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Synthesis and biological evaluation of cajanonic acid A derivatives as potential PPARγ antagonists
Jian-Ta Wang1, Jin-Gang Peng2, Jing Xia2
1State Key Laboratory of Functions and Applications of Medicinal Plants, Guizhou Medical University, Guiyang 550014, China; School of Basic Medical Sciences, Guizhou Medical University, Guiyang 550025, China; Guizhou Provincial Engineering Technology Research Center for Chemical Drug R&D, Guizhou Medical Univeristy, Guiyang 550004, China.
Abstract:
Four series of cajanonic acid A (CAA) derivatives have been designed and synthesized. The newly prepared compounds have been screened for glucose consumption activity in HepG2 cell lines and PPARγ antagonistic activity in HEK293 cell lines. Compound 26g bearing a tetrahydroisoquinolinone scaffold showed the most potent PPARγ antagonistic and hypoglycemic activities. An oral glucose tolerance test (OGTT) was performed and the results further confirmed that 26g was a potent hypoglycemic agent. In addition, the possible binding modes for compound 26g in the PPARγ protein have been investigated in this study.
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