BDBM50510098 CHEMBL4515706

SMILES [#6]-[#8]-c1ccc(\[#6]=[#6]\c2c(-[#6]\[#6]=[#6](\[#6])-[#6])c(-[#8])cc(-[#8])c2-[#6]\[#6]=[#6](\[#6])-[#6])cc1-[#8]

InChI Key InChIKey=YXGUAWGFVSUAKU-UHFFFAOYSA-N

Data  3 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 3 hits for monomerid = 50510098   

TargetProstaglandin G/H synthase 1(Sheep)
Czech Academy of Sciences

Curated by ChEMBL
LigandPNGBDBM50510098(CHEMBL4515706)
Affinity DataIC50: 900nMAssay Description:Inhibition of ram seminal vesicle COX1 assessed as reduction in PGE2 production using arachidonic acid substrate by ELISAMore data for this Ligand-Target Pair
In Depth
Date in BDB:
2/20/2021
Entry Details Article
PubMed
TargetPolyunsaturated fatty acid 5-lipoxygenase(Human)
Czech Academy of Sciences

Curated by ChEMBL
LigandPNGBDBM50510098(CHEMBL4515706)
Affinity DataIC50: 900nMAssay Description:Inhibition of human recombinant 5-LOX assessed as reduction in leukotriene B4 synthesis using arachidonic acid substrate by ELISAMore data for this Ligand-Target Pair
In Depth
Date in BDB:
2/20/2021
Entry Details Article
PubMed
TargetProstaglandin G/H synthase 2(Human)
Czech Academy of Sciences

Curated by ChEMBL
LigandPNGBDBM50510098(CHEMBL4515706)
Affinity DataIC50: 1.47E+4nMAssay Description:Inhibition of human recombinant COX2 assessed as reduction in PGE2 production using arachidonic acid substrate by ELISAMore data for this Ligand-Target Pair
In Depth
Date in BDB:
2/20/2021
Entry Details Article
PubMed