BDBM50334629 2-(4-p-tolyl-1H-1,2,3-triazol-1-yl)cyclohexanone::CHEMBL1642294

SMILES Cc1ccc(cc1)-c1cn(nn1)C1CCCCC1=O

InChI Key InChIKey=GYLRZQXVSISSMM-UHFFFAOYSA-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 = 50334629   

TargetProto-oncogene tyrosine-protein kinase Src(Human)
Institute of Technology and Science

Curated by ChEMBL
LigandPNGBDBM50334629(2-(4-p-tolyl-1H-1,2,3-triazol-1-yl)cyclohexanone |...)
Affinity DataIC50: 3.39E+4nMAssay Description:Inhibition of c-Src after 60 minsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/22/2011
Entry Details Article
PubMed
TargetCholecystokinin(Human)
Institute of Technology and Science

Curated by ChEMBL
LigandPNGBDBM50334629(2-(4-p-tolyl-1H-1,2,3-triazol-1-yl)cyclohexanone |...)
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of human CckMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/22/2011
Entry Details Article
PubMed
TargetEpidermal growth factor receptor(Human)
Institute of Technology and Science

Curated by ChEMBL
LigandPNGBDBM50334629(2-(4-p-tolyl-1H-1,2,3-triazol-1-yl)cyclohexanone |...)
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of human EGFRMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/22/2011
Entry Details Article
PubMed
TargetTyrosine-protein kinase Lck(Human)
Institute of Technology and Science

Curated by ChEMBL
LigandPNGBDBM50334629(2-(4-p-tolyl-1H-1,2,3-triazol-1-yl)cyclohexanone |...)
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of human activated LckMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/22/2011
Entry Details Article
PubMed