Target Validation Information
Target ID T14834
Target Name Cytosolic phospholipase A2
Target Type
Discontinued
Drug Potency against Target [3,4''']biflavone Drug Info IC50 = 8420 nM [529028]
[6,4''']biflavone Drug Info IC50 = 11900 nM [529028]
WAY-196025 Drug Info IC50 = 10 nM [529940]
ECOPLADIB Drug Info IC50 = 150 nM [529940]
EFIPLADIB Drug Info IC50 = 40 nM [529940]
4-(2-oxohexadecanamido)butanoic acid Drug Info IC50 = 4400 nM [528680]
ARACHIDONYL TRIFLUOROMETHYLKETONE Drug Info IC50 = 2300 nM [530576]
1-Imidazol-1-yl-3-(4-octylphenoxy)propan-2-one Drug Info IC50 = 500 nM [530576]
[4',4''']-biflavone Drug Info IC50 = 6000 nM [529028]
[6,3''']biflavone Drug Info IC50 = 16800 nM [529028]
AR-C70484XX Drug Info IC50 = 11 nM [530576]
References
Ref 529028Bioorg Med Chem. 2007 Nov 15;15(22):7138-43. Epub 2007 Aug 22.Inhibitory effect of synthetic C-C biflavones on various phospholipase A(2)s activity.
Ref 529028Bioorg Med Chem. 2007 Nov 15;15(22):7138-43. Epub 2007 Aug 22.Inhibitory effect of synthetic C-C biflavones on various phospholipase A(2)s activity.
Ref 529940J Med Chem. 2009 Feb 26;52(4):1156-71.Reactions of functionalized sulfonamides: application to lowering the lipophilicity of cytosolic phospholipase A2alpha inhibitors.
Ref 529940J Med Chem. 2009 Feb 26;52(4):1156-71.Reactions of functionalized sulfonamides: application to lowering the lipophilicity of cytosolic phospholipase A2alpha inhibitors.
Ref 529940J Med Chem. 2009 Feb 26;52(4):1156-71.Reactions of functionalized sulfonamides: application to lowering the lipophilicity of cytosolic phospholipase A2alpha inhibitors.
Ref 528680J Med Chem. 2007 Mar 22;50(6):1380-400. Epub 2007 Feb 17.Discovery of Ecopladib, an indole inhibitor of cytosolic phospholipase A2alpha.
Ref 530576Bioorg Med Chem. 2010 Jan 15;18(2):945-52. Epub 2009 Nov 17.1-Indol-1-yl-propan-2-ones and related heterocyclic compounds as dual inhibitors of cytosolic phospholipase A(2)alpha and fatty acid amidehydrolase.
Ref 530576Bioorg Med Chem. 2010 Jan 15;18(2):945-52. Epub 2009 Nov 17.1-Indol-1-yl-propan-2-ones and related heterocyclic compounds as dual inhibitors of cytosolic phospholipase A(2)alpha and fatty acid amidehydrolase.
Ref 529028Bioorg Med Chem. 2007 Nov 15;15(22):7138-43. Epub 2007 Aug 22.Inhibitory effect of synthetic C-C biflavones on various phospholipase A(2)s activity.
Ref 529028Bioorg Med Chem. 2007 Nov 15;15(22):7138-43. Epub 2007 Aug 22.Inhibitory effect of synthetic C-C biflavones on various phospholipase A(2)s activity.
Ref 530576Bioorg Med Chem. 2010 Jan 15;18(2):945-52. Epub 2009 Nov 17.1-Indol-1-yl-propan-2-ones and related heterocyclic compounds as dual inhibitors of cytosolic phospholipase A(2)alpha and fatty acid amidehydrolase.

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