rimonabant


SMILES Clc1ccc(cc1)c1c(C)c(nn1c1ccc(cc1Cl)Cl)C(=O)NN1CCCCC1
InChIKey JZCPYUJPEARBJL-UHFFFAOYSA-N

Chemical properties

Hydrogen bond acceptors 4
Hydrogen bond donors 1
Rotatable bonds 4
Molecular weight (Da) 462.1

Drug properties

Molecular type Small molecule
Endogenous/Surrogate Surrogate
Approved drug Yes

Bioactivities

Receptor Activity Source
GTP Uniprot Species Family Class Type Min Avg Max Database
5-HT2A 5HT2A Human 5-Hydroxytryptamine A pKi 7.2 7.2 7.2 Guide to Pharmacology
5-HT2B 5HT2B Human 5-Hydroxytryptamine A pKi 7.3 7.95 8.6 Guide to Pharmacology
5-HT2C 5HT2C Human 5-Hydroxytryptamine A pKi 6.9 7.0 7.1 Guide to Pharmacology
5-HT1B 5HT1B Rat 5-Hydroxytryptamine A pKi 6.4 6.4 6.4 ChEMBL
5-HT2B 5HT2B Human 5-Hydroxytryptamine A pKi 7.29 7.29 7.29 ChEMBL
5-HT1A 5HT1A Rat 5-Hydroxytryptamine A pKi 6.19 6.19 6.19 ChEMBL
5-HT6 5HT6R Human 5-Hydroxytryptamine A pKi 6.53 6.53 6.53 ChEMBL
5-HT2C 5HT2C Human 5-Hydroxytryptamine A pKi 6.97 6.97 6.97 ChEMBL
Receptor Activity Source
GTP Uniprot Species Family Class Type Min Avg Max Database
5-HT1B 5HT1B Rat 5-Hydroxytryptamine A pIC50 6.38 6.38 6.38 ChEMBL
5-HT2B 5HT2B Human 5-Hydroxytryptamine A pIC50 7.09 7.09 7.09 ChEMBL
5-HT1A 5HT1A Rat 5-Hydroxytryptamine A pIC50 5.95 5.95 5.95 ChEMBL
5-HT6 5HT6R Human 5-Hydroxytryptamine A pIC50 6.19 6.19 6.19 ChEMBL
5-HT2C 5HT2C Human 5-Hydroxytryptamine A pIC50 6.69 6.69 6.69 ChEMBL