BDBM4030 1-methyl-2-{[1-methyl-5-nitro-3-(phenylcarbamoyl)-1H-indol-2-yl]disulfanyl}-5-nitro-N-phenyl-1H-indole-3-carboxamide::dithiobis(1H-indole-3-carboxamide) deriv. 10o

SMILES Cn1c(SSc2c(C(=O)Nc3ccccc3)c3cc(ccc3n2C)[N+]([O-])=O)c(C(=O)Nc2ccccc2)c2cc(ccc12)[N+]([O-])=O

InChI Key InChIKey=MGEHDKGYSLPVOE-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 = 4030   

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

LigandPNGBDBM4030(1-methyl-2-{[1-methyl-5-nitro-3-(phenylcarbamoyl)-...)
Affinity DataIC50:  7.20E+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

LigandPNGBDBM4030(1-methyl-2-{[1-methyl-5-nitro-3-(phenylcarbamoyl)-...)
Affinity DataIC50:  5.00E+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