BDBM3954 (5-methoxy-1-phenyl-1H-1,3-benzodiazol-6-yl)methanol::5-Substituted 1-Phenylbenzimidazole 43::6-Hydroxymethyl-5-methoxy-1-phenylbenzimidazole Hydrochloride

SMILES COc1cc2ncn(-c3ccccc3)c2cc1CO

InChI Key InChIKey=LGRRHBCWSVNDAX-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 = 3954   

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

LigandPNGBDBM3954((5-methoxy-1-phenyl-1H-1,3-benzodiazol-6-yl)methan...)
Affinity DataIC50: 370nMAssay 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

LigandPNGBDBM3954((5-methoxy-1-phenyl-1H-1,3-benzodiazol-6-yl)methan...)
Affinity DataIC50: 1.10E+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
TargetProto-oncogene tyrosine-protein kinase Src(Human)
University of Auckland

LigandPNGBDBM3954((5-methoxy-1-phenyl-1H-1,3-benzodiazol-6-yl)methan...)
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