methylhistaprodifen


SMILES CNCCc1cnc([nH]1)CCC(c1ccccc1)c1ccccc1
InChIKey YMVWDVNGNLXSKR-UHFFFAOYSA-N

Chemical properties

Hydrogen bond acceptors 2
Hydrogen bond donors 2
Rotatable bonds 8
Molecular weight (Da) 319.2

Drug properties

Molecular type Small molecule
Physiological/Surrogate Surrogate
Approved drug No

Database connections

Ligand site mutations H1

Bioactivities

Receptor Activity Source
GTP Uniprot Species Family Class Type Min Avg Max Database
H1 HRH1 Rat Histamine A pKd 8.02 8.02 8.02 ChEMBL
β1 B0FL73 Guinea pig Adrenoceptors A pKd 4.84 4.84 4.84 ChEMBL
H1 HRH1 Guinea pig Histamine A pKd 8.75 8.92 9.13 ChEMBL
5-HT1B 5HT1B Human 5-Hydroxytryptamine A pKd 5.09 5.09 5.09 ChEMBL
H1 HRH1 Human Histamine A pKi 6.4 6.4 6.4 Guide to Pharmacology
α1D ADA1D Rat Adrenoceptors A pKd 5.24 5.24 5.24 ChEMBL
Receptor Activity Source
GTP Uniprot Species Family Class Type Min Avg Max Database
H1 HRH1 Rat Histamine A pEC50 6.8 6.8 6.8 ChEMBL
H1 HRH1 Guinea pig Histamine A pEC50 6.31 7.06 7.4 ChEMBL