Zhongnan Wu, Yubo Zhang, Wen Li, Nenghua Chen, Qianwen Niu, Yingying Li, Qingguo Li, Dan Yang, Yaolan Li, Guocai Wang
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Four new ent-kaurane diterpenes with chiral epoxyangelate moieties, (2'R,3'R)-3α-(2',3'-epoxyangeloyloxy)-kaur-16-en-19-oic acid (1), (2'S,3'S)-3α-(2',3'-epoxyangeloyloxy)-kaur-16-en-19-oic acid (2), (2'S,3'S)-3α-(2',3'-epoxyangeloyloxy)-kaur-16-en-19-oic acid (3) and (2'R,3'S)-3α-(2',3'-epoxyangeloyloxy)-kaur-16-en-19-oic acid (4), along with eight known diterpenes (5-12), were isolated from Wedelia prostrata. The absolute configurations of the new structures were determined by X-ray crystallography, ECD calculations and chemical methods. All compounds were evaluated for their cytotoxicity activities on human HepG-2 cells, with IC50 values of 11.72±0.22 μmol/L to 54.75±1.12 μmol/L.