BDBM50279040 CHEMBL4161755

SMILES COc1ccc2n(C(=O)c3ccc(Cl)cc3)c3CC(C)(C)CC(=O)c3c2c1

InChI Key InChIKey=CKMGIAVCGSOXAT-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 = 50279040   

TargetProstaglandin G/H synthase 2(Homo sapiens (Human))
Damanhour University

Curated by ChEMBL
LigandPNGBDBM50279040(CHEMBL4161755)
Affinity DataIC50:  970nMAssay Description:Inhibition of Dexamethasone stimulated transcriptional activity in CHO cells expressing glucocorticoid receptorMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProstaglandin G/H synthase 1/2(RAT)
Damanhour University

Curated by ChEMBL
LigandPNGBDBM50279040(CHEMBL4161755)
Affinity DataIC50:  141nMAssay Description:Binding affinity towards Alpha-1A adrenergic receptor in rat denuded thoracic aortaMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProstaglandin G/H synthase 1/2(Homo sapiens (Human))
Damanhour University

Curated by ChEMBL
LigandPNGBDBM50279040(CHEMBL4161755)
Affinity DataIC50:  50nMAssay Description:Binding affinity towards Alpha-1A adrenergic receptor in rat denuded thoracic aortaMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProstaglandin G/H synthase 1(Homo sapiens (Human))
Damanhour University

Curated by ChEMBL
LigandPNGBDBM50279040(CHEMBL4161755)
Affinity DataIC50:  2.01E+5nMAssay Description:Inhibition of human COX-1 using [14C]-arachidonic acid as substrate preincubated for 5 mins followed by substrate addition measured after 2 mins by t...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed