tropisetron


SMILES CN1[C@@H]2CC[C@H]1C[C@H](C2)OC(=O)c1c[nH]c2c1cccc2
InChIKey ZNRGQMMCGHDTEI-ITGUQSILSA-N

Chemical properties

Hydrogen bond acceptors 3
Hydrogen bond donors 1
Rotatable bonds 2
Molecular weight (Da) 284.2

Drug properties

Molecular type Small molecule
Physiological/Surrogate Surrogate
Approved drug Yes

Bioactivities

Receptor Activity Source
GTP Uniprot Species Family Class Type Min Avg Max Database
5-HT4 5HT4R Human 5-Hydroxytryptamine A pKi 6.3 6.7 7.1 Guide to Pharmacology
5-HT4 5HT4R Rat 5-Hydroxytryptamine A pKi 6.8 6.8 6.8 Guide to Pharmacology
5-HT4 5HT4R Mouse 5-Hydroxytryptamine A pKi 7.1 7.1 7.1 Guide to Pharmacology
5-HT4 5HT4R Rat 5-Hydroxytryptamine A pKi 7.2 7.2 7.2 ChEMBL
5-HT4 5HT4R Human 5-Hydroxytryptamine A pKi 6.7 6.7 6.7 ChEMBL
5-HT4 5HT4R Guinea pig 5-Hydroxytryptamine A pKi 6.9 7.08 7.27 ChEMBL
5-HT4 5HT4R Guinea pig 5-Hydroxytryptamine A pKd 5.7 5.7 5.7 ChEMBL
M5 ACM5 Human Acetylcholine (muscarinic) A pKi 5.61 5.61 5.61 ChEMBL
5-HT1A 5HT1A Human 5-Hydroxytryptamine A pKi 8.28 8.28 8.28 ChEMBL
Receptor Activity Source
GTP Uniprot Species Family Class Type Min Avg Max Database
5-HT4 5HT4R Guinea pig 5-Hydroxytryptamine A pIC50 5.5 6.0 6.49 ChEMBL
M1 ACM1 Rat Acetylcholine (muscarinic) A Potency 5.1 5.22 5.35 ChEMBL
M5 ACM5 Human Acetylcholine (muscarinic) A pIC50 5.46 5.46 5.46 ChEMBL