BDBM4006 1 H-indole-3-alkanamide deriv. 10o::N-(2-phenylethyl)-3-{2-[(3-{2-[(2-phenylethyl)carbamoyl]ethyl}-1H-indol-2-yl)disulfanyl]-1H-indol-3-yl}propanamide

SMILES O=C(CCc1c(SSc2[nH]c3ccccc3c2CCC(=O)NCCc2ccccc2)[nH]c2ccccc12)NCCc1ccccc1

InChI Key InChIKey=MPGQFAMKTLPOPX-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 = 4006   

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

LigandPNGBDBM4006(N-(2-phenylethyl)-3-{2-[(3-{2-[(2-phenylethyl)carb...)
Affinity DataIC50: 1.40E+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:
4/20/2005
Entry Details Article
PubMed
TargetEpidermal growth factor receptor(Human)
University of Auckland

LigandPNGBDBM4006(N-(2-phenylethyl)-3-{2-[(3-{2-[(2-phenylethyl)carb...)
Affinity DataIC50: 2.40E+4nMpH: 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