BDBM3951 5-Methoxy-1-phenylbenzimidazole-6-carboxylic Acid::5-Substituted 1-Phenylbenzimidazole 40::5-methoxy-1-phenyl-1H-1,3-benzodiazole-6-carboxylic acid

SMILES COc1cc2ncn(-c3ccccc3)c2cc1C(O)=O

InChI Key InChIKey=KUEFIOPBQNNRCA-UHFFFAOYSA-N

Data  3 IC50

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 3 hits for monomerid = 3951   

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

LigandPNGBDBM3951(5-methoxy-1-phenyl-1H-1,3-benzodiazole-6-carboxyli...)
Affinity DataIC50: 2.10E+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
TargetFibroblast growth factor receptor 1(Human)
University of Auckland

LigandPNGBDBM3951(5-methoxy-1-phenyl-1H-1,3-benzodiazole-6-carboxyli...)
Affinity DataIC50: 5.00E+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

LigandPNGBDBM3951(5-methoxy-1-phenyl-1H-1,3-benzodiazole-6-carboxyli...)
Affinity DataIC50: 5.00E+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