BDBM4041 1-methyl-2-{[1-methyl-3-(phenylcarbamoyl)-1H-pyrrolo[2,3-b]pyridin-2-yl]disulfanyl}-N-phenyl-1H-pyrrolo[2,3-b]pyridine-3-carboxamide::2,2 -dithiobis(l,3-dihydro-1-methyl-N-phenyl-2H-pyrrolo[2,3-b]pyridme-3-carboxde)::dithiobis(1H-indole-3-carboxamide) deriv. 10z

SMILES Cn1c(SSc2c(C(=O)Nc3ccccc3)c3cccnc3n2C)c(C(=O)Nc2ccccc2)c2cccnc12

InChI Key InChIKey=HCTZFBVISJHBHE-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 = 4041   

TargetEpidermal growth factor receptor(Human)
University of Auckland

LigandPNGBDBM4041(1-methyl-2-{[1-methyl-3-(phenylcarbamoyl)-1H-pyrro...)
Affinity DataIC50: 2.23E+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 DepthDetails Article
PubMed
TargetTyrosine-protein kinase transforming protein Src(Avian sarcoma virus)
University of Auckland

LigandPNGBDBM4041(1-methyl-2-{[1-methyl-3-(phenylcarbamoyl)-1H-pyrro...)
Affinity DataIC50: 5.20E+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 Article
PubMed