Isolation and Cytotoxic Activity of Selaginellin Derivatives and Biflavonoids from Selaginella tamariscina

被引:66
|
作者
Zhang, Guo-gang [1 ]
Jing, Ying [1 ]
Zhang, Hong-mei [1 ]
Ma, En-long [2 ]
Guan, Jin [3 ]
Xue, Feng-ning [1 ]
Liu, Hong-xia [1 ]
Sun, Xiao-ya [1 ]
机构
[1] Shenyang Pharmaceut Univ, Coll Tradit Chinese Mat Med, Shenyang 110016, Peoples R China
[2] Shenyang Pharmaceut Univ, Sch Life Sci & Biopharmaceut, Shenyang 110016, Peoples R China
[3] Shenyang Inst Chem Technol, Coll Appl Chem, Shenyang, Peoples R China
关键词
Selaginella tamariscina; Selaginellaceae; selaginellin; biflavonoid; cytotoxic activity; NATURAL PIGMENT; PULVINATA; MAXIM;
D O I
10.1055/s-0031-1298175
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Five selaginellin derivatives, including two new selaginellins termed selaginellins M (1) and N (2), and three previously identified compounds, selaginellin (3), selaginellin A (4), and selaginellin C (5), were isolated from the Selaginella tamariscina (Beauv.) Spring plant. In addition, four known biflavonoids, namely neocryptomerin (6), hinokiflavone (7), pulvinatabiflavone (8), and 7''-O-methylamentoflavone (9), were also isolated. The structures of new compounds 1 and 2 were elucidated by spectroscopic analysis. The cytotoxic activity of compounds 1-9 was evaluated against a small panel of human cancer cell lines, including U251 (human glioma cells), HeLa (human cervical carcinoma cells), and MCF-7 (human breast cancer cells). The two new selaginellins, selaginellins M (1) and N (2), showed medium activity against the human cancer cell lines.
引用
收藏
页码:390 / 392
页数:3
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