N6-PHENYLADENOSINE


SMILES OC[C@H]1O[C@@H](n2cnc3c(Nc4ccccc4)ncnc32)[C@H](O)[C@@H]1O
InChIKey QVUUUSJUORLECR-XNIJJKJLSA-N

Chemical properties

Hydrogen bond acceptors 9
Hydrogen bond donors 4
Rotatable bonds 4
Molecular weight (Da) 343.1

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
A1 AA1R Rat Adenosine A pKi 7.8 8.35 8.52 ChEMBL
Receptor Activity Source
GTP Uniprot Species Family Class Type Min Avg Max Database
A1 AA1R Chicken Adenosine A pIC50 8.34 8.34 8.34 ChEMBL
Y2 NPY2R Human Neuropeptide Y A pIC50 5.33 5.33 5.33 ChEMBL
Y1 NPY1R Human Neuropeptide Y A pIC50 5.11 5.11 5.11 ChEMBL
A1 AA1R Rat Adenosine A pIC50 8.19 8.34 8.48 ChEMBL
RXFP1 RXFP1 Human Relaxin family peptide A Potency 5.05 5.05 5.05 ChEMBL