BDBM50144945 (2R,3R,4R,5R)-2-Hydroxymethyl-4-methoxy-5-(6-methylamino-purin-9-yl)-tetrahydro-furan-3-ol::(2R,3R,4R,5R)-5-(6-amino-9H-purin-9-yl)-2-(hydroxymethyl)-4-methoxy-tetrahydrofuran-3-ol::2'-O-Methyladenosine::CHEMBL73237
SMILES CO[C@@H]1[C@H](O)[C@@H](CO)O[C@H]1n1cnc2c(N)ncnc12
InChI Key InChIKey=FPUGCISOLXNPPC-IOSLPCCCSA-N
Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB
Found 9 hits for monomerid = 50144945
TargetAdenosine receptor A2a(Rattus norvegicus (rat))
National Institute Of Diabetes, Digestive And Kidney Diseases
Curated by PDSP Ki Database
National Institute Of Diabetes, Digestive And Kidney Diseases
Curated by PDSP Ki Database
TargetAdenosine receptor A1(Rattus norvegicus (rat))
National Institute Of Diabetes, Digestive And Kidney Diseases
Curated by PDSP Ki Database
National Institute Of Diabetes, Digestive And Kidney Diseases
Curated by PDSP Ki Database
TargetTransmembrane and immunoglobulin domain-containing 3(RAT)
National Institute Of Diabetes, Digestive And Kidney Diseases
Curated by PDSP Ki Database
National Institute Of Diabetes, Digestive And Kidney Diseases
Curated by PDSP Ki Database
Affinity DataEC50: >3.00E+3nMAssay Description:Agonist activity at human adenosine A1 receptorMore data for this Ligand-Target Pair
Affinity DataIC50: 4.70E+4nMAssay Description:Inhibition HCV NS5B-mediated RNA synthesisMore data for this Ligand-Target Pair
Affinity DataIC50: >3.00E+3nMAssay Description:Antagonist activity at human adenosine A1 receptorMore data for this Ligand-Target Pair
Affinity DataEC50: >5.00E+4nMAssay Description:Inhibition HCV RNA replicationMore data for this Ligand-Target Pair
Affinity DataEC50: >1.00E+5nMAssay Description:Agonist activity at human adenosine A3 receptor after 15 to 30 minsMore data for this Ligand-Target Pair
Affinity DataIC50: 15nMAssay Description:Antagonist activity at human adenosine A3 receptor after 15 to 30 minsMore data for this Ligand-Target Pair