BDBM50393881 CHEMBL2158244
SMILES Fc1ccc(CSc2ccc3C(=O)NC(=O)c3c2)cc1
InChI Key InChIKey=AOGCOHJURUZUAZ-UHFFFAOYSA-N
Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB
Found 6 hits for monomerid = 50393881
Affinity DataKi: 6.30E+3nMAssay Description:For the A2a receptor binding study, the incubation contained 10 mg of the original tissue weight of the striatal membranes, 4 nM [3H]NECA, 50 nM CPA,...More data for this Ligand-Target Pair
Affinity DataKi: 1.27E+4nMAssay Description:For the A2a receptor binding study, the incubation contained 10 mg of the original tissue weight of the striatal membranes, 4 nM [3H]NECA, 50 nM CPA,...More data for this Ligand-Target Pair
Affinity DataKi: 3.67E+4nMAssay Description:For the A2a receptor binding study, the incubation contained 10 mg of the original tissue weight of the striatal membranes, 4 nM [3H]NECA, 50 nM CPA,...More data for this Ligand-Target Pair
TargetAmine oxidase [flavin-containing] A(Homo sapiens (Human))
North-West University
Curated by ChEMBL
North-West University
Curated by ChEMBL
Affinity DataIC50: 958nMAssay Description:Inhibition of human recombinant MAOA using kynuramine as substrate assessed as formation of 4-hydroxyquinoline after 20 mins by fluorescence spectrop...More data for this Ligand-Target Pair
Affinity DataIC50: 290nMpH: 7.4Assay Description:The enzymatic reactions were carried out at pH 7.4 (K2HPO4/KH2PO4 100 mM, made isotonic with KCl) to a final volume of 500 µL. The reactions containe...More data for this Ligand-Target Pair
Affinity DataIC50: 6.80nMAssay Description:Inhibition of human recombinant MAOB using kynuramine as substrate assessed as formation of 4-hydroxyquinoline after 20 mins by fluorescence spectrop...More data for this Ligand-Target Pair