ML 10302


SMILES COc1cc(N)c(cc1C(=O)OCCN1CCCCC1)Cl
InChIKey RVFIAQAAZUEPPE-UHFFFAOYSA-N

Chemical properties

Hydrogen bond acceptors 5
Hydrogen bond donors 1
Rotatable bonds 5
Molecular weight (Da) 312.1

Drug properties

Molecular type Small molecule
Physiological/Surrogate Surrogate
Approved drug No

Database connections

Ligand site mutations 5-HT4

Bioactivities

Receptor Activity Source
GTP Uniprot Species Family Class Type Min Avg Max Database
5-HT4 5HT4R Human 5-Hydroxytryptamine A pKi 7.9 8.45 9.0 Guide to Pharmacology
5-HT4 5HT4R Rat 5-Hydroxytryptamine A pKi 8.97 8.97 8.97 ChEMBL
5-HT4 5HT4R Human 5-Hydroxytryptamine A pKi 7.97 8.31 9.0 ChEMBL
5-HT4 5HT4R Guinea pig 5-Hydroxytryptamine A pKi 8.22 8.22 8.22 ChEMBL
5-HT4 5HT4R Human 5-Hydroxytryptamine A pKi 8.3 8.3 8.3 PDSP Ki database
Receptor Activity Source
GTP Uniprot Species Family Class Type Min Avg Max Database
5-HT4 5HT4R Rat 5-Hydroxytryptamine A pIC50 8.62 8.62 8.62 ChEMBL
5-HT4 5HT4R Human 5-Hydroxytryptamine A pEC50 7.29 7.86 8.6 ChEMBL
5-HT4 5HT4R Guinea pig 5-Hydroxytryptamine A pEC50 8.4 8.4 8.4 ChEMBL
M1 ACM1 Rat Acetylcholine (muscarinic) A Potency 4.6 4.85 5.1 ChEMBL