BDBM3942 4-Bromo-5-hydroxy-1-phenylbenzimidazole Hydrochloride::4-bromo-1-phenyl-1H-1,3-benzodiazol-5-ol::5-Substituted 1-Phenylbenzimidazole 31

SMILES Oc1ccc2n(cnc2c1Br)-c1ccccc1

InChI Key InChIKey=GYFBHWXMWWQUOF-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 = 3942   

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

LigandChemical structure of BindingDB Monomer ID 3942BDBM3942(4-bromo-1-phenyl-1H-1,3-benzodiazol-5-ol | 4-Bromo...)
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

LigandChemical structure of BindingDB Monomer ID 3942BDBM3942(4-bromo-1-phenyl-1H-1,3-benzodiazol-5-ol | 4-Bromo...)
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
TargetFibroblast growth factor receptor 1(Human)
University of Auckland

LigandChemical structure of BindingDB Monomer ID 3942BDBM3942(4-bromo-1-phenyl-1H-1,3-benzodiazol-5-ol | 4-Bromo...)
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