BDBM4008 1 H-indole-3-alkanamide deriv. 10q::2,2-Dithiobis[N-benzyl-N-(trifluoroacetyl)tryptophanamide]::N-benzyl-3-[2-({3-[2-(benzylcarbamoyl)-2-(2,2,2-trifluoroacetamido)ethyl]-1H-indol-2-yl}disulfanyl)-1H-indol-3-yl]-2-(2,2,2-trifluoroacetamido)propanamide

SMILES FC(F)(F)C(=O)NC(Cc1c(SSc2[nH]c3ccccc3c2CC(NC(=O)C(F)(F)F)C(=O)NCc2ccccc2)[nH]c2ccccc12)C(=O)NCc1ccccc1

InChI Key InChIKey=HPPRVVIEPVVPDV-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 = 4008   

TargetEpidermal growth factor receptor(Human)
University of Auckland

LigandPNGBDBM4008(N-benzyl-3-[2-({3-[2-(benzylcarbamoyl)-2-(2,2,2-tr...)
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 Depth
Date in BDB:
4/20/2005
Entry Details Article
PubMed
TargetTyrosine-protein kinase transforming protein Src(Avian sarcoma virus)
University of Auckland

LigandPNGBDBM4008(N-benzyl-3-[2-({3-[2-(benzylcarbamoyl)-2-(2,2,2-tr...)
Affinity DataIC50: 700nMAssay 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:
4/20/2005
Entry Details Article
PubMed