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. Author manuscript; available in PMC: 2012 Sep 1.
Published in final edited form as: Future Med Chem. 2011 Nov;3(15):1909–1934. doi: 10.4155/fmc.11.136

Table 3.

Endogenous lipids, fatty acids and prostaglandin endoperoxide analogs.

Number Compound Structure IC50[μM] Ref.
1 LTC4 graphic file with name nihms338344t1.jpg 5 [26]
2 15-deoxy-Δ12,14-PGJ2 graphic file with name nihms338344t2.jpg 0.3 [73]
3 U-51605 (PGH2 stable analog) graphic file with name nihms338344t3.jpg <10
>100
[73]
[26]
4 U-44069 (PGH2 stable analog) graphic file with name nihms338344t4.jpg NI [26]
5 U-46619 (PGH2 stable analog) graphic file with name nihms338344t5.jpg NI [26]
6 Arachidonic acid graphic file with name nihms338344t6.jpg 0.3 [73]
7 Docosahexaenoic acid graphic file with name nihms338344t7.jpg 0.3 [73]
8 Eicosapentaenoic acid graphic file with name nihms338344t8.jpg 0.3 [73]
9 Palmitic acid graphic file with name nihms338344t9.jpg 2 [73]

Determined by cell-free mPGES-1 activity assays.

NI: No significant inhibition; PGH2: Prostaglandin endoperoxide.