Taraxastane-type triterpenoids from the medicinal and edible plant Cirsium setosum

被引:15
作者
Lin Peng-Cheng [1 ]
Ji Lin-Lin [2 ]
Zhong Xiang-Jian [2 ]
Li Jin-Jie [2 ]
Wang Xin [2 ]
Shang Xiao-Ya [2 ]
Lin Sheng [3 ,4 ]
机构
[1] Qinghai Univ Nationalities, Coll Pharmaceut Sci, Xining 810000, Qinghai, Peoples R China
[2] Beijing Union Univ, Beiijing Key Lab Bioact Subst & Funct Foods, Beijing 100191, Peoples R China
[3] Chinese Acad Med Sci, State Key Lab Bioact Subst & Funct Nat Med, Inst Mat Med, Beijing 100050, Peoples R China
[4] Peking Union Med Coll, Beijing 100050, Peoples R China
基金
中国国家自然科学基金;
关键词
Cirsium setosum; Taraxastane-type triterpenoid; TNF-alpha secretion inhibitory activity; Cytotoxicity;
D O I
10.1016/S1875-5364(19)30005-6
中图分类号
R [医药、卫生];
学科分类号
10 ;
摘要
Guided by TNF-alpha secretion inhibitory activity assay, four taraxastane-type triterpenoids, including two new ones, 22-oxo-20-taraxasten-3 beta, 30-diol (1) and 22 alpha-hydroxy-20-taraxasten-30 beta, 30-triol (2), have been obtained from an active fraction of the petroleum ether-soluble extract of the the medicinal and edible plant Cirsium setosum. Their structures were elucidated by spectroscopic data and CD data analysis. In the TNF-alpha secretion inhibitory activity assay, compounds 1 and 2 were active with the IC50 of 2.6 and 3.8 mu mol.L-1, respectively. In addition, compounds 1 and 2 showed moderately selective cytotoxicity against the human ovarian cancer (A2780) and colon cancer (HCT-8) cell lines.
引用
收藏
页码:22 / 26
页数:5
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