BDBM33832 (2-methoxyphenyl)-[5-[(phenylmethyl)amino]-3-(3-pyridinyl)-1,2,4-triazol-1-yl]methanone::(2-methoxyphenyl)-[5-[(phenylmethyl)amino]-3-pyridin-3-yl-1,2,4-triazol-1-yl]methanone::MLS000679644::N-benzyl-1-(2-methoxybenzoyl)-3-(3-pyridinyl)-1H-1,2,4-triazol-5-amine::SMR000296887::[5-(benzylamino)-3-(3-pyridyl)-1,2,4-triazol-1-yl]-(2-methoxyphenyl)methanone::[5-(benzylamino)-3-pyridin-3-yl-1,2,4-triazol-1-yl]-(2-methoxyphenyl)methanone::cid_2983598
SMILES COc1ccccc1C(=O)n1nc(nc1NCc1ccccc1)-c1cccnc1
InChI Key InChIKey=SXAWRGSTFBQBIN-UHFFFAOYSA-N
Data 3 IC50
Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB
Found 3 hits for monomerid = 33832
Affinity DataIC50: 4.65nMpH: 7.5 T: 2°CAssay Description:HTS was performed using 217,350 compounds of the MLSCN library individually plated into 10ul 1536 compound plates at a concentration of 2.5 mM each, ...More data for this Ligand-Target Pair
Affinity DataIC50: 7nMAssay Description:Inhibition of human thrombin using S-2238 as chromogenic substrate preincubated for 10 mins followed by substrate addition and measured after 10 mins...More data for this Ligand-Target Pair
Affinity DataIC50: 7.90E+3nMAssay Description:Inhibition of human factor Xa using S-2765 as chromogenic substrate preincubated for 10 mins followed by substrate addition and measured after 10 min...More data for this Ligand-Target Pair