
ChEMBL 572 11 1 8 1.0 CCCS(=O)(=O)N1CCN(S(=O)(=O)CCCN2CCC(CNC(=O)c3cccc4c3OCCO4)CC2)CC1 10.1016/j.bmcl.2005.01.039
CHEMBL360245 122092 0 None - 1 Human 10.0 pKi = 10 Binding
Inhibitory constant for human cloned 5-HT4 receptorInhibitory constant for human cloned 5-HT4 receptor
ChEMBL 572 11 1 8 1.0 CCCS(=O)(=O)N1CCN(S(=O)(=O)CCCN2CCC(CNC(=O)c3cccc4c3OCCO4)CC2)CC1 10.1016/j.bmcl.2005.01.039
53319410 56145 0 None - 1 Human 10.0 pKi = 10.0 Binding
Displacement of [3H]GR113808 from human 5HT4 receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [3H]GR113808 from human 5HT4 receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 427 8 1 6 3.2 CCOC(=O)CCCN1CCC(CNC(=O)c2c3n(c4ccccc24)CCCO3)CC1 10.1016/j.bmc.2010.10.011
CHEMBL1632157 56145 0 None - 1 Human 10.0 pKi = 10.0 Binding
Displacement of [3H]GR113808 from human 5HT4 receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [3H]GR113808 from human 5HT4 receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 427 8 1 6 3.2 CCOC(=O)CCCN1CCC(CNC(=O)c2c3n(c4ccccc24)CCCO3)CC1 10.1016/j.bmc.2010.10.011
50898777 56146 0 None 2951 8 Human 10.0 pKi = 10.0 Binding
Displacement of [3H]GR113808 from human 5HT4 receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [3H]GR113808 from human 5HT4 receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 441 9 1 6 3.6 COC(=O)CCCCCN1CCC(CNC(=O)c2c3n(c4ccccc24)CCCO3)CC1 10.1016/j.bmc.2010.10.011
CHEMBL1632158 56146 0 None 2951 8 Human 10.0 pKi = 10.0 Binding
Displacement of [3H]GR113808 from human 5HT4 receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [3H]GR113808 from human 5HT4 receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 441 9 1 6 3.6 COC(=O)CCCCCN1CCC(CNC(=O)c2c3n(c4ccccc24)CCCO3)CC1 10.1016/j.bmc.2010.10.011
10476858 111872 0 None - 1 Rat 10.0 pKi = 10.0 Binding
pKi against 5-hydroxytryptamine 4 receptor in rat striatum membranepKi against 5-hydroxytryptamine 4 receptor in rat striatum membrane
ChEMBL 413 7 3 5 1.2 CS(=O)(=O)NCCN1CCC(CNC(=O)c2cc(Cl)cc3[nH]cnc23)CC1 10.1016/s0960-894x(01)00517-0
CHEMBL329487 111872 0 None - 1 Rat 10.0 pKi = 10.0 Binding
pKi against 5-hydroxytryptamine 4 receptor in rat striatum membranepKi against 5-hydroxytryptamine 4 receptor in rat striatum membrane
ChEMBL 413 7 3 5 1.2 CS(=O)(=O)NCCN1CCC(CNC(=O)c2cc(Cl)cc3[nH]cnc23)CC1 10.1016/s0960-894x(01)00517-0
119376 1811 41 None 1 26 Guinea pig 10.0 pKi = 10.0 Binding
Binding affinity against 5-hydroxytryptamine 4 receptor in guinea pig striatum using [3H]GR-113808 as radioligandBinding affinity against 5-hydroxytryptamine 4 receptor in guinea pig striatum using [3H]GR-113808 as radioligand
ChEMBL 393 7 1 6 1.6 O=C(c1cn(c2c1cccc2)C)OCC1CCN(CC1)CCNS(=O)(=O)C 10.1021/jm981098j
247 1811 41 None 1 26 Guinea pig 10.0 pKi = 10.0 Binding
Binding affinity against 5-hydroxytryptamine 4 receptor in guinea pig striatum using [3H]GR-113808 as radioligandBinding affinity against 5-hydroxytryptamine 4 receptor in guinea pig striatum using [3H]GR-113808 as radioligand
ChEMBL 393 7 1 6 1.6 O=C(c1cn(c2c1cccc2)C)OCC1CCN(CC1)CCNS(=O)(=O)C 10.1021/jm981098j
CHEMBL33884 1811 41 None 1 26 Guinea pig 10.0 pKi = 10.0 Binding
Binding affinity against 5-hydroxytryptamine 4 receptor in guinea pig striatum using [3H]GR-113808 as radioligandBinding affinity against 5-hydroxytryptamine 4 receptor in guinea pig striatum using [3H]GR-113808 as radioligand
ChEMBL 393 7 1 6 1.6 O=C(c1cn(c2c1cccc2)C)OCC1CCN(CC1)CCNS(=O)(=O)C 10.1021/jm981098j
10476858 111872 0 None - 1 Rat 10.0 pKi = 10.0 Binding
Binding affinity to 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatum membraneBinding affinity to 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatum membrane
ChEMBL 413 7 3 5 1.2 CS(=O)(=O)NCCN1CCC(CNC(=O)c2cc(Cl)cc3[nH]cnc23)CC1 10.1021/jm020807x
CHEMBL329487 111872 0 None - 1 Rat 10.0 pKi = 10.0 Binding
Binding affinity to 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatum membraneBinding affinity to 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatum membrane
ChEMBL 413 7 3 5 1.2 CS(=O)(=O)NCCN1CCC(CNC(=O)c2cc(Cl)cc3[nH]cnc23)CC1 10.1021/jm020807x
72698087 103511 0 None 81 3 Human 10.0 pKi = 10.0 Binding
Binding affinity to human 5HT4RBinding affinity to human 5HT4R
ChEMBL 407 5 0 4 5.0 Fc1cccc2c1nc(OCC1CCN(CCC(F)(F)F)CC1)c1cccnc12 10.1016/j.bmc.2013.08.061
CHEMBL3093186 103511 0 None 81 3 Human 10.0 pKi = 10.0 Binding
Binding affinity to human 5HT4RBinding affinity to human 5HT4R
ChEMBL 407 5 0 4 5.0 Fc1cccc2c1nc(OCC1CCN(CCC(F)(F)F)CC1)c1cccnc12 10.1016/j.bmc.2013.08.061
10476858 111872 0 None - 1 Rat 10.0 pKi = 10.0 Binding
In vitro binding affinity to 5-hydroxytryptamine 4 receptor in rat striatum membraneIn vitro binding affinity to 5-hydroxytryptamine 4 receptor in rat striatum membrane
ChEMBL 413 7 3 5 1.2 CS(=O)(=O)NCCN1CCC(CNC(=O)c2cc(Cl)cc3[nH]cnc23)CC1 10.1016/s0960-894x(01)00517-0
CHEMBL329487 111872 0 None - 1 Rat 10.0 pKi = 10.0 Binding
In vitro binding affinity to 5-hydroxytryptamine 4 receptor in rat striatum membraneIn vitro binding affinity to 5-hydroxytryptamine 4 receptor in rat striatum membrane
ChEMBL 413 7 3 5 1.2 CS(=O)(=O)NCCN1CCC(CNC(=O)c2cc(Cl)cc3[nH]cnc23)CC1 10.1016/s0960-894x(01)00517-0
46935743 90390 0 None - 1 Human 9.9 pKi = 9.9 Binding
Displacement of [3H]GR113808 from human 5-HT4B receptor expressed in HEK293 cells after 1 hr by liquid scintillation counting analysisDisplacement of [3H]GR113808 from human 5-HT4B receptor expressed in HEK293 cells after 1 hr by liquid scintillation counting analysis
ChEMBL 490 7 1 6 4.9 CC(C)(C(=O)O)c1ccc(CN2CCC(COC(=O)c3c4n(c5ccccc35)CCCO4)CC2)cc1 10.1016/j.ejmech.2013.03.060
CHEMBL2391994 90390 0 None - 1 Human 9.9 pKi = 9.9 Binding
Displacement of [3H]GR113808 from human 5-HT4B receptor expressed in HEK293 cells after 1 hr by liquid scintillation counting analysisDisplacement of [3H]GR113808 from human 5-HT4B receptor expressed in HEK293 cells after 1 hr by liquid scintillation counting analysis
ChEMBL 490 7 1 6 4.9 CC(C)(C(=O)O)c1ccc(CN2CCC(COC(=O)c3c4n(c5ccccc35)CCCO4)CC2)cc1 10.1016/j.ejmech.2013.03.060
21268037 62267 0 None - 1 Human 9.9 pKi = 9.9 Binding
Inhibitory constant for human cloned 5-HT4 receptorInhibitory constant for human cloned 5-HT4 receptor
ChEMBL 493 8 1 6 2.7 CC1(C)CCN(S(=O)(=O)CCCN2CCC(CNC(=O)c3cccc4c3OCCO4)CC2)CC1 10.1016/j.bmcl.2005.01.039
CHEMBL178285 62267 0 None - 1 Human 9.9 pKi = 9.9 Binding
Inhibitory constant for human cloned 5-HT4 receptorInhibitory constant for human cloned 5-HT4 receptor
ChEMBL 493 8 1 6 2.7 CC1(C)CCN(S(=O)(=O)CCCN2CCC(CNC(=O)c3cccc4c3OCCO4)CC2)CC1 10.1016/j.bmcl.2005.01.039
21268031 62670 0 None - 1 Human 9.9 pKi = 9.9 Binding
Inhibitory constant for human cloned 5-HT4 receptorInhibitory constant for human cloned 5-HT4 receptor
ChEMBL 508 8 1 7 0.8 CC(=O)N1CCN(S(=O)(=O)CCCN2CCC(CNC(=O)c3cccc4c3OCCO4)CC2)CC1 10.1016/j.bmcl.2005.01.039
CHEMBL178669 62670 0 None - 1 Human 9.9 pKi = 9.9 Binding
Inhibitory constant for human cloned 5-HT4 receptorInhibitory constant for human cloned 5-HT4 receptor
ChEMBL 508 8 1 7 0.8 CC(=O)N1CCN(S(=O)(=O)CCCN2CCC(CNC(=O)c3cccc4c3OCCO4)CC2)CC1 10.1016/j.bmcl.2005.01.039
44390214 63136 0 None - 1 Human 9.9 pKi = 9.9 Binding
Inhibitory constant for human cloned 5-HT4 receptorInhibitory constant for human cloned 5-HT4 receptor
ChEMBL 572 10 1 8 1.0 CC(C)S(=O)(=O)N1CCN(S(=O)(=O)CCCN2CCC(CNC(=O)c3cccc4c3OCCO4)CC2)CC1 10.1016/j.bmcl.2005.01.039
CHEMBL179833 63136 0 None - 1 Human 9.9 pKi = 9.9 Binding
Inhibitory constant for human cloned 5-HT4 receptorInhibitory constant for human cloned 5-HT4 receptor
ChEMBL 572 10 1 8 1.0 CC(C)S(=O)(=O)N1CCN(S(=O)(=O)CCCN2CCC(CNC(=O)c3cccc4c3OCCO4)CC2)CC1 10.1016/j.bmcl.2005.01.039
9952994 106487 0 None - 1 Rat 9.9 pKi = 9.9 Binding
Binding affinity at 5-hydroxytryptamine 4 receptor in rat striatum by [3H]GR-113808 displacement.Binding affinity at 5-hydroxytryptamine 4 receptor in rat striatum by [3H]GR-113808 displacement.
ChEMBL 366 6 1 5 3.5 CCCCN1CCC(COC(=O)c2cc(Cl)c(N)c3c2OCC3)CC1 10.1016/0960-894X(96)00002-9
CHEMBL315071 106487 0 None - 1 Rat 9.9 pKi = 9.9 Binding
Binding affinity at 5-hydroxytryptamine 4 receptor in rat striatum by [3H]GR-113808 displacement.Binding affinity at 5-hydroxytryptamine 4 receptor in rat striatum by [3H]GR-113808 displacement.
ChEMBL 366 6 1 5 3.5 CCCCN1CCC(COC(=O)c2cc(Cl)c(N)c3c2OCC3)CC1 10.1016/0960-894X(96)00002-9
50898775 56154 0 None - 1 Human 9.9 pKi = 9.9 Binding
Displacement of [3H]GR113808 from human 5HT4 receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [3H]GR113808 from human 5HT4 receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 517 11 1 6 5.2 O=C(CCCCCN1CCC(CNC(=O)c2c3n(c4ccccc24)CCCO3)CC1)OCc1ccccc1 10.1016/j.bmc.2010.10.011
CHEMBL1632167 56154 0 None - 1 Human 9.9 pKi = 9.9 Binding
Displacement of [3H]GR113808 from human 5HT4 receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [3H]GR113808 from human 5HT4 receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 517 11 1 6 5.2 O=C(CCCCCN1CCC(CNC(=O)c2c3n(c4ccccc24)CCCO3)CC1)OCc1ccccc1 10.1016/j.bmc.2010.10.011
119376 1811 41 None -2 26 Rat 9.8 pKi = 9.8 Binding
Binding affinity at 5-hydroxytryptamine 4 receptor in rat striatal membranes by [3H]GR-113808 displacement.Binding affinity at 5-hydroxytryptamine 4 receptor in rat striatal membranes by [3H]GR-113808 displacement.
ChEMBL 393 7 1 6 1.6 O=C(c1cn(c2c1cccc2)C)OCC1CCN(CC1)CCNS(=O)(=O)C 10.1021/jm960853v
247 1811 41 None -2 26 Rat 9.8 pKi = 9.8 Binding
Binding affinity at 5-hydroxytryptamine 4 receptor in rat striatal membranes by [3H]GR-113808 displacement.Binding affinity at 5-hydroxytryptamine 4 receptor in rat striatal membranes by [3H]GR-113808 displacement.
ChEMBL 393 7 1 6 1.6 O=C(c1cn(c2c1cccc2)C)OCC1CCN(CC1)CCNS(=O)(=O)C 10.1021/jm960853v
CHEMBL33884 1811 41 None -2 26 Rat 9.8 pKi = 9.8 Binding
Binding affinity at 5-hydroxytryptamine 4 receptor in rat striatal membranes by [3H]GR-113808 displacement.Binding affinity at 5-hydroxytryptamine 4 receptor in rat striatal membranes by [3H]GR-113808 displacement.
ChEMBL 393 7 1 6 1.6 O=C(c1cn(c2c1cccc2)C)OCC1CCN(CC1)CCNS(=O)(=O)C 10.1021/jm960853v
119376 1811 41 None -2 26 Rat 9.8 pKi = 9.8 Binding
Binding affinity towards 5-hydroxytryptamine 4 receptor was determined in rat striatal membranes using [3H]GR-113808 as radioligandBinding affinity towards 5-hydroxytryptamine 4 receptor was determined in rat striatal membranes using [3H]GR-113808 as radioligand
ChEMBL 393 7 1 6 1.6 O=C(c1cn(c2c1cccc2)C)OCC1CCN(CC1)CCNS(=O)(=O)C 10.1021/jm960320m
247 1811 41 None -2 26 Rat 9.8 pKi = 9.8 Binding
Binding affinity towards 5-hydroxytryptamine 4 receptor was determined in rat striatal membranes using [3H]GR-113808 as radioligandBinding affinity towards 5-hydroxytryptamine 4 receptor was determined in rat striatal membranes using [3H]GR-113808 as radioligand
ChEMBL 393 7 1 6 1.6 O=C(c1cn(c2c1cccc2)C)OCC1CCN(CC1)CCNS(=O)(=O)C 10.1021/jm960320m
CHEMBL33884 1811 41 None -2 26 Rat 9.8 pKi = 9.8 Binding
Binding affinity towards 5-hydroxytryptamine 4 receptor was determined in rat striatal membranes using [3H]GR-113808 as radioligandBinding affinity towards 5-hydroxytryptamine 4 receptor was determined in rat striatal membranes using [3H]GR-113808 as radioligand
ChEMBL 393 7 1 6 1.6 O=C(c1cn(c2c1cccc2)C)OCC1CCN(CC1)CCNS(=O)(=O)C 10.1021/jm960320m
90667896 109041 0 None - 1 Rat 9.8 pKi = 9.8 Binding
Displacement of [3H]GR113808 from 5-HT4 receptor in rat striatal membranes after 30 mins by liquid scintillation spectrometric analysisDisplacement of [3H]GR113808 from 5-HT4 receptor in rat striatal membranes after 30 mins by liquid scintillation spectrometric analysis
ChEMBL 330 6 2 3 3.3 CCCCN1CCC(CNC(=S)c2cccc3[nH]cnc23)CC1 10.1039/C0MD00258E
CHEMBL3221571 109041 0 None - 1 Rat 9.8 pKi = 9.8 Binding
Displacement of [3H]GR113808 from 5-HT4 receptor in rat striatal membranes after 30 mins by liquid scintillation spectrometric analysisDisplacement of [3H]GR113808 from 5-HT4 receptor in rat striatal membranes after 30 mins by liquid scintillation spectrometric analysis
ChEMBL 330 6 2 3 3.3 CCCCN1CCC(CNC(=S)c2cccc3[nH]cnc23)CC1 10.1039/C0MD00258E
53354764 3015 30 None 1 2 Human 9.8 pKi = 9.8 Binding
Displacement of [3H]GR113808 from human 5HT4D receptor expressed in HEK293 cells after 30 mins by liquid scintillation countingDisplacement of [3H]GR113808 from human 5HT4D receptor expressed in HEK293 cells after 30 mins by liquid scintillation counting
ChEMBL 432 7 1 8 2.6 OC1(CCOCC1)CN1CCC(CC1)COc1noc2c1c(ccc2)O[C@H]1COCC1 10.1021/jm300953p
9059 3015 30 None 1 2 Human 9.8 pKi = 9.8 Binding
Displacement of [3H]GR113808 from human 5HT4D receptor expressed in HEK293 cells after 30 mins by liquid scintillation countingDisplacement of [3H]GR113808 from human 5HT4D receptor expressed in HEK293 cells after 30 mins by liquid scintillation counting
ChEMBL 432 7 1 8 2.6 OC1(CCOCC1)CN1CCC(CC1)COc1noc2c1c(ccc2)O[C@H]1COCC1 10.1021/jm300953p
CHEMBL2152922 3015 30 None 1 2 Human 9.8 pKi = 9.8 Binding
Displacement of [3H]GR113808 from human 5HT4D receptor expressed in HEK293 cells after 30 mins by liquid scintillation countingDisplacement of [3H]GR113808 from human 5HT4D receptor expressed in HEK293 cells after 30 mins by liquid scintillation counting
ChEMBL 432 7 1 8 2.6 OC1(CCOCC1)CN1CCC(CC1)COc1noc2c1c(ccc2)O[C@H]1COCC1 10.1021/jm300953p
DB12675 3015 30 None 1 2 Human 9.8 pKi = 9.8 Binding
Displacement of [3H]GR113808 from human 5HT4D receptor expressed in HEK293 cells after 30 mins by liquid scintillation countingDisplacement of [3H]GR113808 from human 5HT4D receptor expressed in HEK293 cells after 30 mins by liquid scintillation counting
ChEMBL 432 7 1 8 2.6 OC1(CCOCC1)CN1CCC(CC1)COc1noc2c1c(ccc2)O[C@H]1COCC1 10.1021/jm300953p
119376 1811 41 None -1 26 Human 9.8 pKi = 9.8 Binding
Binding affinity at 5HT4 receptorBinding affinity at 5HT4 receptor
ChEMBL 393 7 1 6 1.6 O=C(c1cn(c2c1cccc2)C)OCC1CCN(CC1)CCNS(=O)(=O)C 10.1016/j.bmc.2008.11.045
247 1811 41 None -1 26 Human 9.8 pKi = 9.8 Binding
Binding affinity at 5HT4 receptorBinding affinity at 5HT4 receptor
ChEMBL 393 7 1 6 1.6 O=C(c1cn(c2c1cccc2)C)OCC1CCN(CC1)CCNS(=O)(=O)C 10.1016/j.bmc.2008.11.045
CHEMBL33884 1811 41 None -1 26 Human 9.8 pKi = 9.8 Binding
Binding affinity at 5HT4 receptorBinding affinity at 5HT4 receptor
ChEMBL 393 7 1 6 1.6 O=C(c1cn(c2c1cccc2)C)OCC1CCN(CC1)CCNS(=O)(=O)C 10.1016/j.bmc.2008.11.045
177336 3071 45 None 6 3 Human 9.8 pKi = 9.8 Binding
Displacement of [3H](1-(2-(methylsulfonamido)ethyl)piperidin-4-yl)methyl 1-methyl-1H-indole-3-carboxylate from human 5HT4R expressed in HEK293 cellsDisplacement of [3H](1-(2-(methylsulfonamido)ethyl)piperidin-4-yl)methyl 1-methyl-1H-indole-3-carboxylate from human 5HT4R expressed in HEK293 cells
ChEMBL 369 6 1 4 3.7 CCCCN1CCC(CC1)CNC(=O)c1c2OCCCn2c2c1cccc2 10.1021/jm300573d
225 3071 45 None 6 3 Human 9.8 pKi = 9.8 Binding
Displacement of [3H](1-(2-(methylsulfonamido)ethyl)piperidin-4-yl)methyl 1-methyl-1H-indole-3-carboxylate from human 5HT4R expressed in HEK293 cellsDisplacement of [3H](1-(2-(methylsulfonamido)ethyl)piperidin-4-yl)methyl 1-methyl-1H-indole-3-carboxylate from human 5HT4R expressed in HEK293 cells
ChEMBL 369 6 1 4 3.7 CCCCN1CCC(CC1)CNC(=O)c1c2OCCCn2c2c1cccc2 10.1021/jm300573d
CHEMBL356359 3071 45 None 6 3 Human 9.8 pKi = 9.8 Binding
Displacement of [3H](1-(2-(methylsulfonamido)ethyl)piperidin-4-yl)methyl 1-methyl-1H-indole-3-carboxylate from human 5HT4R expressed in HEK293 cellsDisplacement of [3H](1-(2-(methylsulfonamido)ethyl)piperidin-4-yl)methyl 1-methyl-1H-indole-3-carboxylate from human 5HT4R expressed in HEK293 cells
ChEMBL 369 6 1 4 3.7 CCCCN1CCC(CC1)CNC(=O)c1c2OCCCn2c2c1cccc2 10.1021/jm300573d
DB04873 3071 45 None 6 3 Human 9.8 pKi = 9.8 Binding
Displacement of [3H](1-(2-(methylsulfonamido)ethyl)piperidin-4-yl)methyl 1-methyl-1H-indole-3-carboxylate from human 5HT4R expressed in HEK293 cellsDisplacement of [3H](1-(2-(methylsulfonamido)ethyl)piperidin-4-yl)methyl 1-methyl-1H-indole-3-carboxylate from human 5HT4R expressed in HEK293 cells
ChEMBL 369 6 1 4 3.7 CCCCN1CCC(CC1)CNC(=O)c1c2OCCCn2c2c1cccc2 10.1021/jm300573d
21252894 84173 0 None - 1 Human 9.8 pKi = 9.8 Binding
Displacement of [3H](1-(2-(methylsulfonamido)ethyl)piperidin-4-yl)methyl 1-methyl-1H-indole-3-carboxylate from human 5HT4R expressed in HEK293 cellsDisplacement of [3H](1-(2-(methylsulfonamido)ethyl)piperidin-4-yl)methyl 1-methyl-1H-indole-3-carboxylate from human 5HT4R expressed in HEK293 cells
ChEMBL 410 7 1 4 5.0 CC(C)n1nc(C(=O)NCC2CCN(CCC3CCCCC3)CC2)c2ccccc21 10.1021/jm300573d
CHEMBL2179699 84173 0 None - 1 Human 9.8 pKi = 9.8 Binding
Displacement of [3H](1-(2-(methylsulfonamido)ethyl)piperidin-4-yl)methyl 1-methyl-1H-indole-3-carboxylate from human 5HT4R expressed in HEK293 cellsDisplacement of [3H](1-(2-(methylsulfonamido)ethyl)piperidin-4-yl)methyl 1-methyl-1H-indole-3-carboxylate from human 5HT4R expressed in HEK293 cells
ChEMBL 410 7 1 4 5.0 CC(C)n1nc(C(=O)NCC2CCN(CCC3CCCCC3)CC2)c2ccccc21 10.1021/jm300573d
CHEMBL2221066 84173 0 None - 1 Human 9.8 pKi = 9.8 Binding
Displacement of [3H](1-(2-(methylsulfonamido)ethyl)piperidin-4-yl)methyl 1-methyl-1H-indole-3-carboxylate from human 5HT4R expressed in HEK293 cellsDisplacement of [3H](1-(2-(methylsulfonamido)ethyl)piperidin-4-yl)methyl 1-methyl-1H-indole-3-carboxylate from human 5HT4R expressed in HEK293 cells
ChEMBL 410 7 1 4 5.0 CC(C)n1nc(C(=O)NCC2CCN(CCC3CCCCC3)CC2)c2ccccc21 10.1021/jm300573d
11317280 63647 0 None - 1 Human 9.8 pKi = 9.8 Binding
Inhibitory constant for human cloned 5-HT4 receptorInhibitory constant for human cloned 5-HT4 receptor
ChEMBL 466 8 2 7 0.5 O=C(NCC1CCN(CCCS(=O)(=O)N2CCNCC2)CC1)c1cccc2c1OCCO2 10.1016/j.bmcl.2005.01.039
CHEMBL180697 63647 0 None - 1 Human 9.8 pKi = 9.8 Binding
Inhibitory constant for human cloned 5-HT4 receptorInhibitory constant for human cloned 5-HT4 receptor
ChEMBL 466 8 2 7 0.5 O=C(NCC1CCN(CCCS(=O)(=O)N2CCNCC2)CC1)c1cccc2c1OCCO2 10.1016/j.bmcl.2005.01.039
44390243 64153 0 None - 1 Human 9.8 pKi = 9.8 Binding
Inhibitory constant for human cloned 5-HT4 receptorInhibitory constant for human cloned 5-HT4 receptor
ChEMBL 557 10 1 8 1.8 O=C(NCC1CCN(CCCS(=O)(=O)N2CCN(Cc3cccnc3)CC2)CC1)c1cccc2c1OCCO2 10.1016/j.bmcl.2005.01.039
CHEMBL181415 64153 0 None - 1 Human 9.8 pKi = 9.8 Binding
Inhibitory constant for human cloned 5-HT4 receptorInhibitory constant for human cloned 5-HT4 receptor
ChEMBL 557 10 1 8 1.8 O=C(NCC1CCN(CCCS(=O)(=O)N2CCN(Cc3cccnc3)CC2)CC1)c1cccc2c1OCCO2 10.1016/j.bmcl.2005.01.039
11493559 73066 0 None - 1 Guinea pig 9.7 pKi = 9.7 Binding
Displacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatumDisplacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatum
ChEMBL 324 4 1 5 2.6 COc1cc(N)c(Cl)cc1C(=O)OC[C@@H]1CCN2CCC[C@@H]12 10.1021/jm0509501
CHEMBL201621 73066 0 None - 1 Guinea pig 9.7 pKi = 9.7 Binding
Displacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatumDisplacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatum
ChEMBL 324 4 1 5 2.6 COc1cc(N)c(Cl)cc1C(=O)OC[C@@H]1CCN2CCC[C@@H]12 10.1021/jm0509501
44407083 73562 0 None 6 2 Guinea pig 9.7 pKi = 9.7 Binding
Displacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatumDisplacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatum
ChEMBL 284 3 1 3 2.8 O=C(OC[C@@H]1CCN2CCC[C@@H]12)c1c[nH]c2ccccc12 10.1021/jm0509501
CHEMBL201946 73562 0 None 6 2 Guinea pig 9.7 pKi = 9.7 Binding
Displacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatumDisplacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatum
ChEMBL 284 3 1 3 2.8 O=C(OC[C@@H]1CCN2CCC[C@@H]12)c1c[nH]c2ccccc12 10.1021/jm0509501
53317702 56147 0 None - 1 Human 9.7 pKi = 9.7 Binding
Displacement of [3H]GR113808 from human 5HT4 receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [3H]GR113808 from human 5HT4 receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 497 13 1 6 5.2 COC(=O)CCCCCCCCCN1CCC(CNC(=O)c2c3n(c4ccccc24)CCCO3)CC1 10.1016/j.bmc.2010.10.011
CHEMBL1632159 56147 0 None - 1 Human 9.7 pKi = 9.7 Binding
Displacement of [3H]GR113808 from human 5HT4 receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [3H]GR113808 from human 5HT4 receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 497 13 1 6 5.2 COC(=O)CCCCCCCCCN1CCC(CNC(=O)c2c3n(c4ccccc24)CCCO3)CC1 10.1016/j.bmc.2010.10.011
9823412 84187 0 None 398 2 Human 9.7 pKi = 9.7 Binding
Displacement of [3H](1-(2-(methylsulfonamido)ethyl)piperidin-4-yl)methyl 1-methyl-1H-indole-3-carboxylate from human 5HT4R expressed in HEK293 cellsDisplacement of [3H](1-(2-(methylsulfonamido)ethyl)piperidin-4-yl)methyl 1-methyl-1H-indole-3-carboxylate from human 5HT4R expressed in HEK293 cells
ChEMBL 419 7 2 5 3.9 CC(C)n1nc(C(=O)NCC2CCN(CCc3ccc(N)cc3)CC2)c2ccccc21 10.1021/jm300573d
CHEMBL2221193 84187 0 None 398 2 Human 9.7 pKi = 9.7 Binding
Displacement of [3H](1-(2-(methylsulfonamido)ethyl)piperidin-4-yl)methyl 1-methyl-1H-indole-3-carboxylate from human 5HT4R expressed in HEK293 cellsDisplacement of [3H](1-(2-(methylsulfonamido)ethyl)piperidin-4-yl)methyl 1-methyl-1H-indole-3-carboxylate from human 5HT4R expressed in HEK293 cells
ChEMBL 419 7 2 5 3.9 CC(C)n1nc(C(=O)NCC2CCN(CCc3ccc(N)cc3)CC2)c2ccccc21 10.1021/jm300573d
CHEMBL3216126 84187 0 None 398 2 Human 9.7 pKi = 9.7 Binding
Displacement of [3H](1-(2-(methylsulfonamido)ethyl)piperidin-4-yl)methyl 1-methyl-1H-indole-3-carboxylate from human 5HT4R expressed in HEK293 cellsDisplacement of [3H](1-(2-(methylsulfonamido)ethyl)piperidin-4-yl)methyl 1-methyl-1H-indole-3-carboxylate from human 5HT4R expressed in HEK293 cells
ChEMBL 419 7 2 5 3.9 CC(C)n1nc(C(=O)NCC2CCN(CCc3ccc(N)cc3)CC2)c2ccccc21 10.1021/jm300573d
118712569 113732 0 None - 1 Human 9.7 pKi = 9.7 Binding
Displacement of [3H]GR113808 from human 5HT4b receptor expressed in HEK293 cell membranesDisplacement of [3H]GR113808 from human 5HT4b receptor expressed in HEK293 cell membranes
ChEMBL 496 7 2 6 3.4 CS(=O)(=O)Nc1ccc(CN2CCC(CNC(=O)c3c4n(c5ccccc35)CCCO4)CC2)cc1 10.1016/j.bmcl.2014.06.083
CHEMBL3329803 113732 0 None - 1 Human 9.7 pKi = 9.7 Binding
Displacement of [3H]GR113808 from human 5HT4b receptor expressed in HEK293 cell membranesDisplacement of [3H]GR113808 from human 5HT4b receptor expressed in HEK293 cell membranes
ChEMBL 496 7 2 6 3.4 CS(=O)(=O)Nc1ccc(CN2CCC(CNC(=O)c3c4n(c5ccccc35)CCCO4)CC2)cc1 10.1016/j.bmcl.2014.06.083
118712572 113735 0 None - 1 Human 9.7 pKi = 9.7 Binding
Displacement of [3H]GR113808 from human 5HT4b receptor expressed in HEK293 cell membranesDisplacement of [3H]GR113808 from human 5HT4b receptor expressed in HEK293 cell membranes
ChEMBL 564 8 2 6 5.1 O=C(NCC1CCN(Cc2ccc(NS(=O)(=O)C3CCCCC3)cc2)CC1)c1c2n(c3ccccc13)CCCO2 10.1016/j.bmcl.2014.06.083
CHEMBL3329806 113735 0 None - 1 Human 9.7 pKi = 9.7 Binding
Displacement of [3H]GR113808 from human 5HT4b receptor expressed in HEK293 cell membranesDisplacement of [3H]GR113808 from human 5HT4b receptor expressed in HEK293 cell membranes
ChEMBL 564 8 2 6 5.1 O=C(NCC1CCN(Cc2ccc(NS(=O)(=O)C3CCCCC3)cc2)CC1)c1c2n(c3ccccc13)CCCO2 10.1016/j.bmcl.2014.06.083
118712573 113736 0 None - 1 Human 9.7 pKi = 9.7 Binding
Displacement of [3H]GR113808 from human 5HT4b receptor expressed in HEK293 cell membranesDisplacement of [3H]GR113808 from human 5HT4b receptor expressed in HEK293 cell membranes
ChEMBL 459 7 2 6 2.5 CS(=O)(=O)Nc1ccc(CN2CCC(CNC(=O)c3cccc4c3OCCO4)CC2)cc1 10.1016/j.bmcl.2014.06.083
CHEMBL3329807 113736 0 None - 1 Human 9.7 pKi = 9.7 Binding
Displacement of [3H]GR113808 from human 5HT4b receptor expressed in HEK293 cell membranesDisplacement of [3H]GR113808 from human 5HT4b receptor expressed in HEK293 cell membranes
ChEMBL 459 7 2 6 2.5 CS(=O)(=O)Nc1ccc(CN2CCC(CNC(=O)c3cccc4c3OCCO4)CC2)cc1 10.1016/j.bmcl.2014.06.083
118712575 113738 0 None - 1 Human 9.7 pKi = 9.7 Binding
Displacement of [3H]GR113808 from human 5HT4b receptor expressed in HEK293 cell membranesDisplacement of [3H]GR113808 from human 5HT4b receptor expressed in HEK293 cell membranes
ChEMBL 501 9 2 6 3.5 CC(C)CS(=O)(=O)Nc1ccc(CN2CCC(CNC(=O)c3cccc4c3OCCO4)CC2)cc1 10.1016/j.bmcl.2014.06.083
CHEMBL3329809 113738 0 None - 1 Human 9.7 pKi = 9.7 Binding
Displacement of [3H]GR113808 from human 5HT4b receptor expressed in HEK293 cell membranesDisplacement of [3H]GR113808 from human 5HT4b receptor expressed in HEK293 cell membranes
ChEMBL 501 9 2 6 3.5 CC(C)CS(=O)(=O)Nc1ccc(CN2CCC(CNC(=O)c3cccc4c3OCCO4)CC2)cc1 10.1016/j.bmcl.2014.06.083
44390192 64440 0 None - 1 Human 9.7 pKi = 9.7 Binding
Inhibitory constant for human cloned 5-HT4 receptorInhibitory constant for human cloned 5-HT4 receptor
ChEMBL 465 8 1 6 2.1 O=C(NCC1CCN(CCCS(=O)(=O)N2CCCCC2)CC1)c1cccc2c1OCCO2 10.1016/j.bmcl.2005.01.039
CHEMBL181928 64440 0 None - 1 Human 9.7 pKi = 9.7 Binding
Inhibitory constant for human cloned 5-HT4 receptorInhibitory constant for human cloned 5-HT4 receptor
ChEMBL 465 8 1 6 2.1 O=C(NCC1CCN(CCCS(=O)(=O)N2CCCCC2)CC1)c1cccc2c1OCCO2 10.1016/j.bmcl.2005.01.039
72698088 103512 0 None 20 5 Human 9.7 pKi = 9.7 Binding
Binding affinity to human 5HT4RBinding affinity to human 5HT4R
ChEMBL 421 6 0 4 5.4 Fc1cccc2c1nc(OCC1CCN(CCCC(F)(F)F)CC1)c1cccnc12 10.1016/j.bmc.2013.08.061
CHEMBL3093187 103512 0 None 20 5 Human 9.7 pKi = 9.7 Binding
Binding affinity to human 5HT4RBinding affinity to human 5HT4R
ChEMBL 421 6 0 4 5.4 Fc1cccc2c1nc(OCC1CCN(CCCC(F)(F)F)CC1)c1cccnc12 10.1016/j.bmc.2013.08.061
72545049 105246 0 None - 1 Rat 9.7 pKi = 9.7 Binding
Displacement of [3H]GR113808 from 5HT4 receptor in Sprague-Dawley rat striatal membranes after 1 hr by gamma countingDisplacement of [3H]GR113808 from 5HT4 receptor in Sprague-Dawley rat striatal membranes after 1 hr by gamma counting
ChEMBL 372 5 1 6 2.5 Nc1c(Cl)cc(C(=O)OCC2CCN(CCF)CC2)c2c1OCCO2 10.1016/j.bmcl.2013.09.097
CHEMBL3126109 105246 0 None - 1 Rat 9.7 pKi = 9.7 Binding
Displacement of [3H]GR113808 from 5HT4 receptor in Sprague-Dawley rat striatal membranes after 1 hr by gamma countingDisplacement of [3H]GR113808 from 5HT4 receptor in Sprague-Dawley rat striatal membranes after 1 hr by gamma counting
ChEMBL 372 5 1 6 2.5 Nc1c(Cl)cc(C(=O)OCC2CCN(CCF)CC2)c2c1OCCO2 10.1016/j.bmcl.2013.09.097
257 3437 9 None 1 4 Guinea pig 9.7 pKi = 9.7 Binding
Displacement of [3H]GR113808 from 5HT4 receptor in guinea pig striatal membranesDisplacement of [3H]GR113808 from 5HT4 receptor in guinea pig striatal membranes
ChEMBL 474 6 1 6 3.3 CCCCN1CCC(CC1)COC(=O)c1cc(I)c(c2c1OCCO2)N 10.1021/jm100668r
5311423 3437 9 None 1 4 Guinea pig 9.7 pKi = 9.7 Binding
Displacement of [3H]GR113808 from 5HT4 receptor in guinea pig striatal membranesDisplacement of [3H]GR113808 from 5HT4 receptor in guinea pig striatal membranes
ChEMBL 474 6 1 6 3.3 CCCCN1CCC(CC1)COC(=O)c1cc(I)c(c2c1OCCO2)N 10.1021/jm100668r
CHEMBL114112 3437 9 None 1 4 Guinea pig 9.7 pKi = 9.7 Binding
Displacement of [3H]GR113808 from 5HT4 receptor in guinea pig striatal membranesDisplacement of [3H]GR113808 from 5HT4 receptor in guinea pig striatal membranes
ChEMBL 474 6 1 6 3.3 CCCCN1CCC(CC1)COC(=O)c1cc(I)c(c2c1OCCO2)N 10.1021/jm100668r
49783421 17606 0 None 51 2 Guinea pig 9.7 pKi = 9.7 Binding
Displacement of [3H]GR113808 from 5HT4 receptor in guinea pig striatal membranesDisplacement of [3H]GR113808 from 5HT4 receptor in guinea pig striatal membranes
ChEMBL 352 9 1 5 3.3 CCCCN1CCC(COC(=O)c2ccc(N)c(OCCF)c2)CC1 10.1021/jm100668r
CHEMBL1258786 17606 0 None 51 2 Guinea pig 9.7 pKi = 9.7 Binding
Displacement of [3H]GR113808 from 5HT4 receptor in guinea pig striatal membranesDisplacement of [3H]GR113808 from 5HT4 receptor in guinea pig striatal membranes
ChEMBL 352 9 1 5 3.3 CCCCN1CCC(COC(=O)c2ccc(N)c(OCCF)c2)CC1 10.1021/jm100668r
71459269 82547 0 None 10 8 Human 9.6 pKi = 9.6 Binding
Displacement of radioligand from human 5HT4R by Cerep protocol based assayDisplacement of radioligand from human 5HT4R by Cerep protocol based assay
ChEMBL 555 7 0 4 6.3 Fc1cccc2c1nc(OCC1CCN(CCCc3ccc(I)cc3)CC1)c1cccnc12 10.1021/jm300943r
CHEMBL2181166 82547 0 None 10 8 Human 9.6 pKi = 9.6 Binding
Displacement of radioligand from human 5HT4R by Cerep protocol based assayDisplacement of radioligand from human 5HT4R by Cerep protocol based assay
ChEMBL 555 7 0 4 6.3 Fc1cccc2c1nc(OCC1CCN(CCCc3ccc(I)cc3)CC1)c1cccnc12 10.1021/jm300943r
53320711 56150 0 None - 1 Human 9.6 pKi = 9.6 Binding
Displacement of [3H]GR113808 from human 5HT4 receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [3H]GR113808 from human 5HT4 receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 455 7 1 6 4.0 CC(C)(C)OC(=O)CCCN1CCC(CNC(=O)c2c3n(c4ccccc24)CCCO3)CC1 10.1016/j.bmc.2010.10.011
CHEMBL1632162 56150 0 None - 1 Human 9.6 pKi = 9.6 Binding
Displacement of [3H]GR113808 from human 5HT4 receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [3H]GR113808 from human 5HT4 receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 455 7 1 6 4.0 CC(C)(C)OC(=O)CCCN1CCC(CNC(=O)c2c3n(c4ccccc24)CCCO3)CC1 10.1016/j.bmc.2010.10.011
17984294 84185 0 None 39 2 Human 9.6 pKi = 9.6 Binding
Displacement of [3H](1-(2-(methylsulfonamido)ethyl)piperidin-4-yl)methyl 1-methyl-1H-indole-3-carboxylate from human 5HT4R expressed in HEK293 cellsDisplacement of [3H](1-(2-(methylsulfonamido)ethyl)piperidin-4-yl)methyl 1-methyl-1H-indole-3-carboxylate from human 5HT4R expressed in HEK293 cells
ChEMBL 420 7 2 5 4.0 CC(C)n1nc(C(=O)NCC2CCN(CCc3ccc(O)cc3)CC2)c2ccccc21 10.1021/jm300573d
CHEMBL2179704 84185 0 None 39 2 Human 9.6 pKi = 9.6 Binding
Displacement of [3H](1-(2-(methylsulfonamido)ethyl)piperidin-4-yl)methyl 1-methyl-1H-indole-3-carboxylate from human 5HT4R expressed in HEK293 cellsDisplacement of [3H](1-(2-(methylsulfonamido)ethyl)piperidin-4-yl)methyl 1-methyl-1H-indole-3-carboxylate from human 5HT4R expressed in HEK293 cells
ChEMBL 420 7 2 5 4.0 CC(C)n1nc(C(=O)NCC2CCN(CCc3ccc(O)cc3)CC2)c2ccccc21 10.1021/jm300573d
CHEMBL2221162 84185 0 None 39 2 Human 9.6 pKi = 9.6 Binding
Displacement of [3H](1-(2-(methylsulfonamido)ethyl)piperidin-4-yl)methyl 1-methyl-1H-indole-3-carboxylate from human 5HT4R expressed in HEK293 cellsDisplacement of [3H](1-(2-(methylsulfonamido)ethyl)piperidin-4-yl)methyl 1-methyl-1H-indole-3-carboxylate from human 5HT4R expressed in HEK293 cells
ChEMBL 420 7 2 5 4.0 CC(C)n1nc(C(=O)NCC2CCN(CCc3ccc(O)cc3)CC2)c2ccccc21 10.1021/jm300573d
119376 1811 41 None -1 26 Human 9.6 pKi = 9.6 Binding
Displacement of [3H]GR113808 from human 5HT4b receptor expressed in HEK293 cell membranesDisplacement of [3H]GR113808 from human 5HT4b receptor expressed in HEK293 cell membranes
ChEMBL 393 7 1 6 1.6 O=C(c1cn(c2c1cccc2)C)OCC1CCN(CC1)CCNS(=O)(=O)C 10.1016/j.bmcl.2014.06.083
247 1811 41 None -1 26 Human 9.6 pKi = 9.6 Binding
Displacement of [3H]GR113808 from human 5HT4b receptor expressed in HEK293 cell membranesDisplacement of [3H]GR113808 from human 5HT4b receptor expressed in HEK293 cell membranes
ChEMBL 393 7 1 6 1.6 O=C(c1cn(c2c1cccc2)C)OCC1CCN(CC1)CCNS(=O)(=O)C 10.1016/j.bmcl.2014.06.083
CHEMBL33884 1811 41 None -1 26 Human 9.6 pKi = 9.6 Binding
Displacement of [3H]GR113808 from human 5HT4b receptor expressed in HEK293 cell membranesDisplacement of [3H]GR113808 from human 5HT4b receptor expressed in HEK293 cell membranes
ChEMBL 393 7 1 6 1.6 O=C(c1cn(c2c1cccc2)C)OCC1CCN(CC1)CCNS(=O)(=O)C 10.1016/j.bmcl.2014.06.083
118712574 113737 0 None - 1 Human 9.6 pKi = 9.6 Binding
Displacement of [3H]GR113808 from human 5HT4b receptor expressed in HEK293 cell membranesDisplacement of [3H]GR113808 from human 5HT4b receptor expressed in HEK293 cell membranes
ChEMBL 501 10 2 6 3.6 CCCCS(=O)(=O)Nc1ccc(CN2CCC(CNC(=O)c3cccc4c3OCCO4)CC2)cc1 10.1016/j.bmcl.2014.06.083
CHEMBL3329808 113737 0 None - 1 Human 9.6 pKi = 9.6 Binding
Displacement of [3H]GR113808 from human 5HT4b receptor expressed in HEK293 cell membranesDisplacement of [3H]GR113808 from human 5HT4b receptor expressed in HEK293 cell membranes
ChEMBL 501 10 2 6 3.6 CCCCS(=O)(=O)Nc1ccc(CN2CCC(CNC(=O)c3cccc4c3OCCO4)CC2)cc1 10.1016/j.bmcl.2014.06.083
177336 3071 45 None 6 3 Human 9.6 pKi = 9.6 Binding
Inhibitory constant for human cloned 5-HT4 receptorInhibitory constant for human cloned 5-HT4 receptor
ChEMBL 369 6 1 4 3.7 CCCCN1CCC(CC1)CNC(=O)c1c2OCCCn2c2c1cccc2 10.1016/j.bmcl.2005.01.039
225 3071 45 None 6 3 Human 9.6 pKi = 9.6 Binding
Inhibitory constant for human cloned 5-HT4 receptorInhibitory constant for human cloned 5-HT4 receptor
ChEMBL 369 6 1 4 3.7 CCCCN1CCC(CC1)CNC(=O)c1c2OCCCn2c2c1cccc2 10.1016/j.bmcl.2005.01.039
CHEMBL356359 3071 45 None 6 3 Human 9.6 pKi = 9.6 Binding
Inhibitory constant for human cloned 5-HT4 receptorInhibitory constant for human cloned 5-HT4 receptor
ChEMBL 369 6 1 4 3.7 CCCCN1CCC(CC1)CNC(=O)c1c2OCCCn2c2c1cccc2 10.1016/j.bmcl.2005.01.039
DB04873 3071 45 None 6 3 Human 9.6 pKi = 9.6 Binding
Inhibitory constant for human cloned 5-HT4 receptorInhibitory constant for human cloned 5-HT4 receptor
ChEMBL 369 6 1 4 3.7 CCCCN1CCC(CC1)CNC(=O)c1c2OCCCn2c2c1cccc2 10.1016/j.bmcl.2005.01.039
9869791 63595 12 None - 1 Human 9.6 pKi = 9.6 Binding
Inhibitory constant for human cloned 5-HT4 receptorInhibitory constant for human cloned 5-HT4 receptor
ChEMBL 480 8 1 7 0.9 CN1CCN(S(=O)(=O)CCCN2CCC(CNC(=O)c3cccc4c3OCCO4)CC2)CC1 10.1016/j.bmcl.2005.01.039
CHEMBL180632 63595 12 None - 1 Human 9.6 pKi = 9.6 Binding
Inhibitory constant for human cloned 5-HT4 receptorInhibitory constant for human cloned 5-HT4 receptor
ChEMBL 480 8 1 7 0.9 CN1CCN(S(=O)(=O)CCCN2CCC(CNC(=O)c3cccc4c3OCCO4)CC2)CC1 10.1016/j.bmcl.2005.01.039
44390227 122297 0 None - 1 Human 9.6 pKi = 9.6 Binding
Inhibitory constant for human cloned 5-HT4 receptorInhibitory constant for human cloned 5-HT4 receptor
ChEMBL 543 9 1 8 1.8 O=C(NCC1CCN(CCCS(=O)(=O)N2CCN(c3ccccn3)CC2)CC1)c1cccc2c1OCCO2 10.1016/j.bmcl.2005.01.039
CHEMBL360531 122297 0 None - 1 Human 9.6 pKi = 9.6 Binding
Inhibitory constant for human cloned 5-HT4 receptorInhibitory constant for human cloned 5-HT4 receptor
ChEMBL 543 9 1 8 1.8 O=C(NCC1CCN(CCCS(=O)(=O)N2CCN(c3ccccn3)CC2)CC1)c1cccc2c1OCCO2 10.1016/j.bmcl.2005.01.039
10831066 188249 3 None - 1 Rat 9.6 pKi = 9.6 Binding
Binding affinity at 5-hydroxytryptamine 4 receptor in rat striatal membranes by [3H]GR-113808 displacement.Binding affinity at 5-hydroxytryptamine 4 receptor in rat striatal membranes by [3H]GR-113808 displacement.
ChEMBL 340 5 1 5 3.1 COc1cc(N)c(Cl)cc1C(=O)OCCN1C[C@@H](C)C[C@@H](C)C1 10.1021/jm960853v
CHEMBL50660 188249 3 None - 1 Rat 9.6 pKi = 9.6 Binding
Binding affinity at 5-hydroxytryptamine 4 receptor in rat striatal membranes by [3H]GR-113808 displacement.Binding affinity at 5-hydroxytryptamine 4 receptor in rat striatal membranes by [3H]GR-113808 displacement.
ChEMBL 340 5 1 5 3.1 COc1cc(N)c(Cl)cc1C(=O)OCCN1C[C@@H](C)C[C@@H](C)C1 10.1021/jm960853v
249 2528 3 None -1 2 Rat 9.6 pKi = 9.6 Binding
Binding affinity towards 5-hydroxytryptamine 4 receptor was determined in rat striatal membranes using [3H]GR-113808 as radioligandBinding affinity towards 5-hydroxytryptamine 4 receptor was determined in rat striatal membranes using [3H]GR-113808 as radioligand
ChEMBL 340 5 1 5 3.1 COc1cc(N)c(cc1C(=O)OCCN1CC(C)CC(C1)C)Cl 10.1021/jm960320m
9905972 2528 3 None -1 2 Rat 9.6 pKi = 9.6 Binding
Binding affinity towards 5-hydroxytryptamine 4 receptor was determined in rat striatal membranes using [3H]GR-113808 as radioligandBinding affinity towards 5-hydroxytryptamine 4 receptor was determined in rat striatal membranes using [3H]GR-113808 as radioligand
ChEMBL 340 5 1 5 3.1 COc1cc(N)c(cc1C(=O)OCCN1CC(C)CC(C1)C)Cl 10.1021/jm960320m
CHEMBL155917 2528 3 None -1 2 Rat 9.6 pKi = 9.6 Binding
Binding affinity towards 5-hydroxytryptamine 4 receptor was determined in rat striatal membranes using [3H]GR-113808 as radioligandBinding affinity towards 5-hydroxytryptamine 4 receptor was determined in rat striatal membranes using [3H]GR-113808 as radioligand
ChEMBL 340 5 1 5 3.1 COc1cc(N)c(cc1C(=O)OCCN1CC(C)CC(C1)C)Cl 10.1021/jm960320m
71457409 82549 0 None 17 6 Human 9.6 pKi = 9.6 Binding
Displacement of radioligand from human 5HT4R by Cerep protocol based assayDisplacement of radioligand from human 5HT4R by Cerep protocol based assay
ChEMBL 461 5 0 4 4.9 CCCN1CCC(COc2nc3c(I)cccc3c3ncccc23)CC1 10.1021/jm300943r
CHEMBL2181168 82549 0 None 17 6 Human 9.6 pKi = 9.6 Binding
Displacement of radioligand from human 5HT4R by Cerep protocol based assayDisplacement of radioligand from human 5HT4R by Cerep protocol based assay
ChEMBL 461 5 0 4 4.9 CCCN1CCC(COc2nc3c(I)cccc3c3ncccc23)CC1 10.1021/jm300943r
71450132 82265 0 None - 1 Human 9.6 pKi = 9.6 Binding
Displacement of [3H]GR113808 from human 5HT4D receptor expressed in HEK293 cells after 30 mins by liquid scintillation countingDisplacement of [3H]GR113808 from human 5HT4D receptor expressed in HEK293 cells after 30 mins by liquid scintillation counting
ChEMBL 358 8 0 5 4.7 CCCCN1CCC(COc2noc3cccc(OC4CCC4)c23)CC1 10.1021/jm300953p
CHEMBL2179584 82265 0 None - 1 Human 9.6 pKi = 9.6 Binding
Displacement of [3H]GR113808 from human 5HT4D receptor expressed in HEK293 cells after 30 mins by liquid scintillation countingDisplacement of [3H]GR113808 from human 5HT4D receptor expressed in HEK293 cells after 30 mins by liquid scintillation counting
ChEMBL 358 8 0 5 4.7 CCCCN1CCC(COc2noc3cccc(OC4CCC4)c23)CC1 10.1021/jm300953p
10472977 96106 0 None - 1 Rat 9.5 pKi = 9.5 Binding
pKi against 5-hydroxytryptamine 4 receptor in rat striatum membranepKi against 5-hydroxytryptamine 4 receptor in rat striatum membrane
ChEMBL 348 5 2 3 3.3 CC(C)CN1CCC(CNC(=O)c2cc(Cl)cc3[nH]cnc23)CC1 10.1016/s0960-894x(01)00517-0
CHEMBL262950 96106 0 None - 1 Rat 9.5 pKi = 9.5 Binding
pKi against 5-hydroxytryptamine 4 receptor in rat striatum membranepKi against 5-hydroxytryptamine 4 receptor in rat striatum membrane
ChEMBL 348 5 2 3 3.3 CC(C)CN1CCC(CNC(=O)c2cc(Cl)cc3[nH]cnc23)CC1 10.1016/s0960-894x(01)00517-0
10472977 96106 0 None - 1 Rat 9.5 pKi = 9.5 Binding
Binding affinity to 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatum membraneBinding affinity to 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatum membrane
ChEMBL 348 5 2 3 3.3 CC(C)CN1CCC(CNC(=O)c2cc(Cl)cc3[nH]cnc23)CC1 10.1021/jm020807x
CHEMBL262950 96106 0 None - 1 Rat 9.5 pKi = 9.5 Binding
Binding affinity to 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatum membraneBinding affinity to 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatum membrane
ChEMBL 348 5 2 3 3.3 CC(C)CN1CCC(CNC(=O)c2cc(Cl)cc3[nH]cnc23)CC1 10.1021/jm020807x
71462651 82268 0 None - 1 Human 9.5 pKi = 9.5 Binding
Displacement of [3H]GR113808 from human 5HT4D receptor expressed in HEK293 cells after 30 mins by liquid scintillation countingDisplacement of [3H]GR113808 from human 5HT4D receptor expressed in HEK293 cells after 30 mins by liquid scintillation counting
ChEMBL 360 9 0 5 4.8 CCCCN1CCC(COc2noc3cccc(OCC(C)C)c23)CC1 10.1021/jm300953p
CHEMBL2179587 82268 0 None - 1 Human 9.5 pKi = 9.5 Binding
Displacement of [3H]GR113808 from human 5HT4D receptor expressed in HEK293 cells after 30 mins by liquid scintillation countingDisplacement of [3H]GR113808 from human 5HT4D receptor expressed in HEK293 cells after 30 mins by liquid scintillation counting
ChEMBL 360 9 0 5 4.8 CCCCN1CCC(COc2noc3cccc(OCC(C)C)c23)CC1 10.1021/jm300953p
10472977 96106 0 None - 1 Rat 9.5 pKi = 9.5 Binding
In vitro binding affinity to 5-hydroxytryptamine 4 receptor in rat striatum membraneIn vitro binding affinity to 5-hydroxytryptamine 4 receptor in rat striatum membrane
ChEMBL 348 5 2 3 3.3 CC(C)CN1CCC(CNC(=O)c2cc(Cl)cc3[nH]cnc23)CC1 10.1016/s0960-894x(01)00517-0
CHEMBL262950 96106 0 None - 1 Rat 9.5 pKi = 9.5 Binding
In vitro binding affinity to 5-hydroxytryptamine 4 receptor in rat striatum membraneIn vitro binding affinity to 5-hydroxytryptamine 4 receptor in rat striatum membrane
ChEMBL 348 5 2 3 3.3 CC(C)CN1CCC(CNC(=O)c2cc(Cl)cc3[nH]cnc23)CC1 10.1016/s0960-894x(01)00517-0
76310958 105247 1 None 1 2 Human 9.5 pKi = 9.5 Binding
Binding affinity to 5-HT4 receptor (unknown origin) assessed as inhibition constantBinding affinity to 5-HT4 receptor (unknown origin) assessed as inhibition constant
ChEMBL 340 3 1 6 2.2 CN1CCC(COC(=O)c2cc(Cl)c(N)c3c2OCCO3)CC1 10.1021/acs.jmedchem.2c00633
CHEMBL3126112 105247 1 None 1 2 Human 9.5 pKi = 9.5 Binding
Binding affinity to 5-HT4 receptor (unknown origin) assessed as inhibition constantBinding affinity to 5-HT4 receptor (unknown origin) assessed as inhibition constant
ChEMBL 340 3 1 6 2.2 CN1CCC(COC(=O)c2cc(Cl)c(N)c3c2OCCO3)CC1 10.1021/acs.jmedchem.2c00633
CHEMBL5182119 105247 1 None 1 2 Human 9.5 pKi = 9.5 Binding
Binding affinity to 5-HT4 receptor (unknown origin) assessed as inhibition constantBinding affinity to 5-HT4 receptor (unknown origin) assessed as inhibition constant
ChEMBL 340 3 1 6 2.2 CN1CCC(COC(=O)c2cc(Cl)c(N)c3c2OCCO3)CC1 10.1021/acs.jmedchem.2c00633
53354764 3015 30 None -1 2 Rat 9.5 pKi = 9.5 Binding
Displacement of [3H]GR113808 from 5HT4 receptor in rat striatal membrane after 30 mins by liquid scintillation countingDisplacement of [3H]GR113808 from 5HT4 receptor in rat striatal membrane after 30 mins by liquid scintillation counting
ChEMBL 432 7 1 8 2.6 OC1(CCOCC1)CN1CCC(CC1)COc1noc2c1c(ccc2)O[C@H]1COCC1 10.1021/jm300953p
9059 3015 30 None -1 2 Rat 9.5 pKi = 9.5 Binding
Displacement of [3H]GR113808 from 5HT4 receptor in rat striatal membrane after 30 mins by liquid scintillation countingDisplacement of [3H]GR113808 from 5HT4 receptor in rat striatal membrane after 30 mins by liquid scintillation counting
ChEMBL 432 7 1 8 2.6 OC1(CCOCC1)CN1CCC(CC1)COc1noc2c1c(ccc2)O[C@H]1COCC1 10.1021/jm300953p
CHEMBL2152922 3015 30 None -1 2 Rat 9.5 pKi = 9.5 Binding
Displacement of [3H]GR113808 from 5HT4 receptor in rat striatal membrane after 30 mins by liquid scintillation countingDisplacement of [3H]GR113808 from 5HT4 receptor in rat striatal membrane after 30 mins by liquid scintillation counting
ChEMBL 432 7 1 8 2.6 OC1(CCOCC1)CN1CCC(CC1)COc1noc2c1c(ccc2)O[C@H]1COCC1 10.1021/jm300953p
DB12675 3015 30 None -1 2 Rat 9.5 pKi = 9.5 Binding
Displacement of [3H]GR113808 from 5HT4 receptor in rat striatal membrane after 30 mins by liquid scintillation countingDisplacement of [3H]GR113808 from 5HT4 receptor in rat striatal membrane after 30 mins by liquid scintillation counting
ChEMBL 432 7 1 8 2.6 OC1(CCOCC1)CN1CCC(CC1)COc1noc2c1c(ccc2)O[C@H]1COCC1 10.1021/jm300953p
71712326 90955 0 None - 1 Human 9.5 pKi = 9.5 Binding
Binding affinity to human recombinant 5HT4 receptorBinding affinity to human recombinant 5HT4 receptor
ChEMBL 554 9 3 7 1.7 CC(C)c1nc2c(C(=O)NCC3CCN(CC(O)CN4CCN(S(C)(=O)=O)CC4)CC3)cc(Cl)cc2[nH]1 10.1016/j.bmcl.2013.05.018
CHEMBL2402896 90955 0 None - 1 Human 9.5 pKi = 9.5 Binding
Binding affinity to human recombinant 5HT4 receptorBinding affinity to human recombinant 5HT4 receptor
ChEMBL 554 9 3 7 1.7 CC(C)c1nc2c(C(=O)NCC3CCN(CC(O)CN4CCN(S(C)(=O)=O)CC4)CC3)cc(Cl)cc2[nH]1 10.1016/j.bmcl.2013.05.018
21252889 84153 0 None - 1 Human 9.5 pKi = 9.5 Binding
Displacement of [3H](1-(2-(methylsulfonamido)ethyl)piperidin-4-yl)methyl 1-methyl-1H-indole-3-carboxylate from human 5HT4R expressed in HEK293 cellsDisplacement of [3H](1-(2-(methylsulfonamido)ethyl)piperidin-4-yl)methyl 1-methyl-1H-indole-3-carboxylate from human 5HT4R expressed in HEK293 cells
ChEMBL 421 8 2 6 1.6 CC(C)n1nc(C(=O)NCC2CCN(CCNS(C)(=O)=O)CC2)c2ccccc21 10.1021/jm300573d
CHEMBL2179702 84153 0 None - 1 Human 9.5 pKi = 9.5 Binding
Displacement of [3H](1-(2-(methylsulfonamido)ethyl)piperidin-4-yl)methyl 1-methyl-1H-indole-3-carboxylate from human 5HT4R expressed in HEK293 cellsDisplacement of [3H](1-(2-(methylsulfonamido)ethyl)piperidin-4-yl)methyl 1-methyl-1H-indole-3-carboxylate from human 5HT4R expressed in HEK293 cells
ChEMBL 421 8 2 6 1.6 CC(C)n1nc(C(=O)NCC2CCN(CCNS(C)(=O)=O)CC2)c2ccccc21 10.1021/jm300573d
CHEMBL2220908 84153 0 None - 1 Human 9.5 pKi = 9.5 Binding
Displacement of [3H](1-(2-(methylsulfonamido)ethyl)piperidin-4-yl)methyl 1-methyl-1H-indole-3-carboxylate from human 5HT4R expressed in HEK293 cellsDisplacement of [3H](1-(2-(methylsulfonamido)ethyl)piperidin-4-yl)methyl 1-methyl-1H-indole-3-carboxylate from human 5HT4R expressed in HEK293 cells
ChEMBL 421 8 2 6 1.6 CC(C)n1nc(C(=O)NCC2CCN(CCNS(C)(=O)=O)CC2)c2ccccc21 10.1021/jm300573d
118712580 113742 0 None - 1 Human 9.5 pKi = 9.5 Binding
Displacement of [3H]GR113808 from human 5HT4b receptor expressed in HEK293 cell membranesDisplacement of [3H]GR113808 from human 5HT4b receptor expressed in HEK293 cell membranes
ChEMBL 476 7 1 6 4.7 CC(C(=O)O)c1ccc(CN2CCC(COC(=O)c3c4n(c5ccccc35)CCCO4)CC2)cc1 10.1016/j.bmcl.2014.06.083
CHEMBL3329813 113742 0 None - 1 Human 9.5 pKi = 9.5 Binding
Displacement of [3H]GR113808 from human 5HT4b receptor expressed in HEK293 cell membranesDisplacement of [3H]GR113808 from human 5HT4b receptor expressed in HEK293 cell membranes
ChEMBL 476 7 1 6 4.7 CC(C(=O)O)c1ccc(CN2CCC(COC(=O)c3c4n(c5ccccc35)CCCO4)CC2)cc1 10.1016/j.bmcl.2014.06.083
44390250 63130 0 None - 1 Human 9.5 pKi = 9.5 Binding
Inhibitory constant for human cloned 5-HT4 receptorInhibitory constant for human cloned 5-HT4 receptor
ChEMBL 544 9 1 8 0.2 CS(=O)(=O)N1CCN(S(=O)(=O)CCCN2CCC(CNC(=O)c3cccc4c3OCCO4)CC2)CC1 10.1016/j.bmcl.2005.01.039
CHEMBL179799 63130 0 None - 1 Human 9.5 pKi = 9.5 Binding
Inhibitory constant for human cloned 5-HT4 receptorInhibitory constant for human cloned 5-HT4 receptor
ChEMBL 544 9 1 8 0.2 CS(=O)(=O)N1CCN(S(=O)(=O)CCCN2CCC(CNC(=O)c3cccc4c3OCCO4)CC2)CC1 10.1016/j.bmcl.2005.01.039
10089141 205838 0 None - 1 Rat 9.5 pKi = 9.5 Binding
Binding affinity to 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatum membraneBinding affinity to 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatum membrane
ChEMBL 348 6 2 3 3.5 CCCCN1CCC(CNC(=O)c2cc(Cl)cc3[nH]cnc23)CC1 10.1021/jm020807x
CHEMBL94880 205838 0 None - 1 Rat 9.5 pKi = 9.5 Binding
Binding affinity to 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatum membraneBinding affinity to 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatum membrane
ChEMBL 348 6 2 3 3.5 CCCCN1CCC(CNC(=O)c2cc(Cl)cc3[nH]cnc23)CC1 10.1021/jm020807x
10089141 205838 0 None - 1 Rat 9.5 pKi = 9.5 Binding
Displacement of [3H]GR113808 from 5-HT4 receptor in rat striatal membranes after 30 mins by liquid scintillation spectrometric analysisDisplacement of [3H]GR113808 from 5-HT4 receptor in rat striatal membranes after 30 mins by liquid scintillation spectrometric analysis
ChEMBL 348 6 2 3 3.5 CCCCN1CCC(CNC(=O)c2cc(Cl)cc3[nH]cnc23)CC1 10.1039/C0MD00258E
CHEMBL94880 205838 0 None - 1 Rat 9.5 pKi = 9.5 Binding
Displacement of [3H]GR113808 from 5-HT4 receptor in rat striatal membranes after 30 mins by liquid scintillation spectrometric analysisDisplacement of [3H]GR113808 from 5-HT4 receptor in rat striatal membranes after 30 mins by liquid scintillation spectrometric analysis
ChEMBL 348 6 2 3 3.5 CCCCN1CCC(CNC(=O)c2cc(Cl)cc3[nH]cnc23)CC1 10.1039/C0MD00258E
53354764 3015 30 None 1 2 Human 9.5 pKi = 9.5 Binding
Displacement of [3H]GR113808 from human 5HT4E receptor expressed in CHO cells after 30 mins by liquid scintillation countingDisplacement of [3H]GR113808 from human 5HT4E receptor expressed in CHO cells after 30 mins by liquid scintillation counting
ChEMBL 432 7 1 8 2.6 OC1(CCOCC1)CN1CCC(CC1)COc1noc2c1c(ccc2)O[C@H]1COCC1 10.1021/jm300953p
9059 3015 30 None 1 2 Human 9.5 pKi = 9.5 Binding
Displacement of [3H]GR113808 from human 5HT4E receptor expressed in CHO cells after 30 mins by liquid scintillation countingDisplacement of [3H]GR113808 from human 5HT4E receptor expressed in CHO cells after 30 mins by liquid scintillation counting
ChEMBL 432 7 1 8 2.6 OC1(CCOCC1)CN1CCC(CC1)COc1noc2c1c(ccc2)O[C@H]1COCC1 10.1021/jm300953p
CHEMBL2152922 3015 30 None 1 2 Human 9.5 pKi = 9.5 Binding
Displacement of [3H]GR113808 from human 5HT4E receptor expressed in CHO cells after 30 mins by liquid scintillation countingDisplacement of [3H]GR113808 from human 5HT4E receptor expressed in CHO cells after 30 mins by liquid scintillation counting
ChEMBL 432 7 1 8 2.6 OC1(CCOCC1)CN1CCC(CC1)COc1noc2c1c(ccc2)O[C@H]1COCC1 10.1021/jm300953p
DB12675 3015 30 None 1 2 Human 9.5 pKi = 9.5 Binding
Displacement of [3H]GR113808 from human 5HT4E receptor expressed in CHO cells after 30 mins by liquid scintillation countingDisplacement of [3H]GR113808 from human 5HT4E receptor expressed in CHO cells after 30 mins by liquid scintillation counting
ChEMBL 432 7 1 8 2.6 OC1(CCOCC1)CN1CCC(CC1)COc1noc2c1c(ccc2)O[C@H]1COCC1 10.1021/jm300953p
10089141 205838 0 None - 1 Rat 9.5 pKi = 9.5 Binding
In vitro binding affinity to 5-hydroxytryptamine 4 receptor in rat striatum membraneIn vitro binding affinity to 5-hydroxytryptamine 4 receptor in rat striatum membrane
ChEMBL 348 6 2 3 3.5 CCCCN1CCC(CNC(=O)c2cc(Cl)cc3[nH]cnc23)CC1 10.1016/s0960-894x(01)00517-0
CHEMBL94880 205838 0 None - 1 Rat 9.5 pKi = 9.5 Binding
In vitro binding affinity to 5-hydroxytryptamine 4 receptor in rat striatum membraneIn vitro binding affinity to 5-hydroxytryptamine 4 receptor in rat striatum membrane
ChEMBL 348 6 2 3 3.5 CCCCN1CCC(CNC(=O)c2cc(Cl)cc3[nH]cnc23)CC1 10.1016/s0960-894x(01)00517-0
10089141 205838 0 None - 1 Rat 9.5 pKi = 9.5 Binding
pKi against 5-hydroxytryptamine 4 receptor in rat striatum membranepKi against 5-hydroxytryptamine 4 receptor in rat striatum membrane
ChEMBL 348 6 2 3 3.5 CCCCN1CCC(CNC(=O)c2cc(Cl)cc3[nH]cnc23)CC1 10.1016/s0960-894x(01)00517-0
CHEMBL94880 205838 0 None - 1 Rat 9.5 pKi = 9.5 Binding
pKi against 5-hydroxytryptamine 4 receptor in rat striatum membranepKi against 5-hydroxytryptamine 4 receptor in rat striatum membrane
ChEMBL 348 6 2 3 3.5 CCCCN1CCC(CNC(=O)c2cc(Cl)cc3[nH]cnc23)CC1 10.1016/s0960-894x(01)00517-0
119376 1811 41 None -1 26 Human 9.5 pKi = 9.5 Binding
Binding affinity was determined against cloned 5-hydroxytryptamine 4A receptor isoform expressed in COS-7 cellsBinding affinity was determined against cloned 5-hydroxytryptamine 4A receptor isoform expressed in COS-7 cells
ChEMBL 393 7 1 6 1.6 O=C(c1cn(c2c1cccc2)C)OCC1CCN(CC1)CCNS(=O)(=O)C 10.1021/jm0009538
247 1811 41 None -1 26 Human 9.5 pKi = 9.5 Binding
Binding affinity was determined against cloned 5-hydroxytryptamine 4A receptor isoform expressed in COS-7 cellsBinding affinity was determined against cloned 5-hydroxytryptamine 4A receptor isoform expressed in COS-7 cells
ChEMBL 393 7 1 6 1.6 O=C(c1cn(c2c1cccc2)C)OCC1CCN(CC1)CCNS(=O)(=O)C 10.1021/jm0009538
CHEMBL33884 1811 41 None -1 26 Human 9.5 pKi = 9.5 Binding
Binding affinity was determined against cloned 5-hydroxytryptamine 4A receptor isoform expressed in COS-7 cellsBinding affinity was determined against cloned 5-hydroxytryptamine 4A receptor isoform expressed in COS-7 cells
ChEMBL 393 7 1 6 1.6 O=C(c1cn(c2c1cccc2)C)OCC1CCN(CC1)CCNS(=O)(=O)C 10.1021/jm0009538
49783419 17567 0 None 6 13 Guinea pig 9.5 pKi = 9.5 Binding
Displacement of [3H]GR113808 from 5HT4 receptor in guinea pig striatal membranesDisplacement of [3H]GR113808 from 5HT4 receptor in guinea pig striatal membranes
ChEMBL 366 6 1 6 2.8 CCCCN1CCC(COC(=O)c2cc(F)c(N)c3c2OCCO3)CC1 10.1021/jm100668r
CHEMBL1258671 17567 0 None 6 13 Guinea pig 9.5 pKi = 9.5 Binding
Displacement of [3H]GR113808 from 5HT4 receptor in guinea pig striatal membranesDisplacement of [3H]GR113808 from 5HT4 receptor in guinea pig striatal membranes
ChEMBL 366 6 1 6 2.8 CCCCN1CCC(COC(=O)c2cc(F)c(N)c3c2OCCO3)CC1 10.1021/jm100668r
49783420 17568 0 None 51 2 Guinea pig 9.5 pKi = 9.5 Binding
Displacement of [3H]GR113808 from 5HT4 receptor in guinea pig striatal membranesDisplacement of [3H]GR113808 from 5HT4 receptor in guinea pig striatal membranes
ChEMBL 338 8 1 5 3.2 CCCCN1CCC(COC(=O)c2ccc(N)c(OCF)c2)CC1 10.1021/jm100668r
CHEMBL1258672 17568 0 None 51 2 Guinea pig 9.5 pKi = 9.5 Binding
Displacement of [3H]GR113808 from 5HT4 receptor in guinea pig striatal membranesDisplacement of [3H]GR113808 from 5HT4 receptor in guinea pig striatal membranes
ChEMBL 338 8 1 5 3.2 CCCCN1CCC(COC(=O)c2ccc(N)c(OCF)c2)CC1 10.1021/jm100668r
44461527 204065 0 None - 1 Guinea pig 9.5 pKi = 9.5 Binding
Compound was tested for binding affinity against 5-HT4 receptor in guinea pig striata using [3H]GR-113808 as radioligandCompound was tested for binding affinity against 5-HT4 receptor in guinea pig striata using [3H]GR-113808 as radioligand
ChEMBL 567 14 2 8 4.1 COc1cc(COc2cc(N)c(Cl)cc2C(=O)CCC2CCN(CCCNS(C)(=O)=O)CC2)cc(OC)c1 10.1016/S0960-894X(01)80414-5
CHEMBL82976 204065 0 None - 1 Guinea pig 9.5 pKi = 9.5 Binding
Compound was tested for binding affinity against 5-HT4 receptor in guinea pig striata using [3H]GR-113808 as radioligandCompound was tested for binding affinity against 5-HT4 receptor in guinea pig striata using [3H]GR-113808 as radioligand
ChEMBL 567 14 2 8 4.1 COc1cc(COc2cc(N)c(Cl)cc2C(=O)CCC2CCN(CCCNS(C)(=O)=O)CC2)cc(OC)c1 10.1016/S0960-894X(01)80414-5
53319411 56148 0 None - 1 Human 9.5 pKi = 9.5 Binding
Displacement of [3H]GR113808 from human 5HT4 receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [3H]GR113808 from human 5HT4 receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 525 15 1 6 5.9 COC(=O)CCCCCCCCCCCN1CCC(CNC(=O)c2c3n(c4ccccc24)CCCO3)CC1 10.1016/j.bmc.2010.10.011
CHEMBL1632160 56148 0 None - 1 Human 9.5 pKi = 9.5 Binding
Displacement of [3H]GR113808 from human 5HT4 receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [3H]GR113808 from human 5HT4 receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 525 15 1 6 5.9 COC(=O)CCCCCCCCCCCN1CCC(CNC(=O)c2c3n(c4ccccc24)CCCO3)CC1 10.1016/j.bmc.2010.10.011
53324684 56155 0 None - 1 Human 9.5 pKi = 9.5 Binding
Displacement of [3H]GR113808 from human 5HT4 receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [3H]GR113808 from human 5HT4 receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 561 8 1 8 4.8 CC(C)(C)C(=O)OCOC(=O)c1ccc(CN2CCC(CNC(=O)c3c4n(c5ccccc35)CCCO4)CC2)cc1 10.1016/j.bmc.2010.10.011
CHEMBL1632168 56155 0 None - 1 Human 9.5 pKi = 9.5 Binding
Displacement of [3H]GR113808 from human 5HT4 receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [3H]GR113808 from human 5HT4 receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 561 8 1 8 4.8 CC(C)(C)C(=O)OCOC(=O)c1ccc(CN2CCC(CNC(=O)c3c4n(c5ccccc35)CCCO4)CC2)cc1 10.1016/j.bmc.2010.10.011
11496400 11703 0 None - 1 Guinea pig 9.5 pKi = 9.5 Binding
Displacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatumDisplacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatum
ChEMBL 338 4 2 3 2.3 COc1cc(N)c(Cl)cc1C(=O)NC[C@@H]1CC[N@@+]2(C)CCC[C@@H]12 10.1021/jm0509501
CHEMBL1181946 11703 0 None - 1 Guinea pig 9.5 pKi = 9.5 Binding
Displacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatumDisplacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatum
ChEMBL 338 4 2 3 2.3 COc1cc(N)c(Cl)cc1C(=O)NC[C@@H]1CC[N@@+]2(C)CCC[C@@H]12 10.1021/jm0509501
CHEMBL199866 11703 0 None - 1 Guinea pig 9.5 pKi = 9.5 Binding
Displacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatumDisplacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatum
ChEMBL 338 4 2 3 2.3 COc1cc(N)c(Cl)cc1C(=O)NC[C@@H]1CC[N@@+]2(C)CCC[C@@H]12 10.1021/jm0509501
53354764 3015 30 None 1 2 Human 9.4 pKi = 9.4 Binding
Displacement of [3H]GR113808 from human 5HT4A receptor expressed in HEK293 cells after 30 mins by liquid scintillation countingDisplacement of [3H]GR113808 from human 5HT4A receptor expressed in HEK293 cells after 30 mins by liquid scintillation counting
ChEMBL 432 7 1 8 2.6 OC1(CCOCC1)CN1CCC(CC1)COc1noc2c1c(ccc2)O[C@H]1COCC1 10.1021/jm300953p
9059 3015 30 None 1 2 Human 9.4 pKi = 9.4 Binding
Displacement of [3H]GR113808 from human 5HT4A receptor expressed in HEK293 cells after 30 mins by liquid scintillation countingDisplacement of [3H]GR113808 from human 5HT4A receptor expressed in HEK293 cells after 30 mins by liquid scintillation counting
ChEMBL 432 7 1 8 2.6 OC1(CCOCC1)CN1CCC(CC1)COc1noc2c1c(ccc2)O[C@H]1COCC1 10.1021/jm300953p
CHEMBL2152922 3015 30 None 1 2 Human 9.4 pKi = 9.4 Binding
Displacement of [3H]GR113808 from human 5HT4A receptor expressed in HEK293 cells after 30 mins by liquid scintillation countingDisplacement of [3H]GR113808 from human 5HT4A receptor expressed in HEK293 cells after 30 mins by liquid scintillation counting
ChEMBL 432 7 1 8 2.6 OC1(CCOCC1)CN1CCC(CC1)COc1noc2c1c(ccc2)O[C@H]1COCC1 10.1021/jm300953p
DB12675 3015 30 None 1 2 Human 9.4 pKi = 9.4 Binding
Displacement of [3H]GR113808 from human 5HT4A receptor expressed in HEK293 cells after 30 mins by liquid scintillation countingDisplacement of [3H]GR113808 from human 5HT4A receptor expressed in HEK293 cells after 30 mins by liquid scintillation counting
ChEMBL 432 7 1 8 2.6 OC1(CCOCC1)CN1CCC(CC1)COc1noc2c1c(ccc2)O[C@H]1COCC1 10.1021/jm300953p
53357029 82270 0 None - 1 Human 9.4 pKi = 9.4 Binding
Displacement of [3H]GR113808 from human 5HT4D receptor expressed in HEK293 cells after 30 mins by liquid scintillation countingDisplacement of [3H]GR113808 from human 5HT4D receptor expressed in HEK293 cells after 30 mins by liquid scintillation counting
ChEMBL 418 8 1 7 3.5 CC(C)COc1cccc2onc(OCC3CCN(CC4(O)CCOCC4)CC3)c12 10.1021/jm300953p
CHEMBL2179589 82270 0 None - 1 Human 9.4 pKi = 9.4 Binding
Displacement of [3H]GR113808 from human 5HT4D receptor expressed in HEK293 cells after 30 mins by liquid scintillation countingDisplacement of [3H]GR113808 from human 5HT4D receptor expressed in HEK293 cells after 30 mins by liquid scintillation counting
ChEMBL 418 8 1 7 3.5 CC(C)COc1cccc2onc(OCC3CCN(CC4(O)CCOCC4)CC3)c12 10.1021/jm300953p
11961293 3710 13 None - 1 Human 9.4 pKi = 9.4 Binding
Binding affinity to human recombinant 5HT4 receptorBinding affinity to human recombinant 5HT4 receptor
ChEMBL 455 6 2 5 3.6 COC(=O)N1CCC(CC1)CN1CCC(CC1)CNC(=O)c1cccc2c1nc([nH]2)C(C)C 10.1016/j.bmcl.2013.05.018
8426 3710 13 None - 1 Human 9.4 pKi = 9.4 Binding
Binding affinity to human recombinant 5HT4 receptorBinding affinity to human recombinant 5HT4 receptor
ChEMBL 455 6 2 5 3.6 COC(=O)N1CCC(CC1)CN1CCC(CC1)CNC(=O)c1cccc2c1nc([nH]2)C(C)C 10.1016/j.bmcl.2013.05.018
CHEMBL2402904 3710 13 None - 1 Human 9.4 pKi = 9.4 Binding
Binding affinity to human recombinant 5HT4 receptorBinding affinity to human recombinant 5HT4 receptor
ChEMBL 455 6 2 5 3.6 COC(=O)N1CCC(CC1)CN1CCC(CC1)CNC(=O)c1cccc2c1nc([nH]2)C(C)C 10.1016/j.bmcl.2013.05.018
DB12725 3710 13 None - 1 Human 9.4 pKi = 9.4 Binding
Binding affinity to human recombinant 5HT4 receptorBinding affinity to human recombinant 5HT4 receptor
ChEMBL 455 6 2 5 3.6 COC(=O)N1CCC(CC1)CN1CCC(CC1)CNC(=O)c1cccc2c1nc([nH]2)C(C)C 10.1016/j.bmcl.2013.05.018
21252892 84151 0 None - 1 Human 9.4 pKi = 9.4 Binding
Displacement of [3H](1-(2-(methylsulfonamido)ethyl)piperidin-4-yl)methyl 1-methyl-1H-indole-3-carboxylate from human 5HT4R expressed in HEK293 cellsDisplacement of [3H](1-(2-(methylsulfonamido)ethyl)piperidin-4-yl)methyl 1-methyl-1H-indole-3-carboxylate from human 5HT4R expressed in HEK293 cells
ChEMBL 413 7 1 6 2.4 CC(C)n1nc(C(=O)NCC2CCN(CCN3CCOCC3)CC2)c2ccccc21 10.1021/jm300573d
CHEMBL2220906 84151 0 None - 1 Human 9.4 pKi = 9.4 Binding
Displacement of [3H](1-(2-(methylsulfonamido)ethyl)piperidin-4-yl)methyl 1-methyl-1H-indole-3-carboxylate from human 5HT4R expressed in HEK293 cellsDisplacement of [3H](1-(2-(methylsulfonamido)ethyl)piperidin-4-yl)methyl 1-methyl-1H-indole-3-carboxylate from human 5HT4R expressed in HEK293 cells
ChEMBL 413 7 1 6 2.4 CC(C)n1nc(C(=O)NCC2CCN(CCN3CCOCC3)CC2)c2ccccc21 10.1021/jm300573d
CHEMBL3215681 84151 0 None - 1 Human 9.4 pKi = 9.4 Binding
Displacement of [3H](1-(2-(methylsulfonamido)ethyl)piperidin-4-yl)methyl 1-methyl-1H-indole-3-carboxylate from human 5HT4R expressed in HEK293 cellsDisplacement of [3H](1-(2-(methylsulfonamido)ethyl)piperidin-4-yl)methyl 1-methyl-1H-indole-3-carboxylate from human 5HT4R expressed in HEK293 cells
ChEMBL 413 7 1 6 2.4 CC(C)n1nc(C(=O)NCC2CCN(CCN3CCOCC3)CC2)c2ccccc21 10.1021/jm300573d
177336 3071 45 None 6 3 Human 9.4 pKi = 9.4 Binding
Displacement of [3H]GR113808 from human 5HT4b receptor expressed in HEK293 cell membranesDisplacement of [3H]GR113808 from human 5HT4b receptor expressed in HEK293 cell membranes
ChEMBL 369 6 1 4 3.7 CCCCN1CCC(CC1)CNC(=O)c1c2OCCCn2c2c1cccc2 10.1016/j.bmcl.2014.06.083
225 3071 45 None 6 3 Human 9.4 pKi = 9.4 Binding
Displacement of [3H]GR113808 from human 5HT4b receptor expressed in HEK293 cell membranesDisplacement of [3H]GR113808 from human 5HT4b receptor expressed in HEK293 cell membranes
ChEMBL 369 6 1 4 3.7 CCCCN1CCC(CC1)CNC(=O)c1c2OCCCn2c2c1cccc2 10.1016/j.bmcl.2014.06.083
CHEMBL356359 3071 45 None 6 3 Human 9.4 pKi = 9.4 Binding
Displacement of [3H]GR113808 from human 5HT4b receptor expressed in HEK293 cell membranesDisplacement of [3H]GR113808 from human 5HT4b receptor expressed in HEK293 cell membranes
ChEMBL 369 6 1 4 3.7 CCCCN1CCC(CC1)CNC(=O)c1c2OCCCn2c2c1cccc2 10.1016/j.bmcl.2014.06.083
DB04873 3071 45 None 6 3 Human 9.4 pKi = 9.4 Binding
Displacement of [3H]GR113808 from human 5HT4b receptor expressed in HEK293 cell membranesDisplacement of [3H]GR113808 from human 5HT4b receptor expressed in HEK293 cell membranes
ChEMBL 369 6 1 4 3.7 CCCCN1CCC(CC1)CNC(=O)c1c2OCCCn2c2c1cccc2 10.1016/j.bmcl.2014.06.083
9912434 123335 0 None - 1 Human 9.4 pKi = 9.4 Binding
Inhibitory constant for human cloned 5-HT4 receptorInhibitory constant for human cloned 5-HT4 receptor
ChEMBL 467 8 1 7 1.0 O=C(NCC1CCN(CCCS(=O)(=O)N2CCOCC2)CC1)c1cccc2c1OCCO2 10.1016/j.bmcl.2005.01.039
CHEMBL362582 123335 0 None - 1 Human 9.4 pKi = 9.4 Binding
Inhibitory constant for human cloned 5-HT4 receptorInhibitory constant for human cloned 5-HT4 receptor
ChEMBL 467 8 1 7 1.0 O=C(NCC1CCN(CCCS(=O)(=O)N2CCOCC2)CC1)c1cccc2c1OCCO2 10.1016/j.bmcl.2005.01.039
11522273 140814 0 None 6 2 Guinea pig 9.4 pKi = 9.4 Binding
Displacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatumDisplacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatum
ChEMBL 299 3 0 5 2.2 Cn1nc(C(=O)OC[C@@H]2CCN3CCC[C@@H]23)c2ccccc21 10.1021/jm0509501
CHEMBL383577 140814 0 None 6 2 Guinea pig 9.4 pKi = 9.4 Binding
Displacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatumDisplacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatum
ChEMBL 299 3 0 5 2.2 Cn1nc(C(=O)OC[C@@H]2CCN3CCC[C@@H]23)c2ccccc21 10.1021/jm0509501
119376 1811 41 None -1 26 Human 9.4 pKi = 9.4 Binding
Binding affinity was determined against cloned 5-hydroxytryptamine 4C receptor isoform expressed in COS-7 cellsBinding affinity was determined against cloned 5-hydroxytryptamine 4C receptor isoform expressed in COS-7 cells
ChEMBL 393 7 1 6 1.6 O=C(c1cn(c2c1cccc2)C)OCC1CCN(CC1)CCNS(=O)(=O)C 10.1021/jm0009538
247 1811 41 None -1 26 Human 9.4 pKi = 9.4 Binding
Binding affinity was determined against cloned 5-hydroxytryptamine 4C receptor isoform expressed in COS-7 cellsBinding affinity was determined against cloned 5-hydroxytryptamine 4C receptor isoform expressed in COS-7 cells
ChEMBL 393 7 1 6 1.6 O=C(c1cn(c2c1cccc2)C)OCC1CCN(CC1)CCNS(=O)(=O)C 10.1021/jm0009538
CHEMBL33884 1811 41 None -1 26 Human 9.4 pKi = 9.4 Binding
Binding affinity was determined against cloned 5-hydroxytryptamine 4C receptor isoform expressed in COS-7 cellsBinding affinity was determined against cloned 5-hydroxytryptamine 4C receptor isoform expressed in COS-7 cells
ChEMBL 393 7 1 6 1.6 O=C(c1cn(c2c1cccc2)C)OCC1CCN(CC1)CCNS(=O)(=O)C 10.1021/jm0009538
145988201 166538 0 None - 1 Guinea pig 9.4 pKi = 9.4 Binding
Displacement of [3H]-GR113808 from 5-HT4R in Dunkin-Hartley guinea pig straitum nuclear membranes after 2 hrs by filter binding methodDisplacement of [3H]-GR113808 from 5-HT4R in Dunkin-Hartley guinea pig straitum nuclear membranes after 2 hrs by filter binding method
ChEMBL 366 7 0 4 4.8 CCCCN1CCC(COC(=O)c2cc(C3CC3)nc3ccccc23)CC1 10.1039/C8MD00233A
CHEMBL4289793 166538 0 None - 1 Guinea pig 9.4 pKi = 9.4 Binding
Displacement of [3H]-GR113808 from 5-HT4R in Dunkin-Hartley guinea pig straitum nuclear membranes after 2 hrs by filter binding methodDisplacement of [3H]-GR113808 from 5-HT4R in Dunkin-Hartley guinea pig straitum nuclear membranes after 2 hrs by filter binding method
ChEMBL 366 7 0 4 4.8 CCCCN1CCC(COC(=O)c2cc(C3CC3)nc3ccccc23)CC1 10.1039/C8MD00233A
49783206 17395 0 None 74 2 Guinea pig 9.4 pKi = 9.4 Binding
Displacement of [3H]GR113808 from 5HT4 receptor in guinea pig striatal membranesDisplacement of [3H]GR113808 from 5HT4 receptor in guinea pig striatal membranes
ChEMBL 373 6 1 7 2.6 CCCCN1CCC(COC(=O)c2cc(C#N)c(N)c3c2OCCO3)CC1 10.1021/jm100668r
CHEMBL1258108 17395 0 None 74 2 Guinea pig 9.4 pKi = 9.4 Binding
Displacement of [3H]GR113808 from 5HT4 receptor in guinea pig striatal membranesDisplacement of [3H]GR113808 from 5HT4 receptor in guinea pig striatal membranes
ChEMBL 373 6 1 7 2.6 CCCCN1CCC(COC(=O)c2cc(C#N)c(N)c3c2OCCO3)CC1 10.1021/jm100668r
53354764 3015 30 None 1 2 Human 9.3 pKi = 9.3 Binding
Displacement of [3H]GR113808 from human 5HT4B receptor expressed in HEK293 cells after 30 mins by liquid scintillation countingDisplacement of [3H]GR113808 from human 5HT4B receptor expressed in HEK293 cells after 30 mins by liquid scintillation counting
ChEMBL 432 7 1 8 2.6 OC1(CCOCC1)CN1CCC(CC1)COc1noc2c1c(ccc2)O[C@H]1COCC1 10.1021/jm300953p
9059 3015 30 None 1 2 Human 9.3 pKi = 9.3 Binding
Displacement of [3H]GR113808 from human 5HT4B receptor expressed in HEK293 cells after 30 mins by liquid scintillation countingDisplacement of [3H]GR113808 from human 5HT4B receptor expressed in HEK293 cells after 30 mins by liquid scintillation counting
ChEMBL 432 7 1 8 2.6 OC1(CCOCC1)CN1CCC(CC1)COc1noc2c1c(ccc2)O[C@H]1COCC1 10.1021/jm300953p
CHEMBL2152922 3015 30 None 1 2 Human 9.3 pKi = 9.3 Binding
Displacement of [3H]GR113808 from human 5HT4B receptor expressed in HEK293 cells after 30 mins by liquid scintillation countingDisplacement of [3H]GR113808 from human 5HT4B receptor expressed in HEK293 cells after 30 mins by liquid scintillation counting
ChEMBL 432 7 1 8 2.6 OC1(CCOCC1)CN1CCC(CC1)COc1noc2c1c(ccc2)O[C@H]1COCC1 10.1021/jm300953p
DB12675 3015 30 None 1 2 Human 9.3 pKi = 9.3 Binding
Displacement of [3H]GR113808 from human 5HT4B receptor expressed in HEK293 cells after 30 mins by liquid scintillation countingDisplacement of [3H]GR113808 from human 5HT4B receptor expressed in HEK293 cells after 30 mins by liquid scintillation counting
ChEMBL 432 7 1 8 2.6 OC1(CCOCC1)CN1CCC(CC1)COc1noc2c1c(ccc2)O[C@H]1COCC1 10.1021/jm300953p
44461518 204228 0 None - 1 Guinea pig 9.3 pKi = 9.3 Binding
Compound was tested for binding affinity against 5-HT4 receptor in guinea pig striata using [3H]GR-113808 as radioligandCompound was tested for binding affinity against 5-HT4 receptor in guinea pig striata using [3H]GR-113808 as radioligand
ChEMBL 567 13 1 8 4.1 COc1cc(COc2cc(N)c(Cl)cc2C(=O)CCC2CCN(CCN(C)S(C)(=O)=O)CC2)cc(OC)c1 10.1016/S0960-894X(01)80414-5
CHEMBL84294 204228 0 None - 1 Guinea pig 9.3 pKi = 9.3 Binding
Compound was tested for binding affinity against 5-HT4 receptor in guinea pig striata using [3H]GR-113808 as radioligandCompound was tested for binding affinity against 5-HT4 receptor in guinea pig striata using [3H]GR-113808 as radioligand
ChEMBL 567 13 1 8 4.1 COc1cc(COc2cc(N)c(Cl)cc2C(=O)CCC2CCN(CCN(C)S(C)(=O)=O)CC2)cc(OC)c1 10.1016/S0960-894X(01)80414-5
19081854 104263 0 None - 1 Guinea pig 9.3 pKi = 9.3 Binding
Compound was tested for binding affinity against 5-HT4 receptor in guinea pig striata using [3H]GR-113808 as radioligandCompound was tested for binding affinity against 5-HT4 receptor in guinea pig striata using [3H]GR-113808 as radioligand
ChEMBL 488 12 1 6 6.0 CCCCN1CCC(CCC(=O)c2cc(Cl)c(N)cc2OCc2cc(OC)cc(OC)c2)CC1 10.1016/S0960-894X(01)80414-5
CHEMBL310667 104263 0 None - 1 Guinea pig 9.3 pKi = 9.3 Binding
Compound was tested for binding affinity against 5-HT4 receptor in guinea pig striata using [3H]GR-113808 as radioligandCompound was tested for binding affinity against 5-HT4 receptor in guinea pig striata using [3H]GR-113808 as radioligand
ChEMBL 488 12 1 6 6.0 CCCCN1CCC(CCC(=O)c2cc(Cl)c(N)cc2OCc2cc(OC)cc(OC)c2)CC1 10.1016/S0960-894X(01)80414-5
119376 1811 41 None -1 26 Human 9.3 pKi = 9.3 Binding
Binding affinity to Rluc fused 5HT4 receptor expressed in CHO cellsBinding affinity to Rluc fused 5HT4 receptor expressed in CHO cells
ChEMBL 393 7 1 6 1.6 O=C(c1cn(c2c1cccc2)C)OCC1CCN(CC1)CCNS(=O)(=O)C 10.1021/jm070552t
247 1811 41 None -1 26 Human 9.3 pKi = 9.3 Binding
Binding affinity to Rluc fused 5HT4 receptor expressed in CHO cellsBinding affinity to Rluc fused 5HT4 receptor expressed in CHO cells
ChEMBL 393 7 1 6 1.6 O=C(c1cn(c2c1cccc2)C)OCC1CCN(CC1)CCNS(=O)(=O)C 10.1021/jm070552t
CHEMBL33884 1811 41 None -1 26 Human 9.3 pKi = 9.3 Binding
Binding affinity to Rluc fused 5HT4 receptor expressed in CHO cellsBinding affinity to Rluc fused 5HT4 receptor expressed in CHO cells
ChEMBL 393 7 1 6 1.6 O=C(c1cn(c2c1cccc2)C)OCC1CCN(CC1)CCNS(=O)(=O)C 10.1021/jm070552t
53357011 82261 0 None - 1 Human 9.3 pKi = 9.3 Binding
Displacement of [3H]GR113808 from human 5HT4D receptor expressed in HEK293 cells after 30 mins by liquid scintillation countingDisplacement of [3H]GR113808 from human 5HT4D receptor expressed in HEK293 cells after 30 mins by liquid scintillation counting
ChEMBL 446 7 2 8 2.8 O[C@@H]1CC[C@@H](Oc2cccc3onc(OCC4CCN(CC5(O)CCOCC5)CC4)c23)C1 10.1021/jm300953p
CHEMBL2179580 82261 0 None - 1 Human 9.3 pKi = 9.3 Binding
Displacement of [3H]GR113808 from human 5HT4D receptor expressed in HEK293 cells after 30 mins by liquid scintillation countingDisplacement of [3H]GR113808 from human 5HT4D receptor expressed in HEK293 cells after 30 mins by liquid scintillation counting
ChEMBL 446 7 2 8 2.8 O[C@@H]1CC[C@@H](Oc2cccc3onc(OCC4CCN(CC5(O)CCOCC5)CC4)c23)C1 10.1021/jm300953p
177336 3071 45 None 6 3 Human 9.3 pKi = 9.3 Binding
Binding affinity at 5HT4 receptorBinding affinity at 5HT4 receptor
ChEMBL 369 6 1 4 3.7 CCCCN1CCC(CC1)CNC(=O)c1c2OCCCn2c2c1cccc2 10.1016/j.bmc.2008.11.045
225 3071 45 None 6 3 Human 9.3 pKi = 9.3 Binding
Binding affinity at 5HT4 receptorBinding affinity at 5HT4 receptor
ChEMBL 369 6 1 4 3.7 CCCCN1CCC(CC1)CNC(=O)c1c2OCCCn2c2c1cccc2 10.1016/j.bmc.2008.11.045
CHEMBL356359 3071 45 None 6 3 Human 9.3 pKi = 9.3 Binding
Binding affinity at 5HT4 receptorBinding affinity at 5HT4 receptor
ChEMBL 369 6 1 4 3.7 CCCCN1CCC(CC1)CNC(=O)c1c2OCCCn2c2c1cccc2 10.1016/j.bmc.2008.11.045
DB04873 3071 45 None 6 3 Human 9.3 pKi = 9.3 Binding
Binding affinity at 5HT4 receptorBinding affinity at 5HT4 receptor
ChEMBL 369 6 1 4 3.7 CCCCN1CCC(CC1)CNC(=O)c1c2OCCCn2c2c1cccc2 10.1016/j.bmc.2008.11.045
71714540 90949 0 None - 1 Human 9.3 pKi = 9.3 Binding
Binding affinity to human recombinant 5HT4 receptorBinding affinity to human recombinant 5HT4 receptor
ChEMBL 506 9 3 7 0.5 CCc1nc2c(C(=O)NCC3CCN(CC(O)CN4CCN(S(C)(=O)=O)CC4)CC3)cccc2[nH]1 10.1016/j.bmcl.2013.05.018
CHEMBL2402890 90949 0 None - 1 Human 9.3 pKi = 9.3 Binding
Binding affinity to human recombinant 5HT4 receptorBinding affinity to human recombinant 5HT4 receptor
ChEMBL 506 9 3 7 0.5 CCc1nc2c(C(=O)NCC3CCN(CC(O)CN4CCN(S(C)(=O)=O)CC4)CC3)cccc2[nH]1 10.1016/j.bmcl.2013.05.018
71714541 90950 0 None - 1 Human 9.3 pKi = 9.3 Binding
Binding affinity to human recombinant 5HT4 receptorBinding affinity to human recombinant 5HT4 receptor
ChEMBL 520 9 3 7 1.1 CC(C)c1nc2c(C(=O)NCC3CCN(CC(O)CN4CCN(S(C)(=O)=O)CC4)CC3)cccc2[nH]1 10.1016/j.bmcl.2013.05.018
CHEMBL2402891 90950 0 None - 1 Human 9.3 pKi = 9.3 Binding
Binding affinity to human recombinant 5HT4 receptorBinding affinity to human recombinant 5HT4 receptor
ChEMBL 520 9 3 7 1.1 CC(C)c1nc2c(C(=O)NCC3CCN(CC(O)CN4CCN(S(C)(=O)=O)CC4)CC3)cccc2[nH]1 10.1016/j.bmcl.2013.05.018
71714542 90951 0 None - 1 Human 9.3 pKi = 9.3 Binding
Binding affinity to human recombinant 5HT4 receptorBinding affinity to human recombinant 5HT4 receptor
ChEMBL 518 9 3 7 0.8 CS(=O)(=O)N1CCN(CC(O)CN2CCC(CNC(=O)c3cccc4[nH]c(C5CC5)nc34)CC2)CC1 10.1016/j.bmcl.2013.05.018
CHEMBL2402892 90951 0 None - 1 Human 9.3 pKi = 9.3 Binding
Binding affinity to human recombinant 5HT4 receptorBinding affinity to human recombinant 5HT4 receptor
ChEMBL 518 9 3 7 0.8 CS(=O)(=O)N1CCN(CC(O)CN2CCC(CNC(=O)c3cccc4[nH]c(C5CC5)nc34)CC2)CC1 10.1016/j.bmcl.2013.05.018
66810955 90962 0 None - 1 Human 9.3 pKi = 9.3 Binding
Binding affinity to human recombinant 5HT4 receptorBinding affinity to human recombinant 5HT4 receptor
ChEMBL 475 7 2 5 2.8 CC(C)c1nc2c(C(=O)NCC3CCN(CC4CCN(S(C)(=O)=O)CC4)CC3)cccc2[nH]1 10.1016/j.bmcl.2013.05.018
CHEMBL2402903 90962 0 None - 1 Human 9.3 pKi = 9.3 Binding
Binding affinity to human recombinant 5HT4 receptorBinding affinity to human recombinant 5HT4 receptor
ChEMBL 475 7 2 5 2.8 CC(C)c1nc2c(C(=O)NCC3CCN(CC4CCN(S(C)(=O)=O)CC4)CC3)cccc2[nH]1 10.1016/j.bmcl.2013.05.018
177336 3071 45 None 6 3 Human 9.3 pKi = 9.3 Binding
Binding affinity was determined against 5-hydroxytryptamine 2C receptor using cloned rat receptors expressed in 293 cells radiolabeled with [3H]mesulergineBinding affinity was determined against 5-hydroxytryptamine 2C receptor using cloned rat receptors expressed in 293 cells radiolabeled with [3H]mesulergine
ChEMBL 369 6 1 4 3.7 CCCCN1CCC(CC1)CNC(=O)c1c2OCCCn2c2c1cccc2 10.1021/jm00024a002
225 3071 45 None 6 3 Human 9.3 pKi = 9.3 Binding
Binding affinity was determined against 5-hydroxytryptamine 2C receptor using cloned rat receptors expressed in 293 cells radiolabeled with [3H]mesulergineBinding affinity was determined against 5-hydroxytryptamine 2C receptor using cloned rat receptors expressed in 293 cells radiolabeled with [3H]mesulergine
ChEMBL 369 6 1 4 3.7 CCCCN1CCC(CC1)CNC(=O)c1c2OCCCn2c2c1cccc2 10.1021/jm00024a002
CHEMBL356359 3071 45 None 6 3 Human 9.3 pKi = 9.3 Binding
Binding affinity was determined against 5-hydroxytryptamine 2C receptor using cloned rat receptors expressed in 293 cells radiolabeled with [3H]mesulergineBinding affinity was determined against 5-hydroxytryptamine 2C receptor using cloned rat receptors expressed in 293 cells radiolabeled with [3H]mesulergine
ChEMBL 369 6 1 4 3.7 CCCCN1CCC(CC1)CNC(=O)c1c2OCCCn2c2c1cccc2 10.1021/jm00024a002
DB04873 3071 45 None 6 3 Human 9.3 pKi = 9.3 Binding
Binding affinity was determined against 5-hydroxytryptamine 2C receptor using cloned rat receptors expressed in 293 cells radiolabeled with [3H]mesulergineBinding affinity was determined against 5-hydroxytryptamine 2C receptor using cloned rat receptors expressed in 293 cells radiolabeled with [3H]mesulergine
ChEMBL 369 6 1 4 3.7 CCCCN1CCC(CC1)CNC(=O)c1c2OCCCn2c2c1cccc2 10.1021/jm00024a002
71457299 84184 0 None - 1 Human 9.3 pKi = 9.3 Binding
Displacement of [3H](1-(2-(methylsulfonamido)ethyl)piperidin-4-yl)methyl 1-methyl-1H-indole-3-carboxylate from human 5HT4R expressed in HEK293 cellsDisplacement of [3H](1-(2-(methylsulfonamido)ethyl)piperidin-4-yl)methyl 1-methyl-1H-indole-3-carboxylate from human 5HT4R expressed in HEK293 cells
ChEMBL 385 7 2 5 2.2 CNC(=O)CCN1CCC(CNC(=O)c2nn(C(C)C)c3ccccc23)CC1 10.1021/jm300573d
CHEMBL2179703 84184 0 None - 1 Human 9.3 pKi = 9.3 Binding
Displacement of [3H](1-(2-(methylsulfonamido)ethyl)piperidin-4-yl)methyl 1-methyl-1H-indole-3-carboxylate from human 5HT4R expressed in HEK293 cellsDisplacement of [3H](1-(2-(methylsulfonamido)ethyl)piperidin-4-yl)methyl 1-methyl-1H-indole-3-carboxylate from human 5HT4R expressed in HEK293 cells
ChEMBL 385 7 2 5 2.2 CNC(=O)CCN1CCC(CNC(=O)c2nn(C(C)C)c3ccccc23)CC1 10.1021/jm300573d
CHEMBL2221161 84184 0 None - 1 Human 9.3 pKi = 9.3 Binding
Displacement of [3H](1-(2-(methylsulfonamido)ethyl)piperidin-4-yl)methyl 1-methyl-1H-indole-3-carboxylate from human 5HT4R expressed in HEK293 cellsDisplacement of [3H](1-(2-(methylsulfonamido)ethyl)piperidin-4-yl)methyl 1-methyl-1H-indole-3-carboxylate from human 5HT4R expressed in HEK293 cells
ChEMBL 385 7 2 5 2.2 CNC(=O)CCN1CCC(CNC(=O)c2nn(C(C)C)c3ccccc23)CC1 10.1021/jm300573d
119376 1811 41 None -1 26 Human 9.3 pKi = 9.3 Binding
Binding affinity was determined against cloned 5-hydroxytryptamine 4B receptor isoform expressed in COS-7 cellsBinding affinity was determined against cloned 5-hydroxytryptamine 4B receptor isoform expressed in COS-7 cells
ChEMBL 393 7 1 6 1.6 O=C(c1cn(c2c1cccc2)C)OCC1CCN(CC1)CCNS(=O)(=O)C 10.1021/jm0009538
247 1811 41 None -1 26 Human 9.3 pKi = 9.3 Binding
Binding affinity was determined against cloned 5-hydroxytryptamine 4B receptor isoform expressed in COS-7 cellsBinding affinity was determined against cloned 5-hydroxytryptamine 4B receptor isoform expressed in COS-7 cells
ChEMBL 393 7 1 6 1.6 O=C(c1cn(c2c1cccc2)C)OCC1CCN(CC1)CCNS(=O)(=O)C 10.1021/jm0009538
CHEMBL33884 1811 41 None -1 26 Human 9.3 pKi = 9.3 Binding
Binding affinity was determined against cloned 5-hydroxytryptamine 4B receptor isoform expressed in COS-7 cellsBinding affinity was determined against cloned 5-hydroxytryptamine 4B receptor isoform expressed in COS-7 cells
ChEMBL 393 7 1 6 1.6 O=C(c1cn(c2c1cccc2)C)OCC1CCN(CC1)CCNS(=O)(=O)C 10.1021/jm0009538
44327645 206377 0 None - 1 Rat 9.3 pKi = 9.3 Binding
pKi against 5-hydroxytryptamine 4 receptor in rat striatum membranepKi against 5-hydroxytryptamine 4 receptor in rat striatum membrane
ChEMBL 362 7 2 3 3.8 CCCCCN1CCC(CNC(=O)c2cc(Cl)cc3[nH]cnc23)CC1 10.1016/s0960-894x(01)00517-0
CHEMBL97955 206377 0 None - 1 Rat 9.3 pKi = 9.3 Binding
pKi against 5-hydroxytryptamine 4 receptor in rat striatum membranepKi against 5-hydroxytryptamine 4 receptor in rat striatum membrane
ChEMBL 362 7 2 3 3.8 CCCCCN1CCC(CNC(=O)c2cc(Cl)cc3[nH]cnc23)CC1 10.1016/s0960-894x(01)00517-0
44327645 206377 0 None - 1 Rat 9.3 pKi = 9.3 Binding
Binding affinity to 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatum membraneBinding affinity to 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatum membrane
ChEMBL 362 7 2 3 3.8 CCCCCN1CCC(CNC(=O)c2cc(Cl)cc3[nH]cnc23)CC1 10.1021/jm020807x
CHEMBL97955 206377 0 None - 1 Rat 9.3 pKi = 9.3 Binding
Binding affinity to 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatum membraneBinding affinity to 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatum membrane
ChEMBL 362 7 2 3 3.8 CCCCCN1CCC(CNC(=O)c2cc(Cl)cc3[nH]cnc23)CC1 10.1021/jm020807x
44327645 206377 0 None - 1 Rat 9.3 pKi = 9.3 Binding
In vitro binding affinity to 5-hydroxytryptamine 4 receptor in rat striatum membraneIn vitro binding affinity to 5-hydroxytryptamine 4 receptor in rat striatum membrane
ChEMBL 362 7 2 3 3.8 CCCCCN1CCC(CNC(=O)c2cc(Cl)cc3[nH]cnc23)CC1 10.1016/s0960-894x(01)00517-0
CHEMBL97955 206377 0 None - 1 Rat 9.3 pKi = 9.3 Binding
In vitro binding affinity to 5-hydroxytryptamine 4 receptor in rat striatum membraneIn vitro binding affinity to 5-hydroxytryptamine 4 receptor in rat striatum membrane
ChEMBL 362 7 2 3 3.8 CCCCCN1CCC(CNC(=O)c2cc(Cl)cc3[nH]cnc23)CC1 10.1016/s0960-894x(01)00517-0
49783209 17427 0 None 3 27 Guinea pig 9.2 pKi = 9.2 Binding
Displacement of [3H]GR113808 from 5HT4 receptor in guinea pig striatal membranesDisplacement of [3H]GR113808 from 5HT4 receptor in guinea pig striatal membranes
ChEMBL 396 7 1 6 3.8 CCCCN1CCC(COC(=O)c2cc(Cl)c(NC)c3c2OCCO3)CC1 10.1021/jm100668r
CHEMBL1258223 17427 0 None 3 27 Guinea pig 9.2 pKi = 9.2 Binding
Displacement of [3H]GR113808 from 5HT4 receptor in guinea pig striatal membranesDisplacement of [3H]GR113808 from 5HT4 receptor in guinea pig striatal membranes
ChEMBL 396 7 1 6 3.8 CCCCN1CCC(COC(=O)c2cc(Cl)c(NC)c3c2OCCO3)CC1 10.1021/jm100668r
145987934 166501 0 None - 1 Guinea pig 9.2 pKi = 9.2 Binding
Displacement of [3H]-GR113808 from 5-HT4R in Dunkin-Hartley guinea pig straitum nuclear membranes after 2 hrs by filter binding methodDisplacement of [3H]-GR113808 from 5-HT4R in Dunkin-Hartley guinea pig straitum nuclear membranes after 2 hrs by filter binding method
ChEMBL 356 7 0 5 3.9 CCCCN1CCC(COC(=O)c2cc(OC)nc3ccccc23)CC1 10.1039/C8MD00233A
CHEMBL4289073 166501 0 None - 1 Guinea pig 9.2 pKi = 9.2 Binding
Displacement of [3H]-GR113808 from 5-HT4R in Dunkin-Hartley guinea pig straitum nuclear membranes after 2 hrs by filter binding methodDisplacement of [3H]-GR113808 from 5-HT4R in Dunkin-Hartley guinea pig straitum nuclear membranes after 2 hrs by filter binding method
ChEMBL 356 7 0 5 3.9 CCCCN1CCC(COC(=O)c2cc(OC)nc3ccccc23)CC1 10.1039/C8MD00233A
21252899 84164 0 None - 1 Human 9.2 pKi = 9.2 Binding
Displacement of [3H](1-(2-(methylsulfonamido)ethyl)piperidin-4-yl)methyl 1-methyl-1H-indole-3-carboxylate from human 5HT4R expressed in HEK293 cellsDisplacement of [3H](1-(2-(methylsulfonamido)ethyl)piperidin-4-yl)methyl 1-methyl-1H-indole-3-carboxylate from human 5HT4R expressed in HEK293 cells
ChEMBL 390 6 1 4 4.3 CC(C)n1nc(C(=O)NCC2CCN(Cc3ccccc3)CC2)c2ccccc21 10.1021/jm300573d
CHEMBL2179696 84164 0 None - 1 Human 9.2 pKi = 9.2 Binding
Displacement of [3H](1-(2-(methylsulfonamido)ethyl)piperidin-4-yl)methyl 1-methyl-1H-indole-3-carboxylate from human 5HT4R expressed in HEK293 cellsDisplacement of [3H](1-(2-(methylsulfonamido)ethyl)piperidin-4-yl)methyl 1-methyl-1H-indole-3-carboxylate from human 5HT4R expressed in HEK293 cells
ChEMBL 390 6 1 4 4.3 CC(C)n1nc(C(=O)NCC2CCN(Cc3ccccc3)CC2)c2ccccc21 10.1021/jm300573d
CHEMBL2220973 84164 0 None - 1 Human 9.2 pKi = 9.2 Binding
Displacement of [3H](1-(2-(methylsulfonamido)ethyl)piperidin-4-yl)methyl 1-methyl-1H-indole-3-carboxylate from human 5HT4R expressed in HEK293 cellsDisplacement of [3H](1-(2-(methylsulfonamido)ethyl)piperidin-4-yl)methyl 1-methyl-1H-indole-3-carboxylate from human 5HT4R expressed in HEK293 cells
ChEMBL 390 6 1 4 4.3 CC(C)n1nc(C(=O)NCC2CCN(Cc3ccccc3)CC2)c2ccccc21 10.1021/jm300573d
72697441 92445 0 None - 1 Human 9.2 pKi = 9.2 Binding
Displacement of [3H]GR113808 from human 5HT4B receptor expressed in HEK293 cellsDisplacement of [3H]GR113808 from human 5HT4B receptor expressed in HEK293 cells
ChEMBL 523 7 2 5 5.4 O=C(O)c1ccccc1-c1ccc(CN2CCC(CNC(=O)c3c4n(c5ccccc35)CCCO4)CC2)cc1 10.1016/j.bmc.2013.09.004
CHEMBL2440458 92445 0 None - 1 Human 9.2 pKi = 9.2 Binding
Displacement of [3H]GR113808 from human 5HT4B receptor expressed in HEK293 cellsDisplacement of [3H]GR113808 from human 5HT4B receptor expressed in HEK293 cells
ChEMBL 523 7 2 5 5.4 O=C(O)c1ccccc1-c1ccc(CN2CCC(CNC(=O)c3c4n(c5ccccc35)CCCO4)CC2)cc1 10.1016/j.bmc.2013.09.004
11014701 205895 0 None - 1 Rat 9.2 pKi = 9.2 Binding
Binding affinity to 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatum membraneBinding affinity to 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatum membrane
ChEMBL 392 6 2 3 3.6 CCCCN1CCC(CNC(=O)c2cc(Br)cc3[nH]cnc23)CC1 10.1021/jm020807x
CHEMBL95178 205895 0 None - 1 Rat 9.2 pKi = 9.2 Binding
Binding affinity to 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatum membraneBinding affinity to 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatum membrane
ChEMBL 392 6 2 3 3.6 CCCCN1CCC(CNC(=O)c2cc(Br)cc3[nH]cnc23)CC1 10.1021/jm020807x
11014701 205895 0 None - 1 Rat 9.2 pKi = 9.2 Binding
In vitro binding affinity to 5-hydroxytryptamine 4 receptor in rat striatum membraneIn vitro binding affinity to 5-hydroxytryptamine 4 receptor in rat striatum membrane
ChEMBL 392 6 2 3 3.6 CCCCN1CCC(CNC(=O)c2cc(Br)cc3[nH]cnc23)CC1 10.1016/s0960-894x(01)00517-0
CHEMBL95178 205895 0 None - 1 Rat 9.2 pKi = 9.2 Binding
In vitro binding affinity to 5-hydroxytryptamine 4 receptor in rat striatum membraneIn vitro binding affinity to 5-hydroxytryptamine 4 receptor in rat striatum membrane
ChEMBL 392 6 2 3 3.6 CCCCN1CCC(CNC(=O)c2cc(Br)cc3[nH]cnc23)CC1 10.1016/s0960-894x(01)00517-0
11014701 205895 0 None - 1 Rat 9.2 pKi = 9.2 Binding
pKi against 5-hydroxytryptamine 4 receptor in rat striatum membranepKi against 5-hydroxytryptamine 4 receptor in rat striatum membrane
ChEMBL 392 6 2 3 3.6 CCCCN1CCC(CNC(=O)c2cc(Br)cc3[nH]cnc23)CC1 10.1016/s0960-894x(01)00517-0
CHEMBL95178 205895 0 None - 1 Rat 9.2 pKi = 9.2 Binding
pKi against 5-hydroxytryptamine 4 receptor in rat striatum membranepKi against 5-hydroxytryptamine 4 receptor in rat striatum membrane
ChEMBL 392 6 2 3 3.6 CCCCN1CCC(CNC(=O)c2cc(Br)cc3[nH]cnc23)CC1 10.1016/s0960-894x(01)00517-0
119376 1811 41 None -1 26 Human 9.2 pKi = 9.2 Binding
Binding affinity to YFP fused 5HT4 receptor expressed in CHO cellsBinding affinity to YFP fused 5HT4 receptor expressed in CHO cells
ChEMBL 393 7 1 6 1.6 O=C(c1cn(c2c1cccc2)C)OCC1CCN(CC1)CCNS(=O)(=O)C 10.1021/jm070552t
247 1811 41 None -1 26 Human 9.2 pKi = 9.2 Binding
Binding affinity to YFP fused 5HT4 receptor expressed in CHO cellsBinding affinity to YFP fused 5HT4 receptor expressed in CHO cells
ChEMBL 393 7 1 6 1.6 O=C(c1cn(c2c1cccc2)C)OCC1CCN(CC1)CCNS(=O)(=O)C 10.1021/jm070552t
CHEMBL33884 1811 41 None -1 26 Human 9.2 pKi = 9.2 Binding
Binding affinity to YFP fused 5HT4 receptor expressed in CHO cellsBinding affinity to YFP fused 5HT4 receptor expressed in CHO cells
ChEMBL 393 7 1 6 1.6 O=C(c1cn(c2c1cccc2)C)OCC1CCN(CC1)CCNS(=O)(=O)C 10.1021/jm070552t
11580890 73598 0 None 4 2 Guinea pig 9.2 pKi = 9.2 Binding
Displacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatumDisplacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatum
ChEMBL 302 3 1 3 2.9 O=C(OC[C@@H]1CCN2CCC[C@@H]12)c1c[nH]c2ccc(F)cc12 10.1021/jm0509501
CHEMBL202122 73598 0 None 4 2 Guinea pig 9.2 pKi = 9.2 Binding
Displacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatumDisplacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatum
ChEMBL 302 3 1 3 2.9 O=C(OC[C@@H]1CCN2CCC[C@@H]12)c1c[nH]c2ccc(F)cc12 10.1021/jm0509501
49783415 17496 0 None 3 13 Guinea pig 9.1 pKi = 9.1 Binding
Displacement of [3H]GR113808 from 5HT4 receptor in guinea pig striatal membranesDisplacement of [3H]GR113808 from 5HT4 receptor in guinea pig striatal membranes
ChEMBL 320 7 1 5 2.9 CCCCN1CCC(COC(=O)c2ccc(N)c(OC)c2)CC1 10.1021/jm100668r
CHEMBL1258452 17496 0 None 3 13 Guinea pig 9.1 pKi = 9.1 Binding
Displacement of [3H]GR113808 from 5HT4 receptor in guinea pig striatal membranesDisplacement of [3H]GR113808 from 5HT4 receptor in guinea pig striatal membranes
ChEMBL 320 7 1 5 2.9 CCCCN1CCC(COC(=O)c2ccc(N)c(OC)c2)CC1 10.1021/jm100668r
71451951 82266 0 None - 1 Human 9.1 pKi = 9.1 Binding
Displacement of [3H]GR113808 from human 5HT4D receptor expressed in HEK293 cells after 30 mins by liquid scintillation countingDisplacement of [3H]GR113808 from human 5HT4D receptor expressed in HEK293 cells after 30 mins by liquid scintillation counting
ChEMBL 372 8 0 5 5.0 CCCCN1CCC(COc2noc3cccc(OC4CCCC4)c23)CC1 10.1021/jm300953p
CHEMBL2179585 82266 0 None - 1 Human 9.1 pKi = 9.1 Binding
Displacement of [3H]GR113808 from human 5HT4D receptor expressed in HEK293 cells after 30 mins by liquid scintillation countingDisplacement of [3H]GR113808 from human 5HT4D receptor expressed in HEK293 cells after 30 mins by liquid scintillation counting
ChEMBL 372 8 0 5 5.0 CCCCN1CCC(COc2noc3cccc(OC4CCCC4)c23)CC1 10.1021/jm300953p
5145950 201794 4 None 5 2 Guinea pig 9.1 pKi = 9.1 Binding
Compound was tested for binding affinity against 5-HT4 receptor in guinea pig striata using [3H]GR-113808 as radioligandCompound was tested for binding affinity against 5-HT4 receptor in guinea pig striata using [3H]GR-113808 as radioligand
ChEMBL 553 13 2 8 3.7 COc1cc(COc2cc(N)c(Cl)cc2C(=O)CCC2CCN(CCNS(C)(=O)=O)CC2)cc(OC)c1 10.1016/S0960-894X(01)80414-5
CHEMBL586946 201794 4 None 5 2 Guinea pig 9.1 pKi = 9.1 Binding
Compound was tested for binding affinity against 5-HT4 receptor in guinea pig striata using [3H]GR-113808 as radioligandCompound was tested for binding affinity against 5-HT4 receptor in guinea pig striata using [3H]GR-113808 as radioligand
ChEMBL 553 13 2 8 3.7 COc1cc(COc2cc(N)c(Cl)cc2C(=O)CCC2CCN(CCNS(C)(=O)=O)CC2)cc(OC)c1 10.1016/S0960-894X(01)80414-5
CHEMBL66114 201794 4 None 5 2 Guinea pig 9.1 pKi = 9.1 Binding
Compound was tested for binding affinity against 5-HT4 receptor in guinea pig striata using [3H]GR-113808 as radioligandCompound was tested for binding affinity against 5-HT4 receptor in guinea pig striata using [3H]GR-113808 as radioligand
ChEMBL 553 13 2 8 3.7 COc1cc(COc2cc(N)c(Cl)cc2C(=O)CCC2CCN(CCNS(C)(=O)=O)CC2)cc(OC)c1 10.1016/S0960-894X(01)80414-5
53322003 56149 0 None - 1 Human 9.1 pKi = 9.1 Binding
Displacement of [3H]GR113808 from human 5HT4 receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [3H]GR113808 from human 5HT4 receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 427 5 1 6 3.2 CC(C)(C)OC(=O)CN1CCC(CNC(=O)c2c3n(c4ccccc24)CCCO3)CC1 10.1016/j.bmc.2010.10.011
CHEMBL1632161 56149 0 None - 1 Human 9.1 pKi = 9.1 Binding
Displacement of [3H]GR113808 from human 5HT4 receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [3H]GR113808 from human 5HT4 receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 427 5 1 6 3.2 CC(C)(C)OC(=O)CN1CCC(CNC(=O)c2c3n(c4ccccc24)CCCO3)CC1 10.1016/j.bmc.2010.10.011
71712327 90956 0 None - 1 Human 9.1 pKi = 9.1 Binding
Binding affinity to human recombinant 5HT4 receptorBinding affinity to human recombinant 5HT4 receptor
ChEMBL 490 8 2 6 1.7 CC(C)c1nc2c(C(=O)NCC3CCN(CCN4CCN(S(C)(=O)=O)CC4)CC3)cccc2[nH]1 10.1016/j.bmcl.2013.05.018
CHEMBL2402897 90956 0 None - 1 Human 9.1 pKi = 9.1 Binding
Binding affinity to human recombinant 5HT4 receptorBinding affinity to human recombinant 5HT4 receptor
ChEMBL 490 8 2 6 1.7 CC(C)c1nc2c(C(=O)NCC3CCN(CCN4CCN(S(C)(=O)=O)CC4)CC3)cccc2[nH]1 10.1016/j.bmcl.2013.05.018
9886435 92441 0 None -1 2 Guinea pig 9.1 pKi = 9.1 Binding
Displacement of [125I]SB207710 from 5-HT4 receptor in guinea pig brain membranesDisplacement of [125I]SB207710 from 5-HT4 receptor in guinea pig brain membranes
ChEMBL 385 6 2 5 2.6 CC(O)CCN1CCC(CNC(=O)c2c3n(c4ccccc24)CCCO3)CC1 10.1016/j.bmc.2013.09.004
CHEMBL2440453 92441 0 None -1 2 Guinea pig 9.1 pKi = 9.1 Binding
Displacement of [125I]SB207710 from 5-HT4 receptor in guinea pig brain membranesDisplacement of [125I]SB207710 from 5-HT4 receptor in guinea pig brain membranes
ChEMBL 385 6 2 5 2.6 CC(O)CCN1CCC(CNC(=O)c2c3n(c4ccccc24)CCCO3)CC1 10.1016/j.bmc.2013.09.004
9886435 92441 0 None 1 2 Human 9.1 pKi = 9.1 Binding
Displacement of [125I]SB207710 from human recombinant 5-HT4 receptorDisplacement of [125I]SB207710 from human recombinant 5-HT4 receptor
ChEMBL 385 6 2 5 2.6 CC(O)CCN1CCC(CNC(=O)c2c3n(c4ccccc24)CCCO3)CC1 10.1016/j.bmc.2013.09.004
CHEMBL2440453 92441 0 None 1 2 Human 9.1 pKi = 9.1 Binding
Displacement of [125I]SB207710 from human recombinant 5-HT4 receptorDisplacement of [125I]SB207710 from human recombinant 5-HT4 receptor
ChEMBL 385 6 2 5 2.6 CC(O)CCN1CCC(CNC(=O)c2c3n(c4ccccc24)CCCO3)CC1 10.1016/j.bmc.2013.09.004
68490431 82316 0 None - 1 Human 9.1 pKi = 9.1 Binding
Displacement of [3H](1-(2-(methylsulfonamido)ethyl)piperidin-4-yl)methyl 1-methyl-1H-indole-3-carboxylate from human 5HT4R expressed in HEK293 cellsDisplacement of [3H](1-(2-(methylsulfonamido)ethyl)piperidin-4-yl)methyl 1-methyl-1H-indole-3-carboxylate from human 5HT4R expressed in HEK293 cells
ChEMBL 448 8 2 5 4.0 CC(C)n1nc(C(=O)NCC2CCN(CCc3ccc(C(=O)O)cc3)CC2)c2ccccc21 10.1021/jm300573d
CHEMBL2179707 82316 0 None - 1 Human 9.1 pKi = 9.1 Binding
Displacement of [3H](1-(2-(methylsulfonamido)ethyl)piperidin-4-yl)methyl 1-methyl-1H-indole-3-carboxylate from human 5HT4R expressed in HEK293 cellsDisplacement of [3H](1-(2-(methylsulfonamido)ethyl)piperidin-4-yl)methyl 1-methyl-1H-indole-3-carboxylate from human 5HT4R expressed in HEK293 cells
ChEMBL 448 8 2 5 4.0 CC(C)n1nc(C(=O)NCC2CCN(CCc3ccc(C(=O)O)cc3)CC2)c2ccccc21 10.1021/jm300573d
21252902 84152 0 None - 1 Human 9.1 pKi = 9.1 Binding
Displacement of [3H](1-(2-(methylsulfonamido)ethyl)piperidin-4-yl)methyl 1-methyl-1H-indole-3-carboxylate from human 5HT4R expressed in HEK293 cellsDisplacement of [3H](1-(2-(methylsulfonamido)ethyl)piperidin-4-yl)methyl 1-methyl-1H-indole-3-carboxylate from human 5HT4R expressed in HEK293 cells
ChEMBL 385 8 1 5 3.0 CC(C)n1nc(C(=O)NCC2CCN(CCCN(C)C)CC2)c2ccccc21 10.1021/jm300573d
CHEMBL2179701 84152 0 None - 1 Human 9.1 pKi = 9.1 Binding
Displacement of [3H](1-(2-(methylsulfonamido)ethyl)piperidin-4-yl)methyl 1-methyl-1H-indole-3-carboxylate from human 5HT4R expressed in HEK293 cellsDisplacement of [3H](1-(2-(methylsulfonamido)ethyl)piperidin-4-yl)methyl 1-methyl-1H-indole-3-carboxylate from human 5HT4R expressed in HEK293 cells
ChEMBL 385 8 1 5 3.0 CC(C)n1nc(C(=O)NCC2CCN(CCCN(C)C)CC2)c2ccccc21 10.1021/jm300573d
CHEMBL2220907 84152 0 None - 1 Human 9.1 pKi = 9.1 Binding
Displacement of [3H](1-(2-(methylsulfonamido)ethyl)piperidin-4-yl)methyl 1-methyl-1H-indole-3-carboxylate from human 5HT4R expressed in HEK293 cellsDisplacement of [3H](1-(2-(methylsulfonamido)ethyl)piperidin-4-yl)methyl 1-methyl-1H-indole-3-carboxylate from human 5HT4R expressed in HEK293 cells
ChEMBL 385 8 1 5 3.0 CC(C)n1nc(C(=O)NCC2CCN(CCCN(C)C)CC2)c2ccccc21 10.1021/jm300573d
70694780 76063 0 None - 1 Human 9.1 pKi = 9.1 Binding
Displacement of [3H]GR113808 from human recombinant 5HT4C receptor expressed in HEK293 cellsDisplacement of [3H]GR113808 from human recombinant 5HT4C receptor expressed in HEK293 cells
ChEMBL 509 12 1 6 5.0 COC[C@@H]1CCCN1CCCCCCN1[C@H]2CC[C@@H]1C[C@H](NC(=O)c1nn(C(C)C)c3ccccc13)C2 10.1016/j.bmcl.2012.05.034
CHEMBL2059582 76063 0 None - 1 Human 9.1 pKi = 9.1 Binding
Displacement of [3H]GR113808 from human recombinant 5HT4C receptor expressed in HEK293 cellsDisplacement of [3H]GR113808 from human recombinant 5HT4C receptor expressed in HEK293 cells
ChEMBL 509 12 1 6 5.0 COC[C@@H]1CCCN1CCCCCCN1[C@H]2CC[C@@H]1C[C@H](NC(=O)c1nn(C(C)C)c3ccccc13)C2 10.1016/j.bmcl.2012.05.034
252 3290 1 None -1 2 Human 9.1 pKi = 9.1 Binding
Inhibitory constant for human cloned 5-HT4 receptorInhibitory constant for human cloned 5-HT4 receptor
ChEMBL 332 6 1 4 2.7 CCCCN1CCC(CC1)CNC(=O)c1cccc2c1OCCO2 10.1016/j.bmcl.2005.01.039
44391713 3290 1 None -1 2 Human 9.1 pKi = 9.1 Binding
Inhibitory constant for human cloned 5-HT4 receptorInhibitory constant for human cloned 5-HT4 receptor
ChEMBL 332 6 1 4 2.7 CCCCN1CCC(CC1)CNC(=O)c1cccc2c1OCCO2 10.1016/j.bmcl.2005.01.039
CHEMBL182590 3290 1 None -1 2 Human 9.1 pKi = 9.1 Binding
Inhibitory constant for human cloned 5-HT4 receptorInhibitory constant for human cloned 5-HT4 receptor
ChEMBL 332 6 1 4 2.7 CCCCN1CCC(CC1)CNC(=O)c1cccc2c1OCCO2 10.1016/j.bmcl.2005.01.039
11508052 73489 0 None 4 2 Guinea pig 9.1 pKi = 9.1 Binding
Displacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatumDisplacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatum
ChEMBL 285 3 1 4 2.2 O=C(OC[C@@H]1CCN2CCC[C@@H]12)c1[nH]nc2ccccc12 10.1021/jm0509501
CHEMBL201878 73489 0 None 4 2 Guinea pig 9.1 pKi = 9.1 Binding
Displacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatumDisplacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatum
ChEMBL 285 3 1 4 2.2 O=C(OC[C@@H]1CCN2CCC[C@@H]12)c1[nH]nc2ccccc12 10.1021/jm0509501
19081848 204150 0 None - 1 Guinea pig 9.1 pKi = 9.1 Binding
Compound was tested for binding affinity against 5-HT4 receptor in guinea pig striata using [3H]GR-113808 as radioligandCompound was tested for binding affinity against 5-HT4 receptor in guinea pig striata using [3H]GR-113808 as radioligand
ChEMBL 502 13 1 6 6.4 CCCCCN1CCC(CCC(=O)c2cc(Cl)c(N)cc2OCc2cc(OC)cc(OC)c2)CC1 10.1016/S0960-894X(01)80414-5
CHEMBL83755 204150 0 None - 1 Guinea pig 9.1 pKi = 9.1 Binding
Compound was tested for binding affinity against 5-HT4 receptor in guinea pig striata using [3H]GR-113808 as radioligandCompound was tested for binding affinity against 5-HT4 receptor in guinea pig striata using [3H]GR-113808 as radioligand
ChEMBL 502 13 1 6 6.4 CCCCCN1CCC(CCC(=O)c2cc(Cl)c(N)cc2OCc2cc(OC)cc(OC)c2)CC1 10.1016/S0960-894X(01)80414-5
145981672 165995 0 None - 1 Guinea pig 9.1 pKi = 9.1 Binding
Displacement of [3H]-GR113808 from 5-HT4R in Dunkin-Hartley guinea pig straitum nuclear membranes after 2 hrs by filter binding methodDisplacement of [3H]-GR113808 from 5-HT4R in Dunkin-Hartley guinea pig straitum nuclear membranes after 2 hrs by filter binding method
ChEMBL 360 6 0 4 4.6 CCCCN1CCC(COC(=O)c2cc(Cl)nc3ccccc23)CC1 10.1039/C8MD00233A
CHEMBL4279446 165995 0 None - 1 Guinea pig 9.1 pKi = 9.1 Binding
Displacement of [3H]-GR113808 from 5-HT4R in Dunkin-Hartley guinea pig straitum nuclear membranes after 2 hrs by filter binding methodDisplacement of [3H]-GR113808 from 5-HT4R in Dunkin-Hartley guinea pig straitum nuclear membranes after 2 hrs by filter binding method
ChEMBL 360 6 0 4 4.6 CCCCN1CCC(COC(=O)c2cc(Cl)nc3ccccc23)CC1 10.1039/C8MD00233A
49783417 17532 0 None 18 2 Guinea pig 9.0 pKi = 9.0 Binding
Displacement of [3H]GR113808 from 5HT4 receptor in guinea pig striatal membranesDisplacement of [3H]GR113808 from 5HT4 receptor in guinea pig striatal membranes
ChEMBL 306 6 1 5 2.6 CCCN1CCC(COC(=O)c2ccc(N)c(OC)c2)CC1 10.1021/jm100668r
CHEMBL1258560 17532 0 None 18 2 Guinea pig 9.0 pKi = 9.0 Binding
Displacement of [3H]GR113808 from 5HT4 receptor in guinea pig striatal membranesDisplacement of [3H]GR113808 from 5HT4 receptor in guinea pig striatal membranes
ChEMBL 306 6 1 5 2.6 CCCN1CCC(COC(=O)c2ccc(N)c(OC)c2)CC1 10.1021/jm100668r
9973683 119302 0 None - 1 Rat 9.0 pKi = 9.0 Binding
Binding affinity towards 5-hydroxytryptamine 4 receptor was determined in rat striatal membranes using [3H]GR-113808 as radioligandBinding affinity towards 5-hydroxytryptamine 4 receptor was determined in rat striatal membranes using [3H]GR-113808 as radioligand
ChEMBL 326 5 1 5 3.0 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCCCCC1 10.1021/jm960320m
CHEMBL348311 119302 0 None - 1 Rat 9.0 pKi = 9.0 Binding
Binding affinity towards 5-hydroxytryptamine 4 receptor was determined in rat striatal membranes using [3H]GR-113808 as radioligandBinding affinity towards 5-hydroxytryptamine 4 receptor was determined in rat striatal membranes using [3H]GR-113808 as radioligand
ChEMBL 326 5 1 5 3.0 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCCCCC1 10.1021/jm960320m
10381762 49038 0 None - 1 Rat 9.0 pKi = 9.0 Binding
Binding affinity towards 5-hydroxytryptamine 4 receptor was determined in rat striatal membranes using [3H]GR-113808 as radioligandBinding affinity towards 5-hydroxytryptamine 4 receptor was determined in rat striatal membranes using [3H]GR-113808 as radioligand
ChEMBL 326 5 1 5 2.8 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCCC(C)C1 10.1021/jm960320m
CHEMBL156349 49038 0 None - 1 Rat 9.0 pKi = 9.0 Binding
Binding affinity towards 5-hydroxytryptamine 4 receptor was determined in rat striatal membranes using [3H]GR-113808 as radioligandBinding affinity towards 5-hydroxytryptamine 4 receptor was determined in rat striatal membranes using [3H]GR-113808 as radioligand
ChEMBL 326 5 1 5 2.8 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCCC(C)C1 10.1021/jm960320m
44213662 204871 0 None - 1 Rat 9.0 pKi = 9.0 Binding
Binding affinity at 5-hydroxytryptamine 4 receptor in rat striatum by [3H]GR-113808 displacement.Binding affinity at 5-hydroxytryptamine 4 receptor in rat striatum by [3H]GR-113808 displacement.
ChEMBL 324 4 1 5 2.5 Nc1c(Cl)cc(C(=O)OCCN2CCCCC2)c2c1CCO2 10.1016/0960-894X(96)00002-9
CHEMBL88973 204871 0 None - 1 Rat 9.0 pKi = 9.0 Binding
Binding affinity at 5-hydroxytryptamine 4 receptor in rat striatum by [3H]GR-113808 displacement.Binding affinity at 5-hydroxytryptamine 4 receptor in rat striatum by [3H]GR-113808 displacement.
ChEMBL 324 4 1 5 2.5 Nc1c(Cl)cc(C(=O)OCCN2CCCCC2)c2c1CCO2 10.1016/0960-894X(96)00002-9
118734523 118175 0 None - 1 Guinea pig 9.0 pKi = 9.0 Binding
Displacement of [3H]GR113808 from 5-HT4R in guinea pig brain membranes incubated for 30 mins by radioligand binding assayDisplacement of [3H]GR113808 from 5-HT4R in guinea pig brain membranes incubated for 30 mins by radioligand binding assay
ChEMBL 394 6 1 5 4.4 COc1cc(N)c(Cl)cc1C(=O)OCC1CCN(CC2CCCCC2)CC1 10.1021/acs.jmedchem.5b00115
CHEMBL3417008 118175 0 None - 1 Guinea pig 9.0 pKi = 9.0 Binding
Displacement of [3H]GR113808 from 5-HT4R in guinea pig brain membranes incubated for 30 mins by radioligand binding assayDisplacement of [3H]GR113808 from 5-HT4R in guinea pig brain membranes incubated for 30 mins by radioligand binding assay
ChEMBL 394 6 1 5 4.4 COc1cc(N)c(Cl)cc1C(=O)OCC1CCN(CC2CCCCC2)CC1 10.1021/acs.jmedchem.5b00115
71462650 82267 0 None - 1 Human 9.0 pKi = 9.0 Binding
Displacement of [3H]GR113808 from human 5HT4D receptor expressed in HEK293 cells after 30 mins by liquid scintillation countingDisplacement of [3H]GR113808 from human 5HT4D receptor expressed in HEK293 cells after 30 mins by liquid scintillation counting
ChEMBL 372 9 0 5 4.9 CCCCN1CCC(COc2noc3cccc(OCC4CCC4)c23)CC1 10.1021/jm300953p
CHEMBL2179586 82267 0 None - 1 Human 9.0 pKi = 9.0 Binding
Displacement of [3H]GR113808 from human 5HT4D receptor expressed in HEK293 cells after 30 mins by liquid scintillation countingDisplacement of [3H]GR113808 from human 5HT4D receptor expressed in HEK293 cells after 30 mins by liquid scintillation counting
ChEMBL 372 9 0 5 4.9 CCCCN1CCC(COc2noc3cccc(OCC4CCC4)c23)CC1 10.1021/jm300953p
71712466 90810 0 None - 1 Human 9.0 pKi = 9 Binding
Binding affinity to human recombinant 5HT4 receptorBinding affinity to human recombinant 5HT4 receptor
ChEMBL 439 6 2 4 3.4 CC(=O)N1CCC(CN2CCC(CNC(=O)c3cccc4[nH]c(C(C)C)nc34)CC2)CC1 10.1016/j.bmcl.2013.05.018
CHEMBL2401750 90810 0 None - 1 Human 9.0 pKi = 9 Binding
Binding affinity to human recombinant 5HT4 receptorBinding affinity to human recombinant 5HT4 receptor
ChEMBL 439 6 2 4 3.4 CC(=O)N1CCC(CN2CCC(CNC(=O)c3cccc4[nH]c(C(C)C)nc34)CC2)CC1 10.1016/j.bmcl.2013.05.018
15295138 50789 0 None - 1 Rat 9.0 pKi = 9 Binding
Binding affinity towards 5-hydroxytryptamine 4 receptor was determined in rat striatal membranes using [3H]GR-113808 as radioligandBinding affinity towards 5-hydroxytryptamine 4 receptor was determined in rat striatal membranes using [3H]GR-113808 as radioligand
ChEMBL 328 5 2 6 1.5 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCCC(O)C1 10.1021/jm960320m
CHEMBL157880 50789 0 None - 1 Rat 9.0 pKi = 9 Binding
Binding affinity towards 5-hydroxytryptamine 4 receptor was determined in rat striatal membranes using [3H]GR-113808 as radioligandBinding affinity towards 5-hydroxytryptamine 4 receptor was determined in rat striatal membranes using [3H]GR-113808 as radioligand
ChEMBL 328 5 2 6 1.5 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCCC(O)C1 10.1021/jm960320m
235 2527 36 None -4 3 Human 9.0 pKi = 9 Binding
Binding affinity towards cloned human 5-hydroxytryptamine 4E receptor expressed in C6 glial cells using [3H]GR-113808 as radioligandBinding affinity towards cloned human 5-hydroxytryptamine 4E receptor expressed in C6 glial cells using [3H]GR-113808 as radioligand
ChEMBL 312 5 1 5 2.6 COc1cc(N)c(cc1C(=O)OCCN1CCCCC1)Cl 10.1021/jm0307887
5311299 2527 36 None -4 3 Human 9.0 pKi = 9 Binding
Binding affinity towards cloned human 5-hydroxytryptamine 4E receptor expressed in C6 glial cells using [3H]GR-113808 as radioligandBinding affinity towards cloned human 5-hydroxytryptamine 4E receptor expressed in C6 glial cells using [3H]GR-113808 as radioligand
ChEMBL 312 5 1 5 2.6 COc1cc(N)c(cc1C(=O)OCCN1CCCCC1)Cl 10.1021/jm0307887
CHEMBL286136 2527 36 None -4 3 Human 9.0 pKi = 9 Binding
Binding affinity towards cloned human 5-hydroxytryptamine 4E receptor expressed in C6 glial cells using [3H]GR-113808 as radioligandBinding affinity towards cloned human 5-hydroxytryptamine 4E receptor expressed in C6 glial cells using [3H]GR-113808 as radioligand
ChEMBL 312 5 1 5 2.6 COc1cc(N)c(cc1C(=O)OCCN1CCCCC1)Cl 10.1021/jm0307887
9800656 15375 0 None - 1 Human 9.0 pKi = 9 Binding
Binding affinity was determined against cloned 5-hydroxytryptamine 4E receptor isoform expressed in C6 glial cells incubated with 0.2 nM [3H]GR-113808Binding affinity was determined against cloned 5-hydroxytryptamine 4E receptor isoform expressed in C6 glial cells incubated with 0.2 nM [3H]GR-113808
ChEMBL 391 6 1 8 1.7 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCN(c2ncccn2)CC1 10.1021/jm0009538
CHEMBL121913 15375 0 None - 1 Human 9.0 pKi = 9 Binding
Binding affinity was determined against cloned 5-hydroxytryptamine 4E receptor isoform expressed in C6 glial cells incubated with 0.2 nM [3H]GR-113808Binding affinity was determined against cloned 5-hydroxytryptamine 4E receptor isoform expressed in C6 glial cells incubated with 0.2 nM [3H]GR-113808
ChEMBL 391 6 1 8 1.7 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCN(c2ncccn2)CC1 10.1021/jm0009538
118712570 113733 0 None - 1 Human 9.0 pKi = 9 Binding
Displacement of [3H]GR113808 from human 5HT4b receptor expressed in HEK293 cell membranesDisplacement of [3H]GR113808 from human 5HT4b receptor expressed in HEK293 cell membranes
ChEMBL 538 10 2 6 4.6 CCCCS(=O)(=O)Nc1ccc(CN2CCC(CNC(=O)c3c4n(c5ccccc35)CCCO4)CC2)cc1 10.1016/j.bmcl.2014.06.083
CHEMBL3329804 113733 0 None - 1 Human 9.0 pKi = 9 Binding
Displacement of [3H]GR113808 from human 5HT4b receptor expressed in HEK293 cell membranesDisplacement of [3H]GR113808 from human 5HT4b receptor expressed in HEK293 cell membranes
ChEMBL 538 10 2 6 4.6 CCCCS(=O)(=O)Nc1ccc(CN2CCC(CNC(=O)c3c4n(c5ccccc35)CCCO4)CC2)cc1 10.1016/j.bmcl.2014.06.083
70696825 76059 0 None - 1 Human 9.0 pKi = 9 Binding
Displacement of [3H]GR113808 from human recombinant 5HT4C receptor expressed in HEK293 cellsDisplacement of [3H]GR113808 from human recombinant 5HT4C receptor expressed in HEK293 cells
ChEMBL 479 10 1 5 5.4 CC(C)n1nc(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CCCCCCN2CCCCC2)c2ccccc21 10.1016/j.bmcl.2012.05.034
CHEMBL2059578 76059 0 None - 1 Human 9.0 pKi = 9 Binding
Displacement of [3H]GR113808 from human recombinant 5HT4C receptor expressed in HEK293 cellsDisplacement of [3H]GR113808 from human recombinant 5HT4C receptor expressed in HEK293 cells
ChEMBL 479 10 1 5 5.4 CC(C)n1nc(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CCCCCCN2CCCCC2)c2ccccc21 10.1016/j.bmcl.2012.05.034
70696826 76061 0 None - 1 Human 9.0 pKi = 9 Binding
Displacement of [3H]GR113808 from human recombinant 5HT4C receptor expressed in HEK293 cellsDisplacement of [3H]GR113808 from human recombinant 5HT4C receptor expressed in HEK293 cells
ChEMBL 467 11 1 5 5.2 CC(C)N(C)CCCCCCN1[C@H]2CC[C@@H]1C[C@H](NC(=O)c1nn(C(C)C)c3ccccc13)C2 10.1016/j.bmcl.2012.05.034
CHEMBL2059580 76061 0 None - 1 Human 9.0 pKi = 9 Binding
Displacement of [3H]GR113808 from human recombinant 5HT4C receptor expressed in HEK293 cellsDisplacement of [3H]GR113808 from human recombinant 5HT4C receptor expressed in HEK293 cells
ChEMBL 467 11 1 5 5.2 CC(C)N(C)CCCCCCN1[C@H]2CC[C@@H]1C[C@H](NC(=O)c1nn(C(C)C)c3ccccc13)C2 10.1016/j.bmcl.2012.05.034
255 3433 13 None 1 2 Guinea pig 9.0 pKi = 9 Binding
In vitro by displacement of [3H]GR-113808 from 5-hydroxytryptamine 4 receptor on guinea pig striatal membraneIn vitro by displacement of [3H]GR-113808 from 5-hydroxytryptamine 4 receptor on guinea pig striatal membrane
ChEMBL 272 4 1 3 2.8 O=C(c1c[nH]c2c1cccc2)OCCN1CCCCC1 10.1021/jm960442e
3272300 3433 13 None 1 2 Guinea pig 9.0 pKi = 9 Binding
In vitro by displacement of [3H]GR-113808 from 5-hydroxytryptamine 4 receptor on guinea pig striatal membraneIn vitro by displacement of [3H]GR-113808 from 5-hydroxytryptamine 4 receptor on guinea pig striatal membrane
ChEMBL 272 4 1 3 2.8 O=C(c1c[nH]c2c1cccc2)OCCN1CCCCC1 10.1021/jm960442e
CHEMBL1255781 3433 13 None 1 2 Guinea pig 9.0 pKi = 9 Binding
In vitro by displacement of [3H]GR-113808 from 5-hydroxytryptamine 4 receptor on guinea pig striatal membraneIn vitro by displacement of [3H]GR-113808 from 5-hydroxytryptamine 4 receptor on guinea pig striatal membrane
ChEMBL 272 4 1 3 2.8 O=C(c1c[nH]c2c1cccc2)OCCN1CCCCC1 10.1021/jm960442e
10615668 186101 0 None - 1 Rat 9.0 pKi = 9.0 Binding
Binding affinity at 5-hydroxytryptamine 4 receptor in rat striatal membranes by [3H]GR-113808 displacement.Binding affinity at 5-hydroxytryptamine 4 receptor in rat striatal membranes by [3H]GR-113808 displacement.
ChEMBL 320 6 1 4 3.6 CCOc1ccccc1NC(=O)OCCN1C[C@@H](C)C[C@@H](C)C1 10.1021/jm960853v
CHEMBL48836 186101 0 None - 1 Rat 9.0 pKi = 9.0 Binding
Binding affinity at 5-hydroxytryptamine 4 receptor in rat striatal membranes by [3H]GR-113808 displacement.Binding affinity at 5-hydroxytryptamine 4 receptor in rat striatal membranes by [3H]GR-113808 displacement.
ChEMBL 320 6 1 4 3.6 CCOc1ccccc1NC(=O)OCCN1C[C@@H](C)C[C@@H](C)C1 10.1021/jm960853v
10690483 49035 0 None - 1 Rat 9.0 pKi = 9.0 Binding
Binding affinity towards 5-hydroxytryptamine 4 receptor was determined in rat striatal membranes using [3H]GR-113808 as radioligandBinding affinity towards 5-hydroxytryptamine 4 receptor was determined in rat striatal membranes using [3H]GR-113808 as radioligand
ChEMBL 369 6 2 6 1.7 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCC(NC(C)=O)CC1 10.1021/jm960320m
CHEMBL156348 49035 0 None - 1 Rat 9.0 pKi = 9.0 Binding
Binding affinity towards 5-hydroxytryptamine 4 receptor was determined in rat striatal membranes using [3H]GR-113808 as radioligandBinding affinity towards 5-hydroxytryptamine 4 receptor was determined in rat striatal membranes using [3H]GR-113808 as radioligand
ChEMBL 369 6 2 6 1.7 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCC(NC(C)=O)CC1 10.1021/jm960320m
235 2527 36 None 4 3 Rat 9.0 pKi = 9.0 Binding
Binding affinity against 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatumBinding affinity against 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatum
ChEMBL 312 5 1 5 2.6 COc1cc(N)c(cc1C(=O)OCCN1CCCCC1)Cl 10.1016/S0960-894X(01)80508-4
5311299 2527 36 None 4 3 Rat 9.0 pKi = 9.0 Binding
Binding affinity against 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatumBinding affinity against 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatum
ChEMBL 312 5 1 5 2.6 COc1cc(N)c(cc1C(=O)OCCN1CCCCC1)Cl 10.1016/S0960-894X(01)80508-4
CHEMBL286136 2527 36 None 4 3 Rat 9.0 pKi = 9.0 Binding
Binding affinity against 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatumBinding affinity against 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatum
ChEMBL 312 5 1 5 2.6 COc1cc(N)c(cc1C(=O)OCCN1CCCCC1)Cl 10.1016/S0960-894X(01)80508-4
235 2527 36 None 4 3 Rat 9.0 pKi = 9.0 Binding
Binding affinity at 5-hydroxytryptamine 4 receptor in rat striatal membranes by [3H]GR-113808 displacement.Binding affinity at 5-hydroxytryptamine 4 receptor in rat striatal membranes by [3H]GR-113808 displacement.
ChEMBL 312 5 1 5 2.6 COc1cc(N)c(cc1C(=O)OCCN1CCCCC1)Cl 10.1021/jm960853v
5311299 2527 36 None 4 3 Rat 9.0 pKi = 9.0 Binding
Binding affinity at 5-hydroxytryptamine 4 receptor in rat striatal membranes by [3H]GR-113808 displacement.Binding affinity at 5-hydroxytryptamine 4 receptor in rat striatal membranes by [3H]GR-113808 displacement.
ChEMBL 312 5 1 5 2.6 COc1cc(N)c(cc1C(=O)OCCN1CCCCC1)Cl 10.1021/jm960853v
CHEMBL286136 2527 36 None 4 3 Rat 9.0 pKi = 9.0 Binding
Binding affinity at 5-hydroxytryptamine 4 receptor in rat striatal membranes by [3H]GR-113808 displacement.Binding affinity at 5-hydroxytryptamine 4 receptor in rat striatal membranes by [3H]GR-113808 displacement.
ChEMBL 312 5 1 5 2.6 COc1cc(N)c(cc1C(=O)OCCN1CCCCC1)Cl 10.1021/jm960853v
235 2527 36 None 4 3 Rat 9.0 pKi = 9.0 Binding
Binding affinity towards 5-hydroxytryptamine 4 receptor was determined in rat striatal membranes using [3H]GR-113808 as radioligandBinding affinity towards 5-hydroxytryptamine 4 receptor was determined in rat striatal membranes using [3H]GR-113808 as radioligand
ChEMBL 312 5 1 5 2.6 COc1cc(N)c(cc1C(=O)OCCN1CCCCC1)Cl 10.1021/jm960320m
5311299 2527 36 None 4 3 Rat 9.0 pKi = 9.0 Binding
Binding affinity towards 5-hydroxytryptamine 4 receptor was determined in rat striatal membranes using [3H]GR-113808 as radioligandBinding affinity towards 5-hydroxytryptamine 4 receptor was determined in rat striatal membranes using [3H]GR-113808 as radioligand
ChEMBL 312 5 1 5 2.6 COc1cc(N)c(cc1C(=O)OCCN1CCCCC1)Cl 10.1021/jm960320m
CHEMBL286136 2527 36 None 4 3 Rat 9.0 pKi = 9.0 Binding
Binding affinity towards 5-hydroxytryptamine 4 receptor was determined in rat striatal membranes using [3H]GR-113808 as radioligandBinding affinity towards 5-hydroxytryptamine 4 receptor was determined in rat striatal membranes using [3H]GR-113808 as radioligand
ChEMBL 312 5 1 5 2.6 COc1cc(N)c(cc1C(=O)OCCN1CCCCC1)Cl 10.1021/jm960320m
53320712 56158 0 None - 1 Human 9.0 pKi = 9.0 Binding
Displacement of [3H]GR113808 from human 5HT4 receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [3H]GR113808 from human 5HT4 receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 385 6 2 5 2.3 O=C(O)CCN1CCC(CNC(=O)c2c3n(c4ccccc24)CCCO3)CC1 10.1016/j.bmc.2010.10.011
CHEMBL1632171 56158 0 None - 1 Human 9.0 pKi = 9.0 Binding
Displacement of [3H]GR113808 from human 5HT4 receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [3H]GR113808 from human 5HT4 receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 385 6 2 5 2.3 O=C(O)CCN1CCC(CNC(=O)c2c3n(c4ccccc24)CCCO3)CC1 10.1016/j.bmc.2010.10.011
71454555 79224 0 None - 1 Rat 8.9 pKi = 8.9 Binding
Binding affinity at 5-hydroxytryptamine 4 receptor in rat striatal membranes by [3H]GR-113808 displacement.Binding affinity at 5-hydroxytryptamine 4 receptor in rat striatal membranes by [3H]GR-113808 displacement.
ChEMBL 320 6 1 4 3.6 CCOc1ccccc1NC(=O)OCCN1C[C@H](C)C[C@@H](C)C1 10.1021/jm960853v
CHEMBL2115017 79224 0 None - 1 Rat 8.9 pKi = 8.9 Binding
Binding affinity at 5-hydroxytryptamine 4 receptor in rat striatal membranes by [3H]GR-113808 displacement.Binding affinity at 5-hydroxytryptamine 4 receptor in rat striatal membranes by [3H]GR-113808 displacement.
ChEMBL 320 6 1 4 3.6 CCOc1ccccc1NC(=O)OCCN1C[C@H](C)C[C@@H](C)C1 10.1021/jm960853v
71462776 82550 0 None 11 7 Human 8.9 pKi = 8.9 Binding
Displacement of radioligand from human 5HT4R by Cerep protocol based assayDisplacement of radioligand from human 5HT4R by Cerep protocol based assay
ChEMBL 460 5 0 3 5.5 CCCN1CCC(COc2nc3c(I)cccc3c3ccccc23)CC1 10.1021/jm300943r
CHEMBL2181169 82550 0 None 11 7 Human 8.9 pKi = 8.9 Binding
Displacement of radioligand from human 5HT4R by Cerep protocol based assayDisplacement of radioligand from human 5HT4R by Cerep protocol based assay
ChEMBL 460 5 0 3 5.5 CCCN1CCC(COc2nc3c(I)cccc3c3ccccc23)CC1 10.1021/jm300943r
71712325 90954 0 None - 1 Human 8.9 pKi = 8.9 Binding
Binding affinity to human recombinant 5HT4 receptorBinding affinity to human recombinant 5HT4 receptor
ChEMBL 554 9 3 7 1.6 CS(=O)(=O)N1CCN(CC(O)CN2CCC(CNC(=O)c3cccc4[nH]c(-c5ccccc5)nc34)CC2)CC1 10.1016/j.bmcl.2013.05.018
CHEMBL2402895 90954 0 None - 1 Human 8.9 pKi = 8.9 Binding
Binding affinity to human recombinant 5HT4 receptorBinding affinity to human recombinant 5HT4 receptor
ChEMBL 554 9 3 7 1.6 CS(=O)(=O)N1CCN(CC(O)CN2CCC(CNC(=O)c3cccc4[nH]c(-c5ccccc5)nc34)CC2)CC1 10.1016/j.bmcl.2013.05.018
71712463 90959 0 None - 1 Human 8.9 pKi = 8.9 Binding
Binding affinity to human recombinant 5HT4 receptorBinding affinity to human recombinant 5HT4 receptor
ChEMBL 465 9 3 6 1.4 CC(C)c1nc2c(C(=O)NCC3CCN(CC(O)CN(C)S(C)(=O)=O)CC3)cccc2[nH]1 10.1016/j.bmcl.2013.05.018
CHEMBL2402900 90959 0 None - 1 Human 8.9 pKi = 8.9 Binding
Binding affinity to human recombinant 5HT4 receptorBinding affinity to human recombinant 5HT4 receptor
ChEMBL 465 9 3 6 1.4 CC(C)c1nc2c(C(=O)NCC3CCN(CC(O)CN(C)S(C)(=O)=O)CC3)cccc2[nH]1 10.1016/j.bmcl.2013.05.018
11293856 84186 0 None 794 2 Human 8.9 pKi = 8.9 Binding
Displacement of [3H](1-(2-(methylsulfonamido)ethyl)piperidin-4-yl)methyl 1-methyl-1H-indole-3-carboxylate from human 5HT4R expressed in HEK293 cellsDisplacement of [3H](1-(2-(methylsulfonamido)ethyl)piperidin-4-yl)methyl 1-methyl-1H-indole-3-carboxylate from human 5HT4R expressed in HEK293 cells
ChEMBL 449 8 1 6 4.2 CC(C)n1nc(C(=O)NCC2CCN(CCc3ccc([N+](=O)[O-])cc3)CC2)c2ccccc21 10.1021/jm300573d
CHEMBL2179705 84186 0 None 794 2 Human 8.9 pKi = 8.9 Binding
Displacement of [3H](1-(2-(methylsulfonamido)ethyl)piperidin-4-yl)methyl 1-methyl-1H-indole-3-carboxylate from human 5HT4R expressed in HEK293 cellsDisplacement of [3H](1-(2-(methylsulfonamido)ethyl)piperidin-4-yl)methyl 1-methyl-1H-indole-3-carboxylate from human 5HT4R expressed in HEK293 cells
ChEMBL 449 8 1 6 4.2 CC(C)n1nc(C(=O)NCC2CCN(CCc3ccc([N+](=O)[O-])cc3)CC2)c2ccccc21 10.1021/jm300573d
CHEMBL2221192 84186 0 None 794 2 Human 8.9 pKi = 8.9 Binding
Displacement of [3H](1-(2-(methylsulfonamido)ethyl)piperidin-4-yl)methyl 1-methyl-1H-indole-3-carboxylate from human 5HT4R expressed in HEK293 cellsDisplacement of [3H](1-(2-(methylsulfonamido)ethyl)piperidin-4-yl)methyl 1-methyl-1H-indole-3-carboxylate from human 5HT4R expressed in HEK293 cells
ChEMBL 449 8 1 6 4.2 CC(C)n1nc(C(=O)NCC2CCN(CCc3ccc([N+](=O)[O-])cc3)CC2)c2ccccc21 10.1021/jm300573d
53322004 56152 0 None - 1 Human 8.9 pKi = 8.9 Binding
Displacement of [3H]GR113808 from human 5HT4 receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [3H]GR113808 from human 5HT4 receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 477 10 1 7 4.1 CCOP(=O)(CCN1CCC(CNC(=O)c2c3n(c4ccccc24)CCCO3)CC1)OCC 10.1016/j.bmc.2010.10.011
CHEMBL1632164 56152 0 None - 1 Human 8.9 pKi = 8.9 Binding
Displacement of [3H]GR113808 from human 5HT4 receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [3H]GR113808 from human 5HT4 receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 477 10 1 7 4.1 CCOP(=O)(CCN1CCC(CNC(=O)c2c3n(c4ccccc24)CCCO3)CC1)OCC 10.1016/j.bmc.2010.10.011
118712576 113739 0 None - 1 Human 8.9 pKi = 8.9 Binding
Displacement of [3H]GR113808 from human 5HT4b receptor expressed in HEK293 cell membranesDisplacement of [3H]GR113808 from human 5HT4b receptor expressed in HEK293 cell membranes
ChEMBL 527 8 2 6 4.2 O=C(NCC1CCN(Cc2ccc(NS(=O)(=O)C3CCCCC3)cc2)CC1)c1cccc2c1OCCO2 10.1016/j.bmcl.2014.06.083
CHEMBL3329810 113739 0 None - 1 Human 8.9 pKi = 8.9 Binding
Displacement of [3H]GR113808 from human 5HT4b receptor expressed in HEK293 cell membranesDisplacement of [3H]GR113808 from human 5HT4b receptor expressed in HEK293 cell membranes
ChEMBL 527 8 2 6 4.2 O=C(NCC1CCN(Cc2ccc(NS(=O)(=O)C3CCCCC3)cc2)CC1)c1cccc2c1OCCO2 10.1016/j.bmcl.2014.06.083
118712578 113740 0 None - 1 Human 8.9 pKi = 8.9 Binding
Displacement of [3H]GR113808 from human 5HT4b receptor expressed in HEK293 cell membranesDisplacement of [3H]GR113808 from human 5HT4b receptor expressed in HEK293 cell membranes
ChEMBL 440 6 1 6 3.8 O=C(OCC1CCN(CC2CCC(C(=O)O)C2)CC1)c1c2n(c3ccccc13)CCCO2 10.1016/j.bmcl.2014.06.083
CHEMBL3329811 113740 0 None - 1 Human 8.9 pKi = 8.9 Binding
Displacement of [3H]GR113808 from human 5HT4b receptor expressed in HEK293 cell membranesDisplacement of [3H]GR113808 from human 5HT4b receptor expressed in HEK293 cell membranes
ChEMBL 440 6 1 6 3.8 O=C(OCC1CCN(CC2CCC(C(=O)O)C2)CC1)c1c2n(c3ccccc13)CCCO2 10.1016/j.bmcl.2014.06.083
118712579 113741 0 None - 1 Human 8.9 pKi = 8.9 Binding
Displacement of [3H]GR113808 from human 5HT4b receptor expressed in HEK293 cell membranesDisplacement of [3H]GR113808 from human 5HT4b receptor expressed in HEK293 cell membranes
ChEMBL 454 6 1 6 4.2 O=C(OCC1CCN(CC2CCCC(C(=O)O)C2)CC1)c1c2n(c3ccccc13)CCCO2 10.1016/j.bmcl.2014.06.083
CHEMBL3329812 113741 0 None - 1 Human 8.9 pKi = 8.9 Binding
Displacement of [3H]GR113808 from human 5HT4b receptor expressed in HEK293 cell membranesDisplacement of [3H]GR113808 from human 5HT4b receptor expressed in HEK293 cell membranes
ChEMBL 454 6 1 6 4.2 O=C(OCC1CCN(CC2CCCC(C(=O)O)C2)CC1)c1c2n(c3ccccc13)CCCO2 10.1016/j.bmcl.2014.06.083
44248186 193790 0 None - 1 Human 8.9 pKi = 8.9 Binding
Displacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 567 15 3 5 6.1 COc1cc(N)c(Cl)cc1C(=O)NC1CCN(CCCCCCCCN(C)CCc2c[nH]c3ccccc23)CC1 10.1021/jm900881j
CHEMBL552484 193790 0 None - 1 Human 8.9 pKi = 8.9 Binding
Displacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 567 15 3 5 6.1 COc1cc(N)c(Cl)cc1C(=O)NC1CCN(CCCCCCCCN(C)CCc2c[nH]c3ccccc23)CC1 10.1021/jm900881j
10524522 15350 0 None - 1 Human 8.9 pKi = 8.9 Binding
Binding affinity was determined against cloned 5-hydroxytryptamine 4E receptor isoform expressed in C6 glial cells incubated with 0.2 nM [3H]GR-113808Binding affinity was determined against cloned 5-hydroxytryptamine 4E receptor isoform expressed in C6 glial cells incubated with 0.2 nM [3H]GR-113808
ChEMBL 391 6 1 8 1.7 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCN(c2cnccn2)CC1 10.1021/jm0009538
CHEMBL121776 15350 0 None - 1 Human 8.9 pKi = 8.9 Binding
Binding affinity was determined against cloned 5-hydroxytryptamine 4E receptor isoform expressed in C6 glial cells incubated with 0.2 nM [3H]GR-113808Binding affinity was determined against cloned 5-hydroxytryptamine 4E receptor isoform expressed in C6 glial cells incubated with 0.2 nM [3H]GR-113808
ChEMBL 391 6 1 8 1.7 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCN(c2cnccn2)CC1 10.1021/jm0009538
10548505 112605 0 None - 1 Human 8.9 pKi = 8.9 Binding
Binding affinity was determined against cloned 5-hydroxytryptamine 4E receptor isoform expressed in C6 glial cells incubated with 0.2 nM [3H]GR-113808Binding affinity was determined against cloned 5-hydroxytryptamine 4E receptor isoform expressed in C6 glial cells incubated with 0.2 nM [3H]GR-113808
ChEMBL 391 6 1 8 1.7 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCN(c2cccnn2)CC1 10.1021/jm0009538
CHEMBL331396 112605 0 None - 1 Human 8.9 pKi = 8.9 Binding
Binding affinity was determined against cloned 5-hydroxytryptamine 4E receptor isoform expressed in C6 glial cells incubated with 0.2 nM [3H]GR-113808Binding affinity was determined against cloned 5-hydroxytryptamine 4E receptor isoform expressed in C6 glial cells incubated with 0.2 nM [3H]GR-113808
ChEMBL 391 6 1 8 1.7 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCN(c2cccnn2)CC1 10.1021/jm0009538
133999 73966 6 None 5 2 Guinea pig 8.9 pKi = 8.9 Binding
Displacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatumDisplacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatum
ChEMBL 318 3 1 4 2.2 O=C(NC[C@@H]1CCN2CCC[C@@H]12)c1cc(Cl)cn2ccnc12 10.1021/jm0509501
CHEMBL202434 73966 6 None 5 2 Guinea pig 8.9 pKi = 8.9 Binding
Displacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatumDisplacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatum
ChEMBL 318 3 1 4 2.2 O=C(NC[C@@H]1CCN2CCC[C@@H]12)c1cc(Cl)cn2ccnc12 10.1021/jm0509501
52945318 17361 0 None - 1 Human 8.9 pKi = 8.9 Binding
Displacement of [3H]GR113808 from human recombinant 5HT4 receptor expressed in HEK293 cellsDisplacement of [3H]GR113808 from human recombinant 5HT4 receptor expressed in HEK293 cells
ChEMBL 348 6 1 6 2.7 CCCCN1CCC(COC(=O)c2ccc(N)c3c2OCCO3)CC1 10.1021/jm100668r
CHEMBL1257991 17361 0 None - 1 Human 8.9 pKi = 8.9 Binding
Displacement of [3H]GR113808 from human recombinant 5HT4 receptor expressed in HEK293 cellsDisplacement of [3H]GR113808 from human recombinant 5HT4 receptor expressed in HEK293 cells
ChEMBL 348 6 1 6 2.7 CCCCN1CCC(COC(=O)c2ccc(N)c3c2OCCO3)CC1 10.1021/jm100668r
44592414 178591 0 None - 1 Human 8.9 pKi = 8.9 Binding
Binding affinity at 5HT4 receptorBinding affinity at 5HT4 receptor
ChEMBL 332 3 2 3 2.8 C[C@@]12CCCN1CC[C@H]2CNC(=O)c1cc(Cl)cc2nc[nH]c12 10.1016/j.bmc.2008.11.045
CHEMBL472219 178591 0 None - 1 Human 8.9 pKi = 8.9 Binding
Binding affinity at 5HT4 receptorBinding affinity at 5HT4 receptor
ChEMBL 332 3 2 3 2.8 C[C@@]12CCCN1CC[C@H]2CNC(=O)c1cc(Cl)cc2nc[nH]c12 10.1016/j.bmc.2008.11.045
9905514 119177 0 None - 1 Rat 8.9 pKi = 8.9 Binding
Binding affinity towards 5-hydroxytryptamine 4 receptor was determined in rat striatal membranes using [3H]GR-113808 as radioligandBinding affinity towards 5-hydroxytryptamine 4 receptor was determined in rat striatal membranes using [3H]GR-113808 as radioligand
ChEMBL 328 5 2 6 1.5 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCC(O)CC1 10.1021/jm960320m
CHEMBL347235 119177 0 None - 1 Rat 8.9 pKi = 8.9 Binding
Binding affinity towards 5-hydroxytryptamine 4 receptor was determined in rat striatal membranes using [3H]GR-113808 as radioligandBinding affinity towards 5-hydroxytryptamine 4 receptor was determined in rat striatal membranes using [3H]GR-113808 as radioligand
ChEMBL 328 5 2 6 1.5 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCC(O)CC1 10.1021/jm960320m
10570203 49286 0 None - 1 Rat 8.9 pKi = 8.9 Binding
Binding affinity towards 5-hydroxytryptamine 4 receptor was determined in rat striatal membranes using [3H]GR-113808 as radioligandBinding affinity towards 5-hydroxytryptamine 4 receptor was determined in rat striatal membranes using [3H]GR-113808 as radioligand
ChEMBL 355 6 2 6 1.3 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCC(C(N)=O)CC1 10.1021/jm960320m
CHEMBL156554 49286 0 None - 1 Rat 8.9 pKi = 8.9 Binding
Binding affinity towards 5-hydroxytryptamine 4 receptor was determined in rat striatal membranes using [3H]GR-113808 as radioligandBinding affinity towards 5-hydroxytryptamine 4 receptor was determined in rat striatal membranes using [3H]GR-113808 as radioligand
ChEMBL 355 6 2 6 1.3 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCC(C(N)=O)CC1 10.1021/jm960320m
10644148 113325 0 None - 1 Human 8.8 pKi = 8.8 Binding
Binding affinity was determined against cloned 5-hydroxytryptamine 4E receptor isoform expressed in C6 glial cells incubated with 0.2 nM [3H]GR-113808Binding affinity was determined against cloned 5-hydroxytryptamine 4E receptor isoform expressed in C6 glial cells incubated with 0.2 nM [3H]GR-113808
ChEMBL 390 6 1 7 2.3 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCN(c2ccccn2)CC1 10.1021/jm0009538
CHEMBL332553 113325 0 None - 1 Human 8.8 pKi = 8.8 Binding
Binding affinity was determined against cloned 5-hydroxytryptamine 4E receptor isoform expressed in C6 glial cells incubated with 0.2 nM [3H]GR-113808Binding affinity was determined against cloned 5-hydroxytryptamine 4E receptor isoform expressed in C6 glial cells incubated with 0.2 nM [3H]GR-113808
ChEMBL 390 6 1 7 2.3 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCN(c2ccccn2)CC1 10.1021/jm0009538
145980826 166098 0 None - 1 Guinea pig 8.8 pKi = 8.8 Binding
Displacement of [3H]-GR113808 from 5-HT4R in Dunkin-Hartley guinea pig straitum nuclear membranes after 2 hrs by filter binding methodDisplacement of [3H]-GR113808 from 5-HT4R in Dunkin-Hartley guinea pig straitum nuclear membranes after 2 hrs by filter binding method
ChEMBL 326 6 0 4 3.9 CCCCN1CCC(COC(=O)c2ccnc3ccccc23)CC1 10.1039/C8MD00233A
CHEMBL4281416 166098 0 None - 1 Guinea pig 8.8 pKi = 8.8 Binding
Displacement of [3H]-GR113808 from 5-HT4R in Dunkin-Hartley guinea pig straitum nuclear membranes after 2 hrs by filter binding methodDisplacement of [3H]-GR113808 from 5-HT4R in Dunkin-Hartley guinea pig straitum nuclear membranes after 2 hrs by filter binding method
ChEMBL 326 6 0 4 3.9 CCCCN1CCC(COC(=O)c2ccnc3ccccc23)CC1 10.1039/C8MD00233A
11166796 82264 0 None 2 2 Rat 8.8 pKi = 8.8 Binding
Displacement of [3H]GR113808 from 5HT4 receptor in rat striatal membrane after 30 mins by liquid scintillation countingDisplacement of [3H]GR113808 from 5HT4 receptor in rat striatal membrane after 30 mins by liquid scintillation counting
ChEMBL 448 5 2 7 2.3 CC(C)n1c(=O)n(C(=O)NCC2CCN(CC3(O)CCOCC3)CC2)c2cc(F)ccc21 10.1021/jm300953p
CHEMBL2179583 82264 0 None 2 2 Rat 8.8 pKi = 8.8 Binding
Displacement of [3H]GR113808 from 5HT4 receptor in rat striatal membrane after 30 mins by liquid scintillation countingDisplacement of [3H]GR113808 from 5HT4 receptor in rat striatal membrane after 30 mins by liquid scintillation counting
ChEMBL 448 5 2 7 2.3 CC(C)n1c(=O)n(C(=O)NCC2CCN(CC3(O)CCOCC3)CC2)c2cc(F)ccc21 10.1021/jm300953p
50898778 56161 0 None - 1 Human 8.8 pKi = 8.8 Binding
Displacement of [3H]GR113808 from human 5HT4 receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [3H]GR113808 from human 5HT4 receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 427 9 2 5 3.5 O=C(O)CCCCCN1CCC(CNC(=O)c2c3n(c4ccccc24)CCCO3)CC1 10.1016/j.bmc.2010.10.011
CHEMBL1632174 56161 0 None - 1 Human 8.8 pKi = 8.8 Binding
Displacement of [3H]GR113808 from human 5HT4 receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [3H]GR113808 from human 5HT4 receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 427 9 2 5 3.5 O=C(O)CCCCCN1CCC(CNC(=O)c2c3n(c4ccccc24)CCCO3)CC1 10.1016/j.bmc.2010.10.011
71712328 90957 0 None - 1 Human 8.8 pKi = 8.8 Binding
Binding affinity to human recombinant 5HT4 receptorBinding affinity to human recombinant 5HT4 receptor
ChEMBL 470 7 2 6 2.5 COC(=O)N1CCN(CCN2CCC(CNC(=O)c3cccc4[nH]c(C(C)C)nc34)CC2)CC1 10.1016/j.bmcl.2013.05.018
CHEMBL2402898 90957 0 None - 1 Human 8.8 pKi = 8.8 Binding
Binding affinity to human recombinant 5HT4 receptorBinding affinity to human recombinant 5HT4 receptor
ChEMBL 470 7 2 6 2.5 COC(=O)N1CCN(CCN2CCC(CNC(=O)c3cccc4[nH]c(C(C)C)nc34)CC2)CC1 10.1016/j.bmcl.2013.05.018
177336 3071 45 None -6 3 Guinea pig 8.8 pKi = 8.8 Binding
Displacement of [125I]SB207710 from 5-HT4 receptor in guinea pig brain membranesDisplacement of [125I]SB207710 from 5-HT4 receptor in guinea pig brain membranes
ChEMBL 369 6 1 4 3.7 CCCCN1CCC(CC1)CNC(=O)c1c2OCCCn2c2c1cccc2 10.1016/j.bmc.2013.09.004
225 3071 45 None -6 3 Guinea pig 8.8 pKi = 8.8 Binding
Displacement of [125I]SB207710 from 5-HT4 receptor in guinea pig brain membranesDisplacement of [125I]SB207710 from 5-HT4 receptor in guinea pig brain membranes
ChEMBL 369 6 1 4 3.7 CCCCN1CCC(CC1)CNC(=O)c1c2OCCCn2c2c1cccc2 10.1016/j.bmc.2013.09.004
CHEMBL356359 3071 45 None -6 3 Guinea pig 8.8 pKi = 8.8 Binding
Displacement of [125I]SB207710 from 5-HT4 receptor in guinea pig brain membranesDisplacement of [125I]SB207710 from 5-HT4 receptor in guinea pig brain membranes
ChEMBL 369 6 1 4 3.7 CCCCN1CCC(CC1)CNC(=O)c1c2OCCCn2c2c1cccc2 10.1016/j.bmc.2013.09.004
DB04873 3071 45 None -6 3 Guinea pig 8.8 pKi = 8.8 Binding
Displacement of [125I]SB207710 from 5-HT4 receptor in guinea pig brain membranesDisplacement of [125I]SB207710 from 5-HT4 receptor in guinea pig brain membranes
ChEMBL 369 6 1 4 3.7 CCCCN1CCC(CC1)CNC(=O)c1c2OCCCn2c2c1cccc2 10.1016/j.bmc.2013.09.004
177336 3071 45 None 6 3 Human 8.8 pKi = 8.8 Binding
Displacement of [125I]SB207710 from human recombinant 5-HT4 receptorDisplacement of [125I]SB207710 from human recombinant 5-HT4 receptor
ChEMBL 369 6 1 4 3.7 CCCCN1CCC(CC1)CNC(=O)c1c2OCCCn2c2c1cccc2 10.1016/j.bmc.2013.09.004
225 3071 45 None 6 3 Human 8.8 pKi = 8.8 Binding
Displacement of [125I]SB207710 from human recombinant 5-HT4 receptorDisplacement of [125I]SB207710 from human recombinant 5-HT4 receptor
ChEMBL 369 6 1 4 3.7 CCCCN1CCC(CC1)CNC(=O)c1c2OCCCn2c2c1cccc2 10.1016/j.bmc.2013.09.004
CHEMBL356359 3071 45 None 6 3 Human 8.8 pKi = 8.8 Binding
Displacement of [125I]SB207710 from human recombinant 5-HT4 receptorDisplacement of [125I]SB207710 from human recombinant 5-HT4 receptor
ChEMBL 369 6 1 4 3.7 CCCCN1CCC(CC1)CNC(=O)c1c2OCCCn2c2c1cccc2 10.1016/j.bmc.2013.09.004
DB04873 3071 45 None 6 3 Human 8.8 pKi = 8.8 Binding
Displacement of [125I]SB207710 from human recombinant 5-HT4 receptorDisplacement of [125I]SB207710 from human recombinant 5-HT4 receptor
ChEMBL 369 6 1 4 3.7 CCCCN1CCC(CC1)CNC(=O)c1c2OCCCn2c2c1cccc2 10.1016/j.bmc.2013.09.004
118712577 113642 0 None - 1 Human 8.8 pKi = 8.8 Binding
Displacement of [3H]GR113808 from human 5HT4b receptor expressed in HEK293 cell membranesDisplacement of [3H]GR113808 from human 5HT4b receptor expressed in HEK293 cell membranes
ChEMBL 464 6 1 6 3.5 O=C(OCC1CCN(CC2C3CC4C2C4C3C(=O)O)CC1)c1c2n(c3ccccc13)CCCO2 10.1016/j.bmcl.2014.06.083
CHEMBL3329226 113642 0 None - 1 Human 8.8 pKi = 8.8 Binding
Displacement of [3H]GR113808 from human 5HT4b receptor expressed in HEK293 cell membranesDisplacement of [3H]GR113808 from human 5HT4b receptor expressed in HEK293 cell membranes
ChEMBL 464 6 1 6 3.5 O=C(OCC1CCN(CC2C3CC4C2C4C3C(=O)O)CC1)c1c2n(c3ccccc13)CCCO2 10.1016/j.bmcl.2014.06.083
70688535 76065 0 None - 1 Human 8.8 pKi = 8.8 Binding
Displacement of [3H]GR113808 from human recombinant 5HT4C receptor expressed in HEK293 cellsDisplacement of [3H]GR113808 from human recombinant 5HT4C receptor expressed in HEK293 cells
ChEMBL 586 13 2 7 4.2 CC(C)n1nc(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CCCCCCN2CCC(CNS(C)(=O)=O)CC2)c2ccccc21 10.1016/j.bmcl.2012.05.034
CHEMBL2059584 76065 0 None - 1 Human 8.8 pKi = 8.8 Binding
Displacement of [3H]GR113808 from human recombinant 5HT4C receptor expressed in HEK293 cellsDisplacement of [3H]GR113808 from human recombinant 5HT4C receptor expressed in HEK293 cells
ChEMBL 586 13 2 7 4.2 CC(C)n1nc(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CCCCCCN2CCC(CNS(C)(=O)=O)CC2)c2ccccc21 10.1016/j.bmcl.2012.05.034
44248184 194488 0 None - 1 Human 8.8 pKi = 8.8 Binding
Displacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 525 12 3 5 5.0 COc1cc(N)c(Cl)cc1C(=O)NC1CCN(CCCCCN(C)CCc2c[nH]c3ccccc23)CC1 10.1021/jm900881j
CHEMBL561278 194488 0 None - 1 Human 8.8 pKi = 8.8 Binding
Displacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 525 12 3 5 5.0 COc1cc(N)c(Cl)cc1C(=O)NC1CCN(CCCCCN(C)CCc2c[nH]c3ccccc23)CC1 10.1021/jm900881j
11166796 82264 0 None -2 2 Human 8.8 pKi = 8.8 Binding
Displacement of [3H]GR113808 from human 5HT4D receptor expressed in HEK293 cells after 30 mins by liquid scintillation countingDisplacement of [3H]GR113808 from human 5HT4D receptor expressed in HEK293 cells after 30 mins by liquid scintillation counting
ChEMBL 448 5 2 7 2.3 CC(C)n1c(=O)n(C(=O)NCC2CCN(CC3(O)CCOCC3)CC2)c2cc(F)ccc21 10.1021/jm300953p
CHEMBL2179583 82264 0 None -2 2 Human 8.8 pKi = 8.8 Binding
Displacement of [3H]GR113808 from human 5HT4D receptor expressed in HEK293 cells after 30 mins by liquid scintillation countingDisplacement of [3H]GR113808 from human 5HT4D receptor expressed in HEK293 cells after 30 mins by liquid scintillation counting
ChEMBL 448 5 2 7 2.3 CC(C)n1c(=O)n(C(=O)NCC2CCN(CC3(O)CCOCC3)CC2)c2cc(F)ccc21 10.1021/jm300953p
10854687 48292 0 None - 1 Rat 8.8 pKi = 8.8 Binding
Binding affinity towards 5-hydroxytryptamine 4 receptor was determined in rat striatal membranes using [3H]GR-113808 as radioligandBinding affinity towards 5-hydroxytryptamine 4 receptor was determined in rat striatal membranes using [3H]GR-113808 as radioligand
ChEMBL 340 5 1 5 3.2 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCCC(C)(C)C1 10.1021/jm960320m
CHEMBL155682 48292 0 None - 1 Rat 8.8 pKi = 8.8 Binding
Binding affinity towards 5-hydroxytryptamine 4 receptor was determined in rat striatal membranes using [3H]GR-113808 as radioligandBinding affinity towards 5-hydroxytryptamine 4 receptor was determined in rat striatal membranes using [3H]GR-113808 as radioligand
ChEMBL 340 5 1 5 3.2 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCCC(C)(C)C1 10.1021/jm960320m
42636941 178371 0 None - 1 Guinea pig 8.8 pKi = 8.8 Binding
Displacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatum membraneDisplacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatum membrane
ChEMBL 343 5 0 5 4.4 CCCN1CCC(COc2nc3scc(C)c3n3cccc23)CC1 10.1016/j.bmc.2008.11.045
CHEMBL470432 178371 0 None - 1 Guinea pig 8.8 pKi = 8.8 Binding
Displacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatum membraneDisplacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatum membrane
ChEMBL 343 5 0 5 4.4 CCCN1CCC(COc2nc3scc(C)c3n3cccc23)CC1 10.1016/j.bmc.2008.11.045
23202543 203684 0 None - 1 Guinea pig 8.8 pKi = 8.8 Binding
Compound was tested for binding affinity against 5-HT4 receptor in guinea pig striata using [3H]GR-113808 as radioligandCompound was tested for binding affinity against 5-HT4 receptor in guinea pig striata using [3H]GR-113808 as radioligand
ChEMBL 493 11 2 6 3.7 CS(=O)(=O)NCCN1CCC(CCC(=O)c2cc(Cl)c(N)cc2OCc2ccccc2)CC1 10.1016/S0960-894X(01)80414-5
CHEMBL80026 203684 0 None - 1 Guinea pig 8.8 pKi = 8.8 Binding
Compound was tested for binding affinity against 5-HT4 receptor in guinea pig striata using [3H]GR-113808 as radioligandCompound was tested for binding affinity against 5-HT4 receptor in guinea pig striata using [3H]GR-113808 as radioligand
ChEMBL 493 11 2 6 3.7 CS(=O)(=O)NCCN1CCC(CCC(=O)c2cc(Cl)c(N)cc2OCc2ccccc2)CC1 10.1016/S0960-894X(01)80414-5
44323244 12279 0 None - 1 Rat 8.7 pKi = 8.7 Binding
Binding affinity at 5-hydroxytryptamine 4 receptor in rat striatum by [3H]GR-113808 displacement.Binding affinity at 5-hydroxytryptamine 4 receptor in rat striatum by [3H]GR-113808 displacement.
ChEMBL 378 5 2 3 3.0 CCCC[N+]12CCC(CC1)[C@H](NC(=O)c1cc(Cl)c(N)c3c1OCC3)C2 10.1016/0960-894X(96)00002-9
CHEMBL1185621 12279 0 None - 1 Rat 8.7 pKi = 8.7 Binding
Binding affinity at 5-hydroxytryptamine 4 receptor in rat striatum by [3H]GR-113808 displacement.Binding affinity at 5-hydroxytryptamine 4 receptor in rat striatum by [3H]GR-113808 displacement.
ChEMBL 378 5 2 3 3.0 CCCC[N+]12CCC(CC1)[C@H](NC(=O)c1cc(Cl)c(N)c3c1OCC3)C2 10.1016/0960-894X(96)00002-9
CHEMBL423504 12279 0 None - 1 Rat 8.7 pKi = 8.7 Binding
Binding affinity at 5-hydroxytryptamine 4 receptor in rat striatum by [3H]GR-113808 displacement.Binding affinity at 5-hydroxytryptamine 4 receptor in rat striatum by [3H]GR-113808 displacement.
ChEMBL 378 5 2 3 3.0 CCCC[N+]12CCC(CC1)[C@H](NC(=O)c1cc(Cl)c(N)c3c1OCC3)C2 10.1016/0960-894X(96)00002-9
22708808 205334 0 None - 1 Rat 8.7 pKi = 8.7 Binding
Binding affinity at 5-hydroxytryptamine 4 receptor in rat striatum by [3H]GR-113808 displacement.Binding affinity at 5-hydroxytryptamine 4 receptor in rat striatum by [3H]GR-113808 displacement.
ChEMBL 365 6 2 4 3.1 CCCCN1CCC(CNC(=O)c2cc(Cl)c(N)c3c2OCC3)CC1 10.1016/0960-894X(96)00002-9
CHEMBL91771 205334 0 None - 1 Rat 8.7 pKi = 8.7 Binding
Binding affinity at 5-hydroxytryptamine 4 receptor in rat striatum by [3H]GR-113808 displacement.Binding affinity at 5-hydroxytryptamine 4 receptor in rat striatum by [3H]GR-113808 displacement.
ChEMBL 365 6 2 4 3.1 CCCCN1CCC(CNC(=O)c2cc(Cl)c(N)c3c2OCC3)CC1 10.1016/0960-894X(96)00002-9
162662474 181472 0 None - 1 Guinea pig 8.7 pKi = 8.7 Binding
Displacement of [3H]-GR113808 from guinea pig brain 5HT4 receptor in presence of serotonin incubated for 30 minsDisplacement of [3H]-GR113808 from guinea pig brain 5HT4 receptor in presence of serotonin incubated for 30 mins
ChEMBL 494 10 3 7 3.2 COc1cc(N)c(Cl)cc1C(=O)CCC1CCN(CCNS(=O)(=O)c2ccc(N)cc2)CC1 10.1016/j.ejmech.2016.05.048
CHEMBL4781228 181472 0 None - 1 Guinea pig 8.7 pKi = 8.7 Binding
Displacement of [3H]-GR113808 from guinea pig brain 5HT4 receptor in presence of serotonin incubated for 30 minsDisplacement of [3H]-GR113808 from guinea pig brain 5HT4 receptor in presence of serotonin incubated for 30 mins
ChEMBL 494 10 3 7 3.2 COc1cc(N)c(Cl)cc1C(=O)CCC1CCN(CCNS(=O)(=O)c2ccc(N)cc2)CC1 10.1016/j.ejmech.2016.05.048
71714544 90953 0 None - 1 Human 8.7 pKi = 8.7 Binding
Binding affinity to human recombinant 5HT4 receptorBinding affinity to human recombinant 5HT4 receptor
ChEMBL 542 9 3 7 1.1 CC(F)(F)c1nc2c(C(=O)NCC3CCN(CC(O)CN4CCN(S(C)(=O)=O)CC4)CC3)cccc2[nH]1 10.1016/j.bmcl.2013.05.018
CHEMBL2402894 90953 0 None - 1 Human 8.7 pKi = 8.7 Binding
Binding affinity to human recombinant 5HT4 receptorBinding affinity to human recombinant 5HT4 receptor
ChEMBL 542 9 3 7 1.1 CC(F)(F)c1nc2c(C(=O)NCC3CCN(CC(O)CN4CCN(S(C)(=O)=O)CC4)CC3)cccc2[nH]1 10.1016/j.bmcl.2013.05.018
44628200 82307 0 None 1584 2 Human 8.7 pKi = 8.7 Binding
Displacement of [3H](1-(2-(methylsulfonamido)ethyl)piperidin-4-yl)methyl 1-methyl-1H-indole-3-carboxylate from human 5HT4R expressed in HEK293 cellsDisplacement of [3H](1-(2-(methylsulfonamido)ethyl)piperidin-4-yl)methyl 1-methyl-1H-indole-3-carboxylate from human 5HT4R expressed in HEK293 cells
ChEMBL 456 7 1 5 5.0 CC(=O)Nc1ccc(CCN2CCC(COc3nc4ccccc4c4cn(C)cc34)CC2)cc1 10.1021/jm300573d
CHEMBL2179670 82307 0 None 1584 2 Human 8.7 pKi = 8.7 Binding
Displacement of [3H](1-(2-(methylsulfonamido)ethyl)piperidin-4-yl)methyl 1-methyl-1H-indole-3-carboxylate from human 5HT4R expressed in HEK293 cellsDisplacement of [3H](1-(2-(methylsulfonamido)ethyl)piperidin-4-yl)methyl 1-methyl-1H-indole-3-carboxylate from human 5HT4R expressed in HEK293 cells
ChEMBL 456 7 1 5 5.0 CC(=O)Nc1ccc(CCN2CCC(COc3nc4ccccc4c4cn(C)cc34)CC2)cc1 10.1021/jm300573d
44628198 82311 0 None - 1 Human 8.7 pKi = 8.7 Binding
Displacement of [3H](1-(2-(methylsulfonamido)ethyl)piperidin-4-yl)methyl 1-methyl-1H-indole-3-carboxylate from human 5HT4R expressed in HEK293 cellsDisplacement of [3H](1-(2-(methylsulfonamido)ethyl)piperidin-4-yl)methyl 1-methyl-1H-indole-3-carboxylate from human 5HT4R expressed in HEK293 cells
ChEMBL 443 7 1 5 4.8 Cn1cc2c(OCC3CCN(CCc4ccc(C(=O)O)cc4)CC3)nc3ccccc3c2c1 10.1021/jm300573d
CHEMBL2179674 82311 0 None - 1 Human 8.7 pKi = 8.7 Binding
Displacement of [3H](1-(2-(methylsulfonamido)ethyl)piperidin-4-yl)methyl 1-methyl-1H-indole-3-carboxylate from human 5HT4R expressed in HEK293 cellsDisplacement of [3H](1-(2-(methylsulfonamido)ethyl)piperidin-4-yl)methyl 1-methyl-1H-indole-3-carboxylate from human 5HT4R expressed in HEK293 cells
ChEMBL 443 7 1 5 4.8 Cn1cc2c(OCC3CCN(CCc4ccc(C(=O)O)cc4)CC3)nc3ccccc3c2c1 10.1021/jm300573d
44629279 82312 0 None 39 2 Human 8.7 pKi = 8.7 Binding
Displacement of [3H](1-(2-(methylsulfonamido)ethyl)piperidin-4-yl)methyl 1-methyl-1H-indole-3-carboxylate from human 5HT4R expressed in HEK293 cellsDisplacement of [3H](1-(2-(methylsulfonamido)ethyl)piperidin-4-yl)methyl 1-methyl-1H-indole-3-carboxylate from human 5HT4R expressed in HEK293 cells
ChEMBL 399 6 0 4 5.1 Cn1cc2c(OCC3CCN(CCc4ccccc4)CC3)nc3ccccc3c2c1 10.1021/jm300573d
CHEMBL2179678 82312 0 None 39 2 Human 8.7 pKi = 8.7 Binding
Displacement of [3H](1-(2-(methylsulfonamido)ethyl)piperidin-4-yl)methyl 1-methyl-1H-indole-3-carboxylate from human 5HT4R expressed in HEK293 cellsDisplacement of [3H](1-(2-(methylsulfonamido)ethyl)piperidin-4-yl)methyl 1-methyl-1H-indole-3-carboxylate from human 5HT4R expressed in HEK293 cells
ChEMBL 399 6 0 4 5.1 Cn1cc2c(OCC3CCN(CCc4ccccc4)CC3)nc3ccccc3c2c1 10.1021/jm300573d
53320713 56159 0 None - 1 Human 8.7 pKi = 8.7 Binding
Displacement of [3H]GR113808 from human 5HT4 receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [3H]GR113808 from human 5HT4 receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 399 7 2 5 2.7 O=C(O)CCCN1CCC(CNC(=O)c2c3n(c4ccccc24)CCCO3)CC1 10.1016/j.bmc.2010.10.011
CHEMBL1632172 56159 0 None - 1 Human 8.7 pKi = 8.7 Binding
Displacement of [3H]GR113808 from human 5HT4 receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [3H]GR113808 from human 5HT4 receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 399 7 2 5 2.7 O=C(O)CCCN1CCC(CNC(=O)c2c3n(c4ccccc24)CCCO3)CC1 10.1016/j.bmc.2010.10.011
70682173 76058 0 None - 1 Human 8.7 pKi = 8.7 Binding
Displacement of [3H]GR113808 from human recombinant 5HT4C receptor expressed in HEK293 cellsDisplacement of [3H]GR113808 from human recombinant 5HT4C receptor expressed in HEK293 cells
ChEMBL 453 7 2 6 3.2 CC(C)n1nc(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CC(O)CN2CCCCC2)c2ccccc21 10.1016/j.bmcl.2012.05.034
CHEMBL2059577 76058 0 None - 1 Human 8.7 pKi = 8.7 Binding
Displacement of [3H]GR113808 from human recombinant 5HT4C receptor expressed in HEK293 cellsDisplacement of [3H]GR113808 from human recombinant 5HT4C receptor expressed in HEK293 cells
ChEMBL 453 7 2 6 3.2 CC(C)n1nc(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CC(O)CN2CCCCC2)c2ccccc21 10.1016/j.bmcl.2012.05.034
44248189 91900499 193177 0 None - 1 Human 8.7 pKi = 8.7 Binding
Displacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 549 12 2 6 4.2 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CCCCCCCN2CCC[C@@H]2C(N)=O)cc2ccccc21 10.1021/jm900881j
CHEMBL539713 193177 0 None - 1 Human 8.7 pKi = 8.7 Binding
Displacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 549 12 2 6 4.2 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CCCCCCCN2CCC[C@@H]2C(N)=O)cc2ccccc21 10.1021/jm900881j
44248315 194247 0 None - 1 Human 8.7 pKi = 8.7 Binding
Displacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 522 11 1 6 4.6 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CCCCCCCN2CCOCC2)cc2ccccc21 10.1021/jm900881j
CHEMBL559322 194247 0 None - 1 Human 8.7 pKi = 8.7 Binding
Displacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 522 11 1 6 4.6 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CCCCCCCN2CCOCC2)cc2ccccc21 10.1021/jm900881j
9819953 120797 0 None - 1 Guinea pig 8.0 pKi = 8 Binding
Ability to displace [3H]GR-113808 from 5-hydroxytryptamine 4 receptorAbility to displace [3H]GR-113808 from 5-hydroxytryptamine 4 receptor
ChEMBL 353 6 1 4 4.5 CCCCN1CCC(COc2nc3ccccc3c3c2CCCN3)CC1 10.1021/jm020954v
CHEMBL35808 120797 0 None - 1 Guinea pig 8.0 pKi = 8 Binding
Ability to displace [3H]GR-113808 from 5-hydroxytryptamine 4 receptorAbility to displace [3H]GR-113808 from 5-hydroxytryptamine 4 receptor
ChEMBL 353 6 1 4 4.5 CCCCN1CCC(COc2nc3ccccc3c3c2CCCN3)CC1 10.1021/jm020954v
11520655 132310 0 None - 1 Human 8.0 pKi = 8 Binding
Binding affinity for 5-HT4 receptor using [3H]GR-113808Binding affinity for 5-HT4 receptor using [3H]GR-113808
ChEMBL 792 19 4 12 4.4 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCC(CCNC(=O)CCC(=O)NCCC2CCN(CCOC(=O)c3cc(Cl)c(N)cc3OC)CC2)CC1 10.1021/jm050234z
CHEMBL370181 132310 0 None - 1 Human 8.0 pKi = 8 Binding
Binding affinity for 5-HT4 receptor using [3H]GR-113808Binding affinity for 5-HT4 receptor using [3H]GR-113808
ChEMBL 792 19 4 12 4.4 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCC(CCNC(=O)CCC(=O)NCCC2CCN(CCOC(=O)c3cc(Cl)c(N)cc3OC)CC2)CC1 10.1021/jm050234z
17755141 78715 0 None - 1 Human 8.0 pKi = 8 Binding
Binding affinity to Rluc fused 5HT4 receptor expressed in CHO cellsBinding affinity to Rluc fused 5HT4 receptor expressed in CHO cells
ChEMBL 1183 28 4 16 9.0 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCC(NC(=O)CCCN(CCCc2ccc(CCCN(CCCC(=O)NC3CCN(CCOC(=O)c4cc(Cl)c(N)cc4OC)CC3)C(=O)OC(C)(C)C)cc2)C(=O)OC(C)(C)C)CC1 10.1021/jm070552t
CHEMBL2113289 78715 0 None - 1 Human 8.0 pKi = 8 Binding
Binding affinity to Rluc fused 5HT4 receptor expressed in CHO cellsBinding affinity to Rluc fused 5HT4 receptor expressed in CHO cells
ChEMBL 1183 28 4 16 9.0 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCC(NC(=O)CCCN(CCCc2ccc(CCCN(CCCC(=O)NC3CCN(CCOC(=O)c4cc(Cl)c(N)cc4OC)CC3)C(=O)OC(C)(C)C)cc2)C(=O)OC(C)(C)C)CC1 10.1021/jm070552t
17755141 78715 0 None - 1 Human 8.0 pKi = 8 Binding
Binding affinity to YFP fused 5HT4 receptor expressed in CHO cellsBinding affinity to YFP fused 5HT4 receptor expressed in CHO cells
ChEMBL 1183 28 4 16 9.0 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCC(NC(=O)CCCN(CCCc2ccc(CCCN(CCCC(=O)NC3CCN(CCOC(=O)c4cc(Cl)c(N)cc4OC)CC3)C(=O)OC(C)(C)C)cc2)C(=O)OC(C)(C)C)CC1 10.1021/jm070552t
CHEMBL2113289 78715 0 None - 1 Human 8.0 pKi = 8 Binding
Binding affinity to YFP fused 5HT4 receptor expressed in CHO cellsBinding affinity to YFP fused 5HT4 receptor expressed in CHO cells
ChEMBL 1183 28 4 16 9.0 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCC(NC(=O)CCCN(CCCc2ccc(CCCN(CCCC(=O)NC3CCN(CCOC(=O)c4cc(Cl)c(N)cc4OC)CC3)C(=O)OC(C)(C)C)cc2)C(=O)OC(C)(C)C)CC1 10.1021/jm070552t
44628201 82309 0 None 3 2 Human 8.0 pKi = 8 Binding
Displacement of [3H](1-(2-(methylsulfonamido)ethyl)piperidin-4-yl)methyl 1-methyl-1H-indole-3-carboxylate from human 5HT4R expressed in HEK293 cellsDisplacement of [3H](1-(2-(methylsulfonamido)ethyl)piperidin-4-yl)methyl 1-methyl-1H-indole-3-carboxylate from human 5HT4R expressed in HEK293 cells
ChEMBL 429 7 1 5 4.6 Cn1cc2c(OCC3CCN(CCc4ccc(CO)cc4)CC3)nc3ccccc3c2c1 10.1021/jm300573d
CHEMBL2179672 82309 0 None 3 2 Human 8.0 pKi = 8 Binding
Displacement of [3H](1-(2-(methylsulfonamido)ethyl)piperidin-4-yl)methyl 1-methyl-1H-indole-3-carboxylate from human 5HT4R expressed in HEK293 cellsDisplacement of [3H](1-(2-(methylsulfonamido)ethyl)piperidin-4-yl)methyl 1-methyl-1H-indole-3-carboxylate from human 5HT4R expressed in HEK293 cells
ChEMBL 429 7 1 5 4.6 Cn1cc2c(OCC3CCN(CCc4ccc(CO)cc4)CC3)nc3ccccc3c2c1 10.1021/jm300573d
11225102 76071 2 None - 1 Human 8.0 pKi = 8 Binding
Displacement of [3H]GR113808 from human recombinant 5HT4C receptor expressed in HEK293 cellsDisplacement of [3H]GR113808 from human recombinant 5HT4C receptor expressed in HEK293 cells
ChEMBL 466 6 1 6 2.5 CC(=O)N1CCN(CCN2[C@H]3CC[C@@H]2C[C@H](NC(=O)c2nn(C(C)C)c4ccccc24)C3)CC1 10.1016/j.bmcl.2012.05.034
CHEMBL2059590 76071 2 None - 1 Human 8.0 pKi = 8 Binding
Displacement of [3H]GR113808 from human recombinant 5HT4C receptor expressed in HEK293 cellsDisplacement of [3H]GR113808 from human recombinant 5HT4C receptor expressed in HEK293 cells
ChEMBL 466 6 1 6 2.5 CC(=O)N1CCN(CCN2[C@H]3CC[C@@H]2C[C@H](NC(=O)c2nn(C(C)C)c4ccccc24)C3)CC1 10.1016/j.bmcl.2012.05.034
11225102 76071 2 None - 1 Human 8.0 pKi = 8 Binding
Displacement of [3H]GR113808 from human recombinant 5HT4c receptor expressed in HEK293 cellsDisplacement of [3H]GR113808 from human recombinant 5HT4c receptor expressed in HEK293 cells
ChEMBL 466 6 1 6 2.5 CC(=O)N1CCN(CCN2[C@H]3CC[C@@H]2C[C@H](NC(=O)c2nn(C(C)C)c4ccccc24)C3)CC1 10.1016/j.bmcl.2012.08.051
CHEMBL2059590 76071 2 None - 1 Human 8.0 pKi = 8 Binding
Displacement of [3H]GR113808 from human recombinant 5HT4c receptor expressed in HEK293 cellsDisplacement of [3H]GR113808 from human recombinant 5HT4c receptor expressed in HEK293 cells
ChEMBL 466 6 1 6 2.5 CC(=O)N1CCN(CCN2[C@H]3CC[C@@H]2C[C@H](NC(=O)c2nn(C(C)C)c4ccccc24)C3)CC1 10.1016/j.bmcl.2012.08.051
44248679 193926 0 None - 1 Human 8.0 pKi = 8 Binding
Displacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 599 12 1 7 3.8 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CCCCCCCN2CCN(S(C)(=O)=O)CC2)cc2ccccc21 10.1021/jm900881j
CHEMBL555693 193926 0 None - 1 Human 8.0 pKi = 8 Binding
Displacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 599 12 1 7 3.8 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CCCCCCCN2CCN(S(C)(=O)=O)CC2)cc2ccccc21 10.1021/jm900881j
44248925 194746 0 None - 1 Human 8.0 pKi = 8 Binding
Displacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 436 9 2 5 3.8 COc1cc(N)c(Cl)cc1C(=O)NC1CCN(CCCCCN2CCCCC2)CC1 10.1021/jm900881j
CHEMBL562902 194746 0 None - 1 Human 8.0 pKi = 8 Binding
Displacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 436 9 2 5 3.8 COc1cc(N)c(Cl)cc1C(=O)NC1CCN(CCCCCN2CCCCC2)CC1 10.1021/jm900881j
10712297 186526 0 None - 1 Rat 8.0 pKi = 8.0 Binding
Binding affinity (Ki+/-SEM) against 5-hydroxytryptamine 4 receptor from cheng Prusoff equation by using [3H]GR-113808 in rat striatumBinding affinity (Ki+/-SEM) against 5-hydroxytryptamine 4 receptor from cheng Prusoff equation by using [3H]GR-113808 in rat striatum
ChEMBL 341 5 2 5 3.2 COc1cc(N)c(Cl)cc1NC(=O)OCCN1CCCC(C)C1 10.1021/jm960853v
CHEMBL49155 186526 0 None - 1 Rat 8.0 pKi = 8.0 Binding
Binding affinity (Ki+/-SEM) against 5-hydroxytryptamine 4 receptor from cheng Prusoff equation by using [3H]GR-113808 in rat striatumBinding affinity (Ki+/-SEM) against 5-hydroxytryptamine 4 receptor from cheng Prusoff equation by using [3H]GR-113808 in rat striatum
ChEMBL 341 5 2 5 3.2 COc1cc(N)c(Cl)cc1NC(=O)OCCN1CCCC(C)C1 10.1021/jm960853v
10688750 206645 0 None - 1 Guinea pig 8.0 pKi = 8.0 Binding
Binding affinity against 5-hydroxytryptamine 4 receptor in guinea pig striatum using [3H]GR-113808 as radioligandBinding affinity against 5-hydroxytryptamine 4 receptor in guinea pig striatum using [3H]GR-113808 as radioligand
ChEMBL 343 4 1 6 0.9 CN1CCN(CCNC(=O)n2c(=O)n(C3CC3)c3ccccc32)CC1 10.1021/jm981098j
CHEMBL99590 206645 0 None - 1 Guinea pig 8.0 pKi = 8.0 Binding
Binding affinity against 5-hydroxytryptamine 4 receptor in guinea pig striatum using [3H]GR-113808 as radioligandBinding affinity against 5-hydroxytryptamine 4 receptor in guinea pig striatum using [3H]GR-113808 as radioligand
ChEMBL 343 4 1 6 0.9 CN1CCN(CCNC(=O)n2c(=O)n(C3CC3)c3ccccc32)CC1 10.1021/jm981098j
44281102 116215 0 None - 1 Rat 8.0 pKi = 8.0 Binding
Binding affinity against 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatumBinding affinity against 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatum
ChEMBL 312 4 1 5 2.6 CCN1CCC(OC(=O)c2cc(Cl)c(N)cc2OC)CC1 10.1016/S0960-894X(01)80508-4
CHEMBL33732 116215 0 None - 1 Rat 8.0 pKi = 8.0 Binding
Binding affinity against 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatumBinding affinity against 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatum
ChEMBL 312 4 1 5 2.6 CCN1CCC(OC(=O)c2cc(Cl)c(N)cc2OC)CC1 10.1016/S0960-894X(01)80508-4
10584 1435 0 None -1 2 Human 8.0 pKi = 8.0 Binding
Agonist activity at 5-HT4R (unknown origin)Agonist activity at 5-HT4R (unknown origin)
ChEMBL 392 7 1 4 5.2 COc1cc(N)c(cc1C(=O)CCC1CCN(CC1)CC1CCCCC1)Cl 10.1016/j.ejmech.2018.10.064
86582973 1435 0 None -1 2 Human 8.0 pKi = 8.0 Binding
Agonist activity at 5-HT4R (unknown origin)Agonist activity at 5-HT4R (unknown origin)
ChEMBL 392 7 1 4 5.2 COc1cc(N)c(cc1C(=O)CCC1CCN(CC1)CC1CCCCC1)Cl 10.1016/j.ejmech.2018.10.064
CHEMBL3417009 1435 0 None -1 2 Human 8.0 pKi = 8.0 Binding
Agonist activity at 5-HT4R (unknown origin)Agonist activity at 5-HT4R (unknown origin)
ChEMBL 392 7 1 4 5.2 COc1cc(N)c(cc1C(=O)CCC1CCN(CC1)CC1CCCCC1)Cl 10.1016/j.ejmech.2018.10.064
10584 1435 0 None -1 2 Human 8.0 pKi = 8.0 Binding
Displacement of [3H]GR113808 from human 5-HT4 receptor expressed in Chem-1 cell membrane incubated for 60 mins by radiometric scintillation counting analysisDisplacement of [3H]GR113808 from human 5-HT4 receptor expressed in Chem-1 cell membrane incubated for 60 mins by radiometric scintillation counting analysis
ChEMBL 392 7 1 4 5.2 COc1cc(N)c(cc1C(=O)CCC1CCN(CC1)CC1CCCCC1)Cl 10.1016/j.bmcl.2022.128873
86582973 1435 0 None -1 2 Human 8.0 pKi = 8.0 Binding
Displacement of [3H]GR113808 from human 5-HT4 receptor expressed in Chem-1 cell membrane incubated for 60 mins by radiometric scintillation counting analysisDisplacement of [3H]GR113808 from human 5-HT4 receptor expressed in Chem-1 cell membrane incubated for 60 mins by radiometric scintillation counting analysis
ChEMBL 392 7 1 4 5.2 COc1cc(N)c(cc1C(=O)CCC1CCN(CC1)CC1CCCCC1)Cl 10.1016/j.bmcl.2022.128873
CHEMBL3417009 1435 0 None -1 2 Human 8.0 pKi = 8.0 Binding
Displacement of [3H]GR113808 from human 5-HT4 receptor expressed in Chem-1 cell membrane incubated for 60 mins by radiometric scintillation counting analysisDisplacement of [3H]GR113808 from human 5-HT4 receptor expressed in Chem-1 cell membrane incubated for 60 mins by radiometric scintillation counting analysis
ChEMBL 392 7 1 4 5.2 COc1cc(N)c(cc1C(=O)CCC1CCN(CC1)CC1CCCCC1)Cl 10.1016/j.bmcl.2022.128873
9881054 126531 0 None - 1 Guinea pig 8.0 pKi = 8.0 Binding
Ability to displace [3H]GR-113808 from 5-hydroxytryptamine 4 receptorAbility to displace [3H]GR-113808 from 5-hydroxytryptamine 4 receptor
ChEMBL 339 4 1 4 4.1 CCN1CCC(COc2nc3ccccc3c3c2CCCCN3)CC1 10.1021/jm020954v
CHEMBL36558 126531 0 None - 1 Guinea pig 8.0 pKi = 8.0 Binding
Ability to displace [3H]GR-113808 from 5-hydroxytryptamine 4 receptorAbility to displace [3H]GR-113808 from 5-hydroxytryptamine 4 receptor
ChEMBL 339 4 1 4 4.1 CCN1CCC(COc2nc3ccccc3c3c2CCCCN3)CC1 10.1021/jm020954v
235 2527 36 None -4 3 Human 8.0 pKi = 8.0 Binding
Binding affinity was determined against cloned 5-hydroxytryptamine 4B receptor isoform expressed in COS-7 cellsBinding affinity was determined against cloned 5-hydroxytryptamine 4B receptor isoform expressed in COS-7 cells
ChEMBL 312 5 1 5 2.6 COc1cc(N)c(cc1C(=O)OCCN1CCCCC1)Cl 10.1021/jm0009538
5311299 2527 36 None -4 3 Human 8.0 pKi = 8.0 Binding
Binding affinity was determined against cloned 5-hydroxytryptamine 4B receptor isoform expressed in COS-7 cellsBinding affinity was determined against cloned 5-hydroxytryptamine 4B receptor isoform expressed in COS-7 cells
ChEMBL 312 5 1 5 2.6 COc1cc(N)c(cc1C(=O)OCCN1CCCCC1)Cl 10.1021/jm0009538
CHEMBL286136 2527 36 None -4 3 Human 8.0 pKi = 8.0 Binding
Binding affinity was determined against cloned 5-hydroxytryptamine 4B receptor isoform expressed in COS-7 cellsBinding affinity was determined against cloned 5-hydroxytryptamine 4B receptor isoform expressed in COS-7 cells
ChEMBL 312 5 1 5 2.6 COc1cc(N)c(cc1C(=O)OCCN1CCCCC1)Cl 10.1021/jm0009538
240 931 39 None -11 25 Human 7.0 pKi = 7 Binding
Binding affinity to human recombinant 5HT4 receptorBinding affinity to human recombinant 5HT4 receptor
ChEMBL 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N 10.1016/j.bmcl.2013.05.018
2769 931 39 None -11 25 Human 7.0 pKi = 7 Binding
Binding affinity to human recombinant 5HT4 receptorBinding affinity to human recombinant 5HT4 receptor
ChEMBL 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N 10.1016/j.bmcl.2013.05.018
44279790 931 39 None -11 25 Human 7.0 pKi = 7 Binding
Binding affinity to human recombinant 5HT4 receptorBinding affinity to human recombinant 5HT4 receptor
ChEMBL 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N 10.1016/j.bmcl.2013.05.018
660 931 39 None -11 25 Human 7.0 pKi = 7 Binding
Binding affinity to human recombinant 5HT4 receptorBinding affinity to human recombinant 5HT4 receptor
ChEMBL 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N 10.1016/j.bmcl.2013.05.018
CHEMBL1729 931 39 None -11 25 Human 7.0 pKi = 7 Binding
Binding affinity to human recombinant 5HT4 receptorBinding affinity to human recombinant 5HT4 receptor
ChEMBL 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N 10.1016/j.bmcl.2013.05.018
CHEMBL560739 931 39 None -11 25 Human 7.0 pKi = 7 Binding
Binding affinity to human recombinant 5HT4 receptorBinding affinity to human recombinant 5HT4 receptor
ChEMBL 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N 10.1016/j.bmcl.2013.05.018
DB00604 931 39 None -11 25 Human 7.0 pKi = 7 Binding
Binding affinity to human recombinant 5HT4 receptorBinding affinity to human recombinant 5HT4 receptor
ChEMBL 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N 10.1016/j.bmcl.2013.05.018
5 139 66 None -190 54 Guinea pig 7.0 pKi = 7 Binding
Displacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatumDisplacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatum
ChEMBL 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 10.1021/jm900018b
5 139 66 None -190 54 Guinea pig 7.0 pKi = 7 Binding
Displacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatumDisplacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatum
ChEMBL 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 10.1021/jm901126m
5202 139 66 None -190 54 Guinea pig 7.0 pKi = 7 Binding
Displacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatumDisplacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatum
ChEMBL 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 10.1021/jm900018b
5202 139 66 None -190 54 Guinea pig 7.0 pKi = 7 Binding
Displacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatumDisplacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatum
ChEMBL 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 10.1021/jm901126m
CHEMBL39 139 66 None -190 54 Guinea pig 7.0 pKi = 7 Binding
Displacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatumDisplacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatum
ChEMBL 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 10.1021/jm900018b
CHEMBL39 139 66 None -190 54 Guinea pig 7.0 pKi = 7 Binding
Displacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatumDisplacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatum
ChEMBL 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 10.1021/jm901126m
DB08839 139 66 None -190 54 Guinea pig 7.0 pKi = 7 Binding
Displacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatumDisplacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatum
ChEMBL 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 10.1021/jm900018b
DB08839 139 66 None -190 54 Guinea pig 7.0 pKi = 7 Binding
Displacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatumDisplacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatum
ChEMBL 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 10.1021/jm901126m
71457412 82561 0 None - 1 Guinea pig 7.0 pKi = 7 Binding
Displacement of [3H]GR113808 from 5HT4R in guinea pig striatal membranesDisplacement of [3H]GR113808 from 5HT4R in guinea pig striatal membranes
ChEMBL 348 5 0 3 5.2 CCCN1CCC(COc2nc3c(C)cccc3c3ccccc23)CC1 10.1021/jm300943r
CHEMBL2181186 82561 0 None - 1 Guinea pig 7.0 pKi = 7 Binding
Displacement of [3H]GR113808 from 5HT4R in guinea pig striatal membranesDisplacement of [3H]GR113808 from 5HT4R in guinea pig striatal membranes
ChEMBL 348 5 0 3 5.2 CCCN1CCC(COc2nc3c(C)cccc3c3ccccc23)CC1 10.1021/jm300943r
5311047 203055 30 None -5 2 Human 7.0 pKi = 7 Binding
Displacement of [3H]GR113808 from human recombinant 5HT4C receptor expressed in HEK293 cellsDisplacement of [3H]GR113808 from human recombinant 5HT4C receptor expressed in HEK293 cells
ChEMBL 465 9 2 6 3.4 COc1cc(N)c(Cl)cc1C(=O)N[C@H]1CCN(CCCOc2ccc(F)cc2)C[C@H]1OC 10.1016/j.bmcl.2012.05.034
CHEMBL74656 203055 30 None -5 2 Human 7.0 pKi = 7 Binding
Displacement of [3H]GR113808 from human recombinant 5HT4C receptor expressed in HEK293 cellsDisplacement of [3H]GR113808 from human recombinant 5HT4C receptor expressed in HEK293 cells
ChEMBL 465 9 2 6 3.4 COc1cc(N)c(Cl)cc1C(=O)N[C@H]1CCN(CCCOc2ccc(F)cc2)C[C@H]1OC 10.1016/j.bmcl.2012.05.034
70682705 77150 0 None - 1 Human 7.0 pKi = 7 Binding
Displacement of [3H]GR113808 from human recombinant 5HT4c receptor expressed in HEK293 cellsDisplacement of [3H]GR113808 from human recombinant 5HT4c receptor expressed in HEK293 cells
ChEMBL 483 7 3 6 1.9 CNC(=O)N(C)CC(O)CN1[C@H]2CC[C@@H]1C[C@H](NC(=O)c1cc3ccccc3n(C(C)C)c1=O)C2 10.1016/j.bmcl.2012.08.051
CHEMBL2087329 77150 0 None - 1 Human 7.0 pKi = 7 Binding
Displacement of [3H]GR113808 from human recombinant 5HT4c receptor expressed in HEK293 cellsDisplacement of [3H]GR113808 from human recombinant 5HT4c receptor expressed in HEK293 cells
ChEMBL 483 7 3 6 1.9 CNC(=O)N(C)CC(O)CN1[C@H]2CC[C@@H]1C[C@H](NC(=O)c1cc3ccccc3n(C(C)C)c1=O)C2 10.1016/j.bmcl.2012.08.051
70686942 77151 0 None - 1 Human 7.0 pKi = 7 Binding
Displacement of [3H]GR113808 from human recombinant 5HT4c receptor expressed in HEK293 cellsDisplacement of [3H]GR113808 from human recombinant 5HT4c receptor expressed in HEK293 cells
ChEMBL 483 7 3 6 1.9 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CC(O)CNC(=O)N(C)C)cc2ccccc21 10.1016/j.bmcl.2012.08.051
CHEMBL2087330 77151 0 None - 1 Human 7.0 pKi = 7 Binding
Displacement of [3H]GR113808 from human recombinant 5HT4c receptor expressed in HEK293 cellsDisplacement of [3H]GR113808 from human recombinant 5HT4c receptor expressed in HEK293 cells
ChEMBL 483 7 3 6 1.9 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CC(O)CNC(=O)N(C)C)cc2ccccc21 10.1016/j.bmcl.2012.08.051
5311047 203055 30 None -5 2 Human 7.0 pKi = 7 Binding
Displacement of [3H]GR113808 from human recombinant 5HT4c receptor expressed in HEK293 cellsDisplacement of [3H]GR113808 from human recombinant 5HT4c receptor expressed in HEK293 cells
ChEMBL 465 9 2 6 3.4 COc1cc(N)c(Cl)cc1C(=O)N[C@H]1CCN(CCCOc2ccc(F)cc2)C[C@H]1OC 10.1016/j.bmcl.2012.08.051
CHEMBL74656 203055 30 None -5 2 Human 7.0 pKi = 7 Binding
Displacement of [3H]GR113808 from human recombinant 5HT4c receptor expressed in HEK293 cellsDisplacement of [3H]GR113808 from human recombinant 5HT4c receptor expressed in HEK293 cells
ChEMBL 465 9 2 6 3.4 COc1cc(N)c(Cl)cc1C(=O)N[C@H]1CCN(CCCOc2ccc(F)cc2)C[C@H]1OC 10.1016/j.bmcl.2012.08.051
44248797 194039 0 None - 1 Human 7.0 pKi = 7 Binding
Displacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 353 7 2 4 3.3 CCCCCN1CCC(NC(=O)c2cc(Cl)c(N)cc2OC)CC1 10.1021/jm900881j
CHEMBL557053 194039 0 None - 1 Human 7.0 pKi = 7 Binding
Displacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 353 7 2 4 3.3 CCCCCN1CCC(NC(=O)c2cc(Cl)c(N)cc2OC)CC1 10.1021/jm900881j
5 139 66 None -190 54 Guinea pig 7.0 pKi = 7 Binding
The compound was tested for the binding affinity against 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand.The compound was tested for the binding affinity against 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand.
ChEMBL 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 10.1021/jm990151g
5202 139 66 None -190 54 Guinea pig 7.0 pKi = 7 Binding
The compound was tested for the binding affinity against 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand.The compound was tested for the binding affinity against 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand.
ChEMBL 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 10.1021/jm990151g
CHEMBL39 139 66 None -190 54 Guinea pig 7.0 pKi = 7 Binding
The compound was tested for the binding affinity against 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand.The compound was tested for the binding affinity against 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand.
ChEMBL 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 10.1021/jm990151g
DB08839 139 66 None -190 54 Guinea pig 7.0 pKi = 7 Binding
The compound was tested for the binding affinity against 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand.The compound was tested for the binding affinity against 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand.
ChEMBL 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 10.1021/jm990151g
118712568 113731 0 None - 1 Human 6.0 pKi = 6 Binding
Displacement of [3H]GR113808 from human 5HT4b receptor expressed in HEK293 cell membranesDisplacement of [3H]GR113808 from human 5HT4b receptor expressed in HEK293 cell membranes
ChEMBL 516 9 3 4 4.8 O=C(NCC1CCN(Cc2ccc(NS(=O)(=O)Cc3ccccc3)cc2)CC1)c1c[nH]c2ccccc12 10.1016/j.bmcl.2014.06.083
CHEMBL3329802 113731 0 None - 1 Human 6.0 pKi = 6 Binding
Displacement of [3H]GR113808 from human 5HT4b receptor expressed in HEK293 cell membranesDisplacement of [3H]GR113808 from human 5HT4b receptor expressed in HEK293 cell membranes
ChEMBL 516 9 3 4 4.8 O=C(NCC1CCN(Cc2ccc(NS(=O)(=O)Cc3ccccc3)cc2)CC1)c1c[nH]c2ccccc12 10.1016/j.bmcl.2014.06.083
44249189 91900488 193731 0 None - 1 Human 6.0 pKi = 6 Binding
Displacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 447 6 2 6 2.2 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CCS(=O)(=O)O)cc2ccccc21 10.1021/jm900881j
CHEMBL552075 193731 0 None - 1 Human 6.0 pKi = 6 Binding
Displacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 447 6 2 6 2.2 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CCS(=O)(=O)O)cc2ccccc21 10.1021/jm900881j
44248310 194881 0 None - 1 Human 6.0 pKi = 6 Binding
Displacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 512 6 1 6 3.6 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CCN2C(=O)c3ccccc3C2=O)cc2ccccc21 10.1021/jm900881j
CHEMBL563799 194881 0 None - 1 Human 6.0 pKi = 6 Binding
Displacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 512 6 1 6 3.6 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CCN2C(=O)c3ccccc3C2=O)cc2ccccc21 10.1021/jm900881j
44575 195839 1 None - 1 Human 6.0 pKi = 6 Binding
Displacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 311 4 2 4 2.1 CCN1CCC(NC(=O)c2cc(Cl)c(N)cc2OC)CC1 10.1021/jm900881j
CHEMBL570074 195839 1 None - 1 Human 6.0 pKi = 6 Binding
Displacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 311 4 2 4 2.1 CCN1CCC(NC(=O)c2cc(Cl)c(N)cc2OC)CC1 10.1021/jm900881j
15544715 112298 1 None - 1 Rat 6.0 pKi = 6 Binding
pKi against 5-hydroxytryptamine 4 receptor in rat striatum membranepKi against 5-hydroxytryptamine 4 receptor in rat striatum membrane
ChEMBL 272 3 2 3 1.8 CCN1CCC(NC(=O)c2cccc3[nH]cnc23)CC1 10.1016/s0960-894x(01)00517-0
CHEMBL330605 112298 1 None - 1 Rat 6.0 pKi = 6 Binding
pKi against 5-hydroxytryptamine 4 receptor in rat striatum membranepKi against 5-hydroxytryptamine 4 receptor in rat striatum membrane
ChEMBL 272 3 2 3 1.8 CCN1CCC(NC(=O)c2cccc3[nH]cnc23)CC1 10.1016/s0960-894x(01)00517-0
44327586 163279 1 None - 1 Rat 6.0 pKi = 6 Binding
pKi against 5-hydroxytryptamine 4 receptor in rat striatum membranepKi against 5-hydroxytryptamine 4 receptor in rat striatum membrane
ChEMBL 286 4 2 3 2.2 CCCN1CCC(NC(=O)c2cccc3[nH]cnc23)CC1 10.1016/s0960-894x(01)00517-0
CHEMBL420638 163279 1 None - 1 Rat 6.0 pKi = 6 Binding
pKi against 5-hydroxytryptamine 4 receptor in rat striatum membranepKi against 5-hydroxytryptamine 4 receptor in rat striatum membrane
ChEMBL 286 4 2 3 2.2 CCCN1CCC(NC(=O)c2cccc3[nH]cnc23)CC1 10.1016/s0960-894x(01)00517-0
15544721 98516 4 None - 1 Rat 5.0 pKi = 5 Binding
pKi against 5-hydroxytryptamine 4 receptor in rat striatum membranepKi against 5-hydroxytryptamine 4 receptor in rat striatum membrane
ChEMBL 259 2 1 4 1.8 CN1CCC(OC(=O)c2cccc3[nH]cnc23)CC1 10.1016/s0960-894x(01)00517-0
CHEMBL279823 98516 4 None - 1 Rat 5.0 pKi = 5 Binding
pKi against 5-hydroxytryptamine 4 receptor in rat striatum membranepKi against 5-hydroxytryptamine 4 receptor in rat striatum membrane
ChEMBL 259 2 1 4 1.8 CN1CCC(OC(=O)c2cccc3[nH]cnc23)CC1 10.1016/s0960-894x(01)00517-0
155525723 170519 0 None - 1 Human 7.0 pKi = 7 Binding
Binding affinity to recombinant human brain 5HT4 receptor by radio ligand binding assayBinding affinity to recombinant human brain 5HT4 receptor by radio ligand binding assay
ChEMBL 515 11 3 7 4.2 COc1cc(/C=C/C(=O)NCCN2CCC(CCC(=O)c3cc(Cl)c(N)cc3OC)CC2)ccc1O 10.1016/j.ejmech.2019.111596
CHEMBL4457426 170519 0 None - 1 Human 7.0 pKi = 7 Binding
Binding affinity to recombinant human brain 5HT4 receptor by radio ligand binding assayBinding affinity to recombinant human brain 5HT4 receptor by radio ligand binding assay
ChEMBL 515 11 3 7 4.2 COc1cc(/C=C/C(=O)NCCN2CCC(CCC(=O)c3cc(Cl)c(N)cc3OC)CC2)ccc1O 10.1016/j.ejmech.2019.111596
71461048 82560 0 None -3 2 Guinea pig 7.0 pKi = 7 Binding
Displacement of [3H]GR113808 from 5HT4R in guinea pig striatal membranesDisplacement of [3H]GR113808 from 5HT4R in guinea pig striatal membranes
ChEMBL 352 5 0 3 5.0 CCCN1CCC(COc2nc3cc(F)ccc3c3ccccc23)CC1 10.1021/jm300943r
CHEMBL2181185 82560 0 None -3 2 Guinea pig 7.0 pKi = 7 Binding
Displacement of [3H]GR113808 from 5HT4R in guinea pig striatal membranesDisplacement of [3H]GR113808 from 5HT4R in guinea pig striatal membranes
ChEMBL 352 5 0 3 5.0 CCCN1CCC(COc2nc3cc(F)ccc3c3ccccc23)CC1 10.1021/jm300943r
10712151 119660 0 None - 1 Rat 7.0 pKi = 7.0 Binding
Binding affinity towards 5-hydroxytryptamine 4 receptor was determined in rat striatal membranes using [3H]GR-113808 as radioligandBinding affinity towards 5-hydroxytryptamine 4 receptor was determined in rat striatal membranes using [3H]GR-113808 as radioligand
ChEMBL 339 5 2 4 2.6 COc1cc(N)c(Cl)cc1C(=O)NCCN1CC(C)CC(C)C1 10.1021/jm960320m
CHEMBL351557 119660 0 None - 1 Rat 7.0 pKi = 7.0 Binding
Binding affinity towards 5-hydroxytryptamine 4 receptor was determined in rat striatal membranes using [3H]GR-113808 as radioligandBinding affinity towards 5-hydroxytryptamine 4 receptor was determined in rat striatal membranes using [3H]GR-113808 as radioligand
ChEMBL 339 5 2 4 2.6 COc1cc(N)c(Cl)cc1C(=O)NCCN1CC(C)CC(C)C1 10.1021/jm960320m
10832327 4157 0 None - 1 Guinea pig 7.0 pKi = 7.0 Binding
Binding affinity against 5-hydroxytryptamine 4 receptor in guinea pig striatum using [3H]GR-113808 as radioligandBinding affinity against 5-hydroxytryptamine 4 receptor in guinea pig striatum using [3H]GR-113808 as radioligand
ChEMBL 359 5 1 6 1.6 CCN1CCN(CCNC(=O)n2c(=O)n(C(C)C)c3ccccc32)CC1 10.1021/jm981098j
CHEMBL100317 4157 0 None - 1 Guinea pig 7.0 pKi = 7.0 Binding
Binding affinity against 5-hydroxytryptamine 4 receptor in guinea pig striatum using [3H]GR-113808 as radioligandBinding affinity against 5-hydroxytryptamine 4 receptor in guinea pig striatum using [3H]GR-113808 as radioligand
ChEMBL 359 5 1 6 1.6 CCN1CCN(CCNC(=O)n2c(=O)n(C(C)C)c3ccccc32)CC1 10.1021/jm981098j
2780 110040 32 None -20 11 Rat 7.0 pKi = 7.0 Binding
Binding affinity against 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatumBinding affinity against 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatum
ChEMBL 373 5 2 4 3.3 COc1cc(N)c(Cl)cc1C(=O)NC1CCN(Cc2ccccc2)CC1 10.1016/0960-894X(95)00115-A
CHEMBL325109 110040 32 None -20 11 Rat 7.0 pKi = 7.0 Binding
Binding affinity against 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatumBinding affinity against 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatum
ChEMBL 373 5 2 4 3.3 COc1cc(N)c(Cl)cc1C(=O)NC1CCN(Cc2ccccc2)CC1 10.1016/0960-894X(95)00115-A
2780 110040 32 None -20 11 Guinea pig 7.0 pKi = 7.0 Binding
Inhibition of [3H]GR-113808 binding to guinea pig striatum 5-hydroxytryptamine 4 receptorInhibition of [3H]GR-113808 binding to guinea pig striatum 5-hydroxytryptamine 4 receptor
ChEMBL 373 5 2 4 3.3 COc1cc(N)c(Cl)cc1C(=O)NC1CCN(Cc2ccccc2)CC1 10.1021/jm020270n
CHEMBL325109 110040 32 None -20 11 Guinea pig 7.0 pKi = 7.0 Binding
Inhibition of [3H]GR-113808 binding to guinea pig striatum 5-hydroxytryptamine 4 receptorInhibition of [3H]GR-113808 binding to guinea pig striatum 5-hydroxytryptamine 4 receptor
ChEMBL 373 5 2 4 3.3 COc1cc(N)c(Cl)cc1C(=O)NC1CCN(Cc2ccccc2)CC1 10.1021/jm020270n
5 139 66 None -288 54 Human 6.0 pKi = 6.0 Binding
Displacement of [3H]GR-113808 from human 5HT4 isoform E receptor expressed in rat C6 cells by liquid scintillation countingDisplacement of [3H]GR-113808 from human 5HT4 isoform E receptor expressed in rat C6 cells by liquid scintillation counting
ChEMBL 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 10.1021/jm801327q
5202 139 66 None -288 54 Human 6.0 pKi = 6.0 Binding
Displacement of [3H]GR-113808 from human 5HT4 isoform E receptor expressed in rat C6 cells by liquid scintillation countingDisplacement of [3H]GR-113808 from human 5HT4 isoform E receptor expressed in rat C6 cells by liquid scintillation counting
ChEMBL 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 10.1021/jm801327q
CHEMBL39 139 66 None -288 54 Human 6.0 pKi = 6.0 Binding
Displacement of [3H]GR-113808 from human 5HT4 isoform E receptor expressed in rat C6 cells by liquid scintillation countingDisplacement of [3H]GR-113808 from human 5HT4 isoform E receptor expressed in rat C6 cells by liquid scintillation counting
ChEMBL 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 10.1021/jm801327q
DB08839 139 66 None -288 54 Human 6.0 pKi = 6.0 Binding
Displacement of [3H]GR-113808 from human 5HT4 isoform E receptor expressed in rat C6 cells by liquid scintillation countingDisplacement of [3H]GR-113808 from human 5HT4 isoform E receptor expressed in rat C6 cells by liquid scintillation counting
ChEMBL 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 10.1021/jm801327q
118734520 118172 0 None - 1 Guinea pig 7.0 pKi = 7.0 Binding
Displacement of [3H]GR113808 from 5-HT4R in guinea pig brain membranes incubated for 30 mins by radioligand binding assayDisplacement of [3H]GR113808 from 5-HT4R in guinea pig brain membranes incubated for 30 mins by radioligand binding assay
ChEMBL 421 8 1 5 5.4 CO/N=C(\CCC1CCN(CC2CCCCC2)CC1)c1cc(Cl)c(N)cc1OC 10.1021/acs.jmedchem.5b00115
CHEMBL3417005 118172 0 None - 1 Guinea pig 7.0 pKi = 7.0 Binding
Displacement of [3H]GR113808 from 5-HT4R in guinea pig brain membranes incubated for 30 mins by radioligand binding assayDisplacement of [3H]GR113808 from 5-HT4R in guinea pig brain membranes incubated for 30 mins by radioligand binding assay
ChEMBL 421 8 1 5 5.4 CO/N=C(\CCC1CCN(CC2CCCCC2)CC1)c1cc(Cl)c(N)cc1OC 10.1021/acs.jmedchem.5b00115
90644475 111790 0 None - 1 Guinea pig 7.0 pKi = 7.0 Binding
Displacement of [3H]GR113808 from Dunkin-Hartley guinea pig brain striatum 5HT4R after 30 minsDisplacement of [3H]GR113808 from Dunkin-Hartley guinea pig brain striatum 5HT4R after 30 mins
ChEMBL 357 4 0 4 3.4 O=C1c2cccc3nc(Cl)cc(c23)C(=O)N1CCCN1CCCCC1 10.1016/j.ejmech.2014.05.015
CHEMBL3291080 111790 0 None - 1 Guinea pig 7.0 pKi = 7.0 Binding
Displacement of [3H]GR113808 from Dunkin-Hartley guinea pig brain striatum 5HT4R after 30 minsDisplacement of [3H]GR113808 from Dunkin-Hartley guinea pig brain striatum 5HT4R after 30 mins
ChEMBL 357 4 0 4 3.4 O=C1c2cccc3nc(Cl)cc(c23)C(=O)N1CCCN1CCCCC1 10.1016/j.ejmech.2014.05.015
136118638 75963 0 None -1 3 Human 6.0 pKi = 6.0 Binding
Displacement of [3H]GR113808 from human recombinant 5HT4 receptorDisplacement of [3H]GR113808 from human recombinant 5HT4 receptor
ChEMBL 335 1 2 3 3.1 CSC1=NC(=O)/C(=C/c2c[nH]c3cccc(Br)c23)N1 10.1016/j.bmc.2013.09.011
CHEMBL2058698 75963 0 None -1 3 Human 6.0 pKi = 6.0 Binding
Displacement of [3H]GR113808 from human recombinant 5HT4 receptorDisplacement of [3H]GR113808 from human recombinant 5HT4 receptor
ChEMBL 335 1 2 3 3.1 CSC1=NC(=O)/C(=C/c2c[nH]c3cccc(Br)c23)N1 10.1016/j.bmc.2013.09.011
10594888 4113 0 None - 1 Guinea pig 7.0 pKi = 7.0 Binding
Binding affinity against 5-hydroxytryptamine 4 receptor in guinea pig striatum using [3H]GR-113808 as radioligandBinding affinity against 5-hydroxytryptamine 4 receptor in guinea pig striatum using [3H]GR-113808 as radioligand
ChEMBL 363 4 1 6 1.3 CC(C)n1c(=O)n(C(=O)NCCN2CCN(C)CC2)c2cc(F)ccc21 10.1021/jm981098j
CHEMBL100088 4113 0 None - 1 Guinea pig 7.0 pKi = 7.0 Binding
Binding affinity against 5-hydroxytryptamine 4 receptor in guinea pig striatum using [3H]GR-113808 as radioligandBinding affinity against 5-hydroxytryptamine 4 receptor in guinea pig striatum using [3H]GR-113808 as radioligand
ChEMBL 363 4 1 6 1.3 CC(C)n1c(=O)n(C(=O)NCCN2CCN(C)CC2)c2cc(F)ccc21 10.1021/jm981098j
5 139 66 None -288 54 Human 7.0 pKi = 7.0 Binding
Displacement of [3H]GR-113808 from human recombinant 5HT4b receptor expressed in HEK293 cells by scintillation countingDisplacement of [3H]GR-113808 from human recombinant 5HT4b receptor expressed in HEK293 cells by scintillation counting
ChEMBL 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 10.1016/j.ejmech.2009.01.015
5202 139 66 None -288 54 Human 7.0 pKi = 7.0 Binding
Displacement of [3H]GR-113808 from human recombinant 5HT4b receptor expressed in HEK293 cells by scintillation countingDisplacement of [3H]GR-113808 from human recombinant 5HT4b receptor expressed in HEK293 cells by scintillation counting
ChEMBL 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 10.1016/j.ejmech.2009.01.015
CHEMBL39 139 66 None -288 54 Human 7.0 pKi = 7.0 Binding
Displacement of [3H]GR-113808 from human recombinant 5HT4b receptor expressed in HEK293 cells by scintillation countingDisplacement of [3H]GR-113808 from human recombinant 5HT4b receptor expressed in HEK293 cells by scintillation counting
ChEMBL 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 10.1016/j.ejmech.2009.01.015
DB08839 139 66 None -288 54 Human 7.0 pKi = 7.0 Binding
Displacement of [3H]GR-113808 from human recombinant 5HT4b receptor expressed in HEK293 cells by scintillation countingDisplacement of [3H]GR-113808 from human recombinant 5HT4b receptor expressed in HEK293 cells by scintillation counting
ChEMBL 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 10.1016/j.ejmech.2009.01.015
11686484 132321 0 None - 1 Human 8.0 pKi = 8.0 Binding
Binding affinity for 5-HT4 receptor using [3H]GR-113808Binding affinity for 5-HT4 receptor using [3H]GR-113808
ChEMBL 806 20 4 12 4.8 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCC(CCNC(=O)CCCC(=O)NCCC2CCN(CCOC(=O)c3cc(Cl)c(N)cc3OC)CC2)CC1 10.1021/jm050234z
CHEMBL370182 132321 0 None - 1 Human 8.0 pKi = 8.0 Binding
Binding affinity for 5-HT4 receptor using [3H]GR-113808Binding affinity for 5-HT4 receptor using [3H]GR-113808
ChEMBL 806 20 4 12 4.8 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCC(CCNC(=O)CCCC(=O)NCCC2CCN(CCOC(=O)c3cc(Cl)c(N)cc3OC)CC2)CC1 10.1021/jm050234z
11629240 140544 0 None - 1 Human 8.0 pKi = 8.0 Binding
Binding affinity for 5-HT4 receptor using [3H]GR-113808Binding affinity for 5-HT4 receptor using [3H]GR-113808
ChEMBL 806 20 4 12 4.8 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCC(CNC(=O)CCCCCC(=O)NCC2CCN(CCOC(=O)c3cc(Cl)c(N)cc3OC)CC2)CC1 10.1021/jm050234z
CHEMBL382543 140544 0 None - 1 Human 8.0 pKi = 8.0 Binding
Binding affinity for 5-HT4 receptor using [3H]GR-113808Binding affinity for 5-HT4 receptor using [3H]GR-113808
ChEMBL 806 20 4 12 4.8 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCC(CNC(=O)CCCCCC(=O)NCC2CCN(CCOC(=O)c3cc(Cl)c(N)cc3OC)CC2)CC1 10.1021/jm050234z
49783421 17606 0 None -51 2 Human 8.0 pKi = 8.0 Binding
Displacement of [3H]GR113808 from human recombinant 5HT4 receptor expressed in HEK293 cellsDisplacement of [3H]GR113808 from human recombinant 5HT4 receptor expressed in HEK293 cells
ChEMBL 352 9 1 5 3.3 CCCCN1CCC(COC(=O)c2ccc(N)c(OCCF)c2)CC1 10.1021/jm100668r
CHEMBL1258786 17606 0 None -51 2 Human 8.0 pKi = 8.0 Binding
Displacement of [3H]GR113808 from human recombinant 5HT4 receptor expressed in HEK293 cellsDisplacement of [3H]GR113808 from human recombinant 5HT4 receptor expressed in HEK293 cells
ChEMBL 352 9 1 5 3.3 CCCCN1CCC(COC(=O)c2ccc(N)c(OCCF)c2)CC1 10.1021/jm100668r
44592282 178627 0 None - 1 Guinea pig 8.0 pKi = 8.0 Binding
Displacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatum membraneDisplacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatum membrane
ChEMBL 355 6 0 5 4.5 C=CCCN1CCC(COc2nc3scc(C)c3n3cccc23)CC1 10.1016/j.bmc.2008.11.045
CHEMBL472481 178627 0 None - 1 Guinea pig 8.0 pKi = 8.0 Binding
Displacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatum membraneDisplacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatum membrane
ChEMBL 355 6 0 5 4.5 C=CCCN1CCC(COc2nc3scc(C)c3n3cccc23)CC1 10.1016/j.bmc.2008.11.045
15544716 110907 0 None - 1 Rat 7.9 pKi = 7.9 Binding
Binding affinity to 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatum membraneBinding affinity to 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatum membrane
ChEMBL 379 7 3 5 0.6 CS(=O)(=O)NCCN1CCC(CNC(=O)c2cccc3[nH]cnc23)CC1 10.1021/jm020807x
CHEMBL327192 110907 0 None - 1 Rat 7.9 pKi = 7.9 Binding
Binding affinity to 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatum membraneBinding affinity to 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatum membrane
ChEMBL 379 7 3 5 0.6 CS(=O)(=O)NCCN1CCC(CNC(=O)c2cccc3[nH]cnc23)CC1 10.1021/jm020807x
15544716 110907 0 None - 1 Rat 7.9 pKi = 7.9 Binding
In vitro binding affinity to 5-hydroxytryptamine 4 receptor in rat striatum membraneIn vitro binding affinity to 5-hydroxytryptamine 4 receptor in rat striatum membrane
ChEMBL 379 7 3 5 0.6 CS(=O)(=O)NCCN1CCC(CNC(=O)c2cccc3[nH]cnc23)CC1 10.1016/s0960-894x(01)00517-0
CHEMBL327192 110907 0 None - 1 Rat 7.9 pKi = 7.9 Binding
In vitro binding affinity to 5-hydroxytryptamine 4 receptor in rat striatum membraneIn vitro binding affinity to 5-hydroxytryptamine 4 receptor in rat striatum membrane
ChEMBL 379 7 3 5 0.6 CS(=O)(=O)NCCN1CCC(CNC(=O)c2cccc3[nH]cnc23)CC1 10.1016/s0960-894x(01)00517-0
15544716 110907 0 None - 1 Rat 7.9 pKi = 7.9 Binding
pKi against 5-hydroxytryptamine 4 receptor in rat striatum membranepKi against 5-hydroxytryptamine 4 receptor in rat striatum membrane
ChEMBL 379 7 3 5 0.6 CS(=O)(=O)NCCN1CCC(CNC(=O)c2cccc3[nH]cnc23)CC1 10.1016/s0960-894x(01)00517-0
CHEMBL327192 110907 0 None - 1 Rat 7.9 pKi = 7.9 Binding
pKi against 5-hydroxytryptamine 4 receptor in rat striatum membranepKi against 5-hydroxytryptamine 4 receptor in rat striatum membrane
ChEMBL 379 7 3 5 0.6 CS(=O)(=O)NCCN1CCC(CNC(=O)c2cccc3[nH]cnc23)CC1 10.1016/s0960-894x(01)00517-0
10739944 78345 0 None - 1 Human 7.9 pKi = 7.9 Binding
Binding affinity was determined against cloned 5-hydroxytryptamine 4E receptor isoform expressed in C6 glial cells incubated with 0.2 nM [3H]GR-113808Binding affinity was determined against cloned 5-hydroxytryptamine 4E receptor isoform expressed in C6 glial cells incubated with 0.2 nM [3H]GR-113808
ChEMBL 403 7 1 6 3.3 COc1cc(N)c(Cl)cc1C(=O)OCCCN1CCN(c2ccccc2)CC1 10.1021/jm0009538
CHEMBL2112621 78345 0 None - 1 Human 7.9 pKi = 7.9 Binding
Binding affinity was determined against cloned 5-hydroxytryptamine 4E receptor isoform expressed in C6 glial cells incubated with 0.2 nM [3H]GR-113808Binding affinity was determined against cloned 5-hydroxytryptamine 4E receptor isoform expressed in C6 glial cells incubated with 0.2 nM [3H]GR-113808
ChEMBL 403 7 1 6 3.3 COc1cc(N)c(Cl)cc1C(=O)OCCCN1CCN(c2ccccc2)CC1 10.1021/jm0009538
44592148 178277 0 None - 1 Guinea pig 7.9 pKi = 7.9 Binding
Displacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatum membraneDisplacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatum membrane
ChEMBL 329 5 0 5 4.1 CCCN1CCC(COc2nc3sccc3n3cccc23)CC1 10.1016/j.bmc.2008.11.045
CHEMBL469582 178277 0 None - 1 Guinea pig 7.9 pKi = 7.9 Binding
Displacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatum membraneDisplacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatum membrane
ChEMBL 329 5 0 5 4.1 CCCN1CCC(COc2nc3sccc3n3cccc23)CC1 10.1016/j.bmc.2008.11.045
243 3153 85 None 12 34 Human 7.0 pKi = 7.0 Binding
Tested for selectivity for 5-hydroxytryptamine 4 receptorTested for selectivity for 5-hydroxytryptamine 4 receptor
ChEMBL 367 6 2 5 2.1 COCCCN1CCC(CC1)NC(=O)c1cc(Cl)c(c2c1OCC2)N 10.1021/jm020099f
3052762 3153 85 None 12 34 Human 7.0 pKi = 7.0 Binding
Tested for selectivity for 5-hydroxytryptamine 4 receptorTested for selectivity for 5-hydroxytryptamine 4 receptor
ChEMBL 367 6 2 5 2.1 COCCCN1CCC(CC1)NC(=O)c1cc(Cl)c(c2c1OCC2)N 10.1021/jm020099f
3502 3153 85 None 12 34 Human 7.0 pKi = 7.0 Binding
Tested for selectivity for 5-hydroxytryptamine 4 receptorTested for selectivity for 5-hydroxytryptamine 4 receptor
ChEMBL 367 6 2 5 2.1 COCCCN1CCC(CC1)NC(=O)c1cc(Cl)c(c2c1OCC2)N 10.1021/jm020099f
CHEMBL117287 3153 85 None 12 34 Human 7.0 pKi = 7.0 Binding
Tested for selectivity for 5-hydroxytryptamine 4 receptorTested for selectivity for 5-hydroxytryptamine 4 receptor
ChEMBL 367 6 2 5 2.1 COCCCN1CCC(CC1)NC(=O)c1cc(Cl)c(c2c1OCC2)N 10.1021/jm020099f
DB06480 3153 85 None 12 34 Human 7.0 pKi = 7.0 Binding
Tested for selectivity for 5-hydroxytryptamine 4 receptorTested for selectivity for 5-hydroxytryptamine 4 receptor
ChEMBL 367 6 2 5 2.1 COCCCN1CCC(CC1)NC(=O)c1cc(Cl)c(c2c1OCC2)N 10.1021/jm020099f
44582815 172657 0 None - 1 Human 7.0 pKi = 7.0 Binding
Displacement of [3H]GR-113808 from human 5HT4 isoform E receptor expressed in rat C6 cells by liquid scintillation countingDisplacement of [3H]GR-113808 from human 5HT4 isoform E receptor expressed in rat C6 cells by liquid scintillation counting
ChEMBL 621 11 3 9 3.9 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCC(NC(=O)CCCCN2C(=O)c3cccc4c(N)ccc(c34)C2=O)CC1 10.1021/jm801327q
CHEMBL452353 172657 0 None - 1 Human 7.0 pKi = 7.0 Binding
Displacement of [3H]GR-113808 from human 5HT4 isoform E receptor expressed in rat C6 cells by liquid scintillation countingDisplacement of [3H]GR-113808 from human 5HT4 isoform E receptor expressed in rat C6 cells by liquid scintillation counting
ChEMBL 621 11 3 9 3.9 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCC(NC(=O)CCCCN2C(=O)c3cccc4c(N)ccc(c34)C2=O)CC1 10.1021/jm801327q
11557207 78645 0 None - 1 Human 7.0 pKi = 7.0 Binding
Binding affinity for 5-HT4 receptor using [3H]GR-113808Binding affinity for 5-HT4 receptor using [3H]GR-113808
ChEMBL 1203 39 7 18 10.7 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCC(NC(=O)CCCCCCCCCCNc2nc(NCCCCCCCCCCC(=O)NC3CCN(CCOC(=O)c4cc(Cl)c(N)cc4OC)CC3)nc(NCc3ccccc3)n2)CC1 10.1021/jm050234z
CHEMBL2113160 78645 0 None - 1 Human 7.0 pKi = 7.0 Binding
Binding affinity for 5-HT4 receptor using [3H]GR-113808Binding affinity for 5-HT4 receptor using [3H]GR-113808
ChEMBL 1203 39 7 18 10.7 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCC(NC(=O)CCCCCCCCCCNc2nc(NCCCCCCCCCCC(=O)NC3CCN(CCOC(=O)c4cc(Cl)c(N)cc4OC)CC3)nc(NCc3ccccc3)n2)CC1 10.1021/jm050234z
10925529 206161 0 None - 1 Rat 6.9 pKi = 6.9 Binding
pKi against 5-hydroxytryptamine 4 receptor in rat striatum membranepKi against 5-hydroxytryptamine 4 receptor in rat striatum membrane
ChEMBL 329 6 3 4 2.4 CCCCN1CCC(CNC(=O)c2ccc(N)c3[nH]cnc23)CC1 10.1016/s0960-894x(01)00517-0
CHEMBL96667 206161 0 None - 1 Rat 6.9 pKi = 6.9 Binding
pKi against 5-hydroxytryptamine 4 receptor in rat striatum membranepKi against 5-hydroxytryptamine 4 receptor in rat striatum membrane
ChEMBL 329 6 3 4 2.4 CCCCN1CCC(CNC(=O)c2ccc(N)c3[nH]cnc23)CC1 10.1016/s0960-894x(01)00517-0
132164 204922 8 None - 1 Rat 6.9 pKi = 6.9 Binding
Binding affinity at 5-hydroxytryptamine 4 receptor in rat striatum by [3H]GR-113808 displacement.Binding affinity at 5-hydroxytryptamine 4 receptor in rat striatum by [3H]GR-113808 displacement.
ChEMBL 321 2 2 4 1.7 Nc1c(Cl)cc(C(=O)N[C@H]2CN3CCC2CC3)c2c1CCO2 10.1016/0960-894X(96)00002-9
CHEMBL89259 204922 8 None - 1 Rat 6.9 pKi = 6.9 Binding
Binding affinity at 5-hydroxytryptamine 4 receptor in rat striatum by [3H]GR-113808 displacement.Binding affinity at 5-hydroxytryptamine 4 receptor in rat striatum by [3H]GR-113808 displacement.
ChEMBL 321 2 2 4 1.7 Nc1c(Cl)cc(C(=O)N[C@H]2CN3CCC2CC3)c2c1CCO2 10.1016/0960-894X(96)00002-9
10925529 206161 0 None - 1 Rat 6.9 pKi = 6.9 Binding
Binding affinity to 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatum membraneBinding affinity to 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatum membrane
ChEMBL 329 6 3 4 2.4 CCCCN1CCC(CNC(=O)c2ccc(N)c3[nH]cnc23)CC1 10.1021/jm020807x
CHEMBL96667 206161 0 None - 1 Rat 6.9 pKi = 6.9 Binding
Binding affinity to 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatum membraneBinding affinity to 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatum membrane
ChEMBL 329 6 3 4 2.4 CCCCN1CCC(CNC(=O)c2ccc(N)c3[nH]cnc23)CC1 10.1021/jm020807x
71457408 82548 0 None - 1 Guinea pig 6.9 pKi = 6.9 Binding
Displacement of [3H]GR113808 from 5HT4R in guinea pig striatal membranesDisplacement of [3H]GR113808 from 5HT4R in guinea pig striatal membranes
ChEMBL 536 7 0 3 6.7 Ic1ccc(CCCN2CCC(COc3nc4ccccc4c4ccccc34)CC2)cc1 10.1021/jm300943r
CHEMBL2181167 82548 0 None - 1 Guinea pig 6.9 pKi = 6.9 Binding
Displacement of [3H]GR113808 from 5HT4R in guinea pig striatal membranesDisplacement of [3H]GR113808 from 5HT4R in guinea pig striatal membranes
ChEMBL 536 7 0 3 6.7 Ic1ccc(CCCN2CCC(COc3nc4ccccc4c4ccccc34)CC2)cc1 10.1021/jm300943r
10925529 206161 0 None - 1 Rat 6.9 pKi = 6.9 Binding
In vitro binding affinity to 5-hydroxytryptamine 4 receptor in rat striatum membraneIn vitro binding affinity to 5-hydroxytryptamine 4 receptor in rat striatum membrane
ChEMBL 329 6 3 4 2.4 CCCCN1CCC(CNC(=O)c2ccc(N)c3[nH]cnc23)CC1 10.1016/s0960-894x(01)00517-0
CHEMBL96667 206161 0 None - 1 Rat 6.9 pKi = 6.9 Binding
In vitro binding affinity to 5-hydroxytryptamine 4 receptor in rat striatum membraneIn vitro binding affinity to 5-hydroxytryptamine 4 receptor in rat striatum membrane
ChEMBL 329 6 3 4 2.4 CCCCN1CCC(CNC(=O)c2ccc(N)c3[nH]cnc23)CC1 10.1016/s0960-894x(01)00517-0
136118650 75970 0 None -7 3 Human 5.9 pKi = 5.9 Binding
Displacement of [3H]GR113808 from human recombinant 5HT4 receptorDisplacement of [3H]GR113808 from human recombinant 5HT4 receptor
ChEMBL 318 1 3 2 2.0 C/N=C1\NC(=O)/C(=C/c2c[nH]c3cc(Br)ccc23)N1 10.1016/j.bmc.2013.09.011
CHEMBL2058705 75970 0 None -7 3 Human 5.9 pKi = 5.9 Binding
Displacement of [3H]GR113808 from human recombinant 5HT4 receptorDisplacement of [3H]GR113808 from human recombinant 5HT4 receptor
ChEMBL 318 1 3 2 2.0 C/N=C1\NC(=O)/C(=C/c2c[nH]c3cc(Br)ccc23)N1 10.1016/j.bmc.2013.09.011
11039391 204561 0 None - 1 Human 6.9 pKi = 6.9 Binding
Binding affinity towards cloned human 5-hydroxytryptamine 4E receptor expressed in C6 glial cells using [3H]GR-113808 as radioligandBinding affinity towards cloned human 5-hydroxytryptamine 4E receptor expressed in C6 glial cells using [3H]GR-113808 as radioligand
ChEMBL 617 11 2 9 2.8 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCN(C(=O)CCNS(=O)(=O)c2cccc3c(N(C)C)cccc23)CC1 10.1021/jm0307887
CHEMBL86985 204561 0 None - 1 Human 6.9 pKi = 6.9 Binding
Binding affinity towards cloned human 5-hydroxytryptamine 4E receptor expressed in C6 glial cells using [3H]GR-113808 as radioligandBinding affinity towards cloned human 5-hydroxytryptamine 4E receptor expressed in C6 glial cells using [3H]GR-113808 as radioligand
ChEMBL 617 11 2 9 2.8 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCN(C(=O)CCNS(=O)(=O)c2cccc3c(N(C)C)cccc23)CC1 10.1021/jm0307887
42618251 186352 0 None - 1 Human 7.9 pKi = 7.9 Binding
Displacement of [3H]GR-113808 from human 5HT4 isoform E receptor expressed in rat C6 cells by liquid scintillation countingDisplacement of [3H]GR-113808 from human 5HT4 isoform E receptor expressed in rat C6 cells by liquid scintillation counting
ChEMBL 530 14 3 7 3.7 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCC(NC(=O)CCCNCCCc2ccccc2)CC1 10.1021/jm801327q
CHEMBL490050 186352 0 None - 1 Human 7.9 pKi = 7.9 Binding
Displacement of [3H]GR-113808 from human 5HT4 isoform E receptor expressed in rat C6 cells by liquid scintillation countingDisplacement of [3H]GR-113808 from human 5HT4 isoform E receptor expressed in rat C6 cells by liquid scintillation counting
ChEMBL 530 14 3 7 3.7 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCC(NC(=O)CCCNCCCc2ccccc2)CC1 10.1021/jm801327q
49783418 17533 0 None - 1 Human 7.9 pKi = 7.9 Binding
Displacement of [3H]GR113808 from human recombinant 5HT4 receptor expressed in HEK293 cellsDisplacement of [3H]GR113808 from human recombinant 5HT4 receptor expressed in HEK293 cells
ChEMBL 334 8 1 5 3.3 CCCCCN1CCC(COC(=O)c2ccc(N)c(OC)c2)CC1 10.1021/jm100668r
CHEMBL1258561 17533 0 None - 1 Human 7.9 pKi = 7.9 Binding
Displacement of [3H]GR113808 from human recombinant 5HT4 receptor expressed in HEK293 cellsDisplacement of [3H]GR113808 from human recombinant 5HT4 receptor expressed in HEK293 cells
ChEMBL 334 8 1 5 3.3 CCCCCN1CCC(COC(=O)c2ccc(N)c(OC)c2)CC1 10.1021/jm100668r
162652829 179806 0 None - 1 Guinea pig 7.9 pKi = 7.9 Binding
Displacement of [3H]-GR113808 from guinea pig brain 5HT4 receptor in presence of serotonin incubated for 30 minsDisplacement of [3H]-GR113808 from guinea pig brain 5HT4 receptor in presence of serotonin incubated for 30 mins
ChEMBL 508 11 1 7 4.5 COc1ccc(S(=O)(=O)CCCN2CCC(CCC(=O)c3cc(Cl)c(N)cc3OC)CC2)cc1 10.1016/j.ejmech.2016.05.048
CHEMBL4751840 179806 0 None - 1 Guinea pig 7.9 pKi = 7.9 Binding
Displacement of [3H]-GR113808 from guinea pig brain 5HT4 receptor in presence of serotonin incubated for 30 minsDisplacement of [3H]-GR113808 from guinea pig brain 5HT4 receptor in presence of serotonin incubated for 30 mins
ChEMBL 508 11 1 7 4.5 COc1ccc(S(=O)(=O)CCCN2CCC(CCC(=O)c3cc(Cl)c(N)cc3OC)CC2)cc1 10.1016/j.ejmech.2016.05.048
162650788 179607 0 None - 1 Guinea pig 7.9 pKi = 7.9 Binding
Displacement of [3H]-GR113808 from guinea pig brain 5HT4 receptor in presence of serotonin incubated for 30 minsDisplacement of [3H]-GR113808 from guinea pig brain 5HT4 receptor in presence of serotonin incubated for 30 mins
ChEMBL 509 11 2 7 3.6 COc1ccc(S(=O)(=O)NCCN2CCC(CCC(=O)c3cc(Cl)c(N)cc3OC)CC2)cc1 10.1016/j.ejmech.2016.05.048
CHEMBL4749344 179607 0 None - 1 Guinea pig 7.9 pKi = 7.9 Binding
Displacement of [3H]-GR113808 from guinea pig brain 5HT4 receptor in presence of serotonin incubated for 30 minsDisplacement of [3H]-GR113808 from guinea pig brain 5HT4 receptor in presence of serotonin incubated for 30 mins
ChEMBL 509 11 2 7 3.6 COc1ccc(S(=O)(=O)NCCN2CCC(CCC(=O)c3cc(Cl)c(N)cc3OC)CC2)cc1 10.1016/j.ejmech.2016.05.048
10270343 118534 0 None - 1 Guinea pig 7.9 pKi = 7.9 Binding
Ability to displace [3H]GR-113808 from 5-hydroxytryptamine 4 receptorAbility to displace [3H]GR-113808 from 5-hydroxytryptamine 4 receptor
ChEMBL 367 7 1 4 4.9 CCCCCN1CCC(COc2nc3ccccc3c3c2CCCN3)CC1 10.1021/jm020954v
CHEMBL34263 118534 0 None - 1 Guinea pig 7.9 pKi = 7.9 Binding
Ability to displace [3H]GR-113808 from 5-hydroxytryptamine 4 receptorAbility to displace [3H]GR-113808 from 5-hydroxytryptamine 4 receptor
ChEMBL 367 7 1 4 4.9 CCCCCN1CCC(COc2nc3ccccc3c3c2CCCN3)CC1 10.1021/jm020954v
10408029 16283 0 None - 1 Human 7.9 pKi = 7.9 Binding
Binding affinity was determined against cloned 5-hydroxytryptamine 4C receptor isoform expressed in COS-7 cellsBinding affinity was determined against cloned 5-hydroxytryptamine 4C receptor isoform expressed in COS-7 cells
ChEMBL 389 6 1 6 2.9 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCN(c2ccccc2)CC1 10.1021/jm0009538
CHEMBL123377 16283 0 None - 1 Human 7.9 pKi = 7.9 Binding
Binding affinity was determined against cloned 5-hydroxytryptamine 4C receptor isoform expressed in COS-7 cellsBinding affinity was determined against cloned 5-hydroxytryptamine 4C receptor isoform expressed in COS-7 cells
ChEMBL 389 6 1 6 2.9 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCN(c2ccccc2)CC1 10.1021/jm0009538
71714543 90952 0 None - 1 Human 7.9 pKi = 7.9 Binding
Binding affinity to human recombinant 5HT4 receptorBinding affinity to human recombinant 5HT4 receptor
ChEMBL 534 8 3 7 1.2 CC(C)(C)c1nc2c(C(=O)NCC3CCN(CC(O)CN4CCN(S(C)(=O)=O)CC4)CC3)cccc2[nH]1 10.1016/j.bmcl.2013.05.018
CHEMBL2402893 90952 0 None - 1 Human 7.9 pKi = 7.9 Binding
Binding affinity to human recombinant 5HT4 receptorBinding affinity to human recombinant 5HT4 receptor
ChEMBL 534 8 3 7 1.2 CC(C)(C)c1nc2c(C(=O)NCC3CCN(CC(O)CN4CCN(S(C)(=O)=O)CC4)CC3)cccc2[nH]1 10.1016/j.bmcl.2013.05.018
11168006 76070 0 None - 1 Human 7.9 pKi = 7.9 Binding
Displacement of [3H]GR113808 from human recombinant 5HT4C receptor expressed in HEK293 cellsDisplacement of [3H]GR113808 from human recombinant 5HT4C receptor expressed in HEK293 cells
ChEMBL 502 7 1 7 1.9 CC(C)n1nc(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CCN2CCN(S(C)(=O)=O)CC2)c2ccccc21 10.1016/j.bmcl.2012.05.034
CHEMBL2059589 76070 0 None - 1 Human 7.9 pKi = 7.9 Binding
Displacement of [3H]GR113808 from human recombinant 5HT4C receptor expressed in HEK293 cellsDisplacement of [3H]GR113808 from human recombinant 5HT4C receptor expressed in HEK293 cells
ChEMBL 502 7 1 7 1.9 CC(C)n1nc(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CCN2CCN(S(C)(=O)=O)CC2)c2ccccc21 10.1016/j.bmcl.2012.05.034
44224237 193122 7 None - 1 Human 7.9 pKi = 7.9 Binding
Displacement of [3H]GR113808 from human recombinant 5HT4C receptor expressed in HEK293 cellsDisplacement of [3H]GR113808 from human recombinant 5HT4C receptor expressed in HEK293 cells
ChEMBL 559 8 2 8 1.2 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3C[C@@H](O)CN2CCN(S(C)(=O)=O)CC2)cc2ccccc21 10.1016/j.bmcl.2012.05.034
CHEMBL538635 193122 7 None - 1 Human 7.9 pKi = 7.9 Binding
Displacement of [3H]GR113808 from human recombinant 5HT4C receptor expressed in HEK293 cellsDisplacement of [3H]GR113808 from human recombinant 5HT4C receptor expressed in HEK293 cells
ChEMBL 559 8 2 8 1.2 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3C[C@@H](O)CN2CCN(S(C)(=O)=O)CC2)cc2ccccc21 10.1016/j.bmcl.2012.05.034
44224237 193122 7 None - 1 Human 7.9 pKi = 7.9 Binding
Displacement of [3H]GR113808 from human recombinant 5HT4c receptor expressed in HEK293 cellsDisplacement of [3H]GR113808 from human recombinant 5HT4c receptor expressed in HEK293 cells
ChEMBL 559 8 2 8 1.2 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3C[C@@H](O)CN2CCN(S(C)(=O)=O)CC2)cc2ccccc21 10.1016/j.bmcl.2012.08.051
CHEMBL538635 193122 7 None - 1 Human 7.9 pKi = 7.9 Binding
Displacement of [3H]GR113808 from human recombinant 5HT4c receptor expressed in HEK293 cellsDisplacement of [3H]GR113808 from human recombinant 5HT4c receptor expressed in HEK293 cells
ChEMBL 559 8 2 8 1.2 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3C[C@@H](O)CN2CCN(S(C)(=O)=O)CC2)cc2ccccc21 10.1016/j.bmcl.2012.08.051
44224237 193122 7 None - 1 Human 7.9 pKi = 7.9 Binding
Displacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 559 8 2 8 1.2 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3C[C@@H](O)CN2CCN(S(C)(=O)=O)CC2)cc2ccccc21 10.1021/jm900881j
CHEMBL538635 193122 7 None - 1 Human 7.9 pKi = 7.9 Binding
Displacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 559 8 2 8 1.2 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3C[C@@H](O)CN2CCN(S(C)(=O)=O)CC2)cc2ccccc21 10.1021/jm900881j
10291662 119698 0 None - 1 Guinea pig 7.9 pKi = 7.9 Binding
Ability to displace [3H]GR-113808 from 5-hydroxytryptamine 4 receptorAbility to displace [3H]GR-113808 from 5-hydroxytryptamine 4 receptor
ChEMBL 353 5 1 4 4.5 CCCN1CCC(COc2nc3ccccc3c3c2CCCCN3)CC1 10.1021/jm020954v
CHEMBL35196 119698 0 None - 1 Guinea pig 7.9 pKi = 7.9 Binding
Ability to displace [3H]GR-113808 from 5-hydroxytryptamine 4 receptorAbility to displace [3H]GR-113808 from 5-hydroxytryptamine 4 receptor
ChEMBL 353 5 1 4 4.5 CCCN1CCC(COc2nc3ccccc3c3c2CCCCN3)CC1 10.1021/jm020954v
155565664 175030 0 None - 1 Human 7.9 pKi = 7.9 Binding
Binding affinity to recombinant human brain 5HT4 receptor by radio ligand binding assayBinding affinity to recombinant human brain 5HT4 receptor by radio ligand binding assay
ChEMBL 432 8 2 6 4.5 COc1ccc(CN2CCC(CCC(=O)c3cc(Cl)c(N)cc3OC)CC2)cc1O 10.1016/j.ejmech.2019.111596
CHEMBL4580044 175030 0 None - 1 Human 7.9 pKi = 7.9 Binding
Binding affinity to recombinant human brain 5HT4 receptor by radio ligand binding assayBinding affinity to recombinant human brain 5HT4 receptor by radio ligand binding assay
ChEMBL 432 8 2 6 4.5 COc1ccc(CN2CCC(CCC(=O)c3cc(Cl)c(N)cc3OC)CC2)cc1O 10.1016/j.ejmech.2019.111596
44592186 178281 0 None - 1 Guinea pig 7.9 pKi = 7.9 Binding
Displacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatum membraneDisplacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatum membrane
ChEMBL 329 5 0 5 4.1 Cc1csc2nc(OCCCN3CCCCC3)c3cccn3c12 10.1016/j.bmc.2008.11.045
CHEMBL469593 178281 0 None - 1 Guinea pig 7.9 pKi = 7.9 Binding
Displacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatum membraneDisplacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatum membrane
ChEMBL 329 5 0 5 4.1 Cc1csc2nc(OCCCN3CCCCC3)c3cccn3c12 10.1016/j.bmc.2008.11.045
4595 176141 102 None -3 15 Rat 5.9 pKi = 5.9 Binding
The binding affinity was measured on 5-hydroxytryptamine 4 receptor using [3H]- GR-113808 as radioligand.The binding affinity was measured on 5-hydroxytryptamine 4 receptor using [3H]- GR-113808 as radioligand.
ChEMBL 293 2 0 4 3.1 Cc1nccn1CC1CCc2c(c3ccccc3n2C)C1=O 10.1021/jm00075a026
CHEMBL46 176141 102 None -3 15 Rat 5.9 pKi = 5.9 Binding
The binding affinity was measured on 5-hydroxytryptamine 4 receptor using [3H]- GR-113808 as radioligand.The binding affinity was measured on 5-hydroxytryptamine 4 receptor using [3H]- GR-113808 as radioligand.
ChEMBL 293 2 0 4 3.1 Cc1nccn1CC1CCc2c(c3ccccc3n2C)C1=O 10.1021/jm00075a026
145957594 161429 0 None - 1 Guinea pig 6.9 pKi = 6.9 Binding
Displacement of [3H]GR113808 from serotonin 5-HT4 receptor in Dunkin-Hartley guinea pigs striatal nuclei membranes incubated for 2 hrs by liquid scintillation countingDisplacement of [3H]GR113808 from serotonin 5-HT4 receptor in Dunkin-Hartley guinea pigs striatal nuclei membranes incubated for 2 hrs by liquid scintillation counting
ChEMBL 791 33 3 15 2.3 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCC(NC(=O)NCCOCCOCCOCCOCCOCCOCCOCCOCCN=[N+]=[N-])CC1 10.1039/C6MD00458J
CHEMBL4159138 161429 0 None - 1 Guinea pig 6.9 pKi = 6.9 Binding
Displacement of [3H]GR113808 from serotonin 5-HT4 receptor in Dunkin-Hartley guinea pigs striatal nuclei membranes incubated for 2 hrs by liquid scintillation countingDisplacement of [3H]GR113808 from serotonin 5-HT4 receptor in Dunkin-Hartley guinea pigs striatal nuclei membranes incubated for 2 hrs by liquid scintillation counting
ChEMBL 791 33 3 15 2.3 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCC(NC(=O)NCCOCCOCCOCCOCCOCCOCCOCCOCCN=[N+]=[N-])CC1 10.1039/C6MD00458J
118734521 118173 0 None - 1 Guinea pig 6.9 pKi = 6.9 Binding
Displacement of [3H]GR113808 from 5-HT4R in guinea pig brain membranes incubated for 30 mins by radioligand binding assayDisplacement of [3H]GR113808 from 5-HT4R in guinea pig brain membranes incubated for 30 mins by radioligand binding assay
ChEMBL 394 7 2 4 5.0 COc1cc(N)c(Cl)cc1C(O)CCC1CCN(CC2CCCCC2)CC1 10.1021/acs.jmedchem.5b00115
CHEMBL3417006 118173 0 None - 1 Guinea pig 6.9 pKi = 6.9 Binding
Displacement of [3H]GR113808 from 5-HT4R in guinea pig brain membranes incubated for 30 mins by radioligand binding assayDisplacement of [3H]GR113808 from 5-HT4R in guinea pig brain membranes incubated for 30 mins by radioligand binding assay
ChEMBL 394 7 2 4 5.0 COc1cc(N)c(Cl)cc1C(O)CCC1CCN(CC2CCCCC2)CC1 10.1021/acs.jmedchem.5b00115
10567201 183683 0 None - 1 Rat 6.9 pKi = 6.9 Binding
Binding affinity (Ki+/-SEM) against 5-hydroxytryptamine 4 receptor from cheng Prusoff equation by using [3H]GR-113808 in rat striatumBinding affinity (Ki+/-SEM) against 5-hydroxytryptamine 4 receptor from cheng Prusoff equation by using [3H]GR-113808 in rat striatum
ChEMBL 313 5 2 5 2.6 COc1cc(N)c(Cl)cc1NC(=O)OCCN1CCCC1 10.1021/jm960853v
CHEMBL48379 183683 0 None - 1 Rat 6.9 pKi = 6.9 Binding
Binding affinity (Ki+/-SEM) against 5-hydroxytryptamine 4 receptor from cheng Prusoff equation by using [3H]GR-113808 in rat striatumBinding affinity (Ki+/-SEM) against 5-hydroxytryptamine 4 receptor from cheng Prusoff equation by using [3H]GR-113808 in rat striatum
ChEMBL 313 5 2 5 2.6 COc1cc(N)c(Cl)cc1NC(=O)OCCN1CCCC1 10.1021/jm960853v
260 3808 49 None -45 6 Guinea pig 6.9 pKi = 6.9 Binding
Binding affinity towards 5-hydroxytryptamine 4 receptor in striatum membranes of guinea-pig brain was evaluatedBinding affinity towards 5-hydroxytryptamine 4 receptor in striatum membranes of guinea-pig brain was evaluated
ChEMBL 284 2 1 3 3.0 CN1[C@@H]2CC[C@H]1C[C@H](C2)OC(=O)c1c[nH]c2c1cccc2 10.1016/s0960-894x(01)00693-x
2775 3808 49 None -45 6 Guinea pig 6.9 pKi = 6.9 Binding
Binding affinity towards 5-hydroxytryptamine 4 receptor in striatum membranes of guinea-pig brain was evaluatedBinding affinity towards 5-hydroxytryptamine 4 receptor in striatum membranes of guinea-pig brain was evaluated
ChEMBL 284 2 1 3 3.0 CN1[C@@H]2CC[C@H]1C[C@H](C2)OC(=O)c1c[nH]c2c1cccc2 10.1016/s0960-894x(01)00693-x
656665 3808 49 None -45 6 Guinea pig 6.9 pKi = 6.9 Binding
Binding affinity towards 5-hydroxytryptamine 4 receptor in striatum membranes of guinea-pig brain was evaluatedBinding affinity towards 5-hydroxytryptamine 4 receptor in striatum membranes of guinea-pig brain was evaluated
ChEMBL 284 2 1 3 3.0 CN1[C@@H]2CC[C@H]1C[C@H](C2)OC(=O)c1c[nH]c2c1cccc2 10.1016/s0960-894x(01)00693-x
CHEMBL56564 3808 49 None -45 6 Guinea pig 6.9 pKi = 6.9 Binding
Binding affinity towards 5-hydroxytryptamine 4 receptor in striatum membranes of guinea-pig brain was evaluatedBinding affinity towards 5-hydroxytryptamine 4 receptor in striatum membranes of guinea-pig brain was evaluated
ChEMBL 284 2 1 3 3.0 CN1[C@@H]2CC[C@H]1C[C@H](C2)OC(=O)c1c[nH]c2c1cccc2 10.1016/s0960-894x(01)00693-x
DB11699 3808 49 None -45 6 Guinea pig 6.9 pKi = 6.9 Binding
Binding affinity towards 5-hydroxytryptamine 4 receptor in striatum membranes of guinea-pig brain was evaluatedBinding affinity towards 5-hydroxytryptamine 4 receptor in striatum membranes of guinea-pig brain was evaluated
ChEMBL 284 2 1 3 3.0 CN1[C@@H]2CC[C@H]1C[C@H](C2)OC(=O)c1c[nH]c2c1cccc2 10.1016/s0960-894x(01)00693-x
240 931 39 None -11 25 Human 6.9 pKi = 6.9 Binding
Binding affinity to serotonin 5-HT4 receptor (unknown origin)Binding affinity to serotonin 5-HT4 receptor (unknown origin)
ChEMBL 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N 10.1016/j.bmcl.2013.05.018
2769 931 39 None -11 25 Human 6.9 pKi = 6.9 Binding
Binding affinity to serotonin 5-HT4 receptor (unknown origin)Binding affinity to serotonin 5-HT4 receptor (unknown origin)
ChEMBL 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N 10.1016/j.bmcl.2013.05.018
44279790 931 39 None -11 25 Human 6.9 pKi = 6.9 Binding
Binding affinity to serotonin 5-HT4 receptor (unknown origin)Binding affinity to serotonin 5-HT4 receptor (unknown origin)
ChEMBL 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N 10.1016/j.bmcl.2013.05.018
660 931 39 None -11 25 Human 6.9 pKi = 6.9 Binding
Binding affinity to serotonin 5-HT4 receptor (unknown origin)Binding affinity to serotonin 5-HT4 receptor (unknown origin)
ChEMBL 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N 10.1016/j.bmcl.2013.05.018
CHEMBL1729 931 39 None -11 25 Human 6.9 pKi = 6.9 Binding
Binding affinity to serotonin 5-HT4 receptor (unknown origin)Binding affinity to serotonin 5-HT4 receptor (unknown origin)
ChEMBL 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N 10.1016/j.bmcl.2013.05.018
CHEMBL560739 931 39 None -11 25 Human 6.9 pKi = 6.9 Binding
Binding affinity to serotonin 5-HT4 receptor (unknown origin)Binding affinity to serotonin 5-HT4 receptor (unknown origin)
ChEMBL 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N 10.1016/j.bmcl.2013.05.018
DB00604 931 39 None -11 25 Human 6.9 pKi = 6.9 Binding
Binding affinity to serotonin 5-HT4 receptor (unknown origin)Binding affinity to serotonin 5-HT4 receptor (unknown origin)
ChEMBL 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N 10.1016/j.bmcl.2013.05.018
44629348 84160 0 None -1 2 Human 6.9 pKi = 6.9 Binding
Displacement of [3H](1-(2-(methylsulfonamido)ethyl)piperidin-4-yl)methyl 1-methyl-1H-indole-3-carboxylate from human 5HT4R expressed in HEK293 cellsDisplacement of [3H](1-(2-(methylsulfonamido)ethyl)piperidin-4-yl)methyl 1-methyl-1H-indole-3-carboxylate from human 5HT4R expressed in HEK293 cells
ChEMBL 427 7 0 4 6.1 CC(C)n1cc2c(OCC3CCN(CCc4ccccc4)CC3)nc3ccccc3c2c1 10.1021/jm300573d
CHEMBL2179677 84160 0 None -1 2 Human 6.9 pKi = 6.9 Binding
Displacement of [3H](1-(2-(methylsulfonamido)ethyl)piperidin-4-yl)methyl 1-methyl-1H-indole-3-carboxylate from human 5HT4R expressed in HEK293 cellsDisplacement of [3H](1-(2-(methylsulfonamido)ethyl)piperidin-4-yl)methyl 1-methyl-1H-indole-3-carboxylate from human 5HT4R expressed in HEK293 cells
ChEMBL 427 7 0 4 6.1 CC(C)n1cc2c(OCC3CCN(CCc4ccccc4)CC3)nc3ccccc3c2c1 10.1021/jm300573d
CHEMBL2220955 84160 0 None -1 2 Human 6.9 pKi = 6.9 Binding
Displacement of [3H](1-(2-(methylsulfonamido)ethyl)piperidin-4-yl)methyl 1-methyl-1H-indole-3-carboxylate from human 5HT4R expressed in HEK293 cellsDisplacement of [3H](1-(2-(methylsulfonamido)ethyl)piperidin-4-yl)methyl 1-methyl-1H-indole-3-carboxylate from human 5HT4R expressed in HEK293 cells
ChEMBL 427 7 0 4 6.1 CC(C)n1cc2c(OCC3CCN(CCc4ccccc4)CC3)nc3ccccc3c2c1 10.1021/jm300573d
44249315 193505 0 None - 1 Human 6.9 pKi = 6.9 Binding
Displacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 331 4 2 6 0.8 CC(C)n1c(=O)n(C(=O)NCCN2CCNCC2)c2ccccc21 10.1021/jm900881j
CHEMBL550459 193505 0 None - 1 Human 6.9 pKi = 6.9 Binding
Displacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 331 4 2 6 0.8 CC(C)n1c(=O)n(C(=O)NCCN2CCNCC2)c2ccccc21 10.1021/jm900881j
44248066 193516 0 None - 1 Human 6.9 pKi = 6.9 Binding
Displacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 473 7 2 7 0.7 COc1cc(N)c(Cl)cc1C(=O)NC1CCN(CCN2CCN(S(C)(=O)=O)CC2)CC1 10.1021/jm900881j
CHEMBL550530 193516 0 None - 1 Human 6.9 pKi = 6.9 Binding
Displacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 473 7 2 7 0.7 COc1cc(N)c(Cl)cc1C(=O)NC1CCN(CCN2CCN(S(C)(=O)=O)CC2)CC1 10.1021/jm900881j
44249055 91900481 193748 0 None - 1 Human 6.9 pKi = 6.9 Binding
Displacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 367 4 1 4 3.3 CCN1[C@H]2CC[C@@H]1C[C@H](NC(=O)c1cc3ccccc3n(C(C)C)c1=O)C2 10.1021/jm900881j
CHEMBL552218 193748 0 None - 1 Human 6.9 pKi = 6.9 Binding
Displacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 367 4 1 4 3.3 CCN1[C@H]2CC[C@@H]1C[C@H](NC(=O)c1cc3ccccc3n(C(C)C)c1=O)C2 10.1021/jm900881j
10643698 193781 0 None - 1 Human 6.9 pKi = 6.9 Binding
Displacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 383 5 2 5 2.3 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CCO)cc2ccccc21 10.1021/jm900881j
CHEMBL552420 193781 0 None - 1 Human 6.9 pKi = 6.9 Binding
Displacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 383 5 2 5 2.3 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CCO)cc2ccccc21 10.1021/jm900881j
3233 3456 40 None -933 12 Human 5.9 pKi = 5.9 Binding
Binding affinity towards 5-hydroxytryptamine 4 receptorBinding affinity towards 5-hydroxytryptamine 4 receptor
ChEMBL 352 5 1 4 2.7 CC1CCN(CC1)CC[C@H]1CCCN1S(=O)(=O)c1cccc(c1)O 10.1021/jm991151j
3247 3456 40 None -933 12 Human 5.9 pKi = 5.9 Binding
Binding affinity towards 5-hydroxytryptamine 4 receptorBinding affinity towards 5-hydroxytryptamine 4 receptor
ChEMBL 352 5 1 4 2.7 CC1CCN(CC1)CC[C@H]1CCCN1S(=O)(=O)c1cccc(c1)O 10.1021/jm991151j
6604889 3456 40 None -933 12 Human 5.9 pKi = 5.9 Binding
Binding affinity towards 5-hydroxytryptamine 4 receptorBinding affinity towards 5-hydroxytryptamine 4 receptor
ChEMBL 352 5 1 4 2.7 CC1CCN(CC1)CC[C@H]1CCCN1S(=O)(=O)c1cccc(c1)O 10.1021/jm991151j
CHEMBL282199 3456 40 None -933 12 Human 5.9 pKi = 5.9 Binding
Binding affinity towards 5-hydroxytryptamine 4 receptorBinding affinity towards 5-hydroxytryptamine 4 receptor
ChEMBL 352 5 1 4 2.7 CC1CCN(CC1)CC[C@H]1CCCN1S(=O)(=O)c1cccc(c1)O 10.1021/jm991151j
DB13988 3456 40 None -933 12 Human 5.9 pKi = 5.9 Binding
Binding affinity towards 5-hydroxytryptamine 4 receptorBinding affinity towards 5-hydroxytryptamine 4 receptor
ChEMBL 352 5 1 4 2.7 CC1CCN(CC1)CC[C@H]1CCCN1S(=O)(=O)c1cccc(c1)O 10.1021/jm991151j
44249179 193155 1 None - 1 Human 5.9 pKi = 5.9 Binding
Displacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 312 5 3 5 0.6 COc1cc(N)c(Cl)cc1C(=O)NCCN1CCNCC1 10.1021/jm900881j
CHEMBL539212 193155 1 None - 1 Human 5.9 pKi = 5.9 Binding
Displacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 312 5 3 5 0.6 COc1cc(N)c(Cl)cc1C(=O)NCCN1CCNCC1 10.1021/jm900881j
3157 1442 69 None -27 12 Guinea pig 6.9 pKi = 6.9 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
ChEMBL 451 4 2 8 1.5 COc1cc2nc([nH]c(=N)c2cc1OC)N1CCN(CC1)C(=O)C1COc2c(O1)cccc2 nan
7170 1442 69 None -27 12 Guinea pig 6.9 pKi = 6.9 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
ChEMBL 451 4 2 8 1.5 COc1cc2nc([nH]c(=N)c2cc1OC)N1CCN(CC1)C(=O)C1COc2c(O1)cccc2 nan
954 1442 69 None -27 12 Guinea pig 6.9 pKi = 6.9 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
ChEMBL 451 4 2 8 1.5 COc1cc2nc([nH]c(=N)c2cc1OC)N1CCN(CC1)C(=O)C1COc2c(O1)cccc2 nan
CHEMBL707 1442 69 None -27 12 Guinea pig 6.9 pKi = 6.9 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
ChEMBL 451 4 2 8 1.5 COc1cc2nc([nH]c(=N)c2cc1OC)N1CCN(CC1)C(=O)C1COc2c(O1)cccc2 nan
DB00590 1442 69 None -27 12 Guinea pig 6.9 pKi = 6.9 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
ChEMBL 451 4 2 8 1.5 COc1cc2nc([nH]c(=N)c2cc1OC)N1CCN(CC1)C(=O)C1COc2c(O1)cccc2 nan
49845575 19163 0 None - 1 Guinea pig 6.9 pKi = 6.9 Binding
Displacement of [3H]GR113808 from 5HT4 receptor in guinea pig striatal membranesDisplacement of [3H]GR113808 from 5HT4 receptor in guinea pig striatal membranes
ChEMBL 467 5 0 5 4.9 Cc1csc2nc(OCC3CCN(C/C=C/I)CC3)c3cccn3c12 10.1016/j.ejmech.2010.07.052
CHEMBL1290805 19163 0 None - 1 Guinea pig 6.9 pKi = 6.9 Binding
Displacement of [3H]GR113808 from 5HT4 receptor in guinea pig striatal membranesDisplacement of [3H]GR113808 from 5HT4 receptor in guinea pig striatal membranes
ChEMBL 467 5 0 5 4.9 Cc1csc2nc(OCC3CCN(C/C=C/I)CC3)c3cccn3c12 10.1016/j.ejmech.2010.07.052
11577105 71820 0 None - 1 Human 7.9 pKi = 7.9 Binding
Binding affinity for 5-HT4 receptor using [3H]GR-113808Binding affinity for 5-HT4 receptor using [3H]GR-113808
ChEMBL 510 16 3 7 4.1 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCC(NC(=O)CCCCCCCCCCN)CC1 10.1021/jm050234z
CHEMBL197965 71820 0 None - 1 Human 7.9 pKi = 7.9 Binding
Binding affinity for 5-HT4 receptor using [3H]GR-113808Binding affinity for 5-HT4 receptor using [3H]GR-113808
ChEMBL 510 16 3 7 4.1 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCC(NC(=O)CCCCCCCCCCN)CC1 10.1021/jm050234z
11593090 71850 0 None - 1 Human 7.9 pKi = 7.9 Binding
Binding affinity for 5-HT4 receptor using [3H]GR-113808Binding affinity for 5-HT4 receptor using [3H]GR-113808
ChEMBL 834 22 4 12 5.6 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCC(CCNC(=O)CCCCCC(=O)NCCC2CCN(CCOC(=O)c3cc(Cl)c(N)cc3OC)CC2)CC1 10.1021/jm050234z
CHEMBL198052 71850 0 None - 1 Human 7.9 pKi = 7.9 Binding
Binding affinity for 5-HT4 receptor using [3H]GR-113808Binding affinity for 5-HT4 receptor using [3H]GR-113808
ChEMBL 834 22 4 12 5.6 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCC(CCNC(=O)CCCCCC(=O)NCCC2CCN(CCOC(=O)c3cc(Cl)c(N)cc3OC)CC2)CC1 10.1021/jm050234z
44404964 72127 0 None - 1 Human 7.9 pKi = 7.9 Binding
Binding affinity for 5-HT4 receptor using [3H]GR-113808Binding affinity for 5-HT4 receptor using [3H]GR-113808
ChEMBL 736 15 5 12 2.9 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCC(C(=O)NCCCNC(=O)C2CCN(CCOC(=O)c3cc(Cl)c(N)cc3O)CC2)CC1 10.1021/jm050234z
CHEMBL198921 72127 0 None - 1 Human 7.9 pKi = 7.9 Binding
Binding affinity for 5-HT4 receptor using [3H]GR-113808Binding affinity for 5-HT4 receptor using [3H]GR-113808
ChEMBL 736 15 5 12 2.9 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCC(C(=O)NCCCNC(=O)C2CCN(CCOC(=O)c3cc(Cl)c(N)cc3O)CC2)CC1 10.1021/jm050234z
130946 201070 2 None - 1 Human 7.9 pKi = 7.9 Binding
Binding affinity to 5HT4 receptorBinding affinity to 5HT4 receptor
ChEMBL 328 2 1 5 2.0 CCn1c(=O)n(C(=O)NC2CC3CCC(C2)N3C)c2ccccc21 10.1016/j.bmc.2008.12.025
CHEMBL62023 201070 2 None - 1 Human 7.9 pKi = 7.9 Binding
Binding affinity to 5HT4 receptorBinding affinity to 5HT4 receptor
ChEMBL 328 2 1 5 2.0 CCn1c(=O)n(C(=O)NC2CC3CCC(C2)N3C)c2ccccc21 10.1016/j.bmc.2008.12.025
145955141 162140 0 None - 1 Guinea pig 7.9 pKi = 7.9 Binding
Displacement of [3H]GR113808 from serotonin 5-HT4 receptor in Dunkin-Hartley guinea pigs striatal nuclei membranes incubated for 2 hrs by liquid scintillation countingDisplacement of [3H]GR113808 from serotonin 5-HT4 receptor in Dunkin-Hartley guinea pigs striatal nuclei membranes incubated for 2 hrs by liquid scintillation counting
ChEMBL 426 9 3 6 2.7 CCCCNC(=O)NC1CCN(CCOC(=O)c2cc(Cl)c(N)cc2OC)CC1 10.1039/C6MD00458J
CHEMBL4170461 162140 0 None - 1 Guinea pig 7.9 pKi = 7.9 Binding
Displacement of [3H]GR113808 from serotonin 5-HT4 receptor in Dunkin-Hartley guinea pigs striatal nuclei membranes incubated for 2 hrs by liquid scintillation countingDisplacement of [3H]GR113808 from serotonin 5-HT4 receptor in Dunkin-Hartley guinea pigs striatal nuclei membranes incubated for 2 hrs by liquid scintillation counting
ChEMBL 426 9 3 6 2.7 CCCCNC(=O)NC1CCN(CCOC(=O)c2cc(Cl)c(N)cc2OC)CC1 10.1039/C6MD00458J
9858485 122615 0 None - 1 Guinea pig 7.9 pKi = 7.9 Binding
Ability to displace [3H]GR-113808 from 5-hydroxytryptamine 4 receptorAbility to displace [3H]GR-113808 from 5-hydroxytryptamine 4 receptor
ChEMBL 325 4 1 4 3.7 CCN1CCC(COc2nc3ccccc3c3c2CCCN3)CC1 10.1021/jm020954v
CHEMBL36120 122615 0 None - 1 Guinea pig 7.9 pKi = 7.9 Binding
Ability to displace [3H]GR-113808 from 5-hydroxytryptamine 4 receptorAbility to displace [3H]GR-113808 from 5-hydroxytryptamine 4 receptor
ChEMBL 325 4 1 4 3.7 CCN1CCC(COc2nc3ccccc3c3c2CCCN3)CC1 10.1021/jm020954v
71462777 82552 0 None -1 4 Guinea pig 7.9 pKi = 7.9 Binding
Displacement of [3H]GR113808 from 5HT4R in guinea pig striatal membranesDisplacement of [3H]GR113808 from 5HT4R in guinea pig striatal membranes
ChEMBL 335 5 0 4 4.3 CCCN1CCC(COc2nc3ccccc3c3ncccc23)CC1 10.1021/jm300943r
CHEMBL2181171 82552 0 None -1 4 Guinea pig 7.9 pKi = 7.9 Binding
Displacement of [3H]GR113808 from 5HT4R in guinea pig striatal membranesDisplacement of [3H]GR113808 from 5HT4R in guinea pig striatal membranes
ChEMBL 335 5 0 4 4.3 CCCN1CCC(COc2nc3ccccc3c3ncccc23)CC1 10.1021/jm300943r
10045643 206344 0 None - 1 Guinea pig 7.9 pKi = 7.9 Binding
Binding affinity against 5-hydroxytryptamine 4 receptor in guinea pig striatum using [3H]GR-113808 as radioligandBinding affinity against 5-hydroxytryptamine 4 receptor in guinea pig striatum using [3H]GR-113808 as radioligand
ChEMBL 385 7 1 6 2.1 CCCCN1CCN(CCNC(=O)n2c(=O)n(C3CC3)c3ccccc32)CC1 10.1021/jm981098j
CHEMBL97755 206344 0 None - 1 Guinea pig 7.9 pKi = 7.9 Binding
Binding affinity against 5-hydroxytryptamine 4 receptor in guinea pig striatum using [3H]GR-113808 as radioligandBinding affinity against 5-hydroxytryptamine 4 receptor in guinea pig striatum using [3H]GR-113808 as radioligand
ChEMBL 385 7 1 6 2.1 CCCCN1CCN(CCNC(=O)n2c(=O)n(C3CC3)c3ccccc32)CC1 10.1021/jm981098j
71462776 82550 0 None -11 7 Guinea pig 7.9 pKi = 7.9 Binding
Displacement of [3H]GR113808 from 5HT4R in guinea pig striatal membranesDisplacement of [3H]GR113808 from 5HT4R in guinea pig striatal membranes
ChEMBL 460 5 0 3 5.5 CCCN1CCC(COc2nc3c(I)cccc3c3ccccc23)CC1 10.1021/jm300943r
CHEMBL2181169 82550 0 None -11 7 Guinea pig 7.9 pKi = 7.9 Binding
Displacement of [3H]GR113808 from 5HT4R in guinea pig striatal membranesDisplacement of [3H]GR113808 from 5HT4R in guinea pig striatal membranes
ChEMBL 460 5 0 3 5.5 CCCN1CCC(COc2nc3c(I)cccc3c3ccccc23)CC1 10.1021/jm300943r
9839847 206505 0 None - 1 Rat 7.9 pKi = 7.9 Binding
Binding affinity to 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatum membraneBinding affinity to 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatum membrane
ChEMBL 314 6 2 3 2.8 CCCCN1CCC(CNC(=O)c2cccc3[nH]cnc23)CC1 10.1021/jm020807x
CHEMBL98734 206505 0 None - 1 Rat 7.9 pKi = 7.9 Binding
Binding affinity to 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatum membraneBinding affinity to 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatum membrane
ChEMBL 314 6 2 3 2.8 CCCCN1CCC(CNC(=O)c2cccc3[nH]cnc23)CC1 10.1021/jm020807x
9839847 206505 0 None - 1 Rat 7.9 pKi = 7.9 Binding
Displacement of [3H]GR113808 from 5-HT4 receptor in rat striatal membranes after 30 mins by liquid scintillation spectrometric analysisDisplacement of [3H]GR113808 from 5-HT4 receptor in rat striatal membranes after 30 mins by liquid scintillation spectrometric analysis
ChEMBL 314 6 2 3 2.8 CCCCN1CCC(CNC(=O)c2cccc3[nH]cnc23)CC1 10.1039/C0MD00258E
CHEMBL98734 206505 0 None - 1 Rat 7.9 pKi = 7.9 Binding
Displacement of [3H]GR113808 from 5-HT4 receptor in rat striatal membranes after 30 mins by liquid scintillation spectrometric analysisDisplacement of [3H]GR113808 from 5-HT4 receptor in rat striatal membranes after 30 mins by liquid scintillation spectrometric analysis
ChEMBL 314 6 2 3 2.8 CCCCN1CCC(CNC(=O)c2cccc3[nH]cnc23)CC1 10.1039/C0MD00258E
9839847 206505 0 None - 1 Rat 7.9 pKi = 7.9 Binding
In vitro binding affinity to 5-hydroxytryptamine 4 receptor in rat striatum membraneIn vitro binding affinity to 5-hydroxytryptamine 4 receptor in rat striatum membrane
ChEMBL 314 6 2 3 2.8 CCCCN1CCC(CNC(=O)c2cccc3[nH]cnc23)CC1 10.1016/s0960-894x(01)00517-0
CHEMBL98734 206505 0 None - 1 Rat 7.9 pKi = 7.9 Binding
In vitro binding affinity to 5-hydroxytryptamine 4 receptor in rat striatum membraneIn vitro binding affinity to 5-hydroxytryptamine 4 receptor in rat striatum membrane
ChEMBL 314 6 2 3 2.8 CCCCN1CCC(CNC(=O)c2cccc3[nH]cnc23)CC1 10.1016/s0960-894x(01)00517-0
9839847 206505 0 None - 1 Rat 7.9 pKi = 7.9 Binding
pKi against 5-hydroxytryptamine 4 receptor in rat striatum membranepKi against 5-hydroxytryptamine 4 receptor in rat striatum membrane
ChEMBL 314 6 2 3 2.8 CCCCN1CCC(CNC(=O)c2cccc3[nH]cnc23)CC1 10.1016/s0960-894x(01)00517-0
CHEMBL98734 206505 0 None - 1 Rat 7.9 pKi = 7.9 Binding
pKi against 5-hydroxytryptamine 4 receptor in rat striatum membranepKi against 5-hydroxytryptamine 4 receptor in rat striatum membrane
ChEMBL 314 6 2 3 2.8 CCCCN1CCC(CNC(=O)c2cccc3[nH]cnc23)CC1 10.1016/s0960-894x(01)00517-0
6604914 99919 2 None 1 2 Rat 6.9 pKi = 6.9 Binding
Binding affinity at 5-hydroxytryptamine 4 receptor in rat striatum by [3H]GR-113808 displacement.Binding affinity at 5-hydroxytryptamine 4 receptor in rat striatum by [3H]GR-113808 displacement.
ChEMBL 309 3 2 4 1.8 COc1cc(N)c(Cl)cc1C(=O)N[C@@H]1CN2CCC1CC2 10.1016/0960-894X(96)00002-9
CHEMBL28992 99919 2 None 1 2 Rat 6.9 pKi = 6.9 Binding
Binding affinity at 5-hydroxytryptamine 4 receptor in rat striatum by [3H]GR-113808 displacement.Binding affinity at 5-hydroxytryptamine 4 receptor in rat striatum by [3H]GR-113808 displacement.
ChEMBL 309 3 2 4 1.8 COc1cc(N)c(Cl)cc1C(=O)N[C@@H]1CN2CCC1CC2 10.1016/0960-894X(96)00002-9
151537 162114 43 None - 1 Guinea pig 5.9 pKi = 5.9 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
ChEMBL 543 5 6 12 0.0 COc1cccc2c1C(=O)c1c(O)c3c(c(O)c1C2=O)C[C@@](O)(C(=O)CO)C[C@@H]3O[C@H]1C[C@H](N)[C@@H](O)[C@H](C)O1 nan
41867 162114 43 None - 1 Guinea pig 5.9 pKi = 5.9 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
ChEMBL 543 5 6 12 0.0 COc1cccc2c1C(=O)c1c(O)c3c(c(O)c1C2=O)C[C@@](O)(C(=O)CO)C[C@@H]3O[C@H]1C[C@H](N)[C@@H](O)[C@H](C)O1 nan
CHEMBL417 162114 43 None - 1 Guinea pig 5.9 pKi = 5.9 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
ChEMBL 543 5 6 12 0.0 COc1cccc2c1C(=O)c1c(O)c3c(c(O)c1C2=O)C[C@@](O)(C(=O)CO)C[C@@H]3O[C@H]1C[C@H](N)[C@@H](O)[C@H](C)O1 nan
5991 202221 68 None 2 5 Guinea pig 5.9 pKi = 5.9 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
ChEMBL 296 0 2 2 3.6 C#C[C@]1(O)CC[C@H]2[C@@H]3CCc4cc(O)ccc4[C@H]3CC[C@@]21C nan
CHEMBL691 202221 68 None 2 5 Guinea pig 5.9 pKi = 5.9 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
ChEMBL 296 0 2 2 3.6 C#C[C@]1(O)CC[C@H]2[C@@H]3CCc4cc(O)ccc4[C@H]3CC[C@@]21C nan
203435 163552 2 None - 1 Rat 6.9 pKi = 6.9 Binding
Binding affinity towards 5-hydroxytryptamine 4 receptor was determined in rat striatal membranes using [3H]GR-113808 as radioligandBinding affinity towards 5-hydroxytryptamine 4 receptor was determined in rat striatal membranes using [3H]GR-113808 as radioligand
ChEMBL 311 5 2 4 2.1 COc1cc(N)c(Cl)cc1C(=O)NCCN1CCCCC1 10.1021/jm960320m
CHEMBL420969 163552 2 None - 1 Rat 6.9 pKi = 6.9 Binding
Binding affinity towards 5-hydroxytryptamine 4 receptor was determined in rat striatal membranes using [3H]GR-113808 as radioligandBinding affinity towards 5-hydroxytryptamine 4 receptor was determined in rat striatal membranes using [3H]GR-113808 as radioligand
ChEMBL 311 5 2 4 2.1 COc1cc(N)c(Cl)cc1C(=O)NCCN1CCCCC1 10.1021/jm960320m
44404968 72010 0 None - 1 Human 7.9 pKi = 7.9 Binding
Binding affinity for 5-HT4 receptor using [3H]GR-113808Binding affinity for 5-HT4 receptor using [3H]GR-113808
ChEMBL 711 20 3 8 6.4 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCC(NC(=O)CCCCCCCCCCC(=O)NC2CCN(Cc3ccccc3)CC2)CC1 10.1021/jm050234z
CHEMBL198504 72010 0 None - 1 Human 7.9 pKi = 7.9 Binding
Binding affinity for 5-HT4 receptor using [3H]GR-113808Binding affinity for 5-HT4 receptor using [3H]GR-113808
ChEMBL 711 20 3 8 6.4 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCC(NC(=O)CCCCCCCCCCC(=O)NC2CCN(Cc3ccccc3)CC2)CC1 10.1021/jm050234z
42618250 168894 0 None - 1 Human 7.9 pKi = 7.9 Binding
Displacement of [3H]GR-113808 from human 5HT4 isoform E receptor expressed in rat C6 cells by liquid scintillation countingDisplacement of [3H]GR-113808 from human 5HT4 isoform E receptor expressed in rat C6 cells by liquid scintillation counting
ChEMBL 982 28 6 14 5.7 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCC(NC(=O)CCCNCCCc2ccc(CCCNCCCC(=O)NC3CCN(CCOC(=O)c4cc(Cl)c(N)cc4OC)CC3)cc2)CC1 10.1021/jm801327q
CHEMBL442869 168894 0 None - 1 Human 7.9 pKi = 7.9 Binding
Displacement of [3H]GR-113808 from human 5HT4 isoform E receptor expressed in rat C6 cells by liquid scintillation countingDisplacement of [3H]GR-113808 from human 5HT4 isoform E receptor expressed in rat C6 cells by liquid scintillation counting
ChEMBL 982 28 6 14 5.7 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCC(NC(=O)CCCNCCCc2ccc(CCCNCCCC(=O)NC3CCN(CCOC(=O)c4cc(Cl)c(N)cc4OC)CC3)cc2)CC1 10.1021/jm801327q
72698085 103509 0 None - 1 Guinea pig 7.9 pKi = 7.9 Binding
Displacement of [3H]GR113808 from 5HT4R in guinea pig striatal membranesDisplacement of [3H]GR113808 from 5HT4R in guinea pig striatal membranes
ChEMBL 420 6 0 3 6.0 Fc1cccc2c1nc(OCC1CCN(CCCC(F)(F)F)CC1)c1ccccc12 10.1016/j.bmc.2013.08.061
CHEMBL3093184 103509 0 None - 1 Guinea pig 7.9 pKi = 7.9 Binding
Displacement of [3H]GR113808 from 5HT4R in guinea pig striatal membranesDisplacement of [3H]GR113808 from 5HT4R in guinea pig striatal membranes
ChEMBL 420 6 0 3 6.0 Fc1cccc2c1nc(OCC1CCN(CCCC(F)(F)F)CC1)c1ccccc12 10.1016/j.bmc.2013.08.061
10408029 16283 0 None - 1 Human 7.8 pKi = 7.8 Binding
Binding affinity was determined against cloned 5-hydroxytryptamine 4E receptor isoform expressed in C6 glial cells incubated with 0.2 nM [3H]GR-113808Binding affinity was determined against cloned 5-hydroxytryptamine 4E receptor isoform expressed in C6 glial cells incubated with 0.2 nM [3H]GR-113808
ChEMBL 389 6 1 6 2.9 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCN(c2ccccc2)CC1 10.1021/jm0009538
CHEMBL123377 16283 0 None - 1 Human 7.8 pKi = 7.8 Binding
Binding affinity was determined against cloned 5-hydroxytryptamine 4E receptor isoform expressed in C6 glial cells incubated with 0.2 nM [3H]GR-113808Binding affinity was determined against cloned 5-hydroxytryptamine 4E receptor isoform expressed in C6 glial cells incubated with 0.2 nM [3H]GR-113808
ChEMBL 389 6 1 6 2.9 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCN(c2ccccc2)CC1 10.1021/jm0009538
118734516 118168 0 None - 1 Guinea pig 7.8 pKi = 7.8 Binding
Displacement of [3H]GR113808 from 5-HT4R in guinea pig brain membranes incubated for 30 mins by radioligand binding assayDisplacement of [3H]GR113808 from 5-HT4R in guinea pig brain membranes incubated for 30 mins by radioligand binding assay
ChEMBL 386 7 1 4 4.8 COc1cc(N)c(Cl)cc1C(=O)CCC1CCN(Cc2ccccc2)CC1 10.1021/acs.jmedchem.5b00115
CHEMBL3417001 118168 0 None - 1 Guinea pig 7.8 pKi = 7.8 Binding
Displacement of [3H]GR113808 from 5-HT4R in guinea pig brain membranes incubated for 30 mins by radioligand binding assayDisplacement of [3H]GR113808 from 5-HT4R in guinea pig brain membranes incubated for 30 mins by radioligand binding assay
ChEMBL 386 7 1 4 4.8 COc1cc(N)c(Cl)cc1C(=O)CCC1CCN(Cc2ccccc2)CC1 10.1021/acs.jmedchem.5b00115
240 931 39 None -4 25 Guinea pig 7.8 pKi = 7.8 Binding
Inhibition of [3H]GR-113808 binding to guinea pig striatum 5-hydroxytryptamine 4 receptorInhibition of [3H]GR-113808 binding to guinea pig striatum 5-hydroxytryptamine 4 receptor
ChEMBL 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N 10.1021/jm020270n
2769 931 39 None -4 25 Guinea pig 7.8 pKi = 7.8 Binding
Inhibition of [3H]GR-113808 binding to guinea pig striatum 5-hydroxytryptamine 4 receptorInhibition of [3H]GR-113808 binding to guinea pig striatum 5-hydroxytryptamine 4 receptor
ChEMBL 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N 10.1021/jm020270n
44279790 931 39 None -4 25 Guinea pig 7.8 pKi = 7.8 Binding
Inhibition of [3H]GR-113808 binding to guinea pig striatum 5-hydroxytryptamine 4 receptorInhibition of [3H]GR-113808 binding to guinea pig striatum 5-hydroxytryptamine 4 receptor
ChEMBL 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N 10.1021/jm020270n
660 931 39 None -4 25 Guinea pig 7.8 pKi = 7.8 Binding
Inhibition of [3H]GR-113808 binding to guinea pig striatum 5-hydroxytryptamine 4 receptorInhibition of [3H]GR-113808 binding to guinea pig striatum 5-hydroxytryptamine 4 receptor
ChEMBL 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N 10.1021/jm020270n
CHEMBL1729 931 39 None -4 25 Guinea pig 7.8 pKi = 7.8 Binding
Inhibition of [3H]GR-113808 binding to guinea pig striatum 5-hydroxytryptamine 4 receptorInhibition of [3H]GR-113808 binding to guinea pig striatum 5-hydroxytryptamine 4 receptor
ChEMBL 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N 10.1021/jm020270n
CHEMBL560739 931 39 None -4 25 Guinea pig 7.8 pKi = 7.8 Binding
Inhibition of [3H]GR-113808 binding to guinea pig striatum 5-hydroxytryptamine 4 receptorInhibition of [3H]GR-113808 binding to guinea pig striatum 5-hydroxytryptamine 4 receptor
ChEMBL 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N 10.1021/jm020270n
DB00604 931 39 None -4 25 Guinea pig 7.8 pKi = 7.8 Binding
Inhibition of [3H]GR-113808 binding to guinea pig striatum 5-hydroxytryptamine 4 receptorInhibition of [3H]GR-113808 binding to guinea pig striatum 5-hydroxytryptamine 4 receptor
ChEMBL 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N 10.1021/jm020270n
10545215 188395 0 None - 1 Rat 7.8 pKi = 7.8 Binding
Binding affinity (Ki+/-SEM) against 5-hydroxytryptamine 4 receptor from cheng Prusoff equation by using [3H]GR-113808 in rat striatumBinding affinity (Ki+/-SEM) against 5-hydroxytryptamine 4 receptor from cheng Prusoff equation by using [3H]GR-113808 in rat striatum
ChEMBL 341 5 2 5 3.4 COc1cc(N)c(Cl)cc1NC(=O)OCCN1CCCCCC1 10.1021/jm960853v
CHEMBL50852 188395 0 None - 1 Rat 7.8 pKi = 7.8 Binding
Binding affinity (Ki+/-SEM) against 5-hydroxytryptamine 4 receptor from cheng Prusoff equation by using [3H]GR-113808 in rat striatumBinding affinity (Ki+/-SEM) against 5-hydroxytryptamine 4 receptor from cheng Prusoff equation by using [3H]GR-113808 in rat striatum
ChEMBL 341 5 2 5 3.4 COc1cc(N)c(Cl)cc1NC(=O)OCCN1CCCCCC1 10.1021/jm960853v
118734508 117993 0 None - 1 Guinea pig 7.8 pKi = 7.8 Binding
Displacement of [3H]GR113808 from 5-HT4R in guinea pig brain membranes incubated for 30 mins by radioligand binding assayDisplacement of [3H]GR113808 from 5-HT4R in guinea pig brain membranes incubated for 30 mins by radioligand binding assay
ChEMBL 350 7 1 4 4.0 COc1cc(N)c(Cl)cc1C(=O)CCC1CCN(CC2CC2)CC1 10.1021/acs.jmedchem.5b00115
CHEMBL3414597 117993 0 None - 1 Guinea pig 7.8 pKi = 7.8 Binding
Displacement of [3H]GR113808 from 5-HT4R in guinea pig brain membranes incubated for 30 mins by radioligand binding assayDisplacement of [3H]GR113808 from 5-HT4R in guinea pig brain membranes incubated for 30 mins by radioligand binding assay
ChEMBL 350 7 1 4 4.0 COc1cc(N)c(Cl)cc1C(=O)CCC1CCN(CC2CC2)CC1 10.1021/acs.jmedchem.5b00115
42646835 193484 2 None - 1 Human 6.8 pKi = 6.8 Binding
Displacement of [3H]GR-113808 from human 5HT4b receptor expressed in COS7 cell membrane by scintillation countingDisplacement of [3H]GR-113808 from human 5HT4b receptor expressed in COS7 cell membrane by scintillation counting
ChEMBL 261 4 2 4 1.5 COc1ccc2[nH]cc(CNN3CCOCC3)c2c1 10.1016/j.ejmech.2009.01.015
CHEMBL550302 193484 2 None - 1 Human 6.8 pKi = 6.8 Binding
Displacement of [3H]GR-113808 from human 5HT4b receptor expressed in COS7 cell membrane by scintillation countingDisplacement of [3H]GR-113808 from human 5HT4b receptor expressed in COS7 cell membrane by scintillation counting
ChEMBL 261 4 2 4 1.5 COc1ccc2[nH]cc(CNN3CCOCC3)c2c1 10.1016/j.ejmech.2009.01.015
119584 2557 99 None -1 6 Guinea pig 6.8 pKi = 6.8 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
ChEMBL 421 7 2 5 3.1 CCOc1cc(N)c(cc1C(=O)NCC1OCCN(C1)Cc1ccc(cc1)F)Cl nan
1848 2557 99 None -1 6 Guinea pig 6.8 pKi = 6.8 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
ChEMBL 421 7 2 5 3.1 CCOc1cc(N)c(cc1C(=O)NCC1OCCN(C1)Cc1ccc(cc1)F)Cl nan
242 2557 99 None -1 6 Guinea pig 6.8 pKi = 6.8 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
ChEMBL 421 7 2 5 3.1 CCOc1cc(N)c(cc1C(=O)NCC1OCCN(C1)Cc1ccc(cc1)F)Cl nan
CHEMBL60889 2557 99 None -1 6 Guinea pig 6.8 pKi = 6.8 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
ChEMBL 421 7 2 5 3.1 CCOc1cc(N)c(cc1C(=O)NCC1OCCN(C1)Cc1ccc(cc1)F)Cl nan
DB11675 2557 99 None -1 6 Guinea pig 6.8 pKi = 6.8 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
ChEMBL 421 7 2 5 3.1 CCOc1cc(N)c(cc1C(=O)NCC1OCCN(C1)Cc1ccc(cc1)F)Cl nan
145991736 166291 0 None - 1 Guinea pig 6.8 pKi = 6.8 Binding
Displacement of [3H]-GR113808 from 5-HT4R in Dunkin-Hartley guinea pig straitum nuclear membranes after 2 hrs by filter binding methodDisplacement of [3H]-GR113808 from 5-HT4R in Dunkin-Hartley guinea pig straitum nuclear membranes after 2 hrs by filter binding method
ChEMBL 355 7 1 4 3.5 CCCCN1CCC(CNC(=O)c2cc(OC)c3ccccc3n2)CC1 10.1039/C8MD00233A
CHEMBL4285302 166291 0 None - 1 Guinea pig 6.8 pKi = 6.8 Binding
Displacement of [3H]-GR113808 from 5-HT4R in Dunkin-Hartley guinea pig straitum nuclear membranes after 2 hrs by filter binding methodDisplacement of [3H]-GR113808 from 5-HT4R in Dunkin-Hartley guinea pig straitum nuclear membranes after 2 hrs by filter binding method
ChEMBL 355 7 1 4 3.5 CCCCN1CCC(CNC(=O)c2cc(OC)c3ccccc3n2)CC1 10.1039/C8MD00233A
145979545 166174 0 None - 1 Guinea pig 7.8 pKi = 7.8 Binding
Displacement of [3H]-GR113808 from 5-HT4R in Dunkin-Hartley guinea pig straitum nuclear membranes after 2 hrs by filter binding methodDisplacement of [3H]-GR113808 from 5-HT4R in Dunkin-Hartley guinea pig straitum nuclear membranes after 2 hrs by filter binding method
ChEMBL 314 5 0 5 2.9 COc1cc(C(=O)OCCN2CCCCC2)c2ccccc2n1 10.1039/C8MD00233A
CHEMBL4283020 166174 0 None - 1 Guinea pig 7.8 pKi = 7.8 Binding
Displacement of [3H]-GR113808 from 5-HT4R in Dunkin-Hartley guinea pig straitum nuclear membranes after 2 hrs by filter binding methodDisplacement of [3H]-GR113808 from 5-HT4R in Dunkin-Hartley guinea pig straitum nuclear membranes after 2 hrs by filter binding method
ChEMBL 314 5 0 5 2.9 COc1cc(C(=O)OCCN2CCCCC2)c2ccccc2n1 10.1039/C8MD00233A
70695321 77147 0 None - 1 Human 7.8 pKi = 7.8 Binding
Displacement of [3H]GR113808 from human recombinant 5HT4c receptor expressed in HEK293 cellsDisplacement of [3H]GR113808 from human recombinant 5HT4c receptor expressed in HEK293 cells
ChEMBL 455 7 4 6 1.3 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CC(O)CNC(N)=O)cc2ccccc21 10.1016/j.bmcl.2012.08.051
CHEMBL2087326 77147 0 None - 1 Human 7.8 pKi = 7.8 Binding
Displacement of [3H]GR113808 from human recombinant 5HT4c receptor expressed in HEK293 cellsDisplacement of [3H]GR113808 from human recombinant 5HT4c receptor expressed in HEK293 cells
ChEMBL 455 7 4 6 1.3 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CC(O)CNC(N)=O)cc2ccccc21 10.1016/j.bmcl.2012.08.051
44247822 91900495 193843 0 None - 1 Human 7.8 pKi = 7.8 Binding
Displacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 571 10 1 7 3.1 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CCCCCN2CCN(S(C)(=O)=O)CC2)cc2ccccc21 10.1021/jm900881j
CHEMBL553685 193843 0 None - 1 Human 7.8 pKi = 7.8 Binding
Displacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 571 10 1 7 3.1 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CCCCCN2CCN(S(C)(=O)=O)CC2)cc2ccccc21 10.1021/jm900881j
44248434 91900496 193966 0 None - 1 Human 7.8 pKi = 7.8 Binding
Displacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 613 13 1 7 4.2 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CCCCCCCCN2CCN(S(C)(=O)=O)CC2)cc2ccccc21 10.1021/jm900881j
CHEMBL556326 193966 0 None - 1 Human 7.8 pKi = 7.8 Binding
Displacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 613 13 1 7 4.2 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CCCCCCCCN2CCN(S(C)(=O)=O)CC2)cc2ccccc21 10.1021/jm900881j
44248070 194151 0 None - 1 Human 7.8 pKi = 7.8 Binding
Displacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 557 13 2 7 3.0 COc1cc(N)c(Cl)cc1C(=O)NC1CCN(CCCCCCCCN2CCN(S(C)(=O)=O)CC2)CC1 10.1021/jm900881j
CHEMBL558261 194151 0 None - 1 Human 7.8 pKi = 7.8 Binding
Displacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 557 13 2 7 3.0 COc1cc(N)c(Cl)cc1C(=O)NC1CCN(CCCCCCCCN2CCN(S(C)(=O)=O)CC2)CC1 10.1021/jm900881j
44248552 91900486 194245 0 None - 1 Human 7.8 pKi = 7.8 Binding
Displacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 554 9 1 6 4.8 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CCCCCN2C(=O)c3ccccc3C2=O)cc2ccccc21 10.1021/jm900881j
CHEMBL559317 194245 0 None - 1 Human 7.8 pKi = 7.8 Binding
Displacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 554 9 1 6 4.8 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CCCCCN2C(=O)c3ccccc3C2=O)cc2ccccc21 10.1021/jm900881j
10615288 186426 0 None - 1 Rat 6.8 pKi = 6.8 Binding
Binding affinity (Ki+/-SEM) against 5-hydroxytryptamine 4 receptor from cheng Prusoff equation by using [3H]GR-113808 in rat striatumBinding affinity (Ki+/-SEM) against 5-hydroxytryptamine 4 receptor from cheng Prusoff equation by using [3H]GR-113808 in rat striatum
ChEMBL 315 7 2 5 2.8 CCN(CC)CCOC(=O)Nc1cc(Cl)c(N)cc1OC 10.1021/jm960853v
CHEMBL49072 186426 0 None - 1 Rat 6.8 pKi = 6.8 Binding
Binding affinity (Ki+/-SEM) against 5-hydroxytryptamine 4 receptor from cheng Prusoff equation by using [3H]GR-113808 in rat striatumBinding affinity (Ki+/-SEM) against 5-hydroxytryptamine 4 receptor from cheng Prusoff equation by using [3H]GR-113808 in rat striatum
ChEMBL 315 7 2 5 2.8 CCN(CC)CCOC(=O)Nc1cc(Cl)c(N)cc1OC 10.1021/jm960853v
134828069 172730 0 None - 1 Human 6.8 pKi = 6.8 Binding
Displacement of [3H]-GR113808 from recombinant human 5-HT4BR expressed in membranes after 60 minsDisplacement of [3H]-GR113808 from recombinant human 5-HT4BR expressed in membranes after 60 mins
ChEMBL 410 7 1 3 5.7 COc1c(C(=O)CCC2CCN(Cc3ccccc3)CC2)cc(Cl)c2[nH]ccc12 10.1016/j.ejmech.2018.10.064
CHEMBL4526050 172730 0 None - 1 Human 6.8 pKi = 6.8 Binding
Displacement of [3H]-GR113808 from recombinant human 5-HT4BR expressed in membranes after 60 minsDisplacement of [3H]-GR113808 from recombinant human 5-HT4BR expressed in membranes after 60 mins
ChEMBL 410 7 1 3 5.7 COc1c(C(=O)CCC2CCN(Cc3ccccc3)CC2)cc(Cl)c2[nH]ccc12 10.1016/j.ejmech.2018.10.064
9819593 98348 2 None 1 2 Rat 5.8 pKi = 5.8 Binding
Binding affinity towards 5-hydroxytryptamine 4 receptor was determined in rat striatal membranes using [3H]GR-113808 as radioligandBinding affinity towards 5-hydroxytryptamine 4 receptor was determined in rat striatal membranes using [3H]GR-113808 as radioligand
ChEMBL 309 3 2 4 1.8 COc1cc(N)c(Cl)cc1C(=O)N[C@H]1CN2CCC1CC2 10.1021/jm960320m
CHEMBL27846 98348 2 None 1 2 Rat 5.8 pKi = 5.8 Binding
Binding affinity towards 5-hydroxytryptamine 4 receptor was determined in rat striatal membranes using [3H]GR-113808 as radioligandBinding affinity towards 5-hydroxytryptamine 4 receptor was determined in rat striatal membranes using [3H]GR-113808 as radioligand
ChEMBL 309 3 2 4 1.8 COc1cc(N)c(Cl)cc1C(=O)N[C@H]1CN2CCC1CC2 10.1021/jm960320m
71461046 82555 0 None - 1 Guinea pig 6.8 pKi = 6.8 Binding
Displacement of [3H]GR113808 from 5HT4R in guinea pig striatal membranesDisplacement of [3H]GR113808 from 5HT4R in guinea pig striatal membranes
ChEMBL 352 5 0 3 5.0 CCCN1CCC(COc2nc3ccccc3c3ccc(F)cc23)CC1 10.1021/jm300943r
CHEMBL2181175 82555 0 None - 1 Guinea pig 6.8 pKi = 6.8 Binding
Displacement of [3H]GR113808 from 5HT4R in guinea pig striatal membranesDisplacement of [3H]GR113808 from 5HT4R in guinea pig striatal membranes
ChEMBL 352 5 0 3 5.0 CCCN1CCC(COc2nc3ccccc3c3ccc(F)cc23)CC1 10.1021/jm300943r
10531 1392 18 None -87 24 Guinea pig 6.8 pKi = 6.8 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
ChEMBL 583 4 3 6 2.1 CN1C[C@@H](C[C@H]2[C@H]1Cc1c[nH]c3c1c2ccc3)C(=O)N[C@]1(C)O[C@@]2(N(C1=O)[C@@H](Cc1ccccc1)C(=O)N1[C@H]2CCC1)O nan
121 1392 18 None -87 24 Guinea pig 6.8 pKi = 6.8 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
ChEMBL 583 4 3 6 2.1 CN1C[C@@H](C[C@H]2[C@H]1Cc1c[nH]c3c1c2ccc3)C(=O)N[C@]1(C)O[C@@]2(N(C1=O)[C@@H](Cc1ccccc1)C(=O)N1[C@H]2CCC1)O nan
888 1392 18 None -87 24 Guinea pig 6.8 pKi = 6.8 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
ChEMBL 583 4 3 6 2.1 CN1C[C@@H](C[C@H]2[C@H]1Cc1c[nH]c3c1c2ccc3)C(=O)N[C@]1(C)O[C@@]2(N(C1=O)[C@@H](Cc1ccccc1)C(=O)N1[C@H]2CCC1)O nan
CHEMBL1732 1392 18 None -87 24 Guinea pig 6.8 pKi = 6.8 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
ChEMBL 583 4 3 6 2.1 CN1C[C@@H](C[C@H]2[C@H]1Cc1c[nH]c3c1c2ccc3)C(=O)N[C@]1(C)O[C@@]2(N(C1=O)[C@@H](Cc1ccccc1)C(=O)N1[C@H]2CCC1)O nan
DB00320 1392 18 None -87 24 Guinea pig 6.8 pKi = 6.8 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
ChEMBL 583 4 3 6 2.1 CN1C[C@@H](C[C@H]2[C@H]1Cc1c[nH]c3c1c2ccc3)C(=O)N[C@]1(C)O[C@@]2(N(C1=O)[C@@H](Cc1ccccc1)C(=O)N1[C@H]2CCC1)O nan
108182 4068 18 None -1 16 Rat 6.8 pKi = 6.8 Binding
Displacement of [3H]GR-113808 from rat striatum 5-hydroxytryptamine 4 receptorDisplacement of [3H]GR-113808 from rat striatum 5-hydroxytryptamine 4 receptor
ChEMBL 309 3 2 4 1.8 COc1cc(N)c(cc1C(=O)NC1CN2CCC1CC2)Cl 10.1016/0960-894X(96)00200-4
245 4068 18 None -1 16 Rat 6.8 pKi = 6.8 Binding
Displacement of [3H]GR-113808 from rat striatum 5-hydroxytryptamine 4 receptorDisplacement of [3H]GR-113808 from rat striatum 5-hydroxytryptamine 4 receptor
ChEMBL 309 3 2 4 1.8 COc1cc(N)c(cc1C(=O)NC1CN2CCC1CC2)Cl 10.1016/0960-894X(96)00200-4
CHEMBL18041 4068 18 None -1 16 Rat 6.8 pKi = 6.8 Binding
Displacement of [3H]GR-113808 from rat striatum 5-hydroxytryptamine 4 receptorDisplacement of [3H]GR-113808 from rat striatum 5-hydroxytryptamine 4 receptor
ChEMBL 309 3 2 4 1.8 COc1cc(N)c(cc1C(=O)NC1CN2CCC1CC2)Cl 10.1016/0960-894X(96)00200-4
9906933 34243 0 None - 1 Guinea pig 6.8 pKi = 6.8 Binding
Binding affinity for 5-hydroxytryptamine 4 receptor by displacement of [3H]GR-113808 from guinea pig brain striatum.Binding affinity for 5-hydroxytryptamine 4 receptor by displacement of [3H]GR-113808 from guinea pig brain striatum.
ChEMBL 360 3 1 4 3.6 CC(C)n1cnc2c(C(=O)NC3CC4CCC(C3)N4C)cc(Cl)cc21 10.1016/0960-894X(96)00052-2
CHEMBL142852 34243 0 None - 1 Guinea pig 6.8 pKi = 6.8 Binding
Binding affinity for 5-hydroxytryptamine 4 receptor by displacement of [3H]GR-113808 from guinea pig brain striatum.Binding affinity for 5-hydroxytryptamine 4 receptor by displacement of [3H]GR-113808 from guinea pig brain striatum.
ChEMBL 360 3 1 4 3.6 CC(C)n1cnc2c(C(=O)NC3CC4CCC(C3)N4C)cc(Cl)cc21 10.1016/0960-894X(96)00052-2
15231247 91900477 193979 0 None - 1 Human 6.8 pKi = 6.8 Binding
Displacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 309 3 3 4 1.9 COc1cc(N)c(Cl)cc1C(=O)N[C@@H]1C[C@@H]2CC[C@H](C1)N2 10.1021/jm900881j
CHEMBL556438 193979 0 None - 1 Human 6.8 pKi = 6.8 Binding
Displacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 309 3 3 4 1.9 COc1cc(N)c(Cl)cc1C(=O)N[C@@H]1C[C@@H]2CC[C@H](C1)N2 10.1021/jm900881j
42499 193268 20 None - 1 Human 5.8 pKi = 5.8 Binding
Displacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 283 3 3 4 1.4 COc1cc(N)c(Cl)cc1C(=O)NC1CCNCC1 10.1021/jm900881j
CHEMBL541969 193268 20 None - 1 Human 5.8 pKi = 5.8 Binding
Displacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 283 3 3 4 1.4 COc1cc(N)c(Cl)cc1C(=O)NC1CCNCC1 10.1021/jm900881j
44248794 193840 0 None - 1 Human 5.8 pKi = 5.8 Binding
Displacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 302 2 2 5 1.7 CC(C)n1c(=O)n(C(=O)NC2CCNCC2)c2ccccc21 10.1021/jm900881j
CHEMBL553658 193840 0 None - 1 Human 5.8 pKi = 5.8 Binding
Displacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 302 2 2 5 1.7 CC(C)n1c(=O)n(C(=O)NC2CCNCC2)c2ccccc21 10.1021/jm900881j
44247817 91900489 194301 0 None - 1 Human 5.8 pKi = 5.8 Binding
Displacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 489 9 2 6 3.4 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CCCCCS(=O)(=O)O)cc2ccccc21 10.1021/jm900881j
CHEMBL559746 194301 0 None - 1 Human 5.8 pKi = 5.8 Binding
Displacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 489 9 2 6 3.4 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CCCCCS(=O)(=O)O)cc2ccccc21 10.1021/jm900881j
9935387 98983 0 None -1995 14 Human 5.8 pKi = 5.8 Binding
The compound was tested for the binding affinity towards human cloned 5-hydroxytryptamine 4 receptor in HeLa cells, using [3H]LSD as radioligandThe compound was tested for the binding affinity towards human cloned 5-hydroxytryptamine 4 receptor in HeLa cells, using [3H]LSD as radioligand
ChEMBL 491 5 1 6 5.0 COc1ccc(NS(=O)(=O)c2sc3ccc(Cl)cc3c2C)cc1N1CCN2CCC[C@@H]2C1 10.1016/s0960-894x(02)00172-5
CHEMBL282971 98983 0 None -1995 14 Human 5.8 pKi = 5.8 Binding
The compound was tested for the binding affinity towards human cloned 5-hydroxytryptamine 4 receptor in HeLa cells, using [3H]LSD as radioligandThe compound was tested for the binding affinity towards human cloned 5-hydroxytryptamine 4 receptor in HeLa cells, using [3H]LSD as radioligand
ChEMBL 491 5 1 6 5.0 COc1ccc(NS(=O)(=O)c2sc3ccc(Cl)cc3c2C)cc1N1CCN2CCC[C@@H]2C1 10.1016/s0960-894x(02)00172-5
44247949 193444 0 None - 1 Human 4.8 pKi = 4.8 Binding
Displacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 475 12 3 6 3.4 COc1cc(N)c(Cl)cc1C(=O)NC1CCN(CCCCCCCCS(=O)(=O)O)CC1 10.1021/jm900881j
CHEMBL549998 193444 0 None - 1 Human 4.8 pKi = 4.8 Binding
Displacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 475 12 3 6 3.4 COc1cc(N)c(Cl)cc1C(=O)NC1CCN(CCCCCCCCS(=O)(=O)O)CC1 10.1021/jm900881j
11600413 67184 0 None - 1 Human 7.8 pKi = 7.8 Binding
Binding affinity for 5-HT4 receptor using [3H]GR-113808Binding affinity for 5-HT4 receptor using [3H]GR-113808
ChEMBL 876 25 4 12 6.7 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCC(CNC(=O)CCCCCCCCCCC(=O)NCC2CCN(CCOC(=O)c3cc(Cl)c(N)cc3OC)CC2)CC1 10.1021/jm050234z
CHEMBL189580 67184 0 None - 1 Human 7.8 pKi = 7.8 Binding
Binding affinity for 5-HT4 receptor using [3H]GR-113808Binding affinity for 5-HT4 receptor using [3H]GR-113808
ChEMBL 876 25 4 12 6.7 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCC(CNC(=O)CCCCCCCCCCC(=O)NCC2CCN(CCOC(=O)c3cc(Cl)c(N)cc3OC)CC2)CC1 10.1021/jm050234z
44404962 72200 0 None - 1 Human 7.8 pKi = 7.8 Binding
Binding affinity for 5-HT4 receptor using [3H]GR-113808Binding affinity for 5-HT4 receptor using [3H]GR-113808
ChEMBL 834 22 5 12 5.9 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCC(NC(=O)CCCCCCCCCCC(=O)NC2CCN(CCOC(=O)c3cc(Cl)c(N)cc3O)CC2)CC1 10.1021/jm050234z
CHEMBL199150 72200 0 None - 1 Human 7.8 pKi = 7.8 Binding
Binding affinity for 5-HT4 receptor using [3H]GR-113808Binding affinity for 5-HT4 receptor using [3H]GR-113808
ChEMBL 834 22 5 12 5.9 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCC(NC(=O)CCCCCCCCCCC(=O)NC2CCN(CCOC(=O)c3cc(Cl)c(N)cc3O)CC2)CC1 10.1021/jm050234z
44592076 172155 0 None - 1 Guinea pig 7.8 pKi = 7.8 Binding
Displacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatum membraneDisplacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatum membrane
ChEMBL 317 8 0 5 4.1 CCN(CC)CCCCOc1nc2ccsc2n2cccc12 10.1016/j.bmc.2008.11.045
CHEMBL450595 172155 0 None - 1 Guinea pig 7.8 pKi = 7.8 Binding
Displacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatum membraneDisplacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatum membrane
ChEMBL 317 8 0 5 4.1 CCN(CC)CCCCOc1nc2ccsc2n2cccc12 10.1016/j.bmc.2008.11.045
44592108 178508 0 None - 1 Guinea pig 7.8 pKi = 7.8 Binding
Displacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatum membraneDisplacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatum membrane
ChEMBL 329 5 0 5 4.1 CCCN1CCC(COc2nc3ccsc3n3cccc23)CC1 10.1016/j.bmc.2008.11.045
CHEMBL471662 178508 0 None - 1 Guinea pig 7.8 pKi = 7.8 Binding
Displacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatum membraneDisplacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatum membrane
ChEMBL 329 5 0 5 4.1 CCCN1CCC(COc2nc3ccsc3n3cccc23)CC1 10.1016/j.bmc.2008.11.045
10292429 119697 0 None - 1 Guinea pig 7.8 pKi = 7.8 Binding
Ability to displace [3H]GR-113808 from 5-hydroxytryptamine 4 receptorAbility to displace [3H]GR-113808 from 5-hydroxytryptamine 4 receptor
ChEMBL 367 6 1 4 4.9 CCCCN1CCC(COc2nc3ccccc3c3c2CCCCN3)CC1 10.1021/jm020954v
CHEMBL35195 119697 0 None - 1 Guinea pig 7.8 pKi = 7.8 Binding
Ability to displace [3H]GR-113808 from 5-hydroxytryptamine 4 receptorAbility to displace [3H]GR-113808 from 5-hydroxytryptamine 4 receptor
ChEMBL 367 6 1 4 4.9 CCCCN1CCC(COc2nc3ccccc3c3c2CCCCN3)CC1 10.1021/jm020954v
162676850 182938 0 None - 1 Guinea pig 7.8 pKi = 7.8 Binding
Displacement of [3H]-GR113808 from guinea pig brain 5HT4 receptor in presence of serotonin incubated for 30 minsDisplacement of [3H]-GR113808 from guinea pig brain 5HT4 receptor in presence of serotonin incubated for 30 mins
ChEMBL 635 10 2 6 5.1 COc1cc(N)c(Cl)cc1C(=O)CCC1CCN(CCNS(=O)(=O)c2cc(Br)ccc2Br)CC1 10.1016/j.ejmech.2016.05.048
CHEMBL4799839 182938 0 None - 1 Guinea pig 7.8 pKi = 7.8 Binding
Displacement of [3H]-GR113808 from guinea pig brain 5HT4 receptor in presence of serotonin incubated for 30 minsDisplacement of [3H]-GR113808 from guinea pig brain 5HT4 receptor in presence of serotonin incubated for 30 mins
ChEMBL 635 10 2 6 5.1 COc1cc(N)c(Cl)cc1C(=O)CCC1CCN(CCNS(=O)(=O)c2cc(Br)ccc2Br)CC1 10.1016/j.ejmech.2016.05.048
10645103 163789 0 None - 1 Human 7.8 pKi = 7.8 Binding
Binding affinity was determined against cloned 5-hydroxytryptamine 4E receptor isoform expressed in C6 glial cells incubated with 0.2 nM [3H]GR-113808Binding affinity was determined against cloned 5-hydroxytryptamine 4E receptor isoform expressed in C6 glial cells incubated with 0.2 nM [3H]GR-113808
ChEMBL 407 6 1 6 3.0 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCN(c2ccccc2F)CC1 10.1021/jm0009538
CHEMBL421256 163789 0 None - 1 Human 7.8 pKi = 7.8 Binding
Binding affinity was determined against cloned 5-hydroxytryptamine 4E receptor isoform expressed in C6 glial cells incubated with 0.2 nM [3H]GR-113808Binding affinity was determined against cloned 5-hydroxytryptamine 4E receptor isoform expressed in C6 glial cells incubated with 0.2 nM [3H]GR-113808
ChEMBL 407 6 1 6 3.0 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCN(c2ccccc2F)CC1 10.1021/jm0009538
10546395 4141 0 None - 1 Guinea pig 7.8 pKi = 7.8 Binding
Binding affinity against 5-hydroxytryptamine 4 receptor in guinea pig striatum using [3H]GR-113808 as radioligandBinding affinity against 5-hydroxytryptamine 4 receptor in guinea pig striatum using [3H]GR-113808 as radioligand
ChEMBL 359 6 1 6 1.4 CCCN1CCN(CCNC(=O)n2c(=O)n(CC)c3ccccc32)CC1 10.1021/jm981098j
CHEMBL100199 4141 0 None - 1 Guinea pig 7.8 pKi = 7.8 Binding
Binding affinity against 5-hydroxytryptamine 4 receptor in guinea pig striatum using [3H]GR-113808 as radioligandBinding affinity against 5-hydroxytryptamine 4 receptor in guinea pig striatum using [3H]GR-113808 as radioligand
ChEMBL 359 6 1 6 1.4 CCCN1CCN(CCNC(=O)n2c(=O)n(CC)c3ccccc32)CC1 10.1021/jm981098j
10645984 18629 0 None - 1 Human 6.8 pKi = 6.8 Binding
Binding affinity was determined against cloned 5-hydroxytryptamine 4E receptor isoform expressed in C6 glial cells incubated with 0.2 nM [3H]GR-113808Binding affinity was determined against cloned 5-hydroxytryptamine 4E receptor isoform expressed in C6 glial cells incubated with 0.2 nM [3H]GR-113808
ChEMBL 423 6 1 6 3.6 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCN(c2cccc(Cl)c2)CC1 10.1021/jm0009538
CHEMBL127876 18629 0 None - 1 Human 6.8 pKi = 6.8 Binding
Binding affinity was determined against cloned 5-hydroxytryptamine 4E receptor isoform expressed in C6 glial cells incubated with 0.2 nM [3H]GR-113808Binding affinity was determined against cloned 5-hydroxytryptamine 4E receptor isoform expressed in C6 glial cells incubated with 0.2 nM [3H]GR-113808
ChEMBL 423 6 1 6 3.6 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCN(c2cccc(Cl)c2)CC1 10.1021/jm0009538
11841878 67255 5 None - 1 Rat 6.8 pKi = 6.8 Binding
Displacement of [3H]GR-113808 from rat striatum 5-hydroxytryptamine 4 receptorDisplacement of [3H]GR-113808 from rat striatum 5-hydroxytryptamine 4 receptor
ChEMBL 332 2 2 3 3.0 CN1C2CCCC1CC(NC(=O)c1cc(Cl)cc3[nH]cnc13)C2 10.1016/0960-894X(96)00200-4
CHEMBL19022 67255 5 None - 1 Rat 6.8 pKi = 6.8 Binding
Displacement of [3H]GR-113808 from rat striatum 5-hydroxytryptamine 4 receptorDisplacement of [3H]GR-113808 from rat striatum 5-hydroxytryptamine 4 receptor
ChEMBL 332 2 2 3 3.0 CN1C2CCCC1CC(NC(=O)c1cc(Cl)cc3[nH]cnc13)C2 10.1016/0960-894X(96)00200-4
11841878 67255 5 None - 1 Rat 6.8 pKi = 6.8 Binding
In vitro affinity at serotonergic 5-hydroxytryptamine 4 receptor by radioligand binding assay using [3H]GR-113808 in rat striatum membranes.In vitro affinity at serotonergic 5-hydroxytryptamine 4 receptor by radioligand binding assay using [3H]GR-113808 in rat striatum membranes.
ChEMBL 332 2 2 3 3.0 CN1C2CCCC1CC(NC(=O)c1cc(Cl)cc3[nH]cnc13)C2 10.1021/jm991076c
CHEMBL19022 67255 5 None - 1 Rat 6.8 pKi = 6.8 Binding
In vitro affinity at serotonergic 5-hydroxytryptamine 4 receptor by radioligand binding assay using [3H]GR-113808 in rat striatum membranes.In vitro affinity at serotonergic 5-hydroxytryptamine 4 receptor by radioligand binding assay using [3H]GR-113808 in rat striatum membranes.
ChEMBL 332 2 2 3 3.0 CN1C2CCCC1CC(NC(=O)c1cc(Cl)cc3[nH]cnc13)C2 10.1021/jm991076c
10859701 67241 0 None - 1 Rat 6.8 pKi = 6.8 Binding
Displacement of [3H]GR-113808 from rat striatum 5-hydroxytryptamine 4 receptorDisplacement of [3H]GR-113808 from rat striatum 5-hydroxytryptamine 4 receptor
ChEMBL 304 2 2 3 2.0 O=C(NC1CN2CCC1CC2)c1cc(Cl)cc2nc[nH]c12 10.1016/0960-894X(96)00200-4
CHEMBL19006 67241 0 None - 1 Rat 6.8 pKi = 6.8 Binding
Displacement of [3H]GR-113808 from rat striatum 5-hydroxytryptamine 4 receptorDisplacement of [3H]GR-113808 from rat striatum 5-hydroxytryptamine 4 receptor
ChEMBL 304 2 2 3 2.0 O=C(NC1CN2CCC1CC2)c1cc(Cl)cc2nc[nH]c12 10.1016/0960-894X(96)00200-4
10859701 67241 0 None - 1 Rat 6.8 pKi = 6.8 Binding
In vitro affinity at serotonergic 5-hydroxytryptamine 4 receptor by radioligand binding assay using [3H]GR-113808 in rat striatum membranes.In vitro affinity at serotonergic 5-hydroxytryptamine 4 receptor by radioligand binding assay using [3H]GR-113808 in rat striatum membranes.
ChEMBL 304 2 2 3 2.0 O=C(NC1CN2CCC1CC2)c1cc(Cl)cc2nc[nH]c12 10.1021/jm991076c
CHEMBL19006 67241 0 None - 1 Rat 6.8 pKi = 6.8 Binding
In vitro affinity at serotonergic 5-hydroxytryptamine 4 receptor by radioligand binding assay using [3H]GR-113808 in rat striatum membranes.In vitro affinity at serotonergic 5-hydroxytryptamine 4 receptor by radioligand binding assay using [3H]GR-113808 in rat striatum membranes.
ChEMBL 304 2 2 3 2.0 O=C(NC1CN2CCC1CC2)c1cc(Cl)cc2nc[nH]c12 10.1021/jm991076c
11841879 120500 6 None - 1 Rat 6.8 pKi = 6.8 Binding
In vitro affinity at serotonergic 5-hydroxytryptamine 4 receptor by radioligand binding assay using [3H]GR-113808 in rat striatum membranes.In vitro affinity at serotonergic 5-hydroxytryptamine 4 receptor by radioligand binding assay using [3H]GR-113808 in rat striatum membranes.
ChEMBL 348 2 2 3 2.1 O=C(NC1CN2CCC1CC2)c1cc(Br)cc2nc[nH]c12 10.1021/jm991076c
CHEMBL356521 120500 6 None - 1 Rat 6.8 pKi = 6.8 Binding
In vitro affinity at serotonergic 5-hydroxytryptamine 4 receptor by radioligand binding assay using [3H]GR-113808 in rat striatum membranes.In vitro affinity at serotonergic 5-hydroxytryptamine 4 receptor by radioligand binding assay using [3H]GR-113808 in rat striatum membranes.
ChEMBL 348 2 2 3 2.1 O=C(NC1CN2CCC1CC2)c1cc(Br)cc2nc[nH]c12 10.1021/jm991076c
9924349 175294 0 None - 1 Human 6.8 pKi = 6.8 Binding
Displacement of [3H]-GR113808 from recombinant human 5-HT4BR expressed in membranes after 60 minsDisplacement of [3H]-GR113808 from recombinant human 5-HT4BR expressed in membranes after 60 mins
ChEMBL 346 6 1 2 5.0 O=C(CCC1CCN(Cc2ccccc2)CC1)c1ccc2[nH]ccc2c1 10.1016/j.ejmech.2018.10.064
CHEMBL4585990 175294 0 None - 1 Human 6.8 pKi = 6.8 Binding
Displacement of [3H]-GR113808 from recombinant human 5-HT4BR expressed in membranes after 60 minsDisplacement of [3H]-GR113808 from recombinant human 5-HT4BR expressed in membranes after 60 mins
ChEMBL 346 6 1 2 5.0 O=C(CCC1CCN(Cc2ccccc2)CC1)c1ccc2[nH]ccc2c1 10.1016/j.ejmech.2018.10.064
9905225 205216 0 None - 1 Rat 7.8 pKi = 7.8 Binding
Binding affinity at 5-hydroxytryptamine 4 receptor in rat striatum by [3H]GR-113808 displacement.Binding affinity at 5-hydroxytryptamine 4 receptor in rat striatum by [3H]GR-113808 displacement.
ChEMBL 321 2 2 4 1.7 Nc1c(Cl)cc(C(=O)N[C@@H]2CN3CCC2CC3)c2c1CCO2 10.1016/0960-894X(96)00002-9
CHEMBL91147 205216 0 None - 1 Rat 7.8 pKi = 7.8 Binding
Binding affinity at 5-hydroxytryptamine 4 receptor in rat striatum by [3H]GR-113808 displacement.Binding affinity at 5-hydroxytryptamine 4 receptor in rat striatum by [3H]GR-113808 displacement.
ChEMBL 321 2 2 4 1.7 Nc1c(Cl)cc(C(=O)N[C@@H]2CN3CCC2CC3)c2c1CCO2 10.1016/0960-894X(96)00002-9
240 931 39 None -4 25 Guinea pig 7.8 pKi = 7.8 Binding
Displacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatumDisplacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatum
ChEMBL 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N 10.1021/jm0509501
2769 931 39 None -4 25 Guinea pig 7.8 pKi = 7.8 Binding
Displacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatumDisplacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatum
ChEMBL 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N 10.1021/jm0509501
44279790 931 39 None -4 25 Guinea pig 7.8 pKi = 7.8 Binding
Displacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatumDisplacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatum
ChEMBL 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N 10.1021/jm0509501
660 931 39 None -4 25 Guinea pig 7.8 pKi = 7.8 Binding
Displacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatumDisplacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatum
ChEMBL 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N 10.1021/jm0509501
CHEMBL1729 931 39 None -4 25 Guinea pig 7.8 pKi = 7.8 Binding
Displacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatumDisplacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatum
ChEMBL 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N 10.1021/jm0509501
CHEMBL560739 931 39 None -4 25 Guinea pig 7.8 pKi = 7.8 Binding
Displacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatumDisplacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatum
ChEMBL 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N 10.1021/jm0509501
DB00604 931 39 None -4 25 Guinea pig 7.8 pKi = 7.8 Binding
Displacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatumDisplacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatum
ChEMBL 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N 10.1021/jm0509501
49783417 17532 0 None -18 2 Human 7.8 pKi = 7.8 Binding
Displacement of [3H]GR113808 from human recombinant 5HT4 receptor expressed in HEK293 cellsDisplacement of [3H]GR113808 from human recombinant 5HT4 receptor expressed in HEK293 cells
ChEMBL 306 6 1 5 2.6 CCCN1CCC(COC(=O)c2ccc(N)c(OC)c2)CC1 10.1021/jm100668r
CHEMBL1258560 17532 0 None -18 2 Human 7.8 pKi = 7.8 Binding
Displacement of [3H]GR113808 from human recombinant 5HT4 receptor expressed in HEK293 cellsDisplacement of [3H]GR113808 from human recombinant 5HT4 receptor expressed in HEK293 cells
ChEMBL 306 6 1 5 2.6 CCCN1CCC(COC(=O)c2ccc(N)c(OC)c2)CC1 10.1021/jm100668r
49783420 17568 0 None -51 2 Human 7.8 pKi = 7.8 Binding
Displacement of [3H]GR113808 from human recombinant 5HT4 receptor expressed in HEK293 cellsDisplacement of [3H]GR113808 from human recombinant 5HT4 receptor expressed in HEK293 cells
ChEMBL 338 8 1 5 3.2 CCCCN1CCC(COC(=O)c2ccc(N)c(OCF)c2)CC1 10.1021/jm100668r
CHEMBL1258672 17568 0 None -51 2 Human 7.8 pKi = 7.8 Binding
Displacement of [3H]GR113808 from human recombinant 5HT4 receptor expressed in HEK293 cellsDisplacement of [3H]GR113808 from human recombinant 5HT4 receptor expressed in HEK293 cells
ChEMBL 338 8 1 5 3.2 CCCCN1CCC(COC(=O)c2ccc(N)c(OCF)c2)CC1 10.1021/jm100668r
71461049 82562 0 None 1 6 Human 7.8 pKi = 7.8 Binding
Displacement of [3H]GR113808 from human recombinant 5HT4R expressed in HEK293T cellsDisplacement of [3H]GR113808 from human recombinant 5HT4R expressed in HEK293T cells
ChEMBL 364 6 0 4 4.9 CCCN1CCC(COc2nc3c(OC)cccc3c3ccccc23)CC1 10.1021/jm300943r
CHEMBL2181187 82562 0 None 1 6 Human 7.8 pKi = 7.8 Binding
Displacement of [3H]GR113808 from human recombinant 5HT4R expressed in HEK293T cellsDisplacement of [3H]GR113808 from human recombinant 5HT4R expressed in HEK293T cells
ChEMBL 364 6 0 4 4.9 CCCN1CCC(COc2nc3c(OC)cccc3c3ccccc23)CC1 10.1021/jm300943r
10669778 116972 0 None - 1 Human 7.8 pKi = 7.8 Binding
Binding affinity was determined against cloned 5-hydroxytryptamine 4E receptor isoform expressed in C6 glial cells incubated with 0.2 nM [3H]GR-113808Binding affinity was determined against cloned 5-hydroxytryptamine 4E receptor isoform expressed in C6 glial cells incubated with 0.2 nM [3H]GR-113808
ChEMBL 419 7 1 7 2.9 COc1ccc(N2CCN(CCOC(=O)c3cc(Cl)c(N)cc3OC)CC2)cc1 10.1021/jm0009538
CHEMBL339936 116972 0 None - 1 Human 7.8 pKi = 7.8 Binding
Binding affinity was determined against cloned 5-hydroxytryptamine 4E receptor isoform expressed in C6 glial cells incubated with 0.2 nM [3H]GR-113808Binding affinity was determined against cloned 5-hydroxytryptamine 4E receptor isoform expressed in C6 glial cells incubated with 0.2 nM [3H]GR-113808
ChEMBL 419 7 1 7 2.9 COc1ccc(N2CCN(CCOC(=O)c3cc(Cl)c(N)cc3OC)CC2)cc1 10.1021/jm0009538
11791805 107054 0 None - 1 Guinea pig 7.8 pKi = 7.8 Binding
Binding affinity against 5-hydroxytryptamine 4 receptor in guinea pig striatum using [3H]GR-113808 as radioligandBinding affinity against 5-hydroxytryptamine 4 receptor in guinea pig striatum using [3H]GR-113808 as radioligand
ChEMBL 345 5 1 6 1.0 CCN1CCN(CCNC(=O)n2c(=O)n(CC)c3ccccc32)CC1 10.1021/jm981098j
CHEMBL318764 107054 0 None - 1 Guinea pig 7.8 pKi = 7.8 Binding
Binding affinity against 5-hydroxytryptamine 4 receptor in guinea pig striatum using [3H]GR-113808 as radioligandBinding affinity against 5-hydroxytryptamine 4 receptor in guinea pig striatum using [3H]GR-113808 as radioligand
ChEMBL 345 5 1 6 1.0 CCN1CCN(CCNC(=O)n2c(=O)n(CC)c3ccccc32)CC1 10.1021/jm981098j
10267187 204772 0 None - 1 Rat 6.8 pKi = 6.8 Binding
Binding affinity at 5-hydroxytryptamine 4 receptor in rat striatum by [3H]GR-113808 displacement.Binding affinity at 5-hydroxytryptamine 4 receptor in rat striatum by [3H]GR-113808 displacement.
ChEMBL 306 2 1 3 2.1 O=C(N[C@@H]1CN2CCC1CC2)c1cc(Cl)cc2c1OCC2 10.1016/0960-894X(96)00002-9
CHEMBL88310 204772 0 None - 1 Rat 6.8 pKi = 6.8 Binding
Binding affinity at 5-hydroxytryptamine 4 receptor in rat striatum by [3H]GR-113808 displacement.Binding affinity at 5-hydroxytryptamine 4 receptor in rat striatum by [3H]GR-113808 displacement.
ChEMBL 306 2 1 3 2.1 O=C(N[C@@H]1CN2CCC1CC2)c1cc(Cl)cc2c1OCC2 10.1016/0960-894X(96)00002-9
10331436 321 7 None -851 6 Human 5.8 pKi = 5.8 Binding
Inhibitory constant against 5-hydroxytryptamine 4 receptor using [3H]GR-113808 radioligandInhibitory constant against 5-hydroxytryptamine 4 receptor using [3H]GR-113808 radioligand
ChEMBL 230 2 2 2 2.4 C[C@@H](Cc1c[nH]c2c1c1CCCOc1cc2)N 10.1021/jm030205t
160 321 7 None -851 6 Human 5.8 pKi = 5.8 Binding
Inhibitory constant against 5-hydroxytryptamine 4 receptor using [3H]GR-113808 radioligandInhibitory constant against 5-hydroxytryptamine 4 receptor using [3H]GR-113808 radioligand
ChEMBL 230 2 2 2 2.4 C[C@@H](Cc1c[nH]c2c1c1CCCOc1cc2)N 10.1021/jm030205t
CHEMBL133455 321 7 None -851 6 Human 5.8 pKi = 5.8 Binding
Inhibitory constant against 5-hydroxytryptamine 4 receptor using [3H]GR-113808 radioligandInhibitory constant against 5-hydroxytryptamine 4 receptor using [3H]GR-113808 radioligand
ChEMBL 230 2 2 2 2.4 C[C@@H](Cc1c[nH]c2c1c1CCCOc1cc2)N 10.1021/jm030205t
11146446 105474 0 None - 1 Human 5.8 pKi = 5.8 Binding
Binding affinity towards cloned human 5-hydroxytryptamine 4E receptor expressed in C6 glial cells using [3H]GR-113808 as radioligandBinding affinity towards cloned human 5-hydroxytryptamine 4E receptor expressed in C6 glial cells using [3H]GR-113808 as radioligand
ChEMBL 603 10 2 9 2.4 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCN(C(=O)CNS(=O)(=O)c2cccc3c(N(C)C)cccc23)CC1 10.1021/jm0307887
CHEMBL312940 105474 0 None - 1 Human 5.8 pKi = 5.8 Binding
Binding affinity towards cloned human 5-hydroxytryptamine 4E receptor expressed in C6 glial cells using [3H]GR-113808 as radioligandBinding affinity towards cloned human 5-hydroxytryptamine 4E receptor expressed in C6 glial cells using [3H]GR-113808 as radioligand
ChEMBL 603 10 2 9 2.4 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCN(C(=O)CNS(=O)(=O)c2cccc3c(N(C)C)cccc23)CC1 10.1021/jm0307887
90666003 108799 0 None - 1 Guinea pig 6.8 pKi = 6.8 Binding
Displacement of [3H]-GR113808 from guinea pig 5HT4 receptor by Grossman's methodDisplacement of [3H]-GR113808 from guinea pig 5HT4 receptor by Grossman's method
ChEMBL 378 5 0 6 4.2 c1cc2c(OCC3CCN(Cc4ccncc4)CC3)nc3ccsc3n2c1 10.1039/C2MD20063E
CHEMBL3218875 108799 0 None - 1 Guinea pig 6.8 pKi = 6.8 Binding
Displacement of [3H]-GR113808 from guinea pig 5HT4 receptor by Grossman's methodDisplacement of [3H]-GR113808 from guinea pig 5HT4 receptor by Grossman's method
ChEMBL 378 5 0 6 4.2 c1cc2c(OCC3CCN(Cc4ccncc4)CC3)nc3ccsc3n2c1 10.1039/C2MD20063E
176155 4101 0 None -1 4 Guinea pig 5.8 pKi = 5.8 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
ChEMBL 377 4 1 3 4.7 C[S+]([O-])c1ccc(-c2nc(-c3ccc(F)cc3)c(-c3ccncc3)[nH]2)cc1 nan
CHEMBL10 4101 0 None -1 4 Guinea pig 5.8 pKi = 5.8 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
ChEMBL 377 4 1 3 4.7 C[S+]([O-])c1ccc(-c2nc(-c3ccc(F)cc3)c(-c3ccncc3)[nH]2)cc1 nan
11714901 133809 0 None - 1 Human 7.8 pKi = 7.8 Binding
Binding affinity for 5-HT4 receptor using [3H]GR-113808Binding affinity for 5-HT4 receptor using [3H]GR-113808
ChEMBL 904 27 4 12 7.5 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCC(CCNC(=O)CCCCCCCCCCC(=O)NCCC2CCN(CCOC(=O)c3cc(Cl)c(N)cc3OC)CC2)CC1 10.1021/jm050234z
CHEMBL371718 133809 0 None - 1 Human 7.8 pKi = 7.8 Binding
Binding affinity for 5-HT4 receptor using [3H]GR-113808Binding affinity for 5-HT4 receptor using [3H]GR-113808
ChEMBL 904 27 4 12 7.5 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCC(CCNC(=O)CCCCCCCCCCC(=O)NCCC2CCN(CCOC(=O)c3cc(Cl)c(N)cc3OC)CC2)CC1 10.1021/jm050234z
162673811 182567 0 None - 1 Guinea pig 7.8 pKi = 7.8 Binding
Displacement of [3H]-GR113808 from guinea pig brain 5HT4 receptor in presence of serotonin incubated for 30 minsDisplacement of [3H]-GR113808 from guinea pig brain 5HT4 receptor in presence of serotonin incubated for 30 mins
ChEMBL 493 10 2 6 3.9 COc1cc(N)c(Cl)cc1C(=O)CCC1CCN(CCNS(=O)(=O)c2ccc(C)cc2)CC1 10.1016/j.ejmech.2016.05.048
CHEMBL4795251 182567 0 None - 1 Guinea pig 7.8 pKi = 7.8 Binding
Displacement of [3H]-GR113808 from guinea pig brain 5HT4 receptor in presence of serotonin incubated for 30 minsDisplacement of [3H]-GR113808 from guinea pig brain 5HT4 receptor in presence of serotonin incubated for 30 mins
ChEMBL 493 10 2 6 3.9 COc1cc(N)c(Cl)cc1C(=O)CCC1CCN(CCNS(=O)(=O)c2ccc(C)cc2)CC1 10.1016/j.ejmech.2016.05.048
44592111 189216 0 None - 1 Guinea pig 7.7 pKi = 7.7 Binding
Displacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatum membraneDisplacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatum membrane
ChEMBL 329 4 0 5 4.0 CC(C)N1CCC(COc2nc3ccsc3n3cccc23)CC1 10.1016/j.bmc.2008.11.045
CHEMBL516340 189216 0 None - 1 Guinea pig 7.7 pKi = 7.7 Binding
Displacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatum membraneDisplacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatum membrane
ChEMBL 329 4 0 5 4.0 CC(C)N1CCC(COc2nc3ccsc3n3cccc23)CC1 10.1016/j.bmc.2008.11.045
162667581 181903 0 None - 1 Guinea pig 7.7 pKi = 7.7 Binding
Displacement of [3H]-GR113808 from guinea pig brain 5HT4 receptor in presence of serotonin incubated for 30 minsDisplacement of [3H]-GR113808 from guinea pig brain 5HT4 receptor in presence of serotonin incubated for 30 mins
ChEMBL 539 12 2 8 3.6 COc1ccc(S(=O)(=O)NCCN2CCC(CCC(=O)c3cc(Cl)c(N)cc3OC)CC2)c(OC)c1 10.1016/j.ejmech.2016.05.048
CHEMBL4786794 181903 0 None - 1 Guinea pig 7.7 pKi = 7.7 Binding
Displacement of [3H]-GR113808 from guinea pig brain 5HT4 receptor in presence of serotonin incubated for 30 minsDisplacement of [3H]-GR113808 from guinea pig brain 5HT4 receptor in presence of serotonin incubated for 30 mins
ChEMBL 539 12 2 8 3.6 COc1ccc(S(=O)(=O)NCCN2CCC(CCC(=O)c3cc(Cl)c(N)cc3OC)CC2)c(OC)c1 10.1016/j.ejmech.2016.05.048
10919426 204498 0 None - 1 Human 6.8 pKi = 6.8 Binding
Binding affinity towards cloned human 5-hydroxytryptamine 4E receptor expressed in C6 glial cells using [3H]GR-113808 as radioligandBinding affinity towards cloned human 5-hydroxytryptamine 4E receptor expressed in C6 glial cells using [3H]GR-113808 as radioligand
ChEMBL 659 14 2 9 4.0 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCN(C(=O)CCCCCNS(=O)(=O)c2cccc3c(N(C)C)cccc23)CC1 10.1021/jm0307887
CHEMBL86624 204498 0 None - 1 Human 6.8 pKi = 6.8 Binding
Binding affinity towards cloned human 5-hydroxytryptamine 4E receptor expressed in C6 glial cells using [3H]GR-113808 as radioligandBinding affinity towards cloned human 5-hydroxytryptamine 4E receptor expressed in C6 glial cells using [3H]GR-113808 as radioligand
ChEMBL 659 14 2 9 4.0 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCN(C(=O)CCCCCNS(=O)(=O)c2cccc3c(N(C)C)cccc23)CC1 10.1021/jm0307887
9856041 23910 2 None -489 8 Human 5.8 pKi = 5.8 Binding
Inhibitory constant against 5-hydroxytryptamine 4 receptor using [3H]GR-113808 radioligandInhibitory constant against 5-hydroxytryptamine 4 receptor using [3H]GR-113808 radioligand
ChEMBL 230 2 2 2 2.4 CC(N)Cc1c[nH]c2ccc3c(c12)CCCO3 10.1021/jm030205t
CHEMBL133868 23910 2 None -489 8 Human 5.8 pKi = 5.8 Binding
Inhibitory constant against 5-hydroxytryptamine 4 receptor using [3H]GR-113808 radioligandInhibitory constant against 5-hydroxytryptamine 4 receptor using [3H]GR-113808 radioligand
ChEMBL 230 2 2 2 2.4 CC(N)Cc1c[nH]c2ccc3c(c12)CCCO3 10.1021/jm030205t
11813759 204573 0 None - 1 Human 6.7 pKi = 6.7 Binding
Binding affinity towards cloned human 5-hydroxytryptamine 4E receptor expressed in C6 glial cells using [3H]GR-113808 as radioligandBinding affinity towards cloned human 5-hydroxytryptamine 4E receptor expressed in C6 glial cells using [3H]GR-113808 as radioligand
ChEMBL 564 8 1 8 4.3 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCC(CN2C(=O)c3cccc4c(N(C)C)ccc(c34)C2=O)CC1 10.1021/jm0307887
CHEMBL87063 204573 0 None - 1 Human 6.7 pKi = 6.7 Binding
Binding affinity towards cloned human 5-hydroxytryptamine 4E receptor expressed in C6 glial cells using [3H]GR-113808 as radioligandBinding affinity towards cloned human 5-hydroxytryptamine 4E receptor expressed in C6 glial cells using [3H]GR-113808 as radioligand
ChEMBL 564 8 1 8 4.3 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCC(CN2C(=O)c3cccc4c(N(C)C)ccc(c34)C2=O)CC1 10.1021/jm0307887
2585 790 100 None -57 22 Guinea pig 6.7 pKi = 6.7 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
ChEMBL 406 10 3 5 3.7 COc1ccccc1OCCNCC(COc1cccc2c1c1ccccc1[nH]2)O nan
522 790 100 None -57 22 Guinea pig 6.7 pKi = 6.7 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
ChEMBL 406 10 3 5 3.7 COc1ccccc1OCCNCC(COc1cccc2c1c1ccccc1[nH]2)O nan
551 790 100 None -57 22 Guinea pig 6.7 pKi = 6.7 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
ChEMBL 406 10 3 5 3.7 COc1ccccc1OCCNCC(COc1cccc2c1c1ccccc1[nH]2)O nan
CHEMBL723 790 100 None -57 22 Guinea pig 6.7 pKi = 6.7 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
ChEMBL 406 10 3 5 3.7 COc1ccccc1OCCNCC(COc1cccc2c1c1ccccc1[nH]2)O nan
DB01136 790 100 None -57 22 Guinea pig 6.7 pKi = 6.7 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
ChEMBL 406 10 3 5 3.7 COc1ccccc1OCCNCC(COc1cccc2c1c1ccccc1[nH]2)O nan
11050452 48882 0 None - 1 Human 6.7 pKi = 6.7 Binding
Binding affinity towards cloned human 5-hydroxytryptamine 4E receptor expressed in C6 glial cells using [3H]GR-113808 as radioligandBinding affinity towards cloned human 5-hydroxytryptamine 4E receptor expressed in C6 glial cells using [3H]GR-113808 as radioligand
ChEMBL 631 12 2 9 3.2 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCN(C(=O)CCCNS(=O)(=O)c2cccc3c(N(C)C)cccc23)CC1 10.1021/jm0307887
CHEMBL156206 48882 0 None - 1 Human 6.7 pKi = 6.7 Binding
Binding affinity towards cloned human 5-hydroxytryptamine 4E receptor expressed in C6 glial cells using [3H]GR-113808 as radioligandBinding affinity towards cloned human 5-hydroxytryptamine 4E receptor expressed in C6 glial cells using [3H]GR-113808 as radioligand
ChEMBL 631 12 2 9 3.2 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCN(C(=O)CCCNS(=O)(=O)c2cccc3c(N(C)C)cccc23)CC1 10.1021/jm0307887
5 139 66 None -117 54 Rat 6.7 pKi = 6.7 Binding
Binding affinity towards 5-hydroxytryptamine 4 receptor was determined in rat striatal membranes using [3H]GR-113808 as radioligandBinding affinity towards 5-hydroxytryptamine 4 receptor was determined in rat striatal membranes using [3H]GR-113808 as radioligand
ChEMBL 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 10.1021/jm960320m
5202 139 66 None -117 54 Rat 6.7 pKi = 6.7 Binding
Binding affinity towards 5-hydroxytryptamine 4 receptor was determined in rat striatal membranes using [3H]GR-113808 as radioligandBinding affinity towards 5-hydroxytryptamine 4 receptor was determined in rat striatal membranes using [3H]GR-113808 as radioligand
ChEMBL 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 10.1021/jm960320m
CHEMBL39 139 66 None -117 54 Rat 6.7 pKi = 6.7 Binding
Binding affinity towards 5-hydroxytryptamine 4 receptor was determined in rat striatal membranes using [3H]GR-113808 as radioligandBinding affinity towards 5-hydroxytryptamine 4 receptor was determined in rat striatal membranes using [3H]GR-113808 as radioligand
ChEMBL 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 10.1021/jm960320m
DB08839 139 66 None -117 54 Rat 6.7 pKi = 6.7 Binding
Binding affinity towards 5-hydroxytryptamine 4 receptor was determined in rat striatal membranes using [3H]GR-113808 as radioligandBinding affinity towards 5-hydroxytryptamine 4 receptor was determined in rat striatal membranes using [3H]GR-113808 as radioligand
ChEMBL 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 10.1021/jm960320m
10615623 156581 0 None - 1 Rat 6.7 pKi = 6.7 Binding
In vitro affinity at serotonergic 5-hydroxytryptamine 4 receptor by radioligand binding assay using [3H]GR-113808 in rat striatum membranes.In vitro affinity at serotonergic 5-hydroxytryptamine 4 receptor by radioligand binding assay using [3H]GR-113808 in rat striatum membranes.
ChEMBL 319 2 3 4 1.6 Nc1c(Cl)cc(C(=O)NC2CN3CCC2CC3)c2[nH]cnc12 10.1021/jm991076c
CHEMBL407493 156581 0 None - 1 Rat 6.7 pKi = 6.7 Binding
In vitro affinity at serotonergic 5-hydroxytryptamine 4 receptor by radioligand binding assay using [3H]GR-113808 in rat striatum membranes.In vitro affinity at serotonergic 5-hydroxytryptamine 4 receptor by radioligand binding assay using [3H]GR-113808 in rat striatum membranes.
ChEMBL 319 2 3 4 1.6 Nc1c(Cl)cc(C(=O)NC2CN3CCC2CC3)c2[nH]cnc12 10.1021/jm991076c
11527897 133776 0 None - 1 Human 7.7 pKi = 7.7 Binding
Binding affinity for 5-HT4 receptor using [3H]GR-113808Binding affinity for 5-HT4 receptor using [3H]GR-113808
ChEMBL 780 18 4 13 2.9 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCC(C(=O)NCCOCCNC(=O)C2CCN(CCOC(=O)c3cc(Cl)c(N)cc3OC)CC2)CC1 10.1021/jm050234z
CHEMBL371707 133776 0 None - 1 Human 7.7 pKi = 7.7 Binding
Binding affinity for 5-HT4 receptor using [3H]GR-113808Binding affinity for 5-HT4 receptor using [3H]GR-113808
ChEMBL 780 18 4 13 2.9 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCC(C(=O)NCCOCCNC(=O)C2CCN(CCOC(=O)c3cc(Cl)c(N)cc3OC)CC2)CC1 10.1021/jm050234z
182593 3343 4 None -1 3 Guinea pig 7.7 pKi = 7.7 Binding
Displacement of [3H]-GR113808 from 5-HT4R in Dunkin-Hartley guinea pig straitum nuclear membranes after 2 hrs by filter binding methodDisplacement of [3H]-GR113808 from 5-HT4R in Dunkin-Hartley guinea pig straitum nuclear membranes after 2 hrs by filter binding method
ChEMBL 326 6 1 5 3.0 COc1cc(N)c(cc1C(=O)OCCCN1CCCCC1)Cl 10.1039/C8MD00233A
254 3343 4 None -1 3 Guinea pig 7.7 pKi = 7.7 Binding
Displacement of [3H]-GR113808 from 5-HT4R in Dunkin-Hartley guinea pig straitum nuclear membranes after 2 hrs by filter binding methodDisplacement of [3H]-GR113808 from 5-HT4R in Dunkin-Hartley guinea pig straitum nuclear membranes after 2 hrs by filter binding method
ChEMBL 326 6 1 5 3.0 COc1cc(N)c(cc1C(=O)OCCCN1CCCCC1)Cl 10.1039/C8MD00233A
CHEMBL83954 3343 4 None -1 3 Guinea pig 7.7 pKi = 7.7 Binding
Displacement of [3H]-GR113808 from 5-HT4R in Dunkin-Hartley guinea pig straitum nuclear membranes after 2 hrs by filter binding methodDisplacement of [3H]-GR113808 from 5-HT4R in Dunkin-Hartley guinea pig straitum nuclear membranes after 2 hrs by filter binding method
ChEMBL 326 6 1 5 3.0 COc1cc(N)c(cc1C(=O)OCCCN1CCCCC1)Cl 10.1039/C8MD00233A
182593 3343 4 None -1 3 Guinea pig 7.7 pKi = 7.7 Binding
Displacement of [3H]GR113808 from Dunkin-Hartley guinea pig brain striatum 5HT4R after 30 minsDisplacement of [3H]GR113808 from Dunkin-Hartley guinea pig brain striatum 5HT4R after 30 mins
ChEMBL 326 6 1 5 3.0 COc1cc(N)c(cc1C(=O)OCCCN1CCCCC1)Cl 10.1016/j.ejmech.2014.05.015
254 3343 4 None -1 3 Guinea pig 7.7 pKi = 7.7 Binding
Displacement of [3H]GR113808 from Dunkin-Hartley guinea pig brain striatum 5HT4R after 30 minsDisplacement of [3H]GR113808 from Dunkin-Hartley guinea pig brain striatum 5HT4R after 30 mins
ChEMBL 326 6 1 5 3.0 COc1cc(N)c(cc1C(=O)OCCCN1CCCCC1)Cl 10.1016/j.ejmech.2014.05.015
CHEMBL83954 3343 4 None -1 3 Guinea pig 7.7 pKi = 7.7 Binding
Displacement of [3H]GR113808 from Dunkin-Hartley guinea pig brain striatum 5HT4R after 30 minsDisplacement of [3H]GR113808 from Dunkin-Hartley guinea pig brain striatum 5HT4R after 30 mins
ChEMBL 326 6 1 5 3.0 COc1cc(N)c(cc1C(=O)OCCCN1CCCCC1)Cl 10.1016/j.ejmech.2014.05.015
182593 3343 4 None -1 3 Guinea pig 7.7 pKi = 7.7 Binding
Displacement of [3H]GR113808 from serotonin 5-HT4 receptor in Dunkin-Hartley guinea pigs striatal nuclei membranes incubated for 2 hrs by liquid scintillation countingDisplacement of [3H]GR113808 from serotonin 5-HT4 receptor in Dunkin-Hartley guinea pigs striatal nuclei membranes incubated for 2 hrs by liquid scintillation counting
ChEMBL 326 6 1 5 3.0 COc1cc(N)c(cc1C(=O)OCCCN1CCCCC1)Cl 10.1039/C6MD00458J
254 3343 4 None -1 3 Guinea pig 7.7 pKi = 7.7 Binding
Displacement of [3H]GR113808 from serotonin 5-HT4 receptor in Dunkin-Hartley guinea pigs striatal nuclei membranes incubated for 2 hrs by liquid scintillation countingDisplacement of [3H]GR113808 from serotonin 5-HT4 receptor in Dunkin-Hartley guinea pigs striatal nuclei membranes incubated for 2 hrs by liquid scintillation counting
ChEMBL 326 6 1 5 3.0 COc1cc(N)c(cc1C(=O)OCCCN1CCCCC1)Cl 10.1039/C6MD00458J
CHEMBL83954 3343 4 None -1 3 Guinea pig 7.7 pKi = 7.7 Binding
Displacement of [3H]GR113808 from serotonin 5-HT4 receptor in Dunkin-Hartley guinea pigs striatal nuclei membranes incubated for 2 hrs by liquid scintillation countingDisplacement of [3H]GR113808 from serotonin 5-HT4 receptor in Dunkin-Hartley guinea pigs striatal nuclei membranes incubated for 2 hrs by liquid scintillation counting
ChEMBL 326 6 1 5 3.0 COc1cc(N)c(cc1C(=O)OCCCN1CCCCC1)Cl 10.1039/C6MD00458J
9861687 188610 0 None - 1 Guinea pig 7.7 pKi = 7.7 Binding
Displacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatum membraneDisplacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatum membrane
ChEMBL 315 4 0 5 3.7 CCN1CCC(COc2nc3ccsc3n3cccc23)CC1 10.1016/j.bmc.2008.11.045
CHEMBL511312 188610 0 None - 1 Guinea pig 7.7 pKi = 7.7 Binding
Displacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatum membraneDisplacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatum membrane
ChEMBL 315 4 0 5 3.7 CCN1CCC(COc2nc3ccsc3n3cccc23)CC1 10.1016/j.bmc.2008.11.045
67251061 82308 0 None 10 2 Human 7.7 pKi = 7.7 Binding
Displacement of [3H](1-(2-(methylsulfonamido)ethyl)piperidin-4-yl)methyl 1-methyl-1H-indole-3-carboxylate from human 5HT4R expressed in HEK293 cellsDisplacement of [3H](1-(2-(methylsulfonamido)ethyl)piperidin-4-yl)methyl 1-methyl-1H-indole-3-carboxylate from human 5HT4R expressed in HEK293 cells
ChEMBL 443 8 0 5 5.2 COCc1ccc(CCN2CCC(COc3nc4ccccc4c4cn(C)cc34)CC2)cc1 10.1021/jm300573d
CHEMBL2179671 82308 0 None 10 2 Human 7.7 pKi = 7.7 Binding
Displacement of [3H](1-(2-(methylsulfonamido)ethyl)piperidin-4-yl)methyl 1-methyl-1H-indole-3-carboxylate from human 5HT4R expressed in HEK293 cellsDisplacement of [3H](1-(2-(methylsulfonamido)ethyl)piperidin-4-yl)methyl 1-methyl-1H-indole-3-carboxylate from human 5HT4R expressed in HEK293 cells
ChEMBL 443 8 0 5 5.2 COCc1ccc(CCN2CCC(COc3nc4ccccc4c4cn(C)cc34)CC2)cc1 10.1021/jm300573d
11842633 3918 17 None - 1 Human 7.7 pKi = 7.7 Binding
Displacement of [3H]GR113808 from human recombinant 5HT4c receptor expressed in HEK293 cellsDisplacement of [3H]GR113808 from human recombinant 5HT4c receptor expressed in HEK293 cells
ChEMBL 504 8 2 7 1.6 O[C@@H](CN(S(=O)(=O)C)C)CN1[C@@H]2CC[C@H]1CC(C2)NC(=O)c1cc2ccccc2n(c1=O)C(C)C 10.1016/j.bmcl.2012.08.051
8425 3918 17 None - 1 Human 7.7 pKi = 7.7 Binding
Displacement of [3H]GR113808 from human recombinant 5HT4c receptor expressed in HEK293 cellsDisplacement of [3H]GR113808 from human recombinant 5HT4c receptor expressed in HEK293 cells
ChEMBL 504 8 2 7 1.6 O[C@@H](CN(S(=O)(=O)C)C)CN1[C@@H]2CC[C@H]1CC(C2)NC(=O)c1cc2ccccc2n(c1=O)C(C)C 10.1016/j.bmcl.2012.08.051
CHEMBL2087337 3918 17 None - 1 Human 7.7 pKi = 7.7 Binding
Displacement of [3H]GR113808 from human recombinant 5HT4c receptor expressed in HEK293 cellsDisplacement of [3H]GR113808 from human recombinant 5HT4c receptor expressed in HEK293 cells
ChEMBL 504 8 2 7 1.6 O[C@@H](CN(S(=O)(=O)C)C)CN1[C@@H]2CC[C@H]1CC(C2)NC(=O)c1cc2ccccc2n(c1=O)C(C)C 10.1016/j.bmcl.2012.08.051
67276168 77155 0 None - 1 Human 7.7 pKi = 7.7 Binding
Displacement of [3H]GR113808 from human recombinant 5HT4c receptor expressed in HEK293 cellsDisplacement of [3H]GR113808 from human recombinant 5HT4c receptor expressed in HEK293 cells
ChEMBL 490 8 3 7 1.2 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CC(O)CNS(C)(=O)=O)cc2ccccc21 10.1016/j.bmcl.2012.08.051
CHEMBL2087334 77155 0 None - 1 Human 7.7 pKi = 7.7 Binding
Displacement of [3H]GR113808 from human recombinant 5HT4c receptor expressed in HEK293 cellsDisplacement of [3H]GR113808 from human recombinant 5HT4c receptor expressed in HEK293 cells
ChEMBL 490 8 3 7 1.2 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CC(O)CNS(C)(=O)=O)cc2ccccc21 10.1016/j.bmcl.2012.08.051
11432106 77156 0 None - 1 Human 7.7 pKi = 7.7 Binding
Displacement of [3H]GR113808 from human recombinant 5HT4c receptor expressed in HEK293 cellsDisplacement of [3H]GR113808 from human recombinant 5HT4c receptor expressed in HEK293 cells
ChEMBL 504 8 2 7 1.6 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CC(O)CN(C)S(C)(=O)=O)cc2ccccc21 10.1016/j.bmcl.2012.08.051
CHEMBL2087335 77156 0 None - 1 Human 7.7 pKi = 7.7 Binding
Displacement of [3H]GR113808 from human recombinant 5HT4c receptor expressed in HEK293 cellsDisplacement of [3H]GR113808 from human recombinant 5HT4c receptor expressed in HEK293 cells
ChEMBL 504 8 2 7 1.6 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CC(O)CN(C)S(C)(=O)=O)cc2ccccc21 10.1016/j.bmcl.2012.08.051
11519716 193824 0 None - 1 Human 7.7 pKi = 7.7 Binding
Displacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 559 8 2 8 1.2 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CC(O)CN2CCN(S(C)(=O)=O)CC2)cc2ccccc21 10.1021/jm900881j
CHEMBL553405 193824 0 None - 1 Human 7.7 pKi = 7.7 Binding
Displacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 559 8 2 8 1.2 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CC(O)CN2CCN(S(C)(=O)=O)CC2)cc2ccccc21 10.1021/jm900881j
44247941 194115 0 None - 1 Human 7.7 pKi = 7.7 Binding
Displacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 498 9 2 6 3.6 COc1cc(N)c(Cl)cc1C(=O)NC1CCN(CCCCCN2C(=O)c3ccccc3C2=O)CC1 10.1021/jm900881j
CHEMBL557867 194115 0 None - 1 Human 7.7 pKi = 7.7 Binding
Displacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 498 9 2 6 3.6 COc1cc(N)c(Cl)cc1C(=O)NC1CCN(CCCCCN2C(=O)c3ccccc3C2=O)CC1 10.1021/jm900881j
71461047 82558 0 None - 1 Guinea pig 5.7 pKi = 5.7 Binding
Displacement of [3H]GR113808 from 5HT4R in guinea pig striatal membranesDisplacement of [3H]GR113808 from 5HT4R in guinea pig striatal membranes
ChEMBL 364 6 0 4 4.9 CCCN1CCC(COc2nc3cc(OC)ccc3c3ccccc23)CC1 10.1021/jm300943r
CHEMBL2181183 82558 0 None - 1 Guinea pig 5.7 pKi = 5.7 Binding
Displacement of [3H]GR113808 from 5HT4R in guinea pig striatal membranesDisplacement of [3H]GR113808 from 5HT4R in guinea pig striatal membranes
ChEMBL 364 6 0 4 4.9 CCCN1CCC(COc2nc3cc(OC)ccc3c3ccccc23)CC1 10.1021/jm300943r
10028436 3476 3 None -954 12 Human 5.7 pKi = 5.7 Binding
Compound was tested for its binding affinity for 5-hydroxytryptamine 4 receptorCompound was tested for its binding affinity for 5-hydroxytryptamine 4 receptor
ChEMBL 487 7 1 4 4.9 Clc1ccc(cc1)OC1CCN(CC1)CC[C@H]1CCCN1S(=O)(=O)c1ccc2c(c1)[nH]cc2 10.1016/s0960-894x(02)00690-x
3237 3476 3 None -954 12 Human 5.7 pKi = 5.7 Binding
Compound was tested for its binding affinity for 5-hydroxytryptamine 4 receptorCompound was tested for its binding affinity for 5-hydroxytryptamine 4 receptor
ChEMBL 487 7 1 4 4.9 Clc1ccc(cc1)OC1CCN(CC1)CC[C@H]1CCCN1S(=O)(=O)c1ccc2c(c1)[nH]cc2 10.1016/s0960-894x(02)00690-x
CHEMBL95104 3476 3 None -954 12 Human 5.7 pKi = 5.7 Binding
Compound was tested for its binding affinity for 5-hydroxytryptamine 4 receptorCompound was tested for its binding affinity for 5-hydroxytryptamine 4 receptor
ChEMBL 487 7 1 4 4.9 Clc1ccc(cc1)OC1CCN(CC1)CC[C@H]1CCCN1S(=O)(=O)c1ccc2c(c1)[nH]cc2 10.1016/s0960-894x(02)00690-x
11177588 94745 3 None -5 3 Human 5.7 pKi = 5.7 Binding
Displacement of [N-methyl-3H]GR-113808 from human 5HT4 receptor expressed in HEK293 cellsDisplacement of [N-methyl-3H]GR-113808 from human 5HT4 receptor expressed in HEK293 cells
ChEMBL 418 5 6 3 1.1 N=C(N)NCCC[C@@H]1NC(=O)/C(=C/c2c[nH]c3cc(Br)ccc23)NC1=O 10.1021/np0601760
CHEMBL255898 94745 3 None -5 3 Human 5.7 pKi = 5.7 Binding
Displacement of [N-methyl-3H]GR-113808 from human 5HT4 receptor expressed in HEK293 cellsDisplacement of [N-methyl-3H]GR-113808 from human 5HT4 receptor expressed in HEK293 cells
ChEMBL 418 5 6 3 1.1 N=C(N)NCCC[C@@H]1NC(=O)/C(=C/c2c[nH]c3cc(Br)ccc23)NC1=O 10.1021/np0601760
118734519 118171 0 None - 1 Guinea pig 6.7 pKi = 6.7 Binding
Displacement of [3H]GR113808 from 5-HT4R in guinea pig brain membranes incubated for 30 mins by radioligand binding assayDisplacement of [3H]GR113808 from 5-HT4R in guinea pig brain membranes incubated for 30 mins by radioligand binding assay
ChEMBL 407 7 2 5 5.2 COc1cc(N)c(Cl)cc1/C(CCC1CCN(CC2CCCCC2)CC1)=N/O 10.1021/acs.jmedchem.5b00115
CHEMBL3417004 118171 0 None - 1 Guinea pig 6.7 pKi = 6.7 Binding
Displacement of [3H]GR113808 from 5-HT4R in guinea pig brain membranes incubated for 30 mins by radioligand binding assayDisplacement of [3H]GR113808 from 5-HT4R in guinea pig brain membranes incubated for 30 mins by radioligand binding assay
ChEMBL 407 7 2 5 5.2 COc1cc(N)c(Cl)cc1/C(CCC1CCN(CC2CCCCC2)CC1)=N/O 10.1021/acs.jmedchem.5b00115
2274 3124 53 None -17 32 Guinea pig 6.7 pKi = 6.7 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
ChEMBL 373 4 0 4 4.6 CN1CCN(CC1)CCCN1c2ccccc2Sc2c1cc(Cl)cc2 nan
4917 3124 53 None -17 32 Guinea pig 6.7 pKi = 6.7 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
ChEMBL 373 4 0 4 4.6 CN1CCN(CC1)CCCN1c2ccccc2Sc2c1cc(Cl)cc2 nan
7279 3124 53 None -17 32 Guinea pig 6.7 pKi = 6.7 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
ChEMBL 373 4 0 4 4.6 CN1CCN(CC1)CCCN1c2ccccc2Sc2c1cc(Cl)cc2 nan
CHEMBL728 3124 53 None -17 32 Guinea pig 6.7 pKi = 6.7 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
ChEMBL 373 4 0 4 4.6 CN1CCN(CC1)CCCN1c2ccccc2Sc2c1cc(Cl)cc2 nan
DB00433 3124 53 None -17 32 Guinea pig 6.7 pKi = 6.7 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
ChEMBL 373 4 0 4 4.6 CN1CCN(CC1)CCCN1c2ccccc2Sc2c1cc(Cl)cc2 nan
10623729 112587 0 None - 1 Human 6.7 pKi = 6.7 Binding
Binding affinity was determined against cloned 5-hydroxytryptamine 4E receptor isoform expressed in C6 glial cells incubated with 0.2 nM [3H]GR-113808Binding affinity was determined against cloned 5-hydroxytryptamine 4E receptor isoform expressed in C6 glial cells incubated with 0.2 nM [3H]GR-113808
ChEMBL 457 6 1 6 3.9 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCN(c2cccc(C(F)(F)F)c2)CC1 10.1021/jm0009538
CHEMBL331264 112587 0 None - 1 Human 6.7 pKi = 6.7 Binding
Binding affinity was determined against cloned 5-hydroxytryptamine 4E receptor isoform expressed in C6 glial cells incubated with 0.2 nM [3H]GR-113808Binding affinity was determined against cloned 5-hydroxytryptamine 4E receptor isoform expressed in C6 glial cells incubated with 0.2 nM [3H]GR-113808
ChEMBL 457 6 1 6 3.9 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCN(c2cccc(C(F)(F)F)c2)CC1 10.1021/jm0009538
260 3808 49 None -38 6 Human 6.7 pKi = 6.7 Binding
Binding affinity at 5HT4 receptorBinding affinity at 5HT4 receptor
ChEMBL 284 2 1 3 3.0 CN1[C@@H]2CC[C@H]1C[C@H](C2)OC(=O)c1c[nH]c2c1cccc2 10.1016/j.bmc.2008.11.045
2775 3808 49 None -38 6 Human 6.7 pKi = 6.7 Binding
Binding affinity at 5HT4 receptorBinding affinity at 5HT4 receptor
ChEMBL 284 2 1 3 3.0 CN1[C@@H]2CC[C@H]1C[C@H](C2)OC(=O)c1c[nH]c2c1cccc2 10.1016/j.bmc.2008.11.045
656665 3808 49 None -38 6 Human 6.7 pKi = 6.7 Binding
Binding affinity at 5HT4 receptorBinding affinity at 5HT4 receptor
ChEMBL 284 2 1 3 3.0 CN1[C@@H]2CC[C@H]1C[C@H](C2)OC(=O)c1c[nH]c2c1cccc2 10.1016/j.bmc.2008.11.045
CHEMBL56564 3808 49 None -38 6 Human 6.7 pKi = 6.7 Binding
Binding affinity at 5HT4 receptorBinding affinity at 5HT4 receptor
ChEMBL 284 2 1 3 3.0 CN1[C@@H]2CC[C@H]1C[C@H](C2)OC(=O)c1c[nH]c2c1cccc2 10.1016/j.bmc.2008.11.045
DB11699 3808 49 None -38 6 Human 6.7 pKi = 6.7 Binding
Binding affinity at 5HT4 receptorBinding affinity at 5HT4 receptor
ChEMBL 284 2 1 3 3.0 CN1[C@@H]2CC[C@H]1C[C@H](C2)OC(=O)c1c[nH]c2c1cccc2 10.1016/j.bmc.2008.11.045
44628269 82310 0 None 3 2 Human 6.7 pKi = 6.7 Binding
Displacement of [3H](1-(2-(methylsulfonamido)ethyl)piperidin-4-yl)methyl 1-methyl-1H-indole-3-carboxylate from human 5HT4R expressed in HEK293 cellsDisplacement of [3H](1-(2-(methylsulfonamido)ethyl)piperidin-4-yl)methyl 1-methyl-1H-indole-3-carboxylate from human 5HT4R expressed in HEK293 cells
ChEMBL 443 7 1 5 4.8 Cn1cc2c(OCC3CCN(CCc4ccccc4C(=O)O)CC3)nc3ccccc3c2c1 10.1021/jm300573d
CHEMBL2179673 82310 0 None 3 2 Human 6.7 pKi = 6.7 Binding
Displacement of [3H](1-(2-(methylsulfonamido)ethyl)piperidin-4-yl)methyl 1-methyl-1H-indole-3-carboxylate from human 5HT4R expressed in HEK293 cellsDisplacement of [3H](1-(2-(methylsulfonamido)ethyl)piperidin-4-yl)methyl 1-methyl-1H-indole-3-carboxylate from human 5HT4R expressed in HEK293 cells
ChEMBL 443 7 1 5 4.8 Cn1cc2c(OCC3CCN(CCc4ccccc4C(=O)O)CC3)nc3ccccc3c2c1 10.1021/jm300573d
44248317 194225 0 None - 1 Human 6.7 pKi = 6.7 Binding
Displacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 559 12 1 7 2.9 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CCCN(C)CCCN(C)S(C)(=O)=O)cc2ccccc21 10.1021/jm900881j
CHEMBL559050 194225 0 None - 1 Human 6.7 pKi = 6.7 Binding
Displacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 559 12 1 7 2.9 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CCCN(C)CCCN(C)S(C)(=O)=O)cc2ccccc21 10.1021/jm900881j
20030109 194677 0 None - 1 Human 6.7 pKi = 6.7 Binding
Displacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 327 5 3 5 1.1 COc1cc(N)c(Cl)cc1C(=O)NC1CCN(CCO)CC1 10.1021/jm900881j
CHEMBL562477 194677 0 None - 1 Human 6.7 pKi = 6.7 Binding
Displacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 327 5 3 5 1.1 COc1cc(N)c(Cl)cc1C(=O)NC1CCN(CCO)CC1 10.1021/jm900881j
15295138 50789 0 None - 1 Rat 8.7 pKi = 8.7 Binding
Binding affinity towards 5-hydroxytryptamine 4 receptor was determined in rat striatal membranes using [3H]GR-113808 as radioligandBinding affinity towards 5-hydroxytryptamine 4 receptor was determined in rat striatal membranes using [3H]GR-113808 as radioligand
ChEMBL 328 5 2 6 1.5 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCCC(O)C1 10.1021/jm960320m
CHEMBL157880 50789 0 None - 1 Rat 8.7 pKi = 8.7 Binding
Binding affinity towards 5-hydroxytryptamine 4 receptor was determined in rat striatal membranes using [3H]GR-113808 as radioligandBinding affinity towards 5-hydroxytryptamine 4 receptor was determined in rat striatal membranes using [3H]GR-113808 as radioligand
ChEMBL 328 5 2 6 1.5 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCCC(O)C1 10.1021/jm960320m
10741078 112342 0 None - 1 Human 8.7 pKi = 8.7 Binding
Binding affinity was determined against cloned 5-hydroxytryptamine 4E receptor isoform expressed in C6 glial cells incubated with 0.2 nM [3H]GR-113808Binding affinity was determined against cloned 5-hydroxytryptamine 4E receptor isoform expressed in C6 glial cells incubated with 0.2 nM [3H]GR-113808
ChEMBL 425 6 1 8 2.4 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCN(c2ccc(Cl)nn2)CC1 10.1021/jm0009538
CHEMBL330848 112342 0 None - 1 Human 8.7 pKi = 8.7 Binding
Binding affinity was determined against cloned 5-hydroxytryptamine 4E receptor isoform expressed in C6 glial cells incubated with 0.2 nM [3H]GR-113808Binding affinity was determined against cloned 5-hydroxytryptamine 4E receptor isoform expressed in C6 glial cells incubated with 0.2 nM [3H]GR-113808
ChEMBL 425 6 1 8 2.4 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCN(c2ccc(Cl)nn2)CC1 10.1021/jm0009538
42618252 186098 0 None - 1 Human 8.7 pKi = 8.7 Binding
Displacement of [3H]GR-113808 from human 5HT4 isoform E receptor expressed in rat C6 cells by liquid scintillation countingDisplacement of [3H]GR-113808 from human 5HT4 isoform E receptor expressed in rat C6 cells by liquid scintillation counting
ChEMBL 580 13 3 8 3.0 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCC(CNC(=O)CCCNS(=O)(=O)c2ccc(C)cc2)CC1 10.1021/jm801327q
CHEMBL488325 186098 0 None - 1 Human 8.7 pKi = 8.7 Binding
Displacement of [3H]GR-113808 from human 5HT4 isoform E receptor expressed in rat C6 cells by liquid scintillation countingDisplacement of [3H]GR-113808 from human 5HT4 isoform E receptor expressed in rat C6 cells by liquid scintillation counting
ChEMBL 580 13 3 8 3.0 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCC(CNC(=O)CCCNS(=O)(=O)c2ccc(C)cc2)CC1 10.1021/jm801327q
49783209 17427 0 None -3 27 Human 8.7 pKi = 8.7 Binding
Displacement of [3H]GR113808 from human recombinant 5HT4 receptor expressed in HEK293 cellsDisplacement of [3H]GR113808 from human recombinant 5HT4 receptor expressed in HEK293 cells
ChEMBL 396 7 1 6 3.8 CCCCN1CCC(COC(=O)c2cc(Cl)c(NC)c3c2OCCO3)CC1 10.1021/jm100668r
CHEMBL1258223 17427 0 None -3 27 Human 8.7 pKi = 8.7 Binding
Displacement of [3H]GR113808 from human recombinant 5HT4 receptor expressed in HEK293 cellsDisplacement of [3H]GR113808 from human recombinant 5HT4 receptor expressed in HEK293 cells
ChEMBL 396 7 1 6 3.8 CCCCN1CCC(COC(=O)c2cc(Cl)c(NC)c3c2OCCO3)CC1 10.1021/jm100668r
53321958 56160 0 None - 1 Human 8.7 pKi = 8.7 Binding
Displacement of [3H]GR113808 from human 5HT4 receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [3H]GR113808 from human 5HT4 receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 413 8 2 5 3.1 O=C(O)CCCCN1CCC(CNC(=O)c2c3n(c4ccccc24)CCCO3)CC1 10.1016/j.bmc.2010.10.011
CHEMBL1632173 56160 0 None - 1 Human 8.7 pKi = 8.7 Binding
Displacement of [3H]GR113808 from human 5HT4 receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [3H]GR113808 from human 5HT4 receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 413 8 2 5 3.1 O=C(O)CCCCN1CCC(CNC(=O)c2c3n(c4ccccc24)CCCO3)CC1 10.1016/j.bmc.2010.10.011
49783419 17567 0 None -6 13 Human 8.7 pKi = 8.7 Binding
Displacement of [3H]GR113808 from human recombinant 5HT4 receptor expressed in HEK293 cellsDisplacement of [3H]GR113808 from human recombinant 5HT4 receptor expressed in HEK293 cells
ChEMBL 366 6 1 6 2.8 CCCCN1CCC(COC(=O)c2cc(F)c(N)c3c2OCCO3)CC1 10.1021/jm100668r
CHEMBL1258671 17567 0 None -6 13 Human 8.7 pKi = 8.7 Binding
Displacement of [3H]GR113808 from human recombinant 5HT4 receptor expressed in HEK293 cellsDisplacement of [3H]GR113808 from human recombinant 5HT4 receptor expressed in HEK293 cells
ChEMBL 366 6 1 6 2.8 CCCCN1CCC(COC(=O)c2cc(F)c(N)c3c2OCCO3)CC1 10.1021/jm100668r
5324247 206315 1 None - 1 Rat 8.7 pKi = 8.7 Binding
pKi against 5-hydroxytryptamine 4 receptor in rat striatum membranepKi against 5-hydroxytryptamine 4 receptor in rat striatum membrane
ChEMBL 362 5 1 4 3.3 CC(C)CN1CCC(CNC(=O)c2cc(Cl)cc3c2ncn3C)CC1 10.1016/s0960-894x(01)00517-0
CHEMBL97594 206315 1 None - 1 Rat 8.7 pKi = 8.7 Binding
pKi against 5-hydroxytryptamine 4 receptor in rat striatum membranepKi against 5-hydroxytryptamine 4 receptor in rat striatum membrane
ChEMBL 362 5 1 4 3.3 CC(C)CN1CCC(CNC(=O)c2cc(Cl)cc3c2ncn3C)CC1 10.1016/s0960-894x(01)00517-0
5324247 206315 1 None - 1 Rat 8.7 pKi = 8.7 Binding
Binding affinity to 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatum membraneBinding affinity to 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatum membrane
ChEMBL 362 5 1 4 3.3 CC(C)CN1CCC(CNC(=O)c2cc(Cl)cc3c2ncn3C)CC1 10.1021/jm020807x
CHEMBL97594 206315 1 None - 1 Rat 8.7 pKi = 8.7 Binding
Binding affinity to 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatum membraneBinding affinity to 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatum membrane
ChEMBL 362 5 1 4 3.3 CC(C)CN1CCC(CNC(=O)c2cc(Cl)cc3c2ncn3C)CC1 10.1021/jm020807x
71455625 82551 0 None -54 6 Guinea pig 8.7 pKi = 8.7 Binding
Displacement of [3H]GR113808 from 5HT4R in guinea pig striatal membranesDisplacement of [3H]GR113808 from 5HT4R in guinea pig striatal membranes
ChEMBL 353 5 0 4 4.4 CCCN1CCC(COc2nc3c(F)cccc3c3ncccc23)CC1 10.1016/j.bmc.2013.08.061
71455625 82551 0 None -54 6 Guinea pig 8.7 pKi = 8.7 Binding
Displacement of [3H]GR113808 from 5HT4R in guinea pig striatal membranesDisplacement of [3H]GR113808 from 5HT4R in guinea pig striatal membranes
ChEMBL 353 5 0 4 4.4 CCCN1CCC(COc2nc3c(F)cccc3c3ncccc23)CC1 10.1021/jm300943r
CHEMBL2181170 82551 0 None -54 6 Guinea pig 8.7 pKi = 8.7 Binding
Displacement of [3H]GR113808 from 5HT4R in guinea pig striatal membranesDisplacement of [3H]GR113808 from 5HT4R in guinea pig striatal membranes
ChEMBL 353 5 0 4 4.4 CCCN1CCC(COc2nc3c(F)cccc3c3ncccc23)CC1 10.1016/j.bmc.2013.08.061
CHEMBL2181170 82551 0 None -54 6 Guinea pig 8.7 pKi = 8.7 Binding
Displacement of [3H]GR113808 from 5HT4R in guinea pig striatal membranesDisplacement of [3H]GR113808 from 5HT4R in guinea pig striatal membranes
ChEMBL 353 5 0 4 4.4 CCCN1CCC(COc2nc3c(F)cccc3c3ncccc23)CC1 10.1021/jm300943r
257 3437 9 None -1 4 Human 8.7 pKi = 8.7 Binding
Displacement of [3H]GR113808 from human recombinant 5HT4 receptor expressed in HEK293 cellsDisplacement of [3H]GR113808 from human recombinant 5HT4 receptor expressed in HEK293 cells
ChEMBL 474 6 1 6 3.3 CCCCN1CCC(CC1)COC(=O)c1cc(I)c(c2c1OCCO2)N 10.1021/jm100668r
5311423 3437 9 None -1 4 Human 8.7 pKi = 8.7 Binding
Displacement of [3H]GR113808 from human recombinant 5HT4 receptor expressed in HEK293 cellsDisplacement of [3H]GR113808 from human recombinant 5HT4 receptor expressed in HEK293 cells
ChEMBL 474 6 1 6 3.3 CCCCN1CCC(CC1)COC(=O)c1cc(I)c(c2c1OCCO2)N 10.1021/jm100668r
CHEMBL114112 3437 9 None -1 4 Human 8.7 pKi = 8.7 Binding
Displacement of [3H]GR113808 from human recombinant 5HT4 receptor expressed in HEK293 cellsDisplacement of [3H]GR113808 from human recombinant 5HT4 receptor expressed in HEK293 cells
ChEMBL 474 6 1 6 3.3 CCCCN1CCC(CC1)COC(=O)c1cc(I)c(c2c1OCCO2)N 10.1021/jm100668r
5324247 206315 1 None - 1 Rat 8.7 pKi = 8.7 Binding
In vitro binding affinity to 5-hydroxytryptamine 4 receptor in rat striatum membraneIn vitro binding affinity to 5-hydroxytryptamine 4 receptor in rat striatum membrane
ChEMBL 362 5 1 4 3.3 CC(C)CN1CCC(CNC(=O)c2cc(Cl)cc3c2ncn3C)CC1 10.1016/s0960-894x(01)00517-0
CHEMBL97594 206315 1 None - 1 Rat 8.7 pKi = 8.7 Binding
In vitro binding affinity to 5-hydroxytryptamine 4 receptor in rat striatum membraneIn vitro binding affinity to 5-hydroxytryptamine 4 receptor in rat striatum membrane
ChEMBL 362 5 1 4 3.3 CC(C)CN1CCC(CNC(=O)c2cc(Cl)cc3c2ncn3C)CC1 10.1016/s0960-894x(01)00517-0
118734522 118174 0 None - 1 Guinea pig 8.7 pKi = 8.7 Binding
Displacement of [3H]GR113808 from 5-HT4R in guinea pig brain membranes incubated for 30 mins by radioligand binding assayDisplacement of [3H]GR113808 from 5-HT4R in guinea pig brain membranes incubated for 30 mins by radioligand binding assay
ChEMBL 393 6 2 4 4.0 COc1cc(N)c(Cl)cc1C(=O)NCC1CCN(CC2CCCCC2)CC1 10.1021/acs.jmedchem.5b00115
CHEMBL3417007 118174 0 None - 1 Guinea pig 8.7 pKi = 8.7 Binding
Displacement of [3H]GR113808 from 5-HT4R in guinea pig brain membranes incubated for 30 mins by radioligand binding assayDisplacement of [3H]GR113808 from 5-HT4R in guinea pig brain membranes incubated for 30 mins by radioligand binding assay
ChEMBL 393 6 2 4 4.0 COc1cc(N)c(Cl)cc1C(=O)NCC1CCN(CC2CCCCC2)CC1 10.1021/acs.jmedchem.5b00115
15544728 205819 0 None - 1 Rat 8.6 pKi = 8.6 Binding
pKi against 5-hydroxytryptamine 4 receptor in rat striatum membranepKi against 5-hydroxytryptamine 4 receptor in rat striatum membrane
ChEMBL 414 7 2 6 1.6 CS(=O)(=O)NCCN1CCC(COC(=O)c2cc(Cl)cc3[nH]cnc23)CC1 10.1016/s0960-894x(01)00517-0
CHEMBL94784 205819 0 None - 1 Rat 8.6 pKi = 8.6 Binding
pKi against 5-hydroxytryptamine 4 receptor in rat striatum membranepKi against 5-hydroxytryptamine 4 receptor in rat striatum membrane
ChEMBL 414 7 2 6 1.6 CS(=O)(=O)NCCN1CCC(COC(=O)c2cc(Cl)cc3[nH]cnc23)CC1 10.1016/s0960-894x(01)00517-0
15544728 205819 0 None - 1 Rat 8.6 pKi = 8.6 Binding
Binding affinity to 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatum membraneBinding affinity to 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatum membrane
ChEMBL 414 7 2 6 1.6 CS(=O)(=O)NCCN1CCC(COC(=O)c2cc(Cl)cc3[nH]cnc23)CC1 10.1021/jm020807x
CHEMBL94784 205819 0 None - 1 Rat 8.6 pKi = 8.6 Binding
Binding affinity to 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatum membraneBinding affinity to 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatum membrane
ChEMBL 414 7 2 6 1.6 CS(=O)(=O)NCCN1CCC(COC(=O)c2cc(Cl)cc3[nH]cnc23)CC1 10.1021/jm020807x
15544728 205819 0 None - 1 Rat 8.6 pKi = 8.6 Binding
In vitro binding affinity to 5-hydroxytryptamine 4 receptor in rat striatum membraneIn vitro binding affinity to 5-hydroxytryptamine 4 receptor in rat striatum membrane
ChEMBL 414 7 2 6 1.6 CS(=O)(=O)NCCN1CCC(COC(=O)c2cc(Cl)cc3[nH]cnc23)CC1 10.1016/s0960-894x(01)00517-0
CHEMBL94784 205819 0 None - 1 Rat 8.6 pKi = 8.6 Binding
In vitro binding affinity to 5-hydroxytryptamine 4 receptor in rat striatum membraneIn vitro binding affinity to 5-hydroxytryptamine 4 receptor in rat striatum membrane
ChEMBL 414 7 2 6 1.6 CS(=O)(=O)NCCN1CCC(COC(=O)c2cc(Cl)cc3[nH]cnc23)CC1 10.1016/s0960-894x(01)00517-0
249 2528 3 None -1 2 Rat 8.6 pKi = 8.6 Binding
Binding affinity towards 5-hydroxytryptamine 4 receptor was determined in rat striatal membranes using [3H]GR-113808 as radioligandBinding affinity towards 5-hydroxytryptamine 4 receptor was determined in rat striatal membranes using [3H]GR-113808 as radioligand
ChEMBL 340 5 1 5 3.1 COc1cc(N)c(cc1C(=O)OCCN1CC(C)CC(C1)C)Cl 10.1021/jm960320m
9905972 2528 3 None -1 2 Rat 8.6 pKi = 8.6 Binding
Binding affinity towards 5-hydroxytryptamine 4 receptor was determined in rat striatal membranes using [3H]GR-113808 as radioligandBinding affinity towards 5-hydroxytryptamine 4 receptor was determined in rat striatal membranes using [3H]GR-113808 as radioligand
ChEMBL 340 5 1 5 3.1 COc1cc(N)c(cc1C(=O)OCCN1CC(C)CC(C1)C)Cl 10.1021/jm960320m
CHEMBL155917 2528 3 None -1 2 Rat 8.6 pKi = 8.6 Binding
Binding affinity towards 5-hydroxytryptamine 4 receptor was determined in rat striatal membranes using [3H]GR-113808 as radioligandBinding affinity towards 5-hydroxytryptamine 4 receptor was determined in rat striatal membranes using [3H]GR-113808 as radioligand
ChEMBL 340 5 1 5 3.1 COc1cc(N)c(cc1C(=O)OCCN1CC(C)CC(C1)C)Cl 10.1021/jm960320m
10522209 101226 0 None - 1 Rat 8.6 pKi = 8.6 Binding
Binding affinity (Ki+/-SEM) against 5-hydroxytryptamine 4 receptor from cheng Prusoff equation by using [3H]GR-113808 in rat striatumBinding affinity (Ki+/-SEM) against 5-hydroxytryptamine 4 receptor from cheng Prusoff equation by using [3H]GR-113808 in rat striatum
ChEMBL 355 5 2 5 3.5 COc1cc(N)c(Cl)cc1NC(=O)OCCN1CC(C)CC(C)C1 10.1021/jm960853v
CHEMBL299408 101226 0 None - 1 Rat 8.6 pKi = 8.6 Binding
Binding affinity (Ki+/-SEM) against 5-hydroxytryptamine 4 receptor from cheng Prusoff equation by using [3H]GR-113808 in rat striatumBinding affinity (Ki+/-SEM) against 5-hydroxytryptamine 4 receptor from cheng Prusoff equation by using [3H]GR-113808 in rat striatum
ChEMBL 355 5 2 5 3.5 COc1cc(N)c(Cl)cc1NC(=O)OCCN1CC(C)CC(C)C1 10.1021/jm960853v
49783415 17496 0 None -3 13 Human 8.6 pKi = 8.6 Binding
Displacement of [3H]GR113808 from human recombinant 5HT4 receptor expressed in HEK293 cellsDisplacement of [3H]GR113808 from human recombinant 5HT4 receptor expressed in HEK293 cells
ChEMBL 320 7 1 5 2.9 CCCCN1CCC(COC(=O)c2ccc(N)c(OC)c2)CC1 10.1021/jm100668r
CHEMBL1258452 17496 0 None -3 13 Human 8.6 pKi = 8.6 Binding
Displacement of [3H]GR113808 from human recombinant 5HT4 receptor expressed in HEK293 cellsDisplacement of [3H]GR113808 from human recombinant 5HT4 receptor expressed in HEK293 cells
ChEMBL 320 7 1 5 2.9 CCCCN1CCC(COC(=O)c2ccc(N)c(OC)c2)CC1 10.1021/jm100668r
53318013 56162 0 None - 1 Human 8.6 pKi = 8.6 Binding
Displacement of [3H]GR113808 from human 5HT4 receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [3H]GR113808 from human 5HT4 receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 511 15 2 5 5.9 O=C(O)CCCCCCCCCCCN1CCC(CNC(=O)c2c3n(c4ccccc24)CCCO3)CC1 10.1016/j.bmc.2010.10.011
CHEMBL1632175 56162 0 None - 1 Human 8.6 pKi = 8.6 Binding
Displacement of [3H]GR113808 from human 5HT4 receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [3H]GR113808 from human 5HT4 receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 511 15 2 5 5.9 O=C(O)CCCCCCCCCCCN1CCC(CNC(=O)c2c3n(c4ccccc24)CCCO3)CC1 10.1016/j.bmc.2010.10.011
9800656 15375 0 None - 1 Human 8.6 pKi = 8.6 Binding
Binding affinity was determined against cloned 5-hydroxytryptamine 4C receptor isoform expressed in COS-7 cellsBinding affinity was determined against cloned 5-hydroxytryptamine 4C receptor isoform expressed in COS-7 cells
ChEMBL 391 6 1 8 1.7 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCN(c2ncccn2)CC1 10.1021/jm0009538
CHEMBL121913 15375 0 None - 1 Human 8.6 pKi = 8.6 Binding
Binding affinity was determined against cloned 5-hydroxytryptamine 4C receptor isoform expressed in COS-7 cellsBinding affinity was determined against cloned 5-hydroxytryptamine 4C receptor isoform expressed in COS-7 cells
ChEMBL 391 6 1 8 1.7 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCN(c2ncccn2)CC1 10.1021/jm0009538
118734513 120125 0 None - 1 Guinea pig 8.6 pKi = 8.6 Binding
Displacement of [3H]GR113808 from 5-HT4R in guinea pig brain membranes incubated for 30 mins by radioligand binding assayDisplacement of [3H]GR113808 from 5-HT4R in guinea pig brain membranes incubated for 30 mins by radioligand binding assay
ChEMBL 393 7 2 5 3.6 COc1cc(N)c(Cl)cc1C(=O)CCC1CCN(CC2CCNCC2)CC1 10.1021/acs.jmedchem.5b00115
CHEMBL3416998 120125 0 None - 1 Guinea pig 8.6 pKi = 8.6 Binding
Displacement of [3H]GR113808 from 5-HT4R in guinea pig brain membranes incubated for 30 mins by radioligand binding assayDisplacement of [3H]GR113808 from 5-HT4R in guinea pig brain membranes incubated for 30 mins by radioligand binding assay
ChEMBL 393 7 2 5 3.6 COc1cc(N)c(Cl)cc1C(=O)CCC1CCN(CC2CCNCC2)CC1 10.1021/acs.jmedchem.5b00115
CHEMBL3546835 120125 0 None - 1 Guinea pig 8.6 pKi = 8.6 Binding
Displacement of [3H]GR113808 from 5-HT4R in guinea pig brain membranes incubated for 30 mins by radioligand binding assayDisplacement of [3H]GR113808 from 5-HT4R in guinea pig brain membranes incubated for 30 mins by radioligand binding assay
ChEMBL 393 7 2 5 3.6 COc1cc(N)c(Cl)cc1C(=O)CCC1CCN(CC2CCNCC2)CC1 10.1021/acs.jmedchem.5b00115
71459269 82547 0 None -10 8 Guinea pig 8.6 pKi = 8.6 Binding
Displacement of [3H]GR113808 from 5HT4R in guinea pig striatal membranesDisplacement of [3H]GR113808 from 5HT4R in guinea pig striatal membranes
ChEMBL 555 7 0 4 6.3 Fc1cccc2c1nc(OCC1CCN(CCCc3ccc(I)cc3)CC1)c1cccnc12 10.1021/jm300943r
CHEMBL2181166 82547 0 None -10 8 Guinea pig 8.6 pKi = 8.6 Binding
Displacement of [3H]GR113808 from 5HT4R in guinea pig striatal membranesDisplacement of [3H]GR113808 from 5HT4R in guinea pig striatal membranes
ChEMBL 555 7 0 4 6.3 Fc1cccc2c1nc(OCC1CCN(CCCc3ccc(I)cc3)CC1)c1cccnc12 10.1021/jm300943r
243 3153 85 None 12 34 Human 8.6 pKi = 8.6 Binding
Binding affinity at 5HT4 receptorBinding affinity at 5HT4 receptor
ChEMBL 367 6 2 5 2.1 COCCCN1CCC(CC1)NC(=O)c1cc(Cl)c(c2c1OCC2)N 10.1016/j.bmc.2008.11.045
3052762 3153 85 None 12 34 Human 8.6 pKi = 8.6 Binding
Binding affinity at 5HT4 receptorBinding affinity at 5HT4 receptor
ChEMBL 367 6 2 5 2.1 COCCCN1CCC(CC1)NC(=O)c1cc(Cl)c(c2c1OCC2)N 10.1016/j.bmc.2008.11.045
3502 3153 85 None 12 34 Human 8.6 pKi = 8.6 Binding
Binding affinity at 5HT4 receptorBinding affinity at 5HT4 receptor
ChEMBL 367 6 2 5 2.1 COCCCN1CCC(CC1)NC(=O)c1cc(Cl)c(c2c1OCC2)N 10.1016/j.bmc.2008.11.045
CHEMBL117287 3153 85 None 12 34 Human 8.6 pKi = 8.6 Binding
Binding affinity at 5HT4 receptorBinding affinity at 5HT4 receptor
ChEMBL 367 6 2 5 2.1 COCCCN1CCC(CC1)NC(=O)c1cc(Cl)c(c2c1OCC2)N 10.1016/j.bmc.2008.11.045
DB06480 3153 85 None 12 34 Human 8.6 pKi = 8.6 Binding
Binding affinity at 5HT4 receptorBinding affinity at 5HT4 receptor
ChEMBL 367 6 2 5 2.1 COCCCN1CCC(CC1)NC(=O)c1cc(Cl)c(c2c1OCC2)N 10.1016/j.bmc.2008.11.045
44629350 84159 0 None - 1 Human 8.6 pKi = 8.6 Binding
Displacement of [3H](1-(2-(methylsulfonamido)ethyl)piperidin-4-yl)methyl 1-methyl-1H-indole-3-carboxylate from human 5HT4R expressed in HEK293 cellsDisplacement of [3H](1-(2-(methylsulfonamido)ethyl)piperidin-4-yl)methyl 1-methyl-1H-indole-3-carboxylate from human 5HT4R expressed in HEK293 cells
ChEMBL 408 6 0 6 3.2 Cn1cc2c(OCC3CCN(CCN4CCOCC4)CC3)nc3ccccc3c2c1 10.1021/jm300573d
CHEMBL2179676 84159 0 None - 1 Human 8.6 pKi = 8.6 Binding
Displacement of [3H](1-(2-(methylsulfonamido)ethyl)piperidin-4-yl)methyl 1-methyl-1H-indole-3-carboxylate from human 5HT4R expressed in HEK293 cellsDisplacement of [3H](1-(2-(methylsulfonamido)ethyl)piperidin-4-yl)methyl 1-methyl-1H-indole-3-carboxylate from human 5HT4R expressed in HEK293 cells
ChEMBL 408 6 0 6 3.2 Cn1cc2c(OCC3CCN(CCN4CCOCC4)CC3)nc3ccccc3c2c1 10.1021/jm300573d
CHEMBL2220954 84159 0 None - 1 Human 8.6 pKi = 8.6 Binding
Displacement of [3H](1-(2-(methylsulfonamido)ethyl)piperidin-4-yl)methyl 1-methyl-1H-indole-3-carboxylate from human 5HT4R expressed in HEK293 cellsDisplacement of [3H](1-(2-(methylsulfonamido)ethyl)piperidin-4-yl)methyl 1-methyl-1H-indole-3-carboxylate from human 5HT4R expressed in HEK293 cells
ChEMBL 408 6 0 6 3.2 Cn1cc2c(OCC3CCN(CCN4CCOCC4)CC3)nc3ccccc3c2c1 10.1021/jm300573d
67472601 92443 0 None - 1 Human 8.6 pKi = 8.6 Binding
Displacement of [3H]GR113808 from human 5HT4B receptor expressed in HEK293 cellsDisplacement of [3H]GR113808 from human 5HT4B receptor expressed in HEK293 cells
ChEMBL 548 7 1 8 5.3 O=C(OCC1CCN(Cc2ccc(-c3ccccc3-c3nnn[nH]3)cc2)CC1)c1c2n(c3ccccc13)CCCO2 10.1016/j.bmc.2013.09.004
CHEMBL2440456 92443 0 None - 1 Human 8.6 pKi = 8.6 Binding
Displacement of [3H]GR113808 from human 5HT4B receptor expressed in HEK293 cellsDisplacement of [3H]GR113808 from human 5HT4B receptor expressed in HEK293 cells
ChEMBL 548 7 1 8 5.3 O=C(OCC1CCN(Cc2ccc(-c3ccccc3-c3nnn[nH]3)cc2)CC1)c1c2n(c3ccccc13)CCCO2 10.1016/j.bmc.2013.09.004
70686434 76064 0 None - 1 Human 8.6 pKi = 8.6 Binding
Displacement of [3H]GR113808 from human recombinant 5HT4C receptor expressed in HEK293 cellsDisplacement of [3H]GR113808 from human recombinant 5HT4C receptor expressed in HEK293 cells
ChEMBL 560 10 3 8 2.0 CC(C)n1nc(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CC(O)CN2CCC(CNS(C)(=O)=O)CC2)c2ccccc21 10.1016/j.bmcl.2012.05.034
CHEMBL2059583 76064 0 None - 1 Human 8.6 pKi = 8.6 Binding
Displacement of [3H]GR113808 from human recombinant 5HT4C receptor expressed in HEK293 cellsDisplacement of [3H]GR113808 from human recombinant 5HT4C receptor expressed in HEK293 cells
ChEMBL 560 10 3 8 2.0 CC(C)n1nc(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CC(O)CN2CCC(CNS(C)(=O)=O)CC2)c2ccccc21 10.1016/j.bmcl.2012.05.034
70684288 76067 0 None - 1 Human 8.6 pKi = 8.6 Binding
Displacement of [3H]GR113808 from human recombinant 5HT4C receptor expressed in HEK293 cellsDisplacement of [3H]GR113808 from human recombinant 5HT4C receptor expressed in HEK293 cells
ChEMBL 558 11 1 7 3.5 CC(C)n1nc(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CCCCCCN2CCN(S(C)(=O)=O)CC2)c2ccccc21 10.1016/j.bmcl.2012.05.034
CHEMBL2059586 76067 0 None - 1 Human 8.6 pKi = 8.6 Binding
Displacement of [3H]GR113808 from human recombinant 5HT4C receptor expressed in HEK293 cellsDisplacement of [3H]GR113808 from human recombinant 5HT4C receptor expressed in HEK293 cells
ChEMBL 558 11 1 7 3.5 CC(C)n1nc(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CCCCCCN2CCN(S(C)(=O)=O)CC2)c2ccccc21 10.1016/j.bmcl.2012.05.034
11504722 76069 0 None - 1 Human 8.6 pKi = 8.6 Binding
Displacement of [3H]GR113808 from human recombinant 5HT4C receptor expressed in HEK293 cellsDisplacement of [3H]GR113808 from human recombinant 5HT4C receptor expressed in HEK293 cells
ChEMBL 532 8 2 8 1.3 CC(C)n1nc(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3C[C@@H](O)CN2CCN(S(C)(=O)=O)CC2)c2ccccc21 10.1016/j.bmcl.2012.05.034
CHEMBL2059588 76069 0 None - 1 Human 8.6 pKi = 8.6 Binding
Displacement of [3H]GR113808 from human recombinant 5HT4C receptor expressed in HEK293 cellsDisplacement of [3H]GR113808 from human recombinant 5HT4C receptor expressed in HEK293 cells
ChEMBL 532 8 2 8 1.3 CC(C)n1nc(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3C[C@@H](O)CN2CCN(S(C)(=O)=O)CC2)c2ccccc21 10.1016/j.bmcl.2012.05.034
44248922 193231 0 None - 1 Human 8.6 pKi = 8.6 Binding
Displacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 627 14 2 7 4.5 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CCCCCCCN2CCC(CNS(C)(=O)=O)CC2)cc2ccccc21 10.1021/jm900881j
CHEMBL540981 193231 0 None - 1 Human 8.6 pKi = 8.6 Binding
Displacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 627 14 2 7 4.5 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CCCCCCCN2CCC(CNS(C)(=O)=O)CC2)cc2ccccc21 10.1021/jm900881j
44248921 193576 0 None - 1 Human 8.6 pKi = 8.6 Binding
Displacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 520 11 1 5 5.7 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CCCCCCCN2CCCCC2)cc2ccccc21 10.1021/jm900881j
CHEMBL551013 193576 0 None - 1 Human 8.6 pKi = 8.6 Binding
Displacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 520 11 1 5 5.7 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CCCCCCCN2CCCCC2)cc2ccccc21 10.1021/jm900881j
41585 101150 3 None - 1 Rat 8.6 pKi = 8.6 Binding
Binding affinity at 5-hydroxytryptamine 4 receptor in rat striatal membranes by [3H]GR-113808 displacement.Binding affinity at 5-hydroxytryptamine 4 receptor in rat striatal membranes by [3H]GR-113808 displacement.
ChEMBL 292 6 1 4 3.1 CCOc1ccccc1NC(=O)OCCN1CCCCC1 10.1021/jm960853v
CHEMBL298920 101150 3 None - 1 Rat 8.6 pKi = 8.6 Binding
Binding affinity at 5-hydroxytryptamine 4 receptor in rat striatal membranes by [3H]GR-113808 displacement.Binding affinity at 5-hydroxytryptamine 4 receptor in rat striatal membranes by [3H]GR-113808 displacement.
ChEMBL 292 6 1 4 3.1 CCOc1ccccc1NC(=O)OCCN1CCCCC1 10.1021/jm960853v
10566592 185305 0 None - 1 Rat 8.6 pKi = 8.6 Binding
Binding affinity at 5-hydroxytryptamine 4 receptor in rat striatal membranes by [3H]GR-113808 displacement.Binding affinity at 5-hydroxytryptamine 4 receptor in rat striatal membranes by [3H]GR-113808 displacement.
ChEMBL 306 5 1 4 3.2 COc1ccccc1NC(=O)OCCN1C[C@@H](C)C[C@@H](C)C1 10.1021/jm960853v
CHEMBL48684 185305 0 None - 1 Rat 8.6 pKi = 8.6 Binding
Binding affinity at 5-hydroxytryptamine 4 receptor in rat striatal membranes by [3H]GR-113808 displacement.Binding affinity at 5-hydroxytryptamine 4 receptor in rat striatal membranes by [3H]GR-113808 displacement.
ChEMBL 306 5 1 4 3.2 COc1ccccc1NC(=O)OCCN1C[C@@H](C)C[C@@H](C)C1 10.1021/jm960853v
71451950 82263 5 None -1 2 Human 8.6 pKi = 8.6 Binding
Displacement of [3H]GR113808 from human 5HT4D receptor expressed in HEK293 cells after 30 mins by liquid scintillation countingDisplacement of [3H]GR113808 from human 5HT4D receptor expressed in HEK293 cells after 30 mins by liquid scintillation counting
ChEMBL 433 4 2 5 2.4 CC1(C)C(=O)N(C(=O)NCC2CCN(CC3(O)CCOCC3)CC2)c2cc(F)ccc21 10.1021/jm300953p
CHEMBL2179582 82263 5 None -1 2 Human 8.6 pKi = 8.6 Binding
Displacement of [3H]GR113808 from human 5HT4D receptor expressed in HEK293 cells after 30 mins by liquid scintillation countingDisplacement of [3H]GR113808 from human 5HT4D receptor expressed in HEK293 cells after 30 mins by liquid scintillation counting
ChEMBL 433 4 2 5 2.4 CC1(C)C(=O)N(C(=O)NCC2CCN(CC3(O)CCOCC3)CC2)c2cc(F)ccc21 10.1021/jm300953p
53324017 56157 0 None - 1 Human 8.6 pKi = 8.6 Binding
Displacement of [3H]GR113808 from human 5HT4 receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [3H]GR113808 from human 5HT4 receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 371 5 2 5 2.0 O=C(O)CN1CCC(CNC(=O)c2c3n(c4ccccc24)CCCO3)CC1 10.1016/j.bmc.2010.10.011
CHEMBL1632170 56157 0 None - 1 Human 8.6 pKi = 8.6 Binding
Displacement of [3H]GR113808 from human 5HT4 receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [3H]GR113808 from human 5HT4 receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 371 5 2 5 2.0 O=C(O)CN1CCC(CNC(=O)c2c3n(c4ccccc24)CCCO3)CC1 10.1016/j.bmc.2010.10.011
15544727 106758 0 None - 1 Rat 8.5 pKi = 8.5 Binding
pKi against 5-hydroxytryptamine 4 receptor in rat striatum membranepKi against 5-hydroxytryptamine 4 receptor in rat striatum membrane
ChEMBL 349 6 1 4 3.9 CCCCN1CCC(COC(=O)c2cc(Cl)cc3[nH]cnc23)CC1 10.1016/s0960-894x(01)00517-0
CHEMBL316856 106758 0 None - 1 Rat 8.5 pKi = 8.5 Binding
pKi against 5-hydroxytryptamine 4 receptor in rat striatum membranepKi against 5-hydroxytryptamine 4 receptor in rat striatum membrane
ChEMBL 349 6 1 4 3.9 CCCCN1CCC(COC(=O)c2cc(Cl)cc3[nH]cnc23)CC1 10.1016/s0960-894x(01)00517-0
9881053 119740 0 None - 1 Guinea pig 8.5 pKi = 8.5 Binding
Ability to displace [3H]GR-113808 from 5-hydroxytryptamine 4 receptorAbility to displace [3H]GR-113808 from 5-hydroxytryptamine 4 receptor
ChEMBL 339 5 1 4 4.1 CCCN1CCC(COc2nc3ccccc3c3c2CCCN3)CC1 10.1021/jm020954v
CHEMBL35226 119740 0 None - 1 Guinea pig 8.5 pKi = 8.5 Binding
Ability to displace [3H]GR-113808 from 5-hydroxytryptamine 4 receptorAbility to displace [3H]GR-113808 from 5-hydroxytryptamine 4 receptor
ChEMBL 339 5 1 4 4.1 CCCN1CCC(COc2nc3ccccc3c3c2CCCN3)CC1 10.1021/jm020954v
15544727 106758 0 None - 1 Rat 8.5 pKi = 8.5 Binding
Binding affinity to 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatum membraneBinding affinity to 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatum membrane
ChEMBL 349 6 1 4 3.9 CCCCN1CCC(COC(=O)c2cc(Cl)cc3[nH]cnc23)CC1 10.1021/jm020807x
CHEMBL316856 106758 0 None - 1 Rat 8.5 pKi = 8.5 Binding
Binding affinity to 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatum membraneBinding affinity to 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatum membrane
ChEMBL 349 6 1 4 3.9 CCCCN1CCC(COC(=O)c2cc(Cl)cc3[nH]cnc23)CC1 10.1021/jm020807x
15544727 106758 0 None - 1 Rat 8.5 pKi = 8.5 Binding
In vitro binding affinity to 5-hydroxytryptamine 4 receptor in rat striatum membraneIn vitro binding affinity to 5-hydroxytryptamine 4 receptor in rat striatum membrane
ChEMBL 349 6 1 4 3.9 CCCCN1CCC(COC(=O)c2cc(Cl)cc3[nH]cnc23)CC1 10.1016/s0960-894x(01)00517-0
CHEMBL316856 106758 0 None - 1 Rat 8.5 pKi = 8.5 Binding
In vitro binding affinity to 5-hydroxytryptamine 4 receptor in rat striatum membraneIn vitro binding affinity to 5-hydroxytryptamine 4 receptor in rat striatum membrane
ChEMBL 349 6 1 4 3.9 CCCCN1CCC(COC(=O)c2cc(Cl)cc3[nH]cnc23)CC1 10.1016/s0960-894x(01)00517-0
11622025 143214 0 None - 1 Human 7.7 pKi = 7.7 Binding
Binding affinity for 5-HT4 receptor using [3H]GR-113808Binding affinity for 5-HT4 receptor using [3H]GR-113808
ChEMBL 848 23 4 12 6.1 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCC(NC(=O)CCCCCCCCCCNC(=O)C2CCN(CCOC(=O)c3cc(Cl)c(N)cc3OC)CC2)CC1 10.1021/jm050234z
CHEMBL390075 143214 0 None - 1 Human 7.7 pKi = 7.7 Binding
Binding affinity for 5-HT4 receptor using [3H]GR-113808Binding affinity for 5-HT4 receptor using [3H]GR-113808
ChEMBL 848 23 4 12 6.1 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCC(NC(=O)CCCCCCCCCCNC(=O)C2CCN(CCOC(=O)c3cc(Cl)c(N)cc3OC)CC2)CC1 10.1021/jm050234z
240 931 39 None -4 25 Guinea pig 7.7 pKi = 7.7 Binding
Displacement of [3H]-GR113808 from 5-HT4R in Dunkin-Hartley guinea pig straitum nuclear membranes after 2 hrs by filter binding methodDisplacement of [3H]-GR113808 from 5-HT4R in Dunkin-Hartley guinea pig straitum nuclear membranes after 2 hrs by filter binding method
ChEMBL 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N 10.1039/C8MD00233A
2769 931 39 None -4 25 Guinea pig 7.7 pKi = 7.7 Binding
Displacement of [3H]-GR113808 from 5-HT4R in Dunkin-Hartley guinea pig straitum nuclear membranes after 2 hrs by filter binding methodDisplacement of [3H]-GR113808 from 5-HT4R in Dunkin-Hartley guinea pig straitum nuclear membranes after 2 hrs by filter binding method
ChEMBL 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N 10.1039/C8MD00233A
44279790 931 39 None -4 25 Guinea pig 7.7 pKi = 7.7 Binding
Displacement of [3H]-GR113808 from 5-HT4R in Dunkin-Hartley guinea pig straitum nuclear membranes after 2 hrs by filter binding methodDisplacement of [3H]-GR113808 from 5-HT4R in Dunkin-Hartley guinea pig straitum nuclear membranes after 2 hrs by filter binding method
ChEMBL 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N 10.1039/C8MD00233A
660 931 39 None -4 25 Guinea pig 7.7 pKi = 7.7 Binding
Displacement of [3H]-GR113808 from 5-HT4R in Dunkin-Hartley guinea pig straitum nuclear membranes after 2 hrs by filter binding methodDisplacement of [3H]-GR113808 from 5-HT4R in Dunkin-Hartley guinea pig straitum nuclear membranes after 2 hrs by filter binding method
ChEMBL 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N 10.1039/C8MD00233A
CHEMBL1729 931 39 None -4 25 Guinea pig 7.7 pKi = 7.7 Binding
Displacement of [3H]-GR113808 from 5-HT4R in Dunkin-Hartley guinea pig straitum nuclear membranes after 2 hrs by filter binding methodDisplacement of [3H]-GR113808 from 5-HT4R in Dunkin-Hartley guinea pig straitum nuclear membranes after 2 hrs by filter binding method
ChEMBL 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N 10.1039/C8MD00233A
CHEMBL560739 931 39 None -4 25 Guinea pig 7.7 pKi = 7.7 Binding
Displacement of [3H]-GR113808 from 5-HT4R in Dunkin-Hartley guinea pig straitum nuclear membranes after 2 hrs by filter binding methodDisplacement of [3H]-GR113808 from 5-HT4R in Dunkin-Hartley guinea pig straitum nuclear membranes after 2 hrs by filter binding method
ChEMBL 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N 10.1039/C8MD00233A
DB00604 931 39 None -4 25 Guinea pig 7.7 pKi = 7.7 Binding
Displacement of [3H]-GR113808 from 5-HT4R in Dunkin-Hartley guinea pig straitum nuclear membranes after 2 hrs by filter binding methodDisplacement of [3H]-GR113808 from 5-HT4R in Dunkin-Hartley guinea pig straitum nuclear membranes after 2 hrs by filter binding method
ChEMBL 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N 10.1039/C8MD00233A
240 931 39 None -4 25 Guinea pig 7.7 pKi = 7.7 Binding
Displacement of [3H]GR113808 from Dunkin-Hartley guinea pig brain striatum 5HT4R after 30 minsDisplacement of [3H]GR113808 from Dunkin-Hartley guinea pig brain striatum 5HT4R after 30 mins
ChEMBL 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N 10.1016/j.ejmech.2014.05.015
2769 931 39 None -4 25 Guinea pig 7.7 pKi = 7.7 Binding
Displacement of [3H]GR113808 from Dunkin-Hartley guinea pig brain striatum 5HT4R after 30 minsDisplacement of [3H]GR113808 from Dunkin-Hartley guinea pig brain striatum 5HT4R after 30 mins
ChEMBL 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N 10.1016/j.ejmech.2014.05.015
44279790 931 39 None -4 25 Guinea pig 7.7 pKi = 7.7 Binding
Displacement of [3H]GR113808 from Dunkin-Hartley guinea pig brain striatum 5HT4R after 30 minsDisplacement of [3H]GR113808 from Dunkin-Hartley guinea pig brain striatum 5HT4R after 30 mins
ChEMBL 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N 10.1016/j.ejmech.2014.05.015
660 931 39 None -4 25 Guinea pig 7.7 pKi = 7.7 Binding
Displacement of [3H]GR113808 from Dunkin-Hartley guinea pig brain striatum 5HT4R after 30 minsDisplacement of [3H]GR113808 from Dunkin-Hartley guinea pig brain striatum 5HT4R after 30 mins
ChEMBL 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N 10.1016/j.ejmech.2014.05.015
CHEMBL1729 931 39 None -4 25 Guinea pig 7.7 pKi = 7.7 Binding
Displacement of [3H]GR113808 from Dunkin-Hartley guinea pig brain striatum 5HT4R after 30 minsDisplacement of [3H]GR113808 from Dunkin-Hartley guinea pig brain striatum 5HT4R after 30 mins
ChEMBL 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N 10.1016/j.ejmech.2014.05.015
CHEMBL560739 931 39 None -4 25 Guinea pig 7.7 pKi = 7.7 Binding
Displacement of [3H]GR113808 from Dunkin-Hartley guinea pig brain striatum 5HT4R after 30 minsDisplacement of [3H]GR113808 from Dunkin-Hartley guinea pig brain striatum 5HT4R after 30 mins
ChEMBL 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N 10.1016/j.ejmech.2014.05.015
DB00604 931 39 None -4 25 Guinea pig 7.7 pKi = 7.7 Binding
Displacement of [3H]GR113808 from Dunkin-Hartley guinea pig brain striatum 5HT4R after 30 minsDisplacement of [3H]GR113808 from Dunkin-Hartley guinea pig brain striatum 5HT4R after 30 mins
ChEMBL 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N 10.1016/j.ejmech.2014.05.015
5311047 203055 30 None 5 2 Guinea pig 7.7 pKi = 7.7 Binding
Displacement of [3H]GR113808 from serotonin 5-HT4 receptor in Dunkin-Hartley guinea pigs striatal nuclei membranes incubated for 2 hrs by liquid scintillation countingDisplacement of [3H]GR113808 from serotonin 5-HT4 receptor in Dunkin-Hartley guinea pigs striatal nuclei membranes incubated for 2 hrs by liquid scintillation counting
ChEMBL 465 9 2 6 3.4 COc1cc(N)c(Cl)cc1C(=O)N[C@H]1CCN(CCCOc2ccc(F)cc2)C[C@H]1OC 10.1039/C6MD00458J
CHEMBL74656 203055 30 None 5 2 Guinea pig 7.7 pKi = 7.7 Binding
Displacement of [3H]GR113808 from serotonin 5-HT4 receptor in Dunkin-Hartley guinea pigs striatal nuclei membranes incubated for 2 hrs by liquid scintillation countingDisplacement of [3H]GR113808 from serotonin 5-HT4 receptor in Dunkin-Hartley guinea pigs striatal nuclei membranes incubated for 2 hrs by liquid scintillation counting
ChEMBL 465 9 2 6 3.4 COc1cc(N)c(Cl)cc1C(=O)N[C@H]1CCN(CCCOc2ccc(F)cc2)C[C@H]1OC 10.1039/C6MD00458J
71461050 82564 0 None -6 5 Guinea pig 7.7 pKi = 7.7 Binding
Displacement of [3H]GR113808 from 5HT4R in guinea pig striatal membranesDisplacement of [3H]GR113808 from 5HT4R in guinea pig striatal membranes
ChEMBL 352 5 0 3 5.0 CCCN1CCC(COc2nc3c(F)cccc3c3ccccc23)CC1 10.1016/j.bmc.2013.08.061
71461050 82564 0 None -6 5 Guinea pig 7.7 pKi = 7.7 Binding
Displacement of [3H]GR113808 from 5HT4R in guinea pig striatal membranesDisplacement of [3H]GR113808 from 5HT4R in guinea pig striatal membranes
ChEMBL 352 5 0 3 5.0 CCCN1CCC(COc2nc3c(F)cccc3c3ccccc23)CC1 10.1021/jm300943r
CHEMBL2181189 82564 0 None -6 5 Guinea pig 7.7 pKi = 7.7 Binding
Displacement of [3H]GR113808 from 5HT4R in guinea pig striatal membranesDisplacement of [3H]GR113808 from 5HT4R in guinea pig striatal membranes
ChEMBL 352 5 0 3 5.0 CCCN1CCC(COc2nc3c(F)cccc3c3ccccc23)CC1 10.1016/j.bmc.2013.08.061
CHEMBL2181189 82564 0 None -6 5 Guinea pig 7.7 pKi = 7.7 Binding
Displacement of [3H]GR113808 from 5HT4R in guinea pig striatal membranesDisplacement of [3H]GR113808 from 5HT4R in guinea pig striatal membranes
ChEMBL 352 5 0 3 5.0 CCCN1CCC(COc2nc3c(F)cccc3c3ccccc23)CC1 10.1021/jm300943r
118734517 118169 0 None - 1 Guinea pig 7.7 pKi = 7.7 Binding
Displacement of [3H]GR113808 from 5-HT4R in guinea pig brain membranes incubated for 30 mins by radioligand binding assayDisplacement of [3H]GR113808 from 5-HT4R in guinea pig brain membranes incubated for 30 mins by radioligand binding assay
ChEMBL 387 7 1 5 4.2 COc1cc(N)c(Cl)cc1C(=O)CCC1CCN(Cc2cccnc2)CC1 10.1021/acs.jmedchem.5b00115
CHEMBL3417002 118169 0 None - 1 Guinea pig 7.7 pKi = 7.7 Binding
Displacement of [3H]GR113808 from 5-HT4R in guinea pig brain membranes incubated for 30 mins by radioligand binding assayDisplacement of [3H]GR113808 from 5-HT4R in guinea pig brain membranes incubated for 30 mins by radioligand binding assay
ChEMBL 387 7 1 5 4.2 COc1cc(N)c(Cl)cc1C(=O)CCC1CCN(Cc2cccnc2)CC1 10.1021/acs.jmedchem.5b00115
118734518 118170 0 None - 1 Guinea pig 7.7 pKi = 7.7 Binding
Displacement of [3H]GR113808 from 5-HT4R in guinea pig brain membranes incubated for 30 mins by radioligand binding assayDisplacement of [3H]GR113808 from 5-HT4R in guinea pig brain membranes incubated for 30 mins by radioligand binding assay
ChEMBL 387 7 1 5 4.2 COc1cc(N)c(Cl)cc1C(=O)CCC1CCN(Cc2ccncc2)CC1 10.1021/acs.jmedchem.5b00115
CHEMBL3417003 118170 0 None - 1 Guinea pig 7.7 pKi = 7.7 Binding
Displacement of [3H]GR113808 from 5-HT4R in guinea pig brain membranes incubated for 30 mins by radioligand binding assayDisplacement of [3H]GR113808 from 5-HT4R in guinea pig brain membranes incubated for 30 mins by radioligand binding assay
ChEMBL 387 7 1 5 4.2 COc1cc(N)c(Cl)cc1C(=O)CCC1CCN(Cc2ccncc2)CC1 10.1021/acs.jmedchem.5b00115
44592183 178261 0 None - 1 Guinea pig 7.7 pKi = 7.7 Binding
Displacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatum membraneDisplacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatum membrane
ChEMBL 343 6 0 5 4.4 CCCCN1CCC(COc2nc3sccc3n3cccc23)CC1 10.1016/j.bmc.2008.11.045
CHEMBL469379 178261 0 None - 1 Guinea pig 7.7 pKi = 7.7 Binding
Displacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatum membraneDisplacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatum membrane
ChEMBL 343 6 0 5 4.4 CCCCN1CCC(COc2nc3sccc3n3cccc23)CC1 10.1016/j.bmc.2008.11.045
44592109 178509 0 None - 1 Guinea pig 7.7 pKi = 7.7 Binding
Displacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatum membraneDisplacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatum membrane
ChEMBL 343 6 0 5 4.4 CCCCN1CCC(COc2nc3ccsc3n3cccc23)CC1 10.1016/j.bmc.2008.11.045
CHEMBL471663 178509 0 None - 1 Guinea pig 7.7 pKi = 7.7 Binding
Displacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatum membraneDisplacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatum membrane
ChEMBL 343 6 0 5 4.4 CCCCN1CCC(COc2nc3ccsc3n3cccc23)CC1 10.1016/j.bmc.2008.11.045
11686510 71970 0 None - 1 Human 6.7 pKi = 6.7 Binding
Binding affinity for 5-HT4 receptor using [3H]GR-113808Binding affinity for 5-HT4 receptor using [3H]GR-113808
ChEMBL 820 21 2 12 5.4 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCN(C(=O)CCCCCCCCCCC(=O)N2CCN(CCOC(=O)c3cc(Cl)c(N)cc3OC)CC2)CC1 10.1021/jm050234z
CHEMBL198372 71970 0 None - 1 Human 6.7 pKi = 6.7 Binding
Binding affinity for 5-HT4 receptor using [3H]GR-113808Binding affinity for 5-HT4 receptor using [3H]GR-113808
ChEMBL 820 21 2 12 5.4 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCN(C(=O)CCCCCCCCCCC(=O)N2CCN(CCOC(=O)c3cc(Cl)c(N)cc3OC)CC2)CC1 10.1021/jm050234z
1235483 37767 1 None - 1 Rat 6.7 pKi = 6.7 Binding
In vitro affinity at serotonergic 5-hydroxytryptamine 4 receptor by radioligand binding assay using [3H]GR-113808 in rat striatum membranes.In vitro affinity at serotonergic 5-hydroxytryptamine 4 receptor by radioligand binding assay using [3H]GR-113808 in rat striatum membranes.
ChEMBL 304 2 2 3 2.0 O=C(N[C@H]1CN2CCC1CC2)c1cc(Cl)cc2nc[nH]c12 10.1021/jm991076c
CHEMBL146012 37767 1 None - 1 Rat 6.7 pKi = 6.7 Binding
In vitro affinity at serotonergic 5-hydroxytryptamine 4 receptor by radioligand binding assay using [3H]GR-113808 in rat striatum membranes.In vitro affinity at serotonergic 5-hydroxytryptamine 4 receptor by radioligand binding assay using [3H]GR-113808 in rat striatum membranes.
ChEMBL 304 2 2 3 2.0 O=C(N[C@H]1CN2CCC1CC2)c1cc(Cl)cc2nc[nH]c12 10.1021/jm991076c
31703 193050 59 None 1 3 Guinea pig 5.7 pKi = 5.7 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
ChEMBL 543 5 6 12 0.0 COc1cccc2c1C(=O)c1c(O)c3c(c(O)c1C2=O)C[C@@](O)(C(=O)CO)C[C@@H]3O[C@H]1C[C@H](N)[C@H](O)[C@H](C)O1 nan
CHEMBL359744 193050 59 None 1 3 Guinea pig 5.7 pKi = 5.7 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
ChEMBL 543 5 6 12 0.0 COc1cccc2c1C(=O)c1c(O)c3c(c(O)c1C2=O)C[C@@](O)(C(=O)CO)C[C@@H]3O[C@H]1C[C@H](N)[C@H](O)[C@H](C)O1 nan
CHEMBL53463 193050 59 None 1 3 Guinea pig 5.7 pKi = 5.7 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
ChEMBL 543 5 6 12 0.0 COc1cccc2c1C(=O)c1c(O)c3c(c(O)c1C2=O)C[C@@](O)(C(=O)CO)C[C@@H]3O[C@H]1C[C@H](N)[C@H](O)[C@H](C)O1 nan
71452074 82554 0 None - 1 Guinea pig 6.7 pKi = 6.7 Binding
Displacement of [3H]GR113808 from 5HT4R in guinea pig striatal membranesDisplacement of [3H]GR113808 from 5HT4R in guinea pig striatal membranes
ChEMBL 352 5 0 3 5.0 CCCN1CCC(COc2nc3ccccc3c3cc(F)ccc23)CC1 10.1021/jm300943r
CHEMBL2181173 82554 0 None - 1 Guinea pig 6.7 pKi = 6.7 Binding
Displacement of [3H]GR113808 from 5HT4R in guinea pig striatal membranesDisplacement of [3H]GR113808 from 5HT4R in guinea pig striatal membranes
ChEMBL 352 5 0 3 5.0 CCCN1CCC(COc2nc3ccccc3c3cc(F)ccc23)CC1 10.1021/jm300943r
11650641 71745 0 None - 1 Human 7.7 pKi = 7.7 Binding
Binding affinity for 5-HT4 receptor using [3H]GR-113808Binding affinity for 5-HT4 receptor using [3H]GR-113808
ChEMBL 736 15 4 12 3.1 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCC(NC(=O)CCC(=O)NC2CCN(CCOC(=O)c3cc(Cl)c(N)cc3OC)CC2)CC1 10.1021/jm050234z
CHEMBL197751 71745 0 None - 1 Human 7.7 pKi = 7.7 Binding
Binding affinity for 5-HT4 receptor using [3H]GR-113808Binding affinity for 5-HT4 receptor using [3H]GR-113808
ChEMBL 736 15 4 12 3.1 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCC(NC(=O)CCC(=O)NC2CCN(CCOC(=O)c3cc(Cl)c(N)cc3OC)CC2)CC1 10.1021/jm050234z
132337 3487 8 None -1 2 Guinea pig 7.7 pKi = 7.7 Binding
Inhibition of [3H]GR-113808 binding to guinea pig striatum 5-hydroxytryptamine 4 receptorInhibition of [3H]GR-113808 binding to guinea pig striatum 5-hydroxytryptamine 4 receptor
ChEMBL 323 4 2 4 2.1 COc1cc(N)c(cc1C(=O)NC[C@@H]1CCN2[C@H]1CCC2)Cl 10.1021/jm020270n
238 3487 8 None -1 2 Guinea pig 7.7 pKi = 7.7 Binding
Inhibition of [3H]GR-113808 binding to guinea pig striatum 5-hydroxytryptamine 4 receptorInhibition of [3H]GR-113808 binding to guinea pig striatum 5-hydroxytryptamine 4 receptor
ChEMBL 323 4 2 4 2.1 COc1cc(N)c(cc1C(=O)NC[C@@H]1CCN2[C@H]1CCC2)Cl 10.1021/jm020270n
CHEMBL34291 3487 8 None -1 2 Guinea pig 7.7 pKi = 7.7 Binding
Inhibition of [3H]GR-113808 binding to guinea pig striatum 5-hydroxytryptamine 4 receptorInhibition of [3H]GR-113808 binding to guinea pig striatum 5-hydroxytryptamine 4 receptor
ChEMBL 323 4 2 4 2.1 COc1cc(N)c(cc1C(=O)NC[C@@H]1CCN2[C@H]1CCC2)Cl 10.1021/jm020270n
90666008 108804 0 None - 1 Guinea pig 7.7 pKi = 7.7 Binding
Displacement of [3H]-GR113808 from guinea pig 5HT4 receptor by Grossman's methodDisplacement of [3H]-GR113808 from guinea pig 5HT4 receptor by Grossman's method
ChEMBL 383 5 0 5 5.1 Cc1csc2nc(OCC3CCN(CC4CCCC4)CC3)c3cccn3c12 10.1039/C2MD20063E
CHEMBL3218880 108804 0 None - 1 Guinea pig 7.7 pKi = 7.7 Binding
Displacement of [3H]-GR113808 from guinea pig 5HT4 receptor by Grossman's methodDisplacement of [3H]-GR113808 from guinea pig 5HT4 receptor by Grossman's method
ChEMBL 383 5 0 5 5.1 Cc1csc2nc(OCC3CCN(CC4CCCC4)CC3)c3cccn3c12 10.1039/C2MD20063E
71462781 82565 0 None - 1 Guinea pig 7.7 pKi = 7.7 Binding
Displacement of [3H]GR113808 from 5HT4R in guinea pig striatal membranesDisplacement of [3H]GR113808 from 5HT4R in guinea pig striatal membranes
ChEMBL 352 5 0 3 5.0 CCCN1CCC(COc2nc3ccccc3c3cccc(F)c23)CC1 10.1021/jm300943r
CHEMBL2181190 82565 0 None - 1 Guinea pig 7.7 pKi = 7.7 Binding
Displacement of [3H]GR113808 from 5HT4R in guinea pig striatal membranesDisplacement of [3H]GR113808 from 5HT4R in guinea pig striatal membranes
ChEMBL 352 5 0 3 5.0 CCCN1CCC(COc2nc3ccccc3c3cccc(F)c23)CC1 10.1021/jm300943r
71450247 82563 0 None -4 9 Guinea pig 7.7 pKi = 7.7 Binding
Displacement of [3H]GR113808 from 5HT4R in guinea pig striatal membranesDisplacement of [3H]GR113808 from 5HT4R in guinea pig striatal membranes
ChEMBL 368 5 0 3 5.5 CCCN1CCC(COc2nc3c(Cl)cccc3c3ccccc23)CC1 10.1021/jm300943r
CHEMBL2181188 82563 0 None -4 9 Guinea pig 7.7 pKi = 7.7 Binding
Displacement of [3H]GR113808 from 5HT4R in guinea pig striatal membranesDisplacement of [3H]GR113808 from 5HT4R in guinea pig striatal membranes
ChEMBL 368 5 0 3 5.5 CCCN1CCC(COc2nc3c(Cl)cccc3c3ccccc23)CC1 10.1021/jm300943r
90666002 108798 0 None - 1 Guinea pig 6.7 pKi = 6.7 Binding
Displacement of [3H]-GR113808 from guinea pig 5HT4 receptor by Grossman's methodDisplacement of [3H]-GR113808 from guinea pig 5HT4 receptor by Grossman's method
ChEMBL 407 6 0 6 4.8 COc1ccc(CN2CCC(COc3nc4ccsc4n4cccc34)CC2)cc1 10.1039/C2MD20063E
CHEMBL3218874 108798 0 None - 1 Guinea pig 6.7 pKi = 6.7 Binding
Displacement of [3H]-GR113808 from guinea pig 5HT4 receptor by Grossman's methodDisplacement of [3H]-GR113808 from guinea pig 5HT4 receptor by Grossman's method
ChEMBL 407 6 0 6 4.8 COc1ccc(CN2CCC(COc3nc4ccsc4n4cccc34)CC2)cc1 10.1039/C2MD20063E
10760942 106807 0 None - 1 Guinea pig 6.7 pKi = 6.7 Binding
Binding affinity against 5-hydroxytryptamine 4 receptor in guinea pig striatum using [3H]GR-113808 as radioligandBinding affinity against 5-hydroxytryptamine 4 receptor in guinea pig striatum using [3H]GR-113808 as radioligand
ChEMBL 359 4 1 6 1.5 Cc1cccc2c1n(C(C)C)c(=O)n2C(=O)NCCN1CCN(C)CC1 10.1021/jm981098j
CHEMBL317146 106807 0 None - 1 Guinea pig 6.7 pKi = 6.7 Binding
Binding affinity against 5-hydroxytryptamine 4 receptor in guinea pig striatum using [3H]GR-113808 as radioligandBinding affinity against 5-hydroxytryptamine 4 receptor in guinea pig striatum using [3H]GR-113808 as radioligand
ChEMBL 359 4 1 6 1.5 Cc1cccc2c1n(C(C)C)c(=O)n2C(=O)NCCN1CCN(C)CC1 10.1021/jm981098j
44592283 188678 0 None - 1 Guinea pig 7.7 pKi = 7.7 Binding
Displacement of [3H]-GR113808 from guinea pig 5HT4 receptor by Grossman's methodDisplacement of [3H]-GR113808 from guinea pig 5HT4 receptor by Grossman's method
ChEMBL 391 5 0 5 5.1 Cc1csc2nc(OCC3CCN(Cc4ccccc4)CC3)c3cccn3c12 10.1039/C2MD20063E
CHEMBL511837 188678 0 None - 1 Guinea pig 7.7 pKi = 7.7 Binding
Displacement of [3H]-GR113808 from guinea pig 5HT4 receptor by Grossman's methodDisplacement of [3H]-GR113808 from guinea pig 5HT4 receptor by Grossman's method
ChEMBL 391 5 0 5 5.1 Cc1csc2nc(OCC3CCN(Cc4ccccc4)CC3)c3cccn3c12 10.1039/C2MD20063E
72697940 103513 0 None - 1 Guinea pig 7.7 pKi = 7.7 Binding
Displacement of [3H]GR113808 from 5HT4R in guinea pig striatal membranesDisplacement of [3H]GR113808 from 5HT4R in guinea pig striatal membranes
ChEMBL 406 5 0 3 5.6 Fc1cccc2c1nc(OCC1CCN(CCC(F)(F)F)CC1)c1ccccc12 10.1016/j.bmc.2013.08.061
CHEMBL3093194 103513 0 None - 1 Guinea pig 7.7 pKi = 7.7 Binding
Displacement of [3H]GR113808 from 5HT4R in guinea pig striatal membranesDisplacement of [3H]GR113808 from 5HT4R in guinea pig striatal membranes
ChEMBL 406 5 0 3 5.6 Fc1cccc2c1nc(OCC1CCN(CCC(F)(F)F)CC1)c1ccccc12 10.1016/j.bmc.2013.08.061
11810608 206314 0 None - 1 Rat 7.7 pKi = 7.7 Binding
pKi against 5-hydroxytryptamine 4 receptor in rat striatum membranepKi against 5-hydroxytryptamine 4 receptor in rat striatum membrane
ChEMBL 363 6 3 4 3.0 CCCCN1CCC(CNC(=O)c2cc(Cl)c(N)c3[nH]cnc23)CC1 10.1016/s0960-894x(01)00517-0
CHEMBL97591 206314 0 None - 1 Rat 7.7 pKi = 7.7 Binding
pKi against 5-hydroxytryptamine 4 receptor in rat striatum membranepKi against 5-hydroxytryptamine 4 receptor in rat striatum membrane
ChEMBL 363 6 3 4 3.0 CCCCN1CCC(CNC(=O)c2cc(Cl)c(N)c3[nH]cnc23)CC1 10.1016/s0960-894x(01)00517-0
11810608 206314 0 None - 1 Rat 7.7 pKi = 7.7 Binding
Binding affinity to 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatum membraneBinding affinity to 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatum membrane
ChEMBL 363 6 3 4 3.0 CCCCN1CCC(CNC(=O)c2cc(Cl)c(N)c3[nH]cnc23)CC1 10.1021/jm020807x
CHEMBL97591 206314 0 None - 1 Rat 7.7 pKi = 7.7 Binding
Binding affinity to 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatum membraneBinding affinity to 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatum membrane
ChEMBL 363 6 3 4 3.0 CCCCN1CCC(CNC(=O)c2cc(Cl)c(N)c3[nH]cnc23)CC1 10.1021/jm020807x
11810608 206314 0 None - 1 Rat 7.7 pKi = 7.7 Binding
In vitro binding affinity to 5-hydroxytryptamine 4 receptor in rat striatum membraneIn vitro binding affinity to 5-hydroxytryptamine 4 receptor in rat striatum membrane
ChEMBL 363 6 3 4 3.0 CCCCN1CCC(CNC(=O)c2cc(Cl)c(N)c3[nH]cnc23)CC1 10.1016/s0960-894x(01)00517-0
CHEMBL97591 206314 0 None - 1 Rat 7.7 pKi = 7.7 Binding
In vitro binding affinity to 5-hydroxytryptamine 4 receptor in rat striatum membraneIn vitro binding affinity to 5-hydroxytryptamine 4 receptor in rat striatum membrane
ChEMBL 363 6 3 4 3.0 CCCCN1CCC(CNC(=O)c2cc(Cl)c(N)c3[nH]cnc23)CC1 10.1016/s0960-894x(01)00517-0
162670887 182387 0 None 7 2 Guinea pig 7.7 pKi = 7.7 Binding
Displacement of [3H]-GR113808 from guinea pig brain 5HT4 receptor in presence of serotonin incubated for 30 minsDisplacement of [3H]-GR113808 from guinea pig brain 5HT4 receptor in presence of serotonin incubated for 30 mins
ChEMBL 543 11 2 7 4.2 COc1ccc(S(=O)(=O)NCCN2CCC(CCC(=O)c3cc(Cl)c(N)cc3OC)CC2)cc1Cl 10.1016/j.ejmech.2016.05.048
CHEMBL4793078 182387 0 None 7 2 Guinea pig 7.7 pKi = 7.7 Binding
Displacement of [3H]-GR113808 from guinea pig brain 5HT4 receptor in presence of serotonin incubated for 30 minsDisplacement of [3H]-GR113808 from guinea pig brain 5HT4 receptor in presence of serotonin incubated for 30 mins
ChEMBL 543 11 2 7 4.2 COc1ccc(S(=O)(=O)NCCN2CCC(CCC(=O)c3cc(Cl)c(N)cc3OC)CC2)cc1Cl 10.1016/j.ejmech.2016.05.048
71452073 82553 0 None 17 2 Guinea pig 7.6 pKi = 7.6 Binding
Displacement of [3H]GR113808 from 5HT4R in guinea pig striatal membranesDisplacement of [3H]GR113808 from 5HT4R in guinea pig striatal membranes
ChEMBL 335 5 0 4 4.3 CCCN1CCC(COc2nc3ccccc3c3cnccc23)CC1 10.1021/jm300943r
CHEMBL2181172 82553 0 None 17 2 Guinea pig 7.6 pKi = 7.6 Binding
Displacement of [3H]GR113808 from 5HT4R in guinea pig striatal membranesDisplacement of [3H]GR113808 from 5HT4R in guinea pig striatal membranes
ChEMBL 335 5 0 4 4.3 CCCN1CCC(COc2nc3ccccc3c3cnccc23)CC1 10.1021/jm300943r
136118637 75962 0 None - 1 Human 5.7 pKi = 5.7 Binding
Displacement of [3H]GR113808 from human recombinant 5HT4 receptorDisplacement of [3H]GR113808 from human recombinant 5HT4 receptor
ChEMBL 321 1 3 2 2.3 O=C1NC(=S)N/C1=C\c1c[nH]c2c(Br)cccc12 10.1016/j.bmc.2013.09.011
CHEMBL2058697 75962 0 None - 1 Human 5.7 pKi = 5.7 Binding
Displacement of [3H]GR113808 from human recombinant 5HT4 receptorDisplacement of [3H]GR113808 from human recombinant 5HT4 receptor
ChEMBL 321 1 3 2 2.3 O=C1NC(=S)N/C1=C\c1c[nH]c2c(Br)cccc12 10.1016/j.bmc.2013.09.011
3397 203777 104 None 1 2 Guinea pig 5.7 pKi = 5.7 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
ChEMBL 276 3 1 3 3.2 CC(C)C(=O)Nc1ccc([N+](=O)[O-])c(C(F)(F)F)c1 nan
CHEMBL806 203777 104 None 1 2 Guinea pig 5.7 pKi = 5.7 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
ChEMBL 276 3 1 3 3.2 CC(C)C(=O)Nc1ccc([N+](=O)[O-])c(C(F)(F)F)c1 nan
136118649 75969 0 None -2 4 Human 6.7 pKi = 6.7 Binding
Displacement of [3H]GR113808 from human recombinant 5HT4 receptorDisplacement of [3H]GR113808 from human recombinant 5HT4 receptor
ChEMBL 318 1 3 2 2.0 C/N=C1\NC(=O)/C(=C/c2c[nH]c3ccc(Br)cc23)N1 10.1016/j.bmc.2013.09.011
CHEMBL2058704 75969 0 None -2 4 Human 6.7 pKi = 6.7 Binding
Displacement of [3H]GR113808 from human recombinant 5HT4 receptorDisplacement of [3H]GR113808 from human recombinant 5HT4 receptor
ChEMBL 318 1 3 2 2.0 C/N=C1\NC(=O)/C(=C/c2c[nH]c3ccc(Br)cc23)N1 10.1016/j.bmc.2013.09.011
10618741 165127 0 None - 1 Rat 6.6 pKi = 6.6 Binding
In vitro affinity at serotonergic 5-hydroxytryptamine 4 receptor by radioligand binding assay using [3H]GR-113808 in rat striatum membranes.In vitro affinity at serotonergic 5-hydroxytryptamine 4 receptor by radioligand binding assay using [3H]GR-113808 in rat striatum membranes.
ChEMBL 363 2 3 4 1.7 Nc1c(Br)cc(C(=O)NC2CN3CCC2CC3)c2[nH]cnc12 10.1021/jm991076c
CHEMBL424498 165127 0 None - 1 Rat 6.6 pKi = 6.6 Binding
In vitro affinity at serotonergic 5-hydroxytryptamine 4 receptor by radioligand binding assay using [3H]GR-113808 in rat striatum membranes.In vitro affinity at serotonergic 5-hydroxytryptamine 4 receptor by radioligand binding assay using [3H]GR-113808 in rat striatum membranes.
ChEMBL 363 2 3 4 1.7 Nc1c(Br)cc(C(=O)NC2CN3CCC2CC3)c2[nH]cnc12 10.1021/jm991076c
44281492 118367 2 None - 1 Rat 7.6 pKi = 7.6 Binding
Binding affinity against 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatumBinding affinity against 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatum
ChEMBL 298 3 1 5 2.2 COc1cc(N)c(Cl)cc1C(=O)OC1CCN(C)CC1 10.1016/S0960-894X(01)80508-4
CHEMBL34224 118367 2 None - 1 Rat 7.6 pKi = 7.6 Binding
Binding affinity against 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatumBinding affinity against 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatum
ChEMBL 298 3 1 5 2.2 COc1cc(N)c(Cl)cc1C(=O)OC1CCN(C)CC1 10.1016/S0960-894X(01)80508-4
10408029 16283 0 None - 1 Human 7.6 pKi = 7.6 Binding
Binding affinity was determined against cloned 5-hydroxytryptamine 4A receptor isoform expressed in COS-7 cellsBinding affinity was determined against cloned 5-hydroxytryptamine 4A receptor isoform expressed in COS-7 cells
ChEMBL 389 6 1 6 2.9 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCN(c2ccccc2)CC1 10.1021/jm0009538
CHEMBL123377 16283 0 None - 1 Human 7.6 pKi = 7.6 Binding
Binding affinity was determined against cloned 5-hydroxytryptamine 4A receptor isoform expressed in COS-7 cellsBinding affinity was determined against cloned 5-hydroxytryptamine 4A receptor isoform expressed in COS-7 cells
ChEMBL 389 6 1 6 2.9 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCN(c2ccccc2)CC1 10.1021/jm0009538
10834000 16153 0 None - 1 Human 7.6 pKi = 7.6 Binding
Binding affinity was determined against cloned 5-hydroxytryptamine 4E receptor isoform expressed in C6 glial cells incubated with 0.2 nM [3H]GR-113808Binding affinity was determined against cloned 5-hydroxytryptamine 4E receptor isoform expressed in C6 glial cells incubated with 0.2 nM [3H]GR-113808
ChEMBL 385 6 1 7 1.9 CCOC(=O)N1CCN(CCOC(=O)c2cc(Cl)c(N)cc2OC)CC1 10.1021/jm0009538
CHEMBL122818 16153 0 None - 1 Human 7.6 pKi = 7.6 Binding
Binding affinity was determined against cloned 5-hydroxytryptamine 4E receptor isoform expressed in C6 glial cells incubated with 0.2 nM [3H]GR-113808Binding affinity was determined against cloned 5-hydroxytryptamine 4E receptor isoform expressed in C6 glial cells incubated with 0.2 nM [3H]GR-113808
ChEMBL 385 6 1 7 1.9 CCOC(=O)N1CCN(CCOC(=O)c2cc(Cl)c(N)cc2OC)CC1 10.1021/jm0009538
10669143 113755 0 None - 1 Human 7.6 pKi = 7.6 Binding
Binding affinity was determined against cloned 5-hydroxytryptamine 4E receptor isoform expressed in C6 glial cells incubated with 0.2 nM [3H]GR-113808Binding affinity was determined against cloned 5-hydroxytryptamine 4E receptor isoform expressed in C6 glial cells incubated with 0.2 nM [3H]GR-113808
ChEMBL 407 6 1 6 3.0 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCN(c2ccc(F)cc2)CC1 10.1021/jm0009538
CHEMBL333028 113755 0 None - 1 Human 7.6 pKi = 7.6 Binding
Binding affinity was determined against cloned 5-hydroxytryptamine 4E receptor isoform expressed in C6 glial cells incubated with 0.2 nM [3H]GR-113808Binding affinity was determined against cloned 5-hydroxytryptamine 4E receptor isoform expressed in C6 glial cells incubated with 0.2 nM [3H]GR-113808
ChEMBL 407 6 1 6 3.0 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCN(c2ccc(F)cc2)CC1 10.1021/jm0009538
6604794 37424 7 None - 1 Guinea pig 7.6 pKi = 7.6 Binding
Binding affinity for 5-hydroxytryptamine 4 receptor by displacement of [3H]GR-113808 from guinea pig brain striatum.Binding affinity for 5-hydroxytryptamine 4 receptor by displacement of [3H]GR-113808 from guinea pig brain striatum.
ChEMBL 346 3 1 4 3.1 CC(C)n1cnc2c(C(=O)N[C@H]3CN4CCC3CC4)cc(Cl)cc21 10.1016/0960-894X(96)00052-2
CHEMBL145725 37424 7 None - 1 Guinea pig 7.6 pKi = 7.6 Binding
Binding affinity for 5-hydroxytryptamine 4 receptor by displacement of [3H]GR-113808 from guinea pig brain striatum.Binding affinity for 5-hydroxytryptamine 4 receptor by displacement of [3H]GR-113808 from guinea pig brain striatum.
ChEMBL 346 3 1 4 3.1 CC(C)n1cnc2c(C(=O)N[C@H]3CN4CCC3CC4)cc(Cl)cc21 10.1016/0960-894X(96)00052-2
5 139 66 None -190 54 Guinea pig 6.6 pKi = 6.6 Binding
The compound was tested for their binding affinity towards 5-hydroxytryptamine 4 receptor from guinea pig striatum using [3H]GR-113808 as radioligand.The compound was tested for their binding affinity towards 5-hydroxytryptamine 4 receptor from guinea pig striatum using [3H]GR-113808 as radioligand.
ChEMBL 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 10.1021/jm00014a021
5202 139 66 None -190 54 Guinea pig 6.6 pKi = 6.6 Binding
The compound was tested for their binding affinity towards 5-hydroxytryptamine 4 receptor from guinea pig striatum using [3H]GR-113808 as radioligand.The compound was tested for their binding affinity towards 5-hydroxytryptamine 4 receptor from guinea pig striatum using [3H]GR-113808 as radioligand.
ChEMBL 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 10.1021/jm00014a021
CHEMBL39 139 66 None -190 54 Guinea pig 6.6 pKi = 6.6 Binding
The compound was tested for their binding affinity towards 5-hydroxytryptamine 4 receptor from guinea pig striatum using [3H]GR-113808 as radioligand.The compound was tested for their binding affinity towards 5-hydroxytryptamine 4 receptor from guinea pig striatum using [3H]GR-113808 as radioligand.
ChEMBL 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 10.1021/jm00014a021
DB08839 139 66 None -190 54 Guinea pig 6.6 pKi = 6.6 Binding
The compound was tested for their binding affinity towards 5-hydroxytryptamine 4 receptor from guinea pig striatum using [3H]GR-113808 as radioligand.The compound was tested for their binding affinity towards 5-hydroxytryptamine 4 receptor from guinea pig striatum using [3H]GR-113808 as radioligand.
ChEMBL 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 10.1021/jm00014a021
10069545 56282 0 None -831 3 Rat 6.6 pKi = 6.6 Binding
Binding affinity against 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatumBinding affinity against 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatum
ChEMBL 399 5 2 4 3.9 COc1cc(N)c(Cl)cc1C(=O)NC1CC2CCC(C1)N2Cc1ccccc1 10.1016/0960-894X(95)00115-A
CHEMBL164169 56282 0 None -831 3 Rat 6.6 pKi = 6.6 Binding
Binding affinity against 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatumBinding affinity against 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatum
ChEMBL 399 5 2 4 3.9 COc1cc(N)c(Cl)cc1C(=O)NC1CC2CCC(C1)N2Cc1ccccc1 10.1016/0960-894X(95)00115-A
71462780 82557 0 None - 1 Guinea pig 6.6 pKi = 6.6 Binding
Displacement of [3H]GR113808 from 5HT4R in guinea pig striatal membranesDisplacement of [3H]GR113808 from 5HT4R in guinea pig striatal membranes
ChEMBL 364 6 0 4 4.9 CCCN1CCC(COc2nc3ccc(OC)cc3c3ccccc23)CC1 10.1021/jm300943r
CHEMBL2181181 82557 0 None - 1 Guinea pig 6.6 pKi = 6.6 Binding
Displacement of [3H]GR113808 from 5HT4R in guinea pig striatal membranesDisplacement of [3H]GR113808 from 5HT4R in guinea pig striatal membranes
ChEMBL 364 6 0 4 4.9 CCCN1CCC(COc2nc3ccc(OC)cc3c3ccccc23)CC1 10.1021/jm300943r
10069545 56282 0 None -831 3 Guinea pig 6.6 pKi = 6.6 Binding
Inhibition of [3H]GR-113808 binding to guinea pig striatum 5-hydroxytryptamine 4 receptorInhibition of [3H]GR-113808 binding to guinea pig striatum 5-hydroxytryptamine 4 receptor
ChEMBL 399 5 2 4 3.9 COc1cc(N)c(Cl)cc1C(=O)NC1CC2CCC(C1)N2Cc1ccccc1 10.1021/jm020270n
CHEMBL164169 56282 0 None -831 3 Guinea pig 6.6 pKi = 6.6 Binding
Inhibition of [3H]GR-113808 binding to guinea pig striatum 5-hydroxytryptamine 4 receptorInhibition of [3H]GR-113808 binding to guinea pig striatum 5-hydroxytryptamine 4 receptor
ChEMBL 399 5 2 4 3.9 COc1cc(N)c(Cl)cc1C(=O)NC1CC2CCC(C1)N2Cc1ccccc1 10.1021/jm020270n
136118646 75966 0 None -2 2 Human 5.6 pKi = 5.6 Binding
Displacement of [3H]GR113808 from human recombinant 5HT4 receptorDisplacement of [3H]GR113808 from human recombinant 5HT4 receptor
ChEMBL 335 1 2 3 3.1 CSC1=NC(=O)/C(=C/c2c[nH]c3c(Br)cccc23)N1 10.1016/j.bmc.2013.09.011
CHEMBL2058701 75966 0 None -2 2 Human 5.6 pKi = 5.6 Binding
Displacement of [3H]GR113808 from human recombinant 5HT4 receptorDisplacement of [3H]GR113808 from human recombinant 5HT4 receptor
ChEMBL 335 1 2 3 3.1 CSC1=NC(=O)/C(=C/c2c[nH]c3c(Br)cccc23)N1 10.1016/j.bmc.2013.09.011
136118635 75959 0 None -6 3 Human 5.6 pKi = 5.6 Binding
Displacement of [3H]GR113808 from human recombinant 5HT4 receptorDisplacement of [3H]GR113808 from human recombinant 5HT4 receptor
ChEMBL 321 1 3 2 2.3 O=C1NC(=S)N/C1=C\c1c[nH]c2cccc(Br)c12 10.1016/j.bmc.2013.09.011
CHEMBL2058694 75959 0 None -6 3 Human 5.6 pKi = 5.6 Binding
Displacement of [3H]GR113808 from human recombinant 5HT4 receptorDisplacement of [3H]GR113808 from human recombinant 5HT4 receptor
ChEMBL 321 1 3 2 2.3 O=C1NC(=S)N/C1=C\c1c[nH]c2cccc(Br)c12 10.1016/j.bmc.2013.09.011
11549456 78642 0 None - 1 Human 7.6 pKi = 7.6 Binding
Binding affinity for 5-HT4 receptor using [3H]GR-113808Binding affinity for 5-HT4 receptor using [3H]GR-113808
ChEMBL 736 15 4 12 3.0 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCC(NC(=O)CCNC(=O)C2CCN(CCOC(=O)c3cc(Cl)c(N)cc3OC)CC2)CC1 10.1021/jm050234z
CHEMBL2113157 78642 0 None - 1 Human 7.6 pKi = 7.6 Binding
Binding affinity for 5-HT4 receptor using [3H]GR-113808Binding affinity for 5-HT4 receptor using [3H]GR-113808
ChEMBL 736 15 4 12 3.0 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCC(NC(=O)CCNC(=O)C2CCN(CCOC(=O)c3cc(Cl)c(N)cc3OC)CC2)CC1 10.1021/jm050234z
11146533 106568 0 None - 1 Human 7.6 pKi = 7.6 Binding
Binding affinity towards cloned human 5-hydroxytryptamine 4E receptor expressed in C6 glial cells using [3H]GR-113808 as radioligandBinding affinity towards cloned human 5-hydroxytryptamine 4E receptor expressed in C6 glial cells using [3H]GR-113808 as radioligand
ChEMBL 616 13 2 8 5.2 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCC(CCCCNS(=O)(=O)c2cccc3c(N(C)C)cccc23)CC1 10.1021/jm0307887
CHEMBL315590 106568 0 None - 1 Human 7.6 pKi = 7.6 Binding
Binding affinity towards cloned human 5-hydroxytryptamine 4E receptor expressed in C6 glial cells using [3H]GR-113808 as radioligandBinding affinity towards cloned human 5-hydroxytryptamine 4E receptor expressed in C6 glial cells using [3H]GR-113808 as radioligand
ChEMBL 616 13 2 8 5.2 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCC(CCCCNS(=O)(=O)c2cccc3c(N(C)C)cccc23)CC1 10.1021/jm0307887
162668604 182004 0 None 6 2 Guinea pig 7.6 pKi = 7.6 Binding
Displacement of [3H]-GR113808 from guinea pig brain 5HT4 receptor in presence of serotonin incubated for 30 minsDisplacement of [3H]-GR113808 from guinea pig brain 5HT4 receptor in presence of serotonin incubated for 30 mins
ChEMBL 587 11 2 7 4.4 COc1ccc(S(=O)(=O)NCCN2CCC(CCC(=O)c3cc(Cl)c(N)cc3OC)CC2)cc1Br 10.1016/j.ejmech.2016.05.048
CHEMBL4788022 182004 0 None 6 2 Guinea pig 7.6 pKi = 7.6 Binding
Displacement of [3H]-GR113808 from guinea pig brain 5HT4 receptor in presence of serotonin incubated for 30 minsDisplacement of [3H]-GR113808 from guinea pig brain 5HT4 receptor in presence of serotonin incubated for 30 mins
ChEMBL 587 11 2 7 4.4 COc1ccc(S(=O)(=O)NCCN2CCC(CCC(=O)c3cc(Cl)c(N)cc3OC)CC2)cc1Br 10.1016/j.ejmech.2016.05.048
15544722 205814 1 None - 1 Rat 7.6 pKi = 7.6 Binding
pKi against 5-hydroxytryptamine 4 receptor in rat striatum membranepKi against 5-hydroxytryptamine 4 receptor in rat striatum membrane
ChEMBL 315 6 1 4 3.2 CCCCN1CCC(COC(=O)c2cccc3[nH]cnc23)CC1 10.1016/s0960-894x(01)00517-0
CHEMBL94756 205814 1 None - 1 Rat 7.6 pKi = 7.6 Binding
pKi against 5-hydroxytryptamine 4 receptor in rat striatum membranepKi against 5-hydroxytryptamine 4 receptor in rat striatum membrane
ChEMBL 315 6 1 4 3.2 CCCCN1CCC(COC(=O)c2cccc3[nH]cnc23)CC1 10.1016/s0960-894x(01)00517-0
15544722 205814 1 None - 1 Rat 7.6 pKi = 7.6 Binding
Binding affinity to 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatum membraneBinding affinity to 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatum membrane
ChEMBL 315 6 1 4 3.2 CCCCN1CCC(COC(=O)c2cccc3[nH]cnc23)CC1 10.1021/jm020807x
CHEMBL94756 205814 1 None - 1 Rat 7.6 pKi = 7.6 Binding
Binding affinity to 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatum membraneBinding affinity to 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatum membrane
ChEMBL 315 6 1 4 3.2 CCCCN1CCC(COC(=O)c2cccc3[nH]cnc23)CC1 10.1021/jm020807x
15544722 205814 1 None - 1 Rat 7.6 pKi = 7.6 Binding
In vitro binding affinity to 5-hydroxytryptamine 4 receptor in rat striatum membraneIn vitro binding affinity to 5-hydroxytryptamine 4 receptor in rat striatum membrane
ChEMBL 315 6 1 4 3.2 CCCCN1CCC(COC(=O)c2cccc3[nH]cnc23)CC1 10.1016/s0960-894x(01)00517-0
CHEMBL94756 205814 1 None - 1 Rat 7.6 pKi = 7.6 Binding
In vitro binding affinity to 5-hydroxytryptamine 4 receptor in rat striatum membraneIn vitro binding affinity to 5-hydroxytryptamine 4 receptor in rat striatum membrane
ChEMBL 315 6 1 4 3.2 CCCCN1CCC(COC(=O)c2cccc3[nH]cnc23)CC1 10.1016/s0960-894x(01)00517-0
10811181 162943 0 None - 1 Human 6.6 pKi = 6.6 Binding
Binding affinity was determined against cloned 5-hydroxytryptamine 4E receptor isoform expressed in C6 glial cells incubated with 0.2 nM [3H]GR-113808Binding affinity was determined against cloned 5-hydroxytryptamine 4E receptor isoform expressed in C6 glial cells incubated with 0.2 nM [3H]GR-113808
ChEMBL 403 7 1 6 2.9 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCN(Cc2ccccc2)CC1 10.1021/jm0009538
CHEMBL420166 162943 0 None - 1 Human 6.6 pKi = 6.6 Binding
Binding affinity was determined against cloned 5-hydroxytryptamine 4E receptor isoform expressed in C6 glial cells incubated with 0.2 nM [3H]GR-113808Binding affinity was determined against cloned 5-hydroxytryptamine 4E receptor isoform expressed in C6 glial cells incubated with 0.2 nM [3H]GR-113808
ChEMBL 403 7 1 6 2.9 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCN(Cc2ccccc2)CC1 10.1021/jm0009538
44299805 100615 0 None - 1 Guinea pig 6.6 pKi = 6.6 Binding
Binding affinity towards 5-HT4 receptor in striatum membranes of guinea-pig brain was evaluatedBinding affinity towards 5-HT4 receptor in striatum membranes of guinea-pig brain was evaluated
ChEMBL 324 3 1 5 2.6 COc1cc(N)c(Cl)cc1C(=O)OC1CC2CCC1CN2C 10.1016/s0960-894x(01)00693-x
CHEMBL294894 100615 0 None - 1 Guinea pig 6.6 pKi = 6.6 Binding
Binding affinity towards 5-HT4 receptor in striatum membranes of guinea-pig brain was evaluatedBinding affinity towards 5-HT4 receptor in striatum membranes of guinea-pig brain was evaluated
ChEMBL 324 3 1 5 2.6 COc1cc(N)c(Cl)cc1C(=O)OC1CC2CCC1CN2C 10.1016/s0960-894x(01)00693-x
9947817 4978 0 None -436 9 Human 5.6 pKi = 5.6 Binding
In vitro binding affinity by radioligand binding assay using cell line expressing human 5-hydroxytryptamine 4 receptorIn vitro binding affinity by radioligand binding assay using cell line expressing human 5-hydroxytryptamine 4 receptor
ChEMBL 286 3 2 3 2.7 CCC(=O)Nc1ccc2[nH]cc(C3CCN(C)CC3)c2n1 10.1021/jm030020m
CHEMBL105261 4978 0 None -436 9 Human 5.6 pKi = 5.6 Binding
In vitro binding affinity by radioligand binding assay using cell line expressing human 5-hydroxytryptamine 4 receptorIn vitro binding affinity by radioligand binding assay using cell line expressing human 5-hydroxytryptamine 4 receptor
ChEMBL 286 3 2 3 2.7 CCC(=O)Nc1ccc2[nH]cc(C3CCN(C)CC3)c2n1 10.1021/jm030020m
107 141 116 None -389 30 Human 6.6 pKi = 6.6 Binding
Displacement of [3H]GR-113808 from human recombinant 5HT4b receptor expressed in HEK293 cells by scintillation countingDisplacement of [3H]GR-113808 from human recombinant 5HT4b receptor expressed in HEK293 cells by scintillation counting
ChEMBL 190 3 2 2 1.7 NCCc1c[nH]c2c1cc(OC)cc2 10.1016/j.ejmech.2009.01.015
1833 141 116 None -389 30 Human 6.6 pKi = 6.6 Binding
Displacement of [3H]GR-113808 from human recombinant 5HT4b receptor expressed in HEK293 cells by scintillation countingDisplacement of [3H]GR-113808 from human recombinant 5HT4b receptor expressed in HEK293 cells by scintillation counting
ChEMBL 190 3 2 2 1.7 NCCc1c[nH]c2c1cc(OC)cc2 10.1016/j.ejmech.2009.01.015
CHEMBL8165 141 116 None -389 30 Human 6.6 pKi = 6.6 Binding
Displacement of [3H]GR-113808 from human recombinant 5HT4b receptor expressed in HEK293 cells by scintillation countingDisplacement of [3H]GR-113808 from human recombinant 5HT4b receptor expressed in HEK293 cells by scintillation counting
ChEMBL 190 3 2 2 1.7 NCCc1c[nH]c2c1cc(OC)cc2 10.1016/j.ejmech.2009.01.015
5 139 66 None -288 54 Human 6.6 pKi = 6.6 Binding
Binding affinity to recombinant human brain 5HT4 receptor by radio ligand binding assayBinding affinity to recombinant human brain 5HT4 receptor by radio ligand binding assay
ChEMBL 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 10.1016/j.ejmech.2019.111596
5202 139 66 None -288 54 Human 6.6 pKi = 6.6 Binding
Binding affinity to recombinant human brain 5HT4 receptor by radio ligand binding assayBinding affinity to recombinant human brain 5HT4 receptor by radio ligand binding assay
ChEMBL 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 10.1016/j.ejmech.2019.111596
CHEMBL39 139 66 None -288 54 Human 6.6 pKi = 6.6 Binding
Binding affinity to recombinant human brain 5HT4 receptor by radio ligand binding assayBinding affinity to recombinant human brain 5HT4 receptor by radio ligand binding assay
ChEMBL 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 10.1016/j.ejmech.2019.111596
DB08839 139 66 None -288 54 Human 6.6 pKi = 6.6 Binding
Binding affinity to recombinant human brain 5HT4 receptor by radio ligand binding assayBinding affinity to recombinant human brain 5HT4 receptor by radio ligand binding assay
ChEMBL 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 10.1016/j.ejmech.2019.111596
71459270 82556 0 None - 1 Guinea pig 6.6 pKi = 6.6 Binding
Displacement of [3H]GR113808 from 5HT4R in guinea pig striatal membranesDisplacement of [3H]GR113808 from 5HT4R in guinea pig striatal membranes
ChEMBL 348 5 0 3 5.2 CCCN1CCC(COc2nc3ccc(C)cc3c3ccccc23)CC1 10.1021/jm300943r
CHEMBL2181180 82556 0 None - 1 Guinea pig 6.6 pKi = 6.6 Binding
Displacement of [3H]GR113808 from 5HT4R in guinea pig striatal membranesDisplacement of [3H]GR113808 from 5HT4R in guinea pig striatal membranes
ChEMBL 348 5 0 3 5.2 CCCN1CCC(COc2nc3ccc(C)cc3c3ccccc23)CC1 10.1021/jm300943r
441383 20133 54 None -5 17 Guinea pig 5.6 pKi = 5.6 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
ChEMBL 531 8 0 8 4.5 CC(C)N1CCN(c2ccc(OC[C@H]3CO[C@](Cn4cncn4)(c4ccc(Cl)cc4Cl)O3)cc2)CC1 nan
CHEMBL1306 20133 54 None -5 17 Guinea pig 5.6 pKi = 5.6 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
ChEMBL 531 8 0 8 4.5 CC(C)N1CCN(c2ccc(OC[C@H]3CO[C@](Cn4cncn4)(c4ccc(Cl)cc4Cl)O3)cc2)CC1 nan
155559813 174267 0 None - 1 Human 7.6 pKi = 7.6 Binding
Displacement of [3H]-GR113808 from recombinant human 5-HT4BR expressed in membranes after 60 minsDisplacement of [3H]-GR113808 from recombinant human 5-HT4BR expressed in membranes after 60 mins
ChEMBL 338 6 1 2 5.0 O=C(CCC1CCN(CC2CCCC2)CC1)c1ccc2[nH]ccc2c1 10.1016/j.ejmech.2018.10.064
CHEMBL4562793 174267 0 None - 1 Human 7.6 pKi = 7.6 Binding
Displacement of [3H]-GR113808 from recombinant human 5-HT4BR expressed in membranes after 60 minsDisplacement of [3H]-GR113808 from recombinant human 5-HT4BR expressed in membranes after 60 mins
ChEMBL 338 6 1 2 5.0 O=C(CCC1CCN(CC2CCCC2)CC1)c1ccc2[nH]ccc2c1 10.1016/j.ejmech.2018.10.064
10569278 186667 0 None - 1 Rat 7.6 pKi = 7.6 Binding
Binding affinity (Ki+/-SEM) against 5-hydroxytryptamine 4 receptor from cheng Prusoff equation by using [3H]GR-113808 in rat striatumBinding affinity (Ki+/-SEM) against 5-hydroxytryptamine 4 receptor from cheng Prusoff equation by using [3H]GR-113808 in rat striatum
ChEMBL 341 5 2 5 3.2 COc1cc(N)c(Cl)cc1NC(=O)OCCN1CCC(C)CC1 10.1021/jm960853v
CHEMBL49266 186667 0 None - 1 Rat 7.6 pKi = 7.6 Binding
Binding affinity (Ki+/-SEM) against 5-hydroxytryptamine 4 receptor from cheng Prusoff equation by using [3H]GR-113808 in rat striatumBinding affinity (Ki+/-SEM) against 5-hydroxytryptamine 4 receptor from cheng Prusoff equation by using [3H]GR-113808 in rat striatum
ChEMBL 341 5 2 5 3.2 COc1cc(N)c(Cl)cc1NC(=O)OCCN1CCC(C)CC1 10.1021/jm960853v
70695322 77149 0 None - 1 Human 7.6 pKi = 7.6 Binding
Displacement of [3H]GR113808 from human recombinant 5HT4c receptor expressed in HEK293 cellsDisplacement of [3H]GR113808 from human recombinant 5HT4c receptor expressed in HEK293 cells
ChEMBL 469 7 4 6 1.6 CNC(=O)NCC(O)CN1[C@H]2CC[C@@H]1C[C@H](NC(=O)c1cc3ccccc3n(C(C)C)c1=O)C2 10.1016/j.bmcl.2012.08.051
CHEMBL2087328 77149 0 None - 1 Human 7.6 pKi = 7.6 Binding
Displacement of [3H]GR113808 from human recombinant 5HT4c receptor expressed in HEK293 cellsDisplacement of [3H]GR113808 from human recombinant 5HT4c receptor expressed in HEK293 cells
ChEMBL 469 7 4 6 1.6 CNC(=O)NCC(O)CN1[C@H]2CC[C@@H]1C[C@H](NC(=O)c1cc3ccccc3n(C(C)C)c1=O)C2 10.1016/j.bmcl.2012.08.051
10737191 206578 0 None - 1 Guinea pig 7.6 pKi = 7.6 Binding
Binding affinity against 5-hydroxytryptamine 4 receptor in guinea pig striatum using [3H]GR-113808 as radioligandBinding affinity against 5-hydroxytryptamine 4 receptor in guinea pig striatum using [3H]GR-113808 as radioligand
ChEMBL 359 5 1 6 1.4 CCn1c(=O)n(C(=O)NCCN2CCN(C(C)C)CC2)c2ccccc21 10.1021/jm981098j
CHEMBL99147 206578 0 None - 1 Guinea pig 7.6 pKi = 7.6 Binding
Binding affinity against 5-hydroxytryptamine 4 receptor in guinea pig striatum using [3H]GR-113808 as radioligandBinding affinity against 5-hydroxytryptamine 4 receptor in guinea pig striatum using [3H]GR-113808 as radioligand
ChEMBL 359 5 1 6 1.4 CCn1c(=O)n(C(=O)NCCN2CCN(C(C)C)CC2)c2ccccc21 10.1021/jm981098j
44592110 188578 0 None - 1 Guinea pig 7.6 pKi = 7.6 Binding
Displacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatum membraneDisplacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatum membrane
ChEMBL 357 7 0 5 4.8 CCCCCN1CCC(COc2nc3ccsc3n3cccc23)CC1 10.1016/j.bmc.2008.11.045
CHEMBL511148 188578 0 None - 1 Guinea pig 7.6 pKi = 7.6 Binding
Displacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatum membraneDisplacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatum membrane
ChEMBL 357 7 0 5 4.8 CCCCCN1CCC(COc2nc3ccsc3n3cccc23)CC1 10.1016/j.bmc.2008.11.045
90666005 108801 0 None - 1 Guinea pig 7.6 pKi = 7.6 Binding
Displacement of [3H]-GR113808 from guinea pig 5HT4 receptor by Grossman's methodDisplacement of [3H]-GR113808 from guinea pig 5HT4 receptor by Grossman's method
ChEMBL 355 5 0 5 4.4 c1cc2c(OCC3CCN(CC4CCC4)CC3)nc3ccsc3n2c1 10.1039/C2MD20063E
CHEMBL3218877 108801 0 None - 1 Guinea pig 7.6 pKi = 7.6 Binding
Displacement of [3H]-GR113808 from guinea pig 5HT4 receptor by Grossman's methodDisplacement of [3H]-GR113808 from guinea pig 5HT4 receptor by Grossman's method
ChEMBL 355 5 0 5 4.4 c1cc2c(OCC3CCN(CC4CCC4)CC3)nc3ccsc3n2c1 10.1039/C2MD20063E
6604789 100578 3 None 12 10 Human 6.6 pKi = 6.6 Binding
Binding affinity against 5-hydroxytryptamine 4 receptorBinding affinity against 5-hydroxytryptamine 4 receptor
ChEMBL 311 3 1 4 1.6 Cn1cc(C(=O)C(=O)N[C@H]2CN3CCC2CC3)c2ccccc21 10.1016/0960-894X(95)00308-G
CHEMBL294649 100578 3 None 12 10 Human 6.6 pKi = 6.6 Binding
Binding affinity against 5-hydroxytryptamine 4 receptorBinding affinity against 5-hydroxytryptamine 4 receptor
ChEMBL 311 3 1 4 1.6 Cn1cc(C(=O)C(=O)N[C@H]2CN3CCC2CC3)c2ccccc21 10.1016/0960-894X(95)00308-G
71712613 90948 0 None - 1 Human 6.6 pKi = 6.6 Binding
Binding affinity to human recombinant 5HT4 receptorBinding affinity to human recombinant 5HT4 receptor
ChEMBL 464 7 3 7 -0.3 CS(=O)(=O)N1CCN(CC(O)CN2CCC(NC(=O)c3cccc4[nH]cnc34)CC2)CC1 10.1016/j.bmcl.2013.05.018
CHEMBL2402889 90948 0 None - 1 Human 6.6 pKi = 6.6 Binding
Binding affinity to human recombinant 5HT4 receptorBinding affinity to human recombinant 5HT4 receptor
ChEMBL 464 7 3 7 -0.3 CS(=O)(=O)N1CCN(CC(O)CN2CCC(NC(=O)c3cccc4[nH]cnc34)CC2)CC1 10.1016/j.bmcl.2013.05.018
44248793 91900478 193950 0 None - 1 Human 6.6 pKi = 6.6 Binding
Displacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 339 3 2 4 2.6 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3)cc2ccccc21 10.1021/jm900881j
CHEMBL556235 193950 0 None - 1 Human 6.6 pKi = 6.6 Binding
Displacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 339 3 2 4 2.6 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3)cc2ccccc21 10.1021/jm900881j
44249053 194826 0 None - 1 Human 6.6 pKi = 6.6 Binding
Displacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 394 6 2 5 2.6 COc1cc(N)c(Cl)cc1C(=O)NC1CCN(CCN2CCCCC2)CC1 10.1021/jm900881j
CHEMBL563445 194826 0 None - 1 Human 6.6 pKi = 6.6 Binding
Displacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 394 6 2 5 2.6 COc1cc(N)c(Cl)cc1C(=O)NC1CCN(CCN2CCCCC2)CC1 10.1021/jm900881j
6918647 100278 2 None -501 14 Human 5.6 pKi = 5.6 Binding
Compound was tested for its binding affinity against 5-hydroxytryptamine 4 receptorCompound was tested for its binding affinity against 5-hydroxytryptamine 4 receptor
ChEMBL 439 5 1 5 3.0 COc1ccc(NS(=O)(=O)c2ccc(Br)cc2)cc1N1CCN(C)CC1 10.1021/jm980532e
CHEMBL292759 100278 2 None -501 14 Human 5.6 pKi = 5.6 Binding
Compound was tested for its binding affinity against 5-hydroxytryptamine 4 receptorCompound was tested for its binding affinity against 5-hydroxytryptamine 4 receptor
ChEMBL 439 5 1 5 3.0 COc1ccc(NS(=O)(=O)c2ccc(Br)cc2)cc1N1CCN(C)CC1 10.1021/jm980532e
44247945 194396 0 None - 1 Human 4.6 pKi = 4.6 Binding
Displacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 391 6 3 6 1.0 COc1cc(N)c(Cl)cc1C(=O)NC1CCN(CCS(=O)(=O)O)CC1 10.1021/jm900881j
CHEMBL560597 194396 0 None - 1 Human 4.6 pKi = 4.6 Binding
Displacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 391 6 3 6 1.0 COc1cc(N)c(Cl)cc1C(=O)NC1CCN(CCS(=O)(=O)O)CC1 10.1021/jm900881j
10831381 206299 0 None - 1 Guinea pig 6.6 pKi = 6.6 Binding
Binding affinity against 5-hydroxytryptamine 4 receptor in guinea pig striatum using [3H]GR-113808 as radioligandBinding affinity against 5-hydroxytryptamine 4 receptor in guinea pig striatum using [3H]GR-113808 as radioligand
ChEMBL 345 5 1 6 1.0 CCCn1c(=O)n(C(=O)NCCN2CCN(C)CC2)c2ccccc21 10.1021/jm981098j
CHEMBL97508 206299 0 None - 1 Guinea pig 6.6 pKi = 6.6 Binding
Binding affinity against 5-hydroxytryptamine 4 receptor in guinea pig striatum using [3H]GR-113808 as radioligandBinding affinity against 5-hydroxytryptamine 4 receptor in guinea pig striatum using [3H]GR-113808 as radioligand
ChEMBL 345 5 1 6 1.0 CCCn1c(=O)n(C(=O)NCCN2CCN(C)CC2)c2ccccc21 10.1021/jm981098j
131725 198753 2 None -3 2 Rat 6.6 pKi = 6.6 Binding
Binding affinity towards 5-hydroxytryptamine 4 receptor was determined in rat striatal membranes using [3H]GR-113808 as radioligandBinding affinity towards 5-hydroxytryptamine 4 receptor was determined in rat striatal membranes using [3H]GR-113808 as radioligand
ChEMBL 342 2 1 5 2.6 CC(C)n1c(=O)n(C(=O)NC2CC3CCC(C2)N3C)c2ccccc21 10.1021/jm960320m
CHEMBL59834 198753 2 None -3 2 Rat 6.6 pKi = 6.6 Binding
Binding affinity towards 5-hydroxytryptamine 4 receptor was determined in rat striatal membranes using [3H]GR-113808 as radioligandBinding affinity towards 5-hydroxytryptamine 4 receptor was determined in rat striatal membranes using [3H]GR-113808 as radioligand
ChEMBL 342 2 1 5 2.6 CC(C)n1c(=O)n(C(=O)NC2CC3CCC(C2)N3C)c2ccccc21 10.1021/jm960320m
162649188 179517 0 None - 1 Guinea pig 7.6 pKi = 7.6 Binding
Displacement of [3H]-GR113808 from guinea pig brain 5HT4 receptor in presence of serotonin incubated for 30 minsDisplacement of [3H]-GR113808 from guinea pig brain 5HT4 receptor in presence of serotonin incubated for 30 mins
ChEMBL 523 12 2 7 4.0 COc1ccc(S(=O)(=O)NCCCN2CCC(CCC(=O)c3cc(Cl)c(N)cc3OC)CC2)cc1 10.1016/j.ejmech.2016.05.048
CHEMBL4748287 179517 0 None - 1 Guinea pig 7.6 pKi = 7.6 Binding
Displacement of [3H]-GR113808 from guinea pig brain 5HT4 receptor in presence of serotonin incubated for 30 minsDisplacement of [3H]-GR113808 from guinea pig brain 5HT4 receptor in presence of serotonin incubated for 30 mins
ChEMBL 523 12 2 7 4.0 COc1ccc(S(=O)(=O)NCCCN2CCC(CCC(=O)c3cc(Cl)c(N)cc3OC)CC2)cc1 10.1016/j.ejmech.2016.05.048
15544723 205703 0 None - 1 Rat 7.6 pKi = 7.6 Binding
Binding affinity to 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatum membraneBinding affinity to 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatum membrane
ChEMBL 380 7 2 6 1.0 CS(=O)(=O)NCCN1CCC(COC(=O)c2cccc3[nH]cnc23)CC1 10.1021/jm020807x
CHEMBL94099 205703 0 None - 1 Rat 7.6 pKi = 7.6 Binding
Binding affinity to 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatum membraneBinding affinity to 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatum membrane
ChEMBL 380 7 2 6 1.0 CS(=O)(=O)NCCN1CCC(COC(=O)c2cccc3[nH]cnc23)CC1 10.1021/jm020807x
15544723 205703 0 None - 1 Rat 7.6 pKi = 7.6 Binding
In vitro binding affinity to 5-hydroxytryptamine 4 receptor in rat striatum membraneIn vitro binding affinity to 5-hydroxytryptamine 4 receptor in rat striatum membrane
ChEMBL 380 7 2 6 1.0 CS(=O)(=O)NCCN1CCC(COC(=O)c2cccc3[nH]cnc23)CC1 10.1016/s0960-894x(01)00517-0
CHEMBL94099 205703 0 None - 1 Rat 7.6 pKi = 7.6 Binding
In vitro binding affinity to 5-hydroxytryptamine 4 receptor in rat striatum membraneIn vitro binding affinity to 5-hydroxytryptamine 4 receptor in rat striatum membrane
ChEMBL 380 7 2 6 1.0 CS(=O)(=O)NCCN1CCC(COC(=O)c2cccc3[nH]cnc23)CC1 10.1016/s0960-894x(01)00517-0
15544723 205703 0 None - 1 Rat 7.6 pKi = 7.6 Binding
pKi against 5-hydroxytryptamine 4 receptor in rat striatum membranepKi against 5-hydroxytryptamine 4 receptor in rat striatum membrane
ChEMBL 380 7 2 6 1.0 CS(=O)(=O)NCCN1CCC(COC(=O)c2cccc3[nH]cnc23)CC1 10.1016/s0960-894x(01)00517-0
CHEMBL94099 205703 0 None - 1 Rat 7.6 pKi = 7.6 Binding
pKi against 5-hydroxytryptamine 4 receptor in rat striatum membranepKi against 5-hydroxytryptamine 4 receptor in rat striatum membrane
ChEMBL 380 7 2 6 1.0 CS(=O)(=O)NCCN1CCC(COC(=O)c2cccc3[nH]cnc23)CC1 10.1016/s0960-894x(01)00517-0
107 141 116 None -389 30 Human 7.6 pKi = 7.6 Binding
Displacement of [3H]GR-113808 from human 5HT4b receptor expressed in COS7 cell membrane by scintillation countingDisplacement of [3H]GR-113808 from human 5HT4b receptor expressed in COS7 cell membrane by scintillation counting
ChEMBL 190 3 2 2 1.7 NCCc1c[nH]c2c1cc(OC)cc2 10.1016/j.ejmech.2009.01.015
1833 141 116 None -389 30 Human 7.6 pKi = 7.6 Binding
Displacement of [3H]GR-113808 from human 5HT4b receptor expressed in COS7 cell membrane by scintillation countingDisplacement of [3H]GR-113808 from human 5HT4b receptor expressed in COS7 cell membrane by scintillation counting
ChEMBL 190 3 2 2 1.7 NCCc1c[nH]c2c1cc(OC)cc2 10.1016/j.ejmech.2009.01.015
CHEMBL8165 141 116 None -389 30 Human 7.6 pKi = 7.6 Binding
Displacement of [3H]GR-113808 from human 5HT4b receptor expressed in COS7 cell membrane by scintillation countingDisplacement of [3H]GR-113808 from human 5HT4b receptor expressed in COS7 cell membrane by scintillation counting
ChEMBL 190 3 2 2 1.7 NCCc1c[nH]c2c1cc(OC)cc2 10.1016/j.ejmech.2009.01.015
10741712 206576 0 None - 1 Guinea pig 6.6 pKi = 6.6 Binding
Binding affinity against 5-hydroxytryptamine 4 receptor in guinea pig striatum using [3H]GR-113808 as radioligandBinding affinity against 5-hydroxytryptamine 4 receptor in guinea pig striatum using [3H]GR-113808 as radioligand
ChEMBL 439 6 1 6 2.9 CC(C)n1c(=O)n(C(=O)NCCN2CCN(Cc3ccc(F)cc3)CC2)c2ccccc21 10.1021/jm981098j
CHEMBL99141 206576 0 None - 1 Guinea pig 6.6 pKi = 6.6 Binding
Binding affinity against 5-hydroxytryptamine 4 receptor in guinea pig striatum using [3H]GR-113808 as radioligandBinding affinity against 5-hydroxytryptamine 4 receptor in guinea pig striatum using [3H]GR-113808 as radioligand
ChEMBL 439 6 1 6 2.9 CC(C)n1c(=O)n(C(=O)NCCN2CCN(Cc3ccc(F)cc3)CC2)c2ccccc21 10.1021/jm981098j
10897011 167602 0 None - 1 Human 6.6 pKi = 6.6 Binding
Binding affinity towards cloned human 5-hydroxytryptamine 4E receptor expressed in C6 glial cells using [3H]GR-113808 as radioligandBinding affinity towards cloned human 5-hydroxytryptamine 4E receptor expressed in C6 glial cells using [3H]GR-113808 as radioligand
ChEMBL 560 9 2 8 3.8 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCC(NS(=O)(=O)c2cccc3c(N(C)C)cccc23)CC1 10.1021/jm0307887
CHEMBL433149 167602 0 None - 1 Human 6.6 pKi = 6.6 Binding
Binding affinity towards cloned human 5-hydroxytryptamine 4E receptor expressed in C6 glial cells using [3H]GR-113808 as radioligandBinding affinity towards cloned human 5-hydroxytryptamine 4E receptor expressed in C6 glial cells using [3H]GR-113808 as radioligand
ChEMBL 560 9 2 8 3.8 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCC(NS(=O)(=O)c2cccc3c(N(C)C)cccc23)CC1 10.1021/jm0307887
1043 1552 13 None -2884 28 Guinea pig 6.6 pKi = 6.6 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
ChEMBL 581 4 3 6 2.0 O=C([C@H]1CN(C)[C@H]2C(=C1)c1cccc3c1c(C2)c[nH]3)N[C@]1(C)O[C@@]2(N(C1=O)[C@@H](Cc1ccccc1)C(=O)N1[C@H]2CCC1)O nan
149 1552 13 None -2884 28 Guinea pig 6.6 pKi = 6.6 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
ChEMBL 581 4 3 6 2.0 O=C([C@H]1CN(C)[C@H]2C(=C1)c1cccc3c1c(C2)c[nH]3)N[C@]1(C)O[C@@]2(N(C1=O)[C@@H](Cc1ccccc1)C(=O)N1[C@H]2CCC1)O nan
8223 1552 13 None -2884 28 Guinea pig 6.6 pKi = 6.6 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
ChEMBL 581 4 3 6 2.0 O=C([C@H]1CN(C)[C@H]2C(=C1)c1cccc3c1c(C2)c[nH]3)N[C@]1(C)O[C@@]2(N(C1=O)[C@@H](Cc1ccccc1)C(=O)N1[C@H]2CCC1)O nan
CHEMBL442 1552 13 None -2884 28 Guinea pig 6.6 pKi = 6.6 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
ChEMBL 581 4 3 6 2.0 O=C([C@H]1CN(C)[C@H]2C(=C1)c1cccc3c1c(C2)c[nH]3)N[C@]1(C)O[C@@]2(N(C1=O)[C@@H](Cc1ccccc1)C(=O)N1[C@H]2CCC1)O nan
DB00696 1552 13 None -2884 28 Guinea pig 6.6 pKi = 6.6 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
ChEMBL 581 4 3 6 2.0 O=C([C@H]1CN(C)[C@H]2C(=C1)c1cccc3c1c(C2)c[nH]3)N[C@]1(C)O[C@@]2(N(C1=O)[C@@H](Cc1ccccc1)C(=O)N1[C@H]2CCC1)O nan
11825705 107722 0 None - 1 Rat 7.6 pKi = 7.6 Binding
pKi against 5-hydroxytryptamine 4 receptor in rat striatum membranepKi against 5-hydroxytryptamine 4 receptor in rat striatum membrane
ChEMBL 407 6 3 4 3.2 CCCCN1CCC(CNC(=O)c2cc(Br)c(N)c3[nH]cnc23)CC1 10.1016/s0960-894x(01)00517-0
CHEMBL319663 107722 0 None - 1 Rat 7.6 pKi = 7.6 Binding
pKi against 5-hydroxytryptamine 4 receptor in rat striatum membranepKi against 5-hydroxytryptamine 4 receptor in rat striatum membrane
ChEMBL 407 6 3 4 3.2 CCCCN1CCC(CNC(=O)c2cc(Br)c(N)c3[nH]cnc23)CC1 10.1016/s0960-894x(01)00517-0
11825705 107722 0 None - 1 Rat 7.6 pKi = 7.6 Binding
Binding affinity to 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatum membraneBinding affinity to 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatum membrane
ChEMBL 407 6 3 4 3.2 CCCCN1CCC(CNC(=O)c2cc(Br)c(N)c3[nH]cnc23)CC1 10.1021/jm020807x
CHEMBL319663 107722 0 None - 1 Rat 7.6 pKi = 7.6 Binding
Binding affinity to 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatum membraneBinding affinity to 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatum membrane
ChEMBL 407 6 3 4 3.2 CCCCN1CCC(CNC(=O)c2cc(Br)c(N)c3[nH]cnc23)CC1 10.1021/jm020807x
11825705 107722 0 None - 1 Rat 7.6 pKi = 7.6 Binding
In vitro binding affinity to 5-hydroxytryptamine 4 receptor in rat striatum membraneIn vitro binding affinity to 5-hydroxytryptamine 4 receptor in rat striatum membrane
ChEMBL 407 6 3 4 3.2 CCCCN1CCC(CNC(=O)c2cc(Br)c(N)c3[nH]cnc23)CC1 10.1016/s0960-894x(01)00517-0
CHEMBL319663 107722 0 None - 1 Rat 7.6 pKi = 7.6 Binding
In vitro binding affinity to 5-hydroxytryptamine 4 receptor in rat striatum membraneIn vitro binding affinity to 5-hydroxytryptamine 4 receptor in rat striatum membrane
ChEMBL 407 6 3 4 3.2 CCCCN1CCC(CNC(=O)c2cc(Br)c(N)c3[nH]cnc23)CC1 10.1016/s0960-894x(01)00517-0
850953 38175 2 None - 1 Rat 6.6 pKi = 6.6 Binding
In vitro affinity at serotonergic 5-hydroxytryptamine 4 receptor by radioligand binding assay using [3H]GR-113808 in rat striatum membranes.In vitro affinity at serotonergic 5-hydroxytryptamine 4 receptor by radioligand binding assay using [3H]GR-113808 in rat striatum membranes.
ChEMBL 348 2 2 3 2.1 O=C(N[C@H]1CN2CCC1CC2)c1cc(Br)cc2nc[nH]c12 10.1021/jm991076c
CHEMBL146368 38175 2 None - 1 Rat 6.6 pKi = 6.6 Binding
In vitro affinity at serotonergic 5-hydroxytryptamine 4 receptor by radioligand binding assay using [3H]GR-113808 in rat striatum membranes.In vitro affinity at serotonergic 5-hydroxytryptamine 4 receptor by radioligand binding assay using [3H]GR-113808 in rat striatum membranes.
ChEMBL 348 2 2 3 2.1 O=C(N[C@H]1CN2CCC1CC2)c1cc(Br)cc2nc[nH]c12 10.1021/jm991076c
133 2460 48 None -79 42 Guinea pig 6.6 pKi = 6.6 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
ChEMBL 403 4 1 4 4.1 O=C(OCc1ccccc1)NC[C@H]1CN(C)[C@H]2[C@H](C1)c1cccc3c1c(C2)cn3C nan
1723 2460 48 None -79 42 Guinea pig 6.6 pKi = 6.6 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
ChEMBL 403 4 1 4 4.1 O=C(OCc1ccccc1)NC[C@H]1CN(C)[C@H]2[C@H](C1)c1cccc3c1c(C2)cn3C nan
28693 2460 48 None -79 42 Guinea pig 6.6 pKi = 6.6 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
ChEMBL 403 4 1 4 4.1 O=C(OCc1ccccc1)NC[C@H]1CN(C)[C@H]2[C@H](C1)c1cccc3c1c(C2)cn3C nan
CHEMBL19215 2460 48 None -79 42 Guinea pig 6.6 pKi = 6.6 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
ChEMBL 403 4 1 4 4.1 O=C(OCc1ccccc1)NC[C@H]1CN(C)[C@H]2[C@H](C1)c1cccc3c1c(C2)cn3C nan
DB13520 2460 48 None -79 42 Guinea pig 6.6 pKi = 6.6 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
ChEMBL 403 4 1 4 4.1 O=C(OCc1ccccc1)NC[C@H]1CN(C)[C@H]2[C@H](C1)c1cccc3c1c(C2)cn3C nan
182593 3343 4 None -2 3 Rat 7.6 pKi = 7.6 Binding
Binding affinity towards 5-hydroxytryptamine 4 receptor was determined in rat striatal membranes using [3H]GR-113808 as radioligandBinding affinity towards 5-hydroxytryptamine 4 receptor was determined in rat striatal membranes using [3H]GR-113808 as radioligand
ChEMBL 326 6 1 5 3.0 COc1cc(N)c(cc1C(=O)OCCCN1CCCCC1)Cl 10.1021/jm960320m
254 3343 4 None -2 3 Rat 7.6 pKi = 7.6 Binding
Binding affinity towards 5-hydroxytryptamine 4 receptor was determined in rat striatal membranes using [3H]GR-113808 as radioligandBinding affinity towards 5-hydroxytryptamine 4 receptor was determined in rat striatal membranes using [3H]GR-113808 as radioligand
ChEMBL 326 6 1 5 3.0 COc1cc(N)c(cc1C(=O)OCCCN1CCCCC1)Cl 10.1021/jm960320m
CHEMBL83954 3343 4 None -2 3 Rat 7.6 pKi = 7.6 Binding
Binding affinity towards 5-hydroxytryptamine 4 receptor was determined in rat striatal membranes using [3H]GR-113808 as radioligandBinding affinity towards 5-hydroxytryptamine 4 receptor was determined in rat striatal membranes using [3H]GR-113808 as radioligand
ChEMBL 326 6 1 5 3.0 COc1cc(N)c(cc1C(=O)OCCCN1CCCCC1)Cl 10.1021/jm960320m
10425296 162847 0 None - 1 Rat 6.6 pKi = 6.6 Binding
Binding affinity at 5-hydroxytryptamine 4 receptor in rat striatum by [3H]GR-113808 displacement.Binding affinity at 5-hydroxytryptamine 4 receptor in rat striatum by [3H]GR-113808 displacement.
ChEMBL 306 2 1 3 2.1 O=C(N[C@H]1CN2CCC1CC2)c1cc(Cl)cc2c1OCC2 10.1016/0960-894X(96)00002-9
CHEMBL419496 162847 0 None - 1 Rat 6.6 pKi = 6.6 Binding
Binding affinity at 5-hydroxytryptamine 4 receptor in rat striatum by [3H]GR-113808 displacement.Binding affinity at 5-hydroxytryptamine 4 receptor in rat striatum by [3H]GR-113808 displacement.
ChEMBL 306 2 1 3 2.1 O=C(N[C@H]1CN2CCC1CC2)c1cc(Cl)cc2c1OCC2 10.1016/0960-894X(96)00002-9
9819593 98348 2 None -1 2 Guinea pig 5.6 pKi = 5.6 Binding
Binding affinity for 5-hydroxytryptamine 4 receptor by displacement of [3H]GR-113808 from guinea pig brain striatum.Binding affinity for 5-hydroxytryptamine 4 receptor by displacement of [3H]GR-113808 from guinea pig brain striatum.
ChEMBL 309 3 2 4 1.8 COc1cc(N)c(Cl)cc1C(=O)N[C@H]1CN2CCC1CC2 10.1016/0960-894X(96)00052-2
CHEMBL27846 98348 2 None -1 2 Guinea pig 5.6 pKi = 5.6 Binding
Binding affinity for 5-hydroxytryptamine 4 receptor by displacement of [3H]GR-113808 from guinea pig brain striatum.Binding affinity for 5-hydroxytryptamine 4 receptor by displacement of [3H]GR-113808 from guinea pig brain striatum.
ChEMBL 309 3 2 4 1.8 COc1cc(N)c(Cl)cc1C(=O)N[C@H]1CN2CCC1CC2 10.1016/0960-894X(96)00052-2
90644472 111787 0 None - 1 Guinea pig 6.6 pKi = 6.6 Binding
Displacement of [3H]GR113808 from Dunkin-Hartley guinea pig brain striatum 5HT4R after 30 minsDisplacement of [3H]GR113808 from Dunkin-Hartley guinea pig brain striatum 5HT4R after 30 mins
ChEMBL 339 5 0 4 3.1 COc1cc2c3c(cccc3n1)CN(CCCN1CCCCC1)C2=O 10.1016/j.ejmech.2014.05.015
CHEMBL3291077 111787 0 None - 1 Guinea pig 6.6 pKi = 6.6 Binding
Displacement of [3H]GR113808 from Dunkin-Hartley guinea pig brain striatum 5HT4R after 30 minsDisplacement of [3H]GR113808 from Dunkin-Hartley guinea pig brain striatum 5HT4R after 30 mins
ChEMBL 339 5 0 4 3.1 COc1cc2c3c(cccc3n1)CN(CCCN1CCCCC1)C2=O 10.1016/j.ejmech.2014.05.015
44327605 205758 0 None - 1 Rat 6.5 pKi = 6.5 Binding
pKi against 5-hydroxytryptamine 4 receptor in rat striatum membranepKi against 5-hydroxytryptamine 4 receptor in rat striatum membrane
ChEMBL 300 5 2 3 2.6 CCCCN1CCC(NC(=O)c2cccc3[nH]cnc23)CC1 10.1016/s0960-894x(01)00517-0
CHEMBL94415 205758 0 None - 1 Rat 6.5 pKi = 6.5 Binding
pKi against 5-hydroxytryptamine 4 receptor in rat striatum membranepKi against 5-hydroxytryptamine 4 receptor in rat striatum membrane
ChEMBL 300 5 2 3 2.6 CCCCN1CCC(NC(=O)c2cccc3[nH]cnc23)CC1 10.1016/s0960-894x(01)00517-0
240 931 39 None -11 25 Human 7.5 pKi = 7.5 Binding
Binding affinity towards Serotonin 5-hydroxytryptamine 4 receptorBinding affinity towards Serotonin 5-hydroxytryptamine 4 receptor
ChEMBL 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N 10.1021/jm0205651
2769 931 39 None -11 25 Human 7.5 pKi = 7.5 Binding
Binding affinity towards Serotonin 5-hydroxytryptamine 4 receptorBinding affinity towards Serotonin 5-hydroxytryptamine 4 receptor
ChEMBL 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N 10.1021/jm0205651
44279790 931 39 None -11 25 Human 7.5 pKi = 7.5 Binding
Binding affinity towards Serotonin 5-hydroxytryptamine 4 receptorBinding affinity towards Serotonin 5-hydroxytryptamine 4 receptor
ChEMBL 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N 10.1021/jm0205651
660 931 39 None -11 25 Human 7.5 pKi = 7.5 Binding
Binding affinity towards Serotonin 5-hydroxytryptamine 4 receptorBinding affinity towards Serotonin 5-hydroxytryptamine 4 receptor
ChEMBL 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N 10.1021/jm0205651
CHEMBL1729 931 39 None -11 25 Human 7.5 pKi = 7.5 Binding
Binding affinity towards Serotonin 5-hydroxytryptamine 4 receptorBinding affinity towards Serotonin 5-hydroxytryptamine 4 receptor
ChEMBL 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N 10.1021/jm0205651
CHEMBL560739 931 39 None -11 25 Human 7.5 pKi = 7.5 Binding
Binding affinity towards Serotonin 5-hydroxytryptamine 4 receptorBinding affinity towards Serotonin 5-hydroxytryptamine 4 receptor
ChEMBL 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N 10.1021/jm0205651
DB00604 931 39 None -11 25 Human 7.5 pKi = 7.5 Binding
Binding affinity towards Serotonin 5-hydroxytryptamine 4 receptorBinding affinity towards Serotonin 5-hydroxytryptamine 4 receptor
ChEMBL 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N 10.1021/jm0205651
9906777 92812 0 None - 1 Guinea pig 7.5 pKi = 7.5 Binding
Displacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatumDisplacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatum
ChEMBL 321 3 2 4 1.6 COc1cc(N)c(Cl)cc1C(=O)N[C@@H]1C2CC3CN(C2)CC31 10.1021/jm0509501
CHEMBL2448165 92812 0 None - 1 Guinea pig 7.5 pKi = 7.5 Binding
Displacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatumDisplacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatum
ChEMBL 321 3 2 4 1.6 COc1cc(N)c(Cl)cc1C(=O)N[C@@H]1C2CC3CN(C2)CC31 10.1021/jm0509501
44592185 188807 0 None - 1 Guinea pig 7.5 pKi = 7.5 Binding
Displacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatum membraneDisplacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatum membrane
ChEMBL 327 5 0 5 3.8 C=CCN1CCC(COc2nc3sccc3n3cccc23)CC1 10.1016/j.bmc.2008.11.045
CHEMBL513020 188807 0 None - 1 Guinea pig 7.5 pKi = 7.5 Binding
Displacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatum membraneDisplacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatum membrane
ChEMBL 327 5 0 5 3.8 C=CCN1CCC(COc2nc3sccc3n3cccc23)CC1 10.1016/j.bmc.2008.11.045
5 139 66 None -288 54 Human 7.5 pKi = 7.5 Binding
Displacement of [3H]GR-113808 from human 5HT4b receptor expressed in COS7 cell membrane by scintillation countingDisplacement of [3H]GR-113808 from human 5HT4b receptor expressed in COS7 cell membrane by scintillation counting
ChEMBL 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 10.1016/j.ejmech.2009.01.015
5202 139 66 None -288 54 Human 7.5 pKi = 7.5 Binding
Displacement of [3H]GR-113808 from human 5HT4b receptor expressed in COS7 cell membrane by scintillation countingDisplacement of [3H]GR-113808 from human 5HT4b receptor expressed in COS7 cell membrane by scintillation counting
ChEMBL 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 10.1016/j.ejmech.2009.01.015
CHEMBL39 139 66 None -288 54 Human 7.5 pKi = 7.5 Binding
Displacement of [3H]GR-113808 from human 5HT4b receptor expressed in COS7 cell membrane by scintillation countingDisplacement of [3H]GR-113808 from human 5HT4b receptor expressed in COS7 cell membrane by scintillation counting
ChEMBL 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 10.1016/j.ejmech.2009.01.015
DB08839 139 66 None -288 54 Human 7.5 pKi = 7.5 Binding
Displacement of [3H]GR-113808 from human 5HT4b receptor expressed in COS7 cell membrane by scintillation countingDisplacement of [3H]GR-113808 from human 5HT4b receptor expressed in COS7 cell membrane by scintillation counting
ChEMBL 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 10.1016/j.ejmech.2009.01.015
11724799 10432 0 None - 1 Rat 7.5 pKi = 7.5 Binding
Binding affinity against 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatumBinding affinity against 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatum
ChEMBL 339 0 2 5 1.5 Nc1cc2c(cc1Cl)C(=O)NC1CCN(CCOCCO2)CC1 10.1016/0960-894X(95)00115-A
CHEMBL116913 10432 0 None - 1 Rat 7.5 pKi = 7.5 Binding
Binding affinity against 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatumBinding affinity against 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatum
ChEMBL 339 0 2 5 1.5 Nc1cc2c(cc1Cl)C(=O)NC1CCN(CCOCCO2)CC1 10.1016/0960-894X(95)00115-A
44327605 205758 0 None - 1 Rat 6.5 pKi = 6.5 Binding
Binding affinity to 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatum membraneBinding affinity to 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatum membrane
ChEMBL 300 5 2 3 2.6 CCCCN1CCC(NC(=O)c2cccc3[nH]cnc23)CC1 10.1021/jm020807x
CHEMBL94415 205758 0 None - 1 Rat 6.5 pKi = 6.5 Binding
Binding affinity to 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatum membraneBinding affinity to 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatum membrane
ChEMBL 300 5 2 3 2.6 CCCCN1CCC(NC(=O)c2cccc3[nH]cnc23)CC1 10.1021/jm020807x
44327605 205758 0 None - 1 Rat 6.5 pKi = 6.5 Binding
In vitro binding affinity to 5-hydroxytryptamine 4 receptor in rat striatum membraneIn vitro binding affinity to 5-hydroxytryptamine 4 receptor in rat striatum membrane
ChEMBL 300 5 2 3 2.6 CCCCN1CCC(NC(=O)c2cccc3[nH]cnc23)CC1 10.1016/s0960-894x(01)00517-0
CHEMBL94415 205758 0 None - 1 Rat 6.5 pKi = 6.5 Binding
In vitro binding affinity to 5-hydroxytryptamine 4 receptor in rat striatum membraneIn vitro binding affinity to 5-hydroxytryptamine 4 receptor in rat striatum membrane
ChEMBL 300 5 2 3 2.6 CCCCN1CCC(NC(=O)c2cccc3[nH]cnc23)CC1 10.1016/s0960-894x(01)00517-0
10550242 17075 0 None - 1 Human 6.5 pKi = 6.5 Binding
Binding affinity was determined against cloned 5-hydroxytryptamine 4E receptor isoform expressed in C6 glial cells incubated with 0.2 nM [3H]GR-113808Binding affinity was determined against cloned 5-hydroxytryptamine 4E receptor isoform expressed in C6 glial cells incubated with 0.2 nM [3H]GR-113808
ChEMBL 423 6 1 6 3.6 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCN(c2ccccc2Cl)CC1 10.1021/jm0009538
CHEMBL125670 17075 0 None - 1 Human 6.5 pKi = 6.5 Binding
Binding affinity was determined against cloned 5-hydroxytryptamine 4E receptor isoform expressed in C6 glial cells incubated with 0.2 nM [3H]GR-113808Binding affinity was determined against cloned 5-hydroxytryptamine 4E receptor isoform expressed in C6 glial cells incubated with 0.2 nM [3H]GR-113808
ChEMBL 423 6 1 6 3.6 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCN(c2ccccc2Cl)CC1 10.1021/jm0009538
11629268 71933 0 None - 1 Human 8.5 pKi = 8.5 Binding
Binding affinity for 5-HT4 receptor using [3H]GR-113808Binding affinity for 5-HT4 receptor using [3H]GR-113808
ChEMBL 824 21 4 14 2.9 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCC(C(=O)NCCOCCOCCNC(=O)C2CCN(CCOC(=O)c3cc(Cl)c(N)cc3OC)CC2)CC1 10.1021/jm050234z
CHEMBL198271 71933 0 None - 1 Human 8.5 pKi = 8.5 Binding
Binding affinity for 5-HT4 receptor using [3H]GR-113808Binding affinity for 5-HT4 receptor using [3H]GR-113808
ChEMBL 824 21 4 14 2.9 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCC(C(=O)NCCOCCOCCNC(=O)C2CCN(CCOC(=O)c3cc(Cl)c(N)cc3OC)CC2)CC1 10.1021/jm050234z
11796362 114603 0 None - 1 Human 8.5 pKi = 8.5 Binding
Binding affinity was determined against cloned 5-hydroxytryptamine 4E receptor isoform expressed in C6 glial cells incubated with 0.2 nM [3H]GR-113808Binding affinity was determined against cloned 5-hydroxytryptamine 4E receptor isoform expressed in C6 glial cells incubated with 0.2 nM [3H]GR-113808
ChEMBL 419 7 1 7 2.9 COc1cccc(N2CCN(CCOC(=O)c3cc(Cl)c(N)cc3OC)CC2)c1 10.1021/jm0009538
CHEMBL334325 114603 0 None - 1 Human 8.5 pKi = 8.5 Binding
Binding affinity was determined against cloned 5-hydroxytryptamine 4E receptor isoform expressed in C6 glial cells incubated with 0.2 nM [3H]GR-113808Binding affinity was determined against cloned 5-hydroxytryptamine 4E receptor isoform expressed in C6 glial cells incubated with 0.2 nM [3H]GR-113808
ChEMBL 419 7 1 7 2.9 COc1cccc(N2CCN(CCOC(=O)c3cc(Cl)c(N)cc3OC)CC2)c1 10.1021/jm0009538
118734510 118163 0 None - 1 Guinea pig 8.5 pKi = 8.5 Binding
Displacement of [3H]GR113808 from 5-HT4R in guinea pig brain membranes incubated for 30 mins by radioligand binding assayDisplacement of [3H]GR113808 from 5-HT4R in guinea pig brain membranes incubated for 30 mins by radioligand binding assay
ChEMBL 378 7 1 4 4.8 COc1cc(N)c(Cl)cc1C(=O)CCC1CCN(CC2CCCC2)CC1 10.1021/acs.jmedchem.5b00115
CHEMBL3416996 118163 0 None - 1 Guinea pig 8.5 pKi = 8.5 Binding
Displacement of [3H]GR113808 from 5-HT4R in guinea pig brain membranes incubated for 30 mins by radioligand binding assayDisplacement of [3H]GR113808 from 5-HT4R in guinea pig brain membranes incubated for 30 mins by radioligand binding assay
ChEMBL 378 7 1 4 4.8 COc1cc(N)c(Cl)cc1C(=O)CCC1CCN(CC2CCCC2)CC1 10.1021/acs.jmedchem.5b00115
71461050 82564 0 None 6 5 Human 8.5 pKi = 8.5 Binding
Binding affinity to human 5HT4RBinding affinity to human 5HT4R
ChEMBL 352 5 0 3 5.0 CCCN1CCC(COc2nc3c(F)cccc3c3ccccc23)CC1 10.1016/j.bmc.2013.08.061
CHEMBL2181189 82564 0 None 6 5 Human 8.5 pKi = 8.5 Binding
Binding affinity to human 5HT4RBinding affinity to human 5HT4R
ChEMBL 352 5 0 3 5.0 CCCN1CCC(COc2nc3c(F)cccc3c3ccccc23)CC1 10.1016/j.bmc.2013.08.061
71461050 82564 0 None 6 5 Human 8.5 pKi = 8.5 Binding
Displacement of [3H]GR113808 from human recombinant 5HT4R expressed in HEK293T cellsDisplacement of [3H]GR113808 from human recombinant 5HT4R expressed in HEK293T cells
ChEMBL 352 5 0 3 5.0 CCCN1CCC(COc2nc3c(F)cccc3c3ccccc23)CC1 10.1021/jm300943r
CHEMBL2181189 82564 0 None 6 5 Human 8.5 pKi = 8.5 Binding
Displacement of [3H]GR113808 from human recombinant 5HT4R expressed in HEK293T cellsDisplacement of [3H]GR113808 from human recombinant 5HT4R expressed in HEK293T cells
ChEMBL 352 5 0 3 5.0 CCCN1CCC(COc2nc3c(F)cccc3c3ccccc23)CC1 10.1021/jm300943r
44247820 91900493 193131 0 None - 1 Human 8.5 pKi = 8.5 Binding
Displacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 534 12 1 5 6.1 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CCCCCCCCN2CCCCC2)cc2ccccc21 10.1021/jm900881j
CHEMBL538706 193131 0 None - 1 Human 8.5 pKi = 8.5 Binding
Displacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 534 12 1 5 6.1 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CCCCCCCCN2CCCCC2)cc2ccccc21 10.1021/jm900881j
44248435 193907 0 None - 1 Human 8.5 pKi = 8.5 Binding
Displacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 623 15 2 5 7.3 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CCCCCCCCN(C)CCc2c[nH]c3ccccc23)cc2ccccc21 10.1021/jm900881j
CHEMBL555210 193907 0 None - 1 Human 8.5 pKi = 8.5 Binding
Displacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 623 15 2 5 7.3 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CCCCCCCCN(C)CCc2c[nH]c3ccccc23)cc2ccccc21 10.1021/jm900881j
44247953 194145 0 None - 1 Human 8.5 pKi = 8.5 Binding
Displacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 581 12 2 5 6.1 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CCCCCN(C)CCc2c[nH]c3ccccc23)cc2ccccc21 10.1021/jm900881j
CHEMBL558163 194145 0 None - 1 Human 8.5 pKi = 8.5 Binding
Displacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 581 12 2 5 6.1 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CCCCCN(C)CCc2c[nH]c3ccccc23)cc2ccccc21 10.1021/jm900881j
44249183 194706 0 None - 1 Human 8.5 pKi = 8.5 Binding
Displacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 478 12 2 5 5.0 COc1cc(N)c(Cl)cc1C(=O)NC1CCN(CCCCCCCCN2CCCCC2)CC1 10.1021/jm900881j
CHEMBL562636 194706 0 None - 1 Human 8.5 pKi = 8.5 Binding
Displacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 478 12 2 5 5.0 COc1cc(N)c(Cl)cc1C(=O)NC1CCN(CCCCCCCCN2CCCCC2)CC1 10.1021/jm900881j
162669699 182139 0 None - 1 Guinea pig 8.5 pKi = 8.5 Binding
Displacement of [3H]-GR113808 from guinea pig brain 5HT4 receptor in presence of serotonin incubated for 30 minsDisplacement of [3H]-GR113808 from guinea pig brain 5HT4 receptor in presence of serotonin incubated for 30 mins
ChEMBL 607 12 2 9 3.3 COc1cc(N)c(Cl)cc1C(=O)CCC1CCN(CCNS(=O)(=O)c2ccc(OC)c(N3CCN(C)CC3)c2)CC1 10.1016/j.ejmech.2016.05.048
CHEMBL4789661 182139 0 None - 1 Guinea pig 8.5 pKi = 8.5 Binding
Displacement of [3H]-GR113808 from guinea pig brain 5HT4 receptor in presence of serotonin incubated for 30 minsDisplacement of [3H]-GR113808 from guinea pig brain 5HT4 receptor in presence of serotonin incubated for 30 mins
ChEMBL 607 12 2 9 3.3 COc1cc(N)c(Cl)cc1C(=O)CCC1CCN(CCNS(=O)(=O)c2ccc(OC)c(N3CCN(C)CC3)c2)CC1 10.1016/j.ejmech.2016.05.048
235 2527 36 None -4 3 Human 8.5 pKi = 8.5 Binding
Binding affinity to YFP fused 5HT4 receptor expressed in CHO cellsBinding affinity to YFP fused 5HT4 receptor expressed in CHO cells
ChEMBL 312 5 1 5 2.6 COc1cc(N)c(cc1C(=O)OCCN1CCCCC1)Cl 10.1021/jm070552t
5311299 2527 36 None -4 3 Human 8.5 pKi = 8.5 Binding
Binding affinity to YFP fused 5HT4 receptor expressed in CHO cellsBinding affinity to YFP fused 5HT4 receptor expressed in CHO cells
ChEMBL 312 5 1 5 2.6 COc1cc(N)c(cc1C(=O)OCCN1CCCCC1)Cl 10.1021/jm070552t
CHEMBL286136 2527 36 None -4 3 Human 8.5 pKi = 8.5 Binding
Binding affinity to YFP fused 5HT4 receptor expressed in CHO cellsBinding affinity to YFP fused 5HT4 receptor expressed in CHO cells
ChEMBL 312 5 1 5 2.6 COc1cc(N)c(cc1C(=O)OCCN1CCCCC1)Cl 10.1021/jm070552t
9800656 15375 0 None - 1 Human 8.5 pKi = 8.5 Binding
Binding affinity was determined against cloned 5-hydroxytryptamine 4A receptor isoform expressed in COS-7 cellsBinding affinity was determined against cloned 5-hydroxytryptamine 4A receptor isoform expressed in COS-7 cells
ChEMBL 391 6 1 8 1.7 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCN(c2ncccn2)CC1 10.1021/jm0009538
CHEMBL121913 15375 0 None - 1 Human 8.5 pKi = 8.5 Binding
Binding affinity was determined against cloned 5-hydroxytryptamine 4A receptor isoform expressed in COS-7 cellsBinding affinity was determined against cloned 5-hydroxytryptamine 4A receptor isoform expressed in COS-7 cells
ChEMBL 391 6 1 8 1.7 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCN(c2ncccn2)CC1 10.1021/jm0009538
10715463 16175 0 None - 1 Human 8.5 pKi = 8.5 Binding
Binding affinity was determined against cloned 5-hydroxytryptamine 4E receptor isoform expressed in C6 glial cells incubated with 0.2 nM [3H]GR-113808Binding affinity was determined against cloned 5-hydroxytryptamine 4E receptor isoform expressed in C6 glial cells incubated with 0.2 nM [3H]GR-113808
ChEMBL 390 6 1 7 2.3 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCN(c2ccncc2)CC1 10.1021/jm0009538
CHEMBL122914 16175 0 None - 1 Human 8.5 pKi = 8.5 Binding
Binding affinity was determined against cloned 5-hydroxytryptamine 4E receptor isoform expressed in C6 glial cells incubated with 0.2 nM [3H]GR-113808Binding affinity was determined against cloned 5-hydroxytryptamine 4E receptor isoform expressed in C6 glial cells incubated with 0.2 nM [3H]GR-113808
ChEMBL 390 6 1 7 2.3 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCN(c2ccncc2)CC1 10.1021/jm0009538
71462652 82271 0 None - 1 Human 8.4 pKi = 8.4 Binding
Displacement of [3H]GR113808 from human 5HT4D receptor expressed in HEK293 cells after 30 mins by liquid scintillation countingDisplacement of [3H]GR113808 from human 5HT4D receptor expressed in HEK293 cells after 30 mins by liquid scintillation counting
ChEMBL 434 8 2 8 2.6 CC(C)(O)COc1cccc2onc(OCC3CCN(CC4(O)CCOCC4)CC3)c12 10.1021/jm300953p
CHEMBL2179590 82271 0 None - 1 Human 8.4 pKi = 8.4 Binding
Displacement of [3H]GR113808 from human 5HT4D receptor expressed in HEK293 cells after 30 mins by liquid scintillation countingDisplacement of [3H]GR113808 from human 5HT4D receptor expressed in HEK293 cells after 30 mins by liquid scintillation counting
ChEMBL 434 8 2 8 2.6 CC(C)(O)COc1cccc2onc(OCC3CCN(CC4(O)CCOCC4)CC3)c12 10.1021/jm300953p
235 2527 36 None -4 3 Human 8.4 pKi = 8.4 Binding
Binding affinity was determined against cloned 5-hydroxytryptamine 4D receptor isoform expressed in COS-7 cellsBinding affinity was determined against cloned 5-hydroxytryptamine 4D receptor isoform expressed in COS-7 cells
ChEMBL 312 5 1 5 2.6 COc1cc(N)c(cc1C(=O)OCCN1CCCCC1)Cl 10.1021/jm0009538
5311299 2527 36 None -4 3 Human 8.4 pKi = 8.4 Binding
Binding affinity was determined against cloned 5-hydroxytryptamine 4D receptor isoform expressed in COS-7 cellsBinding affinity was determined against cloned 5-hydroxytryptamine 4D receptor isoform expressed in COS-7 cells
ChEMBL 312 5 1 5 2.6 COc1cc(N)c(cc1C(=O)OCCN1CCCCC1)Cl 10.1021/jm0009538
CHEMBL286136 2527 36 None -4 3 Human 8.4 pKi = 8.4 Binding
Binding affinity was determined against cloned 5-hydroxytryptamine 4D receptor isoform expressed in COS-7 cellsBinding affinity was determined against cloned 5-hydroxytryptamine 4D receptor isoform expressed in COS-7 cells
ChEMBL 312 5 1 5 2.6 COc1cc(N)c(cc1C(=O)OCCN1CCCCC1)Cl 10.1021/jm0009538
183782 3346 15 None 1 14 Guinea pig 8.4 pKi = 8.4 Binding
Displacement of [3H]-GR113808 from 5-HT4R in Dunkin-Hartley guinea pig straitum nuclear membranes after 2 hrs by filter binding methodDisplacement of [3H]-GR113808 from 5-HT4R in Dunkin-Hartley guinea pig straitum nuclear membranes after 2 hrs by filter binding method
ChEMBL 352 8 1 4 4.4 CCCCN1CCC(CC1)CCC(=O)c1cc(Cl)c(cc1OC)N 10.1039/C8MD00233A
237 3346 15 None 1 14 Guinea pig 8.4 pKi = 8.4 Binding
Displacement of [3H]-GR113808 from 5-HT4R in Dunkin-Hartley guinea pig straitum nuclear membranes after 2 hrs by filter binding methodDisplacement of [3H]-GR113808 from 5-HT4R in Dunkin-Hartley guinea pig straitum nuclear membranes after 2 hrs by filter binding method
ChEMBL 352 8 1 4 4.4 CCCCN1CCC(CC1)CCC(=O)c1cc(Cl)c(cc1OC)N 10.1039/C8MD00233A
CHEMBL85251 3346 15 None 1 14 Guinea pig 8.4 pKi = 8.4 Binding
Displacement of [3H]-GR113808 from 5-HT4R in Dunkin-Hartley guinea pig straitum nuclear membranes after 2 hrs by filter binding methodDisplacement of [3H]-GR113808 from 5-HT4R in Dunkin-Hartley guinea pig straitum nuclear membranes after 2 hrs by filter binding method
ChEMBL 352 8 1 4 4.4 CCCCN1CCC(CC1)CCC(=O)c1cc(Cl)c(cc1OC)N 10.1039/C8MD00233A
5145950 201794 4 None -5 2 Rat 8.4 pKi = 8.4 Binding
Displacement of [3H]GR113808 from 5-HT4 receptor in Sprague-Dawley rat striatum after 30 minsDisplacement of [3H]GR113808 from 5-HT4 receptor in Sprague-Dawley rat striatum after 30 mins
ChEMBL 553 13 2 8 3.7 COc1cc(COc2cc(N)c(Cl)cc2C(=O)CCC2CCN(CCNS(C)(=O)=O)CC2)cc(OC)c1 10.1021/jm400766k
CHEMBL586946 201794 4 None -5 2 Rat 8.4 pKi = 8.4 Binding
Displacement of [3H]GR113808 from 5-HT4 receptor in Sprague-Dawley rat striatum after 30 minsDisplacement of [3H]GR113808 from 5-HT4 receptor in Sprague-Dawley rat striatum after 30 mins
ChEMBL 553 13 2 8 3.7 COc1cc(COc2cc(N)c(Cl)cc2C(=O)CCC2CCN(CCNS(C)(=O)=O)CC2)cc(OC)c1 10.1021/jm400766k
CHEMBL66114 201794 4 None -5 2 Rat 8.4 pKi = 8.4 Binding
Displacement of [3H]GR113808 from 5-HT4 receptor in Sprague-Dawley rat striatum after 30 minsDisplacement of [3H]GR113808 from 5-HT4 receptor in Sprague-Dawley rat striatum after 30 mins
ChEMBL 553 13 2 8 3.7 COc1cc(COc2cc(N)c(Cl)cc2C(=O)CCC2CCN(CCNS(C)(=O)=O)CC2)cc(OC)c1 10.1021/jm400766k
118734511 118164 0 None - 1 Guinea pig 8.4 pKi = 8.4 Binding
Displacement of [3H]GR113808 from 5-HT4R in guinea pig brain membranes incubated for 30 mins by radioligand binding assayDisplacement of [3H]GR113808 from 5-HT4R in guinea pig brain membranes incubated for 30 mins by radioligand binding assay
ChEMBL 406 7 1 4 5.6 COc1cc(N)c(Cl)cc1C(=O)CCC1CCN(CC2CCCCCC2)CC1 10.1021/acs.jmedchem.5b00115
CHEMBL3416997 118164 0 None - 1 Guinea pig 8.4 pKi = 8.4 Binding
Displacement of [3H]GR113808 from 5-HT4R in guinea pig brain membranes incubated for 30 mins by radioligand binding assayDisplacement of [3H]GR113808 from 5-HT4R in guinea pig brain membranes incubated for 30 mins by radioligand binding assay
ChEMBL 406 7 1 4 5.6 COc1cc(N)c(Cl)cc1C(=O)CCC1CCN(CC2CCCCCC2)CC1 10.1021/acs.jmedchem.5b00115
71451950 82263 5 None 1 2 Rat 8.4 pKi = 8.4 Binding
Displacement of [3H]GR113808 from 5HT4 receptor in rat striatal membrane after 30 mins by liquid scintillation countingDisplacement of [3H]GR113808 from 5HT4 receptor in rat striatal membrane after 30 mins by liquid scintillation counting
ChEMBL 433 4 2 5 2.4 CC1(C)C(=O)N(C(=O)NCC2CCN(CC3(O)CCOCC3)CC2)c2cc(F)ccc21 10.1021/jm300953p
CHEMBL2179582 82263 5 None 1 2 Rat 8.4 pKi = 8.4 Binding
Displacement of [3H]GR113808 from 5HT4 receptor in rat striatal membrane after 30 mins by liquid scintillation countingDisplacement of [3H]GR113808 from 5HT4 receptor in rat striatal membrane after 30 mins by liquid scintillation counting
ChEMBL 433 4 2 5 2.4 CC1(C)C(=O)N(C(=O)NCC2CCN(CC3(O)CCOCC3)CC2)c2cc(F)ccc21 10.1021/jm300953p
19081885 203633 0 None - 1 Guinea pig 8.4 pKi = 8.4 Binding
Displacement of [3H]GR113808 from serotonin 5-HT4 receptor in Dunkin-Hartley guinea pigs striatal nuclei membranes incubated for 2 hrs by liquid scintillation countingDisplacement of [3H]GR113808 from serotonin 5-HT4 receptor in Dunkin-Hartley guinea pigs striatal nuclei membranes incubated for 2 hrs by liquid scintillation counting
ChEMBL 338 7 1 4 4.0 CCCN1CCC(CCC(=O)c2cc(Cl)c(N)cc2OC)CC1 10.1039/C6MD00458J
CHEMBL79637 203633 0 None - 1 Guinea pig 8.4 pKi = 8.4 Binding
Displacement of [3H]GR113808 from serotonin 5-HT4 receptor in Dunkin-Hartley guinea pigs striatal nuclei membranes incubated for 2 hrs by liquid scintillation countingDisplacement of [3H]GR113808 from serotonin 5-HT4 receptor in Dunkin-Hartley guinea pigs striatal nuclei membranes incubated for 2 hrs by liquid scintillation counting
ChEMBL 338 7 1 4 4.0 CCCN1CCC(CCC(=O)c2cc(Cl)c(N)cc2OC)CC1 10.1039/C6MD00458J
135409453 3714 38 None -2 2 Human 8.4 pKi = 8.4 Binding
Binding affinity at 5HT4 receptorBinding affinity at 5HT4 receptor
ChEMBL 301 7 3 3 2.6 CCCCCN=C(N/N=C/c1c[nH]c2c1cc(OC)cc2)N 10.1016/j.bmc.2008.11.045
226 3714 38 None -2 2 Human 8.4 pKi = 8.4 Binding
Binding affinity at 5HT4 receptorBinding affinity at 5HT4 receptor
ChEMBL 301 7 3 3 2.6 CCCCCN=C(N/N=C/c1c[nH]c2c1cc(OC)cc2)N 10.1016/j.bmc.2008.11.045
CHEMBL76370 3714 38 None -2 2 Human 8.4 pKi = 8.4 Binding
Binding affinity at 5HT4 receptorBinding affinity at 5HT4 receptor
ChEMBL 301 7 3 3 2.6 CCCCCN=C(N/N=C/c1c[nH]c2c1cc(OC)cc2)N 10.1016/j.bmc.2008.11.045
135409453 3714 38 None -2 2 Human 8.4 pKi = 8.4 Binding
Binding affinity to human recombinant 5HT4 receptorBinding affinity to human recombinant 5HT4 receptor
ChEMBL 301 7 3 3 2.6 CCCCCN=C(N/N=C/c1c[nH]c2c1cc(OC)cc2)N 10.1016/j.bmcl.2013.05.018
226 3714 38 None -2 2 Human 8.4 pKi = 8.4 Binding
Binding affinity to human recombinant 5HT4 receptorBinding affinity to human recombinant 5HT4 receptor
ChEMBL 301 7 3 3 2.6 CCCCCN=C(N/N=C/c1c[nH]c2c1cc(OC)cc2)N 10.1016/j.bmcl.2013.05.018
CHEMBL76370 3714 38 None -2 2 Human 8.4 pKi = 8.4 Binding
Binding affinity to human recombinant 5HT4 receptorBinding affinity to human recombinant 5HT4 receptor
ChEMBL 301 7 3 3 2.6 CCCCCN=C(N/N=C/c1c[nH]c2c1cc(OC)cc2)N 10.1016/j.bmcl.2013.05.018
71712464 90960 0 None - 1 Human 8.4 pKi = 8.4 Binding
Binding affinity to human recombinant 5HT4 receptorBinding affinity to human recombinant 5HT4 receptor
ChEMBL 445 8 3 6 2.2 COC(=O)N(C)CC(O)CN1CCC(CNC(=O)c2cccc3[nH]c(C(C)C)nc23)CC1 10.1016/j.bmcl.2013.05.018
CHEMBL2402901 90960 0 None - 1 Human 8.4 pKi = 8.4 Binding
Binding affinity to human recombinant 5HT4 receptorBinding affinity to human recombinant 5HT4 receptor
ChEMBL 445 8 3 6 2.2 COC(=O)N(C)CC(O)CN1CCC(CNC(=O)c2cccc3[nH]c(C(C)C)nc23)CC1 10.1016/j.bmcl.2013.05.018
71712465 90961 0 None - 1 Human 8.4 pKi = 8.4 Binding
Binding affinity to human recombinant 5HT4 receptorBinding affinity to human recombinant 5HT4 receptor
ChEMBL 429 8 3 5 2.0 CC(=O)N(C)CC(O)CN1CCC(CNC(=O)c2cccc3[nH]c(C(C)C)nc23)CC1 10.1016/j.bmcl.2013.05.018
CHEMBL2402902 90961 0 None - 1 Human 8.4 pKi = 8.4 Binding
Binding affinity to human recombinant 5HT4 receptorBinding affinity to human recombinant 5HT4 receptor
ChEMBL 429 8 3 5 2.0 CC(=O)N(C)CC(O)CN1CCC(CNC(=O)c2cccc3[nH]c(C(C)C)nc23)CC1 10.1016/j.bmcl.2013.05.018
72697299 92442 0 None - 1 Human 8.4 pKi = 8.4 Binding
Displacement of [3H]GR113808 from human 5HT4B receptor expressed in HEK293 cellsDisplacement of [3H]GR113808 from human 5HT4B receptor expressed in HEK293 cells
ChEMBL 547 7 2 7 4.9 O=C(NCC1CCN(Cc2ccc(-c3ccccc3-c3nnn[nH]3)cc2)CC1)c1c2n(c3ccccc13)CCCO2 10.1016/j.bmc.2013.09.004
CHEMBL2440455 92442 0 None - 1 Human 8.4 pKi = 8.4 Binding
Displacement of [3H]GR113808 from human 5HT4B receptor expressed in HEK293 cellsDisplacement of [3H]GR113808 from human 5HT4B receptor expressed in HEK293 cells
ChEMBL 547 7 2 7 4.9 O=C(NCC1CCN(Cc2ccc(-c3ccccc3-c3nnn[nH]3)cc2)CC1)c1c2n(c3ccccc13)CCCO2 10.1016/j.bmc.2013.09.004
135409453 3714 38 None -2 2 Human 8.4 pKi = 8.4 Binding
Displacement of [3H]GR113808 from human recombinant 5HT4C receptor expressed in HEK293 cellsDisplacement of [3H]GR113808 from human recombinant 5HT4C receptor expressed in HEK293 cells
ChEMBL 301 7 3 3 2.6 CCCCCN=C(N/N=C/c1c[nH]c2c1cc(OC)cc2)N 10.1016/j.bmcl.2012.05.034
226 3714 38 None -2 2 Human 8.4 pKi = 8.4 Binding
Displacement of [3H]GR113808 from human recombinant 5HT4C receptor expressed in HEK293 cellsDisplacement of [3H]GR113808 from human recombinant 5HT4C receptor expressed in HEK293 cells
ChEMBL 301 7 3 3 2.6 CCCCCN=C(N/N=C/c1c[nH]c2c1cc(OC)cc2)N 10.1016/j.bmcl.2012.05.034
CHEMBL76370 3714 38 None -2 2 Human 8.4 pKi = 8.4 Binding
Displacement of [3H]GR113808 from human recombinant 5HT4C receptor expressed in HEK293 cellsDisplacement of [3H]GR113808 from human recombinant 5HT4C receptor expressed in HEK293 cells
ChEMBL 301 7 3 3 2.6 CCCCCN=C(N/N=C/c1c[nH]c2c1cc(OC)cc2)N 10.1016/j.bmcl.2012.05.034
70688534 76060 0 None - 1 Human 8.4 pKi = 8.4 Binding
Displacement of [3H]GR113808 from human recombinant 5HT4C receptor expressed in HEK293 cellsDisplacement of [3H]GR113808 from human recombinant 5HT4C receptor expressed in HEK293 cells
ChEMBL 441 8 2 6 3.0 CC(C)N(C)CC(O)CN1[C@H]2CC[C@@H]1C[C@H](NC(=O)c1nn(C(C)C)c3ccccc13)C2 10.1016/j.bmcl.2012.05.034
CHEMBL2059579 76060 0 None - 1 Human 8.4 pKi = 8.4 Binding
Displacement of [3H]GR113808 from human recombinant 5HT4C receptor expressed in HEK293 cellsDisplacement of [3H]GR113808 from human recombinant 5HT4C receptor expressed in HEK293 cells
ChEMBL 441 8 2 6 3.0 CC(C)N(C)CC(O)CN1[C@H]2CC[C@@H]1C[C@H](NC(=O)c1nn(C(C)C)c3ccccc13)C2 10.1016/j.bmcl.2012.05.034
11677434 76062 0 None - 1 Human 8.4 pKi = 8.4 Binding
Displacement of [3H]GR113808 from human recombinant 5HT4C receptor expressed in HEK293 cellsDisplacement of [3H]GR113808 from human recombinant 5HT4C receptor expressed in HEK293 cells
ChEMBL 483 9 2 7 2.8 COC[C@@H]1CCCN1CC(O)CN1[C@H]2CC[C@@H]1C[C@H](NC(=O)c1nn(C(C)C)c3ccccc13)C2 10.1016/j.bmcl.2012.05.034
CHEMBL2059581 76062 0 None - 1 Human 8.4 pKi = 8.4 Binding
Displacement of [3H]GR113808 from human recombinant 5HT4C receptor expressed in HEK293 cellsDisplacement of [3H]GR113808 from human recombinant 5HT4C receptor expressed in HEK293 cells
ChEMBL 483 9 2 7 2.8 COC[C@@H]1CCCN1CC(O)CN1[C@H]2CC[C@@H]1C[C@H](NC(=O)c1nn(C(C)C)c3ccccc13)C2 10.1016/j.bmcl.2012.05.034
11606227 76066 0 None - 1 Human 8.4 pKi = 8.4 Binding
Displacement of [3H]GR113808 from human recombinant 5HT4C receptor expressed in HEK293 cellsDisplacement of [3H]GR113808 from human recombinant 5HT4C receptor expressed in HEK293 cells
ChEMBL 532 8 2 8 1.3 CC(C)n1nc(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CC(O)CN2CCN(S(C)(=O)=O)CC2)c2ccccc21 10.1016/j.bmcl.2012.05.034
CHEMBL2059585 76066 0 None - 1 Human 8.4 pKi = 8.4 Binding
Displacement of [3H]GR113808 from human recombinant 5HT4C receptor expressed in HEK293 cellsDisplacement of [3H]GR113808 from human recombinant 5HT4C receptor expressed in HEK293 cells
ChEMBL 532 8 2 8 1.3 CC(C)n1nc(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CC(O)CN2CCN(S(C)(=O)=O)CC2)c2ccccc21 10.1016/j.bmcl.2012.05.034
135409453 3714 38 None -2 2 Human 8.4 pKi = 8.4 Binding
Displacement of [3H]GR113808 from human recombinant 5HT4c receptor expressed in HEK293 cellsDisplacement of [3H]GR113808 from human recombinant 5HT4c receptor expressed in HEK293 cells
ChEMBL 301 7 3 3 2.6 CCCCCN=C(N/N=C/c1c[nH]c2c1cc(OC)cc2)N 10.1016/j.bmcl.2012.08.051
226 3714 38 None -2 2 Human 8.4 pKi = 8.4 Binding
Displacement of [3H]GR113808 from human recombinant 5HT4c receptor expressed in HEK293 cellsDisplacement of [3H]GR113808 from human recombinant 5HT4c receptor expressed in HEK293 cells
ChEMBL 301 7 3 3 2.6 CCCCCN=C(N/N=C/c1c[nH]c2c1cc(OC)cc2)N 10.1016/j.bmcl.2012.08.051
CHEMBL76370 3714 38 None -2 2 Human 8.4 pKi = 8.4 Binding
Displacement of [3H]GR113808 from human recombinant 5HT4c receptor expressed in HEK293 cellsDisplacement of [3H]GR113808 from human recombinant 5HT4c receptor expressed in HEK293 cells
ChEMBL 301 7 3 3 2.6 CCCCCN=C(N/N=C/c1c[nH]c2c1cc(OC)cc2)N 10.1016/j.bmcl.2012.08.051
44248437 193168 0 None - 1 Human 8.4 pKi = 8.4 Binding
Displacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 597 12 1 6 6.1 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CCCCCCCN2CCN(c3ccccc3)CC2)cc2ccccc21 10.1021/jm900881j
CHEMBL539651 193168 0 None - 1 Human 8.4 pKi = 8.4 Binding
Displacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 597 12 1 6 6.1 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CCCCCCCN2CCN(c3ccccc3)CC2)cc2ccccc21 10.1021/jm900881j
10971995 161857 0 None - 1 Guinea pig 7.5 pKi = 7.5 Binding
Displacement of [3H]GR113808 from serotonin 5-HT4 receptor in Dunkin-Hartley guinea pigs striatal nuclei membranes incubated for 2 hrs by liquid scintillation countingDisplacement of [3H]GR113808 from serotonin 5-HT4 receptor in Dunkin-Hartley guinea pigs striatal nuclei membranes incubated for 2 hrs by liquid scintillation counting
ChEMBL 427 6 2 7 3.1 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCC(NC(=O)OC(C)(C)C)CC1 10.1039/C6MD00458J
CHEMBL4165966 161857 0 None - 1 Guinea pig 7.5 pKi = 7.5 Binding
Displacement of [3H]GR113808 from serotonin 5-HT4 receptor in Dunkin-Hartley guinea pigs striatal nuclei membranes incubated for 2 hrs by liquid scintillation countingDisplacement of [3H]GR113808 from serotonin 5-HT4 receptor in Dunkin-Hartley guinea pigs striatal nuclei membranes incubated for 2 hrs by liquid scintillation counting
ChEMBL 427 6 2 7 3.1 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCC(NC(=O)OC(C)(C)C)CC1 10.1039/C6MD00458J
145978961 165999 0 None - 1 Guinea pig 6.5 pKi = 6.5 Binding
Displacement of [3H]-GR113808 from 5-HT4R in Dunkin-Hartley guinea pig straitum nuclear membranes after 2 hrs by filter binding methodDisplacement of [3H]-GR113808 from 5-HT4R in Dunkin-Hartley guinea pig straitum nuclear membranes after 2 hrs by filter binding method
ChEMBL 429 6 1 7 3.4 COc1cc(C(=O)OCCN2CCC(NC(=O)OC(C)(C)C)CC2)c2ccccc2n1 10.1039/C8MD00233A
CHEMBL4279553 165999 0 None - 1 Guinea pig 6.5 pKi = 6.5 Binding
Displacement of [3H]-GR113808 from 5-HT4R in Dunkin-Hartley guinea pig straitum nuclear membranes after 2 hrs by filter binding methodDisplacement of [3H]-GR113808 from 5-HT4R in Dunkin-Hartley guinea pig straitum nuclear membranes after 2 hrs by filter binding method
ChEMBL 429 6 1 7 3.4 COc1cc(C(=O)OCCN2CCC(NC(=O)OC(C)(C)C)CC2)c2ccccc2n1 10.1039/C8MD00233A
10543526 206641 0 None - 1 Guinea pig 6.5 pKi = 6.5 Binding
Binding affinity against 5-hydroxytryptamine 4 receptor in guinea pig striatum using [3H]GR-113808 as radioligandBinding affinity against 5-hydroxytryptamine 4 receptor in guinea pig striatum using [3H]GR-113808 as radioligand
ChEMBL 317 3 1 6 0.1 CN1CCN(CCNC(=O)n2c(=O)n(C)c3ccccc32)CC1 10.1021/jm981098j
CHEMBL99578 206641 0 None - 1 Guinea pig 6.5 pKi = 6.5 Binding
Binding affinity against 5-hydroxytryptamine 4 receptor in guinea pig striatum using [3H]GR-113808 as radioligandBinding affinity against 5-hydroxytryptamine 4 receptor in guinea pig striatum using [3H]GR-113808 as radioligand
ChEMBL 317 3 1 6 0.1 CN1CCN(CCNC(=O)n2c(=O)n(C)c3ccccc32)CC1 10.1021/jm981098j
11714709 78643 0 None - 1 Human 7.5 pKi = 7.5 Binding
Binding affinity for 5-HT4 receptor using [3H]GR-113808Binding affinity for 5-HT4 receptor using [3H]GR-113808
ChEMBL 750 16 4 12 3.4 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCC(NC(=O)CCCNC(=O)C2CCN(CCOC(=O)c3cc(Cl)c(N)cc3OC)CC2)CC1 10.1021/jm050234z
CHEMBL2113158 78643 0 None - 1 Human 7.5 pKi = 7.5 Binding
Binding affinity for 5-HT4 receptor using [3H]GR-113808Binding affinity for 5-HT4 receptor using [3H]GR-113808
ChEMBL 750 16 4 12 3.4 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCC(NC(=O)CCCNC(=O)C2CCN(CCOC(=O)c3cc(Cl)c(N)cc3OC)CC2)CC1 10.1021/jm050234z
11039730 204525 0 None - 1 Human 7.5 pKi = 7.5 Binding
Binding affinity towards cloned human 5-hydroxytryptamine 4E receptor expressed in C6 glial cells using [3H]GR-113808 as radioligandBinding affinity towards cloned human 5-hydroxytryptamine 4E receptor expressed in C6 glial cells using [3H]GR-113808 as radioligand
ChEMBL 687 16 2 9 4.8 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCN(C(=O)CCCCCCCNS(=O)(=O)c2cccc3c(N(C)C)cccc23)CC1 10.1021/jm0307887
CHEMBL86777 204525 0 None - 1 Human 7.5 pKi = 7.5 Binding
Binding affinity towards cloned human 5-hydroxytryptamine 4E receptor expressed in C6 glial cells using [3H]GR-113808 as radioligandBinding affinity towards cloned human 5-hydroxytryptamine 4E receptor expressed in C6 glial cells using [3H]GR-113808 as radioligand
ChEMBL 687 16 2 9 4.8 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCN(C(=O)CCCCCCCNS(=O)(=O)c2cccc3c(N(C)C)cccc23)CC1 10.1021/jm0307887
135409453 3714 38 None -2 2 Human 7.5 pKi = 7.5 Binding
Displacement of [N-methyl-3H]GR-113808 from human 5HT4 receptor expressed in HEK293 cellsDisplacement of [N-methyl-3H]GR-113808 from human 5HT4 receptor expressed in HEK293 cells
ChEMBL 301 7 3 3 2.6 CCCCCN=C(N/N=C/c1c[nH]c2c1cc(OC)cc2)N 10.1021/np0601760
226 3714 38 None -2 2 Human 7.5 pKi = 7.5 Binding
Displacement of [N-methyl-3H]GR-113808 from human 5HT4 receptor expressed in HEK293 cellsDisplacement of [N-methyl-3H]GR-113808 from human 5HT4 receptor expressed in HEK293 cells
ChEMBL 301 7 3 3 2.6 CCCCCN=C(N/N=C/c1c[nH]c2c1cc(OC)cc2)N 10.1021/np0601760
CHEMBL76370 3714 38 None -2 2 Human 7.5 pKi = 7.5 Binding
Displacement of [N-methyl-3H]GR-113808 from human 5HT4 receptor expressed in HEK293 cellsDisplacement of [N-methyl-3H]GR-113808 from human 5HT4 receptor expressed in HEK293 cells
ChEMBL 301 7 3 3 2.6 CCCCCN=C(N/N=C/c1c[nH]c2c1cc(OC)cc2)N 10.1021/np0601760
182593 3343 4 None 1 3 Human 7.5 pKi = 7.5 Binding
Binding affinity at 5HT4 receptorBinding affinity at 5HT4 receptor
ChEMBL 326 6 1 5 3.0 COc1cc(N)c(cc1C(=O)OCCCN1CCCCC1)Cl 10.1016/j.bmc.2008.11.045
254 3343 4 None 1 3 Human 7.5 pKi = 7.5 Binding
Binding affinity at 5HT4 receptorBinding affinity at 5HT4 receptor
ChEMBL 326 6 1 5 3.0 COc1cc(N)c(cc1C(=O)OCCCN1CCCCC1)Cl 10.1016/j.bmc.2008.11.045
CHEMBL83954 3343 4 None 1 3 Human 7.5 pKi = 7.5 Binding
Binding affinity at 5HT4 receptorBinding affinity at 5HT4 receptor
ChEMBL 326 6 1 5 3.0 COc1cc(N)c(cc1C(=O)OCCCN1CCCCC1)Cl 10.1016/j.bmc.2008.11.045
71459132 84144 0 None - 1 Human 7.5 pKi = 7.5 Binding
Displacement of [3H](1-(2-(methylsulfonamido)ethyl)piperidin-4-yl)methyl 1-methyl-1H-indole-3-carboxylate from human 5HT4R expressed in HEK293 cellsDisplacement of [3H](1-(2-(methylsulfonamido)ethyl)piperidin-4-yl)methyl 1-methyl-1H-indole-3-carboxylate from human 5HT4R expressed in HEK293 cells
ChEMBL 419 7 1 3 4.4 CC(C)n1nc(C(=O)NCC2CC[N+](C)(CCc3ccccc3)CC2)c2ccccc21 10.1021/jm300573d
CHEMBL2179698 84144 0 None - 1 Human 7.5 pKi = 7.5 Binding
Displacement of [3H](1-(2-(methylsulfonamido)ethyl)piperidin-4-yl)methyl 1-methyl-1H-indole-3-carboxylate from human 5HT4R expressed in HEK293 cellsDisplacement of [3H](1-(2-(methylsulfonamido)ethyl)piperidin-4-yl)methyl 1-methyl-1H-indole-3-carboxylate from human 5HT4R expressed in HEK293 cells
ChEMBL 419 7 1 3 4.4 CC(C)n1nc(C(=O)NCC2CC[N+](C)(CCc3ccccc3)CC2)c2ccccc21 10.1021/jm300573d
CHEMBL2220893 84144 0 None - 1 Human 7.5 pKi = 7.5 Binding
Displacement of [3H](1-(2-(methylsulfonamido)ethyl)piperidin-4-yl)methyl 1-methyl-1H-indole-3-carboxylate from human 5HT4R expressed in HEK293 cellsDisplacement of [3H](1-(2-(methylsulfonamido)ethyl)piperidin-4-yl)methyl 1-methyl-1H-indole-3-carboxylate from human 5HT4R expressed in HEK293 cells
ChEMBL 419 7 1 3 4.4 CC(C)n1nc(C(=O)NCC2CC[N+](C)(CCc3ccccc3)CC2)c2ccccc21 10.1021/jm300573d
67276466 77145 0 None - 1 Human 7.5 pKi = 7.5 Binding
Displacement of [3H]GR113808 from human recombinant 5HT4c receptor expressed in HEK293 cellsDisplacement of [3H]GR113808 from human recombinant 5HT4c receptor expressed in HEK293 cells
ChEMBL 454 7 3 6 1.8 CC(=O)NCC(O)CN1[C@H]2CC[C@@H]1C[C@H](NC(=O)c1cc3ccccc3n(C(C)C)c1=O)C2 10.1016/j.bmcl.2012.08.051
CHEMBL2087324 77145 0 None - 1 Human 7.5 pKi = 7.5 Binding
Displacement of [3H]GR113808 from human recombinant 5HT4c receptor expressed in HEK293 cellsDisplacement of [3H]GR113808 from human recombinant 5HT4c receptor expressed in HEK293 cells
ChEMBL 454 7 3 6 1.8 CC(=O)NCC(O)CN1[C@H]2CC[C@@H]1C[C@H](NC(=O)c1cc3ccccc3n(C(C)C)c1=O)C2 10.1016/j.bmcl.2012.08.051
44248311 91900487 193957 0 None - 1 Human 7.5 pKi = 7.5 Binding
Displacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 596 12 1 6 5.9 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CCCCCCCCN2C(=O)c3ccccc3C2=O)cc2ccccc21 10.1021/jm900881j
CHEMBL556279 193957 0 None - 1 Human 7.5 pKi = 7.5 Binding
Displacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 596 12 1 6 5.9 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CCCCCCCCN2C(=O)c3ccccc3C2=O)cc2ccccc21 10.1021/jm900881j
39736 183650 8 None - 1 Rat 7.5 pKi = 7.5 Binding
Binding affinity at 5-hydroxytryptamine 4 receptor in rat striatal membranes by [3H]GR-113808 displacement.Binding affinity at 5-hydroxytryptamine 4 receptor in rat striatal membranes by [3H]GR-113808 displacement.
ChEMBL 248 4 1 3 2.7 O=C(Nc1ccccc1)OCCN1CCCCC1 10.1021/jm960853v
CHEMBL48351 183650 8 None - 1 Rat 7.5 pKi = 7.5 Binding
Binding affinity at 5-hydroxytryptamine 4 receptor in rat striatal membranes by [3H]GR-113808 displacement.Binding affinity at 5-hydroxytryptamine 4 receptor in rat striatal membranes by [3H]GR-113808 displacement.
ChEMBL 248 4 1 3 2.7 O=C(Nc1ccccc1)OCCN1CCCCC1 10.1021/jm960853v
71712612 90947 0 None - 1 Human 6.5 pKi = 6.5 Binding
Binding affinity to human recombinant 5HT4 receptorBinding affinity to human recombinant 5HT4 receptor
ChEMBL 490 7 3 7 0.2 CS(=O)(=O)N1CCN(CC(O)CN2[C@H]3CC[C@@H]2C[C@H](NC(=O)c2cccc4[nH]cnc24)C3)CC1 10.1016/j.bmcl.2013.05.018
CHEMBL2402888 90947 0 None - 1 Human 6.5 pKi = 6.5 Binding
Binding affinity to human recombinant 5HT4 receptorBinding affinity to human recombinant 5HT4 receptor
ChEMBL 490 7 3 7 0.2 CS(=O)(=O)N1CCN(CC(O)CN2[C@H]3CC[C@@H]2C[C@H](NC(=O)c2cccc4[nH]cnc24)C3)CC1 10.1016/j.bmcl.2013.05.018
9817713 193169 53 None - 1 Human 6.5 pKi = 6.5 Binding
Displacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 297 4 3 4 1.7 COc1cc(N)c(Cl)cc1C(=O)NCC1CCNCC1 10.1021/jm900881j
CHEMBL539652 193169 53 None - 1 Human 6.5 pKi = 6.5 Binding
Displacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 297 4 3 4 1.7 COc1cc(N)c(Cl)cc1C(=O)NCC1CCNCC1 10.1021/jm900881j
44249316 91900479 193682 0 None - 1 Human 6.5 pKi = 6.5 Binding
Displacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 328 2 2 5 2.2 CC(C)n1c(=O)n(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3)c2ccccc21 10.1021/jm900881j
CHEMBL551820 193682 0 None - 1 Human 6.5 pKi = 6.5 Binding
Displacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 328 2 2 5 2.2 CC(C)n1c(=O)n(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3)c2ccccc21 10.1021/jm900881j
44248796 193844 0 None - 1 Human 6.5 pKi = 6.5 Binding
Displacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 302 5 3 4 0.8 COc1ccc2[nH]cc(C(=O)NCCN3CCNCC3)c2c1 10.1021/jm900881j
CHEMBL553688 193844 0 None - 1 Human 6.5 pKi = 6.5 Binding
Displacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 302 5 3 4 0.8 COc1ccc2[nH]cc(C(=O)NCCN3CCNCC3)c2c1 10.1021/jm900881j
10346043 46856 0 None -3162 3 Human 5.5 pKi = 5.5 Binding
Compound was evaluated for the binding affinity against human cloned 5-hydroxytryptamine 4 receptor in HeLa cells using [3H]-LSD as the radioligandCompound was evaluated for the binding affinity against human cloned 5-hydroxytryptamine 4 receptor in HeLa cells using [3H]-LSD as the radioligand
ChEMBL 503 5 2 5 3.4 COc1ccc(S(=O)(=O)Nc2cc(Br)ccc2Br)cc1N1CCNCC1 10.1016/s0960-894x(00)00597-7
CHEMBL154274 46856 0 None -3162 3 Human 5.5 pKi = 5.5 Binding
Compound was evaluated for the binding affinity against human cloned 5-hydroxytryptamine 4 receptor in HeLa cells using [3H]-LSD as the radioligandCompound was evaluated for the binding affinity against human cloned 5-hydroxytryptamine 4 receptor in HeLa cells using [3H]-LSD as the radioligand
ChEMBL 503 5 2 5 3.4 COc1ccc(S(=O)(=O)Nc2cc(Br)ccc2Br)cc1N1CCNCC1 10.1016/s0960-894x(00)00597-7
6918648 101089 1 None -5128 14 Human 5.5 pKi = 5.5 Binding
Compound was tested for its binding affinity against 5-hydroxytryptamine 4 receptorCompound was tested for its binding affinity against 5-hydroxytryptamine 4 receptor
ChEMBL 465 5 1 6 4.4 COc1ccc(NS(=O)(=O)c2sc3ccc(Cl)cc3c2C)cc1N1CCN(C)CC1 10.1021/jm980532e
CHEMBL29846 101089 1 None -5128 14 Human 5.5 pKi = 5.5 Binding
Compound was tested for its binding affinity against 5-hydroxytryptamine 4 receptorCompound was tested for its binding affinity against 5-hydroxytryptamine 4 receptor
ChEMBL 465 5 1 6 4.4 COc1ccc(NS(=O)(=O)c2sc3ccc(Cl)cc3c2C)cc1N1CCN(C)CC1 10.1021/jm980532e
44249311 193656 0 None - 1 Human 5.5 pKi = 5.5 Binding
Displacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 313 3 2 4 2.1 CC(C)n1c(=O)c(C(=O)NC2CCNCC2)cc2ccccc21 10.1021/jm900881j
CHEMBL551614 193656 0 None - 1 Human 5.5 pKi = 5.5 Binding
Displacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 313 3 2 4 2.1 CC(C)n1c(=O)c(C(=O)NC2CCNCC2)cc2ccccc21 10.1021/jm900881j
44249317 91900480 193671 0 None - 1 Human 5.5 pKi = 5.5 Binding
Displacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 299 3 3 3 2.2 COc1ccc2[nH]cc(C(=O)N[C@@H]3C[C@@H]4CC[C@H](C3)N4)c2c1 10.1021/jm900881j
CHEMBL551743 193671 0 None - 1 Human 5.5 pKi = 5.5 Binding
Displacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 299 3 3 3 2.2 COc1ccc2[nH]cc(C(=O)N[C@@H]3C[C@@H]4CC[C@H](C3)N4)c2c1 10.1021/jm900881j
44249318 194195 0 None - 1 Human 5.5 pKi = 5.5 Binding
Displacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 273 3 3 3 1.7 COc1ccc2[nH]cc(C(=O)NC3CCNCC3)c2c1 10.1021/jm900881j
CHEMBL558757 194195 0 None - 1 Human 5.5 pKi = 5.5 Binding
Displacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 273 3 3 3 1.7 COc1ccc2[nH]cc(C(=O)NC3CCNCC3)c2c1 10.1021/jm900881j
6918648 101089 1 None -5128 14 Human 5.5 pKi = 5.5 Binding
The compound was tested for the binding affinity towards human cloned 5-hydroxytryptamine 4 receptor in HeLa cells, using [3H]LSD as radioligandThe compound was tested for the binding affinity towards human cloned 5-hydroxytryptamine 4 receptor in HeLa cells, using [3H]LSD as radioligand
ChEMBL 465 5 1 6 4.4 COc1ccc(NS(=O)(=O)c2sc3ccc(Cl)cc3c2C)cc1N1CCN(C)CC1 10.1016/s0960-894x(02)00172-5
CHEMBL29846 101089 1 None -5128 14 Human 5.5 pKi = 5.5 Binding
The compound was tested for the binding affinity towards human cloned 5-hydroxytryptamine 4 receptor in HeLa cells, using [3H]LSD as radioligandThe compound was tested for the binding affinity towards human cloned 5-hydroxytryptamine 4 receptor in HeLa cells, using [3H]LSD as radioligand
ChEMBL 465 5 1 6 4.4 COc1ccc(NS(=O)(=O)c2sc3ccc(Cl)cc3c2C)cc1N1CCN(C)CC1 10.1016/s0960-894x(02)00172-5
11841877 39608 1 None - 1 Rat 6.5 pKi = 6.5 Binding
In vitro affinity at serotonergic 5-hydroxytryptamine 4 receptor by radioligand binding assay using [3H]GR-113808 in rat striatum membranes.In vitro affinity at serotonergic 5-hydroxytryptamine 4 receptor by radioligand binding assay using [3H]GR-113808 in rat striatum membranes.
ChEMBL 318 2 2 3 2.6 CN1C2CCC1CC(NC(=O)c1cc(Cl)cc3[nH]cnc13)C2 10.1021/jm991076c
CHEMBL147725 39608 1 None - 1 Rat 6.5 pKi = 6.5 Binding
In vitro affinity at serotonergic 5-hydroxytryptamine 4 receptor by radioligand binding assay using [3H]GR-113808 in rat striatum membranes.In vitro affinity at serotonergic 5-hydroxytryptamine 4 receptor by radioligand binding assay using [3H]GR-113808 in rat striatum membranes.
ChEMBL 318 2 2 3 2.6 CN1C2CCC1CC(NC(=O)c1cc(Cl)cc3[nH]cnc13)C2 10.1021/jm991076c
11093246 111057 0 None - 1 Human 7.5 pKi = 7.5 Binding
Binding affinity towards cloned human 5-hydroxytryptamine 4E receptor expressed in C6 glial cells using [3H]GR-113808 as radioligandBinding affinity towards cloned human 5-hydroxytryptamine 4E receptor expressed in C6 glial cells using [3H]GR-113808 as radioligand
ChEMBL 602 12 2 8 4.8 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCC(CCCNS(=O)(=O)c2cccc3c(N(C)C)cccc23)CC1 10.1021/jm0307887
CHEMBL327999 111057 0 None - 1 Human 7.5 pKi = 7.5 Binding
Binding affinity towards cloned human 5-hydroxytryptamine 4E receptor expressed in C6 glial cells using [3H]GR-113808 as radioligandBinding affinity towards cloned human 5-hydroxytryptamine 4E receptor expressed in C6 glial cells using [3H]GR-113808 as radioligand
ChEMBL 602 12 2 8 4.8 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCC(CCCNS(=O)(=O)c2cccc3c(N(C)C)cccc23)CC1 10.1021/jm0307887
10408029 16283 0 None - 1 Human 7.5 pKi = 7.5 Binding
Binding affinity was determined against cloned 5-hydroxytryptamine 4D receptor isoform expressed in COS-7 cellsBinding affinity was determined against cloned 5-hydroxytryptamine 4D receptor isoform expressed in COS-7 cells
ChEMBL 389 6 1 6 2.9 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCN(c2ccccc2)CC1 10.1021/jm0009538
CHEMBL123377 16283 0 None - 1 Human 7.5 pKi = 7.5 Binding
Binding affinity was determined against cloned 5-hydroxytryptamine 4D receptor isoform expressed in COS-7 cellsBinding affinity was determined against cloned 5-hydroxytryptamine 4D receptor isoform expressed in COS-7 cells
ChEMBL 389 6 1 6 2.9 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCN(c2ccccc2)CC1 10.1021/jm0009538
49783206 17395 0 None -74 2 Human 7.5 pKi = 7.5 Binding
Displacement of [3H]GR113808 from human recombinant 5HT4 receptor expressed in HEK293 cellsDisplacement of [3H]GR113808 from human recombinant 5HT4 receptor expressed in HEK293 cells
ChEMBL 373 6 1 7 2.6 CCCCN1CCC(COC(=O)c2cc(C#N)c(N)c3c2OCCO3)CC1 10.1021/jm100668r
CHEMBL1258108 17395 0 None -74 2 Human 7.5 pKi = 7.5 Binding
Displacement of [3H]GR113808 from human recombinant 5HT4 receptor expressed in HEK293 cellsDisplacement of [3H]GR113808 from human recombinant 5HT4 receptor expressed in HEK293 cells
ChEMBL 373 6 1 7 2.6 CCCCN1CCC(COC(=O)c2cc(C#N)c(N)c3c2OCCO3)CC1 10.1021/jm100668r
71461048 82560 0 None 3 2 Human 7.5 pKi = 7.5 Binding
Displacement of [3H]GR113808 from human recombinant 5HT4R expressed in HEK293T cellsDisplacement of [3H]GR113808 from human recombinant 5HT4R expressed in HEK293T cells
ChEMBL 352 5 0 3 5.0 CCCN1CCC(COc2nc3cc(F)ccc3c3ccccc23)CC1 10.1021/jm300943r
CHEMBL2181185 82560 0 None 3 2 Human 7.5 pKi = 7.5 Binding
Displacement of [3H]GR113808 from human recombinant 5HT4R expressed in HEK293T cellsDisplacement of [3H]GR113808 from human recombinant 5HT4R expressed in HEK293T cells
ChEMBL 352 5 0 3 5.0 CCCN1CCC(COc2nc3cc(F)ccc3c3ccccc23)CC1 10.1021/jm300943r
10667079 205615 0 None - 1 Guinea pig 7.5 pKi = 7.5 Binding
Binding affinity against 5-hydroxytryptamine 4 receptor in guinea pig striatum using [3H]GR-113808 as radioligandBinding affinity against 5-hydroxytryptamine 4 receptor in guinea pig striatum using [3H]GR-113808 as radioligand
ChEMBL 373 7 1 6 1.8 CCCCN1CCN(CCNC(=O)n2c(=O)n(CC)c3ccccc32)CC1 10.1021/jm981098j
CHEMBL93611 205615 0 None - 1 Guinea pig 7.5 pKi = 7.5 Binding
Binding affinity against 5-hydroxytryptamine 4 receptor in guinea pig striatum using [3H]GR-113808 as radioligandBinding affinity against 5-hydroxytryptamine 4 receptor in guinea pig striatum using [3H]GR-113808 as radioligand
ChEMBL 373 7 1 6 1.8 CCCCN1CCN(CCNC(=O)n2c(=O)n(CC)c3ccccc32)CC1 10.1021/jm981098j
44281491 111982 0 None - 1 Rat 7.5 pKi = 7.5 Binding
Binding affinity against 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatumBinding affinity against 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatum
ChEMBL 312 4 1 5 2.6 CCN1CCCC(OC(=O)c2cc(Cl)c(N)cc2OC)C1 10.1016/S0960-894X(01)80508-4
CHEMBL32986 111982 0 None - 1 Rat 7.5 pKi = 7.5 Binding
Binding affinity against 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatumBinding affinity against 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatum
ChEMBL 312 4 1 5 2.6 CCN1CCCC(OC(=O)c2cc(Cl)c(N)cc2OC)C1 10.1016/S0960-894X(01)80508-4
90644478 111791 0 None - 1 Guinea pig 6.5 pKi = 6.5 Binding
Displacement of [3H]GR113808 from Dunkin-Hartley guinea pig brain striatum 5HT4R after 30 minsDisplacement of [3H]GR113808 from Dunkin-Hartley guinea pig brain striatum 5HT4R after 30 mins
ChEMBL 406 5 0 5 3.7 O=C1c2cccc3nc(N4CCCCC4)cc(c23)C(=O)N1CCCN1CCCCC1 10.1016/j.ejmech.2014.05.015
CHEMBL3291083 111791 0 None - 1 Guinea pig 6.5 pKi = 6.5 Binding
Displacement of [3H]GR113808 from Dunkin-Hartley guinea pig brain striatum 5HT4R after 30 minsDisplacement of [3H]GR113808 from Dunkin-Hartley guinea pig brain striatum 5HT4R after 30 mins
ChEMBL 406 5 0 5 3.7 O=C1c2cccc3nc(N4CCCCC4)cc(c23)C(=O)N1CCCN1CCCCC1 10.1016/j.ejmech.2014.05.015
71461049 82562 0 None -2 6 Guinea pig 7.5 pKi = 7.5 Binding
Displacement of [3H]GR113808 from 5HT4R in guinea pig striatal membranesDisplacement of [3H]GR113808 from 5HT4R in guinea pig striatal membranes
ChEMBL 364 6 0 4 4.9 CCCN1CCC(COc2nc3c(OC)cccc3c3ccccc23)CC1 10.1021/jm300943r
CHEMBL2181187 82562 0 None -2 6 Guinea pig 7.5 pKi = 7.5 Binding
Displacement of [3H]GR113808 from 5HT4R in guinea pig striatal membranesDisplacement of [3H]GR113808 from 5HT4R in guinea pig striatal membranes
ChEMBL 364 6 0 4 4.9 CCCN1CCC(COc2nc3c(OC)cccc3c3ccccc23)CC1 10.1021/jm300943r
10018558 50479 0 None - 1 Rat 7.5 pKi = 7.5 Binding
Binding affinity towards 5-hydroxytryptamine 4 receptor was determined in rat striatal membranes using [3H]GR-113808 as radioligandBinding affinity towards 5-hydroxytryptamine 4 receptor was determined in rat striatal membranes using [3H]GR-113808 as radioligand
ChEMBL 314 5 1 6 1.4 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCOCC1 10.1021/jm960320m
CHEMBL157631 50479 0 None - 1 Rat 7.5 pKi = 7.5 Binding
Binding affinity towards 5-hydroxytryptamine 4 receptor was determined in rat striatal membranes using [3H]GR-113808 as radioligandBinding affinity towards 5-hydroxytryptamine 4 receptor was determined in rat striatal membranes using [3H]GR-113808 as radioligand
ChEMBL 314 5 1 6 1.4 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCOCC1 10.1021/jm960320m
44364334 39716 0 None - 1 Rat 6.5 pKi = 6.5 Binding
In vitro affinity at serotonergic 5-hydroxytryptamine 4 receptor by radioligand binding assay using [3H]GR-113808 in rat striatum membranes.In vitro affinity at serotonergic 5-hydroxytryptamine 4 receptor by radioligand binding assay using [3H]GR-113808 in rat striatum membranes.
ChEMBL 319 2 1 4 3.0 CN1C2CCC1CC(OC(=O)c1cc(Cl)cc3[nH]cnc13)C2 10.1021/jm991076c
CHEMBL147827 39716 0 None - 1 Rat 6.5 pKi = 6.5 Binding
In vitro affinity at serotonergic 5-hydroxytryptamine 4 receptor by radioligand binding assay using [3H]GR-113808 in rat striatum membranes.In vitro affinity at serotonergic 5-hydroxytryptamine 4 receptor by radioligand binding assay using [3H]GR-113808 in rat striatum membranes.
ChEMBL 319 2 1 4 3.0 CN1C2CCC1CC(OC(=O)c1cc(Cl)cc3[nH]cnc13)C2 10.1021/jm991076c
54677674 112311 4 None - 1 Human 7.4 pKi = 7.4 Binding
Binding affinity to 5HT4R (unknown origin)Binding affinity to 5HT4R (unknown origin)
ChEMBL 377 6 2 6 3.0 CC(C)n1c(=O)c(C(=O)NCCCN2CCCCC2)c(O)c2ccsc21 10.1016/j.ejmech.2014.05.015
CHEMBL3291085 112311 4 None - 1 Human 7.4 pKi = 7.4 Binding
Binding affinity to 5HT4R (unknown origin)Binding affinity to 5HT4R (unknown origin)
ChEMBL 377 6 2 6 3.0 CC(C)n1c(=O)c(C(=O)NCCCN2CCCCC2)c(O)c2ccsc21 10.1016/j.ejmech.2014.05.015
CHEMBL3306918 112311 4 None - 1 Human 7.4 pKi = 7.4 Binding
Binding affinity to 5HT4R (unknown origin)Binding affinity to 5HT4R (unknown origin)
ChEMBL 377 6 2 6 3.0 CC(C)n1c(=O)c(C(=O)NCCCN2CCCCC2)c(O)c2ccsc21 10.1016/j.ejmech.2014.05.015
11498641 78644 0 None - 1 Human 7.4 pKi = 7.4 Binding
Binding affinity for 5-HT4 receptor using [3H]GR-113808Binding affinity for 5-HT4 receptor using [3H]GR-113808
ChEMBL 736 15 4 12 2.8 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCC(C(=O)NCCNC(=O)C2CCN(CCOC(=O)c3cc(Cl)c(N)cc3OC)CC2)CC1 10.1021/jm050234z
CHEMBL2113159 78644 0 None - 1 Human 7.4 pKi = 7.4 Binding
Binding affinity for 5-HT4 receptor using [3H]GR-113808Binding affinity for 5-HT4 receptor using [3H]GR-113808
ChEMBL 736 15 4 12 2.8 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCC(C(=O)NCCNC(=O)C2CCN(CCOC(=O)c3cc(Cl)c(N)cc3OC)CC2)CC1 10.1021/jm050234z
49783212 17494 0 None - 1 Human 7.4 pKi = 7.4 Binding
Displacement of [3H]GR113808 from human recombinant 5HT4 receptor expressed in HEK293 cellsDisplacement of [3H]GR113808 from human recombinant 5HT4 receptor expressed in HEK293 cells
ChEMBL 387 7 1 7 3.0 CCCCN1CCC(COC(=O)c2cc(C#N)c(NC)c3c2OCCO3)CC1 10.1021/jm100668r
CHEMBL1258450 17494 0 None - 1 Human 7.4 pKi = 7.4 Binding
Displacement of [3H]GR113808 from human recombinant 5HT4 receptor expressed in HEK293 cellsDisplacement of [3H]GR113808 from human recombinant 5HT4 receptor expressed in HEK293 cells
ChEMBL 387 7 1 7 3.0 CCCCN1CCC(COC(=O)c2cc(C#N)c(NC)c3c2OCCO3)CC1 10.1021/jm100668r
44592145 188784 0 None - 1 Guinea pig 7.4 pKi = 7.4 Binding
Displacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatum membraneDisplacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatum membrane
ChEMBL 341 6 0 5 4.2 C=CCCN1CCC(COc2nc3ccsc3n3cccc23)CC1 10.1016/j.bmc.2008.11.045
CHEMBL512841 188784 0 None - 1 Guinea pig 7.4 pKi = 7.4 Binding
Displacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatum membraneDisplacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatum membrane
ChEMBL 341 6 0 5 4.2 C=CCCN1CCC(COc2nc3ccsc3n3cccc23)CC1 10.1016/j.bmc.2008.11.045
5 139 66 None -117 54 Rat 7.4 pKi = 7.4 Binding
Binding affinity at 5-hydroxytryptamine 4 receptor in rat striatum by [3H]GR-113808 displacement.Binding affinity at 5-hydroxytryptamine 4 receptor in rat striatum by [3H]GR-113808 displacement.
ChEMBL 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 10.1016/0960-894X(96)00002-9
5202 139 66 None -117 54 Rat 7.4 pKi = 7.4 Binding
Binding affinity at 5-hydroxytryptamine 4 receptor in rat striatum by [3H]GR-113808 displacement.Binding affinity at 5-hydroxytryptamine 4 receptor in rat striatum by [3H]GR-113808 displacement.
ChEMBL 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 10.1016/0960-894X(96)00002-9
CHEMBL39 139 66 None -117 54 Rat 7.4 pKi = 7.4 Binding
Binding affinity at 5-hydroxytryptamine 4 receptor in rat striatum by [3H]GR-113808 displacement.Binding affinity at 5-hydroxytryptamine 4 receptor in rat striatum by [3H]GR-113808 displacement.
ChEMBL 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 10.1016/0960-894X(96)00002-9
DB08839 139 66 None -117 54 Rat 7.4 pKi = 7.4 Binding
Binding affinity at 5-hydroxytryptamine 4 receptor in rat striatum by [3H]GR-113808 displacement.Binding affinity at 5-hydroxytryptamine 4 receptor in rat striatum by [3H]GR-113808 displacement.
ChEMBL 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 10.1016/0960-894X(96)00002-9
155517675 169622 0 None - 1 Human 7.4 pKi = 7.4 Binding
Displacement of [3H]-GR113808 from recombinant human 5-HT4BR expressed in membranes after 60 minsDisplacement of [3H]-GR113808 from recombinant human 5-HT4BR expressed in membranes after 60 mins
ChEMBL 386 6 1 2 6.1 O=C(CCC1CCN(CC2CCCCC2)CC1)c1cc(Cl)c2[nH]ccc2c1 10.1016/j.ejmech.2018.10.064
CHEMBL4444843 169622 0 None - 1 Human 7.4 pKi = 7.4 Binding
Displacement of [3H]-GR113808 from recombinant human 5-HT4BR expressed in membranes after 60 minsDisplacement of [3H]-GR113808 from recombinant human 5-HT4BR expressed in membranes after 60 mins
ChEMBL 386 6 1 2 6.1 O=C(CCC1CCN(CC2CCCCC2)CC1)c1cc(Cl)c2[nH]ccc2c1 10.1016/j.ejmech.2018.10.064
155545651 172892 0 None - 1 Human 7.4 pKi = 7.4 Binding
Displacement of [3H]-GR113808 from recombinant human 5-HT4BR expressed in membranes after 60 minsDisplacement of [3H]-GR113808 from recombinant human 5-HT4BR expressed in membranes after 60 mins
ChEMBL 352 6 1 2 5.4 O=C(CCC1CCN(CC2CCCCC2)CC1)c1ccc2[nH]ccc2c1 10.1016/j.ejmech.2018.10.064
CHEMBL4529710 172892 0 None - 1 Human 7.4 pKi = 7.4 Binding
Displacement of [3H]-GR113808 from recombinant human 5-HT4BR expressed in membranes after 60 minsDisplacement of [3H]-GR113808 from recombinant human 5-HT4BR expressed in membranes after 60 mins
ChEMBL 352 6 1 2 5.4 O=C(CCC1CCN(CC2CCCCC2)CC1)c1ccc2[nH]ccc2c1 10.1016/j.ejmech.2018.10.064
2353 100643 75 None -1 5 Guinea pig 6.4 pKi = 6.4 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
ChEMBL 336 2 0 4 3.1 COc1ccc2cc3[n+](cc2c1OC)CCc1cc2c(cc1-3)OCO2 nan
CHEMBL12089 100643 75 None -1 5 Guinea pig 6.4 pKi = 6.4 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
ChEMBL 336 2 0 4 3.1 COc1ccc2cc3[n+](cc2c1OC)CCc1cc2c(cc1-3)OCO2 nan
CHEMBL295124 100643 75 None -1 5 Guinea pig 6.4 pKi = 6.4 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
ChEMBL 336 2 0 4 3.1 COc1ccc2cc3[n+](cc2c1OC)CCc1cc2c(cc1-3)OCO2 nan
146025727 171119 0 None -138 27 Human 5.4 pKi = 5.4 Binding
Displacement of [3H]GR113808 from recombinant human 5HT4 receptor stably expressed in HEKT cells measured after 90 mins by microbeta scintillation counting methodDisplacement of [3H]GR113808 from recombinant human 5HT4 receptor stably expressed in HEKT cells measured after 90 mins by microbeta scintillation counting method
ChEMBL 411 3 0 5 6.4 FC(F)(F)c1cc(Oc2nccc3ccsc23)ccc1-c1cccc2nccn12 10.1021/acs.jmedchem.9b00351
CHEMBL4466483 171119 0 None -138 27 Human 5.4 pKi = 5.4 Binding
Displacement of [3H]GR113808 from recombinant human 5HT4 receptor stably expressed in HEKT cells measured after 90 mins by microbeta scintillation counting methodDisplacement of [3H]GR113808 from recombinant human 5HT4 receptor stably expressed in HEKT cells measured after 90 mins by microbeta scintillation counting method
ChEMBL 411 3 0 5 6.4 FC(F)(F)c1cc(Oc2nccc3ccsc23)ccc1-c1cccc2nccn12 10.1021/acs.jmedchem.9b00351
10552840 163729 0 None - 1 Guinea pig 6.4 pKi = 6.4 Binding
Binding affinity against 5-hydroxytryptamine 4 receptor in guinea pig striatum using [3H]GR-113808 as radioligandBinding affinity against 5-hydroxytryptamine 4 receptor in guinea pig striatum using [3H]GR-113808 as radioligand
ChEMBL 483 9 1 7 3.2 CC(C)n1c(=O)n(C(=O)NCCN2CCN(CCCOc3ccc(F)cc3)CC2)c2ccccc21 10.1021/jm981098j
CHEMBL421187 163729 0 None - 1 Guinea pig 6.4 pKi = 6.4 Binding
Binding affinity against 5-hydroxytryptamine 4 receptor in guinea pig striatum using [3H]GR-113808 as radioligandBinding affinity against 5-hydroxytryptamine 4 receptor in guinea pig striatum using [3H]GR-113808 as radioligand
ChEMBL 483 9 1 7 3.2 CC(C)n1c(=O)n(C(=O)NCCN2CCN(CCCOc3ccc(F)cc3)CC2)c2ccccc21 10.1021/jm981098j
136118639 75964 0 None -2 3 Human 5.4 pKi = 5.4 Binding
Displacement of [3H]GR113808 from human recombinant 5HT4 receptorDisplacement of [3H]GR113808 from human recombinant 5HT4 receptor
ChEMBL 335 1 2 3 3.1 CSC1=NC(=O)/C(=C/c2c[nH]c3ccc(Br)cc23)N1 10.1016/j.bmc.2013.09.011
CHEMBL2058699 75964 0 None -2 3 Human 5.4 pKi = 5.4 Binding
Displacement of [3H]GR113808 from human recombinant 5HT4 receptorDisplacement of [3H]GR113808 from human recombinant 5HT4 receptor
ChEMBL 335 1 2 3 3.1 CSC1=NC(=O)/C(=C/c2c[nH]c3ccc(Br)cc23)N1 10.1016/j.bmc.2013.09.011
44592146 187783 0 None - 1 Guinea pig 7.4 pKi = 7.4 Binding
Displacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatum membraneDisplacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatum membrane
ChEMBL 301 3 0 5 3.3 CN1CCC(COc2nc3sccc3n3cccc23)CC1 10.1016/j.bmc.2008.11.045
CHEMBL501309 187783 0 None - 1 Guinea pig 7.4 pKi = 7.4 Binding
Displacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatum membraneDisplacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatum membrane
ChEMBL 301 3 0 5 3.3 CN1CCC(COc2nc3sccc3n3cccc23)CC1 10.1016/j.bmc.2008.11.045
850954 40016 2 None - 1 Rat 7.4 pKi = 7.4 Binding
In vitro affinity at serotonergic 5-hydroxytryptamine 4 receptor by radioligand binding assay using [3H]GR-113808 in rat striatum membranes.In vitro affinity at serotonergic 5-hydroxytryptamine 4 receptor by radioligand binding assay using [3H]GR-113808 in rat striatum membranes.
ChEMBL 348 2 2 3 2.1 O=C(N[C@@H]1CN2CCC1CC2)c1cc(Br)cc2nc[nH]c12 10.1021/jm991076c
CHEMBL148080 40016 2 None - 1 Rat 7.4 pKi = 7.4 Binding
In vitro affinity at serotonergic 5-hydroxytryptamine 4 receptor by radioligand binding assay using [3H]GR-113808 in rat striatum membranes.In vitro affinity at serotonergic 5-hydroxytryptamine 4 receptor by radioligand binding assay using [3H]GR-113808 in rat striatum membranes.
ChEMBL 348 2 2 3 2.1 O=C(N[C@@H]1CN2CCC1CC2)c1cc(Br)cc2nc[nH]c12 10.1021/jm991076c
10643950 107948 0 None - 1 Guinea pig 7.4 pKi = 7.4 Binding
Binding affinity against 5-hydroxytryptamine 4 receptor in guinea pig striatum using [3H]GR-113808 as radioligandBinding affinity against 5-hydroxytryptamine 4 receptor in guinea pig striatum using [3H]GR-113808 as radioligand
ChEMBL 387 7 1 6 2.4 CCCCN1CCN(CCNC(=O)n2c(=O)n(C(C)C)c3ccccc32)CC1 10.1021/jm981098j
CHEMBL319886 107948 0 None - 1 Guinea pig 7.4 pKi = 7.4 Binding
Binding affinity against 5-hydroxytryptamine 4 receptor in guinea pig striatum using [3H]GR-113808 as radioligandBinding affinity against 5-hydroxytryptamine 4 receptor in guinea pig striatum using [3H]GR-113808 as radioligand
ChEMBL 387 7 1 6 2.4 CCCCN1CCN(CCNC(=O)n2c(=O)n(C(C)C)c3ccccc32)CC1 10.1021/jm981098j
44352308 116984 0 None -46 12 Human 6.4 pKi = 6.4 Binding
Binding affinity towards human 5-hydroxytryptamine 4 receptor using [3H]5-HT as radioligandBinding affinity towards human 5-hydroxytryptamine 4 receptor using [3H]5-HT as radioligand
ChEMBL 339 5 2 2 4.0 Cc1[nH]c2cccc(NC(=O)c3ccc(F)cc3)c2c1CCN(C)C 10.1021/jm0155190
CHEMBL339980 116984 0 None -46 12 Human 6.4 pKi = 6.4 Binding
Binding affinity towards human 5-hydroxytryptamine 4 receptor using [3H]5-HT as radioligandBinding affinity towards human 5-hydroxytryptamine 4 receptor using [3H]5-HT as radioligand
ChEMBL 339 5 2 2 4.0 Cc1[nH]c2cccc(NC(=O)c3ccc(F)cc3)c2c1CCN(C)C 10.1021/jm0155190
6604914 99919 2 None 1 2 Rat 6.4 pKi = 6.4 Binding
Binding affinity against 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatumBinding affinity against 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatum
ChEMBL 309 3 2 4 1.8 COc1cc(N)c(Cl)cc1C(=O)N[C@@H]1CN2CCC1CC2 10.1016/0960-894X(95)00115-A
CHEMBL28992 99919 2 None 1 2 Rat 6.4 pKi = 6.4 Binding
Binding affinity against 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatumBinding affinity against 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatum
ChEMBL 309 3 2 4 1.8 COc1cc(N)c(Cl)cc1C(=O)N[C@@H]1CN2CCC1CC2 10.1016/0960-894X(95)00115-A
6604914 99919 2 None 1 2 Rat 6.4 pKi = 6.4 Binding
Binding affinity towards 5-hydroxytryptamine 4 receptor was determined in rat striatal membranes using [3H]GR-113808 as radioligandBinding affinity towards 5-hydroxytryptamine 4 receptor was determined in rat striatal membranes using [3H]GR-113808 as radioligand
ChEMBL 309 3 2 4 1.8 COc1cc(N)c(Cl)cc1C(=O)N[C@@H]1CN2CCC1CC2 10.1021/jm960320m
CHEMBL28992 99919 2 None 1 2 Rat 6.4 pKi = 6.4 Binding
Binding affinity towards 5-hydroxytryptamine 4 receptor was determined in rat striatal membranes using [3H]GR-113808 as radioligandBinding affinity towards 5-hydroxytryptamine 4 receptor was determined in rat striatal membranes using [3H]GR-113808 as radioligand
ChEMBL 309 3 2 4 1.8 COc1cc(N)c(Cl)cc1C(=O)N[C@@H]1CN2CCC1CC2 10.1021/jm960320m
6604914 99919 2 None -1 2 Guinea pig 6.4 pKi = 6.4 Binding
Inhibition of [3H]GR-113808 binding to guinea pig striatum 5-hydroxytryptamine 4 receptorInhibition of [3H]GR-113808 binding to guinea pig striatum 5-hydroxytryptamine 4 receptor
ChEMBL 309 3 2 4 1.8 COc1cc(N)c(Cl)cc1C(=O)N[C@@H]1CN2CCC1CC2 10.1021/jm020270n
CHEMBL28992 99919 2 None -1 2 Guinea pig 6.4 pKi = 6.4 Binding
Inhibition of [3H]GR-113808 binding to guinea pig striatum 5-hydroxytryptamine 4 receptorInhibition of [3H]GR-113808 binding to guinea pig striatum 5-hydroxytryptamine 4 receptor
ChEMBL 309 3 2 4 1.8 COc1cc(N)c(Cl)cc1C(=O)N[C@@H]1CN2CCC1CC2 10.1021/jm020270n
10568248 185396 0 None - 1 Rat 7.4 pKi = 7.4 Binding
Binding affinity (Ki+/-SEM) against 5-hydroxytryptamine 4 receptor from cheng Prusoff equation by using [3H]GR-113808 in rat striatumBinding affinity (Ki+/-SEM) against 5-hydroxytryptamine 4 receptor from cheng Prusoff equation by using [3H]GR-113808 in rat striatum
ChEMBL 327 5 2 5 3.0 COc1cc(N)c(Cl)cc1NC(=O)OCCN1CCCCC1 10.1021/jm960853v
CHEMBL48698 185396 0 None - 1 Rat 7.4 pKi = 7.4 Binding
Binding affinity (Ki+/-SEM) against 5-hydroxytryptamine 4 receptor from cheng Prusoff equation by using [3H]GR-113808 in rat striatumBinding affinity (Ki+/-SEM) against 5-hydroxytryptamine 4 receptor from cheng Prusoff equation by using [3H]GR-113808 in rat striatum
ChEMBL 327 5 2 5 3.0 COc1cc(N)c(Cl)cc1NC(=O)OCCN1CCCCC1 10.1021/jm960853v
145988372 166737 0 None - 1 Guinea pig 7.4 pKi = 7.4 Binding
Displacement of [3H]-GR113808 from 5-HT4R in Dunkin-Hartley guinea pig straitum nuclear membranes after 2 hrs by filter binding methodDisplacement of [3H]-GR113808 from 5-HT4R in Dunkin-Hartley guinea pig straitum nuclear membranes after 2 hrs by filter binding method
ChEMBL 359 6 1 3 4.1 CCCCN1CCC(CNC(=O)c2cc(Cl)c3ccccc3n2)CC1 10.1039/C8MD00233A
CHEMBL4293603 166737 0 None - 1 Guinea pig 7.4 pKi = 7.4 Binding
Displacement of [3H]-GR113808 from 5-HT4R in Dunkin-Hartley guinea pig straitum nuclear membranes after 2 hrs by filter binding methodDisplacement of [3H]-GR113808 from 5-HT4R in Dunkin-Hartley guinea pig straitum nuclear membranes after 2 hrs by filter binding method
ChEMBL 359 6 1 3 4.1 CCCCN1CCC(CNC(=O)c2cc(Cl)c3ccccc3n2)CC1 10.1039/C8MD00233A
10545158 50085 0 None - 1 Rat 7.4 pKi = 7.4 Binding
Binding affinity towards 5-hydroxytryptamine 4 receptor was determined in rat striatal membranes using [3H]GR-113808 as radioligandBinding affinity towards 5-hydroxytryptamine 4 receptor was determined in rat striatal membranes using [3H]GR-113808 as radioligand
ChEMBL 340 5 1 5 3.4 COc1cc(N)c(Cl)cc1C(=O)OCCN1C(C)CCCC1C 10.1021/jm960320m
CHEMBL157233 50085 0 None - 1 Rat 7.4 pKi = 7.4 Binding
Binding affinity towards 5-hydroxytryptamine 4 receptor was determined in rat striatal membranes using [3H]GR-113808 as radioligandBinding affinity towards 5-hydroxytryptamine 4 receptor was determined in rat striatal membranes using [3H]GR-113808 as radioligand
ChEMBL 340 5 1 5 3.4 COc1cc(N)c(Cl)cc1C(=O)OCCN1C(C)CCCC1C 10.1021/jm960320m
10666045 206663 0 None - 1 Guinea pig 7.4 pKi = 7.4 Binding
Binding affinity against 5-hydroxytryptamine 4 receptor in guinea pig striatum using [3H]GR-113808 as radioligandBinding affinity against 5-hydroxytryptamine 4 receptor in guinea pig striatum using [3H]GR-113808 as radioligand
ChEMBL 357 5 1 6 1.3 CN1CCN(CCCNC(=O)n2c(=O)n(C3CC3)c3ccccc32)CC1 10.1021/jm981098j
CHEMBL99723 206663 0 None - 1 Guinea pig 7.4 pKi = 7.4 Binding
Binding affinity against 5-hydroxytryptamine 4 receptor in guinea pig striatum using [3H]GR-113808 as radioligandBinding affinity against 5-hydroxytryptamine 4 receptor in guinea pig striatum using [3H]GR-113808 as radioligand
ChEMBL 357 5 1 6 1.3 CN1CCN(CCCNC(=O)n2c(=O)n(C3CC3)c3ccccc32)CC1 10.1021/jm981098j
67276147 77146 0 None - 1 Human 7.4 pKi = 7.4 Binding
Displacement of [3H]GR113808 from human recombinant 5HT4c receptor expressed in HEK293 cellsDisplacement of [3H]GR113808 from human recombinant 5HT4c receptor expressed in HEK293 cells
ChEMBL 468 7 2 6 2.1 CC(=O)N(C)CC(O)CN1[C@H]2CC[C@@H]1C[C@H](NC(=O)c1cc3ccccc3n(C(C)C)c1=O)C2 10.1016/j.bmcl.2012.08.051
CHEMBL2087325 77146 0 None - 1 Human 7.4 pKi = 7.4 Binding
Displacement of [3H]GR113808 from human recombinant 5HT4c receptor expressed in HEK293 cellsDisplacement of [3H]GR113808 from human recombinant 5HT4c receptor expressed in HEK293 cells
ChEMBL 468 7 2 6 2.1 CC(=O)N(C)CC(O)CN1[C@H]2CC[C@@H]1C[C@H](NC(=O)c1cc3ccccc3n(C(C)C)c1=O)C2 10.1016/j.bmcl.2012.08.051
70684790 77154 0 None - 1 Human 7.4 pKi = 7.4 Binding
Displacement of [3H]GR113808 from human recombinant 5HT4c receptor expressed in HEK293 cellsDisplacement of [3H]GR113808 from human recombinant 5HT4c receptor expressed in HEK293 cells
ChEMBL 484 7 2 7 2.4 COC(=O)N(C)CC(O)CN1[C@H]2CC[C@@H]1C[C@H](NC(=O)c1cc3ccccc3n(C(C)C)c1=O)C2 10.1016/j.bmcl.2012.08.051
CHEMBL2087333 77154 0 None - 1 Human 7.4 pKi = 7.4 Binding
Displacement of [3H]GR113808 from human recombinant 5HT4c receptor expressed in HEK293 cellsDisplacement of [3H]GR113808 from human recombinant 5HT4c receptor expressed in HEK293 cells
ChEMBL 484 7 2 7 2.4 COC(=O)N(C)CC(O)CN1[C@H]2CC[C@@H]1C[C@H](NC(=O)c1cc3ccccc3n(C(C)C)c1=O)C2 10.1016/j.bmcl.2012.08.051
44248191 193230 0 None - 1 Human 7.4 pKi = 7.4 Binding
Displacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 537 8 1 7 3.5 CCOC(=O)N1CCN(CCCN2[C@H]3CC[C@@H]2C[C@H](NC(=O)c2cc4ccccc4n(C(C)C)c2=O)C3)CC1 10.1021/jm900881j
CHEMBL540980 193230 0 None - 1 Human 7.4 pKi = 7.4 Binding
Displacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 537 8 1 7 3.5 CCOC(=O)N1CCN(CCCN2[C@H]3CC[C@@H]2C[C@H](NC(=O)c2cc4ccccc4n(C(C)C)c2=O)C3)CC1 10.1021/jm900881j
44247951 91900497 193243 0 None - 1 Human 7.4 pKi = 7.4 Binding
Displacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 539 9 2 5 5.0 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CCN(C)CCc2c[nH]c3ccccc23)cc2ccccc21 10.1021/jm900881j
CHEMBL541223 193243 0 None - 1 Human 7.4 pKi = 7.4 Binding
Displacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 539 9 2 5 5.0 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CCN(C)CCc2c[nH]c3ccccc23)cc2ccccc21 10.1021/jm900881j
44248076 193374 0 None - 1 Human 7.4 pKi = 7.4 Binding
Displacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 543 8 1 7 2.3 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CCCN2CCN(S(C)(=O)=O)CC2)cc2ccccc21 10.1021/jm900881j
CHEMBL549449 193374 0 None - 1 Human 7.4 pKi = 7.4 Binding
Displacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 543 8 1 7 2.3 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CCCN2CCN(S(C)(=O)=O)CC2)cc2ccccc21 10.1021/jm900881j
44248195 193412 0 None - 1 Human 7.4 pKi = 7.4 Binding
Displacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 466 7 1 6 3.0 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CCCN2CCOCC2)cc2ccccc21 10.1021/jm900881j
CHEMBL549650 193412 0 None - 1 Human 7.4 pKi = 7.4 Binding
Displacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 466 7 1 6 3.0 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CCCN2CCOCC2)cc2ccccc21 10.1021/jm900881j
44248072 194002 0 None - 1 Human 7.4 pKi = 7.4 Binding
Displacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 483 9 3 5 3.8 COc1cc(N)c(Cl)cc1C(=O)NC1CCN(CCN(C)CCc2c[nH]c3ccccc23)CC1 10.1021/jm900881j
CHEMBL556595 194002 0 None - 1 Human 7.4 pKi = 7.4 Binding
Displacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 483 9 3 5 3.8 COc1cc(N)c(Cl)cc1C(=O)NC1CCN(CCN(C)CCc2c[nH]c3ccccc23)CC1 10.1021/jm900881j
44248068 194212 0 None - 1 Human 7.4 pKi = 7.4 Binding
Displacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 515 10 2 7 1.9 COc1cc(N)c(Cl)cc1C(=O)NC1CCN(CCCCCN2CCN(S(C)(=O)=O)CC2)CC1 10.1021/jm900881j
CHEMBL558924 194212 0 None - 1 Human 7.4 pKi = 7.4 Binding
Displacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 515 10 2 7 1.9 COc1cc(N)c(Cl)cc1C(=O)NC1CCN(CCCCCN2CCN(S(C)(=O)=O)CC2)CC1 10.1021/jm900881j
44247943 194274 0 None - 1 Human 7.4 pKi = 7.4 Binding
Displacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 540 12 2 6 4.8 COc1cc(N)c(Cl)cc1C(=O)NC1CCN(CCCCCCCCN2C(=O)c3ccccc3C2=O)CC1 10.1021/jm900881j
CHEMBL559548 194274 0 None - 1 Human 7.4 pKi = 7.4 Binding
Displacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 540 12 2 6 4.8 COc1cc(N)c(Cl)cc1C(=O)NC1CCN(CCCCCCCCN2C(=O)c3ccccc3C2=O)CC1 10.1021/jm900881j
44249188 194438 1 None - 1 Human 7.4 pKi = 7.4 Binding
Displacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 316 3 2 5 1.9 CC(C)n1c(=O)n(C(=O)NCC2CCNCC2)c2ccccc21 10.1021/jm900881j
CHEMBL560940 194438 1 None - 1 Human 7.4 pKi = 7.4 Binding
Displacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 316 3 2 5 1.9 CC(C)n1c(=O)n(C(=O)NCC2CCNCC2)c2ccccc21 10.1021/jm900881j
10337773 101114 0 None 31 10 Human 6.4 pKi = 6.4 Binding
Binding affinity against 5-Hydroxytryptamine 4 receptorBinding affinity against 5-Hydroxytryptamine 4 receptor
ChEMBL 311 3 1 4 1.6 Cn1cc(C(=O)C(=O)N[C@@H]2CN3CCC2CC3)c2ccccc21 10.1016/0960-894X(95)00308-G
CHEMBL298612 101114 0 None 31 10 Human 6.4 pKi = 6.4 Binding
Binding affinity against 5-Hydroxytryptamine 4 receptorBinding affinity against 5-Hydroxytryptamine 4 receptor
ChEMBL 311 3 1 4 1.6 Cn1cc(C(=O)C(=O)N[C@@H]2CN3CCC2CC3)c2ccccc21 10.1016/0960-894X(95)00308-G
67211178 82314 0 None - 1 Human 6.4 pKi = 6.4 Binding
Displacement of [3H](1-(2-(methylsulfonamido)ethyl)piperidin-4-yl)methyl 1-methyl-1H-indole-3-carboxylate from human 5HT4R expressed in HEK293 cellsDisplacement of [3H](1-(2-(methylsulfonamido)ethyl)piperidin-4-yl)methyl 1-methyl-1H-indole-3-carboxylate from human 5HT4R expressed in HEK293 cells
ChEMBL 295 3 1 4 3.1 Cn1cc2c(OCC3CCNCC3)nc3ccccc3c2c1 10.1021/jm300573d
CHEMBL2179680 82314 0 None - 1 Human 6.4 pKi = 6.4 Binding
Displacement of [3H](1-(2-(methylsulfonamido)ethyl)piperidin-4-yl)methyl 1-methyl-1H-indole-3-carboxylate from human 5HT4R expressed in HEK293 cellsDisplacement of [3H](1-(2-(methylsulfonamido)ethyl)piperidin-4-yl)methyl 1-methyl-1H-indole-3-carboxylate from human 5HT4R expressed in HEK293 cells
ChEMBL 295 3 1 4 3.1 Cn1cc2c(OCC3CCNCC3)nc3ccccc3c2c1 10.1021/jm300573d
10493462 200800 0 None - 1 Human 6.4 pKi = 6.4 Binding
Displacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 286 3 2 4 2.1 CC(C)n1nc(C(=O)NC2CCNCC2)c2ccccc21 10.1021/jm900881j
CHEMBL61130 200800 0 None - 1 Human 6.4 pKi = 6.4 Binding
Displacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 286 3 2 4 2.1 CC(C)n1nc(C(=O)NC2CCNCC2)c2ccccc21 10.1021/jm900881j
10413595 161292 0 None -12589 11 Human 5.4 pKi = 5.4 Binding
Compound was evaluated for the binding affinity against human cloned 5-hydroxytryptamine 4 receptor in HeLa cells using [3H]-LSD as the radioligandCompound was evaluated for the binding affinity against human cloned 5-hydroxytryptamine 4 receptor in HeLa cells using [3H]-LSD as the radioligand
ChEMBL 499 4 1 5 2.5 COc1ccc(S(=O)(=O)N2CCc3ccc(I)cc32)cc1N1CCNCC1 10.1016/s0960-894x(00)00597-7
CHEMBL414628 161292 0 None -12589 11 Human 5.4 pKi = 5.4 Binding
Compound was evaluated for the binding affinity against human cloned 5-hydroxytryptamine 4 receptor in HeLa cells using [3H]-LSD as the radioligandCompound was evaluated for the binding affinity against human cloned 5-hydroxytryptamine 4 receptor in HeLa cells using [3H]-LSD as the radioligand
ChEMBL 499 4 1 5 2.5 COc1ccc(S(=O)(=O)N2CCc3ccc(I)cc32)cc1N1CCNCC1 10.1016/s0960-894x(00)00597-7
276 3457 45 None -2691 13 Human 5.4 pKi = 5.4 Binding
Compound was tested for its binding affinity against 5-hydroxytryptamine 4 receptorCompound was tested for its binding affinity against 5-hydroxytryptamine 4 receptor
ChEMBL 451 5 2 6 4.1 COc1ccc(cc1N1CCNCC1)NS(=O)(=O)c1sc2c(c1C)cc(cc2)Cl 10.1021/jm980532e
5312149 3457 45 None -2691 13 Human 5.4 pKi = 5.4 Binding
Compound was tested for its binding affinity against 5-hydroxytryptamine 4 receptorCompound was tested for its binding affinity against 5-hydroxytryptamine 4 receptor
ChEMBL 451 5 2 6 4.1 COc1ccc(cc1N1CCNCC1)NS(=O)(=O)c1sc2c(c1C)cc(cc2)Cl 10.1021/jm980532e
CHEMBL431298 3457 45 None -2691 13 Human 5.4 pKi = 5.4 Binding
Compound was tested for its binding affinity against 5-hydroxytryptamine 4 receptorCompound was tested for its binding affinity against 5-hydroxytryptamine 4 receptor
ChEMBL 451 5 2 6 4.1 COc1ccc(cc1N1CCNCC1)NS(=O)(=O)c1sc2c(c1C)cc(cc2)Cl 10.1021/jm980532e
44248795 195954 0 None - 1 Human 5.4 pKi = 5.4 Binding
Displacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 287 4 3 3 1.9 COc1ccc2[nH]cc(C(=O)NCC3CCNCC3)c2c1 10.1021/jm900881j
CHEMBL570780 195954 0 None - 1 Human 5.4 pKi = 5.4 Binding
Displacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 287 4 3 3 1.9 COc1ccc2[nH]cc(C(=O)NCC3CCNCC3)c2c1 10.1021/jm900881j
276 3457 45 None -2691 13 Human 5.4 pKi = 5.4 Binding
The compound was tested for the binding affinity towards human cloned 5-hydroxytryptamine 4 receptor in HeLa cells, using [3H]LSD as radioligandThe compound was tested for the binding affinity towards human cloned 5-hydroxytryptamine 4 receptor in HeLa cells, using [3H]LSD as radioligand
ChEMBL 451 5 2 6 4.1 COc1ccc(cc1N1CCNCC1)NS(=O)(=O)c1sc2c(c1C)cc(cc2)Cl 10.1016/s0960-894x(02)00172-5
5312149 3457 45 None -2691 13 Human 5.4 pKi = 5.4 Binding
The compound was tested for the binding affinity towards human cloned 5-hydroxytryptamine 4 receptor in HeLa cells, using [3H]LSD as radioligandThe compound was tested for the binding affinity towards human cloned 5-hydroxytryptamine 4 receptor in HeLa cells, using [3H]LSD as radioligand
ChEMBL 451 5 2 6 4.1 COc1ccc(cc1N1CCNCC1)NS(=O)(=O)c1sc2c(c1C)cc(cc2)Cl 10.1016/s0960-894x(02)00172-5
CHEMBL431298 3457 45 None -2691 13 Human 5.4 pKi = 5.4 Binding
The compound was tested for the binding affinity towards human cloned 5-hydroxytryptamine 4 receptor in HeLa cells, using [3H]LSD as radioligandThe compound was tested for the binding affinity towards human cloned 5-hydroxytryptamine 4 receptor in HeLa cells, using [3H]LSD as radioligand
ChEMBL 451 5 2 6 4.1 COc1ccc(cc1N1CCNCC1)NS(=O)(=O)c1sc2c(c1C)cc(cc2)Cl 10.1016/s0960-894x(02)00172-5
145957993 161631 0 None - 1 Guinea pig 8.4 pKi = 8.4 Binding
Displacement of [3H]GR113808 from serotonin 5-HT4 receptor in Dunkin-Hartley guinea pigs striatal nuclei membranes incubated for 2 hrs by liquid scintillation countingDisplacement of [3H]GR113808 from serotonin 5-HT4 receptor in Dunkin-Hartley guinea pigs striatal nuclei membranes incubated for 2 hrs by liquid scintillation counting
ChEMBL 692 19 5 11 1.9 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCC(NC(=O)NCCOCCOCCNC(=O)NCC(=O)OCc2ccccc2)CC1 10.1039/C6MD00458J
CHEMBL4162531 161631 0 None - 1 Guinea pig 8.4 pKi = 8.4 Binding
Displacement of [3H]GR113808 from serotonin 5-HT4 receptor in Dunkin-Hartley guinea pigs striatal nuclei membranes incubated for 2 hrs by liquid scintillation countingDisplacement of [3H]GR113808 from serotonin 5-HT4 receptor in Dunkin-Hartley guinea pigs striatal nuclei membranes incubated for 2 hrs by liquid scintillation counting
ChEMBL 692 19 5 11 1.9 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCC(NC(=O)NCCOCCOCCNC(=O)NCC(=O)OCc2ccccc2)CC1 10.1039/C6MD00458J
145951595 162247 0 None - 1 Guinea pig 8.4 pKi = 8.4 Binding
Displacement of [3H]GR113808 from serotonin 5-HT4 receptor in Dunkin-Hartley guinea pigs striatal nuclei membranes incubated for 2 hrs by liquid scintillation countingDisplacement of [3H]GR113808 from serotonin 5-HT4 receptor in Dunkin-Hartley guinea pigs striatal nuclei membranes incubated for 2 hrs by liquid scintillation counting
ChEMBL 854 21 6 14 2.7 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCC(NC(=O)NCCOCCOCCNC(=O)NC2CCN(CCOC(=O)c3cc(Cl)c(N)cc3OC)CC2)CC1 10.1039/C6MD00458J
CHEMBL4172346 162247 0 None - 1 Guinea pig 8.4 pKi = 8.4 Binding
Displacement of [3H]GR113808 from serotonin 5-HT4 receptor in Dunkin-Hartley guinea pigs striatal nuclei membranes incubated for 2 hrs by liquid scintillation countingDisplacement of [3H]GR113808 from serotonin 5-HT4 receptor in Dunkin-Hartley guinea pigs striatal nuclei membranes incubated for 2 hrs by liquid scintillation counting
ChEMBL 854 21 6 14 2.7 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCC(NC(=O)NCCOCCOCCNC(=O)NC2CCN(CCOC(=O)c3cc(Cl)c(N)cc3OC)CC2)CC1 10.1039/C6MD00458J
9973684 51199 0 None - 1 Rat 8.4 pKi = 8.4 Binding
Binding affinity towards 5-hydroxytryptamine 4 receptor was determined in rat striatal membranes using [3H]GR-113808 as radioligandBinding affinity towards 5-hydroxytryptamine 4 receptor was determined in rat striatal membranes using [3H]GR-113808 as radioligand
ChEMBL 326 5 1 5 2.8 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCC(C)CC1 10.1021/jm960320m
CHEMBL158238 51199 0 None - 1 Rat 8.4 pKi = 8.4 Binding
Binding affinity towards 5-hydroxytryptamine 4 receptor was determined in rat striatal membranes using [3H]GR-113808 as radioligandBinding affinity towards 5-hydroxytryptamine 4 receptor was determined in rat striatal membranes using [3H]GR-113808 as radioligand
ChEMBL 326 5 1 5 2.8 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCC(C)CC1 10.1021/jm960320m
10519226 101517 0 None - 1 Rat 8.4 pKi = 8.4 Binding
Binding affinity at 5-hydroxytryptamine 4 receptor in rat striatal membranes by [3H]GR-113808 displacement.Binding affinity at 5-hydroxytryptamine 4 receptor in rat striatal membranes by [3H]GR-113808 displacement.
ChEMBL 312 5 1 4 3.4 COc1ccc(Cl)cc1NC(=O)OCCN1CCCCC1 10.1021/jm960853v
CHEMBL301510 101517 0 None - 1 Rat 8.4 pKi = 8.4 Binding
Binding affinity at 5-hydroxytryptamine 4 receptor in rat striatal membranes by [3H]GR-113808 displacement.Binding affinity at 5-hydroxytryptamine 4 receptor in rat striatal membranes by [3H]GR-113808 displacement.
ChEMBL 312 5 1 4 3.4 COc1ccc(Cl)cc1NC(=O)OCCN1CCCCC1 10.1021/jm960853v
90666009 108805 0 None - 1 Guinea pig 8.4 pKi = 8.4 Binding
Displacement of [3H]-GR113808 from guinea pig 5HT4 receptor by Grossman's methodDisplacement of [3H]-GR113808 from guinea pig 5HT4 receptor by Grossman's method
ChEMBL 397 5 0 5 5.5 Cc1csc2nc(OCC3CCN(CC4CCCCC4)CC3)c3cccn3c12 10.1039/C2MD20063E
CHEMBL3218881 108805 0 None - 1 Guinea pig 8.4 pKi = 8.4 Binding
Displacement of [3H]-GR113808 from guinea pig 5HT4 receptor by Grossman's methodDisplacement of [3H]-GR113808 from guinea pig 5HT4 receptor by Grossman's method
ChEMBL 397 5 0 5 5.5 Cc1csc2nc(OCC3CCN(CC4CCCCC4)CC3)c3cccn3c12 10.1039/C2MD20063E
72698088 103512 0 None -20 5 Guinea pig 8.4 pKi = 8.4 Binding
Displacement of [3H]GR113808 from 5HT4R in guinea pig striatal membranesDisplacement of [3H]GR113808 from 5HT4R in guinea pig striatal membranes
ChEMBL 421 6 0 4 5.4 Fc1cccc2c1nc(OCC1CCN(CCCC(F)(F)F)CC1)c1cccnc12 10.1016/j.bmc.2013.08.061
CHEMBL3093187 103512 0 None -20 5 Guinea pig 8.4 pKi = 8.4 Binding
Displacement of [3H]GR113808 from 5HT4R in guinea pig striatal membranesDisplacement of [3H]GR113808 from 5HT4R in guinea pig striatal membranes
ChEMBL 421 6 0 4 5.4 Fc1cccc2c1nc(OCC1CCN(CCCC(F)(F)F)CC1)c1cccnc12 10.1016/j.bmc.2013.08.061
11166796 82264 0 None -2 2 Human 8.4 pKi = 8.4 Binding
Displacement of [3H]GR113808 from human 5HT4A receptor expressed in HEK293 cells after 30 mins by liquid scintillation countingDisplacement of [3H]GR113808 from human 5HT4A receptor expressed in HEK293 cells after 30 mins by liquid scintillation counting
ChEMBL 448 5 2 7 2.3 CC(C)n1c(=O)n(C(=O)NCC2CCN(CC3(O)CCOCC3)CC2)c2cc(F)ccc21 10.1021/jm300953p
CHEMBL2179583 82264 0 None -2 2 Human 8.4 pKi = 8.4 Binding
Displacement of [3H]GR113808 from human 5HT4A receptor expressed in HEK293 cells after 30 mins by liquid scintillation countingDisplacement of [3H]GR113808 from human 5HT4A receptor expressed in HEK293 cells after 30 mins by liquid scintillation counting
ChEMBL 448 5 2 7 2.3 CC(C)n1c(=O)n(C(=O)NCC2CCN(CC3(O)CCOCC3)CC2)c2cc(F)ccc21 10.1021/jm300953p
44213661 205348 0 None - 1 Rat 8.4 pKi = 8.4 Binding
Binding affinity at 5-hydroxytryptamine 4 receptor in rat striatum by [3H]GR-113808 displacement.Binding affinity at 5-hydroxytryptamine 4 receptor in rat striatum by [3H]GR-113808 displacement.
ChEMBL 338 5 1 5 2.9 Nc1c(Cl)cc(C(=O)OCCCN2CCCCC2)c2c1CCO2 10.1016/0960-894X(96)00002-9
CHEMBL91842 205348 0 None - 1 Rat 8.4 pKi = 8.4 Binding
Binding affinity at 5-hydroxytryptamine 4 receptor in rat striatum by [3H]GR-113808 displacement.Binding affinity at 5-hydroxytryptamine 4 receptor in rat striatum by [3H]GR-113808 displacement.
ChEMBL 338 5 1 5 2.9 Nc1c(Cl)cc(C(=O)OCCCN2CCCCC2)c2c1CCO2 10.1016/0960-894X(96)00002-9
53357016 82262 0 None - 1 Human 8.4 pKi = 8.4 Binding
Displacement of [3H]GR113808 from human 5HT4D receptor expressed in HEK293 cells after 30 mins by liquid scintillation countingDisplacement of [3H]GR113808 from human 5HT4D receptor expressed in HEK293 cells after 30 mins by liquid scintillation counting
ChEMBL 446 7 1 8 3.0 OC1(CN2CCC(COc3noc4cccc(OC5CCOCC5)c34)CC2)CCOCC1 10.1021/jm300953p
CHEMBL2179581 82262 0 None - 1 Human 8.4 pKi = 8.4 Binding
Displacement of [3H]GR113808 from human 5HT4D receptor expressed in HEK293 cells after 30 mins by liquid scintillation countingDisplacement of [3H]GR113808 from human 5HT4D receptor expressed in HEK293 cells after 30 mins by liquid scintillation counting
ChEMBL 446 7 1 8 3.0 OC1(CN2CCC(COc3noc4cccc(OC5CCOCC5)c34)CC2)CCOCC1 10.1021/jm300953p
49783210 17457 0 None - 1 Human 8.4 pKi = 8.4 Binding
Displacement of [3H]GR113808 from human recombinant 5HT4 receptor expressed in HEK293 cellsDisplacement of [3H]GR113808 from human recombinant 5HT4 receptor expressed in HEK293 cells
ChEMBL 440 7 1 6 3.9 CCCCN1CCC(COC(=O)c2cc(Br)c(NC)c3c2OCCO3)CC1 10.1021/jm100668r
CHEMBL1258338 17457 0 None - 1 Human 8.4 pKi = 8.4 Binding
Displacement of [3H]GR113808 from human recombinant 5HT4 receptor expressed in HEK293 cellsDisplacement of [3H]GR113808 from human recombinant 5HT4 receptor expressed in HEK293 cells
ChEMBL 440 7 1 6 3.9 CCCCN1CCC(COC(=O)c2cc(Br)c(NC)c3c2OCCO3)CC1 10.1021/jm100668r
CHEMBL4172315 211480 0 None - 1 Guinea pig 8.4 pKi = 8.4 Binding
Displacement of [3H]GR113808 from serotonin 5-HT4 receptor in Dunkin-Hartley guinea pigs striatal nuclei membranes incubated for 2 hrs by liquid scintillation countingDisplacement of [3H]GR113808 from serotonin 5-HT4 receptor in Dunkin-Hartley guinea pigs striatal nuclei membranes incubated for 2 hrs by liquid scintillation counting
ChEMBL None None None COc1cc(N)c(Cl)cc1C(=O)OCCN1CCC(NC(=O)NCCOCCOCCOCCOCCOCCOCCOCCOCCn2cc(CNC(=O)NCCCN(CCCCN(CCCNC(=O)NCc3cn(CCOCCOCCOCCOCCOCCOCCOCCOCCNC(=O)NC4CCN(CCOC(=O)c5cc(Cl)c(N)cc5OC)CC4)nn3)CCCNC(=O)NCc3cn(CCOCCOCCOCCOCCOCCOCCOCCOCCNC(=O)NC4CCN(CCOC(=O)c5cc(Cl)c(N)cc5OC)CC4)nn3)CCCNC(=O)NCc3cn(CCOCCOCCOCCOCCOCCOCCOCCOCCNC(=O)NC4CCN(CCOC(=O)c5cc(Cl)c(N)cc5OC)CC4)nn3)nn2)CC1 10.1039/C6MD00458J
71457409 82549 0 None -17 6 Guinea pig 8.3 pKi = 8.3 Binding
Displacement of [3H]GR113808 from 5HT4R in guinea pig striatal membranesDisplacement of [3H]GR113808 from 5HT4R in guinea pig striatal membranes
ChEMBL 461 5 0 4 4.9 CCCN1CCC(COc2nc3c(I)cccc3c3ncccc23)CC1 10.1021/jm300943r
CHEMBL2181168 82549 0 None -17 6 Guinea pig 8.3 pKi = 8.3 Binding
Displacement of [3H]GR113808 from 5HT4R in guinea pig striatal membranesDisplacement of [3H]GR113808 from 5HT4R in guinea pig striatal membranes
ChEMBL 461 5 0 4 4.9 CCCN1CCC(COc2nc3c(I)cccc3c3ncccc23)CC1 10.1021/jm300943r
71451950 82263 5 None -1 2 Human 8.3 pKi = 8.3 Binding
Displacement of [3H]GR113808 from human 5HT4A receptor expressed in HEK293 cells after 30 mins by liquid scintillation countingDisplacement of [3H]GR113808 from human 5HT4A receptor expressed in HEK293 cells after 30 mins by liquid scintillation counting
ChEMBL 433 4 2 5 2.4 CC1(C)C(=O)N(C(=O)NCC2CCN(CC3(O)CCOCC3)CC2)c2cc(F)ccc21 10.1021/jm300953p
CHEMBL2179582 82263 5 None -1 2 Human 8.3 pKi = 8.3 Binding
Displacement of [3H]GR113808 from human 5HT4A receptor expressed in HEK293 cells after 30 mins by liquid scintillation countingDisplacement of [3H]GR113808 from human 5HT4A receptor expressed in HEK293 cells after 30 mins by liquid scintillation counting
ChEMBL 433 4 2 5 2.4 CC1(C)C(=O)N(C(=O)NCC2CCN(CC3(O)CCOCC3)CC2)c2cc(F)ccc21 10.1021/jm300953p
15295138 50789 0 None - 1 Rat 8.3 pKi = 8.3 Binding
Binding affinity towards 5-hydroxytryptamine 4 receptor was determined in rat striatal membranes using [3H]GR-113808 as radioligandBinding affinity towards 5-hydroxytryptamine 4 receptor was determined in rat striatal membranes using [3H]GR-113808 as radioligand
ChEMBL 328 5 2 6 1.5 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCCC(O)C1 10.1021/jm960320m
CHEMBL157880 50789 0 None - 1 Rat 8.3 pKi = 8.3 Binding
Binding affinity towards 5-hydroxytryptamine 4 receptor was determined in rat striatal membranes using [3H]GR-113808 as radioligandBinding affinity towards 5-hydroxytryptamine 4 receptor was determined in rat striatal membranes using [3H]GR-113808 as radioligand
ChEMBL 328 5 2 6 1.5 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCCC(O)C1 10.1021/jm960320m
118734515 118167 0 None - 1 Guinea pig 8.3 pKi = 8.3 Binding
Displacement of [3H]GR113808 from 5-HT4R in guinea pig brain membranes incubated for 30 mins by radioligand binding assayDisplacement of [3H]GR113808 from 5-HT4R in guinea pig brain membranes incubated for 30 mins by radioligand binding assay
ChEMBL 406 7 1 4 5.4 COc1cc(N)c(Cl)cc1C(=O)CCC1CCN(CC2CCCCC2C)CC1 10.1021/acs.jmedchem.5b00115
CHEMBL3417000 118167 0 None - 1 Guinea pig 8.3 pKi = 8.3 Binding
Displacement of [3H]GR113808 from 5-HT4R in guinea pig brain membranes incubated for 30 mins by radioligand binding assayDisplacement of [3H]GR113808 from 5-HT4R in guinea pig brain membranes incubated for 30 mins by radioligand binding assay
ChEMBL 406 7 1 4 5.4 COc1cc(N)c(Cl)cc1C(=O)CCC1CCN(CC2CCCCC2C)CC1 10.1021/acs.jmedchem.5b00115
11166796 82264 0 None -2 2 Human 8.3 pKi = 8.3 Binding
Displacement of [3H]GR113808 from human 5HT4E receptor expressed in CHO cells after 30 mins by liquid scintillation countingDisplacement of [3H]GR113808 from human 5HT4E receptor expressed in CHO cells after 30 mins by liquid scintillation counting
ChEMBL 448 5 2 7 2.3 CC(C)n1c(=O)n(C(=O)NCC2CCN(CC3(O)CCOCC3)CC2)c2cc(F)ccc21 10.1021/jm300953p
CHEMBL2179583 82264 0 None -2 2 Human 8.3 pKi = 8.3 Binding
Displacement of [3H]GR113808 from human 5HT4E receptor expressed in CHO cells after 30 mins by liquid scintillation countingDisplacement of [3H]GR113808 from human 5HT4E receptor expressed in CHO cells after 30 mins by liquid scintillation counting
ChEMBL 448 5 2 7 2.3 CC(C)n1c(=O)n(C(=O)NCC2CCN(CC3(O)CCOCC3)CC2)c2cc(F)ccc21 10.1021/jm300953p
44374544 52873 0 None - 1 Guinea pig 7.4 pKi = 7.4 Binding
Inhibition of [3H]GR-113808 binding to guinea pig striatum 5-hydroxytryptamine 4 receptorInhibition of [3H]GR-113808 binding to guinea pig striatum 5-hydroxytryptamine 4 receptor
ChEMBL 309 3 2 4 1.8 COc1cc(N)c(Cl)cc1C(=O)NC1CCN2CCC1C2 10.1021/jm020270n
CHEMBL159825 52873 0 None - 1 Guinea pig 7.4 pKi = 7.4 Binding
Inhibition of [3H]GR-113808 binding to guinea pig striatum 5-hydroxytryptamine 4 receptorInhibition of [3H]GR-113808 binding to guinea pig striatum 5-hydroxytryptamine 4 receptor
ChEMBL 309 3 2 4 1.8 COc1cc(N)c(Cl)cc1C(=O)NC1CCN2CCC1C2 10.1021/jm020270n
134828071 173189 0 None - 1 Human 7.4 pKi = 7.4 Binding
Displacement of [3H]-GR113808 from recombinant human 5-HT4BR expressed in membranes after 60 minsDisplacement of [3H]-GR113808 from recombinant human 5-HT4BR expressed in membranes after 60 mins
ChEMBL 416 7 1 3 6.1 COc1c(C(=O)CCC2CCN(CC3CCCCC3)CC2)cc(Cl)c2[nH]ccc12 10.1016/j.ejmech.2018.10.064
CHEMBL4537101 173189 0 None - 1 Human 7.4 pKi = 7.4 Binding
Displacement of [3H]-GR113808 from recombinant human 5-HT4BR expressed in membranes after 60 minsDisplacement of [3H]-GR113808 from recombinant human 5-HT4BR expressed in membranes after 60 mins
ChEMBL 416 7 1 3 6.1 COc1c(C(=O)CCC2CCN(CC3CCCCC3)CC2)cc(Cl)c2[nH]ccc12 10.1016/j.ejmech.2018.10.064
10020895 4637 0 None -524 8 Human 5.4 pKi = 5.4 Binding
In vitro binding affinity by radioligand binding assay using cell line expressing human 5-hydroxytryptamine 4 receptorIn vitro binding affinity by radioligand binding assay using cell line expressing human 5-hydroxytryptamine 4 receptor
ChEMBL 352 3 2 3 3.8 CN1CCC(c2c[nH]c3ccc(NC(=O)c4ccc(F)cc4)nc23)CC1 10.1021/jm030020m
CHEMBL103479 4637 0 None -524 8 Human 5.4 pKi = 5.4 Binding
In vitro binding affinity by radioligand binding assay using cell line expressing human 5-hydroxytryptamine 4 receptorIn vitro binding affinity by radioligand binding assay using cell line expressing human 5-hydroxytryptamine 4 receptor
ChEMBL 352 3 2 3 3.8 CN1CCC(c2c[nH]c3ccc(NC(=O)c4ccc(F)cc4)nc23)CC1 10.1021/jm030020m
71452073 82553 0 None -17 2 Human 6.4 pKi = 6.4 Binding
Displacement of [3H]GR113808 from human recombinant 5HT4R expressed in HEK293T cellsDisplacement of [3H]GR113808 from human recombinant 5HT4R expressed in HEK293T cells
ChEMBL 335 5 0 4 4.3 CCCN1CCC(COc2nc3ccccc3c3cnccc23)CC1 10.1021/jm300943r
CHEMBL2181172 82553 0 None -17 2 Human 6.4 pKi = 6.4 Binding
Displacement of [3H]GR113808 from human recombinant 5HT4R expressed in HEK293T cellsDisplacement of [3H]GR113808 from human recombinant 5HT4R expressed in HEK293T cells
ChEMBL 335 5 0 4 4.3 CCCN1CCC(COc2nc3ccccc3c3cnccc23)CC1 10.1021/jm300943r
44213663 204855 0 None - 1 Rat 7.4 pKi = 7.4 Binding
Binding affinity at 5-hydroxytryptamine 4 receptor in rat striatum by [3H]GR-113808 displacement.Binding affinity at 5-hydroxytryptamine 4 receptor in rat striatum by [3H]GR-113808 displacement.
ChEMBL 323 4 2 4 2.1 Nc1c(Cl)cc(C(=O)NCCN2CCCCC2)c2c1CCO2 10.1016/0960-894X(96)00002-9
CHEMBL88867 204855 0 None - 1 Rat 7.4 pKi = 7.4 Binding
Binding affinity at 5-hydroxytryptamine 4 receptor in rat striatum by [3H]GR-113808 displacement.Binding affinity at 5-hydroxytryptamine 4 receptor in rat striatum by [3H]GR-113808 displacement.
ChEMBL 323 4 2 4 2.1 Nc1c(Cl)cc(C(=O)NCCN2CCCCC2)c2c1CCO2 10.1016/0960-894X(96)00002-9
44592003 188885 0 None - 1 Guinea pig 6.4 pKi = 6.4 Binding
Displacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatum membraneDisplacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatum membrane
ChEMBL 301 4 0 5 3.4 c1cc2c(OCCN3CCCCC3)nc3ccsc3n2c1 10.1016/j.bmc.2008.11.045
CHEMBL513740 188885 0 None - 1 Guinea pig 6.4 pKi = 6.4 Binding
Displacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatum membraneDisplacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatum membrane
ChEMBL 301 4 0 5 3.4 c1cc2c(OCCN3CCCCC3)nc3ccsc3n2c1 10.1016/j.bmc.2008.11.045
44323269 11967 0 None - 1 Rat 6.4 pKi = 6.4 Binding
Binding affinity at 5-hydroxytryptamine 4 receptor in rat striatum by [3H]GR-113808 displacement.Binding affinity at 5-hydroxytryptamine 4 receptor in rat striatum by [3H]GR-113808 displacement.
ChEMBL 378 5 2 3 3.0 CCCC[N+]12CCC(CC1)[C@@H](NC(=O)c1cc(Cl)c(N)c3c1OCC3)C2 10.1016/0960-894X(96)00002-9
CHEMBL1183709 11967 0 None - 1 Rat 6.4 pKi = 6.4 Binding
Binding affinity at 5-hydroxytryptamine 4 receptor in rat striatum by [3H]GR-113808 displacement.Binding affinity at 5-hydroxytryptamine 4 receptor in rat striatum by [3H]GR-113808 displacement.
ChEMBL 378 5 2 3 3.0 CCCC[N+]12CCC(CC1)[C@@H](NC(=O)c1cc(Cl)c(N)c3c1OCC3)C2 10.1016/0960-894X(96)00002-9
CHEMBL314198 11967 0 None - 1 Rat 6.4 pKi = 6.4 Binding
Binding affinity at 5-hydroxytryptamine 4 receptor in rat striatum by [3H]GR-113808 displacement.Binding affinity at 5-hydroxytryptamine 4 receptor in rat striatum by [3H]GR-113808 displacement.
ChEMBL 378 5 2 3 3.0 CCCC[N+]12CCC(CC1)[C@@H](NC(=O)c1cc(Cl)c(N)c3c1OCC3)C2 10.1016/0960-894X(96)00002-9
6604914 99919 2 None -1 2 Guinea pig 6.4 pKi = 6.4 Binding
Binding affinity for 5-hydroxytryptamine 4 receptor by displacement of [3H]GR-113808 from guinea pig brain striatum.Binding affinity for 5-hydroxytryptamine 4 receptor by displacement of [3H]GR-113808 from guinea pig brain striatum.
ChEMBL 309 3 2 4 1.8 COc1cc(N)c(Cl)cc1C(=O)N[C@@H]1CN2CCC1CC2 10.1016/0960-894X(96)00052-2
CHEMBL28992 99919 2 None -1 2 Guinea pig 6.4 pKi = 6.4 Binding
Binding affinity for 5-hydroxytryptamine 4 receptor by displacement of [3H]GR-113808 from guinea pig brain striatum.Binding affinity for 5-hydroxytryptamine 4 receptor by displacement of [3H]GR-113808 from guinea pig brain striatum.
ChEMBL 309 3 2 4 1.8 COc1cc(N)c(Cl)cc1C(=O)N[C@@H]1CN2CCC1CC2 10.1016/0960-894X(96)00052-2
90644473 111788 0 None - 1 Guinea pig 7.4 pKi = 7.4 Binding
Displacement of [3H]GR113808 from Dunkin-Hartley guinea pig brain striatum 5HT4R after 30 minsDisplacement of [3H]GR113808 from Dunkin-Hartley guinea pig brain striatum 5HT4R after 30 mins
ChEMBL 353 5 0 5 2.7 COc1cc2c3c(cccc3n1)C(=O)N(CCCN1CCCCC1)C2=O 10.1016/j.ejmech.2014.05.015
CHEMBL3291078 111788 0 None - 1 Guinea pig 7.4 pKi = 7.4 Binding
Displacement of [3H]GR113808 from Dunkin-Hartley guinea pig brain striatum 5HT4R after 30 minsDisplacement of [3H]GR113808 from Dunkin-Hartley guinea pig brain striatum 5HT4R after 30 mins
ChEMBL 353 5 0 5 2.7 COc1cc2c3c(cccc3n1)C(=O)N(CCCN1CCCCC1)C2=O 10.1016/j.ejmech.2014.05.015
135446149 206444 0 None - 1 Rat 7.4 pKi = 7.4 Binding
Binding affinity to 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatum membraneBinding affinity to 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatum membrane
ChEMBL 393 7 2 5 3.4 CCCCN1CCC(CNC(=O)c2cc(Cl)c([N+](=O)[O-])c3[nH]cnc23)CC1 10.1021/jm020807x
CHEMBL98397 206444 0 None - 1 Rat 7.4 pKi = 7.4 Binding
Binding affinity to 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatum membraneBinding affinity to 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatum membrane
ChEMBL 393 7 2 5 3.4 CCCCN1CCC(CNC(=O)c2cc(Cl)c([N+](=O)[O-])c3[nH]cnc23)CC1 10.1021/jm020807x
135446149 206444 0 None - 1 Rat 7.4 pKi = 7.4 Binding
In vitro binding affinity to 5-hydroxytryptamine 4 receptor in rat striatum membraneIn vitro binding affinity to 5-hydroxytryptamine 4 receptor in rat striatum membrane
ChEMBL 393 7 2 5 3.4 CCCCN1CCC(CNC(=O)c2cc(Cl)c([N+](=O)[O-])c3[nH]cnc23)CC1 10.1016/s0960-894x(01)00517-0
CHEMBL98397 206444 0 None - 1 Rat 7.4 pKi = 7.4 Binding
In vitro binding affinity to 5-hydroxytryptamine 4 receptor in rat striatum membraneIn vitro binding affinity to 5-hydroxytryptamine 4 receptor in rat striatum membrane
ChEMBL 393 7 2 5 3.4 CCCCN1CCC(CNC(=O)c2cc(Cl)c([N+](=O)[O-])c3[nH]cnc23)CC1 10.1016/s0960-894x(01)00517-0
135446149 206444 0 None - 1 Rat 7.4 pKi = 7.4 Binding
pKi against 5-hydroxytryptamine 4 receptor in rat striatum membranepKi against 5-hydroxytryptamine 4 receptor in rat striatum membrane
ChEMBL 393 7 2 5 3.4 CCCCN1CCC(CNC(=O)c2cc(Cl)c([N+](=O)[O-])c3[nH]cnc23)CC1 10.1016/s0960-894x(01)00517-0
CHEMBL98397 206444 0 None - 1 Rat 7.4 pKi = 7.4 Binding
pKi against 5-hydroxytryptamine 4 receptor in rat striatum membranepKi against 5-hydroxytryptamine 4 receptor in rat striatum membrane
ChEMBL 393 7 2 5 3.4 CCCCN1CCC(CNC(=O)c2cc(Cl)c([N+](=O)[O-])c3[nH]cnc23)CC1 10.1016/s0960-894x(01)00517-0
90666006 108802 0 None - 1 Guinea pig 7.4 pKi = 7.4 Binding
Displacement of [3H]-GR113808 from guinea pig 5HT4 receptor by Grossman's methodDisplacement of [3H]-GR113808 from guinea pig 5HT4 receptor by Grossman's method
ChEMBL 369 5 0 5 4.8 c1cc2c(OCC3CCN(CC4CCCC4)CC3)nc3ccsc3n2c1 10.1039/C2MD20063E
CHEMBL3218878 108802 0 None - 1 Guinea pig 7.4 pKi = 7.4 Binding
Displacement of [3H]-GR113808 from guinea pig 5HT4 receptor by Grossman's methodDisplacement of [3H]-GR113808 from guinea pig 5HT4 receptor by Grossman's method
ChEMBL 369 5 0 5 4.8 c1cc2c(OCC3CCN(CC4CCCC4)CC3)nc3ccsc3n2c1 10.1039/C2MD20063E
10566528 161591 0 None - 1 Rat 6.4 pKi = 6.4 Binding
Displacement of [3H]GR-113808 from rat striatum 5-hydroxytryptamine 4 receptorDisplacement of [3H]GR-113808 from rat striatum 5-hydroxytryptamine 4 receptor
ChEMBL 305 2 1 4 2.5 O=C(OC1CN2CCC1CC2)c1cc(Cl)cc2nc[nH]c12 10.1016/0960-894X(96)00200-4
CHEMBL416172 161591 0 None - 1 Rat 6.4 pKi = 6.4 Binding
Displacement of [3H]GR-113808 from rat striatum 5-hydroxytryptamine 4 receptorDisplacement of [3H]GR-113808 from rat striatum 5-hydroxytryptamine 4 receptor
ChEMBL 305 2 1 4 2.5 O=C(OC1CN2CCC1CC2)c1cc(Cl)cc2nc[nH]c12 10.1016/0960-894X(96)00200-4
10566528 161591 0 None - 1 Rat 6.4 pKi = 6.4 Binding
In vitro affinity at serotonergic 5-hydroxytryptamine 4 receptor by radioligand binding assay using [3H]GR-113808 in rat striatum membranes.In vitro affinity at serotonergic 5-hydroxytryptamine 4 receptor by radioligand binding assay using [3H]GR-113808 in rat striatum membranes.
ChEMBL 305 2 1 4 2.5 O=C(OC1CN2CCC1CC2)c1cc(Cl)cc2nc[nH]c12 10.1021/jm991076c
CHEMBL416172 161591 0 None - 1 Rat 6.4 pKi = 6.4 Binding
In vitro affinity at serotonergic 5-hydroxytryptamine 4 receptor by radioligand binding assay using [3H]GR-113808 in rat striatum membranes.In vitro affinity at serotonergic 5-hydroxytryptamine 4 receptor by radioligand binding assay using [3H]GR-113808 in rat striatum membranes.
ChEMBL 305 2 1 4 2.5 O=C(OC1CN2CCC1CC2)c1cc(Cl)cc2nc[nH]c12 10.1021/jm991076c
240 931 39 None -4 25 Guinea pig 7.4 pKi = 7.4 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
ChEMBL 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N nan
2769 931 39 None -4 25 Guinea pig 7.4 pKi = 7.4 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
ChEMBL 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N nan
44279790 931 39 None -4 25 Guinea pig 7.4 pKi = 7.4 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
ChEMBL 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N nan
660 931 39 None -4 25 Guinea pig 7.4 pKi = 7.4 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
ChEMBL 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N nan
CHEMBL1729 931 39 None -4 25 Guinea pig 7.4 pKi = 7.4 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
ChEMBL 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N nan
CHEMBL560739 931 39 None -4 25 Guinea pig 7.4 pKi = 7.4 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
ChEMBL 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N nan
DB00604 931 39 None -4 25 Guinea pig 7.4 pKi = 7.4 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
ChEMBL 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N nan
41581 189231 4 None - 1 Rat 6.3 pKi = 6.3 Binding
Binding affinity at 5-hydroxytryptamine 4 receptor in rat striatal membranes by [3H]GR-113808 displacement.Binding affinity at 5-hydroxytryptamine 4 receptor in rat striatal membranes by [3H]GR-113808 displacement.
ChEMBL 278 5 1 4 2.7 COc1cccc(NC(=O)OCCN2CCCCC2)c1 10.1021/jm960853v
CHEMBL51647 189231 4 None - 1 Rat 6.3 pKi = 6.3 Binding
Binding affinity at 5-hydroxytryptamine 4 receptor in rat striatal membranes by [3H]GR-113808 displacement.Binding affinity at 5-hydroxytryptamine 4 receptor in rat striatal membranes by [3H]GR-113808 displacement.
ChEMBL 278 5 1 4 2.7 COc1cccc(NC(=O)OCCN2CCCCC2)c1 10.1021/jm960853v
44404969 71918 0 None - 1 Human 7.3 pKi = 7.3 Binding
Binding affinity for 5-HT4 receptor using [3H]GR-113808Binding affinity for 5-HT4 receptor using [3H]GR-113808
ChEMBL 930 18 4 13 6.8 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCC(NC(=O)CCc2ccc3c(c2)oc2cc(CCC(=O)NC4CCN(CCOC(=O)c5cc(Cl)c(N)cc5OC)CC4)ccc23)CC1 10.1021/jm050234z
CHEMBL198226 71918 0 None - 1 Human 7.3 pKi = 7.3 Binding
Binding affinity for 5-HT4 receptor using [3H]GR-113808Binding affinity for 5-HT4 receptor using [3H]GR-113808
ChEMBL 930 18 4 13 6.8 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCC(NC(=O)CCc2ccc3c(c2)oc2cc(CCC(=O)NC4CCN(CCOC(=O)c5cc(Cl)c(N)cc5OC)CC4)ccc23)CC1 10.1021/jm050234z
10802184 53873 0 None - 1 Rat 7.3 pKi = 7.3 Binding
Binding affinity towards 5-hydroxytryptamine 4 receptor was determined in rat striatal membranes using [3H]GR-113808 as radioligandBinding affinity towards 5-hydroxytryptamine 4 receptor was determined in rat striatal membranes using [3H]GR-113808 as radioligand
ChEMBL 272 5 1 5 1.6 COc1cc(N)c(Cl)cc1C(=O)OCCN(C)C 10.1021/jm960320m
CHEMBL160705 53873 0 None - 1 Rat 7.3 pKi = 7.3 Binding
Binding affinity towards 5-hydroxytryptamine 4 receptor was determined in rat striatal membranes using [3H]GR-113808 as radioligandBinding affinity towards 5-hydroxytryptamine 4 receptor was determined in rat striatal membranes using [3H]GR-113808 as radioligand
ChEMBL 272 5 1 5 1.6 COc1cc(N)c(Cl)cc1C(=O)OCCN(C)C 10.1021/jm960320m
135442121 111881 0 None - 1 Rat 7.3 pKi = 7.3 Binding
pKi against 5-hydroxytryptamine 4 receptor in rat striatum membranepKi against 5-hydroxytryptamine 4 receptor in rat striatum membrane
ChEMBL 437 7 2 5 3.5 CCCCN1CCC(CNC(=O)c2cc(Br)c([N+](=O)[O-])c3[nH]cnc23)CC1 10.1016/s0960-894x(01)00517-0
CHEMBL329545 111881 0 None - 1 Rat 7.3 pKi = 7.3 Binding
pKi against 5-hydroxytryptamine 4 receptor in rat striatum membranepKi against 5-hydroxytryptamine 4 receptor in rat striatum membrane
ChEMBL 437 7 2 5 3.5 CCCCN1CCC(CNC(=O)c2cc(Br)c([N+](=O)[O-])c3[nH]cnc23)CC1 10.1016/s0960-894x(01)00517-0
136118648 75968 0 None -9 5 Human 6.3 pKi = 6.3 Binding
Displacement of [3H]GR113808 from human recombinant 5HT4 receptorDisplacement of [3H]GR113808 from human recombinant 5HT4 receptor
ChEMBL 318 1 3 2 2.0 C/N=C1\NC(=O)/C(=C/c2c[nH]c3cccc(Br)c23)N1 10.1016/j.bmc.2013.09.011
CHEMBL2058703 75968 0 None -9 5 Human 6.3 pKi = 6.3 Binding
Displacement of [3H]GR113808 from human recombinant 5HT4 receptorDisplacement of [3H]GR113808 from human recombinant 5HT4 receptor
ChEMBL 318 1 3 2 2.0 C/N=C1\NC(=O)/C(=C/c2c[nH]c3cccc(Br)c23)N1 10.1016/j.bmc.2013.09.011
9797313 101459 1 None -154 3 Rat 7.3 pKi = 7.3 Binding
Binding affinity against 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatumBinding affinity against 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatum
ChEMBL 323 3 2 4 2.3 COc1cc(N)c(Cl)cc1C(=O)NC1CC2CCC(C1)N2C 10.1016/0960-894X(95)00115-A
CHEMBL301039 101459 1 None -154 3 Rat 7.3 pKi = 7.3 Binding
Binding affinity against 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatumBinding affinity against 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatum
ChEMBL 323 3 2 4 2.3 COc1cc(N)c(Cl)cc1C(=O)NC1CC2CCC(C1)N2C 10.1016/0960-894X(95)00115-A
9797313 101459 1 None -151 3 Guinea pig 7.3 pKi = 7.3 Binding
Inhibition of [3H]GR-113808 binding to guinea pig striatum 5-hydroxytryptamine 4 receptorInhibition of [3H]GR-113808 binding to guinea pig striatum 5-hydroxytryptamine 4 receptor
ChEMBL 323 3 2 4 2.3 COc1cc(N)c(Cl)cc1C(=O)NC1CC2CCC(C1)N2C 10.1021/jm020270n
CHEMBL301039 101459 1 None -151 3 Guinea pig 7.3 pKi = 7.3 Binding
Inhibition of [3H]GR-113808 binding to guinea pig striatum 5-hydroxytryptamine 4 receptorInhibition of [3H]GR-113808 binding to guinea pig striatum 5-hydroxytryptamine 4 receptor
ChEMBL 323 3 2 4 2.3 COc1cc(N)c(Cl)cc1C(=O)NC1CC2CCC(C1)N2C 10.1021/jm020270n
135442121 111881 0 None - 1 Rat 7.3 pKi = 7.3 Binding
Binding affinity to 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatum membraneBinding affinity to 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatum membrane
ChEMBL 437 7 2 5 3.5 CCCCN1CCC(CNC(=O)c2cc(Br)c([N+](=O)[O-])c3[nH]cnc23)CC1 10.1021/jm020807x
CHEMBL329545 111881 0 None - 1 Rat 7.3 pKi = 7.3 Binding
Binding affinity to 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatum membraneBinding affinity to 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatum membrane
ChEMBL 437 7 2 5 3.5 CCCCN1CCC(CNC(=O)c2cc(Br)c([N+](=O)[O-])c3[nH]cnc23)CC1 10.1021/jm020807x
135442121 111881 0 None - 1 Rat 7.3 pKi = 7.3 Binding
In vitro binding affinity to 5-hydroxytryptamine 4 receptor in rat striatum membraneIn vitro binding affinity to 5-hydroxytryptamine 4 receptor in rat striatum membrane
ChEMBL 437 7 2 5 3.5 CCCCN1CCC(CNC(=O)c2cc(Br)c([N+](=O)[O-])c3[nH]cnc23)CC1 10.1016/s0960-894x(01)00517-0
CHEMBL329545 111881 0 None - 1 Rat 7.3 pKi = 7.3 Binding
In vitro binding affinity to 5-hydroxytryptamine 4 receptor in rat striatum membraneIn vitro binding affinity to 5-hydroxytryptamine 4 receptor in rat striatum membrane
ChEMBL 437 7 2 5 3.5 CCCCN1CCC(CNC(=O)c2cc(Br)c([N+](=O)[O-])c3[nH]cnc23)CC1 10.1016/s0960-894x(01)00517-0
9797313 101459 1 None -154 3 Rat 7.3 pKi = 7.3 Binding
Binding affinity towards 5-hydroxytryptamine 4 receptor was determined in rat striatal membranes using [3H]GR-113808 as radioligandBinding affinity towards 5-hydroxytryptamine 4 receptor was determined in rat striatal membranes using [3H]GR-113808 as radioligand
ChEMBL 323 3 2 4 2.3 COc1cc(N)c(Cl)cc1C(=O)NC1CC2CCC(C1)N2C 10.1021/jm960320m
CHEMBL301039 101459 1 None -154 3 Rat 7.3 pKi = 7.3 Binding
Binding affinity towards 5-hydroxytryptamine 4 receptor was determined in rat striatal membranes using [3H]GR-113808 as radioligandBinding affinity towards 5-hydroxytryptamine 4 receptor was determined in rat striatal membranes using [3H]GR-113808 as radioligand
ChEMBL 323 3 2 4 2.3 COc1cc(N)c(Cl)cc1C(=O)NC1CC2CCC(C1)N2C 10.1021/jm960320m
44592184 178280 0 None - 1 Guinea pig 7.3 pKi = 7.3 Binding
Displacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatum membraneDisplacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatum membrane
ChEMBL 357 7 0 5 4.8 CCCCCN1CCC(COc2nc3sccc3n3cccc23)CC1 10.1016/j.bmc.2008.11.045
CHEMBL469592 178280 0 None - 1 Guinea pig 7.3 pKi = 7.3 Binding
Displacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatum membraneDisplacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatum membrane
ChEMBL 357 7 0 5 4.8 CCCCCN1CCC(COc2nc3sccc3n3cccc23)CC1 10.1016/j.bmc.2008.11.045
10757374 162542 0 None - 1 Rat 6.3 pKi = 6.3 Binding
Binding affinity against 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatumBinding affinity against 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatum
ChEMBL 310 3 1 5 2.2 COc1cc(N)c(Cl)cc1C(=O)O[C@H]1CN2CCC1CC2 10.1016/S0960-894X(01)80508-4
CHEMBL41769 162542 0 None - 1 Rat 6.3 pKi = 6.3 Binding
Binding affinity against 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatumBinding affinity against 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatum
ChEMBL 310 3 1 5 2.2 COc1cc(N)c(Cl)cc1C(=O)O[C@H]1CN2CCC1CC2 10.1016/S0960-894X(01)80508-4
11520559 71969 0 None - 1 Human 6.3 pKi = 6.3 Binding
Binding affinity for 5-HT4 receptor using [3H]GR-113808Binding affinity for 5-HT4 receptor using [3H]GR-113808
ChEMBL 750 16 2 12 3.4 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCN(C(=O)CCCCCC(=O)N2CCN(CCOC(=O)c3cc(Cl)c(N)cc3OC)CC2)CC1 10.1021/jm050234z
CHEMBL198371 71969 0 None - 1 Human 6.3 pKi = 6.3 Binding
Binding affinity for 5-HT4 receptor using [3H]GR-113808Binding affinity for 5-HT4 receptor using [3H]GR-113808
ChEMBL 750 16 2 12 3.4 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCN(C(=O)CCCCCC(=O)N2CCN(CCOC(=O)c3cc(Cl)c(N)cc3OC)CC2)CC1 10.1021/jm050234z
10757374 162542 0 None - 1 Rat 6.3 pKi = 6.3 Binding
Binding affinity towards 5-hydroxytryptamine 4 receptor was determined in rat striatal membranes using [3H]GR-113808 as radioligandBinding affinity towards 5-hydroxytryptamine 4 receptor was determined in rat striatal membranes using [3H]GR-113808 as radioligand
ChEMBL 310 3 1 5 2.2 COc1cc(N)c(Cl)cc1C(=O)O[C@H]1CN2CCC1CC2 10.1021/jm960320m
CHEMBL41769 162542 0 None - 1 Rat 6.3 pKi = 6.3 Binding
Binding affinity towards 5-hydroxytryptamine 4 receptor was determined in rat striatal membranes using [3H]GR-113808 as radioligandBinding affinity towards 5-hydroxytryptamine 4 receptor was determined in rat striatal membranes using [3H]GR-113808 as radioligand
ChEMBL 310 3 1 5 2.2 COc1cc(N)c(Cl)cc1C(=O)O[C@H]1CN2CCC1CC2 10.1021/jm960320m
9956365 193846 0 None -131 3 Guinea pig 6.3 pKi = 6.3 Binding
In vitro binding affinity at 5-hydroxytryptamine 4 receptor in guinea pig striatum using 3[H]GR-113808 as the radioligandIn vitro binding affinity at 5-hydroxytryptamine 4 receptor in guinea pig striatum using 3[H]GR-113808 as the radioligand
ChEMBL 470 7 2 4 4.1 CNC(=O)Cn1c2c(c3ccccc31)CCN(CCCCC13CCCc4cccc(c41)NC3=O)C2 10.1021/jm0104264
CHEMBL553794 193846 0 None -131 3 Guinea pig 6.3 pKi = 6.3 Binding
In vitro binding affinity at 5-hydroxytryptamine 4 receptor in guinea pig striatum using 3[H]GR-113808 as the radioligandIn vitro binding affinity at 5-hydroxytryptamine 4 receptor in guinea pig striatum using 3[H]GR-113808 as the radioligand
ChEMBL 470 7 2 4 4.1 CNC(=O)Cn1c2c(c3ccccc31)CCN(CCCCC13CCCc4cccc(c41)NC3=O)C2 10.1021/jm0104264
10687803 206616 0 None - 1 Guinea pig 7.3 pKi = 7.3 Binding
Binding affinity against 5-hydroxytryptamine 4 receptor in guinea pig striatum using [3H]GR-113808 as radioligandBinding affinity against 5-hydroxytryptamine 4 receptor in guinea pig striatum using [3H]GR-113808 as radioligand
ChEMBL 329 3 1 6 0.9 CN1CCN(CNC(=O)n2c(=O)n(C3CC3)c3ccccc32)CC1 10.1021/jm981098j
CHEMBL99452 206616 0 None - 1 Guinea pig 7.3 pKi = 7.3 Binding
Binding affinity against 5-hydroxytryptamine 4 receptor in guinea pig striatum using [3H]GR-113808 as radioligandBinding affinity against 5-hydroxytryptamine 4 receptor in guinea pig striatum using [3H]GR-113808 as radioligand
ChEMBL 329 3 1 6 0.9 CN1CCN(CNC(=O)n2c(=O)n(C3CC3)c3ccccc32)CC1 10.1021/jm981098j
155544687 174459 0 None - 1 Human 7.3 pKi = 7.3 Binding
Displacement of [3H]-GR113808 from recombinant human 5-HT4BR expressed in membranes after 60 minsDisplacement of [3H]-GR113808 from recombinant human 5-HT4BR expressed in membranes after 60 mins
ChEMBL 312 7 1 2 4.6 CCCCN1CCC(CCC(=O)c2ccc3[nH]ccc3c2)CC1 10.1016/j.ejmech.2018.10.064
CHEMBL4567394 174459 0 None - 1 Human 7.3 pKi = 7.3 Binding
Displacement of [3H]-GR113808 from recombinant human 5-HT4BR expressed in membranes after 60 minsDisplacement of [3H]-GR113808 from recombinant human 5-HT4BR expressed in membranes after 60 mins
ChEMBL 312 7 1 2 4.6 CCCCN1CCC(CCC(=O)c2ccc3[nH]ccc3c2)CC1 10.1016/j.ejmech.2018.10.064
90665997 108795 0 None - 1 Guinea pig 7.3 pKi = 7.3 Binding
Displacement of [3H]-GR113808 from guinea pig 5HT4 receptor by Grossman's methodDisplacement of [3H]-GR113808 from guinea pig 5HT4 receptor by Grossman's method
ChEMBL 391 6 0 5 4.9 c1ccc(CCN2CCC(COc3nc4ccsc4n4cccc34)CC2)cc1 10.1039/C2MD20063E
CHEMBL3218869 108795 0 None - 1 Guinea pig 7.3 pKi = 7.3 Binding
Displacement of [3H]-GR113808 from guinea pig 5HT4 receptor by Grossman's methodDisplacement of [3H]-GR113808 from guinea pig 5HT4 receptor by Grossman's method
ChEMBL 391 6 0 5 4.9 c1ccc(CCN2CCC(COc3nc4ccsc4n4cccc34)CC2)cc1 10.1039/C2MD20063E
235 2527 36 None -4 3 Human 8.3 pKi = 8.3 Binding
Binding affinity for 5-HT4 receptor using [3H]GR-113808Binding affinity for 5-HT4 receptor using [3H]GR-113808
ChEMBL 312 5 1 5 2.6 COc1cc(N)c(cc1C(=O)OCCN1CCCCC1)Cl 10.1021/jm050234z
5311299 2527 36 None -4 3 Human 8.3 pKi = 8.3 Binding
Binding affinity for 5-HT4 receptor using [3H]GR-113808Binding affinity for 5-HT4 receptor using [3H]GR-113808
ChEMBL 312 5 1 5 2.6 COc1cc(N)c(cc1C(=O)OCCN1CCCCC1)Cl 10.1021/jm050234z
CHEMBL286136 2527 36 None -4 3 Human 8.3 pKi = 8.3 Binding
Binding affinity for 5-HT4 receptor using [3H]GR-113808Binding affinity for 5-HT4 receptor using [3H]GR-113808
ChEMBL 312 5 1 5 2.6 COc1cc(N)c(cc1C(=O)OCCN1CCCCC1)Cl 10.1021/jm050234z
44404965 71741 0 None - 1 Human 8.3 pKi = 8.3 Binding
Binding affinity for 5-HT4 receptor using [3H]GR-113808Binding affinity for 5-HT4 receptor using [3H]GR-113808
ChEMBL 764 17 5 12 3.7 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCC(C(=O)NCCCCCNC(=O)C2CCN(CCOC(=O)c3cc(Cl)c(N)cc3O)CC2)CC1 10.1021/jm050234z
CHEMBL197745 71741 0 None - 1 Human 8.3 pKi = 8.3 Binding
Binding affinity for 5-HT4 receptor using [3H]GR-113808Binding affinity for 5-HT4 receptor using [3H]GR-113808
ChEMBL 764 17 5 12 3.7 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCC(C(=O)NCCCCCNC(=O)C2CCN(CCOC(=O)c3cc(Cl)c(N)cc3O)CC2)CC1 10.1021/jm050234z
44404960 71747 0 None - 1 Human 8.3 pKi = 8.3 Binding
Binding affinity for 5-HT4 receptor using [3H]GR-113808Binding affinity for 5-HT4 receptor using [3H]GR-113808
ChEMBL 736 15 5 12 3.2 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCC(NC(=O)CCCC(=O)NC2CCN(CCOC(=O)c3cc(Cl)c(N)cc3O)CC2)CC1 10.1021/jm050234z
CHEMBL197752 71747 0 None - 1 Human 8.3 pKi = 8.3 Binding
Binding affinity for 5-HT4 receptor using [3H]GR-113808Binding affinity for 5-HT4 receptor using [3H]GR-113808
ChEMBL 736 15 5 12 3.2 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCC(NC(=O)CCCC(=O)NC2CCN(CCOC(=O)c3cc(Cl)c(N)cc3O)CC2)CC1 10.1021/jm050234z
11629247 72049 0 None - 1 Human 8.3 pKi = 8.3 Binding
Binding affinity for 5-HT4 receptor using [3H]GR-113808Binding affinity for 5-HT4 receptor using [3H]GR-113808
ChEMBL 812 16 4 12 4.5 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCC(C(=O)NCc2cccc(CNC(=O)C3CCN(CCOC(=O)c4cc(Cl)c(N)cc4OC)CC3)c2)CC1 10.1021/jm050234z
CHEMBL198668 72049 0 None - 1 Human 8.3 pKi = 8.3 Binding
Binding affinity for 5-HT4 receptor using [3H]GR-113808Binding affinity for 5-HT4 receptor using [3H]GR-113808
ChEMBL 812 16 4 12 4.5 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCC(C(=O)NCc2cccc(CNC(=O)C3CCN(CCOC(=O)c4cc(Cl)c(N)cc4OC)CC3)c2)CC1 10.1021/jm050234z
235 2527 36 None -4 3 Human 8.3 pKi = 8.3 Binding
Displacement of [3H]GR-113808 from human 5HT4 isoform E receptor expressed in rat C6 cells by liquid scintillation countingDisplacement of [3H]GR-113808 from human 5HT4 isoform E receptor expressed in rat C6 cells by liquid scintillation counting
ChEMBL 312 5 1 5 2.6 COc1cc(N)c(cc1C(=O)OCCN1CCCCC1)Cl 10.1021/jm801327q
5311299 2527 36 None -4 3 Human 8.3 pKi = 8.3 Binding
Displacement of [3H]GR-113808 from human 5HT4 isoform E receptor expressed in rat C6 cells by liquid scintillation countingDisplacement of [3H]GR-113808 from human 5HT4 isoform E receptor expressed in rat C6 cells by liquid scintillation counting
ChEMBL 312 5 1 5 2.6 COc1cc(N)c(cc1C(=O)OCCN1CCCCC1)Cl 10.1021/jm801327q
CHEMBL286136 2527 36 None -4 3 Human 8.3 pKi = 8.3 Binding
Displacement of [3H]GR-113808 from human 5HT4 isoform E receptor expressed in rat C6 cells by liquid scintillation countingDisplacement of [3H]GR-113808 from human 5HT4 isoform E receptor expressed in rat C6 cells by liquid scintillation counting
ChEMBL 312 5 1 5 2.6 COc1cc(N)c(cc1C(=O)OCCN1CCCCC1)Cl 10.1021/jm801327q
42618248 186445 0 None - 1 Human 8.3 pKi = 8.3 Binding
Displacement of [3H]GR-113808 from human 5HT4 isoform E receptor expressed in rat C6 cells by liquid scintillation countingDisplacement of [3H]GR-113808 from human 5HT4 isoform E receptor expressed in rat C6 cells by liquid scintillation counting
ChEMBL 479 8 2 6 3.6 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCC(NC(=O)Cc2ccccc2Cl)CC1 10.1021/jm801327q
CHEMBL490852 186445 0 None - 1 Human 8.3 pKi = 8.3 Binding
Displacement of [3H]GR-113808 from human 5HT4 isoform E receptor expressed in rat C6 cells by liquid scintillation countingDisplacement of [3H]GR-113808 from human 5HT4 isoform E receptor expressed in rat C6 cells by liquid scintillation counting
ChEMBL 479 8 2 6 3.6 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCC(NC(=O)Cc2ccccc2Cl)CC1 10.1021/jm801327q
71450247 82563 0 None 4 9 Human 8.3 pKi = 8.3 Binding
Displacement of [3H]GR113808 from human recombinant 5HT4R expressed in HEK293T cellsDisplacement of [3H]GR113808 from human recombinant 5HT4R expressed in HEK293T cells
ChEMBL 368 5 0 3 5.5 CCCN1CCC(COc2nc3c(Cl)cccc3c3ccccc23)CC1 10.1021/jm300943r
CHEMBL2181188 82563 0 None 4 9 Human 8.3 pKi = 8.3 Binding
Displacement of [3H]GR113808 from human recombinant 5HT4R expressed in HEK293T cellsDisplacement of [3H]GR113808 from human recombinant 5HT4R expressed in HEK293T cells
ChEMBL 368 5 0 3 5.5 CCCN1CCC(COc2nc3c(Cl)cccc3c3ccccc23)CC1 10.1021/jm300943r
71712329 90958 0 None - 1 Human 8.3 pKi = 8.3 Binding
Binding affinity to human recombinant 5HT4 receptorBinding affinity to human recombinant 5HT4 receptor
ChEMBL 454 7 2 5 2.3 CC(=O)N1CCN(CCN2CCC(CNC(=O)c3cccc4[nH]c(C(C)C)nc34)CC2)CC1 10.1016/j.bmcl.2013.05.018
CHEMBL2402899 90958 0 None - 1 Human 8.3 pKi = 8.3 Binding
Binding affinity to human recombinant 5HT4 receptorBinding affinity to human recombinant 5HT4 receptor
ChEMBL 454 7 2 5 2.3 CC(=O)N1CCN(CCN2CCC(CNC(=O)c3cccc4[nH]c(C(C)C)nc34)CC2)CC1 10.1016/j.bmcl.2013.05.018
44628133 84158 0 None 50 2 Human 8.3 pKi = 8.3 Binding
Displacement of [3H](1-(2-(methylsulfonamido)ethyl)piperidin-4-yl)methyl 1-methyl-1H-indole-3-carboxylate from human 5HT4R expressed in HEK293 cellsDisplacement of [3H](1-(2-(methylsulfonamido)ethyl)piperidin-4-yl)methyl 1-methyl-1H-indole-3-carboxylate from human 5HT4R expressed in HEK293 cells
ChEMBL 414 6 1 5 4.6 Cn1cc2c(OCC3CCN(CCc4ccc(N)cc4)CC3)nc3ccccc3c2c1 10.1021/jm300573d
CHEMBL2179675 84158 0 None 50 2 Human 8.3 pKi = 8.3 Binding
Displacement of [3H](1-(2-(methylsulfonamido)ethyl)piperidin-4-yl)methyl 1-methyl-1H-indole-3-carboxylate from human 5HT4R expressed in HEK293 cellsDisplacement of [3H](1-(2-(methylsulfonamido)ethyl)piperidin-4-yl)methyl 1-methyl-1H-indole-3-carboxylate from human 5HT4R expressed in HEK293 cells
ChEMBL 414 6 1 5 4.6 Cn1cc2c(OCC3CCN(CCc4ccc(N)cc4)CC3)nc3ccccc3c2c1 10.1021/jm300573d
CHEMBL2220953 84158 0 None 50 2 Human 8.3 pKi = 8.3 Binding
Displacement of [3H](1-(2-(methylsulfonamido)ethyl)piperidin-4-yl)methyl 1-methyl-1H-indole-3-carboxylate from human 5HT4R expressed in HEK293 cellsDisplacement of [3H](1-(2-(methylsulfonamido)ethyl)piperidin-4-yl)methyl 1-methyl-1H-indole-3-carboxylate from human 5HT4R expressed in HEK293 cells
ChEMBL 414 6 1 5 4.6 Cn1cc2c(OCC3CCN(CCc4ccc(N)cc4)CC3)nc3ccccc3c2c1 10.1021/jm300573d
53320666 56163 0 None - 1 Human 8.3 pKi = 8.3 Binding
Displacement of [3H]GR113808 from human 5HT4 receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [3H]GR113808 from human 5HT4 receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 447 6 2 5 3.8 O=C(O)c1ccc(CN2CCC(CNC(=O)c3c4n(c5ccccc35)CCCO4)CC2)cc1 10.1016/j.bmc.2010.10.011
CHEMBL1632176 56163 0 None - 1 Human 8.3 pKi = 8.3 Binding
Displacement of [3H]GR113808 from human 5HT4 receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [3H]GR113808 from human 5HT4 receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 447 6 2 5 3.8 O=C(O)c1ccc(CN2CCC(CNC(=O)c3c4n(c5ccccc35)CCCO4)CC2)cc1 10.1016/j.bmc.2010.10.011
44248319 193823 0 None - 1 Human 8.3 pKi = 8.3 Binding
Displacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 615 16 1 7 4.5 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CCCCCCCN(C)CCCN(C)S(C)(=O)=O)cc2ccccc21 10.1021/jm900881j
CHEMBL553404 193823 0 None - 1 Human 8.3 pKi = 8.3 Binding
Displacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 615 16 1 7 4.5 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CCCCCCCN(C)CCCN(C)S(C)(=O)=O)cc2ccccc21 10.1021/jm900881j
44248680 193909 0 None - 1 Human 8.3 pKi = 8.3 Binding
Displacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 571 10 2 7 3.0 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CCCN2CCC(CNS(C)(=O)=O)CC2)cc2ccccc21 10.1021/jm900881j
CHEMBL555223 193909 0 None - 1 Human 8.3 pKi = 8.3 Binding
Displacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 571 10 2 7 3.0 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CCCN2CCC(CNS(C)(=O)=O)CC2)cc2ccccc21 10.1021/jm900881j
44248313 91900492 194191 0 None - 1 Human 8.3 pKi = 8.3 Binding
Displacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 492 9 1 5 5.0 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CCCCCN2CCCCC2)cc2ccccc21 10.1021/jm900881j
CHEMBL558719 194191 0 None - 1 Human 8.3 pKi = 8.3 Binding
Displacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 492 9 1 5 5.0 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CCCCCN2CCCCC2)cc2ccccc21 10.1021/jm900881j
132337 3487 8 None -1 2 Guinea pig 8.3 pKi = 8.3 Binding
Displacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatumDisplacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatum
ChEMBL 323 4 2 4 2.1 COc1cc(N)c(cc1C(=O)NC[C@@H]1CCN2[C@H]1CCC2)Cl 10.1021/jm0509501
238 3487 8 None -1 2 Guinea pig 8.3 pKi = 8.3 Binding
Displacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatumDisplacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatum
ChEMBL 323 4 2 4 2.1 COc1cc(N)c(cc1C(=O)NC[C@@H]1CCN2[C@H]1CCC2)Cl 10.1021/jm0509501
CHEMBL34291 3487 8 None -1 2 Guinea pig 8.3 pKi = 8.3 Binding
Displacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatumDisplacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatum
ChEMBL 323 4 2 4 2.1 COc1cc(N)c(cc1C(=O)NC[C@@H]1CCN2[C@H]1CCC2)Cl 10.1021/jm0509501
71460941 82269 0 None - 1 Human 8.3 pKi = 8.3 Binding
Displacement of [3H]GR113808 from human 5HT4D receptor expressed in HEK293 cells after 30 mins by liquid scintillation countingDisplacement of [3H]GR113808 from human 5HT4D receptor expressed in HEK293 cells after 30 mins by liquid scintillation counting
ChEMBL 374 8 0 5 5.1 CCCCN1CCC(COc2noc3cccc(OCC(C)(C)C)c23)CC1 10.1021/jm300953p
CHEMBL2179588 82269 0 None - 1 Human 8.3 pKi = 8.3 Binding
Displacement of [3H]GR113808 from human 5HT4D receptor expressed in HEK293 cells after 30 mins by liquid scintillation countingDisplacement of [3H]GR113808 from human 5HT4D receptor expressed in HEK293 cells after 30 mins by liquid scintillation counting
ChEMBL 374 8 0 5 5.1 CCCCN1CCC(COc2noc3cccc(OCC(C)(C)C)c23)CC1 10.1021/jm300953p
258 3511 25 None -2 8 Rat 8.3 pKi = 8.3 Binding
Binding affinity against 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatumBinding affinity against 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatum
ChEMBL 300 7 1 5 2.4 CCN(CCOC(=O)c1cc(Cl)c(cc1OC)N)CC 10.1016/S0960-894X(01)80508-4
5191 3511 25 None -2 8 Rat 8.3 pKi = 8.3 Binding
Binding affinity against 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatumBinding affinity against 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatum
ChEMBL 300 7 1 5 2.4 CCN(CCOC(=O)c1cc(Cl)c(cc1OC)N)CC 10.1016/S0960-894X(01)80508-4
CHEMBL287045 3511 25 None -2 8 Rat 8.3 pKi = 8.3 Binding
Binding affinity against 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatumBinding affinity against 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatum
ChEMBL 300 7 1 5 2.4 CCN(CCOC(=O)c1cc(Cl)c(cc1OC)N)CC 10.1016/S0960-894X(01)80508-4
162663493 181420 0 None 30 4 Guinea pig 8.3 pKi = 8.3 Binding
Displacement of [3H]-GR113808 from guinea pig brain 5HT4 receptor in presence of serotonin incubated for 30 minsDisplacement of [3H]-GR113808 from guinea pig brain 5HT4 receptor in presence of serotonin incubated for 30 mins
ChEMBL 572 10 3 7 3.9 COc1cc(N)c(Cl)cc1C(=O)CCC1CCN(CCNS(=O)(=O)c2ccc(N)c(Br)c2)CC1 10.1016/j.ejmech.2016.05.048
CHEMBL4780536 181420 0 None 30 4 Guinea pig 8.3 pKi = 8.3 Binding
Displacement of [3H]-GR113808 from guinea pig brain 5HT4 receptor in presence of serotonin incubated for 30 minsDisplacement of [3H]-GR113808 from guinea pig brain 5HT4 receptor in presence of serotonin incubated for 30 mins
ChEMBL 572 10 3 7 3.9 COc1cc(N)c(Cl)cc1C(=O)CCC1CCN(CCNS(=O)(=O)c2ccc(N)c(Br)c2)CC1 10.1016/j.ejmech.2016.05.048
10447437 49796 0 None - 1 Rat 8.3 pKi = 8.3 Binding
Binding affinity towards 5-hydroxytryptamine 4 receptor was determined in rat striatal membranes using [3H]GR-113808 as radioligandBinding affinity towards 5-hydroxytryptamine 4 receptor was determined in rat striatal membranes using [3H]GR-113808 as radioligand
ChEMBL 298 5 1 5 2.2 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCCC1 10.1021/jm960320m
CHEMBL156970 49796 0 None - 1 Rat 8.3 pKi = 8.3 Binding
Binding affinity towards 5-hydroxytryptamine 4 receptor was determined in rat striatal membranes using [3H]GR-113808 as radioligandBinding affinity towards 5-hydroxytryptamine 4 receptor was determined in rat striatal membranes using [3H]GR-113808 as radioligand
ChEMBL 298 5 1 5 2.2 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCCC1 10.1021/jm960320m
44592233 188770 0 None - 1 Guinea pig 8.3 pKi = 8.3 Binding
Displacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatum membraneDisplacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatum membrane
ChEMBL 357 6 0 5 4.7 CCCCN1CCC(COc2nc3scc(C)c3n3cccc23)CC1 10.1016/j.bmc.2008.11.045
CHEMBL512679 188770 0 None - 1 Guinea pig 8.3 pKi = 8.3 Binding
Displacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatum membraneDisplacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatum membrane
ChEMBL 357 6 0 5 4.7 CCCCN1CCC(COc2nc3scc(C)c3n3cccc23)CC1 10.1016/j.bmc.2008.11.045
10498232 51091 0 None - 1 Rat 8.3 pKi = 8.3 Binding
Binding affinity towards 5-hydroxytryptamine 4 receptor was determined in rat striatal membranes using [3H]GR-113808 as radioligandBinding affinity towards 5-hydroxytryptamine 4 receptor was determined in rat striatal membranes using [3H]GR-113808 as radioligand
ChEMBL 352 5 1 5 3.2 COc1cc(N)c(Cl)cc1C(=O)OCCN1CC2CCC(CC2)C1 10.1021/jm960320m
CHEMBL158147 51091 0 None - 1 Rat 8.3 pKi = 8.3 Binding
Binding affinity towards 5-hydroxytryptamine 4 receptor was determined in rat striatal membranes using [3H]GR-113808 as radioligandBinding affinity towards 5-hydroxytryptamine 4 receptor was determined in rat striatal membranes using [3H]GR-113808 as radioligand
ChEMBL 352 5 1 5 3.2 COc1cc(N)c(Cl)cc1C(=O)OCCN1CC2CCC(CC2)C1 10.1021/jm960320m
258 3511 25 None -2 8 Rat 8.3 pKi = 8.3 Binding
Binding affinity at 5-hydroxytryptamine 4 receptor in rat striatal membranes by [3H]GR-113808 displacement.Binding affinity at 5-hydroxytryptamine 4 receptor in rat striatal membranes by [3H]GR-113808 displacement.
ChEMBL 300 7 1 5 2.4 CCN(CCOC(=O)c1cc(Cl)c(cc1OC)N)CC 10.1021/jm960853v
5191 3511 25 None -2 8 Rat 8.3 pKi = 8.3 Binding
Binding affinity at 5-hydroxytryptamine 4 receptor in rat striatal membranes by [3H]GR-113808 displacement.Binding affinity at 5-hydroxytryptamine 4 receptor in rat striatal membranes by [3H]GR-113808 displacement.
ChEMBL 300 7 1 5 2.4 CCN(CCOC(=O)c1cc(Cl)c(cc1OC)N)CC 10.1021/jm960853v
CHEMBL287045 3511 25 None -2 8 Rat 8.3 pKi = 8.3 Binding
Binding affinity at 5-hydroxytryptamine 4 receptor in rat striatal membranes by [3H]GR-113808 displacement.Binding affinity at 5-hydroxytryptamine 4 receptor in rat striatal membranes by [3H]GR-113808 displacement.
ChEMBL 300 7 1 5 2.4 CCN(CCOC(=O)c1cc(Cl)c(cc1OC)N)CC 10.1021/jm960853v
258 3511 25 None -2 8 Rat 8.3 pKi = 8.3 Binding
Binding affinity towards 5-hydroxytryptamine 4 receptor was determined in rat striatal membranes using [3H]GR-113808 as radioligandBinding affinity towards 5-hydroxytryptamine 4 receptor was determined in rat striatal membranes using [3H]GR-113808 as radioligand
ChEMBL 300 7 1 5 2.4 CCN(CCOC(=O)c1cc(Cl)c(cc1OC)N)CC 10.1021/jm960320m
5191 3511 25 None -2 8 Rat 8.3 pKi = 8.3 Binding
Binding affinity towards 5-hydroxytryptamine 4 receptor was determined in rat striatal membranes using [3H]GR-113808 as radioligandBinding affinity towards 5-hydroxytryptamine 4 receptor was determined in rat striatal membranes using [3H]GR-113808 as radioligand
ChEMBL 300 7 1 5 2.4 CCN(CCOC(=O)c1cc(Cl)c(cc1OC)N)CC 10.1021/jm960320m
CHEMBL287045 3511 25 None -2 8 Rat 8.3 pKi = 8.3 Binding
Binding affinity towards 5-hydroxytryptamine 4 receptor was determined in rat striatal membranes using [3H]GR-113808 as radioligandBinding affinity towards 5-hydroxytryptamine 4 receptor was determined in rat striatal membranes using [3H]GR-113808 as radioligand
ChEMBL 300 7 1 5 2.4 CCN(CCOC(=O)c1cc(Cl)c(cc1OC)N)CC 10.1021/jm960320m
11166796 82264 0 None -2 2 Human 8.3 pKi = 8.3 Binding
Displacement of [3H]GR113808 from human 5HT4B receptor expressed in HEK293 cells after 30 mins by liquid scintillation countingDisplacement of [3H]GR113808 from human 5HT4B receptor expressed in HEK293 cells after 30 mins by liquid scintillation counting
ChEMBL 448 5 2 7 2.3 CC(C)n1c(=O)n(C(=O)NCC2CCN(CC3(O)CCOCC3)CC2)c2cc(F)ccc21 10.1021/jm300953p
CHEMBL2179583 82264 0 None -2 2 Human 8.3 pKi = 8.3 Binding
Displacement of [3H]GR113808 from human 5HT4B receptor expressed in HEK293 cells after 30 mins by liquid scintillation countingDisplacement of [3H]GR113808 from human 5HT4B receptor expressed in HEK293 cells after 30 mins by liquid scintillation counting
ChEMBL 448 5 2 7 2.3 CC(C)n1c(=O)n(C(=O)NCC2CCN(CC3(O)CCOCC3)CC2)c2cc(F)ccc21 10.1021/jm300953p
235 2527 36 None -4 3 Human 8.3 pKi = 8.3 Binding
Binding affinity was determined against cloned 5-hydroxytryptamine 4E receptor isoform expressed in C6 glial cells incubated with 0.2 nM [3H]GR-113808Binding affinity was determined against cloned 5-hydroxytryptamine 4E receptor isoform expressed in C6 glial cells incubated with 0.2 nM [3H]GR-113808
ChEMBL 312 5 1 5 2.6 COc1cc(N)c(cc1C(=O)OCCN1CCCCC1)Cl 10.1021/jm0009538
5311299 2527 36 None -4 3 Human 8.3 pKi = 8.3 Binding
Binding affinity was determined against cloned 5-hydroxytryptamine 4E receptor isoform expressed in C6 glial cells incubated with 0.2 nM [3H]GR-113808Binding affinity was determined against cloned 5-hydroxytryptamine 4E receptor isoform expressed in C6 glial cells incubated with 0.2 nM [3H]GR-113808
ChEMBL 312 5 1 5 2.6 COc1cc(N)c(cc1C(=O)OCCN1CCCCC1)Cl 10.1021/jm0009538
CHEMBL286136 2527 36 None -4 3 Human 8.3 pKi = 8.3 Binding
Binding affinity was determined against cloned 5-hydroxytryptamine 4E receptor isoform expressed in C6 glial cells incubated with 0.2 nM [3H]GR-113808Binding affinity was determined against cloned 5-hydroxytryptamine 4E receptor isoform expressed in C6 glial cells incubated with 0.2 nM [3H]GR-113808
ChEMBL 312 5 1 5 2.6 COc1cc(N)c(cc1C(=O)OCCN1CCCCC1)Cl 10.1021/jm0009538
235 2527 36 None -4 3 Human 8.2 pKi = 8.2 Binding
Binding affinity to Rluc fused 5HT4 receptor expressed in CHO cellsBinding affinity to Rluc fused 5HT4 receptor expressed in CHO cells
ChEMBL 312 5 1 5 2.6 COc1cc(N)c(cc1C(=O)OCCN1CCCCC1)Cl 10.1021/jm070552t
5311299 2527 36 None -4 3 Human 8.2 pKi = 8.2 Binding
Binding affinity to Rluc fused 5HT4 receptor expressed in CHO cellsBinding affinity to Rluc fused 5HT4 receptor expressed in CHO cells
ChEMBL 312 5 1 5 2.6 COc1cc(N)c(cc1C(=O)OCCN1CCCCC1)Cl 10.1021/jm070552t
CHEMBL286136 2527 36 None -4 3 Human 8.2 pKi = 8.2 Binding
Binding affinity to Rluc fused 5HT4 receptor expressed in CHO cellsBinding affinity to Rluc fused 5HT4 receptor expressed in CHO cells
ChEMBL 312 5 1 5 2.6 COc1cc(N)c(cc1C(=O)OCCN1CCCCC1)Cl 10.1021/jm070552t
155543353 172729 0 None - 1 Human 8.2 pKi = 8.2 Binding
Binding affinity to recombinant human brain 5HT4 receptor by radio ligand binding assayBinding affinity to recombinant human brain 5HT4 receptor by radio ligand binding assay
ChEMBL 418 7 3 6 4.2 COc1cc(N)c(Cl)cc1C(=O)CCC1CCN(Cc2ccc(O)c(O)c2)CC1 10.1016/j.ejmech.2019.111596
CHEMBL4526049 172729 0 None - 1 Human 8.2 pKi = 8.2 Binding
Binding affinity to recombinant human brain 5HT4 receptor by radio ligand binding assayBinding affinity to recombinant human brain 5HT4 receptor by radio ligand binding assay
ChEMBL 418 7 3 6 4.2 COc1cc(N)c(Cl)cc1C(=O)CCC1CCN(Cc2ccc(O)c(O)c2)CC1 10.1016/j.ejmech.2019.111596
11643822 157317 0 None - 1 Human 7.3 pKi = 7.3 Binding
Binding affinity for 5-HT4 receptor using [3H]GR-113808Binding affinity for 5-HT4 receptor using [3H]GR-113808
ChEMBL 1158 38 6 15 8.8 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCC(NC(=O)CCCCCCCCCCN(CCCCCCCCCCC(=O)NC2CCN(CCOC(=O)c3cc(Cl)c(N)cc3OC)CC2)CC(=O)NCC2CCNCC2)CC1 10.1021/jm050234z
CHEMBL408379 157317 0 None - 1 Human 7.3 pKi = 7.3 Binding
Binding affinity for 5-HT4 receptor using [3H]GR-113808Binding affinity for 5-HT4 receptor using [3H]GR-113808
ChEMBL 1158 38 6 15 8.8 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCC(NC(=O)CCCCCCCCCCN(CCCCCCCCCCC(=O)NC2CCN(CCOC(=O)c3cc(Cl)c(N)cc3OC)CC2)CC(=O)NCC2CCNCC2)CC1 10.1021/jm050234z
162652332 179768 0 None - 1 Guinea pig 7.3 pKi = 7.3 Binding
Displacement of [3H]-GR113808 from guinea pig brain 5HT4 receptor in presence of serotonin incubated for 30 minsDisplacement of [3H]-GR113808 from guinea pig brain 5HT4 receptor in presence of serotonin incubated for 30 mins
ChEMBL 550 10 2 8 3.4 COc1cc(N)c(Cl)cc1C(=O)CCC1CCN(CCNS(=O)(=O)c2ccc3c(c2)N(C)CCO3)CC1 10.1016/j.ejmech.2016.05.048
CHEMBL4751353 179768 0 None - 1 Guinea pig 7.3 pKi = 7.3 Binding
Displacement of [3H]-GR113808 from guinea pig brain 5HT4 receptor in presence of serotonin incubated for 30 minsDisplacement of [3H]-GR113808 from guinea pig brain 5HT4 receptor in presence of serotonin incubated for 30 mins
ChEMBL 550 10 2 8 3.4 COc1cc(N)c(Cl)cc1C(=O)CCC1CCN(CCNS(=O)(=O)c2ccc3c(c2)N(C)CCO3)CC1 10.1016/j.ejmech.2016.05.048
49783414 17495 0 None - 1 Human 7.3 pKi = 7.3 Binding
Displacement of [3H]GR113808 from human recombinant 5HT4 receptor expressed in HEK293 cellsDisplacement of [3H]GR113808 from human recombinant 5HT4 receptor expressed in HEK293 cells
ChEMBL 320 7 1 5 2.9 CCCCN1CCC(COC(=O)c2ccc(N)cc2OC)CC1 10.1021/jm100668r
CHEMBL1258451 17495 0 None - 1 Human 7.3 pKi = 7.3 Binding
Displacement of [3H]GR113808 from human recombinant 5HT4 receptor expressed in HEK293 cellsDisplacement of [3H]GR113808 from human recombinant 5HT4 receptor expressed in HEK293 cells
ChEMBL 320 7 1 5 2.9 CCCCN1CCC(COC(=O)c2ccc(N)cc2OC)CC1 10.1021/jm100668r
70691118 77148 0 None - 1 Human 7.3 pKi = 7.3 Binding
Displacement of [3H]GR113808 from human recombinant 5HT4c receptor expressed in HEK293 cellsDisplacement of [3H]GR113808 from human recombinant 5HT4c receptor expressed in HEK293 cells
ChEMBL 469 7 3 6 1.7 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CC(O)CN(C)C(N)=O)cc2ccccc21 10.1016/j.bmcl.2012.08.051
CHEMBL2087327 77148 0 None - 1 Human 7.3 pKi = 7.3 Binding
Displacement of [3H]GR113808 from human recombinant 5HT4c receptor expressed in HEK293 cellsDisplacement of [3H]GR113808 from human recombinant 5HT4c receptor expressed in HEK293 cells
ChEMBL 469 7 3 6 1.7 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CC(O)CN(C)C(N)=O)cc2ccccc21 10.1016/j.bmcl.2012.08.051
70686943 77152 0 None - 1 Human 7.3 pKi = 7.3 Binding
Displacement of [3H]GR113808 from human recombinant 5HT4c receptor expressed in HEK293 cellsDisplacement of [3H]GR113808 from human recombinant 5HT4c receptor expressed in HEK293 cells
ChEMBL 497 7 2 6 2.3 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CC(O)CN(C)C(=O)N(C)C)cc2ccccc21 10.1016/j.bmcl.2012.08.051
CHEMBL2087331 77152 0 None - 1 Human 7.3 pKi = 7.3 Binding
Displacement of [3H]GR113808 from human recombinant 5HT4c receptor expressed in HEK293 cellsDisplacement of [3H]GR113808 from human recombinant 5HT4c receptor expressed in HEK293 cells
ChEMBL 497 7 2 6 2.3 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CC(O)CN(C)C(=O)N(C)C)cc2ccccc21 10.1016/j.bmcl.2012.08.051
70684789 77153 0 None - 1 Human 7.3 pKi = 7.3 Binding
Displacement of [3H]GR113808 from human recombinant 5HT4c receptor expressed in HEK293 cellsDisplacement of [3H]GR113808 from human recombinant 5HT4c receptor expressed in HEK293 cells
ChEMBL 470 7 3 7 2.0 COC(=O)NCC(O)CN1[C@H]2CC[C@@H]1C[C@H](NC(=O)c1cc3ccccc3n(C(C)C)c1=O)C2 10.1016/j.bmcl.2012.08.051
CHEMBL2087332 77153 0 None - 1 Human 7.3 pKi = 7.3 Binding
Displacement of [3H]GR113808 from human recombinant 5HT4c receptor expressed in HEK293 cellsDisplacement of [3H]GR113808 from human recombinant 5HT4c receptor expressed in HEK293 cells
ChEMBL 470 7 3 7 2.0 COC(=O)NCC(O)CN1[C@H]2CC[C@@H]1C[C@H](NC(=O)c1cc3ccccc3n(C(C)C)c1=O)C2 10.1016/j.bmcl.2012.08.051
70695323 77157 0 None - 1 Human 7.3 pKi = 7.3 Binding
Displacement of [3H]GR113808 from human recombinant 5HT4c receptor expressed in HEK293 cellsDisplacement of [3H]GR113808 from human recombinant 5HT4c receptor expressed in HEK293 cells
ChEMBL 504 8 2 7 1.6 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3C[C@H](O)CN(C)S(C)(=O)=O)cc2ccccc21 10.1016/j.bmcl.2012.08.051
CHEMBL2087336 77157 0 None - 1 Human 7.3 pKi = 7.3 Binding
Displacement of [3H]GR113808 from human recombinant 5HT4c receptor expressed in HEK293 cellsDisplacement of [3H]GR113808 from human recombinant 5HT4c receptor expressed in HEK293 cells
ChEMBL 504 8 2 7 1.6 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3C[C@H](O)CN(C)S(C)(=O)=O)cc2ccccc21 10.1016/j.bmcl.2012.08.051
44248923 193267 0 None - 1 Human 7.3 pKi = 7.3 Binding
Displacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 559 8 2 8 1.2 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3C[C@H](O)CN2CCN(S(C)(=O)=O)CC2)cc2ccccc21 10.1021/jm900881j
CHEMBL541968 193267 0 None - 1 Human 7.3 pKi = 7.3 Binding
Displacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 559 8 2 8 1.2 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3C[C@H](O)CN2CCN(S(C)(=O)=O)CC2)cc2ccccc21 10.1021/jm900881j
44248080 91900498 194203 0 None - 1 Human 7.3 pKi = 7.3 Binding
Displacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 493 8 2 6 2.6 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CCCN2CCC[C@@H]2C(N)=O)cc2ccccc21 10.1021/jm900881j
CHEMBL558855 194203 0 None - 1 Human 7.3 pKi = 7.3 Binding
Displacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 493 8 2 6 2.6 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CCCN2CCC[C@@H]2C(N)=O)cc2ccccc21 10.1021/jm900881j
44249057 91900485 194425 0 None - 1 Human 7.3 pKi = 7.3 Binding
Displacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 467 11 2 5 4.6 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CCCCCCCCO)cc2ccccc21 10.1021/jm900881j
CHEMBL560876 194425 0 None - 1 Human 7.3 pKi = 7.3 Binding
Displacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 467 11 2 5 4.6 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CCCCCCCCO)cc2ccccc21 10.1021/jm900881j
5 139 66 None -288 54 Human 6.3 pKi = 6.3 Binding
Displacement of [N-methyl-3H]GR-113808 from human 5HT4 receptor expressed in HEK293 cellsDisplacement of [N-methyl-3H]GR-113808 from human 5HT4 receptor expressed in HEK293 cells
ChEMBL 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 10.1021/np0601760
5202 139 66 None -288 54 Human 6.3 pKi = 6.3 Binding
Displacement of [N-methyl-3H]GR-113808 from human 5HT4 receptor expressed in HEK293 cellsDisplacement of [N-methyl-3H]GR-113808 from human 5HT4 receptor expressed in HEK293 cells
ChEMBL 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 10.1021/np0601760
CHEMBL39 139 66 None -288 54 Human 6.3 pKi = 6.3 Binding
Displacement of [N-methyl-3H]GR-113808 from human 5HT4 receptor expressed in HEK293 cellsDisplacement of [N-methyl-3H]GR-113808 from human 5HT4 receptor expressed in HEK293 cells
ChEMBL 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 10.1021/np0601760
DB08839 139 66 None -288 54 Human 6.3 pKi = 6.3 Binding
Displacement of [N-methyl-3H]GR-113808 from human 5HT4 receptor expressed in HEK293 cellsDisplacement of [N-methyl-3H]GR-113808 from human 5HT4 receptor expressed in HEK293 cells
ChEMBL 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 10.1021/np0601760
118712567 113730 0 None - 1 Human 6.3 pKi = 6.3 Binding
Displacement of [3H]GR113808 from human 5HT4b receptor expressed in HEK293 cell membranesDisplacement of [3H]GR113808 from human 5HT4b receptor expressed in HEK293 cell membranes
ChEMBL 508 8 3 4 4.9 O=C(NCC1CCN(Cc2ccc(NS(=O)(=O)C3CCCCC3)cc2)CC1)c1c[nH]c2ccccc12 10.1016/j.bmcl.2014.06.083
CHEMBL3329801 113730 0 None - 1 Human 6.3 pKi = 6.3 Binding
Displacement of [3H]GR113808 from human 5HT4b receptor expressed in HEK293 cell membranesDisplacement of [3H]GR113808 from human 5HT4b receptor expressed in HEK293 cell membranes
ChEMBL 508 8 3 4 4.9 O=C(NCC1CCN(Cc2ccc(NS(=O)(=O)C3CCCCC3)cc2)CC1)c1c[nH]c2ccccc12 10.1016/j.bmcl.2014.06.083
189 3436 31 None -2089 17 Rat 5.3 pKi = 5.3 Binding
Binding affinity against rat 5-hydroxytryptamine 4 receptorBinding affinity against rat 5-hydroxytryptamine 4 receptor
ChEMBL 292 1 1 3 3.2 O=C(N1CCc2c1cc1ccn(c1c2)C)Nc1cccnc1 10.1021/jm00014a004
5163 3436 31 None -2089 17 Rat 5.3 pKi = 5.3 Binding
Binding affinity against rat 5-hydroxytryptamine 4 receptorBinding affinity against rat 5-hydroxytryptamine 4 receptor
ChEMBL 292 1 1 3 3.2 O=C(N1CCc2c1cc1ccn(c1c2)C)Nc1cccnc1 10.1021/jm00014a004
CHEMBL297784 3436 31 None -2089 17 Rat 5.3 pKi = 5.3 Binding
Binding affinity against rat 5-hydroxytryptamine 4 receptorBinding affinity against rat 5-hydroxytryptamine 4 receptor
ChEMBL 292 1 1 3 3.2 O=C(N1CCc2c1cc1ccn(c1c2)C)Nc1cccnc1 10.1021/jm00014a004
9913554 100523 0 None -6309 14 Human 5.3 pKi = 5.3 Binding
The compound was tested for the binding affinity towards human cloned 5-hydroxytryptamine 4 receptor in HeLa cells, using [3H]LSD as radioligandThe compound was tested for the binding affinity towards human cloned 5-hydroxytryptamine 4 receptor in HeLa cells, using [3H]LSD as radioligand
ChEMBL 491 5 1 6 5.0 COc1ccc(NS(=O)(=O)c2sc3ccc(Cl)cc3c2C)cc1N1CCN2CCC[C@H]2C1 10.1016/s0960-894x(02)00172-5
CHEMBL29433 100523 0 None -6309 14 Human 5.3 pKi = 5.3 Binding
The compound was tested for the binding affinity towards human cloned 5-hydroxytryptamine 4 receptor in HeLa cells, using [3H]LSD as radioligandThe compound was tested for the binding affinity towards human cloned 5-hydroxytryptamine 4 receptor in HeLa cells, using [3H]LSD as radioligand
ChEMBL 491 5 1 6 5.0 COc1ccc(NS(=O)(=O)c2sc3ccc(Cl)cc3c2C)cc1N1CCN2CCC[C@H]2C1 10.1016/s0960-894x(02)00172-5
9928343 102995 0 None - 1 Rat 7.3 pKi = 7.3 Binding
Binding affinity for 5-hydroxytryptamine 4 receptor in rat was determined by rat tunica muscularis mucosae assayBinding affinity for 5-hydroxytryptamine 4 receptor in rat was determined by rat tunica muscularis mucosae assay
ChEMBL 349 4 2 4 2.2 COc1cc(N)c(Cl)cc1C(=O)NCC1C2CC3CC1CN(C3)C2 10.1016/j.bmcl.2004.09.005
CHEMBL3085015 102995 0 None - 1 Rat 7.3 pKi = 7.3 Binding
Binding affinity for 5-hydroxytryptamine 4 receptor in rat was determined by rat tunica muscularis mucosae assayBinding affinity for 5-hydroxytryptamine 4 receptor in rat was determined by rat tunica muscularis mucosae assay
ChEMBL 349 4 2 4 2.2 COc1cc(N)c(Cl)cc1C(=O)NCC1C2CC3CC1CN(C3)C2 10.1016/j.bmcl.2004.09.005
155523661 170337 0 None - 1 Human 7.3 pKi = 7.3 Binding
Displacement of [3H]-GR113808 from recombinant human 5-HT4BR expressed in membranes after 60 minsDisplacement of [3H]-GR113808 from recombinant human 5-HT4BR expressed in membranes after 60 mins
ChEMBL 382 7 1 3 5.4 COc1c(C(=O)CCC2CCN(CC3CCCCC3)CC2)ccc2[nH]ccc12 10.1016/j.ejmech.2018.10.064
CHEMBL4454706 170337 0 None - 1 Human 7.3 pKi = 7.3 Binding
Displacement of [3H]-GR113808 from recombinant human 5-HT4BR expressed in membranes after 60 minsDisplacement of [3H]-GR113808 from recombinant human 5-HT4BR expressed in membranes after 60 mins
ChEMBL 382 7 1 3 5.4 COc1c(C(=O)CCC2CCN(CC3CCCCC3)CC2)ccc2[nH]ccc12 10.1016/j.ejmech.2018.10.064
71453895 82077 0 None - 1 Guinea pig 7.3 pKi = 7.3 Binding
Displacement of [3H]GR113808 from 5HT4R in guinea pig striatal membranesDisplacement of [3H]GR113808 from 5HT4R in guinea pig striatal membranes
ChEMBL 334 5 0 3 4.9 CCCN1CCC(COc2nc3ccccc3c3ccccc23)CC1 10.1016/j.bmc.2013.08.061
71453895 82077 0 None - 1 Guinea pig 7.3 pKi = 7.3 Binding
Displacement of [3H]GR113808 from 5HT4R in guinea pig striatal membranesDisplacement of [3H]GR113808 from 5HT4R in guinea pig striatal membranes
ChEMBL 334 5 0 3 4.9 CCCN1CCC(COc2nc3ccccc3c3ccccc23)CC1 10.1021/jm300943r
CHEMBL2177145 82077 0 None - 1 Guinea pig 7.3 pKi = 7.3 Binding
Displacement of [3H]GR113808 from 5HT4R in guinea pig striatal membranesDisplacement of [3H]GR113808 from 5HT4R in guinea pig striatal membranes
ChEMBL 334 5 0 3 4.9 CCCN1CCC(COc2nc3ccccc3c3ccccc23)CC1 10.1016/j.bmc.2013.08.061
CHEMBL2177145 82077 0 None - 1 Guinea pig 7.3 pKi = 7.3 Binding
Displacement of [3H]GR113808 from 5HT4R in guinea pig striatal membranesDisplacement of [3H]GR113808 from 5HT4R in guinea pig striatal membranes
ChEMBL 334 5 0 3 4.9 CCCN1CCC(COc2nc3ccccc3c3ccccc23)CC1 10.1021/jm300943r
135453290 133083 23 None -169 8 Human 6.3 pKi = 6.3 Binding
Inhibitory activity against 5HT4 receptorInhibitory activity against 5HT4 receptor
ChEMBL 191 2 2 4 1.1 C[C@H](N)Cn1ncc2ccc(O)cc21 10.1021/jm050663x
CHEMBL371300 133083 23 None -169 8 Human 6.3 pKi = 6.3 Binding
Inhibitory activity against 5HT4 receptorInhibitory activity against 5HT4 receptor
ChEMBL 191 2 2 4 1.1 C[C@H](N)Cn1ncc2ccc(O)cc21 10.1021/jm050663x
90644470 111786 0 None - 1 Guinea pig 7.3 pKi = 7.3 Binding
Displacement of [3H]GR113808 from Dunkin-Hartley guinea pig brain striatum 5HT4R after 30 minsDisplacement of [3H]GR113808 from Dunkin-Hartley guinea pig brain striatum 5HT4R after 30 mins
ChEMBL 328 6 0 5 3.3 COc1cc(C(=O)OCCCN2CCCCC2)c2ccccc2n1 10.1016/j.ejmech.2014.05.015
CHEMBL3291075 111786 0 None - 1 Guinea pig 7.3 pKi = 7.3 Binding
Displacement of [3H]GR113808 from Dunkin-Hartley guinea pig brain striatum 5HT4R after 30 minsDisplacement of [3H]GR113808 from Dunkin-Hartley guinea pig brain striatum 5HT4R after 30 mins
ChEMBL 328 6 0 5 3.3 COc1cc(C(=O)OCCCN2CCCCC2)c2ccccc2n1 10.1016/j.ejmech.2014.05.015
44592041 178450 0 None - 1 Guinea pig 7.3 pKi = 7.3 Binding
Displacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatum membraneDisplacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatum membrane
ChEMBL 315 5 0 5 3.8 c1cc2c(OCCCN3CCCCC3)nc3ccsc3n2c1 10.1016/j.bmc.2008.11.045
CHEMBL471234 178450 0 None - 1 Guinea pig 7.3 pKi = 7.3 Binding
Displacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatum membraneDisplacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatum membrane
ChEMBL 315 5 0 5 3.8 c1cc2c(OCCCN3CCCCC3)nc3ccsc3n2c1 10.1016/j.bmc.2008.11.045
44592284 178449 0 None - 1 Guinea pig 7.3 pKi = 7.3 Binding
Displacement of [3H]-GR113808 from guinea pig 5HT4 receptor by Grossman's methodDisplacement of [3H]-GR113808 from guinea pig 5HT4 receptor by Grossman's method
ChEMBL 377 5 0 5 4.8 c1ccc(CN2CCC(COc3nc4ccsc4n4cccc34)CC2)cc1 10.1039/C2MD20063E
CHEMBL471231 178449 0 None - 1 Guinea pig 7.3 pKi = 7.3 Binding
Displacement of [3H]-GR113808 from guinea pig 5HT4 receptor by Grossman's methodDisplacement of [3H]-GR113808 from guinea pig 5HT4 receptor by Grossman's method
ChEMBL 377 5 0 5 4.8 c1ccc(CN2CCC(COc3nc4ccsc4n4cccc34)CC2)cc1 10.1039/C2MD20063E
90666004 108800 0 None - 1 Guinea pig 7.3 pKi = 7.3 Binding
Displacement of [3H]-GR113808 from guinea pig 5HT4 receptor by Grossman's methodDisplacement of [3H]-GR113808 from guinea pig 5HT4 receptor by Grossman's method
ChEMBL 341 5 0 5 4.1 c1cc2c(OCC3CCN(CC4CC4)CC3)nc3ccsc3n2c1 10.1039/C2MD20063E
CHEMBL3218876 108800 0 None - 1 Guinea pig 7.3 pKi = 7.3 Binding
Displacement of [3H]-GR113808 from guinea pig 5HT4 receptor by Grossman's methodDisplacement of [3H]-GR113808 from guinea pig 5HT4 receptor by Grossman's method
ChEMBL 341 5 0 5 4.1 c1cc2c(OCC3CCN(CC4CC4)CC3)nc3ccsc3n2c1 10.1039/C2MD20063E
15544720 66832 0 None - 1 Rat 7.3 pKi = 7.3 Binding
pKi against 5-hydroxytryptamine 4 receptor in rat striatum membranepKi against 5-hydroxytryptamine 4 receptor in rat striatum membrane
ChEMBL 292 2 2 3 2.0 CN1CCC(NC(=O)c2cc(Cl)cc3[nH]cnc23)CC1 10.1016/s0960-894x(01)00517-0
CHEMBL18769 66832 0 None - 1 Rat 7.3 pKi = 7.3 Binding
pKi against 5-hydroxytryptamine 4 receptor in rat striatum membranepKi against 5-hydroxytryptamine 4 receptor in rat striatum membrane
ChEMBL 292 2 2 3 2.0 CN1CCC(NC(=O)c2cc(Cl)cc3[nH]cnc23)CC1 10.1016/s0960-894x(01)00517-0
136118640 75965 0 None -4 3 Human 5.3 pKi = 5.3 Binding
Displacement of [3H]GR113808 from human recombinant 5HT4 receptorDisplacement of [3H]GR113808 from human recombinant 5HT4 receptor
ChEMBL 335 1 2 3 3.1 CSC1=NC(=O)/C(=C/c2c[nH]c3cc(Br)ccc23)N1 10.1016/j.bmc.2013.09.011
CHEMBL2058700 75965 0 None -4 3 Human 5.3 pKi = 5.3 Binding
Displacement of [3H]GR113808 from human recombinant 5HT4 receptorDisplacement of [3H]GR113808 from human recombinant 5HT4 receptor
ChEMBL 335 1 2 3 3.1 CSC1=NC(=O)/C(=C/c2c[nH]c3cc(Br)ccc23)N1 10.1016/j.bmc.2013.09.011
15544720 66832 0 None - 1 Rat 7.3 pKi = 7.3 Binding
Binding affinity to 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatum membraneBinding affinity to 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatum membrane
ChEMBL 292 2 2 3 2.0 CN1CCC(NC(=O)c2cc(Cl)cc3[nH]cnc23)CC1 10.1021/jm020807x
CHEMBL18769 66832 0 None - 1 Rat 7.3 pKi = 7.3 Binding
Binding affinity to 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatum membraneBinding affinity to 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatum membrane
ChEMBL 292 2 2 3 2.0 CN1CCC(NC(=O)c2cc(Cl)cc3[nH]cnc23)CC1 10.1021/jm020807x
260 3808 49 None -45 6 Guinea pig 7.3 pKi = 7.3 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
ChEMBL 284 2 1 3 3.0 CN1[C@@H]2CC[C@H]1C[C@H](C2)OC(=O)c1c[nH]c2c1cccc2 nan
2775 3808 49 None -45 6 Guinea pig 7.3 pKi = 7.3 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
ChEMBL 284 2 1 3 3.0 CN1[C@@H]2CC[C@H]1C[C@H](C2)OC(=O)c1c[nH]c2c1cccc2 nan
656665 3808 49 None -45 6 Guinea pig 7.3 pKi = 7.3 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
ChEMBL 284 2 1 3 3.0 CN1[C@@H]2CC[C@H]1C[C@H](C2)OC(=O)c1c[nH]c2c1cccc2 nan
CHEMBL56564 3808 49 None -45 6 Guinea pig 7.3 pKi = 7.3 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
ChEMBL 284 2 1 3 3.0 CN1[C@@H]2CC[C@H]1C[C@H](C2)OC(=O)c1c[nH]c2c1cccc2 nan
DB11699 3808 49 None -45 6 Guinea pig 7.3 pKi = 7.3 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
ChEMBL 284 2 1 3 3.0 CN1[C@@H]2CC[C@H]1C[C@H](C2)OC(=O)c1c[nH]c2c1cccc2 nan
15544720 66832 0 None - 1 Rat 7.3 pKi = 7.3 Binding
Displacement of [3H]GR-113808 from rat striatum 5-hydroxytryptamine 4 receptorDisplacement of [3H]GR-113808 from rat striatum 5-hydroxytryptamine 4 receptor
ChEMBL 292 2 2 3 2.0 CN1CCC(NC(=O)c2cc(Cl)cc3[nH]cnc23)CC1 10.1016/0960-894X(96)00200-4
CHEMBL18769 66832 0 None - 1 Rat 7.3 pKi = 7.3 Binding
Displacement of [3H]GR-113808 from rat striatum 5-hydroxytryptamine 4 receptorDisplacement of [3H]GR-113808 from rat striatum 5-hydroxytryptamine 4 receptor
ChEMBL 292 2 2 3 2.0 CN1CCC(NC(=O)c2cc(Cl)cc3[nH]cnc23)CC1 10.1016/0960-894X(96)00200-4
15544720 66832 0 None - 1 Rat 7.3 pKi = 7.3 Binding
In vitro binding affinity to 5-hydroxytryptamine 4 receptor in rat striatum membraneIn vitro binding affinity to 5-hydroxytryptamine 4 receptor in rat striatum membrane
ChEMBL 292 2 2 3 2.0 CN1CCC(NC(=O)c2cc(Cl)cc3[nH]cnc23)CC1 10.1016/s0960-894x(01)00517-0
CHEMBL18769 66832 0 None - 1 Rat 7.3 pKi = 7.3 Binding
In vitro binding affinity to 5-hydroxytryptamine 4 receptor in rat striatum membraneIn vitro binding affinity to 5-hydroxytryptamine 4 receptor in rat striatum membrane
ChEMBL 292 2 2 3 2.0 CN1CCC(NC(=O)c2cc(Cl)cc3[nH]cnc23)CC1 10.1016/s0960-894x(01)00517-0
1782 2482 81 None -12 22 Guinea pig 6.3 pKi = 6.3 Binding
Inhibition of [3H]GR-113808 binding to guinea pig striatum 5-hydroxytryptamine 4 receptorInhibition of [3H]GR-113808 binding to guinea pig striatum 5-hydroxytryptamine 4 receptor
ChEMBL 299 7 2 4 2.0 CCN(CCNC(=O)c1cc(Cl)c(cc1OC)N)CC 10.1021/jm020270n
241 2482 81 None -12 22 Guinea pig 6.3 pKi = 6.3 Binding
Inhibition of [3H]GR-113808 binding to guinea pig striatum 5-hydroxytryptamine 4 receptorInhibition of [3H]GR-113808 binding to guinea pig striatum 5-hydroxytryptamine 4 receptor
ChEMBL 299 7 2 4 2.0 CCN(CCNC(=O)c1cc(Cl)c(cc1OC)N)CC 10.1021/jm020270n
4168 2482 81 None -12 22 Guinea pig 6.3 pKi = 6.3 Binding
Inhibition of [3H]GR-113808 binding to guinea pig striatum 5-hydroxytryptamine 4 receptorInhibition of [3H]GR-113808 binding to guinea pig striatum 5-hydroxytryptamine 4 receptor
ChEMBL 299 7 2 4 2.0 CCN(CCNC(=O)c1cc(Cl)c(cc1OC)N)CC 10.1021/jm020270n
CHEMBL86 2482 81 None -12 22 Guinea pig 6.3 pKi = 6.3 Binding
Inhibition of [3H]GR-113808 binding to guinea pig striatum 5-hydroxytryptamine 4 receptorInhibition of [3H]GR-113808 binding to guinea pig striatum 5-hydroxytryptamine 4 receptor
ChEMBL 299 7 2 4 2.0 CCN(CCNC(=O)c1cc(Cl)c(cc1OC)N)CC 10.1021/jm020270n
DB01233 2482 81 None -12 22 Guinea pig 6.3 pKi = 6.3 Binding
Inhibition of [3H]GR-113808 binding to guinea pig striatum 5-hydroxytryptamine 4 receptorInhibition of [3H]GR-113808 binding to guinea pig striatum 5-hydroxytryptamine 4 receptor
ChEMBL 299 7 2 4 2.0 CCN(CCNC(=O)c1cc(Cl)c(cc1OC)N)CC 10.1021/jm020270n
10408029 16283 0 None - 1 Human 7.3 pKi = 7.3 Binding
Binding affinity was determined against cloned 5-hydroxytryptamine 4B receptor isoform expressed in COS-7 cellsBinding affinity was determined against cloned 5-hydroxytryptamine 4B receptor isoform expressed in COS-7 cells
ChEMBL 389 6 1 6 2.9 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCN(c2ccccc2)CC1 10.1021/jm0009538
CHEMBL123377 16283 0 None - 1 Human 7.3 pKi = 7.3 Binding
Binding affinity was determined against cloned 5-hydroxytryptamine 4B receptor isoform expressed in COS-7 cellsBinding affinity was determined against cloned 5-hydroxytryptamine 4B receptor isoform expressed in COS-7 cells
ChEMBL 389 6 1 6 2.9 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCN(c2ccccc2)CC1 10.1021/jm0009538
10744356 11268 0 None - 1 Guinea pig 7.3 pKi = 7.3 Binding
Binding affinity against 5-hydroxytryptamine 4 receptor in guinea pig striatum using [3H]GR-113808 as radioligandBinding affinity against 5-hydroxytryptamine 4 receptor in guinea pig striatum using [3H]GR-113808 as radioligand
ChEMBL 386 6 1 5 1.9 C=CC[N+]1(C)CCN(CCNC(=O)n2c(=O)n(C(C)C)c3ccccc32)CC1 10.1021/jm981098j
CHEMBL1179774 11268 0 None - 1 Guinea pig 7.3 pKi = 7.3 Binding
Binding affinity against 5-hydroxytryptamine 4 receptor in guinea pig striatum using [3H]GR-113808 as radioligandBinding affinity against 5-hydroxytryptamine 4 receptor in guinea pig striatum using [3H]GR-113808 as radioligand
ChEMBL 386 6 1 5 1.9 C=CC[N+]1(C)CCN(CCNC(=O)n2c(=O)n(C(C)C)c3ccccc32)CC1 10.1021/jm981098j
CHEMBL99299 11268 0 None - 1 Guinea pig 7.3 pKi = 7.3 Binding
Binding affinity against 5-hydroxytryptamine 4 receptor in guinea pig striatum using [3H]GR-113808 as radioligandBinding affinity against 5-hydroxytryptamine 4 receptor in guinea pig striatum using [3H]GR-113808 as radioligand
ChEMBL 386 6 1 5 1.9 C=CC[N+]1(C)CCN(CCNC(=O)n2c(=O)n(C(C)C)c3ccccc32)CC1 10.1021/jm981098j
90644474 111789 0 None - 1 Guinea pig 6.3 pKi = 6.3 Binding
Displacement of [3H]GR113808 from Dunkin-Hartley guinea pig brain striatum 5HT4R after 30 minsDisplacement of [3H]GR113808 from Dunkin-Hartley guinea pig brain striatum 5HT4R after 30 mins
ChEMBL 343 4 0 3 3.7 O=C1c2cc(Cl)nc3cccc(c23)CN1CCCN1CCCCC1 10.1016/j.ejmech.2014.05.015
CHEMBL3291079 111789 0 None - 1 Guinea pig 6.3 pKi = 6.3 Binding
Displacement of [3H]GR113808 from Dunkin-Hartley guinea pig brain striatum 5HT4R after 30 minsDisplacement of [3H]GR113808 from Dunkin-Hartley guinea pig brain striatum 5HT4R after 30 mins
ChEMBL 343 4 0 3 3.7 O=C1c2cc(Cl)nc3cccc(c23)CN1CCCN1CCCCC1 10.1016/j.ejmech.2014.05.015
44288600 100648 0 None - 1 Rat 7.2 pKi = 7.2 Binding
Binding affinity for 5-hydroxytryptamine 4 receptor in rat was determined by rat tunica muscularis mucosae assayBinding affinity for 5-hydroxytryptamine 4 receptor in rat was determined by rat tunica muscularis mucosae assay
ChEMBL 335 3 2 4 2.0 COc1cc(N)c(Cl)cc1C(=O)NC1C2CC3CC1CN(C3)C2 10.1016/j.bmcl.2004.09.005
CHEMBL295155 100648 0 None - 1 Rat 7.2 pKi = 7.2 Binding
Binding affinity for 5-hydroxytryptamine 4 receptor in rat was determined by rat tunica muscularis mucosae assayBinding affinity for 5-hydroxytryptamine 4 receptor in rat was determined by rat tunica muscularis mucosae assay
ChEMBL 335 3 2 4 2.0 COc1cc(N)c(Cl)cc1C(=O)NC1C2CC3CC1CN(C3)C2 10.1016/j.bmcl.2004.09.005
44592077 188723 0 None - 1 Guinea pig 7.2 pKi = 7.2 Binding
Displacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatum membraneDisplacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatum membrane
ChEMBL 329 6 0 5 4.2 c1cc2c(OCCCCN3CCCCC3)nc3ccsc3n2c1 10.1016/j.bmc.2008.11.045
CHEMBL512303 188723 0 None - 1 Guinea pig 7.2 pKi = 7.2 Binding
Displacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatum membraneDisplacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatum membrane
ChEMBL 329 6 0 5 4.2 c1cc2c(OCCCCN3CCCCC3)nc3ccsc3n2c1 10.1016/j.bmc.2008.11.045
56850385 71133 0 None -72 3 Rat 6.2 pKi = 6.2 Binding
Displacement of [3H]GR113808 from 5HT4 receptor in Sprague-Dawley albinus rat striatal membranes after 30 mins by scintillation countingDisplacement of [3H]GR113808 from 5HT4 receptor in Sprague-Dawley albinus rat striatal membranes after 30 mins by scintillation counting
ChEMBL 351 7 1 3 3.1 O=C1C2CCCN2C(=O)N1CCCCNCc1ccc2ccccc2c1 10.1021/jm2007886
CHEMBL1926730 71133 0 None -72 3 Rat 6.2 pKi = 6.2 Binding
Displacement of [3H]GR113808 from 5HT4 receptor in Sprague-Dawley albinus rat striatal membranes after 30 mins by scintillation countingDisplacement of [3H]GR113808 from 5HT4 receptor in Sprague-Dawley albinus rat striatal membranes after 30 mins by scintillation counting
ChEMBL 351 7 1 3 3.1 O=C1C2CCCN2C(=O)N1CCCCNCc1ccc2ccccc2c1 10.1021/jm2007886
CHEMBL1962454 71133 0 None -72 3 Rat 6.2 pKi = 6.2 Binding
Displacement of [3H]GR113808 from 5HT4 receptor in Sprague-Dawley albinus rat striatal membranes after 30 mins by scintillation countingDisplacement of [3H]GR113808 from 5HT4 receptor in Sprague-Dawley albinus rat striatal membranes after 30 mins by scintillation counting
ChEMBL 351 7 1 3 3.1 O=C1C2CCCN2C(=O)N1CCCCNCc1ccc2ccccc2c1 10.1021/jm2007886
3277217 178155 5 None -6 2 Guinea pig 5.2 pKi = 5.2 Binding
Displacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatumDisplacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatum
ChEMBL 271 3 1 4 1.4 O=C(O)CN1CCN(c2ccc3ccccc3n2)CC1 10.1021/jm900018b
715494 178155 5 None -6 2 Guinea pig 5.2 pKi = 5.2 Binding
Displacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatumDisplacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatum
ChEMBL 271 3 1 4 1.4 O=C(O)CN1CCN(c2ccc3ccccc3n2)CC1 10.1021/jm900018b
CHEMBL468498 178155 5 None -6 2 Guinea pig 5.2 pKi = 5.2 Binding
Displacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatumDisplacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatum
ChEMBL 271 3 1 4 1.4 O=C(O)CN1CCN(c2ccc3ccccc3n2)CC1 10.1021/jm900018b
11174673 173059 0 None - 1 Human 7.2 pKi = 7.2 Binding
Agonist activity at 5-HT4 receptor (unknown origin)Agonist activity at 5-HT4 receptor (unknown origin)
ChEMBL 321 3 3 5 1.6 Cc1cn2c(N)c(Cl)cc(C(=O)NCC3CCNCC3)c2n1 10.1016/j.ejmech.2019.111569
CHEMBL4533922 173059 0 None - 1 Human 7.2 pKi = 7.2 Binding
Agonist activity at 5-HT4 receptor (unknown origin)Agonist activity at 5-HT4 receptor (unknown origin)
ChEMBL 321 3 3 5 1.6 Cc1cn2c(N)c(Cl)cc(C(=O)NCC3CCNCC3)c2n1 10.1016/j.ejmech.2019.111569
44592107 178507 0 None - 1 Guinea pig 7.2 pKi = 7.2 Binding
Displacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatum membraneDisplacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatum membrane
ChEMBL 301 3 0 5 3.3 CN1CCC(COc2nc3ccsc3n3cccc23)CC1 10.1016/j.bmc.2008.11.045
CHEMBL471661 178507 0 None - 1 Guinea pig 7.2 pKi = 7.2 Binding
Displacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatum membraneDisplacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatum membrane
ChEMBL 301 3 0 5 3.3 CN1CCC(COc2nc3ccsc3n3cccc23)CC1 10.1016/j.bmc.2008.11.045
11135810 204778 0 None - 1 Human 7.2 pKi = 7.2 Binding
Binding affinity towards cloned human 5-hydroxytryptamine 4E receptor expressed in C6 glial cells using [3H]GR-113808 as radioligandBinding affinity towards cloned human 5-hydroxytryptamine 4E receptor expressed in C6 glial cells using [3H]GR-113808 as radioligand
ChEMBL 606 11 1 8 5.5 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCC(CCCCN2C(=O)c3cccc4c(N(C)C)ccc(c34)C2=O)CC1 10.1021/jm0307887
CHEMBL88355 204778 0 None - 1 Human 7.2 pKi = 7.2 Binding
Binding affinity towards cloned human 5-hydroxytryptamine 4E receptor expressed in C6 glial cells using [3H]GR-113808 as radioligandBinding affinity towards cloned human 5-hydroxytryptamine 4E receptor expressed in C6 glial cells using [3H]GR-113808 as radioligand
ChEMBL 606 11 1 8 5.5 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCC(CCCCN2C(=O)c3cccc4c(N(C)C)ccc(c34)C2=O)CC1 10.1021/jm0307887
56850387 71134 0 None -13 3 Rat 6.2 pKi = 6.2 Binding
Displacement of [3H]GR113808 from 5HT4 receptor in Sprague-Dawley albinus rat striatal membranes after 30 mins by scintillation countingDisplacement of [3H]GR113808 from 5HT4 receptor in Sprague-Dawley albinus rat striatal membranes after 30 mins by scintillation counting
ChEMBL 365 8 1 3 3.2 O=C1C2CCCN2C(=O)N1CCCCNCCc1ccc2ccccc2c1 10.1021/jm2007886
CHEMBL1926731 71134 0 None -13 3 Rat 6.2 pKi = 6.2 Binding
Displacement of [3H]GR113808 from 5HT4 receptor in Sprague-Dawley albinus rat striatal membranes after 30 mins by scintillation countingDisplacement of [3H]GR113808 from 5HT4 receptor in Sprague-Dawley albinus rat striatal membranes after 30 mins by scintillation counting
ChEMBL 365 8 1 3 3.2 O=C1C2CCCN2C(=O)N1CCCCNCCc1ccc2ccccc2c1 10.1021/jm2007886
CHEMBL1962455 71134 0 None -13 3 Rat 6.2 pKi = 6.2 Binding
Displacement of [3H]GR113808 from 5HT4 receptor in Sprague-Dawley albinus rat striatal membranes after 30 mins by scintillation countingDisplacement of [3H]GR113808 from 5HT4 receptor in Sprague-Dawley albinus rat striatal membranes after 30 mins by scintillation counting
ChEMBL 365 8 1 3 3.2 O=C1C2CCCN2C(=O)N1CCCCNCCc1ccc2ccccc2c1 10.1021/jm2007886
44404955 132997 0 None - 1 Human 8.2 pKi = 8.2 Binding
Binding affinity for 5-HT4 receptor using [3H]GR-113808Binding affinity for 5-HT4 receptor using [3H]GR-113808
ChEMBL 868 24 4 15 3.2 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCC(C(=O)NCCCOCCOCCOCNC(=O)C2CCN(CCOC(=O)c3cc(Cl)c(N)cc3OC)CC2)CC1 10.1021/jm050234z
CHEMBL370796 132997 0 None - 1 Human 8.2 pKi = 8.2 Binding
Binding affinity for 5-HT4 receptor using [3H]GR-113808Binding affinity for 5-HT4 receptor using [3H]GR-113808
ChEMBL 868 24 4 15 3.2 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCC(C(=O)NCCCOCCOCCOCNC(=O)C2CCN(CCOC(=O)c3cc(Cl)c(N)cc3OC)CC2)CC1 10.1021/jm050234z
235 2527 36 None -5 3 Guinea pig 8.2 pKi = 8.2 Binding
Displacement of [3H]-GR113808 from 5-HT4R in Dunkin-Hartley guinea pig straitum nuclear membranes after 2 hrs by filter binding methodDisplacement of [3H]-GR113808 from 5-HT4R in Dunkin-Hartley guinea pig straitum nuclear membranes after 2 hrs by filter binding method
ChEMBL 312 5 1 5 2.6 COc1cc(N)c(cc1C(=O)OCCN1CCCCC1)Cl 10.1039/C8MD00233A
5311299 2527 36 None -5 3 Guinea pig 8.2 pKi = 8.2 Binding
Displacement of [3H]-GR113808 from 5-HT4R in Dunkin-Hartley guinea pig straitum nuclear membranes after 2 hrs by filter binding methodDisplacement of [3H]-GR113808 from 5-HT4R in Dunkin-Hartley guinea pig straitum nuclear membranes after 2 hrs by filter binding method
ChEMBL 312 5 1 5 2.6 COc1cc(N)c(cc1C(=O)OCCN1CCCCC1)Cl 10.1039/C8MD00233A
CHEMBL286136 2527 36 None -5 3 Guinea pig 8.2 pKi = 8.2 Binding
Displacement of [3H]-GR113808 from 5-HT4R in Dunkin-Hartley guinea pig straitum nuclear membranes after 2 hrs by filter binding methodDisplacement of [3H]-GR113808 from 5-HT4R in Dunkin-Hartley guinea pig straitum nuclear membranes after 2 hrs by filter binding method
ChEMBL 312 5 1 5 2.6 COc1cc(N)c(cc1C(=O)OCCN1CCCCC1)Cl 10.1039/C8MD00233A
42636941 178371 0 None - 1 Guinea pig 8.2 pKi = 8.2 Binding
Displacement of [3H]-GR113808 from guinea pig 5HT4 receptor by Grossman's methodDisplacement of [3H]-GR113808 from guinea pig 5HT4 receptor by Grossman's method
ChEMBL 343 5 0 5 4.4 CCCN1CCC(COc2nc3scc(C)c3n3cccc23)CC1 10.1039/C2MD20063E
CHEMBL470432 178371 0 None - 1 Guinea pig 8.2 pKi = 8.2 Binding
Displacement of [3H]-GR113808 from guinea pig 5HT4 receptor by Grossman's methodDisplacement of [3H]-GR113808 from guinea pig 5HT4 receptor by Grossman's method
ChEMBL 343 5 0 5 4.4 CCCN1CCC(COc2nc3scc(C)c3n3cccc23)CC1 10.1039/C2MD20063E
235 2527 36 None -5 3 Guinea pig 8.2 pKi = 8.2 Binding
Displacement of [3H]GR113808 from serotonin 5-HT4 receptor in Dunkin-Hartley guinea pigs striatal nuclei membranes incubated for 2 hrs by liquid scintillation countingDisplacement of [3H]GR113808 from serotonin 5-HT4 receptor in Dunkin-Hartley guinea pigs striatal nuclei membranes incubated for 2 hrs by liquid scintillation counting
ChEMBL 312 5 1 5 2.6 COc1cc(N)c(cc1C(=O)OCCN1CCCCC1)Cl 10.1039/C6MD00458J
5311299 2527 36 None -5 3 Guinea pig 8.2 pKi = 8.2 Binding
Displacement of [3H]GR113808 from serotonin 5-HT4 receptor in Dunkin-Hartley guinea pigs striatal nuclei membranes incubated for 2 hrs by liquid scintillation countingDisplacement of [3H]GR113808 from serotonin 5-HT4 receptor in Dunkin-Hartley guinea pigs striatal nuclei membranes incubated for 2 hrs by liquid scintillation counting
ChEMBL 312 5 1 5 2.6 COc1cc(N)c(cc1C(=O)OCCN1CCCCC1)Cl 10.1039/C6MD00458J
CHEMBL286136 2527 36 None -5 3 Guinea pig 8.2 pKi = 8.2 Binding
Displacement of [3H]GR113808 from serotonin 5-HT4 receptor in Dunkin-Hartley guinea pigs striatal nuclei membranes incubated for 2 hrs by liquid scintillation countingDisplacement of [3H]GR113808 from serotonin 5-HT4 receptor in Dunkin-Hartley guinea pigs striatal nuclei membranes incubated for 2 hrs by liquid scintillation counting
ChEMBL 312 5 1 5 2.6 COc1cc(N)c(cc1C(=O)OCCN1CCCCC1)Cl 10.1039/C6MD00458J
10764565 48748 0 None - 1 Rat 8.2 pKi = 8.2 Binding
Binding affinity towards 5-hydroxytryptamine 4 receptor was determined in rat striatal membranes using [3H]GR-113808 as radioligandBinding affinity towards 5-hydroxytryptamine 4 receptor was determined in rat striatal membranes using [3H]GR-113808 as radioligand
ChEMBL 339 5 1 4 2.7 COc1cc(N)c(Cl)cc1C(=O)OCC[N+]12CCC(CC1)CC2 10.1021/jm960320m
CHEMBL156088 48748 0 None - 1 Rat 8.2 pKi = 8.2 Binding
Binding affinity towards 5-hydroxytryptamine 4 receptor was determined in rat striatal membranes using [3H]GR-113808 as radioligandBinding affinity towards 5-hydroxytryptamine 4 receptor was determined in rat striatal membranes using [3H]GR-113808 as radioligand
ChEMBL 339 5 1 4 2.7 COc1cc(N)c(Cl)cc1C(=O)OCC[N+]12CCC(CC1)CC2 10.1021/jm960320m
10548275 48247 0 None - 1 Rat 8.2 pKi = 8.2 Binding
Binding affinity towards 5-hydroxytryptamine 4 receptor was determined in rat striatal membranes using [3H]GR-113808 as radioligandBinding affinity towards 5-hydroxytryptamine 4 receptor was determined in rat striatal membranes using [3H]GR-113808 as radioligand
ChEMBL 307 5 1 4 2.1 COc1cc(N)c(Cl)cc1C(=O)OCC[n+]1ccccc1 10.1021/jm960320m
CHEMBL155631 48247 0 None - 1 Rat 8.2 pKi = 8.2 Binding
Binding affinity towards 5-hydroxytryptamine 4 receptor was determined in rat striatal membranes using [3H]GR-113808 as radioligandBinding affinity towards 5-hydroxytryptamine 4 receptor was determined in rat striatal membranes using [3H]GR-113808 as radioligand
ChEMBL 307 5 1 4 2.1 COc1cc(N)c(Cl)cc1C(=O)OCC[n+]1ccccc1 10.1021/jm960320m
162648923 179374 0 None - 1 Guinea pig 8.2 pKi = 8.2 Binding
Displacement of [3H]-GR113808 from guinea pig brain 5HT4 receptor in presence of serotonin incubated for 30 minsDisplacement of [3H]-GR113808 from guinea pig brain 5HT4 receptor in presence of serotonin incubated for 30 mins
ChEMBL 550 10 3 8 2.9 COc1cc(N)c(Cl)cc1C(=O)CCC1CCN(CCNS(=O)(=O)c2ccc3c(c2)NC(=O)CO3)CC1 10.1016/j.ejmech.2016.05.048
CHEMBL4746550 179374 0 None - 1 Guinea pig 8.2 pKi = 8.2 Binding
Displacement of [3H]-GR113808 from guinea pig brain 5HT4 receptor in presence of serotonin incubated for 30 minsDisplacement of [3H]-GR113808 from guinea pig brain 5HT4 receptor in presence of serotonin incubated for 30 mins
ChEMBL 550 10 3 8 2.9 COc1cc(N)c(Cl)cc1C(=O)CCC1CCN(CCNS(=O)(=O)c2ccc3c(c2)NC(=O)CO3)CC1 10.1016/j.ejmech.2016.05.048
44371350 119663 0 None - 1 Rat 8.2 pKi = 8.2 Binding
Binding affinity towards 5-hydroxytryptamine 4 receptor was determined in rat striatal membranes using [3H]GR-113808 as radioligandBinding affinity towards 5-hydroxytryptamine 4 receptor was determined in rat striatal membranes using [3H]GR-113808 as radioligand
ChEMBL 342 5 1 6 2.2 COc1cc(N)c(Cl)cc1C(=O)OCCN1CC(C)OC(C)C1 10.1021/jm960320m
CHEMBL351570 119663 0 None - 1 Rat 8.2 pKi = 8.2 Binding
Binding affinity towards 5-hydroxytryptamine 4 receptor was determined in rat striatal membranes using [3H]GR-113808 as radioligandBinding affinity towards 5-hydroxytryptamine 4 receptor was determined in rat striatal membranes using [3H]GR-113808 as radioligand
ChEMBL 342 5 1 6 2.2 COc1cc(N)c(Cl)cc1C(=O)OCCN1CC(C)OC(C)C1 10.1021/jm960320m
71451950 82263 5 None -1 2 Human 8.2 pKi = 8.2 Binding
Displacement of [3H]GR113808 from human 5HT4E receptor expressed in CHO cells after 30 mins by liquid scintillation countingDisplacement of [3H]GR113808 from human 5HT4E receptor expressed in CHO cells after 30 mins by liquid scintillation counting
ChEMBL 433 4 2 5 2.4 CC1(C)C(=O)N(C(=O)NCC2CCN(CC3(O)CCOCC3)CC2)c2cc(F)ccc21 10.1021/jm300953p
CHEMBL2179582 82263 5 None -1 2 Human 8.2 pKi = 8.2 Binding
Displacement of [3H]GR113808 from human 5HT4E receptor expressed in CHO cells after 30 mins by liquid scintillation countingDisplacement of [3H]GR113808 from human 5HT4E receptor expressed in CHO cells after 30 mins by liquid scintillation counting
ChEMBL 433 4 2 5 2.4 CC1(C)C(=O)N(C(=O)NCC2CCN(CC3(O)CCOCC3)CC2)c2cc(F)ccc21 10.1021/jm300953p
49783208 17426 0 None - 1 Human 8.2 pKi = 8.2 Binding
Displacement of [3H]GR113808 from human recombinant 5HT4 receptor expressed in HEK293 cellsDisplacement of [3H]GR113808 from human recombinant 5HT4 receptor expressed in HEK293 cells
ChEMBL 362 6 1 6 3.0 CCCCN1CCC(COC(=O)c2cc(C)c(N)c3c2OCCO3)CC1 10.1021/jm100668r
CHEMBL1258222 17426 0 None - 1 Human 8.2 pKi = 8.2 Binding
Displacement of [3H]GR113808 from human recombinant 5HT4 receptor expressed in HEK293 cellsDisplacement of [3H]GR113808 from human recombinant 5HT4 receptor expressed in HEK293 cells
ChEMBL 362 6 1 6 3.0 CCCCN1CCC(COC(=O)c2cc(C)c(N)c3c2OCCO3)CC1 10.1021/jm100668r
258 3511 25 None -1 8 Human 8.2 pKi = 8.2 Binding
Binding affinity at 5HT4 receptorBinding affinity at 5HT4 receptor
ChEMBL 300 7 1 5 2.4 CCN(CCOC(=O)c1cc(Cl)c(cc1OC)N)CC 10.1016/j.bmc.2008.11.045
5191 3511 25 None -1 8 Human 8.2 pKi = 8.2 Binding
Binding affinity at 5HT4 receptorBinding affinity at 5HT4 receptor
ChEMBL 300 7 1 5 2.4 CCN(CCOC(=O)c1cc(Cl)c(cc1OC)N)CC 10.1016/j.bmc.2008.11.045
CHEMBL287045 3511 25 None -1 8 Human 8.2 pKi = 8.2 Binding
Binding affinity at 5HT4 receptorBinding affinity at 5HT4 receptor
ChEMBL 300 7 1 5 2.4 CCN(CCOC(=O)c1cc(Cl)c(cc1OC)N)CC 10.1016/j.bmc.2008.11.045
71712611 90946 0 None - 1 Human 8.2 pKi = 8.2 Binding
Binding affinity to human recombinant 5HT4 receptorBinding affinity to human recombinant 5HT4 receptor
ChEMBL 478 8 3 7 -0.1 CS(=O)(=O)N1CCN(CC(O)CN2CCC(CNC(=O)c3cccc4[nH]cnc34)CC2)CC1 10.1016/j.bmcl.2013.05.018
CHEMBL2402887 90946 0 None - 1 Human 8.2 pKi = 8.2 Binding
Binding affinity to human recombinant 5HT4 receptorBinding affinity to human recombinant 5HT4 receptor
ChEMBL 478 8 3 7 -0.1 CS(=O)(=O)N1CCN(CC(O)CN2CCC(CNC(=O)c3cccc4[nH]cnc34)CC2)CC1 10.1016/j.bmcl.2013.05.018
44248439 194518 0 None - 1 Human 8.2 pKi = 8.2 Binding
Displacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 464 7 1 5 4.2 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CCCN2CCCCC2)cc2ccccc21 10.1021/jm900881j
CHEMBL561398 194518 0 None - 1 Human 8.2 pKi = 8.2 Binding
Displacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 464 7 1 5 4.2 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CCCN2CCCCC2)cc2ccccc21 10.1021/jm900881j
44592235 171999 0 None - 1 Guinea pig 8.2 pKi = 8.2 Binding
Displacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatum membraneDisplacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatum membrane
ChEMBL 343 4 0 5 4.4 Cc1csc2nc(OCC3CCN(C(C)C)CC3)c3cccn3c12 10.1016/j.bmc.2008.11.045
CHEMBL448702 171999 0 None - 1 Guinea pig 8.2 pKi = 8.2 Binding
Displacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatum membraneDisplacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatum membrane
ChEMBL 343 4 0 5 4.4 Cc1csc2nc(OCC3CCN(C(C)C)CC3)c3cccn3c12 10.1016/j.bmc.2008.11.045
10584 1435 0 None 1 2 Guinea pig 8.2 pKi = 8.2 Binding
Displacement of [3H]GR113808 from 5-HT4R in guinea pig brain membranes incubated for 30 mins by radioligand binding assayDisplacement of [3H]GR113808 from 5-HT4R in guinea pig brain membranes incubated for 30 mins by radioligand binding assay
ChEMBL 392 7 1 4 5.2 COc1cc(N)c(cc1C(=O)CCC1CCN(CC1)CC1CCCCC1)Cl 10.1021/acs.jmedchem.5b00115
86582973 1435 0 None 1 2 Guinea pig 8.2 pKi = 8.2 Binding
Displacement of [3H]GR113808 from 5-HT4R in guinea pig brain membranes incubated for 30 mins by radioligand binding assayDisplacement of [3H]GR113808 from 5-HT4R in guinea pig brain membranes incubated for 30 mins by radioligand binding assay
ChEMBL 392 7 1 4 5.2 COc1cc(N)c(cc1C(=O)CCC1CCN(CC1)CC1CCCCC1)Cl 10.1021/acs.jmedchem.5b00115
CHEMBL3417009 1435 0 None 1 2 Guinea pig 8.2 pKi = 8.2 Binding
Displacement of [3H]GR113808 from 5-HT4R in guinea pig brain membranes incubated for 30 mins by radioligand binding assayDisplacement of [3H]GR113808 from 5-HT4R in guinea pig brain membranes incubated for 30 mins by radioligand binding assay
ChEMBL 392 7 1 4 5.2 COc1cc(N)c(cc1C(=O)CCC1CCN(CC1)CC1CCCCC1)Cl 10.1021/acs.jmedchem.5b00115
10584 1435 0 None -1 2 Human 8.2 pKi = 8.2 Binding
Displacement of [3H]GR113808 from human 5-HT4R membrane in Tris buffer assessed as inhibitory constant measured after 60 mins by filter binding methodDisplacement of [3H]GR113808 from human 5-HT4R membrane in Tris buffer assessed as inhibitory constant measured after 60 mins by filter binding method
ChEMBL 392 7 1 4 5.2 COc1cc(N)c(cc1C(=O)CCC1CCN(CC1)CC1CCCCC1)Cl 10.1016/j.ejmech.2019.02.076
86582973 1435 0 None -1 2 Human 8.2 pKi = 8.2 Binding
Displacement of [3H]GR113808 from human 5-HT4R membrane in Tris buffer assessed as inhibitory constant measured after 60 mins by filter binding methodDisplacement of [3H]GR113808 from human 5-HT4R membrane in Tris buffer assessed as inhibitory constant measured after 60 mins by filter binding method
ChEMBL 392 7 1 4 5.2 COc1cc(N)c(cc1C(=O)CCC1CCN(CC1)CC1CCCCC1)Cl 10.1016/j.ejmech.2019.02.076
CHEMBL3417009 1435 0 None -1 2 Human 8.2 pKi = 8.2 Binding
Displacement of [3H]GR113808 from human 5-HT4R membrane in Tris buffer assessed as inhibitory constant measured after 60 mins by filter binding methodDisplacement of [3H]GR113808 from human 5-HT4R membrane in Tris buffer assessed as inhibitory constant measured after 60 mins by filter binding method
ChEMBL 392 7 1 4 5.2 COc1cc(N)c(cc1C(=O)CCC1CCN(CC1)CC1CCCCC1)Cl 10.1016/j.ejmech.2019.02.076
10666935 206211 0 None 1 2 Guinea pig 8.2 pKi = 8.2 Binding
Binding affinity against 5-hydroxytryptamine 4 receptor in guinea pig striatum using [3H]GR-113808 as radioligandBinding affinity against 5-hydroxytryptamine 4 receptor in guinea pig striatum using [3H]GR-113808 as radioligand
ChEMBL 371 5 1 6 1.7 CC(C)N1CCN(CCNC(=O)n2c(=O)n(C3CC3)c3ccccc32)CC1 10.1021/jm981098j
CHEMBL97019 206211 0 None 1 2 Guinea pig 8.2 pKi = 8.2 Binding
Binding affinity against 5-hydroxytryptamine 4 receptor in guinea pig striatum using [3H]GR-113808 as radioligandBinding affinity against 5-hydroxytryptamine 4 receptor in guinea pig striatum using [3H]GR-113808 as radioligand
ChEMBL 371 5 1 6 1.7 CC(C)N1CCN(CCNC(=O)n2c(=O)n(C3CC3)c3ccccc32)CC1 10.1021/jm981098j
71451950 82263 5 None -1 2 Human 8.2 pKi = 8.2 Binding
Displacement of [3H]GR113808 from human 5HT4B receptor expressed in HEK293 cells after 30 mins by liquid scintillation countingDisplacement of [3H]GR113808 from human 5HT4B receptor expressed in HEK293 cells after 30 mins by liquid scintillation counting
ChEMBL 433 4 2 5 2.4 CC1(C)C(=O)N(C(=O)NCC2CCN(CC3(O)CCOCC3)CC2)c2cc(F)ccc21 10.1021/jm300953p
CHEMBL2179582 82263 5 None -1 2 Human 8.2 pKi = 8.2 Binding
Displacement of [3H]GR113808 from human 5HT4B receptor expressed in HEK293 cells after 30 mins by liquid scintillation countingDisplacement of [3H]GR113808 from human 5HT4B receptor expressed in HEK293 cells after 30 mins by liquid scintillation counting
ChEMBL 433 4 2 5 2.4 CC1(C)C(=O)N(C(=O)NCC2CCN(CC3(O)CCOCC3)CC2)c2cc(F)ccc21 10.1021/jm300953p
11603514 71146 0 None -5 4 Rat 7.2 pKi = 7.2 Binding
Displacement of [3H]GR113808 from 5HT4 receptor in Sprague-Dawley albinus rat striatal membranes after 30 mins by scintillation countingDisplacement of [3H]GR113808 from 5HT4 receptor in Sprague-Dawley albinus rat striatal membranes after 30 mins by scintillation counting
ChEMBL 390 11 1 5 4.0 O=C1CSC(=O)N1CCCCCCCCNCC1CCc2ccccc2O1 10.1021/jm2007886
CHEMBL1926760 71146 0 None -5 4 Rat 7.2 pKi = 7.2 Binding
Displacement of [3H]GR113808 from 5HT4 receptor in Sprague-Dawley albinus rat striatal membranes after 30 mins by scintillation countingDisplacement of [3H]GR113808 from 5HT4 receptor in Sprague-Dawley albinus rat striatal membranes after 30 mins by scintillation counting
ChEMBL 390 11 1 5 4.0 O=C1CSC(=O)N1CCCCCCCCNCC1CCc2ccccc2O1 10.1021/jm2007886
CHEMBL1962492 71146 0 None -5 4 Rat 7.2 pKi = 7.2 Binding
Displacement of [3H]GR113808 from 5HT4 receptor in Sprague-Dawley albinus rat striatal membranes after 30 mins by scintillation countingDisplacement of [3H]GR113808 from 5HT4 receptor in Sprague-Dawley albinus rat striatal membranes after 30 mins by scintillation counting
ChEMBL 390 11 1 5 4.0 O=C1CSC(=O)N1CCCCCCCCNCC1CCc2ccccc2O1 10.1021/jm2007886
209710 101377 1 None - 1 Rat 7.2 pKi = 7.2 Binding
Binding affinity at 5-hydroxytryptamine 4 receptor in rat striatal membranes by [3H]GR-113808 displacement.Binding affinity at 5-hydroxytryptamine 4 receptor in rat striatal membranes by [3H]GR-113808 displacement.
ChEMBL 282 4 1 3 3.4 O=C(Nc1cccc(Cl)c1)OCCN1CCCCC1 10.1021/jm960853v
CHEMBL300476 101377 1 None - 1 Rat 7.2 pKi = 7.2 Binding
Binding affinity at 5-hydroxytryptamine 4 receptor in rat striatal membranes by [3H]GR-113808 displacement.Binding affinity at 5-hydroxytryptamine 4 receptor in rat striatal membranes by [3H]GR-113808 displacement.
ChEMBL 282 4 1 3 3.4 O=C(Nc1cccc(Cl)c1)OCCN1CCCCC1 10.1021/jm960853v
44240743 6679 15 None - 1 Human 5.2 pKi = 5.2 Binding
Binding affinity to 5HT4 receptorBinding affinity to 5HT4 receptor
ChEMBL 370 7 2 3 4.3 O=C(NCCCCN1CCCCC1)Nc1ccc(-c2ccc(F)cc2)nc1 10.1021/jm901692q
CHEMBL1083787 6679 15 None - 1 Human 5.2 pKi = 5.2 Binding
Binding affinity to 5HT4 receptorBinding affinity to 5HT4 receptor
ChEMBL 370 7 2 3 4.3 O=C(NCCCCN1CCCCC1)Nc1ccc(-c2ccc(F)cc2)nc1 10.1021/jm901692q
136118651 75971 0 None -1 4 Human 6.2 pKi = 6.2 Binding
Displacement of [3H]GR113808 from human recombinant 5HT4 receptorDisplacement of [3H]GR113808 from human recombinant 5HT4 receptor
ChEMBL 318 1 3 2 2.0 C/N=C1\NC(=O)/C(=C/c2c[nH]c3c(Br)cccc23)N1 10.1016/j.bmc.2013.09.011
CHEMBL2058706 75971 0 None -1 4 Human 6.2 pKi = 6.2 Binding
Displacement of [3H]GR113808 from human recombinant 5HT4 receptorDisplacement of [3H]GR113808 from human recombinant 5HT4 receptor
ChEMBL 318 1 3 2 2.0 C/N=C1\NC(=O)/C(=C/c2c[nH]c3c(Br)cccc23)N1 10.1016/j.bmc.2013.09.011
145955685 161918 0 None - 1 Guinea pig 7.2 pKi = 7.2 Binding
Displacement of [3H]GR113808 from serotonin 5-HT4 receptor in Dunkin-Hartley guinea pigs striatal nuclei membranes incubated for 2 hrs by liquid scintillation countingDisplacement of [3H]GR113808 from serotonin 5-HT4 receptor in Dunkin-Hartley guinea pigs striatal nuclei membranes incubated for 2 hrs by liquid scintillation counting
ChEMBL 602 17 6 10 0.3 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCC(NC(=O)NCCOCCOCCNC(=O)NCC(=O)O)CC1 10.1039/C6MD00458J
CHEMBL4167048 161918 0 None - 1 Guinea pig 7.2 pKi = 7.2 Binding
Displacement of [3H]GR113808 from serotonin 5-HT4 receptor in Dunkin-Hartley guinea pigs striatal nuclei membranes incubated for 2 hrs by liquid scintillation countingDisplacement of [3H]GR113808 from serotonin 5-HT4 receptor in Dunkin-Hartley guinea pigs striatal nuclei membranes incubated for 2 hrs by liquid scintillation counting
ChEMBL 602 17 6 10 0.3 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCC(NC(=O)NCCOCCOCCNC(=O)NCC(=O)O)CC1 10.1039/C6MD00458J
44592039 187714 0 None - 1 Guinea pig 6.2 pKi = 6.2 Binding
Displacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatum membraneDisplacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatum membrane
ChEMBL 301 4 1 5 3.5 c1cc2c(OCCC3CCCCN3)nc3ccsc3n2c1 10.1016/j.bmc.2008.11.045
CHEMBL500336 187714 0 None - 1 Guinea pig 6.2 pKi = 6.2 Binding
Displacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatum membraneDisplacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatum membrane
ChEMBL 301 4 1 5 3.5 c1cc2c(OCCC3CCCCN3)nc3ccsc3n2c1 10.1016/j.bmc.2008.11.045
260 3808 49 None -19 6 Rat 7.2 pKi = 7.2 Binding
Displacement of [3H]GR-113808 from rat striatum 5-hydroxytryptamine 4 receptorDisplacement of [3H]GR-113808 from rat striatum 5-hydroxytryptamine 4 receptor
ChEMBL 284 2 1 3 3.0 CN1[C@@H]2CC[C@H]1C[C@H](C2)OC(=O)c1c[nH]c2c1cccc2 10.1016/0960-894X(96)00200-4
2775 3808 49 None -19 6 Rat 7.2 pKi = 7.2 Binding
Displacement of [3H]GR-113808 from rat striatum 5-hydroxytryptamine 4 receptorDisplacement of [3H]GR-113808 from rat striatum 5-hydroxytryptamine 4 receptor
ChEMBL 284 2 1 3 3.0 CN1[C@@H]2CC[C@H]1C[C@H](C2)OC(=O)c1c[nH]c2c1cccc2 10.1016/0960-894X(96)00200-4
656665 3808 49 None -19 6 Rat 7.2 pKi = 7.2 Binding
Displacement of [3H]GR-113808 from rat striatum 5-hydroxytryptamine 4 receptorDisplacement of [3H]GR-113808 from rat striatum 5-hydroxytryptamine 4 receptor
ChEMBL 284 2 1 3 3.0 CN1[C@@H]2CC[C@H]1C[C@H](C2)OC(=O)c1c[nH]c2c1cccc2 10.1016/0960-894X(96)00200-4
CHEMBL56564 3808 49 None -19 6 Rat 7.2 pKi = 7.2 Binding
Displacement of [3H]GR-113808 from rat striatum 5-hydroxytryptamine 4 receptorDisplacement of [3H]GR-113808 from rat striatum 5-hydroxytryptamine 4 receptor
ChEMBL 284 2 1 3 3.0 CN1[C@@H]2CC[C@H]1C[C@H](C2)OC(=O)c1c[nH]c2c1cccc2 10.1016/0960-894X(96)00200-4
DB11699 3808 49 None -19 6 Rat 7.2 pKi = 7.2 Binding
Displacement of [3H]GR-113808 from rat striatum 5-hydroxytryptamine 4 receptorDisplacement of [3H]GR-113808 from rat striatum 5-hydroxytryptamine 4 receptor
ChEMBL 284 2 1 3 3.0 CN1[C@@H]2CC[C@H]1C[C@H](C2)OC(=O)c1c[nH]c2c1cccc2 10.1016/0960-894X(96)00200-4
76313431 102895 0 None - 1 Human 7.2 pKi = 7.2 Binding
Binding affinity at 5HT4 receptorBinding affinity at 5HT4 receptor
ChEMBL 330 2 2 5 1.5 COc1ccc2[nH]c(=O)n(C(=O)N[C@H]3C[C@@H]4CC[C@H](C3)N4C)c2c1 10.1016/j.bmc.2008.11.045
CHEMBL3084582 102895 0 None - 1 Human 7.2 pKi = 7.2 Binding
Binding affinity at 5HT4 receptorBinding affinity at 5HT4 receptor
ChEMBL 330 2 2 5 1.5 COc1ccc2[nH]c(=O)n(C(=O)N[C@H]3C[C@@H]4CC[C@H](C3)N4C)c2c1 10.1016/j.bmc.2008.11.045
9839803 92440 0 None -1 2 Guinea pig 7.2 pKi = 7.2 Binding
Displacement of [125I]SB207710 from 5-HT4 receptor in guinea pig brain membranesDisplacement of [125I]SB207710 from 5-HT4 receptor in guinea pig brain membranes
ChEMBL 313 3 2 4 2.2 O=C(NCC1CCNCC1)c1c2n(c3ccccc13)CCCO2 10.1016/j.bmc.2013.09.004
CHEMBL2440452 92440 0 None -1 2 Guinea pig 7.2 pKi = 7.2 Binding
Displacement of [125I]SB207710 from 5-HT4 receptor in guinea pig brain membranesDisplacement of [125I]SB207710 from 5-HT4 receptor in guinea pig brain membranes
ChEMBL 313 3 2 4 2.2 O=C(NCC1CCNCC1)c1c2n(c3ccccc13)CCCO2 10.1016/j.bmc.2013.09.004
9839803 92440 0 None 1 2 Human 7.2 pKi = 7.2 Binding
Displacement of [125I]SB207710 from human recombinant 5-HT4 receptorDisplacement of [125I]SB207710 from human recombinant 5-HT4 receptor
ChEMBL 313 3 2 4 2.2 O=C(NCC1CCNCC1)c1c2n(c3ccccc13)CCCO2 10.1016/j.bmc.2013.09.004
CHEMBL2440452 92440 0 None 1 2 Human 7.2 pKi = 7.2 Binding
Displacement of [125I]SB207710 from human recombinant 5-HT4 receptorDisplacement of [125I]SB207710 from human recombinant 5-HT4 receptor
ChEMBL 313 3 2 4 2.2 O=C(NCC1CCNCC1)c1c2n(c3ccccc13)CCCO2 10.1016/j.bmc.2013.09.004
44592284 178449 0 None - 1 Guinea pig 7.2 pKi = 7.2 Binding
Displacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatum membraneDisplacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatum membrane
ChEMBL 377 5 0 5 4.8 c1ccc(CN2CCC(COc3nc4ccsc4n4cccc34)CC2)cc1 10.1016/j.bmc.2008.11.045
CHEMBL471231 178449 0 None - 1 Guinea pig 7.2 pKi = 7.2 Binding
Displacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatum membraneDisplacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatum membrane
ChEMBL 377 5 0 5 4.8 c1ccc(CN2CCC(COc3nc4ccsc4n4cccc34)CC2)cc1 10.1016/j.bmc.2008.11.045
10757502 91929739 193455 0 None - 1 Human 7.2 pKi = 7.2 Binding
Displacement of [3H]GR113808 from human recombinant 5HT4C receptor expressed in HEK293 cellsDisplacement of [3H]GR113808 from human recombinant 5HT4C receptor expressed in HEK293 cells
ChEMBL 312 3 2 4 2.6 CC(C)n1nc(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3)c2ccccc21 10.1016/j.bmcl.2012.05.034
CHEMBL550064 193455 0 None - 1 Human 7.2 pKi = 7.2 Binding
Displacement of [3H]GR113808 from human recombinant 5HT4C receptor expressed in HEK293 cellsDisplacement of [3H]GR113808 from human recombinant 5HT4C receptor expressed in HEK293 cells
ChEMBL 312 3 2 4 2.6 CC(C)n1nc(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3)c2ccccc21 10.1016/j.bmcl.2012.05.034
10757502 91929739 193455 0 None - 1 Human 7.2 pKi = 7.2 Binding
Displacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 312 3 2 4 2.6 CC(C)n1nc(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3)c2ccccc21 10.1021/jm900881j
CHEMBL550064 193455 0 None - 1 Human 7.2 pKi = 7.2 Binding
Displacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 312 3 2 4 2.6 CC(C)n1nc(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3)c2ccccc21 10.1021/jm900881j
44248312 91900490 193460 0 None - 1 Human 7.2 pKi = 7.2 Binding
Displacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 531 12 2 6 4.5 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CCCCCCCCS(=O)(=O)O)cc2ccccc21 10.1021/jm900881j
CHEMBL550122 193460 0 None - 1 Human 7.2 pKi = 7.2 Binding
Displacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 531 12 2 6 4.5 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CCCCCCCCS(=O)(=O)O)cc2ccccc21 10.1021/jm900881j
44248187 91900482 193710 0 None - 1 Human 7.2 pKi = 7.2 Binding
Displacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 409 7 1 4 4.5 CCCCCN1[C@H]2CC[C@@H]1C[C@H](NC(=O)c1cc3ccccc3n(C(C)C)c1=O)C2 10.1021/jm900881j
CHEMBL551941 193710 0 None - 1 Human 7.2 pKi = 7.2 Binding
Displacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 409 7 1 4 4.5 CCCCCN1[C@H]2CC[C@@H]1C[C@H](NC(=O)c1cc3ccccc3n(C(C)C)c1=O)C2 10.1021/jm900881j
44247811 193800 0 None - 1 Human 7.2 pKi = 7.2 Binding
Displacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 369 8 3 5 2.3 COc1cc(N)c(Cl)cc1C(=O)NC1CCN(CCCCCO)CC1 10.1021/jm900881j
CHEMBL552693 193800 0 None - 1 Human 7.2 pKi = 7.2 Binding
Displacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 369 8 3 5 2.3 COc1cc(N)c(Cl)cc1C(=O)NC1CCN(CCCCCO)CC1 10.1021/jm900881j
44249056 91900483 194663 0 None - 1 Human 7.2 pKi = 7.2 Binding
Displacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 451 10 1 4 5.7 CCCCCCCCN1[C@H]2CC[C@@H]1C[C@H](NC(=O)c1cc3ccccc3n(C(C)C)c1=O)C2 10.1021/jm900881j
CHEMBL562400 194663 0 None - 1 Human 7.2 pKi = 7.2 Binding
Displacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 451 10 1 4 5.7 CCCCCCCCN1[C@H]2CC[C@@H]1C[C@H](NC(=O)c1cc3ccccc3n(C(C)C)c1=O)C2 10.1021/jm900881j
10574402 91900484 194798 0 None - 1 Human 7.2 pKi = 7.2 Binding
Displacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 425 8 2 5 3.5 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CCCCCO)cc2ccccc21 10.1021/jm900881j
CHEMBL563261 194798 0 None - 1 Human 7.2 pKi = 7.2 Binding
Displacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 425 8 2 5 3.5 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CCCCCO)cc2ccccc21 10.1021/jm900881j
44248433 91900494 195066 0 None - 1 Human 7.2 pKi = 7.2 Binding
Displacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 529 7 1 7 1.9 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CCN2CCN(S(C)(=O)=O)CC2)cc2ccccc21 10.1021/jm900881j
CHEMBL565146 195066 0 None - 1 Human 7.2 pKi = 7.2 Binding
Displacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 529 7 1 7 1.9 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CCN2CCN(S(C)(=O)=O)CC2)cc2ccccc21 10.1021/jm900881j
131725 198753 2 None 3 2 Guinea pig 7.2 pKi = 7.2 Binding
Binding affinity against 5-hydroxytryptamine 4 receptor in guinea pig striatum using [3H]GR-113808 as radioligandBinding affinity against 5-hydroxytryptamine 4 receptor in guinea pig striatum using [3H]GR-113808 as radioligand
ChEMBL 342 2 1 5 2.6 CC(C)n1c(=O)n(C(=O)NC2CC3CCC(C2)N3C)c2ccccc21 10.1021/jm981098j
CHEMBL59834 198753 2 None 3 2 Guinea pig 7.2 pKi = 7.2 Binding
Binding affinity against 5-hydroxytryptamine 4 receptor in guinea pig striatum using [3H]GR-113808 as radioligandBinding affinity against 5-hydroxytryptamine 4 receptor in guinea pig striatum using [3H]GR-113808 as radioligand
ChEMBL 342 2 1 5 2.6 CC(C)n1c(=O)n(C(=O)NC2CC3CCC(C2)N3C)c2ccccc21 10.1021/jm981098j
44247947 193663 0 None - 1 Human 5.2 pKi = 5.2 Binding
Displacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 433 9 3 6 2.2 COc1cc(N)c(Cl)cc1C(=O)NC1CCN(CCCCCS(=O)(=O)O)CC1 10.1021/jm900881j
CHEMBL551678 193663 0 None - 1 Human 5.2 pKi = 5.2 Binding
Displacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 433 9 3 6 2.2 COc1cc(N)c(Cl)cc1C(=O)NC1CCN(CCCCCS(=O)(=O)O)CC1 10.1021/jm900881j
3168 9172 84 None -93 21 Guinea pig 6.2 pKi = 6.2 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
ChEMBL 379 6 1 4 3.7 O=C(CCCN1CC=C(n2c(=O)[nH]c3ccccc32)CC1)c1ccc(F)cc1 nan
CHEMBL1108 9172 84 None -93 21 Guinea pig 6.2 pKi = 6.2 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
ChEMBL 379 6 1 4 3.7 O=C(CCCN1CC=C(n2c(=O)[nH]c3ccccc32)CC1)c1ccc(F)cc1 nan
10347130 204315 0 None - 1 Human 7.2 pKi = 7.2 Binding
Binding affinity towards cloned human 5-hydroxytryptamine 4E receptor expressed in C6 glial cells using [3H]GR-113808 as radioligandBinding affinity towards cloned human 5-hydroxytryptamine 4E receptor expressed in C6 glial cells using [3H]GR-113808 as radioligand
ChEMBL 536 7 2 8 3.8 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCC(CN2C(=O)c3cccc4c(N)ccc(c34)C2=O)CC1 10.1021/jm0307887
CHEMBL85125 204315 0 None - 1 Human 7.2 pKi = 7.2 Binding
Binding affinity towards cloned human 5-hydroxytryptamine 4E receptor expressed in C6 glial cells using [3H]GR-113808 as radioligandBinding affinity towards cloned human 5-hydroxytryptamine 4E receptor expressed in C6 glial cells using [3H]GR-113808 as radioligand
ChEMBL 536 7 2 8 3.8 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCC(CN2C(=O)c3cccc4c(N)ccc(c34)C2=O)CC1 10.1021/jm0307887
10812045 15346 0 None - 1 Human 7.2 pKi = 7.2 Binding
Binding affinity was determined against cloned 5-hydroxytryptamine 4E receptor isoform expressed in C6 glial cells incubated with 0.2 nM [3H]GR-113808Binding affinity was determined against cloned 5-hydroxytryptamine 4E receptor isoform expressed in C6 glial cells incubated with 0.2 nM [3H]GR-113808
ChEMBL 419 7 1 7 2.9 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCN(c2ccccc2OC)CC1 10.1021/jm0009538
CHEMBL121766 15346 0 None - 1 Human 7.2 pKi = 7.2 Binding
Binding affinity was determined against cloned 5-hydroxytryptamine 4E receptor isoform expressed in C6 glial cells incubated with 0.2 nM [3H]GR-113808Binding affinity was determined against cloned 5-hydroxytryptamine 4E receptor isoform expressed in C6 glial cells incubated with 0.2 nM [3H]GR-113808
ChEMBL 419 7 1 7 2.9 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCN(c2ccccc2OC)CC1 10.1021/jm0009538
14403199 116110 0 None - 1 Rat 7.2 pKi = 7.2 Binding
Binding affinity against 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatumBinding affinity against 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatum
ChEMBL 324 3 1 5 2.7 COc1cc(N)c(Cl)cc1C(=O)OC1CC2CCC(C1)N2C 10.1016/S0960-894X(01)80508-4
CHEMBL33676 116110 0 None - 1 Rat 7.2 pKi = 7.2 Binding
Binding affinity against 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatumBinding affinity against 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatum
ChEMBL 324 3 1 5 2.7 COc1cc(N)c(Cl)cc1C(=O)OC1CC2CCC(C1)N2C 10.1016/S0960-894X(01)80508-4
14403199 116110 0 None - 1 Rat 7.2 pKi = 7.2 Binding
Binding affinity towards 5-hydroxytryptamine 4 receptor was determined in rat striatal membranes using [3H]GR-113808 as radioligandBinding affinity towards 5-hydroxytryptamine 4 receptor was determined in rat striatal membranes using [3H]GR-113808 as radioligand
ChEMBL 324 3 1 5 2.7 COc1cc(N)c(Cl)cc1C(=O)OC1CC2CCC(C1)N2C 10.1021/jm960320m
CHEMBL33676 116110 0 None - 1 Rat 7.2 pKi = 7.2 Binding
Binding affinity towards 5-hydroxytryptamine 4 receptor was determined in rat striatal membranes using [3H]GR-113808 as radioligandBinding affinity towards 5-hydroxytryptamine 4 receptor was determined in rat striatal membranes using [3H]GR-113808 as radioligand
ChEMBL 324 3 1 5 2.7 COc1cc(N)c(Cl)cc1C(=O)OC1CC2CCC(C1)N2C 10.1021/jm960320m
10530233 11252 0 None - 1 Guinea pig 7.2 pKi = 7.2 Binding
Binding affinity against 5-hydroxytryptamine 4 receptor in guinea pig striatum using [3H]GR-113808 as radioligandBinding affinity against 5-hydroxytryptamine 4 receptor in guinea pig striatum using [3H]GR-113808 as radioligand
ChEMBL 402 7 1 5 2.5 CCCC[N+]1(C)CCN(CCNC(=O)n2c(=O)n(C(C)C)c3ccccc32)CC1 10.1021/jm981098j
CHEMBL1179716 11252 0 None - 1 Guinea pig 7.2 pKi = 7.2 Binding
Binding affinity against 5-hydroxytryptamine 4 receptor in guinea pig striatum using [3H]GR-113808 as radioligandBinding affinity against 5-hydroxytryptamine 4 receptor in guinea pig striatum using [3H]GR-113808 as radioligand
ChEMBL 402 7 1 5 2.5 CCCC[N+]1(C)CCN(CCNC(=O)n2c(=O)n(C(C)C)c3ccccc32)CC1 10.1021/jm981098j
CHEMBL95968 11252 0 None - 1 Guinea pig 7.2 pKi = 7.2 Binding
Binding affinity against 5-hydroxytryptamine 4 receptor in guinea pig striatum using [3H]GR-113808 as radioligandBinding affinity against 5-hydroxytryptamine 4 receptor in guinea pig striatum using [3H]GR-113808 as radioligand
ChEMBL 402 7 1 5 2.5 CCCC[N+]1(C)CCN(CCNC(=O)n2c(=O)n(C(C)C)c3ccccc32)CC1 10.1021/jm981098j
10381927 162549 1 None 1 2 Guinea pig 5.2 pKi = 5.2 Binding
Displacement of [3H]-GR113808 from 5-HT4 receptor of guinea pig striatumDisplacement of [3H]-GR113808 from 5-HT4 receptor of guinea pig striatum
ChEMBL 329 1 0 3 3.8 CN1CCN(c2nc3ccccc3c3c2CCc2ccccc2-3)CC1 10.1021/jm00014a021
CHEMBL417706 162549 1 None 1 2 Guinea pig 5.2 pKi = 5.2 Binding
Displacement of [3H]-GR113808 from 5-HT4 receptor of guinea pig striatumDisplacement of [3H]-GR113808 from 5-HT4 receptor of guinea pig striatum
ChEMBL 329 1 0 3 3.8 CN1CCN(c2nc3ccccc3c3c2CCc2ccccc2-3)CC1 10.1021/jm00014a021
11799162 11263 0 None - 1 Guinea pig 7.2 pKi = 7.2 Binding
Binding affinity against 5-hydroxytryptamine 4 receptor in guinea pig striatum using [3H]GR-113808 as radioligandBinding affinity against 5-hydroxytryptamine 4 receptor in guinea pig striatum using [3H]GR-113808 as radioligand
ChEMBL 360 4 1 5 1.3 CC(C)n1c(=O)n(C(=O)NCCN2CC[N+](C)(C)CC2)c2ccccc21 10.1021/jm981098j
CHEMBL1179748 11263 0 None - 1 Guinea pig 7.2 pKi = 7.2 Binding
Binding affinity against 5-hydroxytryptamine 4 receptor in guinea pig striatum using [3H]GR-113808 as radioligandBinding affinity against 5-hydroxytryptamine 4 receptor in guinea pig striatum using [3H]GR-113808 as radioligand
ChEMBL 360 4 1 5 1.3 CC(C)n1c(=O)n(C(=O)NCCN2CC[N+](C)(C)CC2)c2ccccc21 10.1021/jm981098j
CHEMBL97903 11263 0 None - 1 Guinea pig 7.2 pKi = 7.2 Binding
Binding affinity against 5-hydroxytryptamine 4 receptor in guinea pig striatum using [3H]GR-113808 as radioligandBinding affinity against 5-hydroxytryptamine 4 receptor in guinea pig striatum using [3H]GR-113808 as radioligand
ChEMBL 360 4 1 5 1.3 CC(C)n1c(=O)n(C(=O)NCCN2CC[N+](C)(C)CC2)c2ccccc21 10.1021/jm981098j
21588627 106140 0 None - 1 Rat 7.2 pKi = 7.2 Binding
pKi against 5-hydroxytryptamine 4 receptor in rat striatum membranepKi against 5-hydroxytryptamine 4 receptor in rat striatum membrane
ChEMBL 438 7 1 4 4.8 CC(C)CN1CCC(CNC(=O)c2cc(Cl)cc3c2ncn3Cc2ccccc2)CC1 10.1016/s0960-894x(01)00517-0
CHEMBL314299 106140 0 None - 1 Rat 7.2 pKi = 7.2 Binding
pKi against 5-hydroxytryptamine 4 receptor in rat striatum membranepKi against 5-hydroxytryptamine 4 receptor in rat striatum membrane
ChEMBL 438 7 1 4 4.8 CC(C)CN1CCC(CNC(=O)c2cc(Cl)cc3c2ncn3Cc2ccccc2)CC1 10.1016/s0960-894x(01)00517-0
21588627 106140 0 None - 1 Rat 7.2 pKi = 7.2 Binding
Binding affinity to 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatum membraneBinding affinity to 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatum membrane
ChEMBL 438 7 1 4 4.8 CC(C)CN1CCC(CNC(=O)c2cc(Cl)cc3c2ncn3Cc2ccccc2)CC1 10.1021/jm020807x
CHEMBL314299 106140 0 None - 1 Rat 7.2 pKi = 7.2 Binding
Binding affinity to 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatum membraneBinding affinity to 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatum membrane
ChEMBL 438 7 1 4 4.8 CC(C)CN1CCC(CNC(=O)c2cc(Cl)cc3c2ncn3Cc2ccccc2)CC1 10.1021/jm020807x
21588627 106140 0 None - 1 Rat 7.2 pKi = 7.2 Binding
In vitro binding affinity to 5-hydroxytryptamine 4 receptor in rat striatum membraneIn vitro binding affinity to 5-hydroxytryptamine 4 receptor in rat striatum membrane
ChEMBL 438 7 1 4 4.8 CC(C)CN1CCC(CNC(=O)c2cc(Cl)cc3c2ncn3Cc2ccccc2)CC1 10.1016/s0960-894x(01)00517-0
CHEMBL314299 106140 0 None - 1 Rat 7.2 pKi = 7.2 Binding
In vitro binding affinity to 5-hydroxytryptamine 4 receptor in rat striatum membraneIn vitro binding affinity to 5-hydroxytryptamine 4 receptor in rat striatum membrane
ChEMBL 438 7 1 4 4.8 CC(C)CN1CCC(CNC(=O)c2cc(Cl)cc3c2ncn3Cc2ccccc2)CC1 10.1016/s0960-894x(01)00517-0
119584 2557 99 None -1 6 Guinea pig 7.2 pKi = 7.2 Binding
Inhibition of [3H]GR-113808 binding to guinea pig striatum 5-hydroxytryptamine 4 receptorInhibition of [3H]GR-113808 binding to guinea pig striatum 5-hydroxytryptamine 4 receptor
ChEMBL 421 7 2 5 3.1 CCOc1cc(N)c(cc1C(=O)NCC1OCCN(C1)Cc1ccc(cc1)F)Cl 10.1021/jm020270n
1848 2557 99 None -1 6 Guinea pig 7.2 pKi = 7.2 Binding
Inhibition of [3H]GR-113808 binding to guinea pig striatum 5-hydroxytryptamine 4 receptorInhibition of [3H]GR-113808 binding to guinea pig striatum 5-hydroxytryptamine 4 receptor
ChEMBL 421 7 2 5 3.1 CCOc1cc(N)c(cc1C(=O)NCC1OCCN(C1)Cc1ccc(cc1)F)Cl 10.1021/jm020270n
242 2557 99 None -1 6 Guinea pig 7.2 pKi = 7.2 Binding
Inhibition of [3H]GR-113808 binding to guinea pig striatum 5-hydroxytryptamine 4 receptorInhibition of [3H]GR-113808 binding to guinea pig striatum 5-hydroxytryptamine 4 receptor
ChEMBL 421 7 2 5 3.1 CCOc1cc(N)c(cc1C(=O)NCC1OCCN(C1)Cc1ccc(cc1)F)Cl 10.1021/jm020270n
CHEMBL60889 2557 99 None -1 6 Guinea pig 7.2 pKi = 7.2 Binding
Inhibition of [3H]GR-113808 binding to guinea pig striatum 5-hydroxytryptamine 4 receptorInhibition of [3H]GR-113808 binding to guinea pig striatum 5-hydroxytryptamine 4 receptor
ChEMBL 421 7 2 5 3.1 CCOc1cc(N)c(cc1C(=O)NCC1OCCN(C1)Cc1ccc(cc1)F)Cl 10.1021/jm020270n
DB11675 2557 99 None -1 6 Guinea pig 7.2 pKi = 7.2 Binding
Inhibition of [3H]GR-113808 binding to guinea pig striatum 5-hydroxytryptamine 4 receptorInhibition of [3H]GR-113808 binding to guinea pig striatum 5-hydroxytryptamine 4 receptor
ChEMBL 421 7 2 5 3.1 CCOc1cc(N)c(cc1C(=O)NCC1OCCN(C1)Cc1ccc(cc1)F)Cl 10.1021/jm020270n
10335971 100442 1 None - 1 Guinea pig 5.2 pKi = 5.2 Binding
The compound was tested for their binding affinity towards 5-hydroxytryptamine 4 receptor from guinea pig striatum using [3H]GR-113808 as radioligand.The compound was tested for their binding affinity towards 5-hydroxytryptamine 4 receptor from guinea pig striatum using [3H]GR-113808 as radioligand.
ChEMBL 317 1 0 4 3.9 CN1CCN(c2nc3ccccc3c3c2oc2ccccc23)CC1 10.1021/jm00014a021
CHEMBL293866 100442 1 None - 1 Guinea pig 5.2 pKi = 5.2 Binding
The compound was tested for their binding affinity towards 5-hydroxytryptamine 4 receptor from guinea pig striatum using [3H]GR-113808 as radioligand.The compound was tested for their binding affinity towards 5-hydroxytryptamine 4 receptor from guinea pig striatum using [3H]GR-113808 as radioligand.
ChEMBL 317 1 0 4 3.9 CN1CCN(c2nc3ccccc3c3c2oc2ccccc23)CC1 10.1021/jm00014a021
71450246 82559 0 None - 1 Guinea pig 6.2 pKi = 6.2 Binding
Displacement of [3H]GR113808 from 5HT4R in guinea pig striatal membranesDisplacement of [3H]GR113808 from 5HT4R in guinea pig striatal membranes
ChEMBL 348 5 0 3 5.2 CCCN1CCC(COc2nc3cc(C)ccc3c3ccccc23)CC1 10.1021/jm300943r
CHEMBL2181184 82559 0 None - 1 Guinea pig 6.2 pKi = 6.2 Binding
Displacement of [3H]GR113808 from 5HT4R in guinea pig striatal membranesDisplacement of [3H]GR113808 from 5HT4R in guinea pig striatal membranes
ChEMBL 348 5 0 3 5.2 CCCN1CCC(COc2nc3cc(C)ccc3c3ccccc23)CC1 10.1021/jm300943r
44404958 72062 0 None - 1 Human 8.2 pKi = 8.2 Binding
Binding affinity for 5-HT4 receptor using [3H]GR-113808Binding affinity for 5-HT4 receptor using [3H]GR-113808
ChEMBL 764 17 5 12 3.9 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCC(C(=O)NCCCCCC(=O)NC2CCN(CCOC(=O)c3cc(Cl)c(N)cc3O)CC2)CC1 10.1021/jm050234z
CHEMBL198719 72062 0 None - 1 Human 8.2 pKi = 8.2 Binding
Binding affinity for 5-HT4 receptor using [3H]GR-113808Binding affinity for 5-HT4 receptor using [3H]GR-113808
ChEMBL 764 17 5 12 3.9 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCC(C(=O)NCCCCCC(=O)NC2CCN(CCOC(=O)c3cc(Cl)c(N)cc3O)CC2)CC1 10.1021/jm050234z
11813852 111525 0 None - 1 Human 8.2 pKi = 8.2 Binding
Binding affinity towards cloned human 5-hydroxytryptamine 4E receptor expressed in C6 glial cells using [3H]GR-113808 as radioligandBinding affinity towards cloned human 5-hydroxytryptamine 4E receptor expressed in C6 glial cells using [3H]GR-113808 as radioligand
ChEMBL 574 10 2 8 4.0 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCC(CNS(=O)(=O)c2cccc3c(N(C)C)cccc23)CC1 10.1021/jm0307887
CHEMBL328918 111525 0 None - 1 Human 8.2 pKi = 8.2 Binding
Binding affinity towards cloned human 5-hydroxytryptamine 4E receptor expressed in C6 glial cells using [3H]GR-113808 as radioligandBinding affinity towards cloned human 5-hydroxytryptamine 4E receptor expressed in C6 glial cells using [3H]GR-113808 as radioligand
ChEMBL 574 10 2 8 4.0 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCC(CNS(=O)(=O)c2cccc3c(N(C)C)cccc23)CC1 10.1021/jm0307887
11596009 73027 0 None - 1 Guinea pig 8.2 pKi = 8.2 Binding
Displacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatumDisplacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatum
ChEMBL 342 3 1 5 2.4 CC(C)n1c(=O)n(C(=O)NC[C@@H]2CCN3CCC[C@@H]23)c2ccccc21 10.1021/jm0509501
CHEMBL201414 73027 0 None - 1 Guinea pig 8.2 pKi = 8.2 Binding
Displacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatumDisplacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatum
ChEMBL 342 3 1 5 2.4 CC(C)n1c(=O)n(C(=O)NC[C@@H]2CCN3CCC[C@@H]23)c2ccccc21 10.1021/jm0509501
9800656 15375 0 None - 1 Human 8.2 pKi = 8.2 Binding
Binding affinity was determined against cloned 5-hydroxytryptamine 4D receptor isoform expressed in COS-7 cellsBinding affinity was determined against cloned 5-hydroxytryptamine 4D receptor isoform expressed in COS-7 cells
ChEMBL 391 6 1 8 1.7 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCN(c2ncccn2)CC1 10.1021/jm0009538
CHEMBL121913 15375 0 None - 1 Human 8.2 pKi = 8.2 Binding
Binding affinity was determined against cloned 5-hydroxytryptamine 4D receptor isoform expressed in COS-7 cellsBinding affinity was determined against cloned 5-hydroxytryptamine 4D receptor isoform expressed in COS-7 cells
ChEMBL 391 6 1 8 1.7 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCN(c2ncccn2)CC1 10.1021/jm0009538
49783211 17458 0 None - 1 Human 8.1 pKi = 8.1 Binding
Displacement of [3H]GR113808 from human recombinant 5HT4 receptor expressed in HEK293 cellsDisplacement of [3H]GR113808 from human recombinant 5HT4 receptor expressed in HEK293 cells
ChEMBL 488 7 1 6 3.8 CCCCN1CCC(COC(=O)c2cc(I)c(NC)c3c2OCCO3)CC1 10.1021/jm100668r
CHEMBL1258339 17458 0 None - 1 Human 8.1 pKi = 8.1 Binding
Displacement of [3H]GR113808 from human recombinant 5HT4 receptor expressed in HEK293 cellsDisplacement of [3H]GR113808 from human recombinant 5HT4 receptor expressed in HEK293 cells
ChEMBL 488 7 1 6 3.8 CCCCN1CCC(COC(=O)c2cc(I)c(NC)c3c2OCCO3)CC1 10.1021/jm100668r
11005668 204916 0 None - 1 Human 8.1 pKi = 8.1 Binding
Binding affinity towards cloned human 5-hydroxytryptamine 4E receptor expressed in C6 glial cells using [3H]GR-113808 as radioligandBinding affinity towards cloned human 5-hydroxytryptamine 4E receptor expressed in C6 glial cells using [3H]GR-113808 as radioligand
ChEMBL 504 9 2 11 3.4 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCC(CNc2ccc([N+](=O)[O-])c3nonc23)CC1 10.1021/jm0307887
CHEMBL89225 204916 0 None - 1 Human 8.1 pKi = 8.1 Binding
Binding affinity towards cloned human 5-hydroxytryptamine 4E receptor expressed in C6 glial cells using [3H]GR-113808 as radioligandBinding affinity towards cloned human 5-hydroxytryptamine 4E receptor expressed in C6 glial cells using [3H]GR-113808 as radioligand
ChEMBL 504 9 2 11 3.4 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCC(CNc2ccc([N+](=O)[O-])c3nonc23)CC1 10.1021/jm0307887
71462777 82552 0 None 1 4 Human 8.1 pKi = 8.1 Binding
Displacement of [3H]GR113808 from human recombinant 5HT4R expressed in HEK293T cellsDisplacement of [3H]GR113808 from human recombinant 5HT4R expressed in HEK293T cells
ChEMBL 335 5 0 4 4.3 CCCN1CCC(COc2nc3ccccc3c3ncccc23)CC1 10.1021/jm300943r
CHEMBL2181171 82552 0 None 1 4 Human 8.1 pKi = 8.1 Binding
Displacement of [3H]GR113808 from human recombinant 5HT4R expressed in HEK293T cellsDisplacement of [3H]GR113808 from human recombinant 5HT4R expressed in HEK293T cells
ChEMBL 335 5 0 4 4.3 CCCN1CCC(COc2nc3ccccc3c3ncccc23)CC1 10.1021/jm300943r
10788092 53306 0 None - 1 Rat 8.1 pKi = 8.1 Binding
Binding affinity towards 5-hydroxytryptamine 4 receptor was determined in rat striatal membranes using [3H]GR-113808 as radioligandBinding affinity towards 5-hydroxytryptamine 4 receptor was determined in rat striatal membranes using [3H]GR-113808 as radioligand
ChEMBL 416 7 1 6 3.7 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCC(C(=O)c2ccccc2)CC1 10.1021/jm960320m
CHEMBL160237 53306 0 None - 1 Rat 8.1 pKi = 8.1 Binding
Binding affinity towards 5-hydroxytryptamine 4 receptor was determined in rat striatal membranes using [3H]GR-113808 as radioligandBinding affinity towards 5-hydroxytryptamine 4 receptor was determined in rat striatal membranes using [3H]GR-113808 as radioligand
ChEMBL 416 7 1 6 3.7 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCC(C(=O)c2ccccc2)CC1 10.1021/jm960320m
162645470 178964 0 None 107 2 Guinea pig 8.1 pKi = 8.1 Binding
Displacement of [3H]-GR113808 from guinea pig brain 5HT4 receptor in presence of serotonin incubated for 30 minsDisplacement of [3H]-GR113808 from guinea pig brain 5HT4 receptor in presence of serotonin incubated for 30 mins
ChEMBL 536 11 3 7 3.5 COc1cc(N)c(Cl)cc1C(=O)CCC1CCN(CCNS(=O)(=O)c2ccc(NC(C)=O)cc2)CC1 10.1016/j.ejmech.2016.05.048
CHEMBL4741579 178964 0 None 107 2 Guinea pig 8.1 pKi = 8.1 Binding
Displacement of [3H]-GR113808 from guinea pig brain 5HT4 receptor in presence of serotonin incubated for 30 minsDisplacement of [3H]-GR113808 from guinea pig brain 5HT4 receptor in presence of serotonin incubated for 30 mins
ChEMBL 536 11 3 7 3.5 COc1cc(N)c(Cl)cc1C(=O)CCC1CCN(CCNS(=O)(=O)c2ccc(NC(C)=O)cc2)CC1 10.1016/j.ejmech.2016.05.048
10449091 119460 0 None - 1 Rat 8.1 pKi = 8.1 Binding
Binding affinity towards 5-hydroxytryptamine 4 receptor was determined in rat striatal membranes using [3H]GR-113808 as radioligandBinding affinity towards 5-hydroxytryptamine 4 receptor was determined in rat striatal membranes using [3H]GR-113808 as radioligand
ChEMBL 326 5 1 5 3.0 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCCCC1C 10.1021/jm960320m
CHEMBL349809 119460 0 None - 1 Rat 8.1 pKi = 8.1 Binding
Binding affinity towards 5-hydroxytryptamine 4 receptor was determined in rat striatal membranes using [3H]GR-113808 as radioligandBinding affinity towards 5-hydroxytryptamine 4 receptor was determined in rat striatal membranes using [3H]GR-113808 as radioligand
ChEMBL 326 5 1 5 3.0 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCCCC1C 10.1021/jm960320m
49780155 16959 0 None - 1 Human 8.1 pKi = 8.1 Binding
Displacement of [3H]GR113808 from human recombinant 5HT4 receptor expressed in HEK293 cellsDisplacement of [3H]GR113808 from human recombinant 5HT4 receptor expressed in HEK293 cells
ChEMBL 393 7 1 8 2.6 CCCCN1CCC(COC(=O)c2cc([N+](=O)[O-])c(N)c3c2OCCO3)CC1 10.1021/jm100668r
CHEMBL1255606 16959 0 None - 1 Human 8.1 pKi = 8.1 Binding
Displacement of [3H]GR113808 from human recombinant 5HT4 receptor expressed in HEK293 cellsDisplacement of [3H]GR113808 from human recombinant 5HT4 receptor expressed in HEK293 cells
ChEMBL 393 7 1 8 2.6 CCCCN1CCC(COC(=O)c2cc([N+](=O)[O-])c(N)c3c2OCCO3)CC1 10.1021/jm100668r
44629280 82313 0 None - 1 Human 8.1 pKi = 8.1 Binding
Displacement of [3H](1-(2-(methylsulfonamido)ethyl)piperidin-4-yl)methyl 1-methyl-1H-indole-3-carboxylate from human 5HT4R expressed in HEK293 cellsDisplacement of [3H](1-(2-(methylsulfonamido)ethyl)piperidin-4-yl)methyl 1-methyl-1H-indole-3-carboxylate from human 5HT4R expressed in HEK293 cells
ChEMBL 351 6 0 4 4.6 CCCCN1CCC(COc2nc3ccccc3c3cn(C)cc23)CC1 10.1021/jm300573d
CHEMBL2179679 82313 0 None - 1 Human 8.1 pKi = 8.1 Binding
Displacement of [3H](1-(2-(methylsulfonamido)ethyl)piperidin-4-yl)methyl 1-methyl-1H-indole-3-carboxylate from human 5HT4R expressed in HEK293 cellsDisplacement of [3H](1-(2-(methylsulfonamido)ethyl)piperidin-4-yl)methyl 1-methyl-1H-indole-3-carboxylate from human 5HT4R expressed in HEK293 cells
ChEMBL 351 6 0 4 4.6 CCCCN1CCC(COc2nc3ccccc3c3cn(C)cc23)CC1 10.1021/jm300573d
11627949 76068 0 None - 1 Human 8.1 pKi = 8.1 Binding
Displacement of [3H]GR113808 from human recombinant 5HT4C receptor expressed in HEK293 cellsDisplacement of [3H]GR113808 from human recombinant 5HT4C receptor expressed in HEK293 cells
ChEMBL 532 8 2 8 1.3 CC(C)n1nc(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3C[C@H](O)CN2CCN(S(C)(=O)=O)CC2)c2ccccc21 10.1016/j.bmcl.2012.05.034
CHEMBL2059587 76068 0 None - 1 Human 8.1 pKi = 8.1 Binding
Displacement of [3H]GR113808 from human recombinant 5HT4C receptor expressed in HEK293 cellsDisplacement of [3H]GR113808 from human recombinant 5HT4C receptor expressed in HEK293 cells
ChEMBL 532 8 2 8 1.3 CC(C)n1nc(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3C[C@H](O)CN2CCN(S(C)(=O)=O)CC2)c2ccccc21 10.1016/j.bmcl.2012.05.034
44248193 193141 0 None - 1 Human 8.1 pKi = 8.1 Binding
Displacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 593 12 1 7 5.0 CCOC(=O)N1CCN(CCCCCCCN2[C@H]3CC[C@@H]2C[C@H](NC(=O)c2cc4ccccc4n(C(C)C)c2=O)C3)CC1 10.1021/jm900881j
CHEMBL538956 193141 0 None - 1 Human 8.1 pKi = 8.1 Binding
Displacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 593 12 1 7 5.0 CCOC(=O)N1CCN(CCCCCCCN2[C@H]3CC[C@@H]2C[C@H](NC(=O)c2cc4ccccc4n(C(C)C)c2=O)C3)CC1 10.1021/jm900881j
21252890 193805 1 None - 1 Human 8.1 pKi = 8.1 Binding
Displacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 300 4 2 4 2.3 CC(C)n1nc(C(=O)NCC2CCNCC2)c2ccccc21 10.1021/jm900881j
CHEMBL552796 193805 1 None - 1 Human 8.1 pKi = 8.1 Binding
Displacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 300 4 2 4 2.3 CC(C)n1nc(C(=O)NCC2CCNCC2)c2ccccc21 10.1021/jm900881j
44248321 193908 0 None - 1 Human 8.1 pKi = 8.1 Binding
Displacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 541 8 1 6 4.5 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CCCN2CCN(c3ccccc3)CC2)cc2ccccc21 10.1021/jm900881j
CHEMBL555222 193908 0 None - 1 Human 8.1 pKi = 8.1 Binding
Displacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 541 8 1 6 4.5 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CCCN2CCN(c3ccccc3)CC2)cc2ccccc21 10.1021/jm900881j
235 2527 36 None -4 3 Human 8.1 pKi = 8.1 Binding
Binding affinity was determined against cloned 5-hydroxytryptamine 4C receptor isoform expressed in COS-7 cellsBinding affinity was determined against cloned 5-hydroxytryptamine 4C receptor isoform expressed in COS-7 cells
ChEMBL 312 5 1 5 2.6 COc1cc(N)c(cc1C(=O)OCCN1CCCCC1)Cl 10.1021/jm0009538
5311299 2527 36 None -4 3 Human 8.1 pKi = 8.1 Binding
Binding affinity was determined against cloned 5-hydroxytryptamine 4C receptor isoform expressed in COS-7 cellsBinding affinity was determined against cloned 5-hydroxytryptamine 4C receptor isoform expressed in COS-7 cells
ChEMBL 312 5 1 5 2.6 COc1cc(N)c(cc1C(=O)OCCN1CCCCC1)Cl 10.1021/jm0009538
CHEMBL286136 2527 36 None -4 3 Human 8.1 pKi = 8.1 Binding
Binding affinity was determined against cloned 5-hydroxytryptamine 4C receptor isoform expressed in COS-7 cellsBinding affinity was determined against cloned 5-hydroxytryptamine 4C receptor isoform expressed in COS-7 cells
ChEMBL 312 5 1 5 2.6 COc1cc(N)c(cc1C(=O)OCCN1CCCCC1)Cl 10.1021/jm0009538
10717193 16603 0 None - 1 Human 6.2 pKi = 6.2 Binding
Binding affinity was determined against cloned 5-hydroxytryptamine 4E receptor isoform expressed in C6 glial cells incubated with 0.2 nM [3H]GR-113808Binding affinity was determined against cloned 5-hydroxytryptamine 4E receptor isoform expressed in C6 glial cells incubated with 0.2 nM [3H]GR-113808
ChEMBL 423 6 1 6 3.6 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCN(c2ccc(Cl)cc2)CC1 10.1021/jm0009538
CHEMBL124485 16603 0 None - 1 Human 6.2 pKi = 6.2 Binding
Binding affinity was determined against cloned 5-hydroxytryptamine 4E receptor isoform expressed in C6 glial cells incubated with 0.2 nM [3H]GR-113808Binding affinity was determined against cloned 5-hydroxytryptamine 4E receptor isoform expressed in C6 glial cells incubated with 0.2 nM [3H]GR-113808
ChEMBL 423 6 1 6 3.6 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCN(c2ccc(Cl)cc2)CC1 10.1021/jm0009538
15544714 65951 4 None - 1 Rat 6.1 pKi = 6.1 Binding
Binding affinity to 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatum membraneBinding affinity to 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatum membrane
ChEMBL 258 2 2 3 1.4 CN1CCC(NC(=O)c2cccc3[nH]cnc23)CC1 10.1021/jm020807x
CHEMBL18473 65951 4 None - 1 Rat 6.1 pKi = 6.1 Binding
Binding affinity to 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatum membraneBinding affinity to 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatum membrane
ChEMBL 258 2 2 3 1.4 CN1CCC(NC(=O)c2cccc3[nH]cnc23)CC1 10.1021/jm020807x
15544714 65951 4 None - 1 Rat 6.1 pKi = 6.1 Binding
Displacement of [3H]GR-113808 from rat striatum 5-hydroxytryptamine 4 receptorDisplacement of [3H]GR-113808 from rat striatum 5-hydroxytryptamine 4 receptor
ChEMBL 258 2 2 3 1.4 CN1CCC(NC(=O)c2cccc3[nH]cnc23)CC1 10.1016/0960-894X(96)00200-4
CHEMBL18473 65951 4 None - 1 Rat 6.1 pKi = 6.1 Binding
Displacement of [3H]GR-113808 from rat striatum 5-hydroxytryptamine 4 receptorDisplacement of [3H]GR-113808 from rat striatum 5-hydroxytryptamine 4 receptor
ChEMBL 258 2 2 3 1.4 CN1CCC(NC(=O)c2cccc3[nH]cnc23)CC1 10.1016/0960-894X(96)00200-4
15544714 65951 4 None - 1 Rat 6.1 pKi = 6.1 Binding
In vitro binding affinity to 5-hydroxytryptamine 4 receptor in rat striatum membraneIn vitro binding affinity to 5-hydroxytryptamine 4 receptor in rat striatum membrane
ChEMBL 258 2 2 3 1.4 CN1CCC(NC(=O)c2cccc3[nH]cnc23)CC1 10.1016/s0960-894x(01)00517-0
CHEMBL18473 65951 4 None - 1 Rat 6.1 pKi = 6.1 Binding
In vitro binding affinity to 5-hydroxytryptamine 4 receptor in rat striatum membraneIn vitro binding affinity to 5-hydroxytryptamine 4 receptor in rat striatum membrane
ChEMBL 258 2 2 3 1.4 CN1CCC(NC(=O)c2cccc3[nH]cnc23)CC1 10.1016/s0960-894x(01)00517-0
1471834 3572 36 None -4 3 Human 7.1 pKi = 7.1 Binding
Binding affinity to human 5HT4Binding affinity to human 5HT4
ChEMBL 366 2 0 2 5.5 O=C1C(=Nc2cccc(c2)C(F)(F)F)c2c(N1c1ccccc1)cccc2 10.1021/jm060001n
6126 3572 36 None -4 3 Human 7.1 pKi = 7.1 Binding
Binding affinity to human 5HT4Binding affinity to human 5HT4
ChEMBL 366 2 0 2 5.5 O=C1C(=Nc2cccc(c2)C(F)(F)F)c2c(N1c1ccccc1)cccc2 10.1021/jm060001n
CHEMBL210288 3572 36 None -4 3 Human 7.1 pKi = 7.1 Binding
Binding affinity to human 5HT4Binding affinity to human 5HT4
ChEMBL 366 2 0 2 5.5 O=C1C(=Nc2cccc(c2)C(F)(F)F)c2c(N1c1ccccc1)cccc2 10.1021/jm060001n
15544714 65951 4 None - 1 Rat 6.1 pKi = 6.1 Binding
pKi against 5-hydroxytryptamine 4 receptor in rat striatum membranepKi against 5-hydroxytryptamine 4 receptor in rat striatum membrane
ChEMBL 258 2 2 3 1.4 CN1CCC(NC(=O)c2cccc3[nH]cnc23)CC1 10.1016/s0960-894x(01)00517-0
CHEMBL18473 65951 4 None - 1 Rat 6.1 pKi = 6.1 Binding
pKi against 5-hydroxytryptamine 4 receptor in rat striatum membranepKi against 5-hydroxytryptamine 4 receptor in rat striatum membrane
ChEMBL 258 2 2 3 1.4 CN1CCC(NC(=O)c2cccc3[nH]cnc23)CC1 10.1016/s0960-894x(01)00517-0
30049 187620 1 None - 1 Rat 6.1 pKi = 6.1 Binding
Binding affinity at 5-hydroxytryptamine 4 receptor in rat striatal membranes by [3H]GR-113808 displacement.Binding affinity at 5-hydroxytryptamine 4 receptor in rat striatal membranes by [3H]GR-113808 displacement.
ChEMBL 282 4 1 3 3.4 O=C(Nc1ccc(Cl)cc1)OCCN1CCCCC1 10.1021/jm960853v
CHEMBL49907 187620 1 None - 1 Rat 6.1 pKi = 6.1 Binding
Binding affinity at 5-hydroxytryptamine 4 receptor in rat striatal membranes by [3H]GR-113808 displacement.Binding affinity at 5-hydroxytryptamine 4 receptor in rat striatal membranes by [3H]GR-113808 displacement.
ChEMBL 282 4 1 3 3.4 O=C(Nc1ccc(Cl)cc1)OCCN1CCCCC1 10.1021/jm960853v
15485875 188143 0 None - 1 Guinea pig 7.1 pKi = 7.1 Binding
Displacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatum membraneDisplacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatum membrane
ChEMBL 301 5 0 5 3.4 c1cc2c(OCCCN3CCCC3)nc3ccsc3n2c1 10.1016/j.bmc.2008.11.045
CHEMBL504904 188143 0 None - 1 Guinea pig 7.1 pKi = 7.1 Binding
Displacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatum membraneDisplacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatum membrane
ChEMBL 301 5 0 5 3.4 c1cc2c(OCCCN3CCCC3)nc3ccsc3n2c1 10.1016/j.bmc.2008.11.045
10664258 206627 0 None - 1 Guinea pig 7.1 pKi = 7.1 Binding
Binding affinity against 5-hydroxytryptamine 4 receptor in guinea pig striatum using [3H]GR-113808 as radioligandBinding affinity against 5-hydroxytryptamine 4 receptor in guinea pig striatum using [3H]GR-113808 as radioligand
ChEMBL 331 4 1 6 0.6 CCn1c(=O)n(C(=O)NCCN2CCN(C)CC2)c2ccccc21 10.1021/jm981098j
CHEMBL99515 206627 0 None - 1 Guinea pig 7.1 pKi = 7.1 Binding
Binding affinity against 5-hydroxytryptamine 4 receptor in guinea pig striatum using [3H]GR-113808 as radioligandBinding affinity against 5-hydroxytryptamine 4 receptor in guinea pig striatum using [3H]GR-113808 as radioligand
ChEMBL 331 4 1 6 0.6 CCn1c(=O)n(C(=O)NCCN2CCN(C)CC2)c2ccccc21 10.1021/jm981098j
90665998 108796 0 None - 1 Guinea pig 7.1 pKi = 7.1 Binding
Displacement of [3H]-GR113808 from guinea pig 5HT4 receptor by Grossman's methodDisplacement of [3H]-GR113808 from guinea pig 5HT4 receptor by Grossman's method
ChEMBL 405 7 0 5 5.3 c1ccc(CCCN2CCC(COc3nc4ccsc4n4cccc34)CC2)cc1 10.1039/C2MD20063E
CHEMBL3218870 108796 0 None - 1 Guinea pig 7.1 pKi = 7.1 Binding
Displacement of [3H]-GR113808 from guinea pig 5HT4 receptor by Grossman's methodDisplacement of [3H]-GR113808 from guinea pig 5HT4 receptor by Grossman's method
ChEMBL 405 7 0 5 5.3 c1ccc(CCCN2CCC(COc3nc4ccsc4n4cccc34)CC2)cc1 10.1039/C2MD20063E
108182 4068 18 None -1 16 Rat 6.1 pKi = 6.1 Binding
Binding affinity against 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatumBinding affinity against 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatum
ChEMBL 309 3 2 4 1.8 COc1cc(N)c(cc1C(=O)NC1CN2CCC1CC2)Cl 10.1016/S0960-894X(01)80508-4
245 4068 18 None -1 16 Rat 6.1 pKi = 6.1 Binding
Binding affinity against 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatumBinding affinity against 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatum
ChEMBL 309 3 2 4 1.8 COc1cc(N)c(cc1C(=O)NC1CN2CCC1CC2)Cl 10.1016/S0960-894X(01)80508-4
CHEMBL18041 4068 18 None -1 16 Rat 6.1 pKi = 6.1 Binding
Binding affinity against 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatumBinding affinity against 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatum
ChEMBL 309 3 2 4 1.8 COc1cc(N)c(cc1C(=O)NC1CN2CCC1CC2)Cl 10.1016/S0960-894X(01)80508-4
139188853 166329 0 None - 1 Guinea pig 7.1 pKi = 7.1 Binding
Displacement of [3H]-GR113808 from 5-HT4R in Dunkin-Hartley guinea pig straitum nuclear membranes after 2 hrs by filter binding methodDisplacement of [3H]-GR113808 from 5-HT4R in Dunkin-Hartley guinea pig straitum nuclear membranes after 2 hrs by filter binding method
ChEMBL 341 6 2 4 3.2 CCCCN1CCC(CNC(=O)c2ccc3cccc(O)c3n2)CC1 10.1039/C8MD00233A
CHEMBL4285988 166329 0 None - 1 Guinea pig 7.1 pKi = 7.1 Binding
Displacement of [3H]-GR113808 from 5-HT4R in Dunkin-Hartley guinea pig straitum nuclear membranes after 2 hrs by filter binding methodDisplacement of [3H]-GR113808 from 5-HT4R in Dunkin-Hartley guinea pig straitum nuclear membranes after 2 hrs by filter binding method
ChEMBL 341 6 2 4 3.2 CCCCN1CCC(CNC(=O)c2ccc3cccc(O)c3n2)CC1 10.1039/C8MD00233A
11966400 205117 0 None - 1 Human 7.1 pKi = 7.1 Binding
Binding affinity towards cloned human 5-hydroxytryptamine 4E receptor expressed in C6 glial cells using [3H]GR-113808 as radioligandBinding affinity towards cloned human 5-hydroxytryptamine 4E receptor expressed in C6 glial cells using [3H]GR-113808 as radioligand
ChEMBL 588 11 2 8 4.4 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCC(CCNS(=O)(=O)c2cccc3c(N(C)C)cccc23)CC1 10.1021/jm0307887
CHEMBL90559 205117 0 None - 1 Human 7.1 pKi = 7.1 Binding
Binding affinity towards cloned human 5-hydroxytryptamine 4E receptor expressed in C6 glial cells using [3H]GR-113808 as radioligandBinding affinity towards cloned human 5-hydroxytryptamine 4E receptor expressed in C6 glial cells using [3H]GR-113808 as radioligand
ChEMBL 588 11 2 8 4.4 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCC(CCNS(=O)(=O)c2cccc3c(N(C)C)cccc23)CC1 10.1021/jm0307887
10779499 37841 0 None - 1 Rat 6.1 pKi = 6.1 Binding
In vitro affinity at serotonergic 5-hydroxytryptamine 4 receptor by radioligand binding assay using [3H]GR-113808 in rat striatum membranes.In vitro affinity at serotonergic 5-hydroxytryptamine 4 receptor by radioligand binding assay using [3H]GR-113808 in rat striatum membranes.
ChEMBL 285 2 3 4 1.0 Nc1ccc(C(=O)NC2CN3CCC2CC3)c2[nH]cnc12 10.1021/jm991076c
CHEMBL146068 37841 0 None - 1 Rat 6.1 pKi = 6.1 Binding
In vitro affinity at serotonergic 5-hydroxytryptamine 4 receptor by radioligand binding assay using [3H]GR-113808 in rat striatum membranes.In vitro affinity at serotonergic 5-hydroxytryptamine 4 receptor by radioligand binding assay using [3H]GR-113808 in rat striatum membranes.
ChEMBL 285 2 3 4 1.0 Nc1ccc(C(=O)NC2CN3CCC2CC3)c2[nH]cnc12 10.1021/jm991076c
44247808 193709 0 None - 1 Human 7.1 pKi = 7.1 Binding
Displacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 395 10 2 4 4.5 CCCCCCCCN1CCC(NC(=O)c2cc(Cl)c(N)cc2OC)CC1 10.1021/jm900881j
CHEMBL551940 193709 0 None - 1 Human 7.1 pKi = 7.1 Binding
Displacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 395 10 2 4 4.5 CCCCCCCCN1CCC(NC(=O)c2cc(Cl)c(N)cc2OC)CC1 10.1021/jm900881j
44247813 193919 0 None - 1 Human 7.1 pKi = 7.1 Binding
Displacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 411 11 3 5 3.5 COc1cc(N)c(Cl)cc1C(=O)NC1CCN(CCCCCCCCO)CC1 10.1021/jm900881j
CHEMBL555447 193919 0 None - 1 Human 7.1 pKi = 7.1 Binding
Displacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 411 11 3 5 3.5 COc1cc(N)c(Cl)cc1C(=O)NC1CCN(CCCCCCCCO)CC1 10.1021/jm900881j
10837280 91900491 194149 0 None - 1 Human 7.1 pKi = 7.1 Binding
Displacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 450 6 1 5 3.8 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CCN2CCCCC2)cc2ccccc21 10.1021/jm900881j
CHEMBL558259 194149 0 None - 1 Human 7.1 pKi = 7.1 Binding
Displacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 450 6 1 5 3.8 CC(C)n1c(=O)c(C(=O)N[C@@H]2C[C@@H]3CC[C@H](C2)N3CCN2CCCCC2)cc2ccccc21 10.1021/jm900881j
9857899 121659 0 None - 1 Guinea pig 7.1 pKi = 7.1 Binding
Ability to displace [3H]GR-113808 from 5-hydroxytryptamine 4 receptorAbility to displace [3H]GR-113808 from 5-hydroxytryptamine 4 receptor
ChEMBL 311 3 1 4 3.3 CN1CCC(COc2nc3ccccc3c3c2CCCN3)CC1 10.1021/jm020954v
CHEMBL35972 121659 0 None - 1 Guinea pig 7.1 pKi = 7.1 Binding
Ability to displace [3H]GR-113808 from 5-hydroxytryptamine 4 receptorAbility to displace [3H]GR-113808 from 5-hydroxytryptamine 4 receptor
ChEMBL 311 3 1 4 3.3 CN1CCC(COc2nc3ccccc3c3c2CCCN3)CC1 10.1021/jm020954v
90666007 108803 0 None - 1 Guinea pig 7.1 pKi = 7.1 Binding
Displacement of [3H]-GR113808 from guinea pig 5HT4 receptor by Grossman's methodDisplacement of [3H]-GR113808 from guinea pig 5HT4 receptor by Grossman's method
ChEMBL 383 5 0 5 5.2 c1cc2c(OCC3CCN(CC4CCCCC4)CC3)nc3ccsc3n2c1 10.1039/C2MD20063E
CHEMBL3218879 108803 0 None - 1 Guinea pig 7.1 pKi = 7.1 Binding
Displacement of [3H]-GR113808 from guinea pig 5HT4 receptor by Grossman's methodDisplacement of [3H]-GR113808 from guinea pig 5HT4 receptor by Grossman's method
ChEMBL 383 5 0 5 5.2 c1cc2c(OCC3CCN(CC4CCCCC4)CC3)nc3ccsc3n2c1 10.1039/C2MD20063E
73354085 92439 0 None -1 2 Guinea pig 6.1 pKi = 6.1 Binding
Displacement of [125I]SB207710 from 5-HT4 receptor in guinea pig brain membranesDisplacement of [125I]SB207710 from 5-HT4 receptor in guinea pig brain membranes
ChEMBL 385 6 2 5 3.4 CCCCN1CCC(CNC(=O)c2c3n(c4cc(O)ccc24)CCCO3)CC1 10.1016/j.bmc.2013.09.004
CHEMBL2440451 92439 0 None -1 2 Guinea pig 6.1 pKi = 6.1 Binding
Displacement of [125I]SB207710 from 5-HT4 receptor in guinea pig brain membranesDisplacement of [125I]SB207710 from 5-HT4 receptor in guinea pig brain membranes
ChEMBL 385 6 2 5 3.4 CCCCN1CCC(CNC(=O)c2c3n(c4cc(O)ccc24)CCCO3)CC1 10.1016/j.bmc.2013.09.004
73354085 92439 0 None 1 2 Human 6.1 pKi = 6.1 Binding
Displacement of [125I]SB207710 from human recombinant 5-HT4 receptorDisplacement of [125I]SB207710 from human recombinant 5-HT4 receptor
ChEMBL 385 6 2 5 3.4 CCCCN1CCC(CNC(=O)c2c3n(c4cc(O)ccc24)CCCO3)CC1 10.1016/j.bmc.2013.09.004
CHEMBL2440451 92439 0 None 1 2 Human 6.1 pKi = 6.1 Binding
Displacement of [125I]SB207710 from human recombinant 5-HT4 receptorDisplacement of [125I]SB207710 from human recombinant 5-HT4 receptor
ChEMBL 385 6 2 5 3.4 CCCCN1CCC(CNC(=O)c2c3n(c4cc(O)ccc24)CCCO3)CC1 10.1016/j.bmc.2013.09.004
44249186 193646 0 None - 1 Human 6.1 pKi = 6.1 Binding
Displacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 327 4 2 4 2.3 CC(C)n1c(=O)c(C(=O)NCC2CCNCC2)cc2ccccc21 10.1021/jm900881j
CHEMBL551535 193646 0 None - 1 Human 6.1 pKi = 6.1 Binding
Displacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 327 4 2 4 2.3 CC(C)n1c(=O)c(C(=O)NCC2CCNCC2)cc2ccccc21 10.1021/jm900881j
44247815 194801 0 None - 1 Human 5.1 pKi = 5.1 Binding
Displacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 456 6 2 6 2.4 COc1cc(N)c(Cl)cc1C(=O)NC1CCN(CCN2C(=O)c3ccccc3C2=O)CC1 10.1021/jm900881j
CHEMBL563276 194801 0 None - 1 Human 5.1 pKi = 5.1 Binding
Displacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation countingDisplacement of [H]GR-113808 from human 5HT4C receptor expressed in HEK293 cells by liquid scintillation counting
ChEMBL 456 6 2 6 2.4 COc1cc(N)c(Cl)cc1C(=O)NC1CCN(CCN2C(=O)c3ccccc3C2=O)CC1 10.1021/jm900881j
24865727 192511 0 None -5011 11 Human 5.1 pKi = 5.1 Binding
Displacement of radioligand from human cloned 5HT4 receptorDisplacement of radioligand from human cloned 5HT4 receptor
ChEMBL 479 7 0 5 4.4 Cc1ccc2c(OCCN3CCC(Cc4cccc(N5CCCS5(=O)=O)c4)CC3)cccc2n1 10.1021/jm8001444
CHEMBL522708 192511 0 None -5011 11 Human 5.1 pKi = 5.1 Binding
Displacement of radioligand from human cloned 5HT4 receptorDisplacement of radioligand from human cloned 5HT4 receptor
ChEMBL 479 7 0 5 4.4 Cc1ccc2c(OCCN3CCC(Cc4cccc(N5CCCS5(=O)=O)c4)CC3)cccc2n1 10.1021/jm8001444
11686414 71405 0 None - 1 Human 8.1 pKi = 8.1 Binding
Binding affinity for 5-HT4 receptor using [3H]GR-113808Binding affinity for 5-HT4 receptor using [3H]GR-113808
ChEMBL 764 17 4 12 3.6 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCC(CNC(=O)CCC(=O)NCC2CCN(CCOC(=O)c3cc(Cl)c(N)cc3OC)CC2)CC1 10.1021/jm050234z
CHEMBL196633 71405 0 None - 1 Human 8.1 pKi = 8.1 Binding
Binding affinity for 5-HT4 receptor using [3H]GR-113808Binding affinity for 5-HT4 receptor using [3H]GR-113808
ChEMBL 764 17 4 12 3.6 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCC(CNC(=O)CCC(=O)NCC2CCN(CCOC(=O)c3cc(Cl)c(N)cc3OC)CC2)CC1 10.1021/jm050234z
44404966 132928 0 None - 1 Human 8.1 pKi = 8.1 Binding
Binding affinity for 5-HT4 receptor using [3H]GR-113808Binding affinity for 5-HT4 receptor using [3H]GR-113808
ChEMBL 834 22 5 12 5.7 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCC(C(=O)NCCCCCCCCCCNC(=O)C2CCN(CCOC(=O)c3cc(Cl)c(N)cc3O)CC2)CC1 10.1021/jm050234z
CHEMBL370646 132928 0 None - 1 Human 8.1 pKi = 8.1 Binding
Binding affinity for 5-HT4 receptor using [3H]GR-113808Binding affinity for 5-HT4 receptor using [3H]GR-113808
ChEMBL 834 22 5 12 5.7 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCC(C(=O)NCCCCCCCCCCNC(=O)C2CCN(CCOC(=O)c3cc(Cl)c(N)cc3O)CC2)CC1 10.1021/jm050234z
145990064 166416 0 None - 1 Guinea pig 8.1 pKi = 8.1 Binding
Displacement of [3H]-GR113808 from 5-HT4R in Dunkin-Hartley guinea pig straitum nuclear membranes after 2 hrs by filter binding methodDisplacement of [3H]-GR113808 from 5-HT4R in Dunkin-Hartley guinea pig straitum nuclear membranes after 2 hrs by filter binding method
ChEMBL 344 6 1 6 2.1 COc1cc(C(=O)OCCN2CCC(CO)CC2)c2ccccc2n1 10.1039/C8MD00233A
CHEMBL4287473 166416 0 None - 1 Guinea pig 8.1 pKi = 8.1 Binding
Displacement of [3H]-GR113808 from 5-HT4R in Dunkin-Hartley guinea pig straitum nuclear membranes after 2 hrs by filter binding methodDisplacement of [3H]-GR113808 from 5-HT4R in Dunkin-Hartley guinea pig straitum nuclear membranes after 2 hrs by filter binding method
ChEMBL 344 6 1 6 2.1 COc1cc(C(=O)OCCN2CCC(CO)CC2)c2ccccc2n1 10.1039/C8MD00233A
9800656 15375 0 None - 1 Human 8.1 pKi = 8.1 Binding
Binding affinity was determined against cloned 5-hydroxytryptamine 4B receptor isoform expressed in COS-7 cellsBinding affinity was determined against cloned 5-hydroxytryptamine 4B receptor isoform expressed in COS-7 cells
ChEMBL 391 6 1 8 1.7 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCN(c2ncccn2)CC1 10.1021/jm0009538
CHEMBL121913 15375 0 None - 1 Human 8.1 pKi = 8.1 Binding
Binding affinity was determined against cloned 5-hydroxytryptamine 4B receptor isoform expressed in COS-7 cellsBinding affinity was determined against cloned 5-hydroxytryptamine 4B receptor isoform expressed in COS-7 cells
ChEMBL 391 6 1 8 1.7 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCN(c2ncccn2)CC1 10.1021/jm0009538
11726706 205990 0 None - 1 Guinea pig 8.1 pKi = 8.1 Binding
Binding affinity against 5-hydroxytryptamine 4 receptor in guinea pig striatum using [3H]GR-113808 as radioligandBinding affinity against 5-hydroxytryptamine 4 receptor in guinea pig striatum using [3H]GR-113808 as radioligand
ChEMBL 371 6 1 6 1.7 CCCN1CCN(CCNC(=O)n2c(=O)n(C3CC3)c3ccccc32)CC1 10.1021/jm981098j
CHEMBL95661 205990 0 None - 1 Guinea pig 8.1 pKi = 8.1 Binding
Binding affinity against 5-hydroxytryptamine 4 receptor in guinea pig striatum using [3H]GR-113808 as radioligandBinding affinity against 5-hydroxytryptamine 4 receptor in guinea pig striatum using [3H]GR-113808 as radioligand
ChEMBL 371 6 1 6 1.7 CCCN1CCN(CCNC(=O)n2c(=O)n(C3CC3)c3ccccc32)CC1 10.1021/jm981098j
162658420 180518 0 None - 1 Guinea pig 8.1 pKi = 8.1 Binding
Displacement of [3H]-GR113808 from guinea pig brain 5HT4 receptor in presence of serotonin incubated for 30 minsDisplacement of [3H]-GR113808 from guinea pig brain 5HT4 receptor in presence of serotonin incubated for 30 mins
ChEMBL 539 12 2 8 3.6 COc1ccc(S(=O)(=O)NCCN2CCC(CCC(=O)c3cc(Cl)c(N)cc3OC)CC2)cc1OC 10.1016/j.ejmech.2016.05.048
CHEMBL4760149 180518 0 None - 1 Guinea pig 8.1 pKi = 8.1 Binding
Displacement of [3H]-GR113808 from guinea pig brain 5HT4 receptor in presence of serotonin incubated for 30 minsDisplacement of [3H]-GR113808 from guinea pig brain 5HT4 receptor in presence of serotonin incubated for 30 mins
ChEMBL 539 12 2 8 3.6 COc1ccc(S(=O)(=O)NCCN2CCC(CCC(=O)c3cc(Cl)c(N)cc3OC)CC2)cc1OC 10.1016/j.ejmech.2016.05.048
118734514 118165 0 None - 1 Guinea pig 8.1 pKi = 8.1 Binding
Displacement of [3H]GR113808 from 5-HT4R in guinea pig brain membranes incubated for 30 mins by radioligand binding assayDisplacement of [3H]GR113808 from 5-HT4R in guinea pig brain membranes incubated for 30 mins by radioligand binding assay
ChEMBL 406 8 1 4 5.6 COc1cc(N)c(Cl)cc1C(=O)CCC1CCN(CCC2CCCCC2)CC1 10.1021/acs.jmedchem.5b00115
CHEMBL3416999 118165 0 None - 1 Guinea pig 8.1 pKi = 8.1 Binding
Displacement of [3H]GR113808 from 5-HT4R in guinea pig brain membranes incubated for 30 mins by radioligand binding assayDisplacement of [3H]GR113808 from 5-HT4R in guinea pig brain membranes incubated for 30 mins by radioligand binding assay
ChEMBL 406 8 1 4 5.6 COc1cc(N)c(Cl)cc1C(=O)CCC1CCN(CCC2CCCCC2)CC1 10.1021/acs.jmedchem.5b00115
44323264 205383 0 None - 1 Rat 8.1 pKi = 8.1 Binding
Binding affinity at 5-hydroxytryptamine 4 receptor in rat striatum by [3H]GR-113808 displacement.Binding affinity at 5-hydroxytryptamine 4 receptor in rat striatum by [3H]GR-113808 displacement.
ChEMBL 322 2 1 5 2.1 Nc1c(Cl)cc(C(=O)O[C@@H]2CN3CCC2CC3)c2c1CCO2 10.1016/0960-894X(96)00002-9
CHEMBL92100 205383 0 None - 1 Rat 8.1 pKi = 8.1 Binding
Binding affinity at 5-hydroxytryptamine 4 receptor in rat striatum by [3H]GR-113808 displacement.Binding affinity at 5-hydroxytryptamine 4 receptor in rat striatum by [3H]GR-113808 displacement.
ChEMBL 322 2 1 5 2.1 Nc1c(Cl)cc(C(=O)O[C@@H]2CN3CCC2CC3)c2c1CCO2 10.1016/0960-894X(96)00002-9
235 2527 36 None -4 3 Human 8.1 pKi = 8.1 Binding
Binding affinity was determined against cloned 5-hydroxytryptamine 4A receptor isoform expressed in COS-7 cellsBinding affinity was determined against cloned 5-hydroxytryptamine 4A receptor isoform expressed in COS-7 cells
ChEMBL 312 5 1 5 2.6 COc1cc(N)c(cc1C(=O)OCCN1CCCCC1)Cl 10.1021/jm0009538
5311299 2527 36 None -4 3 Human 8.1 pKi = 8.1 Binding
Binding affinity was determined against cloned 5-hydroxytryptamine 4A receptor isoform expressed in COS-7 cellsBinding affinity was determined against cloned 5-hydroxytryptamine 4A receptor isoform expressed in COS-7 cells
ChEMBL 312 5 1 5 2.6 COc1cc(N)c(cc1C(=O)OCCN1CCCCC1)Cl 10.1021/jm0009538
CHEMBL286136 2527 36 None -4 3 Human 8.1 pKi = 8.1 Binding
Binding affinity was determined against cloned 5-hydroxytryptamine 4A receptor isoform expressed in COS-7 cellsBinding affinity was determined against cloned 5-hydroxytryptamine 4A receptor isoform expressed in COS-7 cells
ChEMBL 312 5 1 5 2.6 COc1cc(N)c(cc1C(=O)OCCN1CCCCC1)Cl 10.1021/jm0009538
44592281 188829 0 None - 1 Guinea pig 8.1 pKi = 8.1 Binding
Displacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatum membraneDisplacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatum membrane
ChEMBL 341 5 0 5 4.1 C=CCN1CCC(COc2nc3scc(C)c3n3cccc23)CC1 10.1016/j.bmc.2008.11.045
CHEMBL513254 188829 0 None - 1 Guinea pig 8.1 pKi = 8.1 Binding
Displacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatum membraneDisplacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatum membrane
ChEMBL 341 5 0 5 4.1 C=CCN1CCC(COc2nc3scc(C)c3n3cccc23)CC1 10.1016/j.bmc.2008.11.045
162675700 182879 0 None 16 2 Guinea pig 8.1 pKi = 8.1 Binding
Displacement of [3H]-GR113808 from guinea pig brain 5HT4 receptor in presence of serotonin incubated for 30 minsDisplacement of [3H]-GR113808 from guinea pig brain 5HT4 receptor in presence of serotonin incubated for 30 mins
ChEMBL 650 10 3 7 4.7 COc1cc(N)c(Cl)cc1C(=O)CCC1CCN(CCNS(=O)(=O)c2cc(Br)c(N)c(Br)c2)CC1 10.1016/j.ejmech.2016.05.048
CHEMBL4799043 182879 0 None 16 2 Guinea pig 8.1 pKi = 8.1 Binding
Displacement of [3H]-GR113808 from guinea pig brain 5HT4 receptor in presence of serotonin incubated for 30 minsDisplacement of [3H]-GR113808 from guinea pig brain 5HT4 receptor in presence of serotonin incubated for 30 mins
ChEMBL 650 10 3 7 4.7 COc1cc(N)c(Cl)cc1C(=O)CCC1CCN(CCNS(=O)(=O)c2cc(Br)c(N)c(Br)c2)CC1 10.1016/j.ejmech.2016.05.048
44592144 178275 0 None - 1 Guinea pig 8.1 pKi = 8.1 Binding
Displacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatum membraneDisplacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatum membrane
ChEMBL 327 5 0 5 3.8 C=CCN1CCC(COc2nc3ccsc3n3cccc23)CC1 10.1016/j.bmc.2008.11.045
CHEMBL469575 178275 0 None - 1 Guinea pig 8.1 pKi = 8.1 Binding
Displacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatum membraneDisplacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatum membrane
ChEMBL 327 5 0 5 3.8 C=CCN1CCC(COc2nc3ccsc3n3cccc23)CC1 10.1016/j.bmc.2008.11.045
118734509 118162 0 None - 1 Guinea pig 8.1 pKi = 8.1 Binding
Displacement of [3H]GR113808 from 5-HT4R in guinea pig brain membranes incubated for 30 mins by radioligand binding assayDisplacement of [3H]GR113808 from 5-HT4R in guinea pig brain membranes incubated for 30 mins by radioligand binding assay
ChEMBL 364 7 1 4 4.4 COc1cc(N)c(Cl)cc1C(=O)CCC1CCN(CC2CCC2)CC1 10.1021/acs.jmedchem.5b00115
CHEMBL3416995 118162 0 None - 1 Guinea pig 8.1 pKi = 8.1 Binding
Displacement of [3H]GR113808 from 5-HT4R in guinea pig brain membranes incubated for 30 mins by radioligand binding assayDisplacement of [3H]GR113808 from 5-HT4R in guinea pig brain membranes incubated for 30 mins by radioligand binding assay
ChEMBL 364 7 1 4 4.4 COc1cc(N)c(Cl)cc1C(=O)CCC1CCN(CC2CCC2)CC1 10.1021/acs.jmedchem.5b00115
151758 188747 4 None - 1 Rat 8.1 pKi = 8.1 Binding
Binding affinity at 5-hydroxytryptamine 4 receptor in rat striatal membranes by [3H]GR-113808 displacement.Binding affinity at 5-hydroxytryptamine 4 receptor in rat striatal membranes by [3H]GR-113808 displacement.
ChEMBL 278 5 1 4 2.7 COc1ccccc1NC(=O)OCCN1CCCCC1 10.1021/jm960853v
CHEMBL51251 188747 4 None - 1 Rat 8.1 pKi = 8.1 Binding
Binding affinity at 5-hydroxytryptamine 4 receptor in rat striatal membranes by [3H]GR-113808 displacement.Binding affinity at 5-hydroxytryptamine 4 receptor in rat striatal membranes by [3H]GR-113808 displacement.
ChEMBL 278 5 1 4 2.7 COc1ccccc1NC(=O)OCCN1CCCCC1 10.1021/jm960853v
10541689 101583 4 None - 1 Rat 7.1 pKi = 7.1 Binding
Binding affinity at 5-hydroxytryptamine 4 receptor in rat striatal membranes by [3H]GR-113808 displacement.Binding affinity at 5-hydroxytryptamine 4 receptor in rat striatal membranes by [3H]GR-113808 displacement.
ChEMBL 292 6 1 4 3.1 COc1ccccc1NC(=O)OCCCN1CCCCC1 10.1021/jm960853v
CHEMBL301967 101583 4 None - 1 Rat 7.1 pKi = 7.1 Binding
Binding affinity at 5-hydroxytryptamine 4 receptor in rat striatal membranes by [3H]GR-113808 displacement.Binding affinity at 5-hydroxytryptamine 4 receptor in rat striatal membranes by [3H]GR-113808 displacement.
ChEMBL 292 6 1 4 3.1 COc1ccccc1NC(=O)OCCCN1CCCCC1 10.1021/jm960853v
107715 199260 18 None -165 20 Guinea pig 6.1 pKi = 6.1 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
ChEMBL 611 5 3 6 2.7 CC(C)[C@@]1(NC(=O)[C@@H]2C[C@@H]3c4cccc5[nH]cc(c45)C[C@H]3N(C)C2)O[C@@]2(O)[C@@H]3CCCN3C(=O)[C@H](Cc3ccccc3)N2C1=O nan
CHEMBL1255837 199260 18 None -165 20 Guinea pig 6.1 pKi = 6.1 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
ChEMBL 611 5 3 6 2.7 CC(C)[C@@]1(NC(=O)[C@@H]2C[C@@H]3c4cccc5[nH]cc(c45)C[C@H]3N(C)C2)O[C@@]2(O)[C@@H]3CCCN3C(=O)[C@H](Cc3ccccc3)N2C1=O nan
CHEMBL601773 199260 18 None -165 20 Guinea pig 6.1 pKi = 6.1 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
ChEMBL 611 5 3 6 2.7 CC(C)[C@@]1(NC(=O)[C@@H]2C[C@@H]3c4cccc5[nH]cc(c45)C[C@H]3N(C)C2)O[C@@]2(O)[C@@H]3CCCN3C(=O)[C@H](Cc3ccccc3)N2C1=O nan
44299805 100615 0 None - 1 Guinea pig 7.1 pKi = 7.1 Binding
Binding affinity towards 5-hydroxytryptamine 4 receptor in striatum membranes of guinea-pig brain was evaluatedBinding affinity towards 5-hydroxytryptamine 4 receptor in striatum membranes of guinea-pig brain was evaluated
ChEMBL 324 3 1 5 2.6 COc1cc(N)c(Cl)cc1C(=O)OC1CC2CCC1CN2C 10.1016/s0960-894x(01)00693-x
CHEMBL294894 100615 0 None - 1 Guinea pig 7.1 pKi = 7.1 Binding
Binding affinity towards 5-hydroxytryptamine 4 receptor in striatum membranes of guinea-pig brain was evaluatedBinding affinity towards 5-hydroxytryptamine 4 receptor in striatum membranes of guinea-pig brain was evaluated
ChEMBL 324 3 1 5 2.6 COc1cc(N)c(Cl)cc1C(=O)OC1CC2CCC1CN2C 10.1016/s0960-894x(01)00693-x
44573 56698 1 None -1 2 Rat 6.1 pKi = 6.1 Binding
Binding affinity against 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatumBinding affinity against 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatum
ChEMBL 297 3 2 4 1.8 COc1cc(N)c(Cl)cc1C(=O)NC1CCN(C)CC1 10.1016/0960-894X(95)00115-A
CHEMBL164425 56698 1 None -1 2 Rat 6.1 pKi = 6.1 Binding
Binding affinity against 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatumBinding affinity against 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatum
ChEMBL 297 3 2 4 1.8 COc1cc(N)c(Cl)cc1C(=O)NC1CCN(C)CC1 10.1016/0960-894X(95)00115-A
44573 56698 1 None 1 2 Guinea pig 6.1 pKi = 6.1 Binding
Inhibition of [3H]GR-113808 binding to guinea pig striatum 5-hydroxytryptamine 4 receptorInhibition of [3H]GR-113808 binding to guinea pig striatum 5-hydroxytryptamine 4 receptor
ChEMBL 297 3 2 4 1.8 COc1cc(N)c(Cl)cc1C(=O)NC1CCN(C)CC1 10.1021/jm020270n
CHEMBL164425 56698 1 None 1 2 Guinea pig 6.1 pKi = 6.1 Binding
Inhibition of [3H]GR-113808 binding to guinea pig striatum 5-hydroxytryptamine 4 receptorInhibition of [3H]GR-113808 binding to guinea pig striatum 5-hydroxytryptamine 4 receptor
ChEMBL 297 3 2 4 1.8 COc1cc(N)c(Cl)cc1C(=O)NC1CCN(C)CC1 10.1021/jm020270n
119584 2557 99 None -1 6 Guinea pig 7.1 pKi = 7.1 Binding
Tested for affinity against 5-hydroxytryptamine 4 receptor in the myenteric plexus of the guinea pig ileum.Tested for affinity against 5-hydroxytryptamine 4 receptor in the myenteric plexus of the guinea pig ileum.
ChEMBL 421 7 2 5 3.1 CCOc1cc(N)c(cc1C(=O)NCC1OCCN(C1)Cc1ccc(cc1)F)Cl 10.1021/jm020099f
1848 2557 99 None -1 6 Guinea pig 7.1 pKi = 7.1 Binding
Tested for affinity against 5-hydroxytryptamine 4 receptor in the myenteric plexus of the guinea pig ileum.Tested for affinity against 5-hydroxytryptamine 4 receptor in the myenteric plexus of the guinea pig ileum.
ChEMBL 421 7 2 5 3.1 CCOc1cc(N)c(cc1C(=O)NCC1OCCN(C1)Cc1ccc(cc1)F)Cl 10.1021/jm020099f
242 2557 99 None -1 6 Guinea pig 7.1 pKi = 7.1 Binding
Tested for affinity against 5-hydroxytryptamine 4 receptor in the myenteric plexus of the guinea pig ileum.Tested for affinity against 5-hydroxytryptamine 4 receptor in the myenteric plexus of the guinea pig ileum.
ChEMBL 421 7 2 5 3.1 CCOc1cc(N)c(cc1C(=O)NCC1OCCN(C1)Cc1ccc(cc1)F)Cl 10.1021/jm020099f
CHEMBL60889 2557 99 None -1 6 Guinea pig 7.1 pKi = 7.1 Binding
Tested for affinity against 5-hydroxytryptamine 4 receptor in the myenteric plexus of the guinea pig ileum.Tested for affinity against 5-hydroxytryptamine 4 receptor in the myenteric plexus of the guinea pig ileum.
ChEMBL 421 7 2 5 3.1 CCOc1cc(N)c(cc1C(=O)NCC1OCCN(C1)Cc1ccc(cc1)F)Cl 10.1021/jm020099f
DB11675 2557 99 None -1 6 Guinea pig 7.1 pKi = 7.1 Binding
Tested for affinity against 5-hydroxytryptamine 4 receptor in the myenteric plexus of the guinea pig ileum.Tested for affinity against 5-hydroxytryptamine 4 receptor in the myenteric plexus of the guinea pig ileum.
ChEMBL 421 7 2 5 3.1 CCOc1cc(N)c(cc1C(=O)NCC1OCCN(C1)Cc1ccc(cc1)F)Cl 10.1021/jm020099f
49783416 17531 0 None - 1 Human 5.1 pKi = 5.1 Binding
Displacement of [3H]GR113808 from human recombinant 5HT4 receptor expressed in HEK293 cellsDisplacement of [3H]GR113808 from human recombinant 5HT4 receptor expressed in HEK293 cells
ChEMBL 319 7 2 4 2.5 CCCCN1CCC(CNC(=O)c2ccc(N)c(OC)c2)CC1 10.1021/jm100668r
CHEMBL1258559 17531 0 None - 1 Human 5.1 pKi = 5.1 Binding
Displacement of [3H]GR113808 from human recombinant 5HT4 receptor expressed in HEK293 cellsDisplacement of [3H]GR113808 from human recombinant 5HT4 receptor expressed in HEK293 cells
ChEMBL 319 7 2 4 2.5 CCCCN1CCC(CNC(=O)c2ccc(N)c(OC)c2)CC1 10.1021/jm100668r
12861897 76738 0 None -35 2 Guinea pig 6.1 pKi = 6.1 Binding
Inhibition of [3H]GR-113808 binding to guinea pig striatum 5-hydroxytryptamine 4 receptorInhibition of [3H]GR-113808 binding to guinea pig striatum 5-hydroxytryptamine 4 receptor
ChEMBL 347 7 2 4 2.8 COc1cc(N)c(Cl)cc1C(=O)NCCN(C)Cc1ccccc1 10.1021/jm020270n
CHEMBL20748 76738 0 None -35 2 Guinea pig 6.1 pKi = 6.1 Binding
Inhibition of [3H]GR-113808 binding to guinea pig striatum 5-hydroxytryptamine 4 receptorInhibition of [3H]GR-113808 binding to guinea pig striatum 5-hydroxytryptamine 4 receptor
ChEMBL 347 7 2 4 2.8 COc1cc(N)c(Cl)cc1C(=O)NCCN(C)Cc1ccccc1 10.1021/jm020270n
10761897 206009 0 None - 1 Guinea pig 7.1 pKi = 7.1 Binding
Binding affinity against 5-hydroxytryptamine 4 receptor in guinea pig striatum using [3H]GR-113808 as radioligandBinding affinity against 5-hydroxytryptamine 4 receptor in guinea pig striatum using [3H]GR-113808 as radioligand
ChEMBL 373 6 1 6 2.0 CCCN1CCN(CCNC(=O)n2c(=O)n(C(C)C)c3ccccc32)CC1 10.1021/jm981098j
CHEMBL95808 206009 0 None - 1 Guinea pig 7.1 pKi = 7.1 Binding
Binding affinity against 5-hydroxytryptamine 4 receptor in guinea pig striatum using [3H]GR-113808 as radioligandBinding affinity against 5-hydroxytryptamine 4 receptor in guinea pig striatum using [3H]GR-113808 as radioligand
ChEMBL 373 6 1 6 2.0 CCCN1CCN(CCNC(=O)n2c(=O)n(C(C)C)c3ccccc32)CC1 10.1021/jm981098j
10761898 205909 0 None - 1 Guinea pig 7.1 pKi = 7.1 Binding
Binding affinity against 5-hydroxytryptamine 4 receptor in guinea pig striatum using [3H]GR-113808 as radioligandBinding affinity against 5-hydroxytryptamine 4 receptor in guinea pig striatum using [3H]GR-113808 as radioligand
ChEMBL 373 5 1 6 2.0 CC(C)N1CCN(CCNC(=O)n2c(=O)n(C(C)C)c3ccccc32)CC1 10.1021/jm981098j
CHEMBL95235 205909 0 None - 1 Guinea pig 7.1 pKi = 7.1 Binding
Binding affinity against 5-hydroxytryptamine 4 receptor in guinea pig striatum using [3H]GR-113808 as radioligandBinding affinity against 5-hydroxytryptamine 4 receptor in guinea pig striatum using [3H]GR-113808 as radioligand
ChEMBL 373 5 1 6 2.0 CC(C)N1CCN(CCNC(=O)n2c(=O)n(C(C)C)c3ccccc32)CC1 10.1021/jm981098j
45276946 19162 0 None - 1 Guinea pig 6.1 pKi = 6.1 Binding
Displacement of [3H]GR113808 from 5HT4 receptor in guinea pig striatal membranesDisplacement of [3H]GR113808 from 5HT4 receptor in guinea pig striatal membranes
ChEMBL 339 4 0 5 3.6 C#CCN1CCC(COc2nc3scc(C)c3n3cccc23)CC1 10.1016/j.ejmech.2010.07.052
CHEMBL1290804 19162 0 None - 1 Guinea pig 6.1 pKi = 6.1 Binding
Displacement of [3H]GR113808 from 5HT4 receptor in guinea pig striatal membranesDisplacement of [3H]GR113808 from 5HT4 receptor in guinea pig striatal membranes
ChEMBL 339 4 0 5 3.6 C#CCN1CCC(COc2nc3scc(C)c3n3cccc23)CC1 10.1016/j.ejmech.2010.07.052
44404961 132493 0 None - 1 Human 8.1 pKi = 8.1 Binding
Binding affinity for 5-HT4 receptor using [3H]GR-113808Binding affinity for 5-HT4 receptor using [3H]GR-113808
ChEMBL 764 17 5 12 4.0 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCC(NC(=O)CCCCCC(=O)NC2CCN(CCOC(=O)c3cc(Cl)c(N)cc3O)CC2)CC1 10.1021/jm050234z
CHEMBL370227 132493 0 None - 1 Human 8.1 pKi = 8.1 Binding
Binding affinity for 5-HT4 receptor using [3H]GR-113808Binding affinity for 5-HT4 receptor using [3H]GR-113808
ChEMBL 764 17 5 12 4.0 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCC(NC(=O)CCCCCC(=O)NC2CCN(CCOC(=O)c3cc(Cl)c(N)cc3O)CC2)CC1 10.1021/jm050234z
11693471 134716 0 None - 1 Human 8.1 pKi = 8.1 Binding
Binding affinity for 5-HT4 receptor using [3H]GR-113808Binding affinity for 5-HT4 receptor using [3H]GR-113808
ChEMBL 778 18 4 12 4.0 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCC(CNC(=O)CCCC(=O)NCC2CCN(CCOC(=O)c3cc(Cl)c(N)cc3OC)CC2)CC1 10.1021/jm050234z
CHEMBL372479 134716 0 None - 1 Human 8.1 pKi = 8.1 Binding
Binding affinity for 5-HT4 receptor using [3H]GR-113808Binding affinity for 5-HT4 receptor using [3H]GR-113808
ChEMBL 778 18 4 12 4.0 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCC(CNC(=O)CCCC(=O)NCC2CCN(CCOC(=O)c3cc(Cl)c(N)cc3OC)CC2)CC1 10.1021/jm050234z
72698087 103511 0 None -81 3 Guinea pig 8.1 pKi = 8.1 Binding
Displacement of [3H]GR113808 from 5HT4R in guinea pig striatal membranesDisplacement of [3H]GR113808 from 5HT4R in guinea pig striatal membranes
ChEMBL 407 5 0 4 5.0 Fc1cccc2c1nc(OCC1CCN(CCC(F)(F)F)CC1)c1cccnc12 10.1016/j.bmc.2013.08.061
CHEMBL3093186 103511 0 None -81 3 Guinea pig 8.1 pKi = 8.1 Binding
Displacement of [3H]GR113808 from 5HT4R in guinea pig striatal membranesDisplacement of [3H]GR113808 from 5HT4R in guinea pig striatal membranes
ChEMBL 407 5 0 4 5.0 Fc1cccc2c1nc(OCC1CCN(CCC(F)(F)F)CC1)c1cccnc12 10.1016/j.bmc.2013.08.061
CHEMBL4164469 211472 0 None - 1 Guinea pig 8.1 pKi = 8.1 Binding
Displacement of [3H]GR113808 from serotonin 5-HT4 receptor in Dunkin-Hartley guinea pigs striatal nuclei membranes incubated for 2 hrs by liquid scintillation countingDisplacement of [3H]GR113808 from serotonin 5-HT4 receptor in Dunkin-Hartley guinea pigs striatal nuclei membranes incubated for 2 hrs by liquid scintillation counting
ChEMBL None None None COc1cc(N)c(Cl)cc1C(=O)OCCN1CCC(NC(=O)NCCOCCOCCOCCOCCOCCOCCOCCOCCn2cc(CNC(=O)NCCCN(C)CCCNC(=O)NCc3cn(CCOCCOCCOCCOCCOCCOCCOCCOCCNC(=O)NC4CCN(CCOC(=O)c5cc(Cl)c(N)cc5OC)CC4)nn3)nn2)CC1 10.1039/C6MD00458J
10757373 49321 0 None - 1 Rat 8.0 pKi = 8.0 Binding
Binding affinity towards 5-hydroxytryptamine 4 receptor was determined in rat striatal membranes using [3H]GR-113808 as radioligandBinding affinity towards 5-hydroxytryptamine 4 receptor was determined in rat striatal membranes using [3H]GR-113808 as radioligand
ChEMBL 310 5 1 5 2.4 COc1cc(N)c(Cl)cc1C(=O)OCCN1CC=CCC1 10.1021/jm960320m
CHEMBL156579 49321 0 None - 1 Rat 8.0 pKi = 8.0 Binding
Binding affinity towards 5-hydroxytryptamine 4 receptor was determined in rat striatal membranes using [3H]GR-113808 as radioligandBinding affinity towards 5-hydroxytryptamine 4 receptor was determined in rat striatal membranes using [3H]GR-113808 as radioligand
ChEMBL 310 5 1 5 2.4 COc1cc(N)c(Cl)cc1C(=O)OCCN1CC=CCC1 10.1021/jm960320m
49783207 17396 0 None - 1 Human 8.0 pKi = 8.0 Binding
Displacement of [3H]GR113808 from human recombinant 5HT4 receptor expressed in HEK293 cellsDisplacement of [3H]GR113808 from human recombinant 5HT4 receptor expressed in HEK293 cells
ChEMBL 362 7 1 6 3.2 CCCCN1CCC(COC(=O)c2ccc(NC)c3c2OCCO3)CC1 10.1021/jm100668r
CHEMBL1258109 17396 0 None - 1 Human 8.0 pKi = 8.0 Binding
Displacement of [3H]GR113808 from human recombinant 5HT4 receptor expressed in HEK293 cellsDisplacement of [3H]GR113808 from human recombinant 5HT4 receptor expressed in HEK293 cells
ChEMBL 362 7 1 6 3.2 CCCCN1CCC(COC(=O)c2ccc(NC)c3c2OCCO3)CC1 10.1021/jm100668r
11794824 17754 0 None - 1 Human 8.0 pKi = 8.0 Binding
Binding affinity was determined against cloned 5-hydroxytryptamine 4E receptor isoform expressed in C6 glial cells incubated with 0.2 nM [3H]GR-113808Binding affinity was determined against cloned 5-hydroxytryptamine 4E receptor isoform expressed in C6 glial cells incubated with 0.2 nM [3H]GR-113808
ChEMBL 391 6 1 8 1.7 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCN(c2cncnc2)CC1 10.1021/jm0009538
CHEMBL125926 17754 0 None - 1 Human 8.0 pKi = 8.0 Binding
Binding affinity was determined against cloned 5-hydroxytryptamine 4E receptor isoform expressed in C6 glial cells incubated with 0.2 nM [3H]GR-113808Binding affinity was determined against cloned 5-hydroxytryptamine 4E receptor isoform expressed in C6 glial cells incubated with 0.2 nM [3H]GR-113808
ChEMBL 391 6 1 8 1.7 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCN(c2cncnc2)CC1 10.1021/jm0009538
44371317 49793 0 None - 1 Rat 8.0 pKi = 8.0 Binding
Binding affinity towards 5-hydroxytryptamine 4 receptor was determined in rat striatal membranes using [3H]GR-113808 as radioligandBinding affinity towards 5-hydroxytryptamine 4 receptor was determined in rat striatal membranes using [3H]GR-113808 as radioligand
ChEMBL 338 5 1 5 3.1 COc1cc(N)c(Cl)cc1C(=O)OCCN1C2CCCC1CC2 10.1021/jm960320m
CHEMBL156965 49793 0 None - 1 Rat 8.0 pKi = 8.0 Binding
Binding affinity towards 5-hydroxytryptamine 4 receptor was determined in rat striatal membranes using [3H]GR-113808 as radioligandBinding affinity towards 5-hydroxytryptamine 4 receptor was determined in rat striatal membranes using [3H]GR-113808 as radioligand
ChEMBL 338 5 1 5 3.1 COc1cc(N)c(Cl)cc1C(=O)OCCN1C2CCCC1CC2 10.1021/jm960320m
183782 3346 15 None 1 14 Guinea pig 8.0 pKi = 8.0 Binding
Displacement of [3H]GR113808 from 5-HT4R in guinea pig brain membranes incubated for 30 mins by radioligand binding assayDisplacement of [3H]GR113808 from 5-HT4R in guinea pig brain membranes incubated for 30 mins by radioligand binding assay
ChEMBL 352 8 1 4 4.4 CCCCN1CCC(CC1)CCC(=O)c1cc(Cl)c(cc1OC)N 10.1021/acs.jmedchem.5b00115
237 3346 15 None 1 14 Guinea pig 8.0 pKi = 8.0 Binding
Displacement of [3H]GR113808 from 5-HT4R in guinea pig brain membranes incubated for 30 mins by radioligand binding assayDisplacement of [3H]GR113808 from 5-HT4R in guinea pig brain membranes incubated for 30 mins by radioligand binding assay
ChEMBL 352 8 1 4 4.4 CCCCN1CCC(CC1)CCC(=O)c1cc(Cl)c(cc1OC)N 10.1021/acs.jmedchem.5b00115
CHEMBL85251 3346 15 None 1 14 Guinea pig 8.0 pKi = 8.0 Binding
Displacement of [3H]GR113808 from 5-HT4R in guinea pig brain membranes incubated for 30 mins by radioligand binding assayDisplacement of [3H]GR113808 from 5-HT4R in guinea pig brain membranes incubated for 30 mins by radioligand binding assay
ChEMBL 352 8 1 4 4.4 CCCCN1CCC(CC1)CCC(=O)c1cc(Cl)c(cc1OC)N 10.1021/acs.jmedchem.5b00115
183782 3346 15 None -1 14 Human 8.0 pKi = 8.0 Binding
Displacement of [3H]-GR113808 from recombinant human 5-HT4BR expressed in membranes after 60 minsDisplacement of [3H]-GR113808 from recombinant human 5-HT4BR expressed in membranes after 60 mins
ChEMBL 352 8 1 4 4.4 CCCCN1CCC(CC1)CCC(=O)c1cc(Cl)c(cc1OC)N 10.1016/j.ejmech.2018.10.064
237 3346 15 None -1 14 Human 8.0 pKi = 8.0 Binding
Displacement of [3H]-GR113808 from recombinant human 5-HT4BR expressed in membranes after 60 minsDisplacement of [3H]-GR113808 from recombinant human 5-HT4BR expressed in membranes after 60 mins
ChEMBL 352 8 1 4 4.4 CCCCN1CCC(CC1)CCC(=O)c1cc(Cl)c(cc1OC)N 10.1016/j.ejmech.2018.10.064
CHEMBL85251 3346 15 None -1 14 Human 8.0 pKi = 8.0 Binding
Displacement of [3H]-GR113808 from recombinant human 5-HT4BR expressed in membranes after 60 minsDisplacement of [3H]-GR113808 from recombinant human 5-HT4BR expressed in membranes after 60 mins
ChEMBL 352 8 1 4 4.4 CCCCN1CCC(CC1)CCC(=O)c1cc(Cl)c(cc1OC)N 10.1016/j.ejmech.2018.10.064
10584 1435 0 None -1 2 Human 8.0 pKi = 8.0 Binding
Displacement of [3H]-GR113808 from recombinant human 5-HT4BR expressed in membranes after 60 minsDisplacement of [3H]-GR113808 from recombinant human 5-HT4BR expressed in membranes after 60 mins
ChEMBL 392 7 1 4 5.2 COc1cc(N)c(cc1C(=O)CCC1CCN(CC1)CC1CCCCC1)Cl 10.1016/j.ejmech.2018.10.064
86582973 1435 0 None -1 2 Human 8.0 pKi = 8.0 Binding
Displacement of [3H]-GR113808 from recombinant human 5-HT4BR expressed in membranes after 60 minsDisplacement of [3H]-GR113808 from recombinant human 5-HT4BR expressed in membranes after 60 mins
ChEMBL 392 7 1 4 5.2 COc1cc(N)c(cc1C(=O)CCC1CCN(CC1)CC1CCCCC1)Cl 10.1016/j.ejmech.2018.10.064
CHEMBL3417009 1435 0 None -1 2 Human 8.0 pKi = 8.0 Binding
Displacement of [3H]-GR113808 from recombinant human 5-HT4BR expressed in membranes after 60 minsDisplacement of [3H]-GR113808 from recombinant human 5-HT4BR expressed in membranes after 60 mins
ChEMBL 392 7 1 4 5.2 COc1cc(N)c(cc1C(=O)CCC1CCN(CC1)CC1CCCCC1)Cl 10.1016/j.ejmech.2018.10.064
44592188 188670 0 None - 1 Guinea pig 8.0 pKi = 8.0 Binding
Displacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatum membraneDisplacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatum membrane
ChEMBL 329 4 0 5 4.0 CCN1CCC(COc2nc3scc(C)c3n3cccc23)CC1 10.1016/j.bmc.2008.11.045
CHEMBL511794 188670 0 None - 1 Guinea pig 8.0 pKi = 8.0 Binding
Displacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatum membraneDisplacement of [3H]GR-113808 from 5HT4 receptor in guinea pig striatum membrane
ChEMBL 329 4 0 5 4.0 CCN1CCC(COc2nc3scc(C)c3n3cccc23)CC1 10.1016/j.bmc.2008.11.045
9927789 111014 0 None - 1 Rat 8.0 pKi = 8.0 Binding
Binding affinity at 5-hydroxytryptamine 4 receptor in rat striatum by [3H]GR-113808 displacement.Binding affinity at 5-hydroxytryptamine 4 receptor in rat striatum by [3H]GR-113808 displacement.
ChEMBL 337 5 2 4 2.5 Nc1c(Cl)cc(C(=O)NCCCN2CCCCC2)c2c1CCO2 10.1016/0960-894X(96)00002-9
CHEMBL327798 111014 0 None - 1 Rat 8.0 pKi = 8.0 Binding
Binding affinity at 5-hydroxytryptamine 4 receptor in rat striatum by [3H]GR-113808 displacement.Binding affinity at 5-hydroxytryptamine 4 receptor in rat striatum by [3H]GR-113808 displacement.
ChEMBL 337 5 2 4 2.5 Nc1c(Cl)cc(C(=O)NCCCN2CCCCC2)c2c1CCO2 10.1016/0960-894X(96)00002-9
10526438 17113 0 None - 1 Human 8.0 pKi = 8.0 Binding
Binding affinity was determined against cloned 5-hydroxytryptamine 4E receptor isoform expressed in C6 glial cells incubated with 0.2 nM [3H]GR-113808Binding affinity was determined against cloned 5-hydroxytryptamine 4E receptor isoform expressed in C6 glial cells incubated with 0.2 nM [3H]GR-113808
ChEMBL 425 6 1 8 2.4 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCN(c2cnc(Cl)nc2)CC1 10.1021/jm0009538
CHEMBL125716 17113 0 None - 1 Human 8.0 pKi = 8.0 Binding
Binding affinity was determined against cloned 5-hydroxytryptamine 4E receptor isoform expressed in C6 glial cells incubated with 0.2 nM [3H]GR-113808Binding affinity was determined against cloned 5-hydroxytryptamine 4E receptor isoform expressed in C6 glial cells incubated with 0.2 nM [3H]GR-113808
ChEMBL 425 6 1 8 2.4 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCN(c2cnc(Cl)nc2)CC1 10.1021/jm0009538
1782 2482 81 None -11 22 Rat 6.1 pKi = 6.1 Binding
Binding affinity at 5-hydroxytryptamine 4 receptor in rat striatum by [3H]GR-113808 displacement.Binding affinity at 5-hydroxytryptamine 4 receptor in rat striatum by [3H]GR-113808 displacement.
ChEMBL 299 7 2 4 2.0 CCN(CCNC(=O)c1cc(Cl)c(cc1OC)N)CC 10.1016/0960-894X(96)00002-9
241 2482 81 None -11 22 Rat 6.1 pKi = 6.1 Binding
Binding affinity at 5-hydroxytryptamine 4 receptor in rat striatum by [3H]GR-113808 displacement.Binding affinity at 5-hydroxytryptamine 4 receptor in rat striatum by [3H]GR-113808 displacement.
ChEMBL 299 7 2 4 2.0 CCN(CCNC(=O)c1cc(Cl)c(cc1OC)N)CC 10.1016/0960-894X(96)00002-9
4168 2482 81 None -11 22 Rat 6.1 pKi = 6.1 Binding
Binding affinity at 5-hydroxytryptamine 4 receptor in rat striatum by [3H]GR-113808 displacement.Binding affinity at 5-hydroxytryptamine 4 receptor in rat striatum by [3H]GR-113808 displacement.
ChEMBL 299 7 2 4 2.0 CCN(CCNC(=O)c1cc(Cl)c(cc1OC)N)CC 10.1016/0960-894X(96)00002-9
CHEMBL86 2482 81 None -11 22 Rat 6.1 pKi = 6.1 Binding
Binding affinity at 5-hydroxytryptamine 4 receptor in rat striatum by [3H]GR-113808 displacement.Binding affinity at 5-hydroxytryptamine 4 receptor in rat striatum by [3H]GR-113808 displacement.
ChEMBL 299 7 2 4 2.0 CCN(CCNC(=O)c1cc(Cl)c(cc1OC)N)CC 10.1016/0960-894X(96)00002-9
DB01233 2482 81 None -11 22 Rat 6.1 pKi = 6.1 Binding
Binding affinity at 5-hydroxytryptamine 4 receptor in rat striatum by [3H]GR-113808 displacement.Binding affinity at 5-hydroxytryptamine 4 receptor in rat striatum by [3H]GR-113808 displacement.
ChEMBL 299 7 2 4 2.0 CCN(CCNC(=O)c1cc(Cl)c(cc1OC)N)CC 10.1016/0960-894X(96)00002-9
10688893 206646 0 None -1 2 Guinea pig 7.0 pKi = 7.0 Binding
Binding affinity against 5-hydroxytryptamine 4 receptor in guinea pig striatum using [3H]GR-113808 as radioligandBinding affinity against 5-hydroxytryptamine 4 receptor in guinea pig striatum using [3H]GR-113808 as radioligand
ChEMBL 345 4 1 6 1.2 CC(C)n1c(=O)n(C(=O)NCCN2CCN(C)CC2)c2ccccc21 10.1021/jm981098j
CHEMBL99591 206646 0 None -1 2 Guinea pig 7.0 pKi = 7.0 Binding
Binding affinity against 5-hydroxytryptamine 4 receptor in guinea pig striatum using [3H]GR-113808 as radioligandBinding affinity against 5-hydroxytryptamine 4 receptor in guinea pig striatum using [3H]GR-113808 as radioligand
ChEMBL 345 4 1 6 1.2 CC(C)n1c(=O)n(C(=O)NCCN2CCN(C)CC2)c2ccccc21 10.1021/jm981098j
10828800 99726 0 None - 1 Rat 7.0 pKi = 7.0 Binding
Binding affinity against 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatumBinding affinity against 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatum
ChEMBL 310 3 1 5 2.2 COc1cc(N)c(Cl)cc1C(=O)O[C@@H]1CN2CCC1CC2 10.1016/S0960-894X(01)80508-4
CHEMBL288199 99726 0 None - 1 Rat 7.0 pKi = 7.0 Binding
Binding affinity against 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatumBinding affinity against 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatum
ChEMBL 310 3 1 5 2.2 COc1cc(N)c(Cl)cc1C(=O)O[C@@H]1CN2CCC1CC2 10.1016/S0960-894X(01)80508-4
10828800 99726 0 None - 1 Rat 7.0 pKi = 7.0 Binding
Binding affinity towards 5-hydroxytryptamine 4 receptor was determined in rat striatal membranes using [3H]GR-113808 as radioligandBinding affinity towards 5-hydroxytryptamine 4 receptor was determined in rat striatal membranes using [3H]GR-113808 as radioligand
ChEMBL 310 3 1 5 2.2 COc1cc(N)c(Cl)cc1C(=O)O[C@@H]1CN2CCC1CC2 10.1021/jm960320m
CHEMBL288199 99726 0 None - 1 Rat 7.0 pKi = 7.0 Binding
Binding affinity towards 5-hydroxytryptamine 4 receptor was determined in rat striatal membranes using [3H]GR-113808 as radioligandBinding affinity towards 5-hydroxytryptamine 4 receptor was determined in rat striatal membranes using [3H]GR-113808 as radioligand
ChEMBL 310 3 1 5 2.2 COc1cc(N)c(Cl)cc1C(=O)O[C@@H]1CN2CCC1CC2 10.1021/jm960320m
72698086 103510 0 None - 1 Guinea pig 7.0 pKi = 7.0 Binding
Displacement of [3H]GR113808 from 5HT4R in guinea pig striatal membranesDisplacement of [3H]GR113808 from 5HT4R in guinea pig striatal membranes
ChEMBL 375 5 0 4 4.3 Fc1cccc2c1nc(OCC1CCN(CC(F)F)CC1)c1cccnc12 10.1016/j.bmc.2013.08.061
CHEMBL3093185 103510 0 None - 1 Guinea pig 7.0 pKi = 7.0 Binding
Displacement of [3H]GR113808 from 5HT4R in guinea pig striatal membranesDisplacement of [3H]GR113808 from 5HT4R in guinea pig striatal membranes
ChEMBL 375 5 0 4 4.3 Fc1cccc2c1nc(OCC1CCN(CC(F)F)CC1)c1cccnc12 10.1016/j.bmc.2013.08.061
75201901 165872 14 None -676 24 Human 5.0 pKi = 5.0 Binding
Displacement of [3H]GR113808 from recombinant human 5HT4 receptor stably expressed in HEKT cells measured after 90 mins by microbeta scintillation counting methodDisplacement of [3H]GR113808 from recombinant human 5HT4 receptor stably expressed in HEKT cells measured after 90 mins by microbeta scintillation counting method
ChEMBL 356 3 0 6 4.9 Cc1cc(Oc2nccc3occc23)ccc1-c1c(C)ncc2nccn12 10.1021/acs.jmedchem.9b00351
CHEMBL4277264 165872 14 None -676 24 Human 5.0 pKi = 5.0 Binding
Displacement of [3H]GR113808 from recombinant human 5HT4 receptor stably expressed in HEKT cells measured after 90 mins by microbeta scintillation counting methodDisplacement of [3H]GR113808 from recombinant human 5HT4 receptor stably expressed in HEKT cells measured after 90 mins by microbeta scintillation counting method
ChEMBL 356 3 0 6 4.9 Cc1cc(Oc2nccc3occc23)ccc1-c1c(C)ncc2nccn12 10.1021/acs.jmedchem.9b00351
136118647 75967 0 None -3 3 Human 6.0 pKi = 6.0 Binding
Displacement of [3H]GR113808 from human recombinant 5HT4 receptorDisplacement of [3H]GR113808 from human recombinant 5HT4 receptor
ChEMBL 240 1 3 2 1.2 C/N=C1\NC(=O)/C(=C/c2c[nH]c3ccccc23)N1 10.1016/j.bmc.2013.09.011
CHEMBL2058702 75967 0 None -3 3 Human 6.0 pKi = 6.0 Binding
Displacement of [3H]GR113808 from human recombinant 5HT4 receptorDisplacement of [3H]GR113808 from human recombinant 5HT4 receptor
ChEMBL 240 1 3 2 1.2 C/N=C1\NC(=O)/C(=C/c2c[nH]c3ccccc23)N1 10.1016/j.bmc.2013.09.011
44323245 106541 0 None - 1 Rat 7.0 pKi = 7.0 Binding
Binding affinity at 5-hydroxytryptamine 4 receptor in rat striatum by [3H]GR-113808 displacement.Binding affinity at 5-hydroxytryptamine 4 receptor in rat striatum by [3H]GR-113808 displacement.
ChEMBL 322 2 1 5 2.1 Nc1c(Cl)cc(C(=O)O[C@H]2CN3CCC2CC3)c2c1CCO2 10.1016/0960-894X(96)00002-9
CHEMBL315443 106541 0 None - 1 Rat 7.0 pKi = 7.0 Binding
Binding affinity at 5-hydroxytryptamine 4 receptor in rat striatum by [3H]GR-113808 displacement.Binding affinity at 5-hydroxytryptamine 4 receptor in rat striatum by [3H]GR-113808 displacement.
ChEMBL 322 2 1 5 2.1 Nc1c(Cl)cc(C(=O)O[C@H]2CN3CCC2CC3)c2c1CCO2 10.1016/0960-894X(96)00002-9
10930618 106556 0 None - 1 Human 7.0 pKi = 7.0 Binding
Binding affinity towards cloned human 5-hydroxytryptamine 4E receptor expressed in C6 glial cells using [3H]GR-113808 as radioligandBinding affinity towards cloned human 5-hydroxytryptamine 4E receptor expressed in C6 glial cells using [3H]GR-113808 as radioligand
ChEMBL 729 19 2 9 5.9 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCN(C(=O)CCCCCCCCCCNS(=O)(=O)c2cccc3c(N(C)C)cccc23)CC1 10.1021/jm0307887
CHEMBL315526 106556 0 None - 1 Human 7.0 pKi = 7.0 Binding
Binding affinity towards cloned human 5-hydroxytryptamine 4E receptor expressed in C6 glial cells using [3H]GR-113808 as radioligandBinding affinity towards cloned human 5-hydroxytryptamine 4E receptor expressed in C6 glial cells using [3H]GR-113808 as radioligand
ChEMBL 729 19 2 9 5.9 COc1cc(N)c(Cl)cc1C(=O)OCCN1CCN(C(=O)CCCCCCCCCCNS(=O)(=O)c2cccc3c(N(C)C)cccc23)CC1 10.1021/jm0307887
6918107 77787 13 None -1 5 Rat 6.0 pKi = 6.0 Binding
The binding affinity was measured on 5-hydroxytryptamine 4 receptor using [3H]- GR-113808 as radioligand.The binding affinity was measured on 5-hydroxytryptamine 4 receptor using [3H]- GR-113808 as radioligand.
ChEMBL 319 2 0 4 3.5 Cc1nccn1C[C@H]1CCc2c(c3cccc4c3n2CCC4)C1=O 10.1021/jm00075a026
CHEMBL2103778 77787 13 None -1 5 Rat 6.0 pKi = 6.0 Binding
The binding affinity was measured on 5-hydroxytryptamine 4 receptor using [3H]- GR-113808 as radioligand.The binding affinity was measured on 5-hydroxytryptamine 4 receptor using [3H]- GR-113808 as radioligand.
ChEMBL 319 2 0 4 3.5 Cc1nccn1C[C@H]1CCc2c(c3cccc4c3n2CCC4)C1=O 10.1021/jm00075a026
1782 2482 81 None -11 22 Rat 6.0 pKi = 6.0 Binding
Binding affinity against 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatumBinding affinity against 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatum
ChEMBL 299 7 2 4 2.0 CCN(CCNC(=O)c1cc(Cl)c(cc1OC)N)CC 10.1016/0960-894X(95)00115-A
241 2482 81 None -11 22 Rat 6.0 pKi = 6.0 Binding
Binding affinity against 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatumBinding affinity against 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatum
ChEMBL 299 7 2 4 2.0 CCN(CCNC(=O)c1cc(Cl)c(cc1OC)N)CC 10.1016/0960-894X(95)00115-A
4168 2482 81 None -11 22 Rat 6.0 pKi = 6.0 Binding
Binding affinity against 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatumBinding affinity against 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatum
ChEMBL 299 7 2 4 2.0 CCN(CCNC(=O)c1cc(Cl)c(cc1OC)N)CC 10.1016/0960-894X(95)00115-A
CHEMBL86 2482 81 None -11 22 Rat 6.0 pKi = 6.0 Binding
Binding affinity against 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatumBinding affinity against 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatum
ChEMBL 299 7 2 4 2.0 CCN(CCNC(=O)c1cc(Cl)c(cc1OC)N)CC 10.1016/0960-894X(95)00115-A
DB01233 2482 81 None -11 22 Rat 6.0 pKi = 6.0 Binding
Binding affinity against 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatumBinding affinity against 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatum
ChEMBL 299 7 2 4 2.0 CCN(CCNC(=O)c1cc(Cl)c(cc1OC)N)CC 10.1016/0960-894X(95)00115-A
1782 2482 81 None -11 22 Rat 6.0 pKi = 6.0 Binding
Binding affinity against 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatumBinding affinity against 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatum
ChEMBL 299 7 2 4 2.0 CCN(CCNC(=O)c1cc(Cl)c(cc1OC)N)CC 10.1016/S0960-894X(01)80508-4
241 2482 81 None -11 22 Rat 6.0 pKi = 6.0 Binding
Binding affinity against 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatumBinding affinity against 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatum
ChEMBL 299 7 2 4 2.0 CCN(CCNC(=O)c1cc(Cl)c(cc1OC)N)CC 10.1016/S0960-894X(01)80508-4
4168 2482 81 None -11 22 Rat 6.0 pKi = 6.0 Binding
Binding affinity against 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatumBinding affinity against 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatum
ChEMBL 299 7 2 4 2.0 CCN(CCNC(=O)c1cc(Cl)c(cc1OC)N)CC 10.1016/S0960-894X(01)80508-4
CHEMBL86 2482 81 None -11 22 Rat 6.0 pKi = 6.0 Binding
Binding affinity against 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatumBinding affinity against 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatum
ChEMBL 299 7 2 4 2.0 CCN(CCNC(=O)c1cc(Cl)c(cc1OC)N)CC 10.1016/S0960-894X(01)80508-4
DB01233 2482 81 None -11 22 Rat 6.0 pKi = 6.0 Binding
Binding affinity against 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatumBinding affinity against 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatum
ChEMBL 299 7 2 4 2.0 CCN(CCNC(=O)c1cc(Cl)c(cc1OC)N)CC 10.1016/S0960-894X(01)80508-4
90666001 108797 0 None - 1 Guinea pig 7.0 pKi = 7 Binding
Displacement of [3H]-GR113808 from guinea pig 5HT4 receptor by Grossman's methodDisplacement of [3H]-GR113808 from guinea pig 5HT4 receptor by Grossman's method
ChEMBL 395 5 0 5 5.0 Fc1ccc(CN2CCC(COc3nc4ccsc4n4cccc34)CC2)cc1 10.1039/C2MD20063E
CHEMBL3218873 108797 0 None - 1 Guinea pig 7.0 pKi = 7 Binding
Displacement of [3H]-GR113808 from guinea pig 5HT4 receptor by Grossman's methodDisplacement of [3H]-GR113808 from guinea pig 5HT4 receptor by Grossman's method
ChEMBL 395 5 0 5 5.0 Fc1ccc(CN2CCC(COc3nc4ccsc4n4cccc34)CC2)cc1 10.1039/C2MD20063E
5 139 66 None -117 54 Rat 7.7 pKd = 7.7 Binding
UnclassifiedUnclassified
Guide to Pharmacology 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 8813606
5202 139 66 None -117 54 Rat 7.7 pKd = 7.7 Binding
UnclassifiedUnclassified
Guide to Pharmacology 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 8813606
CHEMBL39 139 66 None -117 54 Rat 7.7 pKd = 7.7 Binding
UnclassifiedUnclassified
Guide to Pharmacology 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 8813606
DB08839 139 66 None -117 54 Rat 7.7 pKd = 7.7 Binding
UnclassifiedUnclassified
Guide to Pharmacology 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 8813606
5 139 66 None -288 54 Human 8.6 pKd = 8.6 Binding
UnclassifiedUnclassified
Guide to Pharmacology 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 10646498
5202 139 66 None -288 54 Human 8.6 pKd = 8.6 Binding
UnclassifiedUnclassified
Guide to Pharmacology 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 10646498
CHEMBL39 139 66 None -288 54 Human 8.6 pKd = 8.6 Binding
UnclassifiedUnclassified
Guide to Pharmacology 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 10646498
DB08839 139 66 None -288 54 Human 8.6 pKd = 8.6 Binding
UnclassifiedUnclassified
Guide to Pharmacology 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 10646498
236 3345 0 None -4 2 Rat 9.3 pKd = 9.3 Binding
UnclassifiedUnclassified
Guide to Pharmacology 474 8 1 7 4.2 COc1cc(N)c(cc1C(=O)OCC1CCN(CC1)CCCc1ccc2c(c1)OCCO2)Cl 9225293
239 3345 0 None -4 2 Rat 9.3 pKd = 9.3 Binding
UnclassifiedUnclassified
Guide to Pharmacology 474 8 1 7 4.2 COc1cc(N)c(cc1C(=O)OCC1CCN(CC1)CCCc1ccc2c(c1)OCCO2)Cl 9225293
5311417 3345 0 None -4 2 Rat 9.3 pKd = 9.3 Binding
UnclassifiedUnclassified
Guide to Pharmacology 474 8 1 7 4.2 COc1cc(N)c(cc1C(=O)OCC1CCN(CC1)CCCc1ccc2c(c1)OCCO2)Cl 9225293
CHEMBL1908857 3345 0 None -4 2 Rat 9.3 pKd = 9.3 Binding
UnclassifiedUnclassified
Guide to Pharmacology 474 8 1 7 4.2 COc1cc(N)c(cc1C(=O)OCC1CCN(CC1)CCCc1ccc2c(c1)OCCO2)Cl 9225293
236 3345 0 None 4 2 Guinea pig 9.7 pKd = 9.7 Binding
UnclassifiedUnclassified
Guide to Pharmacology 474 8 1 7 4.2 COc1cc(N)c(cc1C(=O)OCC1CCN(CC1)CCCc1ccc2c(c1)OCCO2)Cl 9225293
239 3345 0 None 4 2 Guinea pig 9.7 pKd = 9.7 Binding
UnclassifiedUnclassified
Guide to Pharmacology 474 8 1 7 4.2 COc1cc(N)c(cc1C(=O)OCC1CCN(CC1)CCCc1ccc2c(c1)OCCO2)Cl 9225293
5311417 3345 0 None 4 2 Guinea pig 9.7 pKd = 9.7 Binding
UnclassifiedUnclassified
Guide to Pharmacology 474 8 1 7 4.2 COc1cc(N)c(cc1C(=O)OCC1CCN(CC1)CCCc1ccc2c(c1)OCCO2)Cl 9225293
CHEMBL1908857 3345 0 None 4 2 Guinea pig 9.7 pKd = 9.7 Binding
UnclassifiedUnclassified
Guide to Pharmacology 474 8 1 7 4.2 COc1cc(N)c(cc1C(=O)OCC1CCN(CC1)CCCc1ccc2c(c1)OCCO2)Cl 9225293
121881 3434 21 3H-GR-113808 2 15 Guinea pig 11.0 pKi = 11 Binding
NoneNone
PDSP KiDatabase 382 6 1 6 3.4 CCCCN1CCC(CC1)COC(=O)c1cc(Cl)c(c2c1OCCO2)N None
256 3434 21 3H-GR-113808 2 15 Guinea pig 11.0 pKi = 11 Binding
NoneNone
PDSP KiDatabase 382 6 1 6 3.4 CCCCN1CCC(CC1)COC(=O)c1cc(Cl)c(c2c1OCCO2)N None
CHEMBL68131 3434 21 3H-GR-113808 2 15 Guinea pig 11.0 pKi = 11 Binding
NoneNone
PDSP KiDatabase 382 6 1 6 3.4 CCCCN1CCC(CC1)COC(=O)c1cc(Cl)c(c2c1OCCO2)N None
119376 1811 41 3H-GR-113808 -1 26 Human 10.7 pKi = 10.7 Binding
NoneNone
PDSP KiDatabase 393 7 1 6 1.6 O=C(c1cn(c2c1cccc2)C)OCC1CCN(CC1)CCNS(=O)(=O)C None
119376 1811 41 3H-GR-113808 -2 26 Rat 10.7 pKi = 10.7 Binding
NoneNone
PDSP KiDatabase 393 7 1 6 1.6 O=C(c1cn(c2c1cccc2)C)OCC1CCN(CC1)CCNS(=O)(=O)C None
247 1811 41 3H-GR-113808 -1 26 Human 10.7 pKi = 10.7 Binding
NoneNone
PDSP KiDatabase 393 7 1 6 1.6 O=C(c1cn(c2c1cccc2)C)OCC1CCN(CC1)CCNS(=O)(=O)C None
247 1811 41 3H-GR-113808 -2 26 Rat 10.7 pKi = 10.7 Binding
NoneNone
PDSP KiDatabase 393 7 1 6 1.6 O=C(c1cn(c2c1cccc2)C)OCC1CCN(CC1)CCNS(=O)(=O)C None
CHEMBL33884 1811 41 3H-GR-113808 -1 26 Human 10.7 pKi = 10.7 Binding
NoneNone
PDSP KiDatabase 393 7 1 6 1.6 O=C(c1cn(c2c1cccc2)C)OCC1CCN(CC1)CCNS(=O)(=O)C None
CHEMBL33884 1811 41 3H-GR-113808 -2 26 Rat 10.7 pKi = 10.7 Binding
NoneNone
PDSP KiDatabase 393 7 1 6 1.6 O=C(c1cn(c2c1cccc2)C)OCC1CCN(CC1)CCNS(=O)(=O)C None
119376 1811 41 3H-GR-113808 -2 26 Rat 10.5 pKi = 10.5 Binding
NoneNone
PDSP KiDatabase 393 7 1 6 1.6 O=C(c1cn(c2c1cccc2)C)OCC1CCN(CC1)CCNS(=O)(=O)C None
247 1811 41 3H-GR-113808 -2 26 Rat 10.5 pKi = 10.5 Binding
NoneNone
PDSP KiDatabase 393 7 1 6 1.6 O=C(c1cn(c2c1cccc2)C)OCC1CCN(CC1)CCNS(=O)(=O)C None
CHEMBL33884 1811 41 3H-GR-113808 -2 26 Rat 10.5 pKi = 10.5 Binding
NoneNone
PDSP KiDatabase 393 7 1 6 1.6 O=C(c1cn(c2c1cccc2)C)OCC1CCN(CC1)CCNS(=O)(=O)C None
119376 1811 41 3H-GR-113808 1 26 Guinea pig 10.2 pKi = 10.2 Binding
NoneNone
PDSP KiDatabase 393 7 1 6 1.6 O=C(c1cn(c2c1cccc2)C)OCC1CCN(CC1)CCNS(=O)(=O)C None
247 1811 41 3H-GR-113808 1 26 Guinea pig 10.2 pKi = 10.2 Binding
NoneNone
PDSP KiDatabase 393 7 1 6 1.6 O=C(c1cn(c2c1cccc2)C)OCC1CCN(CC1)CCNS(=O)(=O)C None
CHEMBL33884 1811 41 3H-GR-113808 1 26 Guinea pig 10.2 pKi = 10.2 Binding
NoneNone
PDSP KiDatabase 393 7 1 6 1.6 O=C(c1cn(c2c1cccc2)C)OCC1CCN(CC1)CCNS(=O)(=O)C None
121881 3434 21 3H-GR-113808 2 15 Guinea pig 10.2 pKi = 10.2 Binding
NoneNone
PDSP KiDatabase 382 6 1 6 3.4 CCCCN1CCC(CC1)COC(=O)c1cc(Cl)c(c2c1OCCO2)N None
256 3434 21 3H-GR-113808 2 15 Guinea pig 10.2 pKi = 10.2 Binding
NoneNone
PDSP KiDatabase 382 6 1 6 3.4 CCCCN1CCC(CC1)COC(=O)c1cc(Cl)c(c2c1OCCO2)N None
CHEMBL68131 3434 21 3H-GR-113808 2 15 Guinea pig 10.2 pKi = 10.2 Binding
NoneNone
PDSP KiDatabase 382 6 1 6 3.4 CCCCN1CCC(CC1)COC(=O)c1cc(Cl)c(c2c1OCCO2)N None
119376 1811 41 3H-GR-113808 -1 26 Human 10.1 pKi = 10.1 Binding
NoneNone
PDSP KiDatabase 393 7 1 6 1.6 O=C(c1cn(c2c1cccc2)C)OCC1CCN(CC1)CCNS(=O)(=O)C None
247 1811 41 3H-GR-113808 -1 26 Human 10.1 pKi = 10.1 Binding
NoneNone
PDSP KiDatabase 393 7 1 6 1.6 O=C(c1cn(c2c1cccc2)C)OCC1CCN(CC1)CCNS(=O)(=O)C None
CHEMBL33884 1811 41 3H-GR-113808 -1 26 Human 10.1 pKi = 10.1 Binding
NoneNone
PDSP KiDatabase 393 7 1 6 1.6 O=C(c1cn(c2c1cccc2)C)OCC1CCN(CC1)CCNS(=O)(=O)C None
121881 3434 21 3H-GR-113808 -2 15 Human 10.0 pKi = 10 Binding
NoneNone
PDSP KiDatabase 382 6 1 6 3.4 CCCCN1CCC(CC1)COC(=O)c1cc(Cl)c(c2c1OCCO2)N None
256 3434 21 3H-GR-113808 -2 15 Human 10.0 pKi = 10 Binding
NoneNone
PDSP KiDatabase 382 6 1 6 3.4 CCCCN1CCC(CC1)COC(=O)c1cc(Cl)c(c2c1OCCO2)N None
CHEMBL68131 3434 21 3H-GR-113808 -2 15 Human 10.0 pKi = 10 Binding
NoneNone
PDSP KiDatabase 382 6 1 6 3.4 CCCCN1CCC(CC1)COC(=O)c1cc(Cl)c(c2c1OCCO2)N None
119376 1811 41 3H-GR-113808 -1 26 Human 9.8 pKi = 9.8 Binding
NoneNone
PDSP KiDatabase 393 7 1 6 1.6 O=C(c1cn(c2c1cccc2)C)OCC1CCN(CC1)CCNS(=O)(=O)C None
247 1811 41 3H-GR-113808 -1 26 Human 9.8 pKi = 9.8 Binding
NoneNone
PDSP KiDatabase 393 7 1 6 1.6 O=C(c1cn(c2c1cccc2)C)OCC1CCN(CC1)CCNS(=O)(=O)C None
CHEMBL33884 1811 41 3H-GR-113808 -1 26 Human 9.8 pKi = 9.8 Binding
NoneNone
PDSP KiDatabase 393 7 1 6 1.6 O=C(c1cn(c2c1cccc2)C)OCC1CCN(CC1)CCNS(=O)(=O)C None
119376 1811 41 3H-GR-113808 -1 26 Mouse 9.7 pKi = 9.7 Binding
NoneNone
PDSP KiDatabase 393 7 1 6 1.6 O=C(c1cn(c2c1cccc2)C)OCC1CCN(CC1)CCNS(=O)(=O)C None
247 1811 41 3H-GR-113808 -1 26 Mouse 9.7 pKi = 9.7 Binding
NoneNone
PDSP KiDatabase 393 7 1 6 1.6 O=C(c1cn(c2c1cccc2)C)OCC1CCN(CC1)CCNS(=O)(=O)C None
CHEMBL33884 1811 41 3H-GR-113808 -1 26 Mouse 9.7 pKi = 9.7 Binding
NoneNone
PDSP KiDatabase 393 7 1 6 1.6 O=C(c1cn(c2c1cccc2)C)OCC1CCN(CC1)CCNS(=O)(=O)C None
119376 1811 41 3H-GR-113808 1 26 Guinea pig 9.6 pKi = 9.6 Binding
NoneNone
PDSP KiDatabase 393 7 1 6 1.6 O=C(c1cn(c2c1cccc2)C)OCC1CCN(CC1)CCNS(=O)(=O)C None
119376 1811 41 3H-GR-113808 -1 26 Human 9.6 pKi = 9.6 Binding
NoneNone
PDSP KiDatabase 393 7 1 6 1.6 O=C(c1cn(c2c1cccc2)C)OCC1CCN(CC1)CCNS(=O)(=O)C None
247 1811 41 3H-GR-113808 1 26 Guinea pig 9.6 pKi = 9.6 Binding
NoneNone
PDSP KiDatabase 393 7 1 6 1.6 O=C(c1cn(c2c1cccc2)C)OCC1CCN(CC1)CCNS(=O)(=O)C None
247 1811 41 3H-GR-113808 -1 26 Human 9.6 pKi = 9.6 Binding
NoneNone
PDSP KiDatabase 393 7 1 6 1.6 O=C(c1cn(c2c1cccc2)C)OCC1CCN(CC1)CCNS(=O)(=O)C None
CHEMBL33884 1811 41 3H-GR-113808 1 26 Guinea pig 9.6 pKi = 9.6 Binding
NoneNone
PDSP KiDatabase 393 7 1 6 1.6 O=C(c1cn(c2c1cccc2)C)OCC1CCN(CC1)CCNS(=O)(=O)C None
CHEMBL33884 1811 41 3H-GR-113808 -1 26 Human 9.6 pKi = 9.6 Binding
NoneNone
PDSP KiDatabase 393 7 1 6 1.6 O=C(c1cn(c2c1cccc2)C)OCC1CCN(CC1)CCNS(=O)(=O)C None
119376 1811 41 3H-GR-113808 1 26 Guinea pig 9.5 pKi = 9.5 Binding
NoneNone
PDSP KiDatabase 393 7 1 6 1.6 O=C(c1cn(c2c1cccc2)C)OCC1CCN(CC1)CCNS(=O)(=O)C None
119376 1811 41 3H-GR-113808 -1 26 Mouse 9.5 pKi = 9.5 Binding
NoneNone
PDSP KiDatabase 393 7 1 6 1.6 O=C(c1cn(c2c1cccc2)C)OCC1CCN(CC1)CCNS(=O)(=O)C None
247 1811 41 3H-GR-113808 1 26 Guinea pig 9.5 pKi = 9.5 Binding
NoneNone
PDSP KiDatabase 393 7 1 6 1.6 O=C(c1cn(c2c1cccc2)C)OCC1CCN(CC1)CCNS(=O)(=O)C None
247 1811 41 3H-GR-113808 -1 26 Mouse 9.5 pKi = 9.5 Binding
NoneNone
PDSP KiDatabase 393 7 1 6 1.6 O=C(c1cn(c2c1cccc2)C)OCC1CCN(CC1)CCNS(=O)(=O)C None
CHEMBL33884 1811 41 3H-GR-113808 1 26 Guinea pig 9.5 pKi = 9.5 Binding
NoneNone
PDSP KiDatabase 393 7 1 6 1.6 O=C(c1cn(c2c1cccc2)C)OCC1CCN(CC1)CCNS(=O)(=O)C None
CHEMBL33884 1811 41 3H-GR-113808 -1 26 Mouse 9.5 pKi = 9.5 Binding
NoneNone
PDSP KiDatabase 393 7 1 6 1.6 O=C(c1cn(c2c1cccc2)C)OCC1CCN(CC1)CCNS(=O)(=O)C None
121881 3434 21 3H-RS 57639 -27 15 Rat 9.5 pKi = 9.5 Binding
NoneNone
PDSP KiDatabase 382 6 1 6 3.4 CCCCN1CCC(CC1)COC(=O)c1cc(Cl)c(c2c1OCCO2)N None
256 3434 21 3H-RS 57639 -27 15 Rat 9.5 pKi = 9.5 Binding
NoneNone
PDSP KiDatabase 382 6 1 6 3.4 CCCCN1CCC(CC1)COC(=O)c1cc(Cl)c(c2c1OCCO2)N None
CHEMBL68131 3434 21 3H-RS 57639 -27 15 Rat 9.5 pKi = 9.5 Binding
NoneNone
PDSP KiDatabase 382 6 1 6 3.4 CCCCN1CCC(CC1)COC(=O)c1cc(Cl)c(c2c1OCCO2)N None
119376 1811 41 3H-GR-113808 1 26 Guinea pig 9.4 pKi = 9.4 Binding
NoneNone
PDSP KiDatabase 393 7 1 6 1.6 O=C(c1cn(c2c1cccc2)C)OCC1CCN(CC1)CCNS(=O)(=O)C None
247 1811 41 3H-GR-113808 1 26 Guinea pig 9.4 pKi = 9.4 Binding
NoneNone
PDSP KiDatabase 393 7 1 6 1.6 O=C(c1cn(c2c1cccc2)C)OCC1CCN(CC1)CCNS(=O)(=O)C None
CHEMBL33884 1811 41 3H-GR-113808 1 26 Guinea pig 9.4 pKi = 9.4 Binding
NoneNone
PDSP KiDatabase 393 7 1 6 1.6 O=C(c1cn(c2c1cccc2)C)OCC1CCN(CC1)CCNS(=O)(=O)C None
121881 3434 21 3H-GR-113808 -27 15 Rat 9.4 pKi = 9.4 Binding
NoneNone
PDSP KiDatabase 382 6 1 6 3.4 CCCCN1CCC(CC1)COC(=O)c1cc(Cl)c(c2c1OCCO2)N None
256 3434 21 3H-GR-113808 -27 15 Rat 9.4 pKi = 9.4 Binding
NoneNone
PDSP KiDatabase 382 6 1 6 3.4 CCCCN1CCC(CC1)COC(=O)c1cc(Cl)c(c2c1OCCO2)N None
CHEMBL68131 3434 21 3H-GR-113808 -27 15 Rat 9.4 pKi = 9.4 Binding
NoneNone
PDSP KiDatabase 382 6 1 6 3.4 CCCCN1CCC(CC1)COC(=O)c1cc(Cl)c(c2c1OCCO2)N None
121881 3434 21 3H-5HT -27 15 Rat 8.9 pKi = 8.9 Binding
NoneNone
PDSP KiDatabase 382 6 1 6 3.4 CCCCN1CCC(CC1)COC(=O)c1cc(Cl)c(c2c1OCCO2)N None
256 3434 21 3H-5HT -27 15 Rat 8.9 pKi = 8.9 Binding
NoneNone
PDSP KiDatabase 382 6 1 6 3.4 CCCCN1CCC(CC1)COC(=O)c1cc(Cl)c(c2c1OCCO2)N None
CHEMBL68131 3434 21 3H-5HT -27 15 Rat 8.9 pKi = 8.9 Binding
NoneNone
PDSP KiDatabase 382 6 1 6 3.4 CCCCN1CCC(CC1)COC(=O)c1cc(Cl)c(c2c1OCCO2)N None
None 214256 0 3H-GR-113808 251 13 Guinea pig 8.8 pKi = 8.8 Binding
NoneNone
PDSP KiDatabase 453 9 2 6 2.6 COC1=CC(=C(C=C1C(=O)CCC2CCN(CC2)CCNS(=O)(=O)C)Cl)N.Cl None
119376 1811 41 3H-GR-113808 -2 26 Rat 8.7 pKi = 8.7 Binding
NoneNone
PDSP KiDatabase 393 7 1 6 1.6 O=C(c1cn(c2c1cccc2)C)OCC1CCN(CC1)CCNS(=O)(=O)C None
247 1811 41 3H-GR-113808 -2 26 Rat 8.7 pKi = 8.7 Binding
NoneNone
PDSP KiDatabase 393 7 1 6 1.6 O=C(c1cn(c2c1cccc2)C)OCC1CCN(CC1)CCNS(=O)(=O)C None
CHEMBL33884 1811 41 3H-GR-113808 -2 26 Rat 8.7 pKi = 8.7 Binding
NoneNone
PDSP KiDatabase 393 7 1 6 1.6 O=C(c1cn(c2c1cccc2)C)OCC1CCN(CC1)CCNS(=O)(=O)C None
183782 3346 15 3H-GR-113808 1 14 Guinea pig 8.7 pKi = 8.7 Binding
NoneNone
PDSP KiDatabase 352 8 1 4 4.4 CCCCN1CCC(CC1)CCC(=O)c1cc(Cl)c(cc1OC)N None
237 3346 15 3H-GR-113808 1 14 Guinea pig 8.7 pKi = 8.7 Binding
NoneNone
PDSP KiDatabase 352 8 1 4 4.4 CCCCN1CCC(CC1)CCC(=O)c1cc(Cl)c(cc1OC)N None
CHEMBL85251 3346 15 3H-GR-113808 1 14 Guinea pig 8.7 pKi = 8.7 Binding
NoneNone
PDSP KiDatabase 352 8 1 4 4.4 CCCCN1CCC(CC1)CCC(=O)c1cc(Cl)c(cc1OC)N None
240 931 39 3H-5HT -8 25 Rat 8.0 pKi = 8 Binding
NoneNone
PDSP KiDatabase 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N None
2769 931 39 3H-5HT -8 25 Rat 8.0 pKi = 8 Binding
NoneNone
PDSP KiDatabase 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N None
44279790 931 39 3H-5HT -8 25 Rat 8.0 pKi = 8 Binding
NoneNone
PDSP KiDatabase 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N None
660 931 39 3H-5HT -8 25 Rat 8.0 pKi = 8 Binding
NoneNone
PDSP KiDatabase 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N None
CHEMBL1729 931 39 3H-5HT -8 25 Rat 8.0 pKi = 8 Binding
NoneNone
PDSP KiDatabase 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N None
CHEMBL560739 931 39 3H-5HT -8 25 Rat 8.0 pKi = 8 Binding
NoneNone
PDSP KiDatabase 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N None
DB00604 931 39 3H-5HT -8 25 Rat 8.0 pKi = 8 Binding
NoneNone
PDSP KiDatabase 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N None
None 214237 0 3H-GR-113808 1 6 Human 8.0 pKi = 8.0 Binding
NoneNone
PDSP KiDatabase 367 2 1 6 2.4 CN1C2CCC1CC(C2)OC(=O)N3C4=C(C=CC(=C4)OC)NC3=O.Cl None
108182 4068 18 3H-5HT -1 16 Rat 7.0 pKi = 7 Binding
NoneNone
PDSP KiDatabase 309 3 2 4 1.8 COc1cc(N)c(cc1C(=O)NC1CN2CCC1CC2)Cl None
245 4068 18 3H-5HT -1 16 Rat 7.0 pKi = 7 Binding
NoneNone
PDSP KiDatabase 309 3 2 4 1.8 COc1cc(N)c(cc1C(=O)NC1CN2CCC1CC2)Cl None
CHEMBL18041 4068 18 3H-5HT -1 16 Rat 7.0 pKi = 7 Binding
NoneNone
PDSP KiDatabase 309 3 2 4 1.8 COc1cc(N)c(cc1C(=O)NC1CN2CCC1CC2)Cl None
57174031 214163 0 3H-5HT -33 19 Rat 7.0 pKi = 7 Binding
NoneNone
PDSP KiDatabase 284 2 1 3 3.0 CN1C2CCC1CC(C2)OC(=O)C3=CNC4=CC=CC=C43 None
3035240 214200 0 3H-GR-113808 -1 5 Guinea pig 7.0 pKi = 7 Binding
NoneNone
PDSP KiDatabase 359 3 2 4 2.6 COC1=CC(=C(C=C1C(=O)NC2CCN3CCCC2C3)Cl)N.Cl None
1809 134 28 3H-5HT -46773 36 Rat 6.0 pKi = 6 Binding
NoneNone
PDSP KiDatabase 203 3 3 2 0.8 NCCc1c[nH]c2c1cc(cc2)C(=O)N None
1809 134 28 3H-GR-113808 -46773 36 Rat 6.0 pKi = 6 Binding
NoneNone
PDSP KiDatabase 203 3 3 2 0.8 NCCc1c[nH]c2c1cc(cc2)C(=O)N None
4 134 28 3H-5HT -46773 36 Rat 6.0 pKi = 6 Binding
NoneNone
PDSP KiDatabase 203 3 3 2 0.8 NCCc1c[nH]c2c1cc(cc2)C(=O)N None
4 134 28 3H-GR-113808 -46773 36 Rat 6.0 pKi = 6 Binding
NoneNone
PDSP KiDatabase 203 3 3 2 0.8 NCCc1c[nH]c2c1cc(cc2)C(=O)N None
CHEMBL18840 134 28 3H-5HT -46773 36 Rat 6.0 pKi = 6 Binding
NoneNone
PDSP KiDatabase 203 3 3 2 0.8 NCCc1c[nH]c2c1cc(cc2)C(=O)N None
CHEMBL18840 134 28 3H-GR-113808 -46773 36 Rat 6.0 pKi = 6 Binding
NoneNone
PDSP KiDatabase 203 3 3 2 0.8 NCCc1c[nH]c2c1cc(cc2)C(=O)N None
107 141 116 3H-GR-113808 -389 30 Human 6.0 pKi = 6 Binding
NoneNone
PDSP KiDatabase 190 3 2 2 1.7 NCCc1c[nH]c2c1cc(OC)cc2 None
1833 141 116 3H-GR-113808 -389 30 Human 6.0 pKi = 6 Binding
NoneNone
PDSP KiDatabase 190 3 2 2 1.7 NCCc1c[nH]c2c1cc(OC)cc2 None
CHEMBL8165 141 116 3H-GR-113808 -389 30 Human 6.0 pKi = 6 Binding
NoneNone
PDSP KiDatabase 190 3 2 2 1.7 NCCc1c[nH]c2c1cc(OC)cc2 None
1220 186 46 3H-GR-113808 -2511 44 Rat 6.0 pKi = 6 Binding
NoneNone
PDSP KiDatabase 247 5 1 2 3.4 CCCN(C1CCc2c(C1)c(O)ccc2)CCC None
31 186 46 3H-GR-113808 -2511 44 Rat 6.0 pKi = 6 Binding
NoneNone
PDSP KiDatabase 247 5 1 2 3.4 CCCN(C1CCc2c(C1)c(O)ccc2)CCC None
7 186 46 3H-GR-113808 -2511 44 Rat 6.0 pKi = 6 Binding
NoneNone
PDSP KiDatabase 247 5 1 2 3.4 CCCN(C1CCc2c(C1)c(O)ccc2)CCC None
CHEMBL56 186 46 3H-GR-113808 -2511 44 Rat 6.0 pKi = 6 Binding
NoneNone
PDSP KiDatabase 247 5 1 2 3.4 CCCN(C1CCc2c(C1)c(O)ccc2)CCC None
202 1480 0 UNDEFINED -9 31 Guinea pig 6.0 pKi = 6 Binding
NoneNone
PDSP KiDatabase 297 6 1 3 4.6 CNCC[C@@H](c1cccs1)Oc1cccc2c1cccc2 None
60835 1480 0 UNDEFINED -9 31 Guinea pig 6.0 pKi = 6 Binding
NoneNone
PDSP KiDatabase 297 6 1 3 4.6 CNCC[C@@H](c1cccs1)Oc1cccc2c1cccc2 None
972 1480 0 UNDEFINED -9 31 Guinea pig 6.0 pKi = 6 Binding
NoneNone
PDSP KiDatabase 297 6 1 3 4.6 CNCC[C@@H](c1cccs1)Oc1cccc2c1cccc2 None
CHEMBL1175 1480 0 UNDEFINED -9 31 Guinea pig 6.0 pKi = 6 Binding
NoneNone
PDSP KiDatabase 297 6 1 3 4.6 CNCC[C@@H](c1cccs1)Oc1cccc2c1cccc2 None
DB00476 1480 0 UNDEFINED -9 31 Guinea pig 6.0 pKi = 6 Binding
NoneNone
PDSP KiDatabase 297 6 1 3 4.6 CNCC[C@@H](c1cccs1)Oc1cccc2c1cccc2 None
1524 2150 89 3H-GR-113808 -724 51 Rat 6.0 pKi = 6 Binding
NoneNone
PDSP KiDatabase 395 5 1 5 2.4 Fc1ccc(cc1)C(=O)C1CCN(CC1)CCn1c(=O)[nH]c2c(c1=O)cccc2 None
197 2150 89 3H-GR-113808 -724 51 Rat 6.0 pKi = 6 Binding
NoneNone
PDSP KiDatabase 395 5 1 5 2.4 Fc1ccc(cc1)C(=O)C1CCN(CC1)CCn1c(=O)[nH]c2c(c1=O)cccc2 None
3822 2150 89 3H-GR-113808 -724 51 Rat 6.0 pKi = 6 Binding
NoneNone
PDSP KiDatabase 395 5 1 5 2.4 Fc1ccc(cc1)C(=O)C1CCN(CC1)CCn1c(=O)[nH]c2c(c1=O)cccc2 None
88 2150 89 3H-GR-113808 -724 51 Rat 6.0 pKi = 6 Binding
NoneNone
PDSP KiDatabase 395 5 1 5 2.4 Fc1ccc(cc1)C(=O)C1CCN(CC1)CCn1c(=O)[nH]c2c(c1=O)cccc2 None
CHEMBL51 2150 89 3H-GR-113808 -724 51 Rat 6.0 pKi = 6 Binding
NoneNone
PDSP KiDatabase 395 5 1 5 2.4 Fc1ccc(cc1)C(=O)C1CCN(CC1)CCn1c(=O)[nH]c2c(c1=O)cccc2 None
DB12465 2150 89 3H-GR-113808 -724 51 Rat 6.0 pKi = 6 Binding
NoneNone
PDSP KiDatabase 395 5 1 5 2.4 Fc1ccc(cc1)C(=O)C1CCN(CC1)CCn1c(=O)[nH]c2c(c1=O)cccc2 None
1621 2396 16 3H-GR-113808 -3235 44 Rat 6.0 pKi = 6 Binding
NoneNone
PDSP KiDatabase 323 3 1 2 2.9 CCN(C(=O)[C@H]1CN(C)[C@H]2C(=C1)c1cccc3c1c(C2)c[nH]3)CC None
17 2396 16 3H-GR-113808 -3235 44 Rat 6.0 pKi = 6 Binding
NoneNone
PDSP KiDatabase 323 3 1 2 2.9 CCN(C(=O)[C@H]1CN(C)[C@H]2C(=C1)c1cccc3c1c(C2)c[nH]3)CC None
5761 2396 16 3H-GR-113808 -3235 44 Rat 6.0 pKi = 6 Binding
NoneNone
PDSP KiDatabase 323 3 1 2 2.9 CCN(C(=O)[C@H]1CN(C)[C@H]2C(=C1)c1cccc3c1c(C2)c[nH]3)CC None
CHEMBL263881 2396 16 3H-GR-113808 -3235 44 Rat 6.0 pKi = 6 Binding
NoneNone
PDSP KiDatabase 323 3 1 2 2.9 CCN(C(=O)[C@H]1CN(C)[C@H]2C(=C1)c1cccc3c1c(C2)c[nH]3)CC None
DB04829 2396 16 3H-GR-113808 -3235 44 Rat 6.0 pKi = 6 Binding
NoneNone
PDSP KiDatabase 323 3 1 2 2.9 CCN(C(=O)[C@H]1CN(C)[C@H]2C(=C1)c1cccc3c1c(C2)c[nH]3)CC None
2543 3651 66 3H-GR-113808 -281 31 Rat 6.0 pKi = 6 Binding
NoneNone
PDSP KiDatabase 295 6 2 3 1.3 CNS(=O)(=O)Cc1ccc2c(c1)c(CCN(C)C)c[nH]2 None
5358 3651 66 3H-GR-113808 -281 31 Rat 6.0 pKi = 6 Binding
NoneNone
PDSP KiDatabase 295 6 2 3 1.3 CNS(=O)(=O)Cc1ccc2c(c1)c(CCN(C)C)c[nH]2 None
54 3651 66 3H-GR-113808 -281 31 Rat 6.0 pKi = 6 Binding
NoneNone
PDSP KiDatabase 295 6 2 3 1.3 CNS(=O)(=O)Cc1ccc2c(c1)c(CCN(C)C)c[nH]2 None
CHEMBL128 3651 66 3H-GR-113808 -281 31 Rat 6.0 pKi = 6 Binding
NoneNone
PDSP KiDatabase 295 6 2 3 1.3 CNS(=O)(=O)Cc1ccc2c(c1)c(CCN(C)C)c[nH]2 None
DB00669 3651 66 3H-GR-113808 -281 31 Rat 6.0 pKi = 6 Binding
NoneNone
PDSP KiDatabase 295 6 2 3 1.3 CNS(=O)(=O)Cc1ccc2c(c1)c(CCN(C)C)c[nH]2 None
108182 4068 18 3H-GR-113808 -1 16 Guinea pig 6.0 pKi = 6 Binding
NoneNone
PDSP KiDatabase 309 3 2 4 1.8 COc1cc(N)c(cc1C(=O)NC1CN2CCC1CC2)Cl None
108182 4068 18 3H-RS 57639 -1 16 Rat 6.0 pKi = 6 Binding
NoneNone
PDSP KiDatabase 309 3 2 4 1.8 COc1cc(N)c(cc1C(=O)NC1CN2CCC1CC2)Cl None
245 4068 18 3H-GR-113808 -1 16 Guinea pig 6.0 pKi = 6 Binding
NoneNone
PDSP KiDatabase 309 3 2 4 1.8 COc1cc(N)c(cc1C(=O)NC1CN2CCC1CC2)Cl None
245 4068 18 3H-RS 57639 -1 16 Rat 6.0 pKi = 6 Binding
NoneNone
PDSP KiDatabase 309 3 2 4 1.8 COc1cc(N)c(cc1C(=O)NC1CN2CCC1CC2)Cl None
CHEMBL18041 4068 18 3H-GR-113808 -1 16 Guinea pig 6.0 pKi = 6 Binding
NoneNone
PDSP KiDatabase 309 3 2 4 1.8 COc1cc(N)c(cc1C(=O)NC1CN2CCC1CC2)Cl None
CHEMBL18041 4068 18 3H-RS 57639 -1 16 Rat 6.0 pKi = 6 Binding
NoneNone
PDSP KiDatabase 309 3 2 4 1.8 COc1cc(N)c(cc1C(=O)NC1CN2CCC1CC2)Cl None
5656 201377 82 UNDEFINED -7 40 Guinea pig 6.0 pKi = 6 Binding
NoneNone
PDSP KiDatabase 277 5 1 3 3.0 COc1ccc(C(CN(C)C)C2(O)CCCCC2)cc1 None
CHEMBL637 201377 82 UNDEFINED -7 40 Guinea pig 6.0 pKi = 6 Binding
NoneNone
PDSP KiDatabase 277 5 1 3 3.0 COc1ccc(C(CN(C)C)C2(O)CCCCC2)cc1 None
54841 201437 51 UNDEFINED -1 28 Guinea pig 6.0 pKi = 6 Binding
NoneNone
PDSP KiDatabase 255 6 1 2 3.7 CNCC[C@@H](Oc1ccccc1C)c1ccccc1 None
CHEMBL641 201437 51 UNDEFINED -1 28 Guinea pig 6.0 pKi = 6 Binding
NoneNone
PDSP KiDatabase 255 6 1 2 3.7 CNCC[C@@H](Oc1ccccc1C)c1ccccc1 None
None 214629 0 UNDEFINED -1122 11 Human 6.0 pKi = 6 Binding
NoneNone
PDSP KiDatabase 243 3 1 4 2.7 CCC1=CC2=C(O1)C=CC3=C2N(N=C3)CC(C)N None
None 215342 0 UNDEFINED - 1 Human 6.0 pKi = 6 Binding
NoneNone
PDSP KiDatabase 394 5 1 4 5.1 CC1=CC(=C(C=C1)OC)NC(=O)OC2CC3CCCC(C2)N3CC4=CC=CC=C4 None
1809 134 28 3H-GR-113808 -87096 36 Guinea pig 5.0 pKi = 5 Binding
NoneNone
PDSP KiDatabase 203 3 3 2 0.8 NCCc1c[nH]c2c1cc(cc2)C(=O)N None
1809 134 28 3H-GR-113808 -109647 36 Human 5.0 pKi = 5 Binding
NoneNone
PDSP KiDatabase 203 3 3 2 0.8 NCCc1c[nH]c2c1cc(cc2)C(=O)N None
1809 134 28 3H-GR-113808 -109647 36 Mouse 5.0 pKi = 5 Binding
NoneNone
PDSP KiDatabase 203 3 3 2 0.8 NCCc1c[nH]c2c1cc(cc2)C(=O)N None
1809 134 28 3H-GR-113808 -46773 36 Rat 5.0 pKi = 5 Binding
NoneNone
PDSP KiDatabase 203 3 3 2 0.8 NCCc1c[nH]c2c1cc(cc2)C(=O)N None
4 134 28 3H-GR-113808 -87096 36 Guinea pig 5.0 pKi = 5 Binding
NoneNone
PDSP KiDatabase 203 3 3 2 0.8 NCCc1c[nH]c2c1cc(cc2)C(=O)N None
4 134 28 3H-GR-113808 -109647 36 Human 5.0 pKi = 5 Binding
NoneNone
PDSP KiDatabase 203 3 3 2 0.8 NCCc1c[nH]c2c1cc(cc2)C(=O)N None
4 134 28 3H-GR-113808 -109647 36 Mouse 5.0 pKi = 5 Binding
NoneNone
PDSP KiDatabase 203 3 3 2 0.8 NCCc1c[nH]c2c1cc(cc2)C(=O)N None
4 134 28 3H-GR-113808 -46773 36 Rat 5.0 pKi = 5 Binding
NoneNone
PDSP KiDatabase 203 3 3 2 0.8 NCCc1c[nH]c2c1cc(cc2)C(=O)N None
CHEMBL18840 134 28 3H-GR-113808 -87096 36 Guinea pig 5.0 pKi = 5 Binding
NoneNone
PDSP KiDatabase 203 3 3 2 0.8 NCCc1c[nH]c2c1cc(cc2)C(=O)N None
CHEMBL18840 134 28 3H-GR-113808 -109647 36 Human 5.0 pKi = 5 Binding
NoneNone
PDSP KiDatabase 203 3 3 2 0.8 NCCc1c[nH]c2c1cc(cc2)C(=O)N None
CHEMBL18840 134 28 3H-GR-113808 -109647 36 Mouse 5.0 pKi = 5 Binding
NoneNone
PDSP KiDatabase 203 3 3 2 0.8 NCCc1c[nH]c2c1cc(cc2)C(=O)N None
CHEMBL18840 134 28 3H-GR-113808 -46773 36 Rat 5.0 pKi = 5 Binding
NoneNone
PDSP KiDatabase 203 3 3 2 0.8 NCCc1c[nH]c2c1cc(cc2)C(=O)N None
1220 186 46 3H-GR-113808 -2511 44 Rat 5.0 pKi = 5 Binding
NoneNone
PDSP KiDatabase 247 5 1 2 3.4 CCCN(C1CCc2c(C1)c(O)ccc2)CCC None
31 186 46 3H-GR-113808 -2511 44 Rat 5.0 pKi = 5 Binding
NoneNone
PDSP KiDatabase 247 5 1 2 3.4 CCCN(C1CCc2c(C1)c(O)ccc2)CCC None
7 186 46 3H-GR-113808 -2511 44 Rat 5.0 pKi = 5 Binding
NoneNone
PDSP KiDatabase 247 5 1 2 3.4 CCCN(C1CCc2c(C1)c(O)ccc2)CCC None
CHEMBL56 186 46 3H-GR-113808 -2511 44 Rat 5.0 pKi = 5 Binding
NoneNone
PDSP KiDatabase 247 5 1 2 3.4 CCCN(C1CCc2c(C1)c(O)ccc2)CCC None
179 396 107 3H-GR-113808 -4365 50 Guinea pig 5.0 pKi = 5 Binding
NoneNone
PDSP KiDatabase 369 7 2 6 1.3 CCN1CCCC1CNC(=O)c1cc(c(cc1OC)N)S(=O)(=O)CC None
2159 396 107 3H-GR-113808 -4365 50 Guinea pig 5.0 pKi = 5 Binding
NoneNone
PDSP KiDatabase 369 7 2 6 1.3 CCN1CCCC1CNC(=O)c1cc(c(cc1OC)N)S(=O)(=O)CC None
963 396 107 3H-GR-113808 -4365 50 Guinea pig 5.0 pKi = 5 Binding
NoneNone
PDSP KiDatabase 369 7 2 6 1.3 CCN1CCCC1CNC(=O)c1cc(c(cc1OC)N)S(=O)(=O)CC None
CHEMBL243712 396 107 3H-GR-113808 -4365 50 Guinea pig 5.0 pKi = 5 Binding
NoneNone
PDSP KiDatabase 369 7 2 6 1.3 CCN1CCCC1CNC(=O)c1cc(c(cc1OC)N)S(=O)(=O)CC None
DB06288 396 107 3H-GR-113808 -4365 50 Guinea pig 5.0 pKi = 5 Binding
NoneNone
PDSP KiDatabase 369 7 2 6 1.3 CCN1CCCC1CNC(=O)c1cc(c(cc1OC)N)S(=O)(=O)CC None
2477 734 54 3H-GR-113808 -1548 28 Rat 5.0 pKi = 5 Binding
NoneNone
PDSP KiDatabase 385 6 0 6 2.1 O=C1CC2(CCCC2)CC(=O)N1CCCCN1CCN(CC1)c1ncccn1 None
36 734 54 3H-GR-113808 -1548 28 Rat 5.0 pKi = 5 Binding
NoneNone
PDSP KiDatabase 385 6 0 6 2.1 O=C1CC2(CCCC2)CC(=O)N1CCCCN1CCN(CC1)c1ncccn1 None
437 734 54 3H-GR-113808 -1548 28 Rat 5.0 pKi = 5 Binding
NoneNone
PDSP KiDatabase 385 6 0 6 2.1 O=C1CC2(CCCC2)CC(=O)N1CCCCN1CCN(CC1)c1ncccn1 None
CHEMBL49 734 54 3H-GR-113808 -1548 28 Rat 5.0 pKi = 5 Binding
NoneNone
PDSP KiDatabase 385 6 0 6 2.1 O=C1CC2(CCCC2)CC(=O)N1CCCCN1CCN(CC1)c1ncccn1 None
DB00490 734 54 3H-GR-113808 -1548 28 Rat 5.0 pKi = 5 Binding
NoneNone
PDSP KiDatabase 385 6 0 6 2.1 O=C1CC2(CCCC2)CC(=O)N1CCCCN1CCN(CC1)c1ncccn1 None
135398737 944 89 3H-GR-113808 -4168 91 Guinea pig 5.0 pKi = 5 Binding
NoneNone
PDSP KiDatabase 326 0 1 4 3.7 CN1CCN(CC1)C1=Nc2cc(Cl)ccc2Nc2c1cccc2 None
38 944 89 3H-GR-113808 -4168 91 Guinea pig 5.0 pKi = 5 Binding
NoneNone
PDSP KiDatabase 326 0 1 4 3.7 CN1CCN(CC1)C1=Nc2cc(Cl)ccc2Nc2c1cccc2 None
722 944 89 3H-GR-113808 -4168 91 Guinea pig 5.0 pKi = 5 Binding
NoneNone
PDSP KiDatabase 326 0 1 4 3.7 CN1CCN(CC1)C1=Nc2cc(Cl)ccc2Nc2c1cccc2 None
CHEMBL42 944 89 3H-GR-113808 -4168 91 Guinea pig 5.0 pKi = 5 Binding
NoneNone
PDSP KiDatabase 326 0 1 4 3.7 CN1CCN(CC1)C1=Nc2cc(Cl)ccc2Nc2c1cccc2 None
DB00363 944 89 3H-GR-113808 -4168 91 Guinea pig 5.0 pKi = 5 Binding
NoneNone
PDSP KiDatabase 326 0 1 4 3.7 CN1CCN(CC1)C1=Nc2cc(Cl)ccc2Nc2c1cccc2 None
107780 1814 50 3H-5HT -10715 17 Guinea pig 5.0 pKi = 5 Binding
NoneNone
PDSP KiDatabase 497 6 1 7 5.0 COc1ccc(cc1N1CCN(CC1)C)NC(=O)c1ccc(cc1)c1ccc(cc1C)c1noc(n1)C None
14 1814 50 3H-5HT -10715 17 Guinea pig 5.0 pKi = 5 Binding
NoneNone
PDSP KiDatabase 497 6 1 7 5.0 COc1ccc(cc1N1CCN(CC1)C)NC(=O)c1ccc(cc1)c1ccc(cc1C)c1noc(n1)C None
CHEMBL15928 1814 50 3H-5HT -10715 17 Guinea pig 5.0 pKi = 5 Binding
NoneNone
PDSP KiDatabase 497 6 1 7 5.0 COc1ccc(cc1N1CCN(CC1)C)NC(=O)c1ccc(cc1)c1ccc(cc1C)c1noc(n1)C None
1353 1880 85 3H-GR-113808 -6918 85 Guinea pig 5.0 pKi = 5 Binding
NoneNone
PDSP KiDatabase 375 6 1 3 4.4 Fc1ccc(cc1)C(=O)CCCN1CCC(CC1)(O)c1ccc(cc1)Cl None
3559 1880 85 3H-GR-113808 -6918 85 Guinea pig 5.0 pKi = 5 Binding
NoneNone
PDSP KiDatabase 375 6 1 3 4.4 Fc1ccc(cc1)C(=O)CCCN1CCC(CC1)(O)c1ccc(cc1)Cl None
86 1880 85 3H-GR-113808 -6918 85 Guinea pig 5.0 pKi = 5 Binding
NoneNone
PDSP KiDatabase 375 6 1 3 4.4 Fc1ccc(cc1)C(=O)CCCN1CCC(CC1)(O)c1ccc(cc1)Cl None
CHEMBL54 1880 85 3H-GR-113808 -6918 85 Guinea pig 5.0 pKi = 5 Binding
NoneNone
PDSP KiDatabase 375 6 1 3 4.4 Fc1ccc(cc1)C(=O)CCCN1CCC(CC1)(O)c1ccc(cc1)Cl None
DB00502 1880 85 3H-GR-113808 -6918 85 Guinea pig 5.0 pKi = 5 Binding
NoneNone
PDSP KiDatabase 375 6 1 3 4.4 Fc1ccc(cc1)C(=O)CCCN1CCC(CC1)(O)c1ccc(cc1)Cl None
2402 3318 58 3H-GR-113808 -660 25 Guinea pig 5.0 pKi = 5 Binding
NoneNone
PDSP KiDatabase 260 7 1 2 3.5 CCCN(CCC)CCc1cccc2c1CC(=N2)O None
5095 3318 58 3H-GR-113808 -660 25 Guinea pig 5.0 pKi = 5 Binding
NoneNone
PDSP KiDatabase 260 7 1 2 3.5 CCCN(CCC)CCc1cccc2c1CC(=N2)O None
7295 3318 58 3H-GR-113808 -660 25 Guinea pig 5.0 pKi = 5 Binding
NoneNone
PDSP KiDatabase 260 7 1 2 3.5 CCCN(CCC)CCc1cccc2c1CC(=N2)O None
CHEMBL589 3318 58 3H-GR-113808 -660 25 Guinea pig 5.0 pKi = 5 Binding
NoneNone
PDSP KiDatabase 260 7 1 2 3.5 CCCN(CCC)CCc1cccc2c1CC(=N2)O None
DB00268 3318 58 3H-GR-113808 -660 25 Guinea pig 5.0 pKi = 5 Binding
NoneNone
PDSP KiDatabase 260 7 1 2 3.5 CCCN(CCC)CCc1cccc2c1CC(=N2)O None
1150 3817 116 3H-5HT -436 24 Mouse 5.0 pKi = 5 Binding
NoneNone
PDSP KiDatabase 160 2 2 1 1.7 NCCc1c[nH]c2c1cccc2 None
125 3817 116 3H-5HT -436 24 Mouse 5.0 pKi = 5 Binding
NoneNone
PDSP KiDatabase 160 2 2 1 1.7 NCCc1c[nH]c2c1cccc2 None
CHEMBL6640 3817 116 3H-5HT -436 24 Mouse 5.0 pKi = 5 Binding
NoneNone
PDSP KiDatabase 160 2 2 1 1.7 NCCc1c[nH]c2c1cccc2 None
DB08653 3817 116 3H-5HT -436 24 Mouse 5.0 pKi = 5 Binding
NoneNone
PDSP KiDatabase 160 2 2 1 1.7 NCCc1c[nH]c2c1cccc2 None
44208932 140176 6 UNDEFINED -120226 37 Human 5.0 pKi = 5 Binding
NoneNone
PDSP KiDatabase 475 5 1 3 6.8 Cc1ccc(Cn2nc(C(=O)NC3C4(C)CCC(C4)C3(C)C)cc2-c2ccc(Cl)c(C)c2)cc1 None
CHEMBL381689 140176 6 UNDEFINED -120226 37 Human 5.0 pKi = 5 Binding
NoneNone
PDSP KiDatabase 475 5 1 3 6.8 Cc1ccc(Cn2nc(C(=O)NC3C4(C)CCC(C4)C3(C)C)cc2-c2ccc(Cl)c(C)c2)cc1 None
None 214571 0 3H-GR-113808 -331 5 Rat 5.0 pKi = 5 Binding
NoneNone
PDSP KiDatabase 390 4 1 4 3.2 C1CN(CCN1CCN2C3=CC=CC=C3NC2=O)C4=CC=C(C=C4)C(F)(F)F None
None 214703 0 Functional -660 27 Rat 5.0 pKi = 5 Binding
NoneNone
PDSP KiDatabase 322 5 2 3 4.1 CC(CC1=CNC2=C1C=C(C=C2)OCC3=CC=CS3)N.Cl None
None 214703 0 UNDEFINED -660 27 Rat 5.0 pKi = 5 Binding
NoneNone
PDSP KiDatabase 322 5 2 3 4.1 CC(CC1=CNC2=C1C=C(C=C2)OCC3=CC=CS3)N.Cl None
108182 4068 18 3H-GR-113808 1 16 Mouse 6.0 pKi = 6.0 Binding
NoneNone
PDSP KiDatabase 309 3 2 4 1.8 COc1cc(N)c(cc1C(=O)NC1CN2CCC1CC2)Cl None
245 4068 18 3H-GR-113808 1 16 Mouse 6.0 pKi = 6.0 Binding
NoneNone
PDSP KiDatabase 309 3 2 4 1.8 COc1cc(N)c(cc1C(=O)NC1CN2CCC1CC2)Cl None
CHEMBL18041 4068 18 3H-GR-113808 1 16 Mouse 6.0 pKi = 6.0 Binding
NoneNone
PDSP KiDatabase 309 3 2 4 1.8 COc1cc(N)c(cc1C(=O)NC1CN2CCC1CC2)Cl None
107 141 116 3H-5HT -257 30 Rat 7.0 pKi = 7.0 Binding
NoneNone
PDSP KiDatabase 190 3 2 2 1.7 NCCc1c[nH]c2c1cc(OC)cc2 None
1833 141 116 3H-5HT -257 30 Rat 7.0 pKi = 7.0 Binding
NoneNone
PDSP KiDatabase 190 3 2 2 1.7 NCCc1c[nH]c2c1cc(OC)cc2 None
CHEMBL8165 141 116 3H-5HT -257 30 Rat 7.0 pKi = 7.0 Binding
NoneNone
PDSP KiDatabase 190 3 2 2 1.7 NCCc1c[nH]c2c1cc(OC)cc2 None
3035240 214200 0 3H-GR-113808 1 5 Rat 7.0 pKi = 7.0 Binding
NoneNone
PDSP KiDatabase 359 3 2 4 2.6 COC1=CC(=C(C=C1C(=O)NC2CCN3CCCC2C3)Cl)N.Cl None
4595 176141 102 3H-GR113808 -3 15 Rat 5.9 pKi = 5.9 Binding
NoneNone
PDSP KiDatabase 293 2 0 4 3.1 Cc1nccn1CC1CCc2c(c3ccccc3n2C)C1=O None
CHEMBL46 176141 102 3H-GR113808 -3 15 Rat 5.9 pKi = 5.9 Binding
NoneNone
PDSP KiDatabase 293 2 0 4 3.1 Cc1nccn1CC1CCc2c(c3ccccc3n2C)C1=O None
240 931 39 3H-GR-113808 -8 25 Rat 6.9 pKi = 6.9 Binding
NoneNone
PDSP KiDatabase 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N None
2769 931 39 3H-GR-113808 -8 25 Rat 6.9 pKi = 6.9 Binding
NoneNone
PDSP KiDatabase 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N None
44279790 931 39 3H-GR-113808 -8 25 Rat 6.9 pKi = 6.9 Binding
NoneNone
PDSP KiDatabase 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N None
660 931 39 3H-GR-113808 -8 25 Rat 6.9 pKi = 6.9 Binding
NoneNone
PDSP KiDatabase 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N None
CHEMBL1729 931 39 3H-GR-113808 -8 25 Rat 6.9 pKi = 6.9 Binding
NoneNone
PDSP KiDatabase 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N None
CHEMBL560739 931 39 3H-GR-113808 -8 25 Rat 6.9 pKi = 6.9 Binding
NoneNone
PDSP KiDatabase 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N None
DB00604 931 39 3H-GR-113808 -8 25 Rat 6.9 pKi = 6.9 Binding
NoneNone
PDSP KiDatabase 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N None
107 141 116 3H-GR-113808 -257 30 Rat 6.9 pKi = 6.9 Binding
NoneNone
PDSP KiDatabase 190 3 2 2 1.7 NCCc1c[nH]c2c1cc(OC)cc2 None
1833 141 116 3H-GR-113808 -257 30 Rat 6.9 pKi = 6.9 Binding
NoneNone
PDSP KiDatabase 190 3 2 2 1.7 NCCc1c[nH]c2c1cc(OC)cc2 None
CHEMBL8165 141 116 3H-GR-113808 -257 30 Rat 6.9 pKi = 6.9 Binding
NoneNone
PDSP KiDatabase 190 3 2 2 1.7 NCCc1c[nH]c2c1cc(OC)cc2 None
5 139 66 3H-GR-113808 -288 54 Human 6.9 pKi = 6.9 Binding
NoneNone
PDSP KiDatabase 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 None
5 139 66 3H-GR-113808 -117 54 Rat 6.9 pKi = 6.9 Binding
NoneNone
PDSP KiDatabase 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 None
5202 139 66 3H-GR-113808 -288 54 Human 6.9 pKi = 6.9 Binding
NoneNone
PDSP KiDatabase 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 None
5202 139 66 3H-GR-113808 -117 54 Rat 6.9 pKi = 6.9 Binding
NoneNone
PDSP KiDatabase 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 None
CHEMBL39 139 66 3H-GR-113808 -288 54 Human 6.9 pKi = 6.9 Binding
NoneNone
PDSP KiDatabase 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 None
CHEMBL39 139 66 3H-GR-113808 -117 54 Rat 6.9 pKi = 6.9 Binding
NoneNone
PDSP KiDatabase 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 None
DB08839 139 66 3H-GR-113808 -288 54 Human 6.9 pKi = 6.9 Binding
NoneNone
PDSP KiDatabase 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 None
DB08839 139 66 3H-GR-113808 -117 54 Rat 6.9 pKi = 6.9 Binding
NoneNone
PDSP KiDatabase 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 None
240 931 39 3H-GR-113808 -8 25 Rat 6.9 pKi = 6.9 Binding
NoneNone
PDSP KiDatabase 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N None
2769 931 39 3H-GR-113808 -8 25 Rat 6.9 pKi = 6.9 Binding
NoneNone
PDSP KiDatabase 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N None
44279790 931 39 3H-GR-113808 -8 25 Rat 6.9 pKi = 6.9 Binding
NoneNone
PDSP KiDatabase 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N None
660 931 39 3H-GR-113808 -8 25 Rat 6.9 pKi = 6.9 Binding
NoneNone
PDSP KiDatabase 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N None
CHEMBL1729 931 39 3H-GR-113808 -8 25 Rat 6.9 pKi = 6.9 Binding
NoneNone
PDSP KiDatabase 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N None
CHEMBL560739 931 39 3H-GR-113808 -8 25 Rat 6.9 pKi = 6.9 Binding
NoneNone
PDSP KiDatabase 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N None
DB00604 931 39 3H-GR-113808 -8 25 Rat 6.9 pKi = 6.9 Binding
NoneNone
PDSP KiDatabase 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N None
108182 4068 18 3H-5HT -1 16 Rat 6.9 pKi = 6.9 Binding
NoneNone
PDSP KiDatabase 309 3 2 4 1.8 COc1cc(N)c(cc1C(=O)NC1CN2CCC1CC2)Cl None
245 4068 18 3H-5HT -1 16 Rat 6.9 pKi = 6.9 Binding
NoneNone
PDSP KiDatabase 309 3 2 4 1.8 COc1cc(N)c(cc1C(=O)NC1CN2CCC1CC2)Cl None
CHEMBL18041 4068 18 3H-5HT -1 16 Rat 6.9 pKi = 6.9 Binding
NoneNone
PDSP KiDatabase 309 3 2 4 1.8 COc1cc(N)c(cc1C(=O)NC1CN2CCC1CC2)Cl None
3035240 214200 0 3H-GR-113808 -1 5 Guinea pig 6.9 pKi = 6.9 Binding
NoneNone
PDSP KiDatabase 359 3 2 4 2.6 COC1=CC(=C(C=C1C(=O)NC2CCN3CCCC2C3)Cl)N.Cl None
108182 4068 18 3H-GR-113808 -1 16 Rat 5.9 pKi = 5.9 Binding
NoneNone
PDSP KiDatabase 309 3 2 4 1.8 COc1cc(N)c(cc1C(=O)NC1CN2CCC1CC2)Cl None
108182 4068 18 3H-RS 57639 -1 16 Rat 5.9 pKi = 5.9 Binding
NoneNone
PDSP KiDatabase 309 3 2 4 1.8 COc1cc(N)c(cc1C(=O)NC1CN2CCC1CC2)Cl None
245 4068 18 3H-GR-113808 -1 16 Rat 5.9 pKi = 5.9 Binding
NoneNone
PDSP KiDatabase 309 3 2 4 1.8 COc1cc(N)c(cc1C(=O)NC1CN2CCC1CC2)Cl None
245 4068 18 3H-RS 57639 -1 16 Rat 5.9 pKi = 5.9 Binding
NoneNone
PDSP KiDatabase 309 3 2 4 1.8 COc1cc(N)c(cc1C(=O)NC1CN2CCC1CC2)Cl None
CHEMBL18041 4068 18 3H-GR-113808 -1 16 Rat 5.9 pKi = 5.9 Binding
NoneNone
PDSP KiDatabase 309 3 2 4 1.8 COc1cc(N)c(cc1C(=O)NC1CN2CCC1CC2)Cl None
CHEMBL18041 4068 18 3H-RS 57639 -1 16 Rat 5.9 pKi = 5.9 Binding
NoneNone
PDSP KiDatabase 309 3 2 4 1.8 COc1cc(N)c(cc1C(=O)NC1CN2CCC1CC2)Cl None
130946 201070 2 UNDEFINED - 1 Human 7.9 pKi = 7.9 Binding
NoneNone
PDSP KiDatabase 328 2 1 5 2.0 CCn1c(=O)n(C(=O)NC2CC3CCC(C2)N3C)c2ccccc21 None
CHEMBL62023 201070 2 UNDEFINED - 1 Human 7.9 pKi = 7.9 Binding
NoneNone
PDSP KiDatabase 328 2 1 5 2.0 CCn1c(=O)n(C(=O)NC2CC3CCC(C2)N3C)c2ccccc21 None
3035240 214200 0 3H-GR-113808 -1 5 Mouse 6.9 pKi = 6.9 Binding
NoneNone
PDSP KiDatabase 359 3 2 4 2.6 COC1=CC(=C(C=C1C(=O)NC2CCN3CCCC2C3)Cl)N.Cl None
108182 4068 18 3H-5HT -1 16 Rat 6.9 pKi = 6.9 Binding
NoneNone
PDSP KiDatabase 309 3 2 4 1.8 COc1cc(N)c(cc1C(=O)NC1CN2CCC1CC2)Cl None
245 4068 18 3H-5HT -1 16 Rat 6.9 pKi = 6.9 Binding
NoneNone
PDSP KiDatabase 309 3 2 4 1.8 COc1cc(N)c(cc1C(=O)NC1CN2CCC1CC2)Cl None
CHEMBL18041 4068 18 3H-5HT -1 16 Rat 6.9 pKi = 6.9 Binding
NoneNone
PDSP KiDatabase 309 3 2 4 1.8 COc1cc(N)c(cc1C(=O)NC1CN2CCC1CC2)Cl None
5 139 66 3H-GR-113808 -117 54 Rat 6.8 pKi = 6.8 Binding
NoneNone
PDSP KiDatabase 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 None
5202 139 66 3H-GR-113808 -117 54 Rat 6.8 pKi = 6.8 Binding
NoneNone
PDSP KiDatabase 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 None
CHEMBL39 139 66 3H-GR-113808 -117 54 Rat 6.8 pKi = 6.8 Binding
NoneNone
PDSP KiDatabase 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 None
DB08839 139 66 3H-GR-113808 -117 54 Rat 6.8 pKi = 6.8 Binding
NoneNone
PDSP KiDatabase 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 None
152 361 18 3H-GR-113808 -89 18 Rat 5.8 pKi = 5.8 Binding
NoneNone
PDSP KiDatabase 190 2 3 2 1.8 CC(Cc1c[nH]c2c1cc(O)cc2)N None
2107 361 18 3H-GR-113808 -89 18 Rat 5.8 pKi = 5.8 Binding
NoneNone
PDSP KiDatabase 190 2 3 2 1.8 CC(Cc1c[nH]c2c1cc(O)cc2)N None
CHEMBL275854 361 18 3H-GR-113808 -89 18 Rat 5.8 pKi = 5.8 Binding
NoneNone
PDSP KiDatabase 190 2 3 2 1.8 CC(Cc1c[nH]c2c1cc(O)cc2)N None
107 141 116 3H-GR-113808 -389 30 Human 6.8 pKi = 6.8 Binding
NoneNone
PDSP KiDatabase 190 3 2 2 1.7 NCCc1c[nH]c2c1cc(OC)cc2 None
1833 141 116 3H-GR-113808 -389 30 Human 6.8 pKi = 6.8 Binding
NoneNone
PDSP KiDatabase 190 3 2 2 1.7 NCCc1c[nH]c2c1cc(OC)cc2 None
CHEMBL8165 141 116 3H-GR-113808 -389 30 Human 6.8 pKi = 6.8 Binding
NoneNone
PDSP KiDatabase 190 3 2 2 1.7 NCCc1c[nH]c2c1cc(OC)cc2 None
5 139 66 3H-GR-113808 -117 54 Rat 6.8 pKi = 6.8 Binding
NoneNone
PDSP KiDatabase 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 None
5202 139 66 3H-GR-113808 -117 54 Rat 6.8 pKi = 6.8 Binding
NoneNone
PDSP KiDatabase 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 None
CHEMBL39 139 66 3H-GR-113808 -117 54 Rat 6.8 pKi = 6.8 Binding
NoneNone
PDSP KiDatabase 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 None
DB08839 139 66 3H-GR-113808 -117 54 Rat 6.8 pKi = 6.8 Binding
NoneNone
PDSP KiDatabase 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 None
240 931 39 3H-GR-113808 -11 25 Human 6.8 pKi = 6.8 Binding
NoneNone
PDSP KiDatabase 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N None
240 931 39 3H-RS 57639 -8 25 Rat 6.8 pKi = 6.8 Binding
NoneNone
PDSP KiDatabase 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N None
2769 931 39 3H-GR-113808 -11 25 Human 6.8 pKi = 6.8 Binding
NoneNone
PDSP KiDatabase 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N None
2769 931 39 3H-RS 57639 -8 25 Rat 6.8 pKi = 6.8 Binding
NoneNone
PDSP KiDatabase 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N None
44279790 931 39 3H-GR-113808 -11 25 Human 6.8 pKi = 6.8 Binding
NoneNone
PDSP KiDatabase 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N None
44279790 931 39 3H-RS 57639 -8 25 Rat 6.8 pKi = 6.8 Binding
NoneNone
PDSP KiDatabase 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N None
660 931 39 3H-GR-113808 -11 25 Human 6.8 pKi = 6.8 Binding
NoneNone
PDSP KiDatabase 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N None
660 931 39 3H-RS 57639 -8 25 Rat 6.8 pKi = 6.8 Binding
NoneNone
PDSP KiDatabase 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N None
CHEMBL1729 931 39 3H-GR-113808 -11 25 Human 6.8 pKi = 6.8 Binding
NoneNone
PDSP KiDatabase 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N None
CHEMBL1729 931 39 3H-RS 57639 -8 25 Rat 6.8 pKi = 6.8 Binding
NoneNone
PDSP KiDatabase 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N None
CHEMBL560739 931 39 3H-GR-113808 -11 25 Human 6.8 pKi = 6.8 Binding
NoneNone
PDSP KiDatabase 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N None
CHEMBL560739 931 39 3H-RS 57639 -8 25 Rat 6.8 pKi = 6.8 Binding
NoneNone
PDSP KiDatabase 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N None
DB00604 931 39 3H-GR-113808 -11 25 Human 6.8 pKi = 6.8 Binding
NoneNone
PDSP KiDatabase 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N None
DB00604 931 39 3H-RS 57639 -8 25 Rat 6.8 pKi = 6.8 Binding
NoneNone
PDSP KiDatabase 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N None
108182 4068 18 3H-GR-113808 -1 16 Guinea pig 6.8 pKi = 6.8 Binding
NoneNone
PDSP KiDatabase 309 3 2 4 1.8 COc1cc(N)c(cc1C(=O)NC1CN2CCC1CC2)Cl None
245 4068 18 3H-GR-113808 -1 16 Guinea pig 6.8 pKi = 6.8 Binding
NoneNone
PDSP KiDatabase 309 3 2 4 1.8 COc1cc(N)c(cc1C(=O)NC1CN2CCC1CC2)Cl None
CHEMBL18041 4068 18 3H-GR-113808 -1 16 Guinea pig 6.8 pKi = 6.8 Binding
NoneNone
PDSP KiDatabase 309 3 2 4 1.8 COc1cc(N)c(cc1C(=O)NC1CN2CCC1CC2)Cl None
57174031 214163 0 3H-GR-113808 -8 19 Mouse 6.8 pKi = 6.8 Binding
NoneNone
PDSP KiDatabase 284 2 1 3 3.0 CN1C2CCC1CC(C2)OC(=O)C3=CNC4=CC=CC=C43 None
None 214237 0 3H-RS 57639 -2 6 Rat 6.8 pKi = 6.8 Binding
NoneNone
PDSP KiDatabase 367 2 1 6 2.4 CN1C2CCC1CC(C2)OC(=O)N3C4=C(C=CC(=C4)OC)NC3=O.Cl None
152 361 18 3H-GR-113808 -208 18 Guinea pig 5.8 pKi = 5.8 Binding
NoneNone
PDSP KiDatabase 190 2 3 2 1.8 CC(Cc1c[nH]c2c1cc(O)cc2)N None
2107 361 18 3H-GR-113808 -208 18 Guinea pig 5.8 pKi = 5.8 Binding
NoneNone
PDSP KiDatabase 190 2 3 2 1.8 CC(Cc1c[nH]c2c1cc(O)cc2)N None
CHEMBL275854 361 18 3H-GR-113808 -208 18 Guinea pig 5.8 pKi = 5.8 Binding
NoneNone
PDSP KiDatabase 190 2 3 2 1.8 CC(Cc1c[nH]c2c1cc(O)cc2)N None
57174031 214163 0 3H-5HT -33 19 Rat 6.8 pKi = 6.8 Binding
NoneNone
PDSP KiDatabase 284 2 1 3 3.0 CN1C2CCC1CC(C2)OC(=O)C3=CNC4=CC=CC=C43 None
3035240 214200 0 3H-GR-113808 -2 5 Human 6.8 pKi = 6.8 Binding
NoneNone
PDSP KiDatabase 359 3 2 4 2.6 COC1=CC(=C(C=C1C(=O)NC2CCN3CCCC2C3)Cl)N.Cl None
None 214237 0 3H-GR-113808 1 6 Human 7.7 pKi = 7.7 Binding
NoneNone
PDSP KiDatabase 367 2 1 6 2.4 CN1C2CCC1CC(C2)OC(=O)N3C4=C(C=CC(=C4)OC)NC3=O.Cl None
108182 4068 18 3H-GR-113808 -1 16 Rat 6.7 pKi = 6.7 Binding
NoneNone
PDSP KiDatabase 309 3 2 4 1.8 COc1cc(N)c(cc1C(=O)NC1CN2CCC1CC2)Cl None
245 4068 18 3H-GR-113808 -1 16 Rat 6.7 pKi = 6.7 Binding
NoneNone
PDSP KiDatabase 309 3 2 4 1.8 COc1cc(N)c(cc1C(=O)NC1CN2CCC1CC2)Cl None
CHEMBL18041 4068 18 3H-GR-113808 -1 16 Rat 6.7 pKi = 6.7 Binding
NoneNone
PDSP KiDatabase 309 3 2 4 1.8 COc1cc(N)c(cc1C(=O)NC1CN2CCC1CC2)Cl None
258 3511 25 3H-5HT -2 8 Rat 7.7 pKi = 7.7 Binding
NoneNone
PDSP KiDatabase 300 7 1 5 2.4 CCN(CCOC(=O)c1cc(Cl)c(cc1OC)N)CC None
258 3511 25 3H-GR-113808 -2 8 Rat 7.7 pKi = 7.7 Binding
NoneNone
PDSP KiDatabase 300 7 1 5 2.4 CCN(CCOC(=O)c1cc(Cl)c(cc1OC)N)CC None
5191 3511 25 3H-5HT -2 8 Rat 7.7 pKi = 7.7 Binding
NoneNone
PDSP KiDatabase 300 7 1 5 2.4 CCN(CCOC(=O)c1cc(Cl)c(cc1OC)N)CC None
5191 3511 25 3H-GR-113808 -2 8 Rat 7.7 pKi = 7.7 Binding
NoneNone
PDSP KiDatabase 300 7 1 5 2.4 CCN(CCOC(=O)c1cc(Cl)c(cc1OC)N)CC None
CHEMBL287045 3511 25 3H-5HT -2 8 Rat 7.7 pKi = 7.7 Binding
NoneNone
PDSP KiDatabase 300 7 1 5 2.4 CCN(CCOC(=O)c1cc(Cl)c(cc1OC)N)CC None
CHEMBL287045 3511 25 3H-GR-113808 -2 8 Rat 7.7 pKi = 7.7 Binding
NoneNone
PDSP KiDatabase 300 7 1 5 2.4 CCN(CCOC(=O)c1cc(Cl)c(cc1OC)N)CC None
108182 4068 18 3H-GR-113808 1 16 Mouse 6.7 pKi = 6.7 Binding
NoneNone
PDSP KiDatabase 309 3 2 4 1.8 COc1cc(N)c(cc1C(=O)NC1CN2CCC1CC2)Cl None
245 4068 18 3H-GR-113808 1 16 Mouse 6.7 pKi = 6.7 Binding
NoneNone
PDSP KiDatabase 309 3 2 4 1.8 COc1cc(N)c(cc1C(=O)NC1CN2CCC1CC2)Cl None
CHEMBL18041 4068 18 3H-GR-113808 1 16 Mouse 6.7 pKi = 6.7 Binding
NoneNone
PDSP KiDatabase 309 3 2 4 1.8 COc1cc(N)c(cc1C(=O)NC1CN2CCC1CC2)Cl None
5 139 66 3H-RS 57639 -117 54 Rat 6.7 pKi = 6.7 Binding
NoneNone
PDSP KiDatabase 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 None
5202 139 66 3H-RS 57639 -117 54 Rat 6.7 pKi = 6.7 Binding
NoneNone
PDSP KiDatabase 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 None
CHEMBL39 139 66 3H-RS 57639 -117 54 Rat 6.7 pKi = 6.7 Binding
NoneNone
PDSP KiDatabase 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 None
DB08839 139 66 3H-RS 57639 -117 54 Rat 6.7 pKi = 6.7 Binding
NoneNone
PDSP KiDatabase 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 None
108182 4068 18 3H-GR-113808 -1 16 Guinea pig 6.7 pKi = 6.7 Binding
NoneNone
PDSP KiDatabase 309 3 2 4 1.8 COc1cc(N)c(cc1C(=O)NC1CN2CCC1CC2)Cl None
245 4068 18 3H-GR-113808 -1 16 Guinea pig 6.7 pKi = 6.7 Binding
NoneNone
PDSP KiDatabase 309 3 2 4 1.8 COc1cc(N)c(cc1C(=O)NC1CN2CCC1CC2)Cl None
CHEMBL18041 4068 18 3H-GR-113808 -1 16 Guinea pig 6.7 pKi = 6.7 Binding
NoneNone
PDSP KiDatabase 309 3 2 4 1.8 COc1cc(N)c(cc1C(=O)NC1CN2CCC1CC2)Cl None
57174031 214163 0 3H-GR-113808 -14 19 Guinea pig 6.7 pKi = 6.7 Binding
NoneNone
PDSP KiDatabase 284 2 1 3 3.0 CN1C2CCC1CC(C2)OC(=O)C3=CNC4=CC=CC=C43 None
57174031 214163 0 3H-GR-113808 -6 19 Human 6.7 pKi = 6.7 Binding
NoneNone
PDSP KiDatabase 284 2 1 3 3.0 CN1C2CCC1CC(C2)OC(=O)C3=CNC4=CC=CC=C43 None
258 3511 25 3H-GR-113808 1 8 Guinea pig 8.6 pKi = 8.6 Binding
NoneNone
PDSP KiDatabase 300 7 1 5 2.4 CCN(CCOC(=O)c1cc(Cl)c(cc1OC)N)CC None
5191 3511 25 3H-GR-113808 1 8 Guinea pig 8.6 pKi = 8.6 Binding
NoneNone
PDSP KiDatabase 300 7 1 5 2.4 CCN(CCOC(=O)c1cc(Cl)c(cc1OC)N)CC None
CHEMBL287045 3511 25 3H-GR-113808 1 8 Guinea pig 8.6 pKi = 8.6 Binding
NoneNone
PDSP KiDatabase 300 7 1 5 2.4 CCN(CCOC(=O)c1cc(Cl)c(cc1OC)N)CC None
5 139 66 3H-5HT -117 54 Rat 6.7 pKi = 6.7 Binding
NoneNone
PDSP KiDatabase 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 None
5202 139 66 3H-5HT -117 54 Rat 6.7 pKi = 6.7 Binding
NoneNone
PDSP KiDatabase 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 None
CHEMBL39 139 66 3H-5HT -117 54 Rat 6.7 pKi = 6.7 Binding
NoneNone
PDSP KiDatabase 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 None
DB08839 139 66 3H-5HT -117 54 Rat 6.7 pKi = 6.7 Binding
NoneNone
PDSP KiDatabase 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 None
130 3444 43 35S-GTPGammaS -562 13 Human 5.7 pKi = 5.7 Binding
NoneNone
PDSP KiDatabase 520 3 0 6 5.6 CN1CCC2(CC1)COc1c2cc2c(c1)CCN2C(=O)c1ccc(cc1)c1ccc(cc1C)c1noc(n1)C None
3378093 3444 43 35S-GTPGammaS -562 13 Human 5.7 pKi = 5.7 Binding
NoneNone
PDSP KiDatabase 520 3 0 6 5.6 CN1CCC2(CC1)COc1c2cc2c(c1)CCN2C(=O)c1ccc(cc1)c1ccc(cc1C)c1noc(n1)C None
CHEMBL281350 3444 43 35S-GTPGammaS -562 13 Human 5.7 pKi = 5.7 Binding
NoneNone
PDSP KiDatabase 520 3 0 6 5.6 CN1CCC2(CC1)COc1c2cc2c(c1)CCN2C(=O)c1ccc(cc1)c1ccc(cc1C)c1noc(n1)C None
None 214237 0 3H-GR-113808 -2 6 Rat 7.7 pKi = 7.7 Binding
NoneNone
PDSP KiDatabase 367 2 1 6 2.4 CN1C2CCC1CC(C2)OC(=O)N3C4=C(C=CC(=C4)OC)NC3=O.Cl None
None 214237 0 3H-ZACOPRIDE -2 6 Rat 6.7 pKi = 6.7 Binding
NoneNone
PDSP KiDatabase 367 2 1 6 2.4 CN1C2CCC1CC(C2)OC(=O)N3C4=C(C=CC(=C4)OC)NC3=O.Cl None
108182 4068 18 3H-GR-113808 1 16 Mouse 6.7 pKi = 6.7 Binding
NoneNone
PDSP KiDatabase 309 3 2 4 1.8 COc1cc(N)c(cc1C(=O)NC1CN2CCC1CC2)Cl None
245 4068 18 3H-GR-113808 1 16 Mouse 6.7 pKi = 6.7 Binding
NoneNone
PDSP KiDatabase 309 3 2 4 1.8 COc1cc(N)c(cc1C(=O)NC1CN2CCC1CC2)Cl None
CHEMBL18041 4068 18 3H-GR-113808 1 16 Mouse 6.7 pKi = 6.7 Binding
NoneNone
PDSP KiDatabase 309 3 2 4 1.8 COc1cc(N)c(cc1C(=O)NC1CN2CCC1CC2)Cl None
None 214195 0 3H-GR-113808 4 2 Mouse 6.7 pKi = 6.7 Binding
NoneNone
PDSP KiDatabase 336 1 2 4 1.9 CN1C2CCC1CC(C2)NC(=O)N3C4=CC=CC=C4NC3=O.Cl None
107 141 116 3H-GR-113808 -457 30 Mouse 6.6 pKi = 6.6 Binding
NoneNone
PDSP KiDatabase 190 3 2 2 1.7 NCCc1c[nH]c2c1cc(OC)cc2 None
1833 141 116 3H-GR-113808 -457 30 Mouse 6.6 pKi = 6.6 Binding
NoneNone
PDSP KiDatabase 190 3 2 2 1.7 NCCc1c[nH]c2c1cc(OC)cc2 None
CHEMBL8165 141 116 3H-GR-113808 -457 30 Mouse 6.6 pKi = 6.6 Binding
NoneNone
PDSP KiDatabase 190 3 2 2 1.7 NCCc1c[nH]c2c1cc(OC)cc2 None
3035240 214200 0 3H-GR-113808 1 5 Rat 6.6 pKi = 6.6 Binding
NoneNone
PDSP KiDatabase 359 3 2 4 2.6 COC1=CC(=C(C=C1C(=O)NC2CCN3CCCC2C3)Cl)N.Cl None
240 931 39 3H-5HT -8 25 Rat 7.6 pKi = 7.6 Binding
NoneNone
PDSP KiDatabase 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N None
2769 931 39 3H-5HT -8 25 Rat 7.6 pKi = 7.6 Binding
NoneNone
PDSP KiDatabase 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N None
44279790 931 39 3H-5HT -8 25 Rat 7.6 pKi = 7.6 Binding
NoneNone
PDSP KiDatabase 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N None
660 931 39 3H-5HT -8 25 Rat 7.6 pKi = 7.6 Binding
NoneNone
PDSP KiDatabase 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N None
CHEMBL1729 931 39 3H-5HT -8 25 Rat 7.6 pKi = 7.6 Binding
NoneNone
PDSP KiDatabase 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N None
CHEMBL560739 931 39 3H-5HT -8 25 Rat 7.6 pKi = 7.6 Binding
NoneNone
PDSP KiDatabase 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N None
DB00604 931 39 3H-5HT -8 25 Rat 7.6 pKi = 7.6 Binding
NoneNone
PDSP KiDatabase 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N None
258 3511 25 3H-RS 57639 -2 8 Rat 7.6 pKi = 7.6 Binding
NoneNone
PDSP KiDatabase 300 7 1 5 2.4 CCN(CCOC(=O)c1cc(Cl)c(cc1OC)N)CC None
5191 3511 25 3H-RS 57639 -2 8 Rat 7.6 pKi = 7.6 Binding
NoneNone
PDSP KiDatabase 300 7 1 5 2.4 CCN(CCOC(=O)c1cc(Cl)c(cc1OC)N)CC None
CHEMBL287045 3511 25 3H-RS 57639 -2 8 Rat 7.6 pKi = 7.6 Binding
NoneNone
PDSP KiDatabase 300 7 1 5 2.4 CCN(CCOC(=O)c1cc(Cl)c(cc1OC)N)CC None
3035240 214200 0 3H-5HT 1 5 Rat 7.6 pKi = 7.6 Binding
NoneNone
PDSP KiDatabase 359 3 2 4 2.6 COC1=CC(=C(C=C1C(=O)NC2CCN3CCCC2C3)Cl)N.Cl None
None 214237 0 3H-GR-113808 -1 6 Guinea pig 7.6 pKi = 7.6 Binding
NoneNone
PDSP KiDatabase 367 2 1 6 2.4 CN1C2CCC1CC(C2)OC(=O)N3C4=C(C=CC(=C4)OC)NC3=O.Cl None
107 141 116 3H-GR-113808 -549 30 Guinea pig 6.6 pKi = 6.6 Binding
NoneNone
PDSP KiDatabase 190 3 2 2 1.7 NCCc1c[nH]c2c1cc(OC)cc2 None
1833 141 116 3H-GR-113808 -549 30 Guinea pig 6.6 pKi = 6.6 Binding
NoneNone
PDSP KiDatabase 190 3 2 2 1.7 NCCc1c[nH]c2c1cc(OC)cc2 None
CHEMBL8165 141 116 3H-GR-113808 -549 30 Guinea pig 6.6 pKi = 6.6 Binding
NoneNone
PDSP KiDatabase 190 3 2 2 1.7 NCCc1c[nH]c2c1cc(OC)cc2 None
108182 4068 18 3H-GR-113808 -1 16 Guinea pig 6.6 pKi = 6.6 Binding
NoneNone
PDSP KiDatabase 309 3 2 4 1.8 COc1cc(N)c(cc1C(=O)NC1CN2CCC1CC2)Cl None
245 4068 18 3H-GR-113808 -1 16 Guinea pig 6.6 pKi = 6.6 Binding
NoneNone
PDSP KiDatabase 309 3 2 4 1.8 COc1cc(N)c(cc1C(=O)NC1CN2CCC1CC2)Cl None
CHEMBL18041 4068 18 3H-GR-113808 -1 16 Guinea pig 6.6 pKi = 6.6 Binding
NoneNone
PDSP KiDatabase 309 3 2 4 1.8 COc1cc(N)c(cc1C(=O)NC1CN2CCC1CC2)Cl None
57174031 214163 0 3H-GR-113808 -33 19 Rat 6.6 pKi = 6.6 Binding
NoneNone
PDSP KiDatabase 284 2 1 3 3.0 CN1C2CCC1CC(C2)OC(=O)C3=CNC4=CC=CC=C43 None
3035240 214200 0 3H-GR-113808 -2 5 Human 6.6 pKi = 6.6 Binding
NoneNone
PDSP KiDatabase 359 3 2 4 2.6 COC1=CC(=C(C=C1C(=O)NC2CCN3CCCC2C3)Cl)N.Cl None
3035240 214200 0 3H-GR-113808 1 5 Rat 6.6 pKi = 6.6 Binding
NoneNone
PDSP KiDatabase 359 3 2 4 2.6 COC1=CC(=C(C=C1C(=O)NC2CCN3CCCC2C3)Cl)N.Cl None
3035240 214200 0 3H-RS 57639 1 5 Rat 6.6 pKi = 6.6 Binding
NoneNone
PDSP KiDatabase 359 3 2 4 2.6 COC1=CC(=C(C=C1C(=O)NC2CCN3CCCC2C3)Cl)N.Cl None
None 214237 0 3H-GR-113808 -1 6 Mouse 7.6 pKi = 7.6 Binding
NoneNone
PDSP KiDatabase 367 2 1 6 2.4 CN1C2CCC1CC(C2)OC(=O)N3C4=C(C=CC(=C4)OC)NC3=O.Cl None
152 361 18 3H-5HT -89 18 Rat 6.6 pKi = 6.6 Binding
NoneNone
PDSP KiDatabase 190 2 3 2 1.8 CC(Cc1c[nH]c2c1cc(O)cc2)N None
2107 361 18 3H-5HT -89 18 Rat 6.6 pKi = 6.6 Binding
NoneNone
PDSP KiDatabase 190 2 3 2 1.8 CC(Cc1c[nH]c2c1cc(O)cc2)N None
CHEMBL275854 361 18 3H-5HT -89 18 Rat 6.6 pKi = 6.6 Binding
NoneNone
PDSP KiDatabase 190 2 3 2 1.8 CC(Cc1c[nH]c2c1cc(O)cc2)N None
3035240 214200 0 3H-5HT 1 5 Rat 7.6 pKi = 7.6 Binding
NoneNone
PDSP KiDatabase 359 3 2 4 2.6 COC1=CC(=C(C=C1C(=O)NC2CCN3CCCC2C3)Cl)N.Cl None
1267 3744 43 3H-GR-113808 -1174 25 Guinea pig 5.6 pKi = 5.6 Binding
NoneNone
PDSP KiDatabase 292 2 2 2 2.8 S=C(N1CCC(CC1)c1cnc[nH]1)NC1CCCCC1 None
3035905 3744 43 3H-GR-113808 -1174 25 Guinea pig 5.6 pKi = 5.6 Binding
NoneNone
PDSP KiDatabase 292 2 2 2 2.8 S=C(N1CCC(CC1)c1cnc[nH]1)NC1CCCCC1 None
CHEMBL260374 3744 43 3H-GR-113808 -1174 25 Guinea pig 5.6 pKi = 5.6 Binding
NoneNone
PDSP KiDatabase 292 2 2 2 2.8 S=C(N1CCC(CC1)c1cnc[nH]1)NC1CCCCC1 None
108182 4068 18 3H-GR-113808 -2 16 Human 6.6 pKi = 6.6 Binding
NoneNone
PDSP KiDatabase 309 3 2 4 1.8 COc1cc(N)c(cc1C(=O)NC1CN2CCC1CC2)Cl None
245 4068 18 3H-GR-113808 -2 16 Human 6.6 pKi = 6.6 Binding
NoneNone
PDSP KiDatabase 309 3 2 4 1.8 COc1cc(N)c(cc1C(=O)NC1CN2CCC1CC2)Cl None
CHEMBL18041 4068 18 3H-GR-113808 -2 16 Human 6.6 pKi = 6.6 Binding
NoneNone
PDSP KiDatabase 309 3 2 4 1.8 COc1cc(N)c(cc1C(=O)NC1CN2CCC1CC2)Cl None
240 931 39 3H-GR113808 -11 25 Human 7.5 pKi = 7.5 Binding
NoneNone
PDSP KiDatabase 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N None
2769 931 39 3H-GR113808 -11 25 Human 7.5 pKi = 7.5 Binding
NoneNone
PDSP KiDatabase 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N None
44279790 931 39 3H-GR113808 -11 25 Human 7.5 pKi = 7.5 Binding
NoneNone
PDSP KiDatabase 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N None
660 931 39 3H-GR113808 -11 25 Human 7.5 pKi = 7.5 Binding
NoneNone
PDSP KiDatabase 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N None
CHEMBL1729 931 39 3H-GR113808 -11 25 Human 7.5 pKi = 7.5 Binding
NoneNone
PDSP KiDatabase 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N None
CHEMBL560739 931 39 3H-GR113808 -11 25 Human 7.5 pKi = 7.5 Binding
NoneNone
PDSP KiDatabase 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N None
DB00604 931 39 3H-GR113808 -11 25 Human 7.5 pKi = 7.5 Binding
NoneNone
PDSP KiDatabase 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N None
119376 1811 41 3H-5HT -2 26 Rat 8.5 pKi = 8.5 Binding
NoneNone
PDSP KiDatabase 393 7 1 6 1.6 O=C(c1cn(c2c1cccc2)C)OCC1CCN(CC1)CCNS(=O)(=O)C None
247 1811 41 3H-5HT -2 26 Rat 8.5 pKi = 8.5 Binding
NoneNone
PDSP KiDatabase 393 7 1 6 1.6 O=C(c1cn(c2c1cccc2)C)OCC1CCN(CC1)CCNS(=O)(=O)C None
CHEMBL33884 1811 41 3H-5HT -2 26 Rat 8.5 pKi = 8.5 Binding
NoneNone
PDSP KiDatabase 393 7 1 6 1.6 O=C(c1cn(c2c1cccc2)C)OCC1CCN(CC1)CCNS(=O)(=O)C None
119376 1811 41 3H-RS 57639 -2 26 Rat 8.4 pKi = 8.4 Binding
NoneNone
PDSP KiDatabase 393 7 1 6 1.6 O=C(c1cn(c2c1cccc2)C)OCC1CCN(CC1)CCNS(=O)(=O)C None
247 1811 41 3H-RS 57639 -2 26 Rat 8.4 pKi = 8.4 Binding
NoneNone
PDSP KiDatabase 393 7 1 6 1.6 O=C(c1cn(c2c1cccc2)C)OCC1CCN(CC1)CCNS(=O)(=O)C None
CHEMBL33884 1811 41 3H-RS 57639 -2 26 Rat 8.4 pKi = 8.4 Binding
NoneNone
PDSP KiDatabase 393 7 1 6 1.6 O=C(c1cn(c2c1cccc2)C)OCC1CCN(CC1)CCNS(=O)(=O)C None
108182 4068 18 3H-GR-113808 1 16 Mouse 6.5 pKi = 6.5 Binding
NoneNone
PDSP KiDatabase 309 3 2 4 1.8 COc1cc(N)c(cc1C(=O)NC1CN2CCC1CC2)Cl None
245 4068 18 3H-GR-113808 1 16 Mouse 6.5 pKi = 6.5 Binding
NoneNone
PDSP KiDatabase 309 3 2 4 1.8 COc1cc(N)c(cc1C(=O)NC1CN2CCC1CC2)Cl None
CHEMBL18041 4068 18 3H-GR-113808 1 16 Mouse 6.5 pKi = 6.5 Binding
NoneNone
PDSP KiDatabase 309 3 2 4 1.8 COc1cc(N)c(cc1C(=O)NC1CN2CCC1CC2)Cl None
240 931 39 3H-GR-113808 -4 25 Guinea pig 7.5 pKi = 7.5 Binding
NoneNone
PDSP KiDatabase 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N None
2769 931 39 3H-GR-113808 -4 25 Guinea pig 7.5 pKi = 7.5 Binding
NoneNone
PDSP KiDatabase 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N None
44279790 931 39 3H-GR-113808 -4 25 Guinea pig 7.5 pKi = 7.5 Binding
NoneNone
PDSP KiDatabase 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N None
660 931 39 3H-GR-113808 -4 25 Guinea pig 7.5 pKi = 7.5 Binding
NoneNone
PDSP KiDatabase 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N None
CHEMBL1729 931 39 3H-GR-113808 -4 25 Guinea pig 7.5 pKi = 7.5 Binding
NoneNone
PDSP KiDatabase 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N None
CHEMBL560739 931 39 3H-GR-113808 -4 25 Guinea pig 7.5 pKi = 7.5 Binding
NoneNone
PDSP KiDatabase 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N None
DB00604 931 39 3H-GR-113808 -4 25 Guinea pig 7.5 pKi = 7.5 Binding
NoneNone
PDSP KiDatabase 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N None
107 141 116 3H-5HT -257 30 Rat 6.5 pKi = 6.5 Binding
NoneNone
PDSP KiDatabase 190 3 2 2 1.7 NCCc1c[nH]c2c1cc(OC)cc2 None
1833 141 116 3H-5HT -257 30 Rat 6.5 pKi = 6.5 Binding
NoneNone
PDSP KiDatabase 190 3 2 2 1.7 NCCc1c[nH]c2c1cc(OC)cc2 None
CHEMBL8165 141 116 3H-5HT -257 30 Rat 6.5 pKi = 6.5 Binding
NoneNone
PDSP KiDatabase 190 3 2 2 1.7 NCCc1c[nH]c2c1cc(OC)cc2 None
108182 4068 18 3H-5HT -1 16 Rat 6.5 pKi = 6.5 Binding
NoneNone
PDSP KiDatabase 309 3 2 4 1.8 COc1cc(N)c(cc1C(=O)NC1CN2CCC1CC2)Cl None
245 4068 18 3H-5HT -1 16 Rat 6.5 pKi = 6.5 Binding
NoneNone
PDSP KiDatabase 309 3 2 4 1.8 COc1cc(N)c(cc1C(=O)NC1CN2CCC1CC2)Cl None
CHEMBL18041 4068 18 3H-5HT -1 16 Rat 6.5 pKi = 6.5 Binding
NoneNone
PDSP KiDatabase 309 3 2 4 1.8 COc1cc(N)c(cc1C(=O)NC1CN2CCC1CC2)Cl None
5 139 66 3H-GR-113808 -288 54 Human 6.5 pKi = 6.5 Binding
NoneNone
PDSP KiDatabase 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 None
5202 139 66 3H-GR-113808 -288 54 Human 6.5 pKi = 6.5 Binding
NoneNone
PDSP KiDatabase 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 None
CHEMBL39 139 66 3H-GR-113808 -288 54 Human 6.5 pKi = 6.5 Binding
NoneNone
PDSP KiDatabase 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 None
DB08839 139 66 3H-GR-113808 -288 54 Human 6.5 pKi = 6.5 Binding
NoneNone
PDSP KiDatabase 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 None
107 141 116 3H-GR-113808 -549 30 Guinea pig 6.5 pKi = 6.5 Binding
NoneNone
PDSP KiDatabase 190 3 2 2 1.7 NCCc1c[nH]c2c1cc(OC)cc2 None
107 141 116 3H-RS 57639 -257 30 Rat 6.5 pKi = 6.5 Binding
NoneNone
PDSP KiDatabase 190 3 2 2 1.7 NCCc1c[nH]c2c1cc(OC)cc2 None
1833 141 116 3H-GR-113808 -549 30 Guinea pig 6.5 pKi = 6.5 Binding
NoneNone
PDSP KiDatabase 190 3 2 2 1.7 NCCc1c[nH]c2c1cc(OC)cc2 None
1833 141 116 3H-RS 57639 -257 30 Rat 6.5 pKi = 6.5 Binding
NoneNone
PDSP KiDatabase 190 3 2 2 1.7 NCCc1c[nH]c2c1cc(OC)cc2 None
CHEMBL8165 141 116 3H-GR-113808 -549 30 Guinea pig 6.5 pKi = 6.5 Binding
NoneNone
PDSP KiDatabase 190 3 2 2 1.7 NCCc1c[nH]c2c1cc(OC)cc2 None
CHEMBL8165 141 116 3H-RS 57639 -257 30 Rat 6.5 pKi = 6.5 Binding
NoneNone
PDSP KiDatabase 190 3 2 2 1.7 NCCc1c[nH]c2c1cc(OC)cc2 None
108182 4068 18 3H-5HT -1 16 Rat 6.5 pKi = 6.5 Binding
NoneNone
PDSP KiDatabase 309 3 2 4 1.8 COc1cc(N)c(cc1C(=O)NC1CN2CCC1CC2)Cl None
245 4068 18 3H-5HT -1 16 Rat 6.5 pKi = 6.5 Binding
NoneNone
PDSP KiDatabase 309 3 2 4 1.8 COc1cc(N)c(cc1C(=O)NC1CN2CCC1CC2)Cl None
CHEMBL18041 4068 18 3H-5HT -1 16 Rat 6.5 pKi = 6.5 Binding
NoneNone
PDSP KiDatabase 309 3 2 4 1.8 COc1cc(N)c(cc1C(=O)NC1CN2CCC1CC2)Cl None
1809 134 28 3H-5HT -46773 36 Rat 5.5 pKi = 5.5 Binding
NoneNone
PDSP KiDatabase 203 3 3 2 0.8 NCCc1c[nH]c2c1cc(cc2)C(=O)N None
1809 134 28 3H-GR-113808 -46773 36 Rat 5.5 pKi = 5.5 Binding
NoneNone
PDSP KiDatabase 203 3 3 2 0.8 NCCc1c[nH]c2c1cc(cc2)C(=O)N None
4 134 28 3H-5HT -46773 36 Rat 5.5 pKi = 5.5 Binding
NoneNone
PDSP KiDatabase 203 3 3 2 0.8 NCCc1c[nH]c2c1cc(cc2)C(=O)N None
4 134 28 3H-GR-113808 -46773 36 Rat 5.5 pKi = 5.5 Binding
NoneNone
PDSP KiDatabase 203 3 3 2 0.8 NCCc1c[nH]c2c1cc(cc2)C(=O)N None
CHEMBL18840 134 28 3H-5HT -46773 36 Rat 5.5 pKi = 5.5 Binding
NoneNone
PDSP KiDatabase 203 3 3 2 0.8 NCCc1c[nH]c2c1cc(cc2)C(=O)N None
CHEMBL18840 134 28 3H-GR-113808 -46773 36 Rat 5.5 pKi = 5.5 Binding
NoneNone
PDSP KiDatabase 203 3 3 2 0.8 NCCc1c[nH]c2c1cc(cc2)C(=O)N None
240 931 39 3H-GR-113808 -5 25 Mouse 7.5 pKi = 7.5 Binding
NoneNone
PDSP KiDatabase 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N None
2769 931 39 3H-GR-113808 -5 25 Mouse 7.5 pKi = 7.5 Binding
NoneNone
PDSP KiDatabase 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N None
44279790 931 39 3H-GR-113808 -5 25 Mouse 7.5 pKi = 7.5 Binding
NoneNone
PDSP KiDatabase 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N None
660 931 39 3H-GR-113808 -5 25 Mouse 7.5 pKi = 7.5 Binding
NoneNone
PDSP KiDatabase 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N None
CHEMBL1729 931 39 3H-GR-113808 -5 25 Mouse 7.5 pKi = 7.5 Binding
NoneNone
PDSP KiDatabase 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N None
CHEMBL560739 931 39 3H-GR-113808 -5 25 Mouse 7.5 pKi = 7.5 Binding
NoneNone
PDSP KiDatabase 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N None
DB00604 931 39 3H-GR-113808 -5 25 Mouse 7.5 pKi = 7.5 Binding
NoneNone
PDSP KiDatabase 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N None
5 139 66 3H-GR-113808 -117 54 Rat 7.4 pKi = 7.4 Binding
NoneNone
PDSP KiDatabase 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 None
5202 139 66 3H-GR-113808 -117 54 Rat 7.4 pKi = 7.4 Binding
NoneNone
PDSP KiDatabase 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 None
CHEMBL39 139 66 3H-GR-113808 -117 54 Rat 7.4 pKi = 7.4 Binding
NoneNone
PDSP KiDatabase 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 None
DB08839 139 66 3H-GR-113808 -117 54 Rat 7.4 pKi = 7.4 Binding
NoneNone
PDSP KiDatabase 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 None
5 139 66 3H-GR-113808 -190 54 Guinea pig 7.4 pKi = 7.4 Binding
NoneNone
PDSP KiDatabase 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 None
5202 139 66 3H-GR-113808 -190 54 Guinea pig 7.4 pKi = 7.4 Binding
NoneNone
PDSP KiDatabase 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 None
CHEMBL39 139 66 3H-GR-113808 -190 54 Guinea pig 7.4 pKi = 7.4 Binding
NoneNone
PDSP KiDatabase 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 None
DB08839 139 66 3H-GR-113808 -190 54 Guinea pig 7.4 pKi = 7.4 Binding
NoneNone
PDSP KiDatabase 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 None
107 141 116 3H-5HT -257 30 Rat 7.4 pKi = 7.4 Binding
NoneNone
PDSP KiDatabase 190 3 2 2 1.7 NCCc1c[nH]c2c1cc(OC)cc2 None
1833 141 116 3H-5HT -257 30 Rat 7.4 pKi = 7.4 Binding
NoneNone
PDSP KiDatabase 190 3 2 2 1.7 NCCc1c[nH]c2c1cc(OC)cc2 None
CHEMBL8165 141 116 3H-5HT -257 30 Rat 7.4 pKi = 7.4 Binding
NoneNone
PDSP KiDatabase 190 3 2 2 1.7 NCCc1c[nH]c2c1cc(OC)cc2 None
107 141 116 3H-GR-113808 -257 30 Rat 6.4 pKi = 6.4 Binding
NoneNone
PDSP KiDatabase 190 3 2 2 1.7 NCCc1c[nH]c2c1cc(OC)cc2 None
1833 141 116 3H-GR-113808 -257 30 Rat 6.4 pKi = 6.4 Binding
NoneNone
PDSP KiDatabase 190 3 2 2 1.7 NCCc1c[nH]c2c1cc(OC)cc2 None
CHEMBL8165 141 116 3H-GR-113808 -257 30 Rat 6.4 pKi = 6.4 Binding
NoneNone
PDSP KiDatabase 190 3 2 2 1.7 NCCc1c[nH]c2c1cc(OC)cc2 None
1782 2482 81 3H-GR-113808 -25 22 Mouse 5.4 pKi = 5.4 Binding
NoneNone
PDSP KiDatabase 299 7 2 4 2.0 CCN(CCNC(=O)c1cc(Cl)c(cc1OC)N)CC None
241 2482 81 3H-GR-113808 -25 22 Mouse 5.4 pKi = 5.4 Binding
NoneNone
PDSP KiDatabase 299 7 2 4 2.0 CCN(CCNC(=O)c1cc(Cl)c(cc1OC)N)CC None
4168 2482 81 3H-GR-113808 -25 22 Mouse 5.4 pKi = 5.4 Binding
NoneNone
PDSP KiDatabase 299 7 2 4 2.0 CCN(CCNC(=O)c1cc(Cl)c(cc1OC)N)CC None
CHEMBL86 2482 81 3H-GR-113808 -25 22 Mouse 5.4 pKi = 5.4 Binding
NoneNone
PDSP KiDatabase 299 7 2 4 2.0 CCN(CCNC(=O)c1cc(Cl)c(cc1OC)N)CC None
DB01233 2482 81 3H-GR-113808 -25 22 Mouse 5.4 pKi = 5.4 Binding
NoneNone
PDSP KiDatabase 299 7 2 4 2.0 CCN(CCNC(=O)c1cc(Cl)c(cc1OC)N)CC None
107 141 116 3H-GR-113808 -257 30 Rat 6.4 pKi = 6.4 Binding
NoneNone
PDSP KiDatabase 190 3 2 2 1.7 NCCc1c[nH]c2c1cc(OC)cc2 None
1833 141 116 3H-GR-113808 -257 30 Rat 6.4 pKi = 6.4 Binding
NoneNone
PDSP KiDatabase 190 3 2 2 1.7 NCCc1c[nH]c2c1cc(OC)cc2 None
CHEMBL8165 141 116 3H-GR-113808 -257 30 Rat 6.4 pKi = 6.4 Binding
NoneNone
PDSP KiDatabase 190 3 2 2 1.7 NCCc1c[nH]c2c1cc(OC)cc2 None
235 2527 36 3H-GR-113808 -4 3 Human 8.3 pKi = 8.3 Binding
NoneNone
PDSP KiDatabase 312 5 1 5 2.6 COc1cc(N)c(cc1C(=O)OCCN1CCCCC1)Cl None
5311299 2527 36 3H-GR-113808 -4 3 Human 8.3 pKi = 8.3 Binding
NoneNone
PDSP KiDatabase 312 5 1 5 2.6 COc1cc(N)c(cc1C(=O)OCCN1CCCCC1)Cl None
CHEMBL286136 2527 36 3H-GR-113808 -4 3 Human 8.3 pKi = 8.3 Binding
NoneNone
PDSP KiDatabase 312 5 1 5 2.6 COc1cc(N)c(cc1C(=O)OCCN1CCCCC1)Cl None
None 214237 0 3H-GR-113808 -2 6 Rat 8.3 pKi = 8.3 Binding
NoneNone
PDSP KiDatabase 367 2 1 6 2.4 CN1C2CCC1CC(C2)OC(=O)N3C4=C(C=CC(=C4)OC)NC3=O.Cl None
441383 20133 54 None -5 17 Guinea pig 8.3 pKi = 8.3 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
Drug Central 531 8 0 8 4.5 CC(C)N1CCN(c2ccc(OC[C@H]3CO[C@](Cn4cncn4)(c4ccc(Cl)cc4Cl)O3)cc2)CC1 None
CHEMBL1306 20133 54 None -5 17 Guinea pig 8.3 pKi = 8.3 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
Drug Central 531 8 0 8 4.5 CC(C)N1CCN(c2ccc(OC[C@H]3CO[C@](Cn4cncn4)(c4ccc(Cl)cc4Cl)O3)cc2)CC1 None
3397 203777 104 None 1 2 Guinea pig 8.3 pKi = 8.3 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
Drug Central 276 3 1 3 3.2 CC(C)C(=O)Nc1ccc([N+](=O)[O-])c(C(F)(F)F)c1 None
CHEMBL806 203777 104 None 1 2 Guinea pig 8.3 pKi = 8.3 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
Drug Central 276 3 1 3 3.2 CC(C)C(=O)Nc1ccc([N+](=O)[O-])c(C(F)(F)F)c1 None
31703 193050 59 None 1 3 Guinea pig 8.3 pKi = 8.3 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
Drug Central 543 5 6 12 0.0 COc1cccc2c1C(=O)c1c(O)c3c(c(O)c1C2=O)C[C@@](O)(C(=O)CO)C[C@@H]3O[C@H]1C[C@H](N)[C@H](O)[C@H](C)O1 None
CHEMBL359744 193050 59 None 1 3 Guinea pig 8.3 pKi = 8.3 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
Drug Central 543 5 6 12 0.0 COc1cccc2c1C(=O)c1c(O)c3c(c(O)c1C2=O)C[C@@](O)(C(=O)CO)C[C@@H]3O[C@H]1C[C@H](N)[C@H](O)[C@H](C)O1 None
CHEMBL53463 193050 59 None 1 3 Guinea pig 8.3 pKi = 8.3 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
Drug Central 543 5 6 12 0.0 COc1cccc2c1C(=O)c1c(O)c3c(c(O)c1C2=O)C[C@@](O)(C(=O)CO)C[C@@H]3O[C@H]1C[C@H](N)[C@H](O)[C@H](C)O1 None
151537 162114 43 None - 1 Guinea pig 8.2 pKi = 8.2 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
Drug Central 543 5 6 12 0.0 COc1cccc2c1C(=O)c1c(O)c3c(c(O)c1C2=O)C[C@@](O)(C(=O)CO)C[C@@H]3O[C@H]1C[C@H](N)[C@@H](O)[C@H](C)O1 None
41867 162114 43 None - 1 Guinea pig 8.2 pKi = 8.2 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
Drug Central 543 5 6 12 0.0 COc1cccc2c1C(=O)c1c(O)c3c(c(O)c1C2=O)C[C@@](O)(C(=O)CO)C[C@@H]3O[C@H]1C[C@H](N)[C@@H](O)[C@H](C)O1 None
CHEMBL417 162114 43 None - 1 Guinea pig 8.2 pKi = 8.2 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
Drug Central 543 5 6 12 0.0 COc1cccc2c1C(=O)c1c(O)c3c(c(O)c1C2=O)C[C@@](O)(C(=O)CO)C[C@@H]3O[C@H]1C[C@H](N)[C@@H](O)[C@H](C)O1 None
5991 202221 68 None 2 5 Guinea pig 8.2 pKi = 8.2 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
Drug Central 296 0 2 2 3.6 C#C[C@]1(O)CC[C@H]2[C@@H]3CCc4cc(O)ccc4[C@H]3CC[C@@]21C None
CHEMBL691 202221 68 None 2 5 Guinea pig 8.2 pKi = 8.2 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
Drug Central 296 0 2 2 3.6 C#C[C@]1(O)CC[C@H]2[C@@H]3CCc4cc(O)ccc4[C@H]3CC[C@@]21C None
4595 176141 102 None -3 15 Rat 8.2 pKi = 8.2 Binding
The binding affinity was measured on 5-hydroxytryptamine 4 receptor using [3H]- GR-113808 as radioligand.The binding affinity was measured on 5-hydroxytryptamine 4 receptor using [3H]- GR-113808 as radioligand.
Drug Central 293 2 0 4 3.1 Cc1nccn1CC1CCc2c(c3ccccc3n2C)C1=O None
CHEMBL46 176141 102 None -3 15 Rat 8.2 pKi = 8.2 Binding
The binding affinity was measured on 5-hydroxytryptamine 4 receptor using [3H]- GR-113808 as radioligand.The binding affinity was measured on 5-hydroxytryptamine 4 receptor using [3H]- GR-113808 as radioligand.
Drug Central 293 2 0 4 3.1 Cc1nccn1CC1CCc2c(c3ccccc3n2C)C1=O None
5 139 66 3H-GR-113808 -190 54 Guinea pig 7.3 pKi = 7.3 Binding
NoneNone
PDSP KiDatabase 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 None
5202 139 66 3H-GR-113808 -190 54 Guinea pig 7.3 pKi = 7.3 Binding
NoneNone
PDSP KiDatabase 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 None
CHEMBL39 139 66 3H-GR-113808 -190 54 Guinea pig 7.3 pKi = 7.3 Binding
NoneNone
PDSP KiDatabase 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 None
DB08839 139 66 3H-GR-113808 -190 54 Guinea pig 7.3 pKi = 7.3 Binding
NoneNone
PDSP KiDatabase 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 None
107 141 116 3H-GR-113808 -389 30 Human 6.3 pKi = 6.3 Binding
NoneNone
PDSP KiDatabase 190 3 2 2 1.7 NCCc1c[nH]c2c1cc(OC)cc2 None
107 141 116 3H-GR-113808 -257 30 Rat 6.3 pKi = 6.3 Binding
NoneNone
PDSP KiDatabase 190 3 2 2 1.7 NCCc1c[nH]c2c1cc(OC)cc2 None
1833 141 116 3H-GR-113808 -389 30 Human 6.3 pKi = 6.3 Binding
NoneNone
PDSP KiDatabase 190 3 2 2 1.7 NCCc1c[nH]c2c1cc(OC)cc2 None
1833 141 116 3H-GR-113808 -257 30 Rat 6.3 pKi = 6.3 Binding
NoneNone
PDSP KiDatabase 190 3 2 2 1.7 NCCc1c[nH]c2c1cc(OC)cc2 None
CHEMBL8165 141 116 3H-GR-113808 -389 30 Human 6.3 pKi = 6.3 Binding
NoneNone
PDSP KiDatabase 190 3 2 2 1.7 NCCc1c[nH]c2c1cc(OC)cc2 None
CHEMBL8165 141 116 3H-GR-113808 -257 30 Rat 6.3 pKi = 6.3 Binding
NoneNone
PDSP KiDatabase 190 3 2 2 1.7 NCCc1c[nH]c2c1cc(OC)cc2 None
1782 2482 81 3H-GR-113808 -12 22 Guinea pig 6.3 pKi = 6.3 Binding
NoneNone
PDSP KiDatabase 299 7 2 4 2.0 CCN(CCNC(=O)c1cc(Cl)c(cc1OC)N)CC None
241 2482 81 3H-GR-113808 -12 22 Guinea pig 6.3 pKi = 6.3 Binding
NoneNone
PDSP KiDatabase 299 7 2 4 2.0 CCN(CCNC(=O)c1cc(Cl)c(cc1OC)N)CC None
4168 2482 81 3H-GR-113808 -12 22 Guinea pig 6.3 pKi = 6.3 Binding
NoneNone
PDSP KiDatabase 299 7 2 4 2.0 CCN(CCNC(=O)c1cc(Cl)c(cc1OC)N)CC None
CHEMBL86 2482 81 3H-GR-113808 -12 22 Guinea pig 6.3 pKi = 6.3 Binding
NoneNone
PDSP KiDatabase 299 7 2 4 2.0 CCN(CCNC(=O)c1cc(Cl)c(cc1OC)N)CC None
DB01233 2482 81 3H-GR-113808 -12 22 Guinea pig 6.3 pKi = 6.3 Binding
NoneNone
PDSP KiDatabase 299 7 2 4 2.0 CCN(CCNC(=O)c1cc(Cl)c(cc1OC)N)CC None
108182 4068 18 3H-GR-113808 -1 16 Guinea pig 6.3 pKi = 6.3 Binding
NoneNone
PDSP KiDatabase 309 3 2 4 1.8 COc1cc(N)c(cc1C(=O)NC1CN2CCC1CC2)Cl None
245 4068 18 3H-GR-113808 -1 16 Guinea pig 6.3 pKi = 6.3 Binding
NoneNone
PDSP KiDatabase 309 3 2 4 1.8 COc1cc(N)c(cc1C(=O)NC1CN2CCC1CC2)Cl None
CHEMBL18041 4068 18 3H-GR-113808 -1 16 Guinea pig 6.3 pKi = 6.3 Binding
NoneNone
PDSP KiDatabase 309 3 2 4 1.8 COc1cc(N)c(cc1C(=O)NC1CN2CCC1CC2)Cl None
57174031 214163 0 3H-GR-113808 -33 19 Rat 6.3 pKi = 6.3 Binding
NoneNone
PDSP KiDatabase 284 2 1 3 3.0 CN1C2CCC1CC(C2)OC(=O)C3=CNC4=CC=CC=C43 None
57174031 214163 0 3H-RS 57639 -33 19 Rat 6.3 pKi = 6.3 Binding
NoneNone
PDSP KiDatabase 284 2 1 3 3.0 CN1C2CCC1CC(C2)OC(=O)C3=CNC4=CC=CC=C43 None
1809 134 28 3H-RS 57639 -46773 36 Rat 5.3 pKi = 5.3 Binding
NoneNone
PDSP KiDatabase 203 3 3 2 0.8 NCCc1c[nH]c2c1cc(cc2)C(=O)N None
4 134 28 3H-RS 57639 -46773 36 Rat 5.3 pKi = 5.3 Binding
NoneNone
PDSP KiDatabase 203 3 3 2 0.8 NCCc1c[nH]c2c1cc(cc2)C(=O)N None
CHEMBL18840 134 28 3H-RS 57639 -46773 36 Rat 5.3 pKi = 5.3 Binding
NoneNone
PDSP KiDatabase 203 3 3 2 0.8 NCCc1c[nH]c2c1cc(cc2)C(=O)N None
None 214461 0 UNDEFINED -467 15 Guinea pig 5.3 pKi = 5.3 Binding
NoneNone
PDSP KiDatabase 438 5 1 4 4.8 C1CC(CCC1CCN2CCC3=C(C2)C=CC(=C3)C#N)NC(=O)C4=CC=NC5=CC=CC=C45 None
240 931 39 3H-GR-113808 -5 25 Mouse 7.3 pKi = 7.3 Binding
NoneNone
PDSP KiDatabase 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N None
2769 931 39 3H-GR-113808 -5 25 Mouse 7.3 pKi = 7.3 Binding
NoneNone
PDSP KiDatabase 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N None
44279790 931 39 3H-GR-113808 -5 25 Mouse 7.3 pKi = 7.3 Binding
NoneNone
PDSP KiDatabase 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N None
660 931 39 3H-GR-113808 -5 25 Mouse 7.3 pKi = 7.3 Binding
NoneNone
PDSP KiDatabase 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N None
CHEMBL1729 931 39 3H-GR-113808 -5 25 Mouse 7.3 pKi = 7.3 Binding
NoneNone
PDSP KiDatabase 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N None
CHEMBL560739 931 39 3H-GR-113808 -5 25 Mouse 7.3 pKi = 7.3 Binding
NoneNone
PDSP KiDatabase 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N None
DB00604 931 39 3H-GR-113808 -5 25 Mouse 7.3 pKi = 7.3 Binding
NoneNone
PDSP KiDatabase 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N None
107 141 116 3H-GR-113808 -457 30 Mouse 6.3 pKi = 6.3 Binding
NoneNone
PDSP KiDatabase 190 3 2 2 1.7 NCCc1c[nH]c2c1cc(OC)cc2 None
1833 141 116 3H-GR-113808 -457 30 Mouse 6.3 pKi = 6.3 Binding
NoneNone
PDSP KiDatabase 190 3 2 2 1.7 NCCc1c[nH]c2c1cc(OC)cc2 None
CHEMBL8165 141 116 3H-GR-113808 -457 30 Mouse 6.3 pKi = 6.3 Binding
NoneNone
PDSP KiDatabase 190 3 2 2 1.7 NCCc1c[nH]c2c1cc(OC)cc2 None
2780 110040 32 3H-GR-113808 -41 11 Mouse 7.3 pKi = 7.3 Binding
NoneNone
PDSP KiDatabase 373 5 2 4 3.3 COc1cc(N)c(Cl)cc1C(=O)NC1CCN(Cc2ccccc2)CC1 None
CHEMBL325109 110040 32 3H-GR-113808 -41 11 Mouse 7.3 pKi = 7.3 Binding
NoneNone
PDSP KiDatabase 373 5 2 4 3.3 COc1cc(N)c(Cl)cc1C(=O)NC1CCN(Cc2ccccc2)CC1 None
None 214502 0 3H-GR-113808 -436 18 Guinea pig 6.3 pKi = 6.3 Binding
NoneNone
PDSP KiDatabase 416 9 3 4 2.8 C1=CC(=CC=C1CCNC(N)SCCCC2=CN=CN2)I None
None 214237 0 3H-GR-113808 -1 6 Mouse 7.3 pKi = 7.3 Binding
NoneNone
PDSP KiDatabase 367 2 1 6 2.4 CN1C2CCC1CC(C2)OC(=O)N3C4=C(C=CC(=C4)OC)NC3=O.Cl None
57174031 214163 0 3H-Cyclic AMP -14 19 Guinea pig 6.3 pKi = 6.3 Binding
NoneNone
PDSP KiDatabase 284 2 1 3 3.0 CN1C2CCC1CC(C2)OC(=O)C3=CNC4=CC=CC=C43 None
57174031 214163 0 3H-GR-113808 -33 19 Rat 6.3 pKi = 6.3 Binding
NoneNone
PDSP KiDatabase 284 2 1 3 3.0 CN1C2CCC1CC(C2)OC(=O)C3=CNC4=CC=CC=C43 None
5 139 66 3H-GR-113808 -288 54 Human 7.3 pKi = 7.3 Binding
NoneNone
PDSP KiDatabase 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 None
5 139 66 3H-GR-113808 -154 54 Mouse 7.3 pKi = 7.3 Binding
NoneNone
PDSP KiDatabase 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 None
5202 139 66 3H-GR-113808 -288 54 Human 7.3 pKi = 7.3 Binding
NoneNone
PDSP KiDatabase 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 None
5202 139 66 3H-GR-113808 -154 54 Mouse 7.3 pKi = 7.3 Binding
NoneNone
PDSP KiDatabase 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 None
CHEMBL39 139 66 3H-GR-113808 -288 54 Human 7.3 pKi = 7.3 Binding
NoneNone
PDSP KiDatabase 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 None
CHEMBL39 139 66 3H-GR-113808 -154 54 Mouse 7.3 pKi = 7.3 Binding
NoneNone
PDSP KiDatabase 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 None
DB08839 139 66 3H-GR-113808 -288 54 Human 7.3 pKi = 7.3 Binding
NoneNone
PDSP KiDatabase 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 None
DB08839 139 66 3H-GR-113808 -154 54 Mouse 7.3 pKi = 7.3 Binding
NoneNone
PDSP KiDatabase 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 None
1782 2482 81 None -25 22 Mouse 8.2 pKi = 8.2 Binding
NoneNone
Drug Central 299 7 2 4 2.0 CCN(CCNC(=O)c1cc(Cl)c(cc1OC)N)CC None
241 2482 81 None -25 22 Mouse 8.2 pKi = 8.2 Binding
NoneNone
Drug Central 299 7 2 4 2.0 CCN(CCNC(=O)c1cc(Cl)c(cc1OC)N)CC None
4168 2482 81 None -25 22 Mouse 8.2 pKi = 8.2 Binding
NoneNone
Drug Central 299 7 2 4 2.0 CCN(CCNC(=O)c1cc(Cl)c(cc1OC)N)CC None
CHEMBL86 2482 81 None -25 22 Mouse 8.2 pKi = 8.2 Binding
NoneNone
Drug Central 299 7 2 4 2.0 CCN(CCNC(=O)c1cc(Cl)c(cc1OC)N)CC None
DB01233 2482 81 None -25 22 Mouse 8.2 pKi = 8.2 Binding
NoneNone
Drug Central 299 7 2 4 2.0 CCN(CCNC(=O)c1cc(Cl)c(cc1OC)N)CC None
1782 2482 81 None -11 22 Rat 8.2 pKi = 8.2 Binding
Binding affinity at 5-hydroxytryptamine 4 receptor in rat striatum by [3H]GR-113808 displacement.Binding affinity at 5-hydroxytryptamine 4 receptor in rat striatum by [3H]GR-113808 displacement.
Drug Central 299 7 2 4 2.0 CCN(CCNC(=O)c1cc(Cl)c(cc1OC)N)CC None
241 2482 81 None -11 22 Rat 8.2 pKi = 8.2 Binding
Binding affinity at 5-hydroxytryptamine 4 receptor in rat striatum by [3H]GR-113808 displacement.Binding affinity at 5-hydroxytryptamine 4 receptor in rat striatum by [3H]GR-113808 displacement.
Drug Central 299 7 2 4 2.0 CCN(CCNC(=O)c1cc(Cl)c(cc1OC)N)CC None
4168 2482 81 None -11 22 Rat 8.2 pKi = 8.2 Binding
Binding affinity at 5-hydroxytryptamine 4 receptor in rat striatum by [3H]GR-113808 displacement.Binding affinity at 5-hydroxytryptamine 4 receptor in rat striatum by [3H]GR-113808 displacement.
Drug Central 299 7 2 4 2.0 CCN(CCNC(=O)c1cc(Cl)c(cc1OC)N)CC None
CHEMBL86 2482 81 None -11 22 Rat 8.2 pKi = 8.2 Binding
Binding affinity at 5-hydroxytryptamine 4 receptor in rat striatum by [3H]GR-113808 displacement.Binding affinity at 5-hydroxytryptamine 4 receptor in rat striatum by [3H]GR-113808 displacement.
Drug Central 299 7 2 4 2.0 CCN(CCNC(=O)c1cc(Cl)c(cc1OC)N)CC None
DB01233 2482 81 None -11 22 Rat 8.2 pKi = 8.2 Binding
Binding affinity at 5-hydroxytryptamine 4 receptor in rat striatum by [3H]GR-113808 displacement.Binding affinity at 5-hydroxytryptamine 4 receptor in rat striatum by [3H]GR-113808 displacement.
Drug Central 299 7 2 4 2.0 CCN(CCNC(=O)c1cc(Cl)c(cc1OC)N)CC None
107715 199260 18 None -165 20 Guinea pig 8.2 pKi = 8.2 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
Drug Central 611 5 3 6 2.7 CC(C)[C@@]1(NC(=O)[C@@H]2C[C@@H]3c4cccc5[nH]cc(c45)C[C@H]3N(C)C2)O[C@@]2(O)[C@@H]3CCCN3C(=O)[C@H](Cc3ccccc3)N2C1=O None
CHEMBL1255837 199260 18 None -165 20 Guinea pig 8.2 pKi = 8.2 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
Drug Central 611 5 3 6 2.7 CC(C)[C@@]1(NC(=O)[C@@H]2C[C@@H]3c4cccc5[nH]cc(c45)C[C@H]3N(C)C2)O[C@@]2(O)[C@@H]3CCCN3C(=O)[C@H](Cc3ccccc3)N2C1=O None
CHEMBL601773 199260 18 None -165 20 Guinea pig 8.2 pKi = 8.2 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
Drug Central 611 5 3 6 2.7 CC(C)[C@@]1(NC(=O)[C@@H]2C[C@@H]3c4cccc5[nH]cc(c45)C[C@H]3N(C)C2)O[C@@]2(O)[C@@H]3CCCN3C(=O)[C@H](Cc3ccccc3)N2C1=O None
3168 9172 84 None -93 21 Guinea pig 8.2 pKi = 8.2 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
Drug Central 379 6 1 4 3.7 O=C(CCCN1CC=C(n2c(=O)[nH]c3ccccc32)CC1)c1ccc(F)cc1 None
CHEMBL1108 9172 84 None -93 21 Guinea pig 8.2 pKi = 8.2 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
Drug Central 379 6 1 4 3.7 O=C(CCCN1CC=C(n2c(=O)[nH]c3ccccc32)CC1)c1ccc(F)cc1 None
1782 2482 81 None -12 22 Guinea pig 8.2 pKi = 8.2 Binding
Inhibition of [3H]GR-113808 binding to guinea pig striatum 5-hydroxytryptamine 4 receptorInhibition of [3H]GR-113808 binding to guinea pig striatum 5-hydroxytryptamine 4 receptor
Drug Central 299 7 2 4 2.0 CCN(CCNC(=O)c1cc(Cl)c(cc1OC)N)CC None
241 2482 81 None -12 22 Guinea pig 8.2 pKi = 8.2 Binding
Inhibition of [3H]GR-113808 binding to guinea pig striatum 5-hydroxytryptamine 4 receptorInhibition of [3H]GR-113808 binding to guinea pig striatum 5-hydroxytryptamine 4 receptor
Drug Central 299 7 2 4 2.0 CCN(CCNC(=O)c1cc(Cl)c(cc1OC)N)CC None
4168 2482 81 None -12 22 Guinea pig 8.2 pKi = 8.2 Binding
Inhibition of [3H]GR-113808 binding to guinea pig striatum 5-hydroxytryptamine 4 receptorInhibition of [3H]GR-113808 binding to guinea pig striatum 5-hydroxytryptamine 4 receptor
Drug Central 299 7 2 4 2.0 CCN(CCNC(=O)c1cc(Cl)c(cc1OC)N)CC None
CHEMBL86 2482 81 None -12 22 Guinea pig 8.2 pKi = 8.2 Binding
Inhibition of [3H]GR-113808 binding to guinea pig striatum 5-hydroxytryptamine 4 receptorInhibition of [3H]GR-113808 binding to guinea pig striatum 5-hydroxytryptamine 4 receptor
Drug Central 299 7 2 4 2.0 CCN(CCNC(=O)c1cc(Cl)c(cc1OC)N)CC None
DB01233 2482 81 None -12 22 Guinea pig 8.2 pKi = 8.2 Binding
Inhibition of [3H]GR-113808 binding to guinea pig striatum 5-hydroxytryptamine 4 receptorInhibition of [3H]GR-113808 binding to guinea pig striatum 5-hydroxytryptamine 4 receptor
Drug Central 299 7 2 4 2.0 CCN(CCNC(=O)c1cc(Cl)c(cc1OC)N)CC None
5 139 66 3H-5HT -117 54 Rat 8.2 pKi = 8.2 Binding
NoneNone
PDSP KiDatabase 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 None
5202 139 66 3H-5HT -117 54 Rat 8.2 pKi = 8.2 Binding
NoneNone
PDSP KiDatabase 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 None
CHEMBL39 139 66 3H-5HT -117 54 Rat 8.2 pKi = 8.2 Binding
NoneNone
PDSP KiDatabase 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 None
DB08839 139 66 3H-5HT -117 54 Rat 8.2 pKi = 8.2 Binding
NoneNone
PDSP KiDatabase 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 None
258 3511 25 3H-GR-113808 1 8 Guinea pig 8.2 pKi = 8.2 Binding
NoneNone
PDSP KiDatabase 300 7 1 5 2.4 CCN(CCOC(=O)c1cc(Cl)c(cc1OC)N)CC None
258 3511 25 3H-GR-113808 -1 8 Human 8.2 pKi = 8.2 Binding
NoneNone
PDSP KiDatabase 300 7 1 5 2.4 CCN(CCOC(=O)c1cc(Cl)c(cc1OC)N)CC None
258 3511 25 3H-GR-113808 -1 8 Mouse 8.2 pKi = 8.2 Binding
NoneNone
PDSP KiDatabase 300 7 1 5 2.4 CCN(CCOC(=O)c1cc(Cl)c(cc1OC)N)CC None
5191 3511 25 3H-GR-113808 1 8 Guinea pig 8.2 pKi = 8.2 Binding
NoneNone
PDSP KiDatabase 300 7 1 5 2.4 CCN(CCOC(=O)c1cc(Cl)c(cc1OC)N)CC None
5191 3511 25 3H-GR-113808 -1 8 Human 8.2 pKi = 8.2 Binding
NoneNone
PDSP KiDatabase 300 7 1 5 2.4 CCN(CCOC(=O)c1cc(Cl)c(cc1OC)N)CC None
5191 3511 25 3H-GR-113808 -1 8 Mouse 8.2 pKi = 8.2 Binding
NoneNone
PDSP KiDatabase 300 7 1 5 2.4 CCN(CCOC(=O)c1cc(Cl)c(cc1OC)N)CC None
CHEMBL287045 3511 25 3H-GR-113808 1 8 Guinea pig 8.2 pKi = 8.2 Binding
NoneNone
PDSP KiDatabase 300 7 1 5 2.4 CCN(CCOC(=O)c1cc(Cl)c(cc1OC)N)CC None
CHEMBL287045 3511 25 3H-GR-113808 -1 8 Human 8.2 pKi = 8.2 Binding
NoneNone
PDSP KiDatabase 300 7 1 5 2.4 CCN(CCOC(=O)c1cc(Cl)c(cc1OC)N)CC None
CHEMBL287045 3511 25 3H-GR-113808 -1 8 Mouse 8.2 pKi = 8.2 Binding
NoneNone
PDSP KiDatabase 300 7 1 5 2.4 CCN(CCOC(=O)c1cc(Cl)c(cc1OC)N)CC None
133 2460 48 None -79 42 Guinea pig 8.2 pKi = 8.2 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
Drug Central 403 4 1 4 4.1 O=C(OCc1ccccc1)NC[C@H]1CN(C)[C@H]2[C@H](C1)c1cccc3c1c(C2)cn3C None
1723 2460 48 None -79 42 Guinea pig 8.2 pKi = 8.2 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
Drug Central 403 4 1 4 4.1 O=C(OCc1ccccc1)NC[C@H]1CN(C)[C@H]2[C@H](C1)c1cccc3c1c(C2)cn3C None
28693 2460 48 None -79 42 Guinea pig 8.2 pKi = 8.2 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
Drug Central 403 4 1 4 4.1 O=C(OCc1ccccc1)NC[C@H]1CN(C)[C@H]2[C@H](C1)c1cccc3c1c(C2)cn3C None
CHEMBL19215 2460 48 None -79 42 Guinea pig 8.2 pKi = 8.2 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
Drug Central 403 4 1 4 4.1 O=C(OCc1ccccc1)NC[C@H]1CN(C)[C@H]2[C@H](C1)c1cccc3c1c(C2)cn3C None
DB13520 2460 48 None -79 42 Guinea pig 8.2 pKi = 8.2 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
Drug Central 403 4 1 4 4.1 O=C(OCc1ccccc1)NC[C@H]1CN(C)[C@H]2[C@H](C1)c1cccc3c1c(C2)cn3C None
11954224 214174 0 None -93 59 Guinea pig 8.2 pKi = 8.2 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
Drug Central 581 4 3 6 2.0 CC1(C(=O)N2C(C(=O)N3CCCC3C2(O1)O)CC4=CC=CC=C4)NC(=O)C5CN(C6CC7=CNC8=CC=CC(=C78)C6=C5)C None
2274 3124 53 None -17 32 Guinea pig 8.2 pKi = 8.2 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
Drug Central 373 4 0 4 4.6 CN1CCN(CC1)CCCN1c2ccccc2Sc2c1cc(Cl)cc2 None
4917 3124 53 None -17 32 Guinea pig 8.2 pKi = 8.2 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
Drug Central 373 4 0 4 4.6 CN1CCN(CC1)CCCN1c2ccccc2Sc2c1cc(Cl)cc2 None
7279 3124 53 None -17 32 Guinea pig 8.2 pKi = 8.2 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
Drug Central 373 4 0 4 4.6 CN1CCN(CC1)CCCN1c2ccccc2Sc2c1cc(Cl)cc2 None
CHEMBL728 3124 53 None -17 32 Guinea pig 8.2 pKi = 8.2 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
Drug Central 373 4 0 4 4.6 CN1CCN(CC1)CCCN1c2ccccc2Sc2c1cc(Cl)cc2 None
DB00433 3124 53 None -17 32 Guinea pig 8.2 pKi = 8.2 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
Drug Central 373 4 0 4 4.6 CN1CCN(CC1)CCCN1c2ccccc2Sc2c1cc(Cl)cc2 None
2585 790 100 None -57 22 Guinea pig 8.2 pKi = 8.2 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
Drug Central 406 10 3 5 3.7 COc1ccccc1OCCNCC(COc1cccc2c1c1ccccc1[nH]2)O None
522 790 100 None -57 22 Guinea pig 8.2 pKi = 8.2 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
Drug Central 406 10 3 5 3.7 COc1ccccc1OCCNCC(COc1cccc2c1c1ccccc1[nH]2)O None
551 790 100 None -57 22 Guinea pig 8.2 pKi = 8.2 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
Drug Central 406 10 3 5 3.7 COc1ccccc1OCCNCC(COc1cccc2c1c1ccccc1[nH]2)O None
CHEMBL723 790 100 None -57 22 Guinea pig 8.2 pKi = 8.2 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
Drug Central 406 10 3 5 3.7 COc1ccccc1OCCNCC(COc1cccc2c1c1ccccc1[nH]2)O None
DB01136 790 100 None -57 22 Guinea pig 8.2 pKi = 8.2 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
Drug Central 406 10 3 5 3.7 COc1ccccc1OCCNCC(COc1cccc2c1c1ccccc1[nH]2)O None
10531 1392 18 None -87 24 Guinea pig 8.2 pKi = 8.2 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
Drug Central 583 4 3 6 2.1 CN1C[C@@H](C[C@H]2[C@H]1Cc1c[nH]c3c1c2ccc3)C(=O)N[C@]1(C)O[C@@]2(N(C1=O)[C@@H](Cc1ccccc1)C(=O)N1[C@H]2CCC1)O None
121 1392 18 None -87 24 Guinea pig 8.2 pKi = 8.2 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
Drug Central 583 4 3 6 2.1 CN1C[C@@H](C[C@H]2[C@H]1Cc1c[nH]c3c1c2ccc3)C(=O)N[C@]1(C)O[C@@]2(N(C1=O)[C@@H](Cc1ccccc1)C(=O)N1[C@H]2CCC1)O None
888 1392 18 None -87 24 Guinea pig 8.2 pKi = 8.2 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
Drug Central 583 4 3 6 2.1 CN1C[C@@H](C[C@H]2[C@H]1Cc1c[nH]c3c1c2ccc3)C(=O)N[C@]1(C)O[C@@]2(N(C1=O)[C@@H](Cc1ccccc1)C(=O)N1[C@H]2CCC1)O None
CHEMBL1732 1392 18 None -87 24 Guinea pig 8.2 pKi = 8.2 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
Drug Central 583 4 3 6 2.1 CN1C[C@@H](C[C@H]2[C@H]1Cc1c[nH]c3c1c2ccc3)C(=O)N[C@]1(C)O[C@@]2(N(C1=O)[C@@H](Cc1ccccc1)C(=O)N1[C@H]2CCC1)O None
DB00320 1392 18 None -87 24 Guinea pig 8.2 pKi = 8.2 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
Drug Central 583 4 3 6 2.1 CN1C[C@@H](C[C@H]2[C@H]1Cc1c[nH]c3c1c2ccc3)C(=O)N[C@]1(C)O[C@@]2(N(C1=O)[C@@H](Cc1ccccc1)C(=O)N1[C@H]2CCC1)O None
57174031 214163 0 None -6 19 Human 8.2 pKi = 8.2 Binding
NoneNone
Drug Central 284 2 1 3 3.0 CN1C2CCC1CC(C2)OC(=O)C3=CNC4=CC=CC=C43 None
57174031 214163 0 None -14 19 Guinea pig 8.2 pKi = 8.2 Binding
Binding affinity towards 5-hydroxytryptamine 4 receptor in striatum membranes of guinea-pig brain was evaluatedBinding affinity towards 5-hydroxytryptamine 4 receptor in striatum membranes of guinea-pig brain was evaluated
Drug Central 284 2 1 3 3.0 CN1C2CCC1CC(C2)OC(=O)C3=CNC4=CC=CC=C43 None
3157 1442 69 None -27 12 Guinea pig 8.2 pKi = 8.2 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
Drug Central 451 4 2 8 1.5 COc1cc2nc([nH]c(=N)c2cc1OC)N1CCN(CC1)C(=O)C1COc2c(O1)cccc2 None
7170 1442 69 None -27 12 Guinea pig 8.2 pKi = 8.2 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
Drug Central 451 4 2 8 1.5 COc1cc2nc([nH]c(=N)c2cc1OC)N1CCN(CC1)C(=O)C1COc2c(O1)cccc2 None
954 1442 69 None -27 12 Guinea pig 8.2 pKi = 8.2 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
Drug Central 451 4 2 8 1.5 COc1cc2nc([nH]c(=N)c2cc1OC)N1CCN(CC1)C(=O)C1COc2c(O1)cccc2 None
CHEMBL707 1442 69 None -27 12 Guinea pig 8.2 pKi = 8.2 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
Drug Central 451 4 2 8 1.5 COc1cc2nc([nH]c(=N)c2cc1OC)N1CCN(CC1)C(=O)C1COc2c(O1)cccc2 None
DB00590 1442 69 None -27 12 Guinea pig 8.2 pKi = 8.2 Binding
DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)DRUGMATRIX: Serotonin (5-Hydroxytryptamine) 5-HT4 radioligand binding (ligand: [3H] GR-113808)
Drug Central 451 4 2 8 1.5 COc1cc2nc([nH]c(=N)c2cc1OC)N1CCN(CC1)C(=O)C1COc2c(O1)cccc2 None
119584 2557 99 None -1 6 Human 8.2 pKi = 8.2 Binding
NoneNone
Drug Central 421 7 2 5 3.1 CCOc1cc(N)c(cc1C(=O)NCC1OCCN(C1)Cc1ccc(cc1)F)Cl None
1848 2557 99 None -1 6 Human 8.2 pKi = 8.2 Binding
NoneNone
Drug Central 421 7 2 5 3.1 CCOc1cc(N)c(cc1C(=O)NCC1OCCN(C1)Cc1ccc(cc1)F)Cl None
242 2557 99 None -1 6 Human 8.2 pKi = 8.2 Binding
NoneNone
Drug Central 421 7 2 5 3.1 CCOc1cc(N)c(cc1C(=O)NCC1OCCN(C1)Cc1ccc(cc1)F)Cl None
CHEMBL60889 2557 99 None -1 6 Human 8.2 pKi = 8.2 Binding
NoneNone
Drug Central 421 7 2 5 3.1 CCOc1cc(N)c(cc1C(=O)NCC1OCCN(C1)Cc1ccc(cc1)F)Cl None
DB11675 2557 99 None -1 6 Human 8.2 pKi = 8.2 Binding
NoneNone
Drug Central 421 7 2 5 3.1 CCOc1cc(N)c(cc1C(=O)NCC1OCCN(C1)Cc1ccc(cc1)F)Cl None
2780 110040 32 None -20 11 Rat 8.2 pKi = 8.2 Binding
Binding affinity against 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatumBinding affinity against 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatum
Drug Central 373 5 2 4 3.3 COc1cc(N)c(Cl)cc1C(=O)NC1CCN(Cc2ccccc2)CC1 None
CHEMBL325109 110040 32 None -20 11 Rat 8.2 pKi = 8.2 Binding
Binding affinity against 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatumBinding affinity against 5-hydroxytryptamine 4 receptor using [3H]GR-113808 as radioligand in rat striatum
Drug Central 373 5 2 4 3.3 COc1cc(N)c(Cl)cc1C(=O)NC1CCN(Cc2ccccc2)CC1 None
2780 110040 32 None -20 11 Guinea pig 8.2 pKi = 8.2 Binding
Inhibition of [3H]GR-113808 binding to guinea pig striatum 5-hydroxytryptamine 4 receptorInhibition of [3H]GR-113808 binding to guinea pig striatum 5-hydroxytryptamine 4 receptor
Drug Central 373 5 2 4 3.3 COc1cc(N)c(Cl)cc1C(=O)NC1CCN(Cc2ccccc2)CC1 None
CHEMBL325109 110040 32 None -20 11 Guinea pig 8.2 pKi = 8.2 Binding
Inhibition of [3H]GR-113808 binding to guinea pig striatum 5-hydroxytryptamine 4 receptorInhibition of [3H]GR-113808 binding to guinea pig striatum 5-hydroxytryptamine 4 receptor
Drug Central 373 5 2 4 3.3 COc1cc(N)c(Cl)cc1C(=O)NC1CCN(Cc2ccccc2)CC1 None
240 931 39 3H-GR-113808 -4 25 Guinea pig 7.2 pKi = 7.2 Binding
NoneNone
PDSP KiDatabase 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N None
240 931 39 3H-GR-113808 -11 25 Human 7.2 pKi = 7.2 Binding
NoneNone
PDSP KiDatabase 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N None
2769 931 39 3H-GR-113808 -4 25 Guinea pig 7.2 pKi = 7.2 Binding
NoneNone
PDSP KiDatabase 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N None
2769 931 39 3H-GR-113808 -11 25 Human 7.2 pKi = 7.2 Binding
NoneNone
PDSP KiDatabase 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N None
44279790 931 39 3H-GR-113808 -4 25 Guinea pig 7.2 pKi = 7.2 Binding
NoneNone
PDSP KiDatabase 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N None
44279790 931 39 3H-GR-113808 -11 25 Human 7.2 pKi = 7.2 Binding
NoneNone
PDSP KiDatabase 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N None
660 931 39 3H-GR-113808 -4 25 Guinea pig 7.2 pKi = 7.2 Binding
NoneNone
PDSP KiDatabase 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N None
660 931 39 3H-GR-113808 -11 25 Human 7.2 pKi = 7.2 Binding
NoneNone
PDSP KiDatabase 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N None
CHEMBL1729 931 39 3H-GR-113808 -4 25 Guinea pig 7.2 pKi = 7.2 Binding
NoneNone
PDSP KiDatabase 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N None
CHEMBL1729 931 39 3H-GR-113808 -11 25 Human 7.2 pKi = 7.2 Binding
NoneNone
PDSP KiDatabase 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N None
CHEMBL560739 931 39 3H-GR-113808 -4 25 Guinea pig 7.2 pKi = 7.2 Binding
NoneNone
PDSP KiDatabase 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N None
CHEMBL560739 931 39 3H-GR-113808 -11 25 Human 7.2 pKi = 7.2 Binding
NoneNone
PDSP KiDatabase 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N None
DB00604 931 39 3H-GR-113808 -4 25 Guinea pig 7.2 pKi = 7.2 Binding
NoneNone
PDSP KiDatabase 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N None
DB00604 931 39 3H-GR-113808 -11 25 Human 7.2 pKi = 7.2 Binding
NoneNone
PDSP KiDatabase 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N None
57174031 214163 0 3H-GR-113808 -14 19 Guinea pig 7.2 pKi = 7.2 Binding
NoneNone
PDSP KiDatabase 284 2 1 3 3.0 CN1C2CCC1CC(C2)OC(=O)C3=CNC4=CC=CC=C43 None
None 214237 0 3H-GR-113808 1 6 Human 7.2 pKi = 7.2 Binding
NoneNone
PDSP KiDatabase 367 2 1 6 2.4 CN1C2CCC1CC(C2)OC(=O)N3C4=C(C=CC(=C4)OC)NC3=O.Cl None
None 214237 0 3H-GR-113808 -2 6 Rat 7.2 pKi = 7.2 Binding
NoneNone
PDSP KiDatabase 367 2 1 6 2.4 CN1C2CCC1CC(C2)OC(=O)N3C4=C(C=CC(=C4)OC)NC3=O.Cl None
107 141 116 3H-GR-113808 -549 30 Guinea pig 6.2 pKi = 6.2 Binding
NoneNone
PDSP KiDatabase 190 3 2 2 1.7 NCCc1c[nH]c2c1cc(OC)cc2 None
1833 141 116 3H-GR-113808 -549 30 Guinea pig 6.2 pKi = 6.2 Binding
NoneNone
PDSP KiDatabase 190 3 2 2 1.7 NCCc1c[nH]c2c1cc(OC)cc2 None
CHEMBL8165 141 116 3H-GR-113808 -549 30 Guinea pig 6.2 pKi = 6.2 Binding
NoneNone
PDSP KiDatabase 190 3 2 2 1.7 NCCc1c[nH]c2c1cc(OC)cc2 None
1782 2482 81 3H-GR-113808 -12 22 Guinea pig 6.2 pKi = 6.2 Binding
NoneNone
PDSP KiDatabase 299 7 2 4 2.0 CCN(CCNC(=O)c1cc(Cl)c(cc1OC)N)CC None
241 2482 81 3H-GR-113808 -12 22 Guinea pig 6.2 pKi = 6.2 Binding
NoneNone
PDSP KiDatabase 299 7 2 4 2.0 CCN(CCNC(=O)c1cc(Cl)c(cc1OC)N)CC None
4168 2482 81 3H-GR-113808 -12 22 Guinea pig 6.2 pKi = 6.2 Binding
NoneNone
PDSP KiDatabase 299 7 2 4 2.0 CCN(CCNC(=O)c1cc(Cl)c(cc1OC)N)CC None
CHEMBL86 2482 81 3H-GR-113808 -12 22 Guinea pig 6.2 pKi = 6.2 Binding
NoneNone
PDSP KiDatabase 299 7 2 4 2.0 CCN(CCNC(=O)c1cc(Cl)c(cc1OC)N)CC None
DB01233 2482 81 3H-GR-113808 -12 22 Guinea pig 6.2 pKi = 6.2 Binding
NoneNone
PDSP KiDatabase 299 7 2 4 2.0 CCN(CCNC(=O)c1cc(Cl)c(cc1OC)N)CC None
1809 134 28 3H-GR-113808 -87096 36 Guinea pig 5.2 pKi = 5.2 Binding
NoneNone
PDSP KiDatabase 203 3 3 2 0.8 NCCc1c[nH]c2c1cc(cc2)C(=O)N None
4 134 28 3H-GR-113808 -87096 36 Guinea pig 5.2 pKi = 5.2 Binding
NoneNone
PDSP KiDatabase 203 3 3 2 0.8 NCCc1c[nH]c2c1cc(cc2)C(=O)N None
CHEMBL18840 134 28 3H-GR-113808 -87096 36 Guinea pig 5.2 pKi = 5.2 Binding
NoneNone
PDSP KiDatabase 203 3 3 2 0.8 NCCc1c[nH]c2c1cc(cc2)C(=O)N None
57174031 214163 0 None -8 19 Mouse 8.2 pKi = 8.2 Binding
NoneNone
Drug Central 284 2 1 3 3.0 CN1C2CCC1CC(C2)OC(=O)C3=CNC4=CC=CC=C43 None
119584 2557 99 None -1 6 Guinea pig 8.2 pKi = 8.2 Binding
Inhibition of [3H]GR-113808 binding to guinea pig striatum 5-hydroxytryptamine 4 receptorInhibition of [3H]GR-113808 binding to guinea pig striatum 5-hydroxytryptamine 4 receptor
Drug Central 421 7 2 5 3.1 CCOc1cc(N)c(cc1C(=O)NCC1OCCN(C1)Cc1ccc(cc1)F)Cl None
1848 2557 99 None -1 6 Guinea pig 8.2 pKi = 8.2 Binding
Inhibition of [3H]GR-113808 binding to guinea pig striatum 5-hydroxytryptamine 4 receptorInhibition of [3H]GR-113808 binding to guinea pig striatum 5-hydroxytryptamine 4 receptor
Drug Central 421 7 2 5 3.1 CCOc1cc(N)c(cc1C(=O)NCC1OCCN(C1)Cc1ccc(cc1)F)Cl None
242 2557 99 None -1 6 Guinea pig 8.2 pKi = 8.2 Binding
Inhibition of [3H]GR-113808 binding to guinea pig striatum 5-hydroxytryptamine 4 receptorInhibition of [3H]GR-113808 binding to guinea pig striatum 5-hydroxytryptamine 4 receptor
Drug Central 421 7 2 5 3.1 CCOc1cc(N)c(cc1C(=O)NCC1OCCN(C1)Cc1ccc(cc1)F)Cl None
CHEMBL60889 2557 99 None -1 6 Guinea pig 8.2 pKi = 8.2 Binding
Inhibition of [3H]GR-113808 binding to guinea pig striatum 5-hydroxytryptamine 4 receptorInhibition of [3H]GR-113808 binding to guinea pig striatum 5-hydroxytryptamine 4 receptor
Drug Central 421 7 2 5 3.1 CCOc1cc(N)c(cc1C(=O)NCC1OCCN(C1)Cc1ccc(cc1)F)Cl None
DB11675 2557 99 None -1 6 Guinea pig 8.2 pKi = 8.2 Binding
Inhibition of [3H]GR-113808 binding to guinea pig striatum 5-hydroxytryptamine 4 receptorInhibition of [3H]GR-113808 binding to guinea pig striatum 5-hydroxytryptamine 4 receptor
Drug Central 421 7 2 5 3.1 CCOc1cc(N)c(cc1C(=O)NCC1OCCN(C1)Cc1ccc(cc1)F)Cl None
57174031 214163 0 None -33 19 Rat 8.1 pKi = 8.1 Binding
Displacement of [3H]GR-113808 from rat striatum 5-hydroxytryptamine 4 receptorDisplacement of [3H]GR-113808 from rat striatum 5-hydroxytryptamine 4 receptor
Drug Central 284 2 1 3 3.0 CN1C2CCC1CC(C2)OC(=O)C3=CNC4=CC=CC=C43 None
240 931 39 None -5 25 Mouse 8.1 pKi = 8.1 Binding
NoneNone
Drug Central 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N None
2769 931 39 None -5 25 Mouse 8.1 pKi = 8.1 Binding
NoneNone
Drug Central 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N None
44279790 931 39 None -5 25 Mouse 8.1 pKi = 8.1 Binding
NoneNone
Drug Central 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N None
660 931 39 None -5 25 Mouse 8.1 pKi = 8.1 Binding
NoneNone
Drug Central 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N None
CHEMBL1729 931 39 None -5 25 Mouse 8.1 pKi = 8.1 Binding
NoneNone
Drug Central 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N None
CHEMBL560739 931 39 None -5 25 Mouse 8.1 pKi = 8.1 Binding
NoneNone
Drug Central 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N None
DB00604 931 39 None -5 25 Mouse 8.1 pKi = 8.1 Binding
NoneNone
Drug Central 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N None
240 931 39 None -11 25 Human 8.1 pKi = 8.1 Binding
Binding affinity towards Serotonin 5-hydroxytryptamine 4 receptorBinding affinity towards Serotonin 5-hydroxytryptamine 4 receptor
Drug Central 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N None
2769 931 39 None -11 25 Human 8.1 pKi = 8.1 Binding
Binding affinity towards Serotonin 5-hydroxytryptamine 4 receptorBinding affinity towards Serotonin 5-hydroxytryptamine 4 receptor
Drug Central 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N None
44279790 931 39 None -11 25 Human 8.1 pKi = 8.1 Binding
Binding affinity towards Serotonin 5-hydroxytryptamine 4 receptorBinding affinity towards Serotonin 5-hydroxytryptamine 4 receptor
Drug Central 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N None
660 931 39 None -11 25 Human 8.1 pKi = 8.1 Binding
Binding affinity towards Serotonin 5-hydroxytryptamine 4 receptorBinding affinity towards Serotonin 5-hydroxytryptamine 4 receptor
Drug Central 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N None
CHEMBL1729 931 39 None -11 25 Human 8.1 pKi = 8.1 Binding
Binding affinity towards Serotonin 5-hydroxytryptamine 4 receptorBinding affinity towards Serotonin 5-hydroxytryptamine 4 receptor
Drug Central 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N None
CHEMBL560739 931 39 None -11 25 Human 8.1 pKi = 8.1 Binding
Binding affinity towards Serotonin 5-hydroxytryptamine 4 receptorBinding affinity towards Serotonin 5-hydroxytryptamine 4 receptor
Drug Central 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N None
DB00604 931 39 None -11 25 Human 8.1 pKi = 8.1 Binding
Binding affinity towards Serotonin 5-hydroxytryptamine 4 receptorBinding affinity towards Serotonin 5-hydroxytryptamine 4 receptor
Drug Central 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N None
258 3511 25 3H-GR-113808 -1 8 Mouse 8.1 pKi = 8.1 Binding
NoneNone
PDSP KiDatabase 300 7 1 5 2.4 CCN(CCOC(=O)c1cc(Cl)c(cc1OC)N)CC None
5191 3511 25 3H-GR-113808 -1 8 Mouse 8.1 pKi = 8.1 Binding
NoneNone
PDSP KiDatabase 300 7 1 5 2.4 CCN(CCOC(=O)c1cc(Cl)c(cc1OC)N)CC None
CHEMBL287045 3511 25 3H-GR-113808 -1 8 Mouse 8.1 pKi = 8.1 Binding
NoneNone
PDSP KiDatabase 300 7 1 5 2.4 CCN(CCOC(=O)c1cc(Cl)c(cc1OC)N)CC None
240 931 39 None -4 25 Guinea pig 8.1 pKi = 8.1 Binding
Inhibition of [3H]GR-113808 binding to guinea pig striatum 5-hydroxytryptamine 4 receptorInhibition of [3H]GR-113808 binding to guinea pig striatum 5-hydroxytryptamine 4 receptor
Drug Central 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N None
2769 931 39 None -4 25 Guinea pig 8.1 pKi = 8.1 Binding
Inhibition of [3H]GR-113808 binding to guinea pig striatum 5-hydroxytryptamine 4 receptorInhibition of [3H]GR-113808 binding to guinea pig striatum 5-hydroxytryptamine 4 receptor
Drug Central 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N None
44279790 931 39 None -4 25 Guinea pig 8.1 pKi = 8.1 Binding
Inhibition of [3H]GR-113808 binding to guinea pig striatum 5-hydroxytryptamine 4 receptorInhibition of [3H]GR-113808 binding to guinea pig striatum 5-hydroxytryptamine 4 receptor
Drug Central 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N None
660 931 39 None -4 25 Guinea pig 8.1 pKi = 8.1 Binding
Inhibition of [3H]GR-113808 binding to guinea pig striatum 5-hydroxytryptamine 4 receptorInhibition of [3H]GR-113808 binding to guinea pig striatum 5-hydroxytryptamine 4 receptor
Drug Central 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N None
CHEMBL1729 931 39 None -4 25 Guinea pig 8.1 pKi = 8.1 Binding
Inhibition of [3H]GR-113808 binding to guinea pig striatum 5-hydroxytryptamine 4 receptorInhibition of [3H]GR-113808 binding to guinea pig striatum 5-hydroxytryptamine 4 receptor
Drug Central 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N None
CHEMBL560739 931 39 None -4 25 Guinea pig 8.1 pKi = 8.1 Binding
Inhibition of [3H]GR-113808 binding to guinea pig striatum 5-hydroxytryptamine 4 receptorInhibition of [3H]GR-113808 binding to guinea pig striatum 5-hydroxytryptamine 4 receptor
Drug Central 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N None
DB00604 931 39 None -4 25 Guinea pig 8.1 pKi = 8.1 Binding
Inhibition of [3H]GR-113808 binding to guinea pig striatum 5-hydroxytryptamine 4 receptorInhibition of [3H]GR-113808 binding to guinea pig striatum 5-hydroxytryptamine 4 receptor
Drug Central 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N None
5 139 66 3H-5HT -117 54 Rat 8.1 pKi = 8.1 Binding
NoneNone
PDSP KiDatabase 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 None
5202 139 66 3H-5HT -117 54 Rat 8.1 pKi = 8.1 Binding
NoneNone
PDSP KiDatabase 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 None
CHEMBL39 139 66 3H-5HT -117 54 Rat 8.1 pKi = 8.1 Binding
NoneNone
PDSP KiDatabase 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 None
DB08839 139 66 3H-5HT -117 54 Rat 8.1 pKi = 8.1 Binding
NoneNone
PDSP KiDatabase 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 None
258 3511 25 3H-GR-113808 1 8 Guinea pig 8.1 pKi = 8.1 Binding
NoneNone
PDSP KiDatabase 300 7 1 5 2.4 CCN(CCOC(=O)c1cc(Cl)c(cc1OC)N)CC None
5191 3511 25 3H-GR-113808 1 8 Guinea pig 8.1 pKi = 8.1 Binding
NoneNone
PDSP KiDatabase 300 7 1 5 2.4 CCN(CCOC(=O)c1cc(Cl)c(cc1OC)N)CC None
CHEMBL287045 3511 25 3H-GR-113808 1 8 Guinea pig 8.1 pKi = 8.1 Binding
NoneNone
PDSP KiDatabase 300 7 1 5 2.4 CCN(CCOC(=O)c1cc(Cl)c(cc1OC)N)CC None
5 139 66 3H-GR-113808 -190 54 Guinea pig 7.1 pKi = 7.1 Binding
NoneNone
PDSP KiDatabase 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 None
5 139 66 3H-GR-113808 -154 54 Mouse 7.1 pKi = 7.1 Binding
NoneNone
PDSP KiDatabase 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 None
5202 139 66 3H-GR-113808 -190 54 Guinea pig 7.1 pKi = 7.1 Binding
NoneNone
PDSP KiDatabase 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 None
5202 139 66 3H-GR-113808 -154 54 Mouse 7.1 pKi = 7.1 Binding
NoneNone
PDSP KiDatabase 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 None
CHEMBL39 139 66 3H-GR-113808 -190 54 Guinea pig 7.1 pKi = 7.1 Binding
NoneNone
PDSP KiDatabase 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 None
CHEMBL39 139 66 3H-GR-113808 -154 54 Mouse 7.1 pKi = 7.1 Binding
NoneNone
PDSP KiDatabase 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 None
DB08839 139 66 3H-GR-113808 -190 54 Guinea pig 7.1 pKi = 7.1 Binding
NoneNone
PDSP KiDatabase 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 None
DB08839 139 66 3H-GR-113808 -154 54 Mouse 7.1 pKi = 7.1 Binding
NoneNone
PDSP KiDatabase 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 None
240 931 39 3H-GR-113808 -8 25 Rat 7.1 pKi = 7.1 Binding
NoneNone
PDSP KiDatabase 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N None
2769 931 39 3H-GR-113808 -8 25 Rat 7.1 pKi = 7.1 Binding
NoneNone
PDSP KiDatabase 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N None
44279790 931 39 3H-GR-113808 -8 25 Rat 7.1 pKi = 7.1 Binding
NoneNone
PDSP KiDatabase 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N None
660 931 39 3H-GR-113808 -8 25 Rat 7.1 pKi = 7.1 Binding
NoneNone
PDSP KiDatabase 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N None
CHEMBL1729 931 39 3H-GR-113808 -8 25 Rat 7.1 pKi = 7.1 Binding
NoneNone
PDSP KiDatabase 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N None
CHEMBL560739 931 39 3H-GR-113808 -8 25 Rat 7.1 pKi = 7.1 Binding
NoneNone
PDSP KiDatabase 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N None
DB00604 931 39 3H-GR-113808 -8 25 Rat 7.1 pKi = 7.1 Binding
NoneNone
PDSP KiDatabase 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N None
None 214237 0 3H-5HT -2 6 Rat 7.1 pKi = 7.1 Binding
NoneNone
PDSP KiDatabase 367 2 1 6 2.4 CN1C2CCC1CC(C2)OC(=O)N3C4=C(C=CC(=C4)OC)NC3=O.Cl None
108182 4068 18 3H-GR-113808 -1 16 Rat 6.1 pKi = 6.1 Binding
NoneNone
PDSP KiDatabase 309 3 2 4 1.8 COc1cc(N)c(cc1C(=O)NC1CN2CCC1CC2)Cl None
108182 4068 18 3H-RS 57639 -1 16 Rat 6.1 pKi = 6.1 Binding
NoneNone
PDSP KiDatabase 309 3 2 4 1.8 COc1cc(N)c(cc1C(=O)NC1CN2CCC1CC2)Cl None
245 4068 18 3H-GR-113808 -1 16 Rat 6.1 pKi = 6.1 Binding
NoneNone
PDSP KiDatabase 309 3 2 4 1.8 COc1cc(N)c(cc1C(=O)NC1CN2CCC1CC2)Cl None
245 4068 18 3H-RS 57639 -1 16 Rat 6.1 pKi = 6.1 Binding
NoneNone
PDSP KiDatabase 309 3 2 4 1.8 COc1cc(N)c(cc1C(=O)NC1CN2CCC1CC2)Cl None
CHEMBL18041 4068 18 3H-GR-113808 -1 16 Rat 6.1 pKi = 6.1 Binding
NoneNone
PDSP KiDatabase 309 3 2 4 1.8 COc1cc(N)c(cc1C(=O)NC1CN2CCC1CC2)Cl None
CHEMBL18041 4068 18 3H-RS 57639 -1 16 Rat 6.1 pKi = 6.1 Binding
NoneNone
PDSP KiDatabase 309 3 2 4 1.8 COc1cc(N)c(cc1C(=O)NC1CN2CCC1CC2)Cl None
240 931 39 None -8 25 Rat 8.1 pKi = 8.1 Binding
NoneNone
Drug Central 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N None
2769 931 39 None -8 25 Rat 8.1 pKi = 8.1 Binding
NoneNone
Drug Central 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N None
44279790 931 39 None -8 25 Rat 8.1 pKi = 8.1 Binding
NoneNone
Drug Central 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N None
660 931 39 None -8 25 Rat 8.1 pKi = 8.1 Binding
NoneNone
Drug Central 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N None
CHEMBL1729 931 39 None -8 25 Rat 8.1 pKi = 8.1 Binding
NoneNone
Drug Central 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N None
CHEMBL560739 931 39 None -8 25 Rat 8.1 pKi = 8.1 Binding
NoneNone
Drug Central 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N None
DB00604 931 39 None -8 25 Rat 8.1 pKi = 8.1 Binding
NoneNone
Drug Central 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N None
135526515 216000 0 None -1 2 Human 8.1 pKi = 8.1 Binding
Binding affinity at 5HT4 receptorBinding affinity at 5HT4 receptor
Drug Central 301 7 4 3 2.8 CCCCCNC(=N)NN=CC1=CNC2=C1C=C(OC)C=C2 None
243 3153 85 None 12 34 Human 8.1 pKi = 8.1 Binding
Binding affinity at 5HT4 receptorBinding affinity at 5HT4 receptor
Drug Central 367 6 2 5 2.1 COCCCN1CCC(CC1)NC(=O)c1cc(Cl)c(c2c1OCC2)N None
3052762 3153 85 None 12 34 Human 8.1 pKi = 8.1 Binding
Binding affinity at 5HT4 receptorBinding affinity at 5HT4 receptor
Drug Central 367 6 2 5 2.1 COCCCN1CCC(CC1)NC(=O)c1cc(Cl)c(c2c1OCC2)N None
3502 3153 85 None 12 34 Human 8.1 pKi = 8.1 Binding
Binding affinity at 5HT4 receptorBinding affinity at 5HT4 receptor
Drug Central 367 6 2 5 2.1 COCCCN1CCC(CC1)NC(=O)c1cc(Cl)c(c2c1OCC2)N None
CHEMBL117287 3153 85 None 12 34 Human 8.1 pKi = 8.1 Binding
Binding affinity at 5HT4 receptorBinding affinity at 5HT4 receptor
Drug Central 367 6 2 5 2.1 COCCCN1CCC(CC1)NC(=O)c1cc(Cl)c(c2c1OCC2)N None
DB06480 3153 85 None 12 34 Human 8.1 pKi = 8.1 Binding
Binding affinity at 5HT4 receptorBinding affinity at 5HT4 receptor
Drug Central 367 6 2 5 2.1 COCCCN1CCC(CC1)NC(=O)c1cc(Cl)c(c2c1OCC2)N None
108182 4068 18 3H-GR-113808 -1 16 Rat 6.1 pKi = 6.1 Binding
NoneNone
PDSP KiDatabase 309 3 2 4 1.8 COc1cc(N)c(cc1C(=O)NC1CN2CCC1CC2)Cl None
245 4068 18 3H-GR-113808 -1 16 Rat 6.1 pKi = 6.1 Binding
NoneNone
PDSP KiDatabase 309 3 2 4 1.8 COc1cc(N)c(cc1C(=O)NC1CN2CCC1CC2)Cl None
CHEMBL18041 4068 18 3H-GR-113808 -1 16 Rat 6.1 pKi = 6.1 Binding
NoneNone
PDSP KiDatabase 309 3 2 4 1.8 COc1cc(N)c(cc1C(=O)NC1CN2CCC1CC2)Cl None
57174031 214163 0 3H-GR-113808 -8 19 Mouse 7.1 pKi = 7.1 Binding
NoneNone
PDSP KiDatabase 284 2 1 3 3.0 CN1C2CCC1CC(C2)OC(=O)C3=CNC4=CC=CC=C43 None
1782 2482 81 3H-GR-113808 -25 22 Mouse 6.1 pKi = 6.1 Binding
NoneNone
PDSP KiDatabase 299 7 2 4 2.0 CCN(CCNC(=O)c1cc(Cl)c(cc1OC)N)CC None
241 2482 81 3H-GR-113808 -25 22 Mouse 6.1 pKi = 6.1 Binding
NoneNone
PDSP KiDatabase 299 7 2 4 2.0 CCN(CCNC(=O)c1cc(Cl)c(cc1OC)N)CC None
4168 2482 81 3H-GR-113808 -25 22 Mouse 6.1 pKi = 6.1 Binding
NoneNone
PDSP KiDatabase 299 7 2 4 2.0 CCN(CCNC(=O)c1cc(Cl)c(cc1OC)N)CC None
CHEMBL86 2482 81 3H-GR-113808 -25 22 Mouse 6.1 pKi = 6.1 Binding
NoneNone
PDSP KiDatabase 299 7 2 4 2.0 CCN(CCNC(=O)c1cc(Cl)c(cc1OC)N)CC None
DB01233 2482 81 3H-GR-113808 -25 22 Mouse 6.1 pKi = 6.1 Binding
NoneNone
PDSP KiDatabase 299 7 2 4 2.0 CCN(CCNC(=O)c1cc(Cl)c(cc1OC)N)CC None
1809 134 28 3H-GR-113808 -46773 36 Rat 5.0 pKi = 5.0 Binding
NoneNone
PDSP KiDatabase 203 3 3 2 0.8 NCCc1c[nH]c2c1cc(cc2)C(=O)N None
4 134 28 3H-GR-113808 -46773 36 Rat 5.0 pKi = 5.0 Binding
NoneNone
PDSP KiDatabase 203 3 3 2 0.8 NCCc1c[nH]c2c1cc(cc2)C(=O)N None
CHEMBL18840 134 28 3H-GR-113808 -46773 36 Rat 5.0 pKi = 5.0 Binding
NoneNone
PDSP KiDatabase 203 3 3 2 0.8 NCCc1c[nH]c2c1cc(cc2)C(=O)N None
3035240 214200 0 3H-GR-113808 -1 5 Mouse 7.0 pKi = 7.0 Binding
NoneNone
PDSP KiDatabase 359 3 2 4 2.6 COC1=CC(=C(C=C1C(=O)NC2CCN3CCCC2C3)Cl)N.Cl None
1809 134 28 3H-GR-113808 -109647 36 Mouse 5.0 pKi = 5.0 Binding
NoneNone
PDSP KiDatabase 203 3 3 2 0.8 NCCc1c[nH]c2c1cc(cc2)C(=O)N None
4 134 28 3H-GR-113808 -109647 36 Mouse 5.0 pKi = 5.0 Binding
NoneNone
PDSP KiDatabase 203 3 3 2 0.8 NCCc1c[nH]c2c1cc(cc2)C(=O)N None
CHEMBL18840 134 28 3H-GR-113808 -109647 36 Mouse 5.0 pKi = 5.0 Binding
NoneNone
PDSP KiDatabase 203 3 3 2 0.8 NCCc1c[nH]c2c1cc(cc2)C(=O)N None
57174031 214163 0 3H-ZACOPRIDE -33 19 Rat 6.0 pKi = 6 Binding
NoneNone
PDSP KiDatabase 284 2 1 3 3.0 CN1C2CCC1CC(C2)OC(=O)C3=CNC4=CC=CC=C43 None
53354764 3015 30 None 1 2 Human 9.8 pKi = 9.8 Binding
Measured at the 5-HT<sub>4d</sub> receptor.Measured at the 5-HT<sub>4d</sub> receptor.
Guide to Pharmacology 432 7 1 8 2.6 OC1(CCOCC1)CN1CCC(CC1)COc1noc2c1c(ccc2)O[C@H]1COCC1 22974325
9059 3015 30 None 1 2 Human 9.8 pKi = 9.8 Binding
Measured at the 5-HT<sub>4d</sub> receptor.Measured at the 5-HT<sub>4d</sub> receptor.
Guide to Pharmacology 432 7 1 8 2.6 OC1(CCOCC1)CN1CCC(CC1)COc1noc2c1c(ccc2)O[C@H]1COCC1 22974325
CHEMBL2152922 3015 30 None 1 2 Human 9.8 pKi = 9.8 Binding
Measured at the 5-HT<sub>4d</sub> receptor.Measured at the 5-HT<sub>4d</sub> receptor.
Guide to Pharmacology 432 7 1 8 2.6 OC1(CCOCC1)CN1CCC(CC1)COc1noc2c1c(ccc2)O[C@H]1COCC1 22974325
DB12675 3015 30 None 1 2 Human 9.8 pKi = 9.8 Binding
Measured at the 5-HT<sub>4d</sub> receptor.Measured at the 5-HT<sub>4d</sub> receptor.
Guide to Pharmacology 432 7 1 8 2.6 OC1(CCOCC1)CN1CCC(CC1)COc1noc2c1c(ccc2)O[C@H]1COCC1 22974325
121881 3434 21 None -2 15 Human 10.1 pKi = 10.1 Binding
UnclassifiedUnclassified
Guide to Pharmacology 382 6 1 6 3.4 CCCCN1CCC(CC1)COC(=O)c1cc(Cl)c(c2c1OCCO2)N 10646498
121881 3434 21 None -2 15 Human 10.1 pKi = 10.1 Binding
UnclassifiedUnclassified
Guide to Pharmacology 382 6 1 6 3.4 CCCCN1CCC(CC1)COC(=O)c1cc(Cl)c(c2c1OCCO2)N 10683202
121881 3434 21 None -2 15 Human 10.1 pKi = 10.1 Binding
UnclassifiedUnclassified
Guide to Pharmacology 382 6 1 6 3.4 CCCCN1CCC(CC1)COC(=O)c1cc(Cl)c(c2c1OCCO2)N 11030734
121881 3434 21 None -2 15 Human 10.1 pKi = 10.1 Binding
UnclassifiedUnclassified
Guide to Pharmacology 382 6 1 6 3.4 CCCCN1CCC(CC1)COC(=O)c1cc(Cl)c(c2c1OCCO2)N 9349523
256 3434 21 None -2 15 Human 10.1 pKi = 10.1 Binding
UnclassifiedUnclassified
Guide to Pharmacology 382 6 1 6 3.4 CCCCN1CCC(CC1)COC(=O)c1cc(Cl)c(c2c1OCCO2)N 10646498
256 3434 21 None -2 15 Human 10.1 pKi = 10.1 Binding
UnclassifiedUnclassified
Guide to Pharmacology 382 6 1 6 3.4 CCCCN1CCC(CC1)COC(=O)c1cc(Cl)c(c2c1OCCO2)N 10683202
256 3434 21 None -2 15 Human 10.1 pKi = 10.1 Binding
UnclassifiedUnclassified
Guide to Pharmacology 382 6 1 6 3.4 CCCCN1CCC(CC1)COC(=O)c1cc(Cl)c(c2c1OCCO2)N 11030734
256 3434 21 None -2 15 Human 10.1 pKi = 10.1 Binding
UnclassifiedUnclassified
Guide to Pharmacology 382 6 1 6 3.4 CCCCN1CCC(CC1)COC(=O)c1cc(Cl)c(c2c1OCCO2)N 9349523
CHEMBL68131 3434 21 None -2 15 Human 10.1 pKi = 10.1 Binding
UnclassifiedUnclassified
Guide to Pharmacology 382 6 1 6 3.4 CCCCN1CCC(CC1)COC(=O)c1cc(Cl)c(c2c1OCCO2)N 10646498
CHEMBL68131 3434 21 None -2 15 Human 10.1 pKi = 10.1 Binding
UnclassifiedUnclassified
Guide to Pharmacology 382 6 1 6 3.4 CCCCN1CCC(CC1)COC(=O)c1cc(Cl)c(c2c1OCCO2)N 10683202
CHEMBL68131 3434 21 None -2 15 Human 10.1 pKi = 10.1 Binding
UnclassifiedUnclassified
Guide to Pharmacology 382 6 1 6 3.4 CCCCN1CCC(CC1)COC(=O)c1cc(Cl)c(c2c1OCCO2)N 11030734
CHEMBL68131 3434 21 None -2 15 Human 10.1 pKi = 10.1 Binding
UnclassifiedUnclassified
Guide to Pharmacology 382 6 1 6 3.4 CCCCN1CCC(CC1)COC(=O)c1cc(Cl)c(c2c1OCCO2)N 9349523
250 3334 5 None 2 13 Human 10.5 pKi = 10.5 Binding
UnclassifiedUnclassified
Guide to Pharmacology 502 10 1 7 5.0 COc1cc(CCCN2CCC(CC2)CCC(=O)c2cc(Cl)c(c3c2OCCO3)N)ccc1OC 15351779
250 3334 5 None 2 13 Human 10.5 pKi = 10.5 Binding
UnclassifiedUnclassified
Guide to Pharmacology 502 10 1 7 5.0 COc1cc(CCCN2CCC(CC2)CCC(=O)c2cc(Cl)c(c3c2OCCO3)N)ccc1OC 9351641
5311416 3334 5 None 2 13 Human 10.5 pKi = 10.5 Binding
UnclassifiedUnclassified
Guide to Pharmacology 502 10 1 7 5.0 COc1cc(CCCN2CCC(CC2)CCC(=O)c2cc(Cl)c(c3c2OCCO3)N)ccc1OC 15351779
5311416 3334 5 None 2 13 Human 10.5 pKi = 10.5 Binding
UnclassifiedUnclassified
Guide to Pharmacology 502 10 1 7 5.0 COc1cc(CCCN2CCC(CC2)CCC(=O)c2cc(Cl)c(c3c2OCCO3)N)ccc1OC 9351641
CHEMBL69733 3334 5 None 2 13 Human 10.5 pKi = 10.5 Binding
UnclassifiedUnclassified
Guide to Pharmacology 502 10 1 7 5.0 COc1cc(CCCN2CCC(CC2)CCC(=O)c2cc(Cl)c(c3c2OCCO3)N)ccc1OC 15351779
CHEMBL69733 3334 5 None 2 13 Human 10.5 pKi = 10.5 Binding
UnclassifiedUnclassified
Guide to Pharmacology 502 10 1 7 5.0 COc1cc(CCCN2CCC(CC2)CCC(=O)c2cc(Cl)c(c3c2OCCO3)N)ccc1OC 9351641
1782 2482 81 None -25 22 Mouse 6.0 pKi = 6 Binding
UnclassifiedUnclassified
Guide to Pharmacology 299 7 2 4 2.0 CCN(CCNC(=O)c1cc(Cl)c(cc1OC)N)CC 8946946
241 2482 81 None -25 22 Mouse 6.0 pKi = 6 Binding
UnclassifiedUnclassified
Guide to Pharmacology 299 7 2 4 2.0 CCN(CCNC(=O)c1cc(Cl)c(cc1OC)N)CC 8946946
4168 2482 81 None -25 22 Mouse 6.0 pKi = 6 Binding
UnclassifiedUnclassified
Guide to Pharmacology 299 7 2 4 2.0 CCN(CCNC(=O)c1cc(Cl)c(cc1OC)N)CC 8946946
CHEMBL86 2482 81 None -25 22 Mouse 6.0 pKi = 6 Binding
UnclassifiedUnclassified
Guide to Pharmacology 299 7 2 4 2.0 CCN(CCNC(=O)c1cc(Cl)c(cc1OC)N)CC 8946946
DB01233 2482 81 None -25 22 Mouse 6.0 pKi = 6 Binding
UnclassifiedUnclassified
Guide to Pharmacology 299 7 2 4 2.0 CCN(CCNC(=O)c1cc(Cl)c(cc1OC)N)CC 8946946
240 931 39 None -11 25 Human 6.9 pKi = 6.9 Binding
UnclassifiedUnclassified
Guide to Pharmacology 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N 10646498
240 931 39 None -11 25 Human 6.9 pKi = 6.9 Binding
UnclassifiedUnclassified
Guide to Pharmacology 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N 10683202
240 931 39 None -11 25 Human 6.9 pKi = 6.9 Binding
UnclassifiedUnclassified
Guide to Pharmacology 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N 11030734
240 931 39 None -11 25 Human 6.9 pKi = 6.9 Binding
UnclassifiedUnclassified
Guide to Pharmacology 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N 11218067
240 931 39 None -11 25 Human 6.9 pKi = 6.9 Binding
UnclassifiedUnclassified
Guide to Pharmacology 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N 7796807
240 931 39 None -11 25 Human 6.9 pKi = 6.9 Binding
UnclassifiedUnclassified
Guide to Pharmacology 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N 9349523
2769 931 39 None -11 25 Human 6.9 pKi = 6.9 Binding
UnclassifiedUnclassified
Guide to Pharmacology 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N 10646498
2769 931 39 None -11 25 Human 6.9 pKi = 6.9 Binding
UnclassifiedUnclassified
Guide to Pharmacology 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N 10683202
2769 931 39 None -11 25 Human 6.9 pKi = 6.9 Binding
UnclassifiedUnclassified
Guide to Pharmacology 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N 11030734
2769 931 39 None -11 25 Human 6.9 pKi = 6.9 Binding
UnclassifiedUnclassified
Guide to Pharmacology 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N 11218067
2769 931 39 None -11 25 Human 6.9 pKi = 6.9 Binding
UnclassifiedUnclassified
Guide to Pharmacology 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N 7796807
2769 931 39 None -11 25 Human 6.9 pKi = 6.9 Binding
UnclassifiedUnclassified
Guide to Pharmacology 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N 9349523
44279790 931 39 None -11 25 Human 6.9 pKi = 6.9 Binding
UnclassifiedUnclassified
Guide to Pharmacology 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N 10646498
44279790 931 39 None -11 25 Human 6.9 pKi = 6.9 Binding
UnclassifiedUnclassified
Guide to Pharmacology 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N 10683202
44279790 931 39 None -11 25 Human 6.9 pKi = 6.9 Binding
UnclassifiedUnclassified
Guide to Pharmacology 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N 11030734
44279790 931 39 None -11 25 Human 6.9 pKi = 6.9 Binding
UnclassifiedUnclassified
Guide to Pharmacology 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N 11218067
44279790 931 39 None -11 25 Human 6.9 pKi = 6.9 Binding
UnclassifiedUnclassified
Guide to Pharmacology 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N 7796807
44279790 931 39 None -11 25 Human 6.9 pKi = 6.9 Binding
UnclassifiedUnclassified
Guide to Pharmacology 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N 9349523
660 931 39 None -11 25 Human 6.9 pKi = 6.9 Binding
UnclassifiedUnclassified
Guide to Pharmacology 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N 10646498
660 931 39 None -11 25 Human 6.9 pKi = 6.9 Binding
UnclassifiedUnclassified
Guide to Pharmacology 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N 10683202
660 931 39 None -11 25 Human 6.9 pKi = 6.9 Binding
UnclassifiedUnclassified
Guide to Pharmacology 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N 11030734
660 931 39 None -11 25 Human 6.9 pKi = 6.9 Binding
UnclassifiedUnclassified
Guide to Pharmacology 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N 11218067
660 931 39 None -11 25 Human 6.9 pKi = 6.9 Binding
UnclassifiedUnclassified
Guide to Pharmacology 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N 7796807
660 931 39 None -11 25 Human 6.9 pKi = 6.9 Binding
UnclassifiedUnclassified
Guide to Pharmacology 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N 9349523
CHEMBL1729 931 39 None -11 25 Human 6.9 pKi = 6.9 Binding
UnclassifiedUnclassified
Guide to Pharmacology 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N 10646498
CHEMBL1729 931 39 None -11 25 Human 6.9 pKi = 6.9 Binding
UnclassifiedUnclassified
Guide to Pharmacology 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N 10683202
CHEMBL1729 931 39 None -11 25 Human 6.9 pKi = 6.9 Binding
UnclassifiedUnclassified
Guide to Pharmacology 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N 11030734
CHEMBL1729 931 39 None -11 25 Human 6.9 pKi = 6.9 Binding
UnclassifiedUnclassified
Guide to Pharmacology 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N 11218067
CHEMBL1729 931 39 None -11 25 Human 6.9 pKi = 6.9 Binding
UnclassifiedUnclassified
Guide to Pharmacology 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N 7796807
CHEMBL1729 931 39 None -11 25 Human 6.9 pKi = 6.9 Binding
UnclassifiedUnclassified
Guide to Pharmacology 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N 9349523
CHEMBL560739 931 39 None -11 25 Human 6.9 pKi = 6.9 Binding
UnclassifiedUnclassified
Guide to Pharmacology 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N 10646498
CHEMBL560739 931 39 None -11 25 Human 6.9 pKi = 6.9 Binding
UnclassifiedUnclassified
Guide to Pharmacology 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N 10683202
CHEMBL560739 931 39 None -11 25 Human 6.9 pKi = 6.9 Binding
UnclassifiedUnclassified
Guide to Pharmacology 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N 11030734
CHEMBL560739 931 39 None -11 25 Human 6.9 pKi = 6.9 Binding
UnclassifiedUnclassified
Guide to Pharmacology 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N 11218067
CHEMBL560739 931 39 None -11 25 Human 6.9 pKi = 6.9 Binding
UnclassifiedUnclassified
Guide to Pharmacology 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N 7796807
CHEMBL560739 931 39 None -11 25 Human 6.9 pKi = 6.9 Binding
UnclassifiedUnclassified
Guide to Pharmacology 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N 9349523
DB00604 931 39 None -11 25 Human 6.9 pKi = 6.9 Binding
UnclassifiedUnclassified
Guide to Pharmacology 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N 10646498
DB00604 931 39 None -11 25 Human 6.9 pKi = 6.9 Binding
UnclassifiedUnclassified
Guide to Pharmacology 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N 10683202
DB00604 931 39 None -11 25 Human 6.9 pKi = 6.9 Binding
UnclassifiedUnclassified
Guide to Pharmacology 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N 11030734
DB00604 931 39 None -11 25 Human 6.9 pKi = 6.9 Binding
UnclassifiedUnclassified
Guide to Pharmacology 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N 11218067
DB00604 931 39 None -11 25 Human 6.9 pKi = 6.9 Binding
UnclassifiedUnclassified
Guide to Pharmacology 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N 7796807
DB00604 931 39 None -11 25 Human 6.9 pKi = 6.9 Binding
UnclassifiedUnclassified
Guide to Pharmacology 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N 9349523
234 654 0 None -1 3 Human 7.3 pKi = 7.3 Binding
UnclassifiedUnclassified
Guide to Pharmacology 342 2 1 5 2.6 CN1[C@@H]2CC[C@H]1CC(C2)NC(=O)n1c(=O)n(c2c1cccc2)C(C)C 9351641
5311029 654 0 None -1 3 Human 7.3 pKi = 7.3 Binding
UnclassifiedUnclassified
Guide to Pharmacology 342 2 1 5 2.6 CN1[C@@H]2CC[C@H]1CC(C2)NC(=O)n1c(=O)n(c2c1cccc2)C(C)C 9351641
11842633 3918 17 None - 1 Human 7.7 pKi = 7.7 Binding
UnclassifiedUnclassified
Guide to Pharmacology 504 8 2 7 1.6 O[C@@H](CN(S(=O)(=O)C)C)CN1[C@@H]2CC[C@H]1CC(C2)NC(=O)c1cc2ccccc2n(c1=O)C(C)C 18415081
11842633 3918 17 None - 1 Human 7.7 pKi = 7.7 Binding
UnclassifiedUnclassified
Guide to Pharmacology 504 8 2 7 1.6 O[C@@H](CN(S(=O)(=O)C)C)CN1[C@@H]2CC[C@H]1CC(C2)NC(=O)c1cc2ccccc2n(c1=O)C(C)C 22959244
8425 3918 17 None - 1 Human 7.7 pKi = 7.7 Binding
UnclassifiedUnclassified
Guide to Pharmacology 504 8 2 7 1.6 O[C@@H](CN(S(=O)(=O)C)C)CN1[C@@H]2CC[C@H]1CC(C2)NC(=O)c1cc2ccccc2n(c1=O)C(C)C 18415081
8425 3918 17 None - 1 Human 7.7 pKi = 7.7 Binding
UnclassifiedUnclassified
Guide to Pharmacology 504 8 2 7 1.6 O[C@@H](CN(S(=O)(=O)C)C)CN1[C@@H]2CC[C@H]1CC(C2)NC(=O)c1cc2ccccc2n(c1=O)C(C)C 22959244
CHEMBL2087337 3918 17 None - 1 Human 7.7 pKi = 7.7 Binding
UnclassifiedUnclassified
Guide to Pharmacology 504 8 2 7 1.6 O[C@@H](CN(S(=O)(=O)C)C)CN1[C@@H]2CC[C@H]1CC(C2)NC(=O)c1cc2ccccc2n(c1=O)C(C)C 18415081
CHEMBL2087337 3918 17 None - 1 Human 7.7 pKi = 7.7 Binding
UnclassifiedUnclassified
Guide to Pharmacology 504 8 2 7 1.6 O[C@@H](CN(S(=O)(=O)C)C)CN1[C@@H]2CC[C@H]1CC(C2)NC(=O)c1cc2ccccc2n(c1=O)C(C)C 22959244
10584 1435 0 None 1 2 Guinea pig 8.2 pKi = 8.2 Binding
UnclassifiedUnclassified
Guide to Pharmacology 392 7 1 4 5.2 COc1cc(N)c(cc1C(=O)CCC1CCN(CC1)CC1CCCCC1)Cl 25157130
86582973 1435 0 None 1 2 Guinea pig 8.2 pKi = 8.2 Binding
UnclassifiedUnclassified
Guide to Pharmacology 392 7 1 4 5.2 COc1cc(N)c(cc1C(=O)CCC1CCN(CC1)CC1CCCCC1)Cl 25157130
CHEMBL3417009 1435 0 None 1 2 Guinea pig 8.2 pKi = 8.2 Binding
UnclassifiedUnclassified
Guide to Pharmacology 392 7 1 4 5.2 COc1cc(N)c(cc1C(=O)CCC1CCN(CC1)CC1CCCCC1)Cl 25157130
45275554 3260 0 None 6 3 Human 8.3 pKi = 8.3 Binding
UnclassifiedUnclassified
Guide to Pharmacology 492 9 3 6 3.7 COc1cc(N)c(cc1C(=O)NCC1CCN(CC1)CC[C@@H](c1ccc(cc1)F)OC(=O)N)Cl 25316608
8427 3260 0 None 6 3 Human 8.3 pKi = 8.3 Binding
UnclassifiedUnclassified
Guide to Pharmacology 492 9 3 6 3.7 COc1cc(N)c(cc1C(=O)NCC1CCN(CC1)CC[C@@H](c1ccc(cc1)F)OC(=O)N)Cl 25316608
CHEMBL3544975 3260 0 None 6 3 Human 8.3 pKi = 8.3 Binding
UnclassifiedUnclassified
Guide to Pharmacology 492 9 3 6 3.7 COc1cc(N)c(cc1C(=O)NCC1CCN(CC1)CC[C@@H](c1ccc(cc1)F)OC(=O)N)Cl 25316608
DB12798 3260 0 None 6 3 Human 8.3 pKi = 8.3 Binding
UnclassifiedUnclassified
Guide to Pharmacology 492 9 3 6 3.7 COc1cc(N)c(cc1C(=O)NCC1CCN(CC1)CC[C@@H](c1ccc(cc1)F)OC(=O)N)Cl 25316608
235 2527 36 None -4 3 Human 8.5 pKi = 8.5 Binding
UnclassifiedUnclassified
Guide to Pharmacology 312 5 1 5 2.6 COc1cc(N)c(cc1C(=O)OCCN1CCCCC1)Cl 10683202
235 2527 36 None -4 3 Human 8.5 pKi = 8.5 Binding
UnclassifiedUnclassified
Guide to Pharmacology 312 5 1 5 2.6 COc1cc(N)c(cc1C(=O)OCCN1CCCCC1)Cl 10821780
235 2527 36 None -4 3 Human 8.5 pKi = 8.5 Binding
UnclassifiedUnclassified
Guide to Pharmacology 312 5 1 5 2.6 COc1cc(N)c(cc1C(=O)OCCN1CCCCC1)Cl 11030734
235 2527 36 None -4 3 Human 8.5 pKi = 8.5 Binding
UnclassifiedUnclassified
Guide to Pharmacology 312 5 1 5 2.6 COc1cc(N)c(cc1C(=O)OCCN1CCCCC1)Cl 12801225
235 2527 36 None -4 3 Human 8.5 pKi = 8.5 Binding
UnclassifiedUnclassified
Guide to Pharmacology 312 5 1 5 2.6 COc1cc(N)c(cc1C(=O)OCCN1CCCCC1)Cl 9603189
5311299 2527 36 None -4 3 Human 8.5 pKi = 8.5 Binding
UnclassifiedUnclassified
Guide to Pharmacology 312 5 1 5 2.6 COc1cc(N)c(cc1C(=O)OCCN1CCCCC1)Cl 10683202
5311299 2527 36 None -4 3 Human 8.5 pKi = 8.5 Binding
UnclassifiedUnclassified
Guide to Pharmacology 312 5 1 5 2.6 COc1cc(N)c(cc1C(=O)OCCN1CCCCC1)Cl 10821780
5311299 2527 36 None -4 3 Human 8.5 pKi = 8.5 Binding
UnclassifiedUnclassified
Guide to Pharmacology 312 5 1 5 2.6 COc1cc(N)c(cc1C(=O)OCCN1CCCCC1)Cl 11030734
5311299 2527 36 None -4 3 Human 8.5 pKi = 8.5 Binding
UnclassifiedUnclassified
Guide to Pharmacology 312 5 1 5 2.6 COc1cc(N)c(cc1C(=O)OCCN1CCCCC1)Cl 12801225
5311299 2527 36 None -4 3 Human 8.5 pKi = 8.5 Binding
UnclassifiedUnclassified
Guide to Pharmacology 312 5 1 5 2.6 COc1cc(N)c(cc1C(=O)OCCN1CCCCC1)Cl 9603189
CHEMBL286136 2527 36 None -4 3 Human 8.5 pKi = 8.5 Binding
UnclassifiedUnclassified
Guide to Pharmacology 312 5 1 5 2.6 COc1cc(N)c(cc1C(=O)OCCN1CCCCC1)Cl 10683202
CHEMBL286136 2527 36 None -4 3 Human 8.5 pKi = 8.5 Binding
UnclassifiedUnclassified
Guide to Pharmacology 312 5 1 5 2.6 COc1cc(N)c(cc1C(=O)OCCN1CCCCC1)Cl 10821780
CHEMBL286136 2527 36 None -4 3 Human 8.5 pKi = 8.5 Binding
UnclassifiedUnclassified
Guide to Pharmacology 312 5 1 5 2.6 COc1cc(N)c(cc1C(=O)OCCN1CCCCC1)Cl 11030734
CHEMBL286136 2527 36 None -4 3 Human 8.5 pKi = 8.5 Binding
UnclassifiedUnclassified
Guide to Pharmacology 312 5 1 5 2.6 COc1cc(N)c(cc1C(=O)OCCN1CCCCC1)Cl 12801225
CHEMBL286136 2527 36 None -4 3 Human 8.5 pKi = 8.5 Binding
UnclassifiedUnclassified
Guide to Pharmacology 312 5 1 5 2.6 COc1cc(N)c(cc1C(=O)OCCN1CCCCC1)Cl 9603189
11961293 3710 13 None - 1 Human 9.4 pKi = 9.4 Binding
UnclassifiedUnclassified
Guide to Pharmacology 455 6 2 5 3.6 COC(=O)N1CCC(CC1)CN1CCC(CC1)CNC(=O)c1cccc2c1nc([nH]2)C(C)C 23756062
8426 3710 13 None - 1 Human 9.4 pKi = 9.4 Binding
UnclassifiedUnclassified
Guide to Pharmacology 455 6 2 5 3.6 COC(=O)N1CCC(CC1)CN1CCC(CC1)CNC(=O)c1cccc2c1nc([nH]2)C(C)C 23756062
CHEMBL2402904 3710 13 None - 1 Human 9.4 pKi = 9.4 Binding
UnclassifiedUnclassified
Guide to Pharmacology 455 6 2 5 3.6 COC(=O)N1CCC(CC1)CN1CCC(CC1)CNC(=O)c1cccc2c1nc([nH]2)C(C)C 23756062
DB12725 3710 13 None - 1 Human 9.4 pKi = 9.4 Binding
UnclassifiedUnclassified
Guide to Pharmacology 455 6 2 5 3.6 COC(=O)N1CCC(CC1)CN1CCC(CC1)CNC(=O)c1cccc2c1nc([nH]2)C(C)C 23756062
119376 1811 41 None -1 26 Human 9.8 pKi = 9.8 Binding
UnclassifiedUnclassified
Guide to Pharmacology 393 7 1 6 1.6 O=C(c1cn(c2c1cccc2)C)OCC1CCN(CC1)CCNS(=O)(=O)C 10646498
119376 1811 41 None -1 26 Human 9.8 pKi = 9.8 Binding
UnclassifiedUnclassified
Guide to Pharmacology 393 7 1 6 1.6 O=C(c1cn(c2c1cccc2)C)OCC1CCN(CC1)CCNS(=O)(=O)C 11030734
119376 1811 41 None -1 26 Human 9.8 pKi = 9.8 Binding
UnclassifiedUnclassified
Guide to Pharmacology 393 7 1 6 1.6 O=C(c1cn(c2c1cccc2)C)OCC1CCN(CC1)CCNS(=O)(=O)C 11218067
119376 1811 41 None -1 26 Human 9.8 pKi = 9.8 Binding
UnclassifiedUnclassified
Guide to Pharmacology 393 7 1 6 1.6 O=C(c1cn(c2c1cccc2)C)OCC1CCN(CC1)CCNS(=O)(=O)C 15351779
119376 1811 41 None -1 26 Human 9.8 pKi = 9.8 Binding
UnclassifiedUnclassified
Guide to Pharmacology 393 7 1 6 1.6 O=C(c1cn(c2c1cccc2)C)OCC1CCN(CC1)CCNS(=O)(=O)C 9349523
119376 1811 41 None -1 26 Human 9.8 pKi = 9.8 Binding
UnclassifiedUnclassified
Guide to Pharmacology 393 7 1 6 1.6 O=C(c1cn(c2c1cccc2)C)OCC1CCN(CC1)CCNS(=O)(=O)C 9351641
119376 1811 41 None -1 26 Human 9.8 pKi = 9.8 Binding
UnclassifiedUnclassified
Guide to Pharmacology 393 7 1 6 1.6 O=C(c1cn(c2c1cccc2)C)OCC1CCN(CC1)CCNS(=O)(=O)C 9603189
247 1811 41 None -1 26 Human 9.8 pKi = 9.8 Binding
UnclassifiedUnclassified
Guide to Pharmacology 393 7 1 6 1.6 O=C(c1cn(c2c1cccc2)C)OCC1CCN(CC1)CCNS(=O)(=O)C 10646498
247 1811 41 None -1 26 Human 9.8 pKi = 9.8 Binding
UnclassifiedUnclassified
Guide to Pharmacology 393 7 1 6 1.6 O=C(c1cn(c2c1cccc2)C)OCC1CCN(CC1)CCNS(=O)(=O)C 11030734
247 1811 41 None -1 26 Human 9.8 pKi = 9.8 Binding
UnclassifiedUnclassified
Guide to Pharmacology 393 7 1 6 1.6 O=C(c1cn(c2c1cccc2)C)OCC1CCN(CC1)CCNS(=O)(=O)C 11218067
247 1811 41 None -1 26 Human 9.8 pKi = 9.8 Binding
UnclassifiedUnclassified
Guide to Pharmacology 393 7 1 6 1.6 O=C(c1cn(c2c1cccc2)C)OCC1CCN(CC1)CCNS(=O)(=O)C 15351779
247 1811 41 None -1 26 Human 9.8 pKi = 9.8 Binding
UnclassifiedUnclassified
Guide to Pharmacology 393 7 1 6 1.6 O=C(c1cn(c2c1cccc2)C)OCC1CCN(CC1)CCNS(=O)(=O)C 9349523
247 1811 41 None -1 26 Human 9.8 pKi = 9.8 Binding
UnclassifiedUnclassified
Guide to Pharmacology 393 7 1 6 1.6 O=C(c1cn(c2c1cccc2)C)OCC1CCN(CC1)CCNS(=O)(=O)C 9351641
247 1811 41 None -1 26 Human 9.8 pKi = 9.8 Binding
UnclassifiedUnclassified
Guide to Pharmacology 393 7 1 6 1.6 O=C(c1cn(c2c1cccc2)C)OCC1CCN(CC1)CCNS(=O)(=O)C 9603189
CHEMBL33884 1811 41 None -1 26 Human 9.8 pKi = 9.8 Binding
UnclassifiedUnclassified
Guide to Pharmacology 393 7 1 6 1.6 O=C(c1cn(c2c1cccc2)C)OCC1CCN(CC1)CCNS(=O)(=O)C 10646498
CHEMBL33884 1811 41 None -1 26 Human 9.8 pKi = 9.8 Binding
UnclassifiedUnclassified
Guide to Pharmacology 393 7 1 6 1.6 O=C(c1cn(c2c1cccc2)C)OCC1CCN(CC1)CCNS(=O)(=O)C 11030734
CHEMBL33884 1811 41 None -1 26 Human 9.8 pKi = 9.8 Binding
UnclassifiedUnclassified
Guide to Pharmacology 393 7 1 6 1.6 O=C(c1cn(c2c1cccc2)C)OCC1CCN(CC1)CCNS(=O)(=O)C 11218067
CHEMBL33884 1811 41 None -1 26 Human 9.8 pKi = 9.8 Binding
UnclassifiedUnclassified
Guide to Pharmacology 393 7 1 6 1.6 O=C(c1cn(c2c1cccc2)C)OCC1CCN(CC1)CCNS(=O)(=O)C 15351779
CHEMBL33884 1811 41 None -1 26 Human 9.8 pKi = 9.8 Binding
UnclassifiedUnclassified
Guide to Pharmacology 393 7 1 6 1.6 O=C(c1cn(c2c1cccc2)C)OCC1CCN(CC1)CCNS(=O)(=O)C 9349523
CHEMBL33884 1811 41 None -1 26 Human 9.8 pKi = 9.8 Binding
UnclassifiedUnclassified
Guide to Pharmacology 393 7 1 6 1.6 O=C(c1cn(c2c1cccc2)C)OCC1CCN(CC1)CCNS(=O)(=O)C 9351641
CHEMBL33884 1811 41 None -1 26 Human 9.8 pKi = 9.8 Binding
UnclassifiedUnclassified
Guide to Pharmacology 393 7 1 6 1.6 O=C(c1cn(c2c1cccc2)C)OCC1CCN(CC1)CCNS(=O)(=O)C 9603189
257 3437 9 None -1 4 Human 10.2 pKi None 10.2 Binding
UnclassifiedUnclassified
Guide to Pharmacology 474 6 1 6 3.3 CCCCN1CCC(CC1)COC(=O)c1cc(I)c(c2c1OCCO2)N 11218067
5311423 3437 9 None -1 4 Human 10.2 pKi None 10.2 Binding
UnclassifiedUnclassified
Guide to Pharmacology 474 6 1 6 3.3 CCCCN1CCC(CC1)COC(=O)c1cc(I)c(c2c1OCCO2)N 11218067
CHEMBL114112 3437 9 None -1 4 Human 10.2 pKi None 10.2 Binding
UnclassifiedUnclassified
Guide to Pharmacology 474 6 1 6 3.3 CCCCN1CCC(CC1)COC(=O)c1cc(I)c(c2c1OCCO2)N 11218067
248 1812 0 None -2 2 Human 10.3 pKi None 10.3 Binding
UnclassifiedUnclassified
Guide to Pharmacology 427 8 2 6 1.7 COc1[nH]c2c(c1C(=O)OCC1CCN(CC1)CCNS(=O)(=O)C)cc(cc2)F 9349523
248 1812 0 None -2 2 Human 10.3 pKi None 10.3 Binding
UnclassifiedUnclassified
Guide to Pharmacology 427 8 2 6 1.7 COc1[nH]c2c(c1C(=O)OCC1CCN(CC1)CCNS(=O)(=O)C)cc(cc2)F 9351641
4284721 1812 0 None -2 2 Human 10.3 pKi None 10.3 Binding
UnclassifiedUnclassified
Guide to Pharmacology 427 8 2 6 1.7 COc1[nH]c2c(c1C(=O)OCC1CCN(CC1)CCNS(=O)(=O)C)cc(cc2)F 9349523
4284721 1812 0 None -2 2 Human 10.3 pKi None 10.3 Binding
UnclassifiedUnclassified
Guide to Pharmacology 427 8 2 6 1.7 COc1[nH]c2c(c1C(=O)OCC1CCN(CC1)CCNS(=O)(=O)C)cc(cc2)F 9351641
CHEMBL471233 1812 0 None -2 2 Human 10.3 pKi None 10.3 Binding
UnclassifiedUnclassified
Guide to Pharmacology 427 8 2 6 1.7 COc1[nH]c2c(c1C(=O)OCC1CCN(CC1)CCNS(=O)(=O)C)cc(cc2)F 9349523
CHEMBL471233 1812 0 None -2 2 Human 10.3 pKi None 10.3 Binding
UnclassifiedUnclassified
Guide to Pharmacology 427 8 2 6 1.7 COc1[nH]c2c(c1C(=O)OCC1CCN(CC1)CCNS(=O)(=O)C)cc(cc2)F 9351641
248 1812 0 None 2 2 Mouse 10.6 pKi None 10.6 Binding
UnclassifiedUnclassified
Guide to Pharmacology 427 8 2 6 1.7 COc1[nH]c2c(c1C(=O)OCC1CCN(CC1)CCNS(=O)(=O)C)cc(cc2)F 8946946
4284721 1812 0 None 2 2 Mouse 10.6 pKi None 10.6 Binding
UnclassifiedUnclassified
Guide to Pharmacology 427 8 2 6 1.7 COc1[nH]c2c(c1C(=O)OCC1CCN(CC1)CCNS(=O)(=O)C)cc(cc2)F 8946946
CHEMBL471233 1812 0 None 2 2 Mouse 10.6 pKi None 10.6 Binding
UnclassifiedUnclassified
Guide to Pharmacology 427 8 2 6 1.7 COc1[nH]c2c(c1C(=O)OCC1CCN(CC1)CCNS(=O)(=O)C)cc(cc2)F 8946946
108182 4068 18 None -2 16 Human 5.8 pKi None 5.8 Binding
UnclassifiedUnclassified
Guide to Pharmacology 309 3 2 4 1.8 COc1cc(N)c(cc1C(=O)NC1CN2CCC1CC2)Cl 7796807
108182 4068 18 None -2 16 Human 5.8 pKi None 5.8 Binding
UnclassifiedUnclassified
Guide to Pharmacology 309 3 2 4 1.8 COc1cc(N)c(cc1C(=O)NC1CN2CCC1CC2)Cl 9351641
108182 4068 18 None -2 16 Human 5.8 pKi None 5.8 Binding
UnclassifiedUnclassified
Guide to Pharmacology 309 3 2 4 1.8 COc1cc(N)c(cc1C(=O)NC1CN2CCC1CC2)Cl 9603189
245 4068 18 None -2 16 Human 5.8 pKi None 5.8 Binding
UnclassifiedUnclassified
Guide to Pharmacology 309 3 2 4 1.8 COc1cc(N)c(cc1C(=O)NC1CN2CCC1CC2)Cl 7796807
245 4068 18 None -2 16 Human 5.8 pKi None 5.8 Binding
UnclassifiedUnclassified
Guide to Pharmacology 309 3 2 4 1.8 COc1cc(N)c(cc1C(=O)NC1CN2CCC1CC2)Cl 9351641
245 4068 18 None -2 16 Human 5.8 pKi None 5.8 Binding
UnclassifiedUnclassified
Guide to Pharmacology 309 3 2 4 1.8 COc1cc(N)c(cc1C(=O)NC1CN2CCC1CC2)Cl 9603189
CHEMBL18041 4068 18 None -2 16 Human 5.8 pKi None 5.8 Binding
UnclassifiedUnclassified
Guide to Pharmacology 309 3 2 4 1.8 COc1cc(N)c(cc1C(=O)NC1CN2CCC1CC2)Cl 7796807
CHEMBL18041 4068 18 None -2 16 Human 5.8 pKi None 5.8 Binding
UnclassifiedUnclassified
Guide to Pharmacology 309 3 2 4 1.8 COc1cc(N)c(cc1C(=O)NC1CN2CCC1CC2)Cl 9351641
CHEMBL18041 4068 18 None -2 16 Human 5.8 pKi None 5.8 Binding
UnclassifiedUnclassified
Guide to Pharmacology 309 3 2 4 1.8 COc1cc(N)c(cc1C(=O)NC1CN2CCC1CC2)Cl 9603189
152 361 18 None -208 18 Human 5.8 pKi None 5.8 Binding
UnclassifiedUnclassified
Guide to Pharmacology 190 2 3 2 1.8 CC(Cc1c[nH]c2c1cc(O)cc2)N 15466450
152 361 18 None -208 18 Human 5.8 pKi None 5.8 Binding
UnclassifiedUnclassified
Guide to Pharmacology 190 2 3 2 1.8 CC(Cc1c[nH]c2c1cc(O)cc2)N 7796807
2107 361 18 None -208 18 Human 5.8 pKi None 5.8 Binding
UnclassifiedUnclassified
Guide to Pharmacology 190 2 3 2 1.8 CC(Cc1c[nH]c2c1cc(O)cc2)N 15466450
2107 361 18 None -208 18 Human 5.8 pKi None 5.8 Binding
UnclassifiedUnclassified
Guide to Pharmacology 190 2 3 2 1.8 CC(Cc1c[nH]c2c1cc(O)cc2)N 7796807
CHEMBL275854 361 18 None -208 18 Human 5.8 pKi None 5.8 Binding
UnclassifiedUnclassified
Guide to Pharmacology 190 2 3 2 1.8 CC(Cc1c[nH]c2c1cc(O)cc2)N 15466450
CHEMBL275854 361 18 None -208 18 Human 5.8 pKi None 5.8 Binding
UnclassifiedUnclassified
Guide to Pharmacology 190 2 3 2 1.8 CC(Cc1c[nH]c2c1cc(O)cc2)N 7796807
152 361 18 None -89 18 Rat 6.1 pKi None 6.1 Binding
UnclassifiedUnclassified
Guide to Pharmacology 190 2 3 2 1.8 CC(Cc1c[nH]c2c1cc(O)cc2)N 8813606
152 361 18 None -89 18 Rat 6.1 pKi None 6.1 Binding
UnclassifiedUnclassified
Guide to Pharmacology 190 2 3 2 1.8 CC(Cc1c[nH]c2c1cc(O)cc2)N 9225293
2107 361 18 None -89 18 Rat 6.1 pKi None 6.1 Binding
UnclassifiedUnclassified
Guide to Pharmacology 190 2 3 2 1.8 CC(Cc1c[nH]c2c1cc(O)cc2)N 8813606
2107 361 18 None -89 18 Rat 6.1 pKi None 6.1 Binding
UnclassifiedUnclassified
Guide to Pharmacology 190 2 3 2 1.8 CC(Cc1c[nH]c2c1cc(O)cc2)N 9225293
CHEMBL275854 361 18 None -89 18 Rat 6.1 pKi None 6.1 Binding
UnclassifiedUnclassified
Guide to Pharmacology 190 2 3 2 1.8 CC(Cc1c[nH]c2c1cc(O)cc2)N 8813606
CHEMBL275854 361 18 None -89 18 Rat 6.1 pKi None 6.1 Binding
UnclassifiedUnclassified
Guide to Pharmacology 190 2 3 2 1.8 CC(Cc1c[nH]c2c1cc(O)cc2)N 9225293
107 141 116 None -389 30 Human 6.2 pKi None 6.2 Binding
UnclassifiedUnclassified
Guide to Pharmacology 190 3 2 2 1.7 NCCc1c[nH]c2c1cc(OC)cc2 10646498
107 141 116 None -389 30 Human 6.2 pKi None 6.2 Binding
UnclassifiedUnclassified
Guide to Pharmacology 190 3 2 2 1.7 NCCc1c[nH]c2c1cc(OC)cc2 10683202
107 141 116 None -389 30 Human 6.2 pKi None 6.2 Binding
UnclassifiedUnclassified
Guide to Pharmacology 190 3 2 2 1.7 NCCc1c[nH]c2c1cc(OC)cc2 11030734
107 141 116 None -389 30 Human 6.2 pKi None 6.2 Binding
UnclassifiedUnclassified
Guide to Pharmacology 190 3 2 2 1.7 NCCc1c[nH]c2c1cc(OC)cc2 11218067
107 141 116 None -389 30 Human 6.2 pKi None 6.2 Binding
UnclassifiedUnclassified
Guide to Pharmacology 190 3 2 2 1.7 NCCc1c[nH]c2c1cc(OC)cc2 9349523
107 141 116 None -389 30 Human 6.2 pKi None 6.2 Binding
UnclassifiedUnclassified
Guide to Pharmacology 190 3 2 2 1.7 NCCc1c[nH]c2c1cc(OC)cc2 9603189
1833 141 116 None -389 30 Human 6.2 pKi None 6.2 Binding
UnclassifiedUnclassified
Guide to Pharmacology 190 3 2 2 1.7 NCCc1c[nH]c2c1cc(OC)cc2 10646498
1833 141 116 None -389 30 Human 6.2 pKi None 6.2 Binding
UnclassifiedUnclassified
Guide to Pharmacology 190 3 2 2 1.7 NCCc1c[nH]c2c1cc(OC)cc2 10683202
1833 141 116 None -389 30 Human 6.2 pKi None 6.2 Binding
UnclassifiedUnclassified
Guide to Pharmacology 190 3 2 2 1.7 NCCc1c[nH]c2c1cc(OC)cc2 11030734
1833 141 116 None -389 30 Human 6.2 pKi None 6.2 Binding
UnclassifiedUnclassified
Guide to Pharmacology 190 3 2 2 1.7 NCCc1c[nH]c2c1cc(OC)cc2 11218067
1833 141 116 None -389 30 Human 6.2 pKi None 6.2 Binding
UnclassifiedUnclassified
Guide to Pharmacology 190 3 2 2 1.7 NCCc1c[nH]c2c1cc(OC)cc2 9349523
1833 141 116 None -389 30 Human 6.2 pKi None 6.2 Binding
UnclassifiedUnclassified
Guide to Pharmacology 190 3 2 2 1.7 NCCc1c[nH]c2c1cc(OC)cc2 9603189
CHEMBL8165 141 116 None -389 30 Human 6.2 pKi None 6.2 Binding
UnclassifiedUnclassified
Guide to Pharmacology 190 3 2 2 1.7 NCCc1c[nH]c2c1cc(OC)cc2 10646498
CHEMBL8165 141 116 None -389 30 Human 6.2 pKi None 6.2 Binding
UnclassifiedUnclassified
Guide to Pharmacology 190 3 2 2 1.7 NCCc1c[nH]c2c1cc(OC)cc2 10683202
CHEMBL8165 141 116 None -389 30 Human 6.2 pKi None 6.2 Binding
UnclassifiedUnclassified
Guide to Pharmacology 190 3 2 2 1.7 NCCc1c[nH]c2c1cc(OC)cc2 11030734
CHEMBL8165 141 116 None -389 30 Human 6.2 pKi None 6.2 Binding
UnclassifiedUnclassified
Guide to Pharmacology 190 3 2 2 1.7 NCCc1c[nH]c2c1cc(OC)cc2 11218067
CHEMBL8165 141 116 None -389 30 Human 6.2 pKi None 6.2 Binding
UnclassifiedUnclassified
Guide to Pharmacology 190 3 2 2 1.7 NCCc1c[nH]c2c1cc(OC)cc2 9349523
CHEMBL8165 141 116 None -389 30 Human 6.2 pKi None 6.2 Binding
UnclassifiedUnclassified
Guide to Pharmacology 190 3 2 2 1.7 NCCc1c[nH]c2c1cc(OC)cc2 9603189
244 3262 0 None -5 3 Human 6.4 pKi None 6.4 Binding
UnclassifiedUnclassified
Guide to Pharmacology 323 3 2 4 2.1 COc1cc(N)c(cc1C(=O)N[C@H]1CCN2C[C@@H]1CCC2)Cl 10683202
244 3262 0 None -5 3 Human 6.4 pKi None 6.4 Binding
UnclassifiedUnclassified
Guide to Pharmacology 323 3 2 4 2.1 COc1cc(N)c(cc1C(=O)N[C@H]1CCN2C[C@@H]1CCC2)Cl 11030734
244 3262 0 None -5 3 Human 6.4 pKi None 6.4 Binding
UnclassifiedUnclassified
Guide to Pharmacology 323 3 2 4 2.1 COc1cc(N)c(cc1C(=O)N[C@H]1CCN2C[C@@H]1CCC2)Cl 11218067
244 3262 0 None -5 3 Human 6.4 pKi None 6.4 Binding
UnclassifiedUnclassified
Guide to Pharmacology 323 3 2 4 2.1 COc1cc(N)c(cc1C(=O)N[C@H]1CCN2C[C@@H]1CCC2)Cl 7796807
244 3262 0 None -5 3 Human 6.4 pKi None 6.4 Binding
UnclassifiedUnclassified
Guide to Pharmacology 323 3 2 4 2.1 COc1cc(N)c(cc1C(=O)N[C@H]1CCN2C[C@@H]1CCC2)Cl 9351641
244 3262 0 None -5 3 Human 6.4 pKi None 6.4 Binding
UnclassifiedUnclassified
Guide to Pharmacology 323 3 2 4 2.1 COc1cc(N)c(cc1C(=O)N[C@H]1CCN2C[C@@H]1CCC2)Cl 9603189
3086547 3262 0 None -5 3 Human 6.4 pKi None 6.4 Binding
UnclassifiedUnclassified
Guide to Pharmacology 323 3 2 4 2.1 COc1cc(N)c(cc1C(=O)N[C@H]1CCN2C[C@@H]1CCC2)Cl 10683202
3086547 3262 0 None -5 3 Human 6.4 pKi None 6.4 Binding
UnclassifiedUnclassified
Guide to Pharmacology 323 3 2 4 2.1 COc1cc(N)c(cc1C(=O)N[C@H]1CCN2C[C@@H]1CCC2)Cl 11030734
3086547 3262 0 None -5 3 Human 6.4 pKi None 6.4 Binding
UnclassifiedUnclassified
Guide to Pharmacology 323 3 2 4 2.1 COc1cc(N)c(cc1C(=O)N[C@H]1CCN2C[C@@H]1CCC2)Cl 11218067
3086547 3262 0 None -5 3 Human 6.4 pKi None 6.4 Binding
UnclassifiedUnclassified
Guide to Pharmacology 323 3 2 4 2.1 COc1cc(N)c(cc1C(=O)N[C@H]1CCN2C[C@@H]1CCC2)Cl 7796807
3086547 3262 0 None -5 3 Human 6.4 pKi None 6.4 Binding
UnclassifiedUnclassified
Guide to Pharmacology 323 3 2 4 2.1 COc1cc(N)c(cc1C(=O)N[C@H]1CCN2C[C@@H]1CCC2)Cl 9351641
3086547 3262 0 None -5 3 Human 6.4 pKi None 6.4 Binding
UnclassifiedUnclassified
Guide to Pharmacology 323 3 2 4 2.1 COc1cc(N)c(cc1C(=O)N[C@H]1CCN2C[C@@H]1CCC2)Cl 9603189
108182 4068 18 None -1 16 Rat 6.4 pKi None 6.4 Binding
UnclassifiedUnclassified
Guide to Pharmacology 309 3 2 4 1.8 COc1cc(N)c(cc1C(=O)NC1CN2CCC1CC2)Cl 8813606
108182 4068 18 None -1 16 Rat 6.4 pKi None 6.4 Binding
UnclassifiedUnclassified
Guide to Pharmacology 309 3 2 4 1.8 COc1cc(N)c(cc1C(=O)NC1CN2CCC1CC2)Cl 9225293
245 4068 18 None -1 16 Rat 6.4 pKi None 6.4 Binding
UnclassifiedUnclassified
Guide to Pharmacology 309 3 2 4 1.8 COc1cc(N)c(cc1C(=O)NC1CN2CCC1CC2)Cl 8813606
245 4068 18 None -1 16 Rat 6.4 pKi None 6.4 Binding
UnclassifiedUnclassified
Guide to Pharmacology 309 3 2 4 1.8 COc1cc(N)c(cc1C(=O)NC1CN2CCC1CC2)Cl 9225293
CHEMBL18041 4068 18 None -1 16 Rat 6.4 pKi None 6.4 Binding
UnclassifiedUnclassified
Guide to Pharmacology 309 3 2 4 1.8 COc1cc(N)c(cc1C(=O)NC1CN2CCC1CC2)Cl 8813606
CHEMBL18041 4068 18 None -1 16 Rat 6.4 pKi None 6.4 Binding
UnclassifiedUnclassified
Guide to Pharmacology 309 3 2 4 1.8 COc1cc(N)c(cc1C(=O)NC1CN2CCC1CC2)Cl 9225293
5 139 66 None -288 54 Human 6.5 pKi None 6.5 Binding
UnclassifiedUnclassified
Guide to Pharmacology 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 10646498
5 139 66 None -288 54 Human 6.5 pKi None 6.5 Binding
UnclassifiedUnclassified
Guide to Pharmacology 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 10683202
5 139 66 None -288 54 Human 6.5 pKi None 6.5 Binding
UnclassifiedUnclassified
Guide to Pharmacology 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 10821780
5 139 66 None -288 54 Human 6.5 pKi None 6.5 Binding
UnclassifiedUnclassified
Guide to Pharmacology 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 11030734
5 139 66 None -288 54 Human 6.5 pKi None 6.5 Binding
UnclassifiedUnclassified
Guide to Pharmacology 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 11218067
5 139 66 None -288 54 Human 6.5 pKi None 6.5 Binding
UnclassifiedUnclassified
Guide to Pharmacology 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 15351779
5 139 66 None -288 54 Human 6.5 pKi None 6.5 Binding
UnclassifiedUnclassified
Guide to Pharmacology 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 15466450
5 139 66 None -288 54 Human 6.5 pKi None 6.5 Binding
UnclassifiedUnclassified
Guide to Pharmacology 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 9349523
5 139 66 None -288 54 Human 6.5 pKi None 6.5 Binding
UnclassifiedUnclassified
Guide to Pharmacology 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 9351641
5 139 66 None -288 54 Human 6.5 pKi None 6.5 Binding
UnclassifiedUnclassified
Guide to Pharmacology 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 9603189
5202 139 66 None -288 54 Human 6.5 pKi None 6.5 Binding
UnclassifiedUnclassified
Guide to Pharmacology 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 10646498
5202 139 66 None -288 54 Human 6.5 pKi None 6.5 Binding
UnclassifiedUnclassified
Guide to Pharmacology 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 10683202
5202 139 66 None -288 54 Human 6.5 pKi None 6.5 Binding
UnclassifiedUnclassified
Guide to Pharmacology 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 10821780
5202 139 66 None -288 54 Human 6.5 pKi None 6.5 Binding
UnclassifiedUnclassified
Guide to Pharmacology 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 11030734
5202 139 66 None -288 54 Human 6.5 pKi None 6.5 Binding
UnclassifiedUnclassified
Guide to Pharmacology 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 11218067
5202 139 66 None -288 54 Human 6.5 pKi None 6.5 Binding
UnclassifiedUnclassified
Guide to Pharmacology 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 15351779
5202 139 66 None -288 54 Human 6.5 pKi None 6.5 Binding
UnclassifiedUnclassified
Guide to Pharmacology 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 15466450
5202 139 66 None -288 54 Human 6.5 pKi None 6.5 Binding
UnclassifiedUnclassified
Guide to Pharmacology 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 9349523
5202 139 66 None -288 54 Human 6.5 pKi None 6.5 Binding
UnclassifiedUnclassified
Guide to Pharmacology 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 9351641
5202 139 66 None -288 54 Human 6.5 pKi None 6.5 Binding
UnclassifiedUnclassified
Guide to Pharmacology 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 9603189
CHEMBL39 139 66 None -288 54 Human 6.5 pKi None 6.5 Binding
UnclassifiedUnclassified
Guide to Pharmacology 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 10646498
CHEMBL39 139 66 None -288 54 Human 6.5 pKi None 6.5 Binding
UnclassifiedUnclassified
Guide to Pharmacology 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 10683202
CHEMBL39 139 66 None -288 54 Human 6.5 pKi None 6.5 Binding
UnclassifiedUnclassified
Guide to Pharmacology 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 10821780
CHEMBL39 139 66 None -288 54 Human 6.5 pKi None 6.5 Binding
UnclassifiedUnclassified
Guide to Pharmacology 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 11030734
CHEMBL39 139 66 None -288 54 Human 6.5 pKi None 6.5 Binding
UnclassifiedUnclassified
Guide to Pharmacology 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 11218067
CHEMBL39 139 66 None -288 54 Human 6.5 pKi None 6.5 Binding
UnclassifiedUnclassified
Guide to Pharmacology 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 15351779
CHEMBL39 139 66 None -288 54 Human 6.5 pKi None 6.5 Binding
UnclassifiedUnclassified
Guide to Pharmacology 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 15466450
CHEMBL39 139 66 None -288 54 Human 6.5 pKi None 6.5 Binding
UnclassifiedUnclassified
Guide to Pharmacology 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 9349523
CHEMBL39 139 66 None -288 54 Human 6.5 pKi None 6.5 Binding
UnclassifiedUnclassified
Guide to Pharmacology 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 9351641
CHEMBL39 139 66 None -288 54 Human 6.5 pKi None 6.5 Binding
UnclassifiedUnclassified
Guide to Pharmacology 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 9603189
DB08839 139 66 None -288 54 Human 6.5 pKi None 6.5 Binding
UnclassifiedUnclassified
Guide to Pharmacology 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 10646498
DB08839 139 66 None -288 54 Human 6.5 pKi None 6.5 Binding
UnclassifiedUnclassified
Guide to Pharmacology 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 10683202
DB08839 139 66 None -288 54 Human 6.5 pKi None 6.5 Binding
UnclassifiedUnclassified
Guide to Pharmacology 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 10821780
DB08839 139 66 None -288 54 Human 6.5 pKi None 6.5 Binding
UnclassifiedUnclassified
Guide to Pharmacology 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 11030734
DB08839 139 66 None -288 54 Human 6.5 pKi None 6.5 Binding
UnclassifiedUnclassified
Guide to Pharmacology 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 11218067
DB08839 139 66 None -288 54 Human 6.5 pKi None 6.5 Binding
UnclassifiedUnclassified
Guide to Pharmacology 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 15351779
DB08839 139 66 None -288 54 Human 6.5 pKi None 6.5 Binding
UnclassifiedUnclassified
Guide to Pharmacology 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 15466450
DB08839 139 66 None -288 54 Human 6.5 pKi None 6.5 Binding
UnclassifiedUnclassified
Guide to Pharmacology 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 9349523
DB08839 139 66 None -288 54 Human 6.5 pKi None 6.5 Binding
UnclassifiedUnclassified
Guide to Pharmacology 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 9351641
DB08839 139 66 None -288 54 Human 6.5 pKi None 6.5 Binding
UnclassifiedUnclassified
Guide to Pharmacology 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 9603189
119584 2557 99 None -1 6 Human 6.6 pKi None 6.6 Binding
UnclassifiedUnclassified
Guide to Pharmacology 421 7 2 5 3.1 CCOc1cc(N)c(cc1C(=O)NCC1OCCN(C1)Cc1ccc(cc1)F)Cl 10646498
1848 2557 99 None -1 6 Human 6.6 pKi None 6.6 Binding
UnclassifiedUnclassified
Guide to Pharmacology 421 7 2 5 3.1 CCOc1cc(N)c(cc1C(=O)NCC1OCCN(C1)Cc1ccc(cc1)F)Cl 10646498
242 2557 99 None -1 6 Human 6.6 pKi None 6.6 Binding
UnclassifiedUnclassified
Guide to Pharmacology 421 7 2 5 3.1 CCOc1cc(N)c(cc1C(=O)NCC1OCCN(C1)Cc1ccc(cc1)F)Cl 10646498
CHEMBL60889 2557 99 None -1 6 Human 6.6 pKi None 6.6 Binding
UnclassifiedUnclassified
Guide to Pharmacology 421 7 2 5 3.1 CCOc1cc(N)c(cc1C(=O)NCC1OCCN(C1)Cc1ccc(cc1)F)Cl 10646498
DB11675 2557 99 None -1 6 Human 6.6 pKi None 6.6 Binding
UnclassifiedUnclassified
Guide to Pharmacology 421 7 2 5 3.1 CCOc1cc(N)c(cc1C(=O)NCC1OCCN(C1)Cc1ccc(cc1)F)Cl 10646498
107 141 116 None -457 30 Mouse 6.6 pKi None 6.6 Binding
UnclassifiedUnclassified
Guide to Pharmacology 190 3 2 2 1.7 NCCc1c[nH]c2c1cc(OC)cc2 8946946
1833 141 116 None -457 30 Mouse 6.6 pKi None 6.6 Binding
UnclassifiedUnclassified
Guide to Pharmacology 190 3 2 2 1.7 NCCc1c[nH]c2c1cc(OC)cc2 8946946
CHEMBL8165 141 116 None -457 30 Mouse 6.6 pKi None 6.6 Binding
UnclassifiedUnclassified
Guide to Pharmacology 190 3 2 2 1.7 NCCc1c[nH]c2c1cc(OC)cc2 8946946
260 3808 49 None -38 6 Human 6.7 pKi None 6.7 Binding
UnclassifiedUnclassified
Guide to Pharmacology 284 2 1 3 3.0 CN1[C@@H]2CC[C@H]1C[C@H](C2)OC(=O)c1c[nH]c2c1cccc2 11218067
260 3808 49 None -38 6 Human 6.7 pKi None 6.7 Binding
UnclassifiedUnclassified
Guide to Pharmacology 284 2 1 3 3.0 CN1[C@@H]2CC[C@H]1C[C@H](C2)OC(=O)c1c[nH]c2c1cccc2 9349523
2775 3808 49 None -38 6 Human 6.7 pKi None 6.7 Binding
UnclassifiedUnclassified
Guide to Pharmacology 284 2 1 3 3.0 CN1[C@@H]2CC[C@H]1C[C@H](C2)OC(=O)c1c[nH]c2c1cccc2 11218067
2775 3808 49 None -38 6 Human 6.7 pKi None 6.7 Binding
UnclassifiedUnclassified
Guide to Pharmacology 284 2 1 3 3.0 CN1[C@@H]2CC[C@H]1C[C@H](C2)OC(=O)c1c[nH]c2c1cccc2 9349523
656665 3808 49 None -38 6 Human 6.7 pKi None 6.7 Binding
UnclassifiedUnclassified
Guide to Pharmacology 284 2 1 3 3.0 CN1[C@@H]2CC[C@H]1C[C@H](C2)OC(=O)c1c[nH]c2c1cccc2 11218067
656665 3808 49 None -38 6 Human 6.7 pKi None 6.7 Binding
UnclassifiedUnclassified
Guide to Pharmacology 284 2 1 3 3.0 CN1[C@@H]2CC[C@H]1C[C@H](C2)OC(=O)c1c[nH]c2c1cccc2 9349523
CHEMBL56564 3808 49 None -38 6 Human 6.7 pKi None 6.7 Binding
UnclassifiedUnclassified
Guide to Pharmacology 284 2 1 3 3.0 CN1[C@@H]2CC[C@H]1C[C@H](C2)OC(=O)c1c[nH]c2c1cccc2 11218067
CHEMBL56564 3808 49 None -38 6 Human 6.7 pKi None 6.7 Binding
UnclassifiedUnclassified
Guide to Pharmacology 284 2 1 3 3.0 CN1[C@@H]2CC[C@H]1C[C@H](C2)OC(=O)c1c[nH]c2c1cccc2 9349523
DB11699 3808 49 None -38 6 Human 6.7 pKi None 6.7 Binding
UnclassifiedUnclassified
Guide to Pharmacology 284 2 1 3 3.0 CN1[C@@H]2CC[C@H]1C[C@H](C2)OC(=O)c1c[nH]c2c1cccc2 11218067
DB11699 3808 49 None -38 6 Human 6.7 pKi None 6.7 Binding
UnclassifiedUnclassified
Guide to Pharmacology 284 2 1 3 3.0 CN1[C@@H]2CC[C@H]1C[C@H](C2)OC(=O)c1c[nH]c2c1cccc2 9349523
108182 4068 18 None 1 16 Mouse 6.7 pKi None 6.7 Binding
UnclassifiedUnclassified
Guide to Pharmacology 309 3 2 4 1.8 COc1cc(N)c(cc1C(=O)NC1CN2CCC1CC2)Cl 8946946
245 4068 18 None 1 16 Mouse 6.7 pKi None 6.7 Binding
UnclassifiedUnclassified
Guide to Pharmacology 309 3 2 4 1.8 COc1cc(N)c(cc1C(=O)NC1CN2CCC1CC2)Cl 8946946
CHEMBL18041 4068 18 None 1 16 Mouse 6.7 pKi None 6.7 Binding
UnclassifiedUnclassified
Guide to Pharmacology 309 3 2 4 1.8 COc1cc(N)c(cc1C(=O)NC1CN2CCC1CC2)Cl 8946946
260 3808 49 None -19 6 Rat 6.8 pKi None 6.8 Binding
UnclassifiedUnclassified
Guide to Pharmacology 284 2 1 3 3.0 CN1[C@@H]2CC[C@H]1C[C@H](C2)OC(=O)c1c[nH]c2c1cccc2 8813606
2775 3808 49 None -19 6 Rat 6.8 pKi None 6.8 Binding
UnclassifiedUnclassified
Guide to Pharmacology 284 2 1 3 3.0 CN1[C@@H]2CC[C@H]1C[C@H](C2)OC(=O)c1c[nH]c2c1cccc2 8813606
656665 3808 49 None -19 6 Rat 6.8 pKi None 6.8 Binding
UnclassifiedUnclassified
Guide to Pharmacology 284 2 1 3 3.0 CN1[C@@H]2CC[C@H]1C[C@H](C2)OC(=O)c1c[nH]c2c1cccc2 8813606
CHEMBL56564 3808 49 None -19 6 Rat 6.8 pKi None 6.8 Binding
UnclassifiedUnclassified
Guide to Pharmacology 284 2 1 3 3.0 CN1[C@@H]2CC[C@H]1C[C@H](C2)OC(=O)c1c[nH]c2c1cccc2 8813606
DB11699 3808 49 None -19 6 Rat 6.8 pKi None 6.8 Binding
UnclassifiedUnclassified
Guide to Pharmacology 284 2 1 3 3.0 CN1[C@@H]2CC[C@H]1C[C@H](C2)OC(=O)c1c[nH]c2c1cccc2 8813606
107 141 116 None -257 30 Rat 6.9 pKi None 6.9 Binding
UnclassifiedUnclassified
Guide to Pharmacology 190 3 2 2 1.7 NCCc1c[nH]c2c1cc(OC)cc2 7796807
107 141 116 None -257 30 Rat 6.9 pKi None 6.9 Binding
UnclassifiedUnclassified
Guide to Pharmacology 190 3 2 2 1.7 NCCc1c[nH]c2c1cc(OC)cc2 8813606
107 141 116 None -257 30 Rat 6.9 pKi None 6.9 Binding
UnclassifiedUnclassified
Guide to Pharmacology 190 3 2 2 1.7 NCCc1c[nH]c2c1cc(OC)cc2 9225293
1833 141 116 None -257 30 Rat 6.9 pKi None 6.9 Binding
UnclassifiedUnclassified
Guide to Pharmacology 190 3 2 2 1.7 NCCc1c[nH]c2c1cc(OC)cc2 7796807
1833 141 116 None -257 30 Rat 6.9 pKi None 6.9 Binding
UnclassifiedUnclassified
Guide to Pharmacology 190 3 2 2 1.7 NCCc1c[nH]c2c1cc(OC)cc2 8813606
1833 141 116 None -257 30 Rat 6.9 pKi None 6.9 Binding
UnclassifiedUnclassified
Guide to Pharmacology 190 3 2 2 1.7 NCCc1c[nH]c2c1cc(OC)cc2 9225293
CHEMBL8165 141 116 None -257 30 Rat 6.9 pKi None 6.9 Binding
UnclassifiedUnclassified
Guide to Pharmacology 190 3 2 2 1.7 NCCc1c[nH]c2c1cc(OC)cc2 7796807
CHEMBL8165 141 116 None -257 30 Rat 6.9 pKi None 6.9 Binding
UnclassifiedUnclassified
Guide to Pharmacology 190 3 2 2 1.7 NCCc1c[nH]c2c1cc(OC)cc2 8813606
CHEMBL8165 141 116 None -257 30 Rat 6.9 pKi None 6.9 Binding
UnclassifiedUnclassified
Guide to Pharmacology 190 3 2 2 1.7 NCCc1c[nH]c2c1cc(OC)cc2 9225293
244 3262 0 None -1 3 Mouse 6.9 pKi None 6.9 Binding
UnclassifiedUnclassified
Guide to Pharmacology 323 3 2 4 2.1 COc1cc(N)c(cc1C(=O)N[C@H]1CCN2C[C@@H]1CCC2)Cl 8946946
3086547 3262 0 None -1 3 Mouse 6.9 pKi None 6.9 Binding
UnclassifiedUnclassified
Guide to Pharmacology 323 3 2 4 2.1 COc1cc(N)c(cc1C(=O)N[C@H]1CCN2C[C@@H]1CCC2)Cl 8946946
244 3262 0 None 1 3 Rat 7.1 pKi None 7.1 Binding
UnclassifiedUnclassified
Guide to Pharmacology 323 3 2 4 2.1 COc1cc(N)c(cc1C(=O)N[C@H]1CCN2C[C@@H]1CCC2)Cl 8813606
244 3262 0 None 1 3 Rat 7.1 pKi None 7.1 Binding
UnclassifiedUnclassified
Guide to Pharmacology 323 3 2 4 2.1 COc1cc(N)c(cc1C(=O)N[C@H]1CCN2C[C@@H]1CCC2)Cl 9225293
3086547 3262 0 None 1 3 Rat 7.1 pKi None 7.1 Binding
UnclassifiedUnclassified
Guide to Pharmacology 323 3 2 4 2.1 COc1cc(N)c(cc1C(=O)N[C@H]1CCN2C[C@@H]1CCC2)Cl 8813606
3086547 3262 0 None 1 3 Rat 7.1 pKi None 7.1 Binding
UnclassifiedUnclassified
Guide to Pharmacology 323 3 2 4 2.1 COc1cc(N)c(cc1C(=O)N[C@H]1CCN2C[C@@H]1CCC2)Cl 9225293
260 3808 49 None -15 6 Mouse 7.1 pKi None 7.1 Binding
UnclassifiedUnclassified
Guide to Pharmacology 284 2 1 3 3.0 CN1[C@@H]2CC[C@H]1C[C@H](C2)OC(=O)c1c[nH]c2c1cccc2 8946946
2775 3808 49 None -15 6 Mouse 7.1 pKi None 7.1 Binding
UnclassifiedUnclassified
Guide to Pharmacology 284 2 1 3 3.0 CN1[C@@H]2CC[C@H]1C[C@H](C2)OC(=O)c1c[nH]c2c1cccc2 8946946
656665 3808 49 None -15 6 Mouse 7.1 pKi None 7.1 Binding
UnclassifiedUnclassified
Guide to Pharmacology 284 2 1 3 3.0 CN1[C@@H]2CC[C@H]1C[C@H](C2)OC(=O)c1c[nH]c2c1cccc2 8946946
CHEMBL56564 3808 49 None -15 6 Mouse 7.1 pKi None 7.1 Binding
UnclassifiedUnclassified
Guide to Pharmacology 284 2 1 3 3.0 CN1[C@@H]2CC[C@H]1C[C@H](C2)OC(=O)c1c[nH]c2c1cccc2 8946946
DB11699 3808 49 None -15 6 Mouse 7.1 pKi None 7.1 Binding
UnclassifiedUnclassified
Guide to Pharmacology 284 2 1 3 3.0 CN1[C@@H]2CC[C@H]1C[C@H](C2)OC(=O)c1c[nH]c2c1cccc2 8946946
5 139 66 None -154 54 Mouse 7.2 pKi None 7.2 Binding
UnclassifiedUnclassified
Guide to Pharmacology 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 8946946
5202 139 66 None -154 54 Mouse 7.2 pKi None 7.2 Binding
UnclassifiedUnclassified
Guide to Pharmacology 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 8946946
CHEMBL39 139 66 None -154 54 Mouse 7.2 pKi None 7.2 Binding
UnclassifiedUnclassified
Guide to Pharmacology 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 8946946
DB08839 139 66 None -154 54 Mouse 7.2 pKi None 7.2 Binding
UnclassifiedUnclassified
Guide to Pharmacology 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 8946946
129928 1302 0 None -5 2 Mouse 7.3 pKi None 7.3 Binding
UnclassifiedUnclassified
Guide to Pharmacology 331 2 1 6 1.9 COc1ccc2c(c1)n(C(=O)OC1CC3CCC(C1)N3C)c(=O)[nH]2 8946946
246 1302 0 None -5 2 Mouse 7.3 pKi None 7.3 Binding
UnclassifiedUnclassified
Guide to Pharmacology 331 2 1 6 1.9 COc1ccc2c(c1)n(C(=O)OC1CC3CCC(C1)N3C)c(=O)[nH]2 8946946
CHEMBL1194556 1302 0 None -5 2 Mouse 7.3 pKi None 7.3 Binding
UnclassifiedUnclassified
Guide to Pharmacology 331 2 1 6 1.9 COc1ccc2c(c1)n(C(=O)OC1CC3CCC(C1)N3C)c(=O)[nH]2 8946946
233 653 0 None -1 2 Human 7.4 pKi None 7.4 Binding
UnclassifiedUnclassified
Guide to Pharmacology 328 2 1 5 2.0 CCn1c(=O)n(c2c1cccc2)C(=O)NC1CC2CC[C@@H](C1)N2C 10683202
233 653 0 None -1 2 Human 7.4 pKi None 7.4 Binding
UnclassifiedUnclassified
Guide to Pharmacology 328 2 1 5 2.0 CCn1c(=O)n(c2c1cccc2)C(=O)NC1CC2CC[C@@H](C1)N2C 11030734
233 653 0 None -1 2 Human 7.4 pKi None 7.4 Binding
UnclassifiedUnclassified
Guide to Pharmacology 328 2 1 5 2.0 CCn1c(=O)n(c2c1cccc2)C(=O)NC1CC2CC[C@@H](C1)N2C 9603189
9929033 653 0 None -1 2 Human 7.4 pKi None 7.4 Binding
UnclassifiedUnclassified
Guide to Pharmacology 328 2 1 5 2.0 CCn1c(=O)n(c2c1cccc2)C(=O)NC1CC2CC[C@@H](C1)N2C 10683202
9929033 653 0 None -1 2 Human 7.4 pKi None 7.4 Binding
UnclassifiedUnclassified
Guide to Pharmacology 328 2 1 5 2.0 CCn1c(=O)n(c2c1cccc2)C(=O)NC1CC2CC[C@@H](C1)N2C 11030734
9929033 653 0 None -1 2 Human 7.4 pKi None 7.4 Binding
UnclassifiedUnclassified
Guide to Pharmacology 328 2 1 5 2.0 CCn1c(=O)n(c2c1cccc2)C(=O)NC1CC2CC[C@@H](C1)N2C 9603189
240 931 39 None -8 25 Rat 7.4 pKi None 7.4 Binding
UnclassifiedUnclassified
Guide to Pharmacology 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N 8813606
240 931 39 None -8 25 Rat 7.4 pKi None 7.4 Binding
UnclassifiedUnclassified
Guide to Pharmacology 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N 9225293
2769 931 39 None -8 25 Rat 7.4 pKi None 7.4 Binding
UnclassifiedUnclassified
Guide to Pharmacology 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N 8813606
2769 931 39 None -8 25 Rat 7.4 pKi None 7.4 Binding
UnclassifiedUnclassified
Guide to Pharmacology 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N 9225293
44279790 931 39 None -8 25 Rat 7.4 pKi None 7.4 Binding
UnclassifiedUnclassified
Guide to Pharmacology 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N 8813606
44279790 931 39 None -8 25 Rat 7.4 pKi None 7.4 Binding
UnclassifiedUnclassified
Guide to Pharmacology 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N 9225293
660 931 39 None -8 25 Rat 7.4 pKi None 7.4 Binding
UnclassifiedUnclassified
Guide to Pharmacology 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N 8813606
660 931 39 None -8 25 Rat 7.4 pKi None 7.4 Binding
UnclassifiedUnclassified
Guide to Pharmacology 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N 9225293
CHEMBL1729 931 39 None -8 25 Rat 7.4 pKi None 7.4 Binding
UnclassifiedUnclassified
Guide to Pharmacology 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N 8813606
CHEMBL1729 931 39 None -8 25 Rat 7.4 pKi None 7.4 Binding
UnclassifiedUnclassified
Guide to Pharmacology 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N 9225293
CHEMBL560739 931 39 None -8 25 Rat 7.4 pKi None 7.4 Binding
UnclassifiedUnclassified
Guide to Pharmacology 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N 8813606
CHEMBL560739 931 39 None -8 25 Rat 7.4 pKi None 7.4 Binding
UnclassifiedUnclassified
Guide to Pharmacology 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N 9225293
DB00604 931 39 None -8 25 Rat 7.4 pKi None 7.4 Binding
UnclassifiedUnclassified
Guide to Pharmacology 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N 8813606
DB00604 931 39 None -8 25 Rat 7.4 pKi None 7.4 Binding
UnclassifiedUnclassified
Guide to Pharmacology 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N 9225293
234 654 0 None -1 3 Mouse 7.4 pKi None 7.4 Binding
UnclassifiedUnclassified
Guide to Pharmacology 342 2 1 5 2.6 CN1[C@@H]2CC[C@H]1CC(C2)NC(=O)n1c(=O)n(c2c1cccc2)C(C)C 8946946
5311029 654 0 None -1 3 Mouse 7.4 pKi None 7.4 Binding
UnclassifiedUnclassified
Guide to Pharmacology 342 2 1 5 2.6 CN1[C@@H]2CC[C@H]1CC(C2)NC(=O)n1c(=O)n(c2c1cccc2)C(C)C 8946946
5 139 66 None -117 54 Rat 7.5 pKi None 7.5 Binding
UnclassifiedUnclassified
Guide to Pharmacology 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 7796807
5 139 66 None -117 54 Rat 7.5 pKi None 7.5 Binding
UnclassifiedUnclassified
Guide to Pharmacology 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 8813606
5 139 66 None -117 54 Rat 7.5 pKi None 7.5 Binding
UnclassifiedUnclassified
Guide to Pharmacology 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 9225293
5202 139 66 None -117 54 Rat 7.5 pKi None 7.5 Binding
UnclassifiedUnclassified
Guide to Pharmacology 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 7796807
5202 139 66 None -117 54 Rat 7.5 pKi None 7.5 Binding
UnclassifiedUnclassified
Guide to Pharmacology 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 8813606
5202 139 66 None -117 54 Rat 7.5 pKi None 7.5 Binding
UnclassifiedUnclassified
Guide to Pharmacology 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 9225293
CHEMBL39 139 66 None -117 54 Rat 7.5 pKi None 7.5 Binding
UnclassifiedUnclassified
Guide to Pharmacology 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 7796807
CHEMBL39 139 66 None -117 54 Rat 7.5 pKi None 7.5 Binding
UnclassifiedUnclassified
Guide to Pharmacology 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 8813606
CHEMBL39 139 66 None -117 54 Rat 7.5 pKi None 7.5 Binding
UnclassifiedUnclassified
Guide to Pharmacology 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 9225293
DB08839 139 66 None -117 54 Rat 7.5 pKi None 7.5 Binding
UnclassifiedUnclassified
Guide to Pharmacology 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 7796807
DB08839 139 66 None -117 54 Rat 7.5 pKi None 7.5 Binding
UnclassifiedUnclassified
Guide to Pharmacology 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 8813606
DB08839 139 66 None -117 54 Rat 7.5 pKi None 7.5 Binding
UnclassifiedUnclassified
Guide to Pharmacology 176 2 3 2 1.4 NCCc1c[nH]c2c1cc(O)cc2 9225293
234 654 0 None 1 3 Rat 7.5 pKi None 7.5 Binding
UnclassifiedUnclassified
Guide to Pharmacology 342 2 1 5 2.6 CN1[C@@H]2CC[C@H]1CC(C2)NC(=O)n1c(=O)n(c2c1cccc2)C(C)C 9225293
5311029 654 0 None 1 3 Rat 7.5 pKi None 7.5 Binding
UnclassifiedUnclassified
Guide to Pharmacology 342 2 1 5 2.6 CN1[C@@H]2CC[C@H]1CC(C2)NC(=O)n1c(=O)n(c2c1cccc2)C(C)C 9225293
233 653 0 None 1 2 Mouse 7.5 pKi None 7.5 Binding
UnclassifiedUnclassified
Guide to Pharmacology 328 2 1 5 2.0 CCn1c(=O)n(c2c1cccc2)C(=O)NC1CC2CC[C@@H](C1)N2C 8946946
9929033 653 0 None 1 2 Mouse 7.5 pKi None 7.5 Binding
UnclassifiedUnclassified
Guide to Pharmacology 328 2 1 5 2.0 CCn1c(=O)n(c2c1cccc2)C(=O)NC1CC2CC[C@@H](C1)N2C 8946946
240 931 39 None -5 25 Mouse 7.5 pKi None 7.5 Binding
UnclassifiedUnclassified
Guide to Pharmacology 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N 8946946
2769 931 39 None -5 25 Mouse 7.5 pKi None 7.5 Binding
UnclassifiedUnclassified
Guide to Pharmacology 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N 8946946
44279790 931 39 None -5 25 Mouse 7.5 pKi None 7.5 Binding
UnclassifiedUnclassified
Guide to Pharmacology 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N 8946946
660 931 39 None -5 25 Mouse 7.5 pKi None 7.5 Binding
UnclassifiedUnclassified
Guide to Pharmacology 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N 8946946
CHEMBL1729 931 39 None -5 25 Mouse 7.5 pKi None 7.5 Binding
UnclassifiedUnclassified
Guide to Pharmacology 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N 8946946
CHEMBL560739 931 39 None -5 25 Mouse 7.5 pKi None 7.5 Binding
UnclassifiedUnclassified
Guide to Pharmacology 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N 8946946
DB00604 931 39 None -5 25 Mouse 7.5 pKi None 7.5 Binding
UnclassifiedUnclassified
Guide to Pharmacology 465 9 2 6 3.4 COC1CN(CCCOc2ccc(cc2)F)CCC1NC(=O)c1cc(Cl)c(cc1OC)N 8946946
258 3511 25 None -2 8 Rat 7.7 pKi None 7.7 Binding
UnclassifiedUnclassified
Guide to Pharmacology 300 7 1 5 2.4 CCN(CCOC(=O)c1cc(Cl)c(cc1OC)N)CC 9225293
5191 3511 25 None -2 8 Rat 7.7 pKi None 7.7 Binding
UnclassifiedUnclassified
Guide to Pharmacology 300 7 1 5 2.4 CCN(CCOC(=O)c1cc(Cl)c(cc1OC)N)CC 9225293
CHEMBL287045 3511 25 None -2 8 Rat 7.7 pKi None 7.7 Binding
UnclassifiedUnclassified
Guide to Pharmacology 300 7 1 5 2.4 CCN(CCOC(=O)c1cc(Cl)c(cc1OC)N)CC 9225293
243 3153 85 None 12 34 Human 7.8 pKi None 7.8 Binding
UnclassifiedUnclassified
Guide to Pharmacology 367 6 2 5 2.1 COCCCN1CCC(CC1)NC(=O)c1cc(Cl)c(c2c1OCC2)N 10646498
243 3153 85 None 12 34 Human 7.8 pKi None 7.8 Binding
UnclassifiedUnclassified
Guide to Pharmacology 367 6 2 5 2.1 COCCCN1CCC(CC1)NC(=O)c1cc(Cl)c(c2c1OCC2)N 11438309
3052762 3153 85 None 12 34 Human 7.8 pKi None 7.8 Binding
UnclassifiedUnclassified
Guide to Pharmacology 367 6 2 5 2.1 COCCCN1CCC(CC1)NC(=O)c1cc(Cl)c(c2c1OCC2)N 10646498
3052762 3153 85 None 12 34 Human 7.8 pKi None 7.8 Binding
UnclassifiedUnclassified
Guide to Pharmacology 367 6 2 5 2.1 COCCCN1CCC(CC1)NC(=O)c1cc(Cl)c(c2c1OCC2)N 11438309
3502 3153 85 None 12 34 Human 7.8 pKi None 7.8 Binding
UnclassifiedUnclassified
Guide to Pharmacology 367 6 2 5 2.1 COCCCN1CCC(CC1)NC(=O)c1cc(Cl)c(c2c1OCC2)N 10646498
3502 3153 85 None 12 34 Human 7.8 pKi None 7.8 Binding
UnclassifiedUnclassified
Guide to Pharmacology 367 6 2 5 2.1 COCCCN1CCC(CC1)NC(=O)c1cc(Cl)c(c2c1OCC2)N 11438309
CHEMBL117287 3153 85 None 12 34 Human 7.8 pKi None 7.8 Binding
UnclassifiedUnclassified
Guide to Pharmacology 367 6 2 5 2.1 COCCCN1CCC(CC1)NC(=O)c1cc(Cl)c(c2c1OCC2)N 10646498
CHEMBL117287 3153 85 None 12 34 Human 7.8 pKi None 7.8 Binding
UnclassifiedUnclassified
Guide to Pharmacology 367 6 2 5 2.1 COCCCN1CCC(CC1)NC(=O)c1cc(Cl)c(c2c1OCC2)N 11438309
DB06480 3153 85 None 12 34 Human 7.8 pKi None 7.8 Binding
UnclassifiedUnclassified
Guide to Pharmacology 367 6 2 5 2.1 COCCCN1CCC(CC1)NC(=O)c1cc(Cl)c(c2c1OCC2)N 10646498
DB06480 3153 85 None 12 34 Human 7.8 pKi None 7.8 Binding
UnclassifiedUnclassified
Guide to Pharmacology 367 6 2 5 2.1 COCCCN1CCC(CC1)NC(=O)c1cc(Cl)c(c2c1OCC2)N 11438309
135409453 3714 38 None -2 2 Human 8.0 pKi None 8 Binding
UnclassifiedUnclassified
Guide to Pharmacology 301 7 3 3 2.6 CCCCCN=C(N/N=C/c1c[nH]c2c1cc(OC)cc2)N 10646498
135409453 3714 38 None -2 2 Human 8.0 pKi None 8 Binding
UnclassifiedUnclassified
Guide to Pharmacology 301 7 3 3 2.6 CCCCCN=C(N/N=C/c1c[nH]c2c1cc(OC)cc2)N 15466450
226 3714 38 None -2 2 Human 8.0 pKi None 8 Binding
UnclassifiedUnclassified
Guide to Pharmacology 301 7 3 3 2.6 CCCCCN=C(N/N=C/c1c[nH]c2c1cc(OC)cc2)N 10646498
226 3714 38 None -2 2 Human 8.0 pKi None 8 Binding
UnclassifiedUnclassified
Guide to Pharmacology 301 7 3 3 2.6 CCCCCN=C(N/N=C/c1c[nH]c2c1cc(OC)cc2)N 15466450
CHEMBL76370 3714 38 None -2 2 Human 8.0 pKi None 8 Binding
UnclassifiedUnclassified
Guide to Pharmacology 301 7 3 3 2.6 CCCCCN=C(N/N=C/c1c[nH]c2c1cc(OC)cc2)N 10646498
CHEMBL76370 3714 38 None -2 2 Human 8.0 pKi None 8 Binding
UnclassifiedUnclassified
Guide to Pharmacology 301 7 3 3 2.6 CCCCCN=C(N/N=C/c1c[nH]c2c1cc(OC)cc2)N 15466450
129928 1302 0 None 5 2 Human 8.0 pKi None 8 Binding
UnclassifiedUnclassified
Guide to Pharmacology 331 2 1 6 1.9 COc1ccc2c(c1)n(C(=O)OC1CC3CCC(C1)N3C)c(=O)[nH]2 9351641
246 1302 0 None 5 2 Human 8.0 pKi None 8 Binding
UnclassifiedUnclassified
Guide to Pharmacology 331 2 1 6 1.9 COc1ccc2c(c1)n(C(=O)OC1CC3CCC(C1)N3C)c(=O)[nH]2 9351641
CHEMBL1194556 1302 0 None 5 2 Human 8.0 pKi None 8 Binding
UnclassifiedUnclassified
Guide to Pharmacology 331 2 1 6 1.9 COc1ccc2c(c1)n(C(=O)OC1CC3CCC(C1)N3C)c(=O)[nH]2 9351641
132337 3487 8 None 1 2 Mouse 8.1 pKi None 8.1 Binding
UnclassifiedUnclassified
Guide to Pharmacology 323 4 2 4 2.1 COc1cc(N)c(cc1C(=O)NC[C@@H]1CCN2[C@H]1CCC2)Cl 8946946
238 3487 8 None 1 2 Mouse 8.1 pKi None 8.1 Binding
UnclassifiedUnclassified
Guide to Pharmacology 323 4 2 4 2.1 COc1cc(N)c(cc1C(=O)NC[C@@H]1CCN2[C@H]1CCC2)Cl 8946946
CHEMBL34291 3487 8 None 1 2 Mouse 8.1 pKi None 8.1 Binding
UnclassifiedUnclassified
Guide to Pharmacology 323 4 2 4 2.1 COc1cc(N)c(cc1C(=O)NC[C@@H]1CCN2[C@H]1CCC2)Cl 8946946
258 3511 25 None -1 8 Mouse 8.1 pKi None 8.1 Binding
UnclassifiedUnclassified
Guide to Pharmacology 300 7 1 5 2.4 CCN(CCOC(=O)c1cc(Cl)c(cc1OC)N)CC 7498967
5191 3511 25 None -1 8 Mouse 8.1 pKi None 8.1 Binding
UnclassifiedUnclassified
Guide to Pharmacology 300 7 1 5 2.4 CCN(CCOC(=O)c1cc(Cl)c(cc1OC)N)CC 7498967
CHEMBL287045 3511 25 None -1 8 Mouse 8.1 pKi None 8.1 Binding
UnclassifiedUnclassified
Guide to Pharmacology 300 7 1 5 2.4 CCN(CCOC(=O)c1cc(Cl)c(cc1OC)N)CC 7498967
182593 3343 4 None 1 3 Human 8.5 pKi None 8.5 Binding
UnclassifiedUnclassified
Guide to Pharmacology 326 6 1 5 3.0 COc1cc(N)c(cc1C(=O)OCCCN1CCCCC1)Cl 10683202
182593 3343 4 None 1 3 Human 8.5 pKi None 8.5 Binding
UnclassifiedUnclassified
Guide to Pharmacology 326 6 1 5 3.0 COc1cc(N)c(cc1C(=O)OCCCN1CCCCC1)Cl 11030734
182593 3343 4 None 1 3 Human 8.5 pKi None 8.5 Binding
UnclassifiedUnclassified
Guide to Pharmacology 326 6 1 5 3.0 COc1cc(N)c(cc1C(=O)OCCCN1CCCCC1)Cl 15351779
254 3343 4 None 1 3 Human 8.5 pKi None 8.5 Binding
UnclassifiedUnclassified
Guide to Pharmacology 326 6 1 5 3.0 COc1cc(N)c(cc1C(=O)OCCCN1CCCCC1)Cl 10683202
254 3343 4 None 1 3 Human 8.5 pKi None 8.5 Binding
UnclassifiedUnclassified
Guide to Pharmacology 326 6 1 5 3.0 COc1cc(N)c(cc1C(=O)OCCCN1CCCCC1)Cl 11030734
254 3343 4 None 1 3 Human 8.5 pKi None 8.5 Binding
UnclassifiedUnclassified
Guide to Pharmacology 326 6 1 5 3.0 COc1cc(N)c(cc1C(=O)OCCCN1CCCCC1)Cl 15351779
CHEMBL83954 3343 4 None 1 3 Human 8.5 pKi None 8.5 Binding
UnclassifiedUnclassified
Guide to Pharmacology 326 6 1 5 3.0 COc1cc(N)c(cc1C(=O)OCCCN1CCCCC1)Cl 10683202
CHEMBL83954 3343 4 None 1 3 Human 8.5 pKi None 8.5 Binding
UnclassifiedUnclassified
Guide to Pharmacology 326 6 1 5 3.0 COc1cc(N)c(cc1C(=O)OCCCN1CCCCC1)Cl 11030734
CHEMBL83954 3343 4 None 1 3 Human 8.5 pKi None 8.5 Binding
UnclassifiedUnclassified
Guide to Pharmacology 326 6 1 5 3.0 COc1cc(N)c(cc1C(=O)OCCCN1CCCCC1)Cl 15351779
183782 3346 15 None -1 14 Human 8.5 pKi None 8.5 Binding
UnclassifiedUnclassified
Guide to Pharmacology 352 8 1 4 4.4 CCCCN1CCC(CC1)CCC(=O)c1cc(Cl)c(cc1OC)N 10683202
183782 3346 15 None -1 14 Human 8.5 pKi None 8.5 Binding
UnclassifiedUnclassified
Guide to Pharmacology 352 8 1 4 4.4 CCCCN1CCC(CC1)CCC(=O)c1cc(Cl)c(cc1OC)N 11030734
237 3346 15 None -1 14 Human 8.5 pKi None 8.5 Binding
UnclassifiedUnclassified
Guide to Pharmacology 352 8 1 4 4.4 CCCCN1CCC(CC1)CCC(=O)c1cc(Cl)c(cc1OC)N 10683202
237 3346 15 None -1 14 Human 8.5 pKi None 8.5 Binding
UnclassifiedUnclassified
Guide to Pharmacology 352 8 1 4 4.4 CCCCN1CCC(CC1)CCC(=O)c1cc(Cl)c(cc1OC)N 11030734
CHEMBL85251 3346 15 None -1 14 Human 8.5 pKi None 8.5 Binding
UnclassifiedUnclassified
Guide to Pharmacology 352 8 1 4 4.4 CCCCN1CCC(CC1)CCC(=O)c1cc(Cl)c(cc1OC)N 10683202
CHEMBL85251 3346 15 None -1 14 Human 8.5 pKi None 8.5 Binding
UnclassifiedUnclassified
Guide to Pharmacology 352 8 1 4 4.4 CCCCN1CCC(CC1)CCC(=O)c1cc(Cl)c(cc1OC)N 11030734
119376 1811 41 None -2 26 Rat 8.6 pKi None 8.6 Binding
UnclassifiedUnclassified
Guide to Pharmacology 393 7 1 6 1.6 O=C(c1cn(c2c1cccc2)C)OCC1CCN(CC1)CCNS(=O)(=O)C 9225293
247 1811 41 None -2 26 Rat 8.6 pKi None 8.6 Binding
UnclassifiedUnclassified
Guide to Pharmacology 393 7 1 6 1.6 O=C(c1cn(c2c1cccc2)C)OCC1CCN(CC1)CCNS(=O)(=O)C 9225293
CHEMBL33884 1811 41 None -2 26 Rat 8.6 pKi None 8.6 Binding
UnclassifiedUnclassified
Guide to Pharmacology 393 7 1 6 1.6 O=C(c1cn(c2c1cccc2)C)OCC1CCN(CC1)CCNS(=O)(=O)C 9225293
236 3345 0 None -4 2 Rat 8.8 pKi None 8.8 Binding
UnclassifiedUnclassified
Guide to Pharmacology 474 8 1 7 4.2 COc1cc(N)c(cc1C(=O)OCC1CCN(CC1)CCCc1ccc2c(c1)OCCO2)Cl 9225293
239 3345 0 None -4 2 Rat 8.8 pKi None 8.8 Binding
UnclassifiedUnclassified
Guide to Pharmacology 474 8 1 7 4.2 COc1cc(N)c(cc1C(=O)OCC1CCN(CC1)CCCc1ccc2c(c1)OCCO2)Cl 9225293
5311417 3345 0 None -4 2 Rat 8.8 pKi None 8.8 Binding
UnclassifiedUnclassified
Guide to Pharmacology 474 8 1 7 4.2 COc1cc(N)c(cc1C(=O)OCC1CCN(CC1)CCCc1ccc2c(c1)OCCO2)Cl 9225293
CHEMBL1908857 3345 0 None -4 2 Rat 8.8 pKi None 8.8 Binding
UnclassifiedUnclassified
Guide to Pharmacology 474 8 1 7 4.2 COc1cc(N)c(cc1C(=O)OCC1CCN(CC1)CCCc1ccc2c(c1)OCCO2)Cl 9225293
255 3433 13 None -1 2 Human 8.8 pKi None 8.8 Binding
UnclassifiedUnclassified
Guide to Pharmacology 272 4 1 3 2.8 O=C(c1c[nH]c2c1cccc2)OCCN1CCCCC1 11218067
3272300 3433 13 None -1 2 Human 8.8 pKi None 8.8 Binding
UnclassifiedUnclassified
Guide to Pharmacology 272 4 1 3 2.8 O=C(c1c[nH]c2c1cccc2)OCCN1CCCCC1 11218067
CHEMBL1255781 3433 13 None -1 2 Human 8.8 pKi None 8.8 Binding
UnclassifiedUnclassified
Guide to Pharmacology 272 4 1 3 2.8 O=C(c1c[nH]c2c1cccc2)OCCN1CCCCC1 11218067
121881 3434 21 None -27 15 Rat 9.2 pKi None 9.2 Binding
UnclassifiedUnclassified
Guide to Pharmacology 382 6 1 6 3.4 CCCCN1CCC(CC1)COC(=O)c1cc(Cl)c(c2c1OCCO2)N 9225293
256 3434 21 None -27 15 Rat 9.2 pKi None 9.2 Binding
UnclassifiedUnclassified
Guide to Pharmacology 382 6 1 6 3.4 CCCCN1CCC(CC1)COC(=O)c1cc(Cl)c(c2c1OCCO2)N 9225293
CHEMBL68131 3434 21 None -27 15 Rat 9.2 pKi None 9.2 Binding
UnclassifiedUnclassified
Guide to Pharmacology 382 6 1 6 3.4 CCCCN1CCC(CC1)COC(=O)c1cc(Cl)c(c2c1OCCO2)N 9225293
29 780 0 None 1584 9 Human 9.2 pKi None 9.2 Binding
UnclassifiedUnclassified
Guide to Pharmacology 456 5 1 8 3.4 Nc1c(Cl)cc(c2c1OCCO2)c1nn(c(=O)o1)C1CCN(CC1)CCc1ccccc1 12130738
9805719 780 0 None 1584 9 Human 9.2 pKi None 9.2 Binding
UnclassifiedUnclassified
Guide to Pharmacology 456 5 1 8 3.4 Nc1c(Cl)cc(c2c1OCCO2)c1nn(c(=O)o1)C1CCN(CC1)CCc1ccccc1 12130738
CHEMBL2027925 780 0 None 1584 9 Human 9.2 pKi None 9.2 Binding
UnclassifiedUnclassified
Guide to Pharmacology 456 5 1 8 3.4 Nc1c(Cl)cc(c2c1OCCO2)c1nn(c(=O)o1)C1CCN(CC1)CCc1ccccc1 12130738
252 3290 1 None 1 2 Mouse 9.3 pKi None 9.3 Binding
UnclassifiedUnclassified
Guide to Pharmacology 332 6 1 4 2.7 CCCCN1CCC(CC1)CNC(=O)c1cccc2c1OCCO2 11976337
44391713 3290 1 None 1 2 Mouse 9.3 pKi None 9.3 Binding
UnclassifiedUnclassified
Guide to Pharmacology 332 6 1 4 2.7 CCCCN1CCC(CC1)CNC(=O)c1cccc2c1OCCO2 11976337
CHEMBL182590 3290 1 None 1 2 Mouse 9.3 pKi None 9.3 Binding
UnclassifiedUnclassified
Guide to Pharmacology 332 6 1 4 2.7 CCCCN1CCC(CC1)CNC(=O)c1cccc2c1OCCO2 11976337
249 2528 3 None 1 2 Human 9.4 pKi None 9.4 Binding
UnclassifiedUnclassified
Guide to Pharmacology 340 5 1 5 3.1 COc1cc(N)c(cc1C(=O)OCCN1CC(C)CC(C1)C)Cl 10683202
249 2528 3 None 1 2 Human 9.4 pKi None 9.4 Binding
UnclassifiedUnclassified
Guide to Pharmacology 340 5 1 5 3.1 COc1cc(N)c(cc1C(=O)OCCN1CC(C)CC(C1)C)Cl 10821780
249 2528 3 None 1 2 Human 9.4 pKi None 9.4 Binding
UnclassifiedUnclassified
Guide to Pharmacology 340 5 1 5 3.1 COc1cc(N)c(cc1C(=O)OCCN1CC(C)CC(C1)C)Cl 11030734
249 2528 3 None 1 2 Human 9.4 pKi None 9.4 Binding
UnclassifiedUnclassified
Guide to Pharmacology 340 5 1 5 3.1 COc1cc(N)c(cc1C(=O)OCCN1CC(C)CC(C1)C)Cl 15466450
249 2528 3 None 1 2 Human 9.4 pKi None 9.4 Binding
UnclassifiedUnclassified
Guide to Pharmacology 340 5 1 5 3.1 COc1cc(N)c(cc1C(=O)OCCN1CC(C)CC(C1)C)Cl 9603189
9905972 2528 3 None 1 2 Human 9.4 pKi None 9.4 Binding
UnclassifiedUnclassified
Guide to Pharmacology 340 5 1 5 3.1 COc1cc(N)c(cc1C(=O)OCCN1CC(C)CC(C1)C)Cl 10683202
9905972 2528 3 None 1 2 Human 9.4 pKi None 9.4 Binding
UnclassifiedUnclassified
Guide to Pharmacology 340 5 1 5 3.1 COc1cc(N)c(cc1C(=O)OCCN1CC(C)CC(C1)C)Cl 10821780
9905972 2528 3 None 1 2 Human 9.4 pKi None 9.4 Binding
UnclassifiedUnclassified
Guide to Pharmacology 340 5 1 5 3.1 COc1cc(N)c(cc1C(=O)OCCN1CC(C)CC(C1)C)Cl 11030734
9905972 2528 3 None 1 2 Human 9.4 pKi None 9.4 Binding
UnclassifiedUnclassified
Guide to Pharmacology 340 5 1 5 3.1 COc1cc(N)c(cc1C(=O)OCCN1CC(C)CC(C1)C)Cl 15466450
9905972 2528 3 None 1 2 Human 9.4 pKi None 9.4 Binding
UnclassifiedUnclassified
Guide to Pharmacology 340 5 1 5 3.1 COc1cc(N)c(cc1C(=O)OCCN1CC(C)CC(C1)C)Cl 9603189
CHEMBL155917 2528 3 None 1 2 Human 9.4 pKi None 9.4 Binding
UnclassifiedUnclassified
Guide to Pharmacology 340 5 1 5 3.1 COc1cc(N)c(cc1C(=O)OCCN1CC(C)CC(C1)C)Cl 10683202
CHEMBL155917 2528 3 None 1 2 Human 9.4 pKi None 9.4 Binding
UnclassifiedUnclassified
Guide to Pharmacology 340 5 1 5 3.1 COc1cc(N)c(cc1C(=O)OCCN1CC(C)CC(C1)C)Cl 10821780
CHEMBL155917 2528 3 None 1 2 Human 9.4 pKi None 9.4 Binding
UnclassifiedUnclassified
Guide to Pharmacology 340 5 1 5 3.1 COc1cc(N)c(cc1C(=O)OCCN1CC(C)CC(C1)C)Cl 11030734
CHEMBL155917 2528 3 None 1 2 Human 9.4 pKi None 9.4 Binding
UnclassifiedUnclassified
Guide to Pharmacology 340 5 1 5 3.1 COc1cc(N)c(cc1C(=O)OCCN1CC(C)CC(C1)C)Cl 15466450
CHEMBL155917 2528 3 None 1 2 Human 9.4 pKi None 9.4 Binding
UnclassifiedUnclassified
Guide to Pharmacology 340 5 1 5 3.1 COc1cc(N)c(cc1C(=O)OCCN1CC(C)CC(C1)C)Cl 9603189
10404587 3338 3 None - 1 Mouse 9.5 pKi None 9.5 Binding
UnclassifiedUnclassified
Guide to Pharmacology 333 6 0 5 3.1 CCCCN1CCC(CC1)COC(=O)c1cccc2c1OCCO2 11976337
251 3338 3 None - 1 Mouse 9.5 pKi None 9.5 Binding
UnclassifiedUnclassified
Guide to Pharmacology 333 6 0 5 3.1 CCCCN1CCC(CC1)COC(=O)c1cccc2c1OCCO2 11976337
CHEMBL130040 3338 3 None - 1 Mouse 9.5 pKi None 9.5 Binding
UnclassifiedUnclassified
Guide to Pharmacology 333 6 0 5 3.1 CCCCN1CCC(CC1)COC(=O)c1cccc2c1OCCO2 11976337
177336 3071 45 None 6 3 Human 9.6 pKi None 9.6 Binding
UnclassifiedUnclassified
Guide to Pharmacology 369 6 1 4 3.7 CCCCN1CCC(CC1)CNC(=O)c1c2OCCCn2c2c1cccc2 11504648
177336 3071 45 None 6 3 Human 9.6 pKi None 9.6 Binding
UnclassifiedUnclassified
Guide to Pharmacology 369 6 1 4 3.7 CCCCN1CCC(CC1)CNC(=O)c1c2OCCCn2c2c1cccc2 15466450
177336 3071 45 None 6 3 Human 9.6 pKi None 9.6 Binding
UnclassifiedUnclassified
Guide to Pharmacology 369 6 1 4 3.7 CCCCN1CCC(CC1)CNC(=O)c1c2OCCCn2c2c1cccc2 9351641
225 3071 45 None 6 3 Human 9.6 pKi None 9.6 Binding
UnclassifiedUnclassified
Guide to Pharmacology 369 6 1 4 3.7 CCCCN1CCC(CC1)CNC(=O)c1c2OCCCn2c2c1cccc2 11504648
225 3071 45 None 6 3 Human 9.6 pKi None 9.6 Binding
UnclassifiedUnclassified
Guide to Pharmacology 369 6 1 4 3.7 CCCCN1CCC(CC1)CNC(=O)c1c2OCCCn2c2c1cccc2 15466450
225 3071 45 None 6 3 Human 9.6 pKi None 9.6 Binding
UnclassifiedUnclassified
Guide to Pharmacology 369 6 1 4 3.7 CCCCN1CCC(CC1)CNC(=O)c1c2OCCCn2c2c1cccc2 9351641
CHEMBL356359 3071 45 None 6 3 Human 9.6 pKi None 9.6 Binding
UnclassifiedUnclassified
Guide to Pharmacology 369 6 1 4 3.7 CCCCN1CCC(CC1)CNC(=O)c1c2OCCCn2c2c1cccc2 11504648
CHEMBL356359 3071 45 None 6 3 Human 9.6 pKi None 9.6 Binding
UnclassifiedUnclassified
Guide to Pharmacology 369 6 1 4 3.7 CCCCN1CCC(CC1)CNC(=O)c1c2OCCCn2c2c1cccc2 15466450
CHEMBL356359 3071 45 None 6 3 Human 9.6 pKi None 9.6 Binding
UnclassifiedUnclassified
Guide to Pharmacology 369 6 1 4 3.7 CCCCN1CCC(CC1)CNC(=O)c1c2OCCCn2c2c1cccc2 9351641
DB04873 3071 45 None 6 3 Human 9.6 pKi None 9.6 Binding
UnclassifiedUnclassified
Guide to Pharmacology 369 6 1 4 3.7 CCCCN1CCC(CC1)CNC(=O)c1c2OCCCn2c2c1cccc2 11504648
DB04873 3071 45 None 6 3 Human 9.6 pKi None 9.6 Binding
UnclassifiedUnclassified
Guide to Pharmacology 369 6 1 4 3.7 CCCCN1CCC(CC1)CNC(=O)c1c2OCCCn2c2c1cccc2 15466450
DB04873 3071 45 None 6 3 Human 9.6 pKi None 9.6 Binding
UnclassifiedUnclassified
Guide to Pharmacology 369 6 1 4 3.7 CCCCN1CCC(CC1)CNC(=O)c1c2OCCCn2c2c1cccc2 9351641
119376 1811 41 None -1 26 Mouse 9.7 pKi None 9.7 Binding
UnclassifiedUnclassified
Guide to Pharmacology 393 7 1 6 1.6 O=C(c1cn(c2c1cccc2)C)OCC1CCN(CC1)CCNS(=O)(=O)C 8946946
247 1811 41 None -1 26 Mouse 9.7 pKi None 9.7 Binding
UnclassifiedUnclassified
Guide to Pharmacology 393 7 1 6 1.6 O=C(c1cn(c2c1cccc2)C)OCC1CCN(CC1)CCNS(=O)(=O)C 8946946
CHEMBL33884 1811 41 None -1 26 Mouse 9.7 pKi None 9.7 Binding
UnclassifiedUnclassified
Guide to Pharmacology 393 7 1 6 1.6 O=C(c1cn(c2c1cccc2)C)OCC1CCN(CC1)CCNS(=O)(=O)C 8946946