BDBM3927 5-Substituted 1-Phenylbenzimidazole 16::5-[2-(N,N-Dimethylamino)ethoxy]-1-phenylbenzimidazole Dihydrochloride::dimethyl({2-[(1-phenyl-1H-1,3-benzodiazol-5-yl)oxy]ethyl})amine

SMILES CN(C)CCOc1ccc2n(cnc2c1)-c1ccccc1

InChI Key InChIKey=WKHHTMXHSFWCIX-UHFFFAOYSA-N

Data  3 IC50

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

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 3 hits for monomerid = 3927   

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

LigandPNGBDBM3927(5-Substituted 1-Phenylbenzimidazole 16 | 5-[2-(N,N...)
Affinity DataIC50:  1.50E+3nMpH: 7.4 T: 2°CAssay 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

LigandPNGBDBM3927(5-Substituted 1-Phenylbenzimidazole 16 | 5-[2-(N,N...)
Affinity DataIC50:  2.80E+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

LigandPNGBDBM3927(5-Substituted 1-Phenylbenzimidazole 16 | 5-[2-(N,N...)
Affinity DataIC50:  4.50E+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