BDBM4002 1 H-indole-3-alkanamide deriv. 10k::2,2 -dithiobis[N-[[4-(methoxycarbonyl)phenyl]methyl]-1H-indole-3-propanamide]::methyl 4-({3-[2-({3-[2-({[4-(methoxycarbonyl)phenyl]methyl}carbamoyl)ethyl]-1H-indol-2-yl}disulfanyl)-1H-indol-3-yl]propanamido}methyl)benzoate

SMILES COC(=O)c1ccc(CNC(=O)CCc2c(SSc3[nH]c4ccccc4c3CCC(=O)NCc3ccc(cc3)C(=O)OC)[nH]c3ccccc23)cc1

InChI Key InChIKey=SEFPCKRFUORUQG-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 = 4002   

TargetEpidermal growth factor receptor(Human)
University of Auckland

LigandPNGBDBM4002(methyl 4-({3-[2-({3-[2-({[4-(methoxycarbonyl)pheny...)
Affinity DataIC50: 4.40E+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
TargetTyrosine-protein kinase transforming protein Src(Avian sarcoma virus)
University of Auckland

LigandPNGBDBM4002(methyl 4-({3-[2-({3-[2-({[4-(methoxycarbonyl)pheny...)
Affinity DataIC50: 1.80E+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 Depth
Date in BDB:
4/20/2005
Entry Details Article
PubMed