BDBM3998 1 H-indole-3-alkanamide deriv. 10g::N-methoxy-3-[2-({3-[2-(methoxycarbamoyl)ethyl]-1H-indol-2-yl}disulfanyl)-1H-indol-3-yl]propanamide

SMILES CONC(=O)CCc1c(SSc2[nH]c3ccccc3c2CCC(=O)NOC)[nH]c2ccccc12

InChI Key InChIKey=BYVXOMRKIJSLRU-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 = 3998   

TargetEpidermal growth factor receptor(Human)
University of Auckland

LigandPNGBDBM3998(N-methoxy-3-[2-({3-[2-(methoxycarbamoyl)ethyl]-1H-...)
Affinity DataIC50: 6.80E+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 DepthDetails Article
PubMed
TargetTyrosine-protein kinase transforming protein Src(Avian sarcoma virus)
University of Auckland

LigandPNGBDBM3998(N-methoxy-3-[2-({3-[2-(methoxycarbamoyl)ethyl]-1H-...)
Affinity DataIC50: 2.90E+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 Article
PubMed