BDBM5171 (2E)-2-[(3,4-dihydroxyphenyl)carbonyl]-3-(1H-indol-3-yl)prop-2-enenitrile::Indole-Containing Inhibitor 5

SMILES Oc1ccc(cc1O)C(=O)C(=C\c1c[nH]c2ccccc12)\C#N

InChI Key InChIKey=TTZDOBVWBQXGDC-KPKJPENVSA-N

Data  4 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 4 hits for monomerid = 5171   

TargetEpidermal growth factor receptor(Homo sapiens (Human))
Hebrew University of Jerusalem

LigandPNGBDBM5171((2E)-2-[(3,4-dihydroxyphenyl)carbonyl]-3-(1H-indol...)
Affinity DataIC50:  3.00E+4nMpH: 7.5 T: 2°CAssay Description:The assay was using Swiss 3T3 cell membranes harboring EGF-R or PDGFR-beta. Receptor autophosphorylation was initiated by addition of [gamma-32P]ATP ...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProtein-tyrosine kinase 6(Homo sapiens (Human))
Yonsei University

Curated by ChEMBL
LigandPNGBDBM5171((2E)-2-[(3,4-dihydroxyphenyl)carbonyl]-3-(1H-indol...)
Affinity DataIC50:  5.32E+4nMAssay Description:Inhibition of PTK6 (unknown origin) expressed in HEK293 cells assessed as decrease in tyrosine phosphorylation by chemiluminescence assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProtein-tyrosine kinase 6(Homo sapiens (Human))
Yonsei University

Curated by ChEMBL
LigandPNGBDBM5171((2E)-2-[(3,4-dihydroxyphenyl)carbonyl]-3-(1H-indol...)
Affinity DataIC50:  2.32E+3nMAssay Description:Inhibition of GST-tagged PTK6 (unknown origin) assessed as phosphorylated tyrosines after 20 mins by ELISAMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPlatelet-derived growth factor receptor beta(Homo sapiens (Human))
Hebrew University of Jerusalem

LigandPNGBDBM5171((2E)-2-[(3,4-dihydroxyphenyl)carbonyl]-3-(1H-indol...)
Affinity DataIC50:  1.00E+3nMAssay Description:The assay was using Swiss 3T3 cell membranes harboring EGF-R or PDGFR-beta. Receptor autophosphorylation was initiated by addition of [gamma-32P]ATP ...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed