BDBM50120136 CHEMBL83008::N*4*-(2-Chloro-6-methyl-phenyl)-imidazo[1,5-a]quinoxaline-4,7-diamine::N4-(2-chloro-6-methylphenyl)imidazo[1,5-a]quinoxaline-4,7-diamine

SMILES Cc1cccc(Cl)c1Nc1nc2cc(N)ccc2n2cncc12

InChI Key InChIKey=VOWKXPVQYBNEJS-UHFFFAOYSA-N

Data  3 IC50

  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 = 50120136   

TargetTyrosine-protein kinase Lck(Human)
Yale University

Curated by ChEMBL
LigandPNGBDBM50120136(N4-(2-chloro-6-methylphenyl)imidazo[1,5-a]quinoxal...)
Affinity DataIC50: 21nMAssay Description:Evaluated for inhibition of human p56 Lck tyrosine kinaseMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/30/2012
Entry Details Article
PubMed
TargetTyrosine-protein kinase Lck(Human)
Yale University

Curated by ChEMBL
LigandPNGBDBM50120136(N4-(2-chloro-6-methylphenyl)imidazo[1,5-a]quinoxal...)
Affinity DataIC50: 21nMAssay Description:50% inhibition of the phosphorylation of an exogenous substrate by human Lck enzyme.More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetTyrosine-protein kinase Lck(Human)
Yale University

Curated by ChEMBL
LigandPNGBDBM50120136(N4-(2-chloro-6-methylphenyl)imidazo[1,5-a]quinoxal...)
Affinity DataIC50: 21nMAssay Description:Inhibition of LckMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/15/2012
Entry Details Article
PubMed