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SMILES Cc1cc(-c2ccccc2)n(n1)-c1ccc(cc1)S(C)(=O)=O

InChI Key InChIKey=IYQBBPZGSNHUDK-UHFFFAOYSA-N

  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 3 hits for monomerid = 50110482   

TargetProstaglandin G/H synthase 1(Homo sapiens (Human))
Laboratoires Innothera

Curated by ChEMBL
LigandPNGBDBM50110482(1-(4-Methanesulfonyl-phenyl)-3-methyl-5-phenyl-1H-...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+4nMAssay Description:The compound was evaluated for its inhibitory activity against Prostaglandin G/H synthase 1 using monocytes-like cellsMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q20864MCPubMed
TargetProstaglandin G/H synthase 2(Homo sapiens (Human))
Laboratoires Innothera

Curated by ChEMBL
LigandPNGBDBM50110482(1-(4-Methanesulfonyl-phenyl)-3-methyl-5-phenyl-1H-...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+4nMAssay Description:The compound was evaluated for its inhibitory activity against Prostaglandin G/H synthase 2 using osteosarcomes cellsMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q20864MCPubMed
TargetPolyunsaturated fatty acid 5-lipoxygenase(Homo sapiens (Human))
Laboratoires Innothera

Curated by ChEMBL
LigandPNGBDBM50110482(1-(4-Methanesulfonyl-phenyl)-3-methyl-5-phenyl-1H-...)copy SMILEScopy InChI
Affinity DataIC50: 4.00E+4nMAssay Description:The compound was evaluated for its inhibitory activity against 5-lipoxygenase using granulocytes-type cellsMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q20864MCPubMed