BDBM4012 1 H-indole-3-alkanamide deriv. 10u::N-benzyl-4-[2-({3-[3-(benzylcarbamoyl)propyl]-1H-indol-2-yl}disulfanyl)-1H-indol-3-yl]butanamide

SMILES O=C(CCCc1c(SSc2[nH]c3ccccc3c2CCCC(=O)NCc2ccccc2)[nH]c2ccccc12)NCc1ccccc1

InChI Key InChIKey=OHULBTKPWJQBHV-UHFFFAOYSA-N

Data  2 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 2 hits for monomerid = 4012   

TargetTyrosine-protein kinase transforming protein Src(Avian sarcoma virus)
University Of Auckland

LigandPNGBDBM4012(1 H-indole-3-alkanamide deriv. 10u | N-benzyl-4-[2...)
Affinity DataIC50:  1.30E+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
TargetEpidermal growth factor receptor(Homo sapiens (Human))
University Of Auckland

LigandPNGBDBM4012(1 H-indole-3-alkanamide deriv. 10u | N-benzyl-4-[2...)
Affinity DataIC50:  1.00E+5nMpH: 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