BDBM53469 MLS001209351::N-[1-(4-Bromo-phenyl)-ethylidene]-N'-(2-methyl-6-piperidin-1-yl-pyrimidin-4-yl)-hydrazine::N-[1-(4-bromophenyl)ethylideneamino]-2-methyl-6-(1-piperidinyl)-4-pyrimidinamine::N-[1-(4-bromophenyl)ethylideneamino]-2-methyl-6-piperidin-1-yl-pyrimidin-4-amine::N-[1-(4-bromophenyl)ethylideneamino]-2-methyl-6-piperidin-1-ylpyrimidin-4-amine::O-acyl oxime isatin derivative, 52::SMR000513418::[1-(4-bromophenyl)ethylideneamino]-(2-methyl-6-piperidino-pyrimidin-4-yl)amine::cid_3099302
SMILES CC(N=Nc1cc(nc(C)n1)N1CCCCC1)c1ccc(Br)cc1
InChI Key InChIKey=BPMFYJYDZFKDCR-UHFFFAOYSA-N
Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB
Found 3 hits for monomerid = 53469
TargetUbiquitin carboxyl-terminal hydrolase isozyme L1(Mus musculus (Mouse))
Brigham and Women'S Hospital
Brigham and Women'S Hospital
Affinity DataIC50: 2.60E+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: 4.67E+4nMAssay 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: 1.60E+4nMpH: 7.6 T: 2°CAssay Description:Inhibition activity and selectivity for UCH-L1 and UCH-L3.More data for this Ligand-Target Pair