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

Data  2 IC50  1 EC50

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
Find this compound or compounds like it in BindingDB:
   Substructure
Similarity at least:  must be >=0.5
Exact match

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

LigandPNGBDBM53469(MLS001209351 | N-[1-(4-Bromo-phenyl)-ethylidene]-N...)
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
In DepthDetails ArticlePubMed
TargetStreptokinase A(Streptococcus pyogenes M1 GAS)
Broad Institute

Curated by PubChem BioAssay
LigandPNGBDBM53469(MLS001209351 | N-[1-(4-Bromo-phenyl)-ethylidene]-N...)
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
In DepthDetails PCBioAssay
TargetUbiquitin carboxyl-terminal hydrolase isozyme L3(Mus musculus (Mouse))
Brigham and Women'S Hospital

LigandPNGBDBM53469(MLS001209351 | N-[1-(4-Bromo-phenyl)-ethylidene]-N...)
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
In DepthDetails ArticlePubMed