morin


SMILES Oc1ccc(c(c1)O)c1oc2cc(O)cc(c2c(=O)c1O)O
InChIKey YXOLAZRVSSWPPT-UHFFFAOYSA-N

Chemical properties

Hydrogen bond acceptors 7
Hydrogen bond donors 5
Rotatable bonds 1
Molecular weight (Da) 302.0

Drug properties

Molecular type Small molecule
Physiological/Surrogate Surrogate
Approved drug No

Database connections

Bioactivities

Receptor Activity Source
GTP Uniprot Species Family Class Type Min Avg Max Database
A2A AA2AR Human Adenosine A pKi 4.8 4.8 4.8 Guide to Pharmacology
A1 AA1R Rat Adenosine A pKi 4.9 4.9 4.9 Guide to Pharmacology
A1 AA1R Rat Adenosine A pKi 4.86 4.86 4.86 ChEMBL
A3 AA3R Human Adenosine A pKi 4.47 4.47 4.47 ChEMBL
Receptor Activity Source
GTP Uniprot Species Family Class Type Min Avg Max Database
GPR35 GPR35 Human A orphans A pEC50 4.95 5.42 5.88 ChEMBL
GPR35 GPR35 Human A orphans A pIC50 5.8 5.8 5.8 ChEMBL
M1 ACM1 Rat Acetylcholine (muscarinic) A Potency 7.7 7.7 7.7 ChEMBL