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. Author manuscript; available in PMC: 2014 Jun 1.
Published in final edited form as: J Nutr Biochem. 2013 Mar 27;24(6):929–939. doi: 10.1016/j.jnutbio.2013.01.006

Fig. 2.

Fig. 2

Chemical structure of naturally occuring agonists of PPARγ. (A) Representative binding mode of the most stable docked orientation of ligands with PPARγ illustrated in ribbon mode. Ligand poses are generated by AutoDock Vina. Cis-9, trans-11 CLA is in red; trans-10, cis-12 CLA is in magenta; PUA is in blue. (B) c-9,t-11 CLA. (C) t-10,c-12 CLA. (D) 2-D PUA. (E) ABA. (F) 2-CAA. (G) JAA. (H) α-ESA. (I) β-ESA. (J) Butyric acid, a type of SCFA.