quinpirole


SMILES CCCN1CCC[C@H]2[C@H]1Cc1cn[nH]c1C2
InChIKey FTSUPYGMFAPCFZ-ZWNOBZJWSA-N

Chemical properties

Hydrogen bond acceptors 2
Hydrogen bond donors 1
Rotatable bonds 2
Molecular weight (Da) 219.2

Drug properties

Molecular type Small molecule
Endogenous/Surrogate Surrogate
Approved drug No

Database connections

Ligand site mutations D2 D3 D4

Bioactivities

Receptor Activity Source
GTP Uniprot Species Family Class Type Min Avg Max Database
D1 DRD1 Pig Dopamine A pKi 4.06 4.1 4.14 ChEMBL
D2 DRD2 Bovine Dopamine A pKi 5.59 6.21 7.23 ChEMBL
D3 DRD3 Rat Dopamine A pKi 8.25 8.25 8.25 ChEMBL
D1 DRD1 Human Dopamine A pKi 4.06 5.34 7.2 ChEMBL
D4 DRD4 Human Dopamine A pKi 7.28 8.07 8.74 ChEMBL
D2 DRD2 Rat Dopamine A pKd 5.17 5.5 5.72 ChEMBL
D2 DRD2 Rat Dopamine A pKi 7.2 7.23 7.27 ChEMBL
5-HT2A 5HT2A Human 5-Hydroxytryptamine A pKi 4.6 4.6 4.6 ChEMBL
D3 DRD3 Human Dopamine A pKi 6.38 7.56 9.39 ChEMBL
D2 DRD2 Human Dopamine A pKi 4.51 6.59 8.26 ChEMBL
D4 DRD4 Human Dopamine A pKi 6.91 7.87 9.64 PDSP Ki database
D2 DRD2 Rat Dopamine A pKi 5.11 6.76 8.1 PDSP Ki database
D3 DRD3 Human Dopamine A pKi 7.37 7.76 9.07 PDSP Ki database
5-HT1A 5HT1A Human 5-Hydroxytryptamine A pKi 5.77 5.77 5.77 PDSP Ki database
5-HT1A 5HT1A Human 5-Hydroxytryptamine A pKi 5.8 5.8 5.8 Guide to Pharmacology
5-HT1B 5HT1B Human 5-Hydroxytryptamine A pKi 5.0 5.0 5.0 PDSP Ki database
5-HT1D 5HT1D Human 5-Hydroxytryptamine A pKi 5.0 5.0 5.0 PDSP Ki database
5-HT2A 5HT2A Human 5-Hydroxytryptamine A pKi 5.0 5.25 5.5 Guide to Pharmacology
5-HT2A 5HT2A Human 5-Hydroxytryptamine A pKi 5.0 5.24 5.48 PDSP Ki database
5-HT2B 5HT2B Human 5-Hydroxytryptamine A pKi 5.0 5.75 6.5 Guide to Pharmacology
5-HT2B 5HT2B Human 5-Hydroxytryptamine A pKi 5.0 5.76 6.52 PDSP Ki database
5-HT2C 5HT2C Human 5-Hydroxytryptamine A pKi 5.0 5.25 5.5 Guide to Pharmacology
5-HT2C 5HT2C Human 5-Hydroxytryptamine A pKi 5.0 5.24 5.48 PDSP Ki database
α1B ADA1B Human Adrenoceptors A pKi 5.0 5.0 5.0 PDSP Ki database
α1D ADA1D Human Adrenoceptors A pKi 5.0 5.0 5.0 PDSP Ki database
α2A ADA2A Human Adrenoceptors A pKi 5.0 5.0 5.0 PDSP Ki database
α2B ADA2B Human Adrenoceptors A pKi 5.6 5.6 5.6 PDSP Ki database
α2C ADA2C Human Adrenoceptors A pKi 5.0 5.0 5.0 PDSP Ki database
β1 ADRB1 Human Adrenoceptors A pKi 5.0 5.0 5.0 PDSP Ki database
β2 ADRB2 Human Adrenoceptors A pKi 4.0 4.0 4.0 ChEMBL
β2 ADRB2 Human Adrenoceptors A pKi 5.0 5.0 5.0 PDSP Ki database
D1 DRD1 Human Dopamine A pKi 5.0 5.0 5.0 PDSP Ki database
D2 DRD2 Human Dopamine A pKi 4.9 6.3 7.7 Guide to Pharmacology
D2 DRD2 Human Dopamine A pKi 5.67 6.55 8.55 PDSP Ki database
D3 DRD3 Human Dopamine A pKi 6.4 7.2 8.0 Guide to Pharmacology
H1 HRH1 Guinea pig Histamine A pKi 5.98 5.98 5.98 PDSP Ki database
D4 DRD4 Human Dopamine A pKi 7.5 7.5 7.5 Guide to Pharmacology
D5 DRD5 Human Dopamine A pKi 5.0 5.0 5.0 PDSP Ki database
D3 DRD3 Rat Dopamine A pKi 7.3 7.55 7.8 Guide to Pharmacology
D3 DRD3 Rat Dopamine A pKi 7.33 7.71 8.29 PDSP Ki database
5-HT2C 5HT2C Rat 5-Hydroxytryptamine A pKi 5.0 5.0 5.0 PDSP Ki database
D2 DRD2 Mouse Dopamine A pKi 6.69 6.69 6.69 PDSP Ki database
D1 DRD1 Bovine Dopamine A pKi 5.0 5.0 5.0 PDSP Ki database
D2 DRD2 Dog Dopamine A pKi 8.32 8.32 8.32 PDSP Ki database
D1 DRD1 Rat Dopamine A pKi 6.0 6.0 6.0 PDSP Ki database
D2 DRD2 Rat Dopamine A pKi 5.2 5.2 5.2 Guide to Pharmacology
Receptor Activity Source
GTP Uniprot Species Family Class Type Min Avg Max Database
D3 DRD3 Rat Dopamine A pEC50 7.1 7.93 8.77 ChEMBL
D3 DRD3 Rat Dopamine A pIC50 7.54 7.57 7.6 ChEMBL
D4 DRD4 Human Dopamine A pEC50 7.08 8.02 8.85 ChEMBL
D2 DRD2 Rat Dopamine A pEC50 7.32 7.95 8.66 ChEMBL
D2 DRD2 Rat Dopamine A pIC50 5.32 5.89 7.0 ChEMBL
D3 DRD3 Human Dopamine A pEC50 6.73 8.47 10.01 ChEMBL
D2 DRD2 Human Dopamine A pEC50 5.55 7.51 8.93 ChEMBL
D2 DRD2 Human Dopamine A pIC50 6.33 6.33 6.33 ChEMBL
TSH TSHR Human Glycoprotein hormone A Potency 5.2 5.2 5.2 ChEMBL
M1 ACM1 Rat Acetylcholine (muscarinic) A Potency 5.65 5.65 5.65 ChEMBL