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. Author manuscript; available in PMC: 2016 Sep 13.
Published in final edited form as: Am J Med Sci. 2016 Feb 23;351(5):513–519. doi: 10.1016/j.amjms.2016.02.030

Figure 1.

Figure 1

(A) Chemical structure of sodium (S)-2-(Z)-(13-(3-pentyl)ureido)-tridec-8(Z)-enamido)succinate, an agonistic orally-active analog of 14,15-epoxyeicosatrienoic acid. (B) Chemical structure of 11-nonyloxy-undec-8(Z)-enoic acid (11,12-ether-EET-8ZE), an analog of 11,12-epoxyeicosatrienoic acid.