BDBM53449 4-(4-bromophenyl)-2-(o-toluoylamino)-3-thenoic acid::4-(4-bromophenyl)-2-[(2-methylbenzoyl)amino]-3-thiophenecarboxylic acid::4-(4-bromophenyl)-2-[(2-methylbenzoyl)amino]thiophene-3-carboxylic acid::4-(4-bromophenyl)-2-[(2-methylphenyl)carbonylamino]thiophene-3-carboxylic acid::4-(4-bromophenyl)-2-[[(2-methylphenyl)-oxomethyl]amino]-3-thiophenecarboxylic acid::MLS001179267::O-acyl oxime isatin derivative, 1::SMR000475976::cid_1724426
SMILES Cc1ccccc1C(=O)Nc1scc(c1C(O)=O)-c1ccc(Br)cc1
InChI Key InChIKey=OFSBARBUGZRRKM-UHFFFAOYSA-N
Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB
Found 3 hits for monomerid = 53449
TargetUbiquitin carboxyl-terminal hydrolase isozyme L1(Mus musculus (Mouse))
Brigham and Women'S Hospital
Brigham and Women'S Hospital
Affinity DataIC50: 6.00E+3nMpH: 7.6 T: 2°CAssay Description:Inhibition activity and selectivity for UCH-L1 and UCH-L3.More data for this Ligand-Target Pair
Affinity DataEC50: 1.50E+5nMAssay Description:Keywords: Group A streptococcus, GAS, streptokinase, expression, virulence, inhibition, dose response, EC50 Assay Overview: The goal of this assa...More data for this Ligand-Target Pair
TargetUbiquitin carboxyl-terminal hydrolase isozyme L3(Mus musculus (Mouse))
Brigham and Women'S Hospital
Brigham and Women'S Hospital
Affinity DataIC50: 3.20E+4nMpH: 7.6 T: 2°CAssay Description:Inhibition activity and selectivity for UCH-L1 and UCH-L3.More data for this Ligand-Target Pair