BDBM3950 5-Hydroxy-6-methyl-1-phenylbenzimidazole Hydrochloride::5-Substituted 1-Phenylbenzimidazole 39::6-methyl-1-phenyl-1H-1,3-benzodiazol-5-ol

SMILES Cc1cc2n(cnc2cc1O)-c1ccccc1

InChI Key InChIKey=UIFBZRWGJYZWIJ-UHFFFAOYSA-N

Data  3 IC50

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

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 3 hits for monomerid = 3950   

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

LigandPNGBDBM3950(5-Hydroxy-6-methyl-1-phenylbenzimidazole Hydrochlo...)
Affinity DataIC50:  2.50E+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 DepthDetails ArticlePubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
University of Auckland

LigandPNGBDBM3950(5-Hydroxy-6-methyl-1-phenylbenzimidazole Hydrochlo...)
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 DepthDetails ArticlePubMed
TargetFibroblast growth factor receptor 1(Homo sapiens (Human))
University of Auckland

LigandPNGBDBM3950(5-Hydroxy-6-methyl-1-phenylbenzimidazole Hydrochlo...)
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 DepthDetails ArticlePubMed