BDBM50294012 (E)-3-(2-(6-(Cyclopropylamino)-9H-purin-9-yl)vinyl)-4-methyl-N-(3-(1H-imidazol-1-yl)-5-(trifluoromethyl)phenyl)benzamide::CHEMBL559826::N-(3-(1H-imidazol-1-yl)-5-(trifluoromethyl)phenyl)-3-(2-(6-(cyclopropylamino)-9H-purin-9-yl)vinyl)-4-methylbenzamide

SMILES Cc1ccc(cc1\C=C\n1cnc2c(NC3CC3)ncnc12)C(=O)Nc1cc(cc(c1)C(F)(F)F)-n1ccnc1

InChI Key InChIKey=VPICTYHNLMNLMP-UHFFFAOYSA-N

Data  3 IC50

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
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Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 3 hits for monomerid = 50294012   

TargetProto-oncogene tyrosine-protein kinase Src(Human)
Ariad Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50294012(N-(3-(1H-imidazol-1-yl)-5-(trifluoromethyl)phenyl)...)
Affinity DataIC50: 8.00E+3nMAssay Description:Inhibition of human Src kinase by TR-FRET assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/26/2010
Entry Details Article
PubMed
TargetTyrosine-protein kinase ABL1(Human)
Ariad Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50294012(N-(3-(1H-imidazol-1-yl)-5-(trifluoromethyl)phenyl)...)
Affinity DataIC50: 1.30E+4nMAssay Description:Inhibition of wild type human Abl kinase by TR-FRET assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/26/2010
Entry Details Article
PubMed
TargetTyrosine-protein kinase ABL1(Human)
Ariad Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50294012(N-(3-(1H-imidazol-1-yl)-5-(trifluoromethyl)phenyl)...)
Affinity DataIC50: 13nMAssay Description:Inhibition of wild type human ABL after 1 hr by TR-FRET assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/21/2010
Entry Details Article
PubMed