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Ligand source activities (1 row/activity)
Ligands | Receptor | Activity | Chemical information | ||||||||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Common name | GPCRdb ID | Reference ligand | Vendors | Species | Assay Type | Activity Type | Activity Relation | Activity Value | p-value (-log) | Fold selectivity | Tested GPCRs | Assay Description | Source | Mol weight | Rot Bonds | H don | H acc | LogP | Smiles | DOI | |
Ligands | Receptor | Activity | Chemical information | ||||||||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Common name | GPCRdb ID | Reference ligand | Vendors | Species | Assay Type | Activity Type | Activity Relation | Activity Value | p-value (-log) | Fold selectivity | Tested GPCRs | Assay Description | Source | Mol weight | Rot Bonds | H don | H acc | LogP | Smiles | DOI | |
CHEMBL1082389 | 6426 | None | 21 | Human | Binding | IC50 | = | 394.00 | 6.41 | - | 2 | Fluorescence Polarization Assays: In another embodiment, Fluorescence Polarization ("FP") based assays may be used to detect and monitor ligand binding. Fluorescence polarization is a versatile laboratory technique for measuring equilibrium binding, nucleic acid hybridization, and enzymatic activity. Fluorescence polarization assays are homogeneous in that they do not require a separation step such as centrifugation, filtration, chromatography, precipitation, or electrophoresis. These assays are done in real time, directly in solution and do not require an immobilized phase. Polarization values can be measured repeatedly and after the addition of reagents since measuring the polarization is rapid and does not destroy the sample. Generally, this technique can be used to measure polarization values of fluorophores from low picomolar to micromolar levels. | ChEMBL | 415.1 | 7 | 1 | 3 | 4.43 | O=C(O)c1ccc(CN(Cc2ccccc2)S(=O)(=O)c2ccc(Cl)cc2)cc1 | - | |
CHEMBL1323541 | 22276 | None | 5 | Human | Binding | IC50 | = | 6136.00 | 5.21 | - | 1 | Fluorescence Polarization Assays: In another embodiment, Fluorescence Polarization ("FP") based assays may be used to detect and monitor ligand binding. Fluorescence polarization is a versatile laboratory technique for measuring equilibrium binding, nucleic acid hybridization, and enzymatic activity. Fluorescence polarization assays are homogeneous in that they do not require a separation step such as centrifugation, filtration, chromatography, precipitation, or electrophoresis. These assays are done in real time, directly in solution and do not require an immobilized phase. Polarization values can be measured repeatedly and after the addition of reagents since measuring the polarization is rapid and does not destroy the sample. Generally, this technique can be used to measure polarization values of fluorophores from low picomolar to micromolar levels. | ChEMBL | 460.2 | 7 | 2 | 3 | 5.75 | COc1ccc(CN(CC2CCC(C(=O)O)CC2)C(=S)Nc2ccc(C)c(Cl)c2)cc1 | - | |
CHEMBL1326627 | 22623 | None | 5 | Human | Binding | IC50 | = | 8852.00 | 5.05 | - | 1 | Fluorescence Polarization Assays: In another embodiment, Fluorescence Polarization ("FP") based assays may be used to detect and monitor ligand binding. Fluorescence polarization is a versatile laboratory technique for measuring equilibrium binding, nucleic acid hybridization, and enzymatic activity. Fluorescence polarization assays are homogeneous in that they do not require a separation step such as centrifugation, filtration, chromatography, precipitation, or electrophoresis. These assays are done in real time, directly in solution and do not require an immobilized phase. Polarization values can be measured repeatedly and after the addition of reagents since measuring the polarization is rapid and does not destroy the sample. Generally, this technique can be used to measure polarization values of fluorophores from low picomolar to micromolar levels. | ChEMBL | 442.2 | 8 | 2 | 4 | 4.79 | COc1ccc(CN(CC2CCC(C(=O)O)CC2)C(=S)Nc2ccccc2OC)cc1 | - | |
CHEMBL1356858 | 26182 | None | 2 | Human | Binding | IC50 | = | 672.00 | 6.17 | - | 1 | Fluorescence Polarization Assays: In another embodiment, Fluorescence Polarization ("FP") based assays may be used to detect and monitor ligand binding. Fluorescence polarization is a versatile laboratory technique for measuring equilibrium binding, nucleic acid hybridization, and enzymatic activity. Fluorescence polarization assays are homogeneous in that they do not require a separation step such as centrifugation, filtration, chromatography, precipitation, or electrophoresis. These assays are done in real time, directly in solution and do not require an immobilized phase. Polarization values can be measured repeatedly and after the addition of reagents since measuring the polarization is rapid and does not destroy the sample. Generally, this technique can be used to measure polarization values of fluorophores from low picomolar to micromolar levels. | ChEMBL | 449.1 | 8 | 0 | 4 | 4.90 | CCOC(=O)C1CCC(CN(Cc2ccccc2)S(=O)(=O)c2ccc(Cl)cc2)CC1 | - | |
CHEMBL1366449 | 27220 | None | 1 | Human | Binding | IC50 | = | 1006.00 | 6.00 | - | 1 | Fluorescence Polarization Assays: In another embodiment, Fluorescence Polarization ("FP") based assays may be used to detect and monitor ligand binding. Fluorescence polarization is a versatile laboratory technique for measuring equilibrium binding, nucleic acid hybridization, and enzymatic activity. Fluorescence polarization assays are homogeneous in that they do not require a separation step such as centrifugation, filtration, chromatography, precipitation, or electrophoresis. These assays are done in real time, directly in solution and do not require an immobilized phase. Polarization values can be measured repeatedly and after the addition of reagents since measuring the polarization is rapid and does not destroy the sample. Generally, this technique can be used to measure polarization values of fluorophores from low picomolar to micromolar levels. | ChEMBL | 365.1 | 3 | 0 | 9 | -0.71 | Cc1nc(SCC(=O)N2CCOCC2)c2c(=O)n(C)c(=O)n(C)c2n1 | - | |
CHEMBL1395308 | 30740 | None | 5 | Human | Binding | IC50 | = | 12623.00 | 4.90 | - | 1 | Fluorescence Polarization Assays: In another embodiment, Fluorescence Polarization ("FP") based assays may be used to detect and monitor ligand binding. Fluorescence polarization is a versatile laboratory technique for measuring equilibrium binding, nucleic acid hybridization, and enzymatic activity. Fluorescence polarization assays are homogeneous in that they do not require a separation step such as centrifugation, filtration, chromatography, precipitation, or electrophoresis. These assays are done in real time, directly in solution and do not require an immobilized phase. Polarization values can be measured repeatedly and after the addition of reagents since measuring the polarization is rapid and does not destroy the sample. Generally, this technique can be used to measure polarization values of fluorophores from low picomolar to micromolar levels. | ChEMBL | 377.1 | 3 | 1 | 6 | 1.49 | Cc1cc2c(cc1S(=O)(=O)Nc1ccc(F)cc1)n(C)c(=O)c(=O)n2C | - | |
CHEMBL1401915 | 31339 | None | 6 | Human | Binding | IC50 | = | 264.00 | 6.58 | - | 1 | Fluorescence Polarization Assays: In another embodiment, Fluorescence Polarization ("FP") based assays may be used to detect and monitor ligand binding. Fluorescence polarization is a versatile laboratory technique for measuring equilibrium binding, nucleic acid hybridization, and enzymatic activity. Fluorescence polarization assays are homogeneous in that they do not require a separation step such as centrifugation, filtration, chromatography, precipitation, or electrophoresis. These assays are done in real time, directly in solution and do not require an immobilized phase. Polarization values can be measured repeatedly and after the addition of reagents since measuring the polarization is rapid and does not destroy the sample. Generally, this technique can be used to measure polarization values of fluorophores from low picomolar to micromolar levels. | ChEMBL | 389.1 | 3 | 1 | 8 | 0.77 | Cn1c(=O)c2cc(S(=O)(=O)Nc3ccc4c(c3)OCO4)ccc2n(C)c1=O | - | |
CHEMBL1419634 | 33419 | None | 7 | Human | Binding | IC50 | = | 935.00 | 6.03 | - | 2 | Fluorescence Polarization Assays: In another embodiment, Fluorescence Polarization ("FP") based assays may be used to detect and monitor ligand binding. Fluorescence polarization is a versatile laboratory technique for measuring equilibrium binding, nucleic acid hybridization, and enzymatic activity. Fluorescence polarization assays are homogeneous in that they do not require a separation step such as centrifugation, filtration, chromatography, precipitation, or electrophoresis. These assays are done in real time, directly in solution and do not require an immobilized phase. Polarization values can be measured repeatedly and after the addition of reagents since measuring the polarization is rapid and does not destroy the sample. Generally, this technique can be used to measure polarization values of fluorophores from low picomolar to micromolar levels. | ChEMBL | 377.1 | 3 | 1 | 6 | 1.49 | Cc1c(F)cccc1NS(=O)(=O)c1ccc2c(c1)c(=O)n(C)c(=O)n2C | - | |
CHEMBL1419634 | 33419 | None | 7 | Human | Binding | IC50 | = | 935.00 | 6.03 | - | 2 | Fluorescence Polarization Assays: In another embodiment, Fluorescence Polarization ("FP") based assays may be used to detect and monitor ligand binding. Fluorescence polarization is a versatile laboratory technique for measuring equilibrium binding, nucleic acid hybridization, and enzymatic activity. Fluorescence polarization assays are homogeneous in that they do not require a separation step such as centrifugation, filtration, chromatography, precipitation, or electrophoresis. These assays are done in real time, directly in solution and do not require an immobilized phase. Polarization values can be measured repeatedly and after the addition of reagents since measuring the polarization is rapid and does not destroy the sample. Generally, this technique can be used to measure polarization values of fluorophores from low picomolar to micromolar levels. | ChEMBL | 377.1 | 3 | 1 | 6 | 1.49 | Cc1c(F)cccc1NS(=O)(=O)c1ccc2c(c1)c(=O)n(C)c(=O)n2C | - | |
CHEMBL1434982 | 35184 | None | 5 | Human | Binding | IC50 | = | 2344.00 | 5.63 | - | 1 | Fluorescence Polarization Assays: In another embodiment, Fluorescence Polarization ("FP") based assays may be used to detect and monitor ligand binding. Fluorescence polarization is a versatile laboratory technique for measuring equilibrium binding, nucleic acid hybridization, and enzymatic activity. Fluorescence polarization assays are homogeneous in that they do not require a separation step such as centrifugation, filtration, chromatography, precipitation, or electrophoresis. These assays are done in real time, directly in solution and do not require an immobilized phase. Polarization values can be measured repeatedly and after the addition of reagents since measuring the polarization is rapid and does not destroy the sample. Generally, this technique can be used to measure polarization values of fluorophores from low picomolar to micromolar levels. | ChEMBL | 493.1 | 8 | 0 | 4 | 5.01 | CCOC(=O)C1CCC(CN(Cc2ccccc2)S(=O)(=O)c2ccc(Br)cc2)CC1 | - | |
CHEMBL1499181 | 42453 | None | 9 | Human | Binding | IC50 | = | 721.00 | 6.14 | - | 2 | Fluorescence Polarization Assays: In another embodiment, Fluorescence Polarization ("FP") based assays may be used to detect and monitor ligand binding. Fluorescence polarization is a versatile laboratory technique for measuring equilibrium binding, nucleic acid hybridization, and enzymatic activity. Fluorescence polarization assays are homogeneous in that they do not require a separation step such as centrifugation, filtration, chromatography, precipitation, or electrophoresis. These assays are done in real time, directly in solution and do not require an immobilized phase. Polarization values can be measured repeatedly and after the addition of reagents since measuring the polarization is rapid and does not destroy the sample. Generally, this technique can be used to measure polarization values of fluorophores from low picomolar to micromolar levels. | ChEMBL | 391.2 | 4 | 0 | 8 | 0.94 | CCc1nc(SCC(=O)N2CCC(C)CC2)c2c(=O)n(C)c(=O)n(C)c2n1 | - | |
CHEMBL1503512 | 42956 | None | 1 | Human | Binding | IC50 | = | 7710.00 | 5.11 | - | 2 | Fluorescence Polarization Assays: In another embodiment, Fluorescence Polarization ("FP") based assays may be used to detect and monitor ligand binding. Fluorescence polarization is a versatile laboratory technique for measuring equilibrium binding, nucleic acid hybridization, and enzymatic activity. Fluorescence polarization assays are homogeneous in that they do not require a separation step such as centrifugation, filtration, chromatography, precipitation, or electrophoresis. These assays are done in real time, directly in solution and do not require an immobilized phase. Polarization values can be measured repeatedly and after the addition of reagents since measuring the polarization is rapid and does not destroy the sample. Generally, this technique can be used to measure polarization values of fluorophores from low picomolar to micromolar levels. | ChEMBL | 403.1 | 3 | 1 | 8 | 0.81 | Cn1c(=O)c(=O)n(C)c2cc(S(=O)(=O)Nc3ccc4c(c3)OCCO4)ccc21 | - | |
CHEMBL1523162 | 44948 | None | 6 | Human | Binding | IC50 | = | 7740.00 | 5.11 | - | 1 | Fluorescence Polarization Assays: In another embodiment, Fluorescence Polarization ("FP") based assays may be used to detect and monitor ligand binding. Fluorescence polarization is a versatile laboratory technique for measuring equilibrium binding, nucleic acid hybridization, and enzymatic activity. Fluorescence polarization assays are homogeneous in that they do not require a separation step such as centrifugation, filtration, chromatography, precipitation, or electrophoresis. These assays are done in real time, directly in solution and do not require an immobilized phase. Polarization values can be measured repeatedly and after the addition of reagents since measuring the polarization is rapid and does not destroy the sample. Generally, this technique can be used to measure polarization values of fluorophores from low picomolar to micromolar levels. | ChEMBL | 381.1 | 7 | 1 | 3 | 3.78 | O=C(O)c1ccc(S(=O)(=O)N(Cc2ccccc2)Cc2ccccc2)cc1 | - | |
CHEMBL1711155 | 59454 | None | 8 | Human | Binding | IC50 | = | 763.00 | 6.12 | - | 1 | Fluorescence Polarization Assays: In another embodiment, Fluorescence Polarization ("FP") based assays may be used to detect and monitor ligand binding. Fluorescence polarization is a versatile laboratory technique for measuring equilibrium binding, nucleic acid hybridization, and enzymatic activity. Fluorescence polarization assays are homogeneous in that they do not require a separation step such as centrifugation, filtration, chromatography, precipitation, or electrophoresis. These assays are done in real time, directly in solution and do not require an immobilized phase. Polarization values can be measured repeatedly and after the addition of reagents since measuring the polarization is rapid and does not destroy the sample. Generally, this technique can be used to measure polarization values of fluorophores from low picomolar to micromolar levels. | ChEMBL | 450.2 | 5 | 0 | 10 | -0.02 | CCOC(=O)N1CCN(C(=O)CSc2nc(CC)nc3c2c(=O)n(C)c(=O)n3C)CC1 | - | |
CHEMBL1870906 | 67053 | None | 1 | Human | Binding | IC50 | = | 14926.00 | 4.83 | - | 1 | Fluorescence Polarization Assays: In another embodiment, Fluorescence Polarization ("FP") based assays may be used to detect and monitor ligand binding. Fluorescence polarization is a versatile laboratory technique for measuring equilibrium binding, nucleic acid hybridization, and enzymatic activity. Fluorescence polarization assays are homogeneous in that they do not require a separation step such as centrifugation, filtration, chromatography, precipitation, or electrophoresis. These assays are done in real time, directly in solution and do not require an immobilized phase. Polarization values can be measured repeatedly and after the addition of reagents since measuring the polarization is rapid and does not destroy the sample. Generally, this technique can be used to measure polarization values of fluorophores from low picomolar to micromolar levels. | ChEMBL | 458.2 | 6 | 0 | 7 | 1.22 | CCN(C(=O)CN(C)S(=O)(=O)c1ccc2c(c1)n(C)c(=O)c(=O)n2C)c1cccc(C)c1 | - | |
CHEMBL22815 | 85616 | None | 46 | Human | Binding | EC50 | = | 950.00 | 6.02 | - | 1 | Agonist activity at human TAS2R14 transfected in HEK293T cells assessed as IP1 accumulation measured after 150 mins by IP1 accumulation assay | ChEMBL | 247.0 | 3 | 2 | 2 | 3.78 | O=C(O)c1ccccc1Nc1cccc(Cl)c1 | https://dx.doi.org/10.1021/acs.jmedchem.2c01997 | |
CHEMBL3088246 | 103810 | None | 0 | Human | Binding | EC50 | = | 230.00 | 6.64 | - | 1 | Agonist activity at human TAS2R14 transfected in HEK293T cells assessed as IP1 accumulation measured after 150 mins by IP1 accumulation assay | ChEMBL | 359.0 | 3 | 2 | 2 | 4.91 | O=C(O)c1ccccc1Nc1cc(Br)cc(C(F)(F)F)c1 | https://dx.doi.org/10.1021/acs.jmedchem.2c01997 | |
CHEMBL3092263 | 103958 | None | 0 | Human | Binding | IC50 | = | 3470.00 | 5.46 | - | 1 | Fluorescence Polarization Assays: In another embodiment, Fluorescence Polarization ("FP") based assays may be used to detect and monitor ligand binding. Fluorescence polarization is a versatile laboratory technique for measuring equilibrium binding, nucleic acid hybridization, and enzymatic activity. Fluorescence polarization assays are homogeneous in that they do not require a separation step such as centrifugation, filtration, chromatography, precipitation, or electrophoresis. These assays are done in real time, directly in solution and do not require an immobilized phase. Polarization values can be measured repeatedly and after the addition of reagents since measuring the polarization is rapid and does not destroy the sample. Generally, this technique can be used to measure polarization values of fluorophores from low picomolar to micromolar levels. | ChEMBL | 417.2 | 8 | 1 | 4 | 4.17 | COc1ccc(CN(CC2CCCCC2)S(=O)(=O)c2ccc(C(=O)O)cc2)cc1 | - | |
CHEMBL3092287 | 103959 | None | 0 | Human | Binding | IC50 | = | 200.00 | 6.70 | - | 2 | Fluorescence Polarization Assays: In another embodiment, Fluorescence Polarization ("FP") based assays may be used to detect and monitor ligand binding. Fluorescence polarization is a versatile laboratory technique for measuring equilibrium binding, nucleic acid hybridization, and enzymatic activity. Fluorescence polarization assays are homogeneous in that they do not require a separation step such as centrifugation, filtration, chromatography, precipitation, or electrophoresis. These assays are done in real time, directly in solution and do not require an immobilized phase. Polarization values can be measured repeatedly and after the addition of reagents since measuring the polarization is rapid and does not destroy the sample. Generally, this technique can be used to measure polarization values of fluorophores from low picomolar to micromolar levels. | ChEMBL | 411.1 | 8 | 1 | 4 | 3.78 | COc1ccc(CN(Cc2ccccc2)S(=O)(=O)c2ccc(C(=O)O)cc2)cc1 | - | |
CHEMBL3092287 | 103959 | None | 0 | Human | Binding | IC50 | = | 220.00 | 6.66 | - | 2 | Fluorescence Polarization Assays: In another embodiment, Fluorescence Polarization ("FP") based assays may be used to detect and monitor ligand binding. Fluorescence polarization is a versatile laboratory technique for measuring equilibrium binding, nucleic acid hybridization, and enzymatic activity. Fluorescence polarization assays are homogeneous in that they do not require a separation step such as centrifugation, filtration, chromatography, precipitation, or electrophoresis. These assays are done in real time, directly in solution and do not require an immobilized phase. Polarization values can be measured repeatedly and after the addition of reagents since measuring the polarization is rapid and does not destroy the sample. Generally, this technique can be used to measure polarization values of fluorophores from low picomolar to micromolar levels. | ChEMBL | 411.1 | 8 | 1 | 4 | 3.78 | COc1ccc(CN(Cc2ccccc2)S(=O)(=O)c2ccc(C(=O)O)cc2)cc1 | - |
Showing 1 to 20 of 183 entries
Ligands | Receptor | Activity | Chemical information | ||||||||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Common name | GPCRdb ID | Reference ligand | Vendors | Species | Assay Type | Activity Type | Activity Relation | Activity Value | p-value (-log) | Fold selectivity | Tested GPCRs | Assay Description | Source | Mol weight | Rot Bonds | H don | H acc | LogP | Smiles | DOI | |
Ligands | Receptor | Activity | Chemical information | ||||||||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Common name | GPCRdb ID | Reference ligand | Vendors | Species | Assay Type | Activity Type | Activity Relation | Activity Value | p-value (-log) | Fold selectivity | Tested GPCRs | Assay Description | Source | Mol weight | Rot Bonds | H don | H acc | LogP | Smiles | DOI | |
(±)-Equol | 3140 | None | 0 | Human | Functional | pEC50 | = | - | 4.33 | 1 | 2 | Unclassified | Guide to Pharmacology | 242.1 | 1 | 2 | 3 | 2.82 | Oc1ccc(C2COc3cc(O)ccc3C2)cc1 | https://pubmed.ncbi.nlm.nih.gov/21942422 | |
(+/-)-Eriodictyol | 1583 | None | 0 | Human | Functional | pEC50 | = | - | 4.21 | - | 1 | Unclassified | Guide to Pharmacology | 288.1 | 1 | 4 | 6 | 2.22 | O=C1CC(c2ccc(O)c(O)c2)Oc2cc(O)cc(O)c21 | https://pubmed.ncbi.nlm.nih.gov/24117141 | |
(-)-α-thujone | 369 | None | 39 | Human | Functional | pEC50 | = | - | 4.82 | 2 | 2 | Unclassified | Guide to Pharmacology | 152.1 | 1 | 0 | 1 | 2.26 | CC(C)[C@]12CC(=O)[C@H](C)[C@H]1C2 | https://pubmed.ncbi.nlm.nih.gov/15178431 | |
aristolochic acid | 471 | None | 0 | Human | Functional | pEC50 | = | - | 6.31 | -6 | 3 | Unclassified | Guide to Pharmacology | 341.1 | 3 | 1 | 6 | 3.34 | COc1cccc2c1cc([N+](=O)[O-])c1c(C(=O)O)cc3c(c12)OCO3 | https://pubmed.ncbi.nlm.nih.gov/30009876 | |
aristolochic acid | 471 | None | 0 | Human | Functional | pEC50 | = | - | 6.31 | -6 | 3 | Unclassified | Guide to Pharmacology | 341.1 | 3 | 1 | 6 | 3.34 | COc1cccc2c1cc([N+](=O)[O-])c1c(C(=O)O)cc3c(c12)OCO3 | https://pubmed.ncbi.nlm.nih.gov/38776963 | |
compound 28.1 [PMID: 36847646] | 1052 | None | 4 | Human | Functional | pEC50 | = | - | 7.14 | - | 4 | Unclassified | Guide to Pharmacology | 321.1 | 3 | 2 | 6 | 2.73 | Cc1cc(C(F)(F)F)nc(Nc2ccccc2-c2nnn[nH]2)n1 | https://pubmed.ncbi.nlm.nih.gov/36847646 | |
coumestrol | 1171 | None | 0 | Human | Functional | pEC50 | = | - | 3.45 | - | 1 | Unclassified | Guide to Pharmacology | 268.0 | 0 | 2 | 5 | 3.10 | O=c1oc2cc(O)ccc2c2oc3cc(O)ccc3c12 | https://pubmed.ncbi.nlm.nih.gov/21942422 | |
datiscetin | 1326 | None | 0 | Human | Functional | pEC50 | = | - | 5.00 | 4 | 2 | Unclassified | Guide to Pharmacology | 286.0 | 1 | 4 | 6 | 2.28 | O=c1c(O)c(-c2ccccc2O)oc2cc(O)cc(O)c12 | https://pubmed.ncbi.nlm.nih.gov/24117141 | |
eriodictyol chalcone | 1584 | None | 0 | Human | Functional | pEC50 | = | - | 4.39 | - | 1 | Unclassified | Guide to Pharmacology | 288.1 | 3 | 5 | 6 | 2.11 | O=C(/C=C/c1ccc(O)c(O)c1)c1c(O)cc(O)cc1O | https://pubmed.ncbi.nlm.nih.gov/24117141 | |
flufenamic acid | 1656 | None | 64 | Human | Functional | pEC50 | = | - | 6.62 | -1 | 11 | Unclassified | Guide to Pharmacology | 281.1 | 3 | 2 | 2 | 4.15 | O=C(O)c1ccccc1Nc1cccc(C(F)(F)F)c1 | https://pubmed.ncbi.nlm.nih.gov/31236627 | |
flufenamic acid | 1656 | None | 64 | Human | Functional | pEC50 | = | - | 6.62 | -1 | 11 | Unclassified | Guide to Pharmacology | 281.1 | 3 | 2 | 2 | 4.15 | O=C(O)c1ccccc1Nc1cccc(C(F)(F)F)c1 | https://pubmed.ncbi.nlm.nih.gov/38776963 | |
flufenamic acid | 1656 | None | 64 | Human | Functional | pEC50 | = | 6.86 | 8.16 | -1 | 11 | calcium imaging in ransfected human embryonic kidney (HEK)-293T | Drug Central | 281.1 | 3 | 2 | 2 | 4.15 | O=C(O)c1ccccc1Nc1cccc(C(F)(F)F)c1 | - | |
genistein | 1784 | None | 76 | Human | Functional | pEC50 | = | - | 4.19 | -64 | 9 | Unclassified | Guide to Pharmacology | 270.1 | 1 | 3 | 5 | 2.58 | O=c1c(-c2ccc(O)cc2)coc2cc(O)cc(O)c12 | https://pubmed.ncbi.nlm.nih.gov/30009876 | |
homoeriodictyol | 1940 | None | 0 | Human | Functional | pEC50 | = | - | 4.19 | - | 1 | Unclassified | Guide to Pharmacology | 302.1 | 2 | 3 | 6 | 2.52 | COc1cc(C2CC(=O)c3c(O)cc(O)cc3O2)ccc1O | https://pubmed.ncbi.nlm.nih.gov/24117141 | |
isoprenaline | 2091 | None | 34 | Human | Functional | EC50 | = | 4.90 | 8.31 | -63 | 49 | Agonist activity at human TAS2R14 expressed in HEK293T cells co-expressing Galpha15 assessed as increase in intracellular calcium level by Calcium-3 dye based fluorescence assay | ChEMBL | 211.1 | 4 | 4 | 4 | 1.13 | CC(C)NCC(O)c1ccc(O)c(O)c1 | - | |
isoprenaline | 2091 | None | 34 | Human | Functional | pEC50 | = | 8.31 | 8.08 | -63 | 49 | Agonist activity at human TAS2R14 expressed in HEK293T cells co-expressing Galpha15 assessed as increase in intracellular calcium level by Calcium-3 dye based fluorescence assay | Drug Central | 211.1 | 4 | 4 | 4 | 1.13 | CC(C)NCC(O)c1ccc(O)c(O)c1 | - | |
isoprenaline | 2091 | None | 34 | Human | Functional | pEC50 | = | 8.31 | 8.08 | -63 | 49 | Agonist activity at human TAS2R14 expressed in HEK293T cells co-expressing Galpha15 assessed as increase in intracellular calcium level by Calcium-3 dye based fluorescence assay | Drug Central | 211.1 | 4 | 4 | 4 | 1.13 | CC(C)NCC(O)c1ccc(O)c(O)c1 | - | |
lupulone | 2384 | None | 0 | Human | Functional | pIC50 | = | - | 5.89 | - | 1 | Unclassified | Guide to Pharmacology | 414.3 | 9 | 2 | 4 | 6.86 | CC(C)=CCC1=C(O)C(CC=C(C)C)(CC=C(C)C)C(=O)C(C(=O)CC(C)C)=C1O | - | |
luteolin | 2386 | None | 74 | Human | Functional | pEC50 | = | - | 5.22 | 1 | 5 | Unclassified | Guide to Pharmacology | 286.0 | 1 | 4 | 6 | 2.28 | O=c1cc(-c2ccc(O)c(O)c2)oc2cc(O)cc(O)c12 | https://pubmed.ncbi.nlm.nih.gov/24117141 | |
N-octanoyl-L-homoserine lactone | 2850 | None | 0 | Human | Functional | pEC50 | = | - | 4.71 | - | 1 | Unclassified | Guide to Pharmacology | - | - | - | - | - | - | https://pubmed.ncbi.nlm.nih.gov/29799189 |
Showing 1 to 20 of 29 entries