BDBM3952 5-Hydroxy-1-phenylbenzimidazole-6-carboxylic Acid::5-Substituted 1-Phenylbenzimidazole 41::5-hydroxy-1-phenyl-1H-1,3-benzodiazole-6-carboxylic acid

SMILES OC(=O)c1cc2n(cnc2cc1O)-c1ccccc1

InChI Key InChIKey=FVMWOYILISEIBR-UHFFFAOYSA-N

Data  3 IC50

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
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Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 3 hits for monomerid = 3952   

TargetPlatelet-derived growth factor receptor beta(Human)
University of Auckland

LigandPNGBDBM3952(5-hydroxy-1-phenyl-1H-1,3-benzodiazole-6-carboxyli...)
Affinity DataIC50: 4.30E+3nMAssay Description:IC50 is the inhibitor concentration which inhibits 50% of kinase activity that catalyzes the transfer of the terminal phosphate from [gamma-32P] labe...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/29/2005
Entry Details Article
PubMed
TargetFibroblast growth factor receptor 1(Human)
University of Auckland

LigandPNGBDBM3952(5-hydroxy-1-phenyl-1H-1,3-benzodiazole-6-carboxyli...)
Affinity DataIC50: 2.20E+4nMAssay Description:IC50 is the inhibitor concentration which inhibits 50% of kinase activity that catalyzes the transfer of the terminal phosphate from [gamma-32P] labe...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/29/2005
Entry Details Article
PubMed
TargetProto-oncogene tyrosine-protein kinase Src(Human)
University of Auckland

LigandPNGBDBM3952(5-hydroxy-1-phenyl-1H-1,3-benzodiazole-6-carboxyli...)
Affinity DataIC50: 3.35E+4nMAssay Description:IC50 is the inhibitor concentration which inhibits 50% of kinase activity that catalyzes the transfer of the terminal phosphate from [gamma-32P] labe...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/29/2005
Entry Details Article
PubMed