Cytotoxic triterpenoid saponins from Lysimachia foenum-graecum

被引:23
|
作者
Dai, Lu-Mei [1 ]
Huang, Ri-Zhen [1 ,2 ]
Zhang, Bin [1 ]
Hua, Jing [1 ]
Wang, Heng-Shan [1 ]
Liang, Dong [1 ]
机构
[1] Guangxi Normal Univ, Sch Chem & Pharmaceut Sci, State Key Lab Chem & Mol Engn Med Resources, Guilin 541004, Peoples R China
[2] Southeast Univ, Sch Chem & Chem Engn, Dept Pharmaceut Engn, Nanjing 211189, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
Lysimachia foenum-graecum; Myrsinaceae; Triterpenoid saponins; Cytotoxic activities; POTENTIAL ANTICANCER AGENTS; IN-VITRO EVALUATION; ARDISIA-MAMILLATA; ACID-DERIVATIVES; CYCLAMEN COUM; DESIGN;
D O I
10.1016/j.phytochem.2017.01.021
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Eleven oleanane-type triterpenoid saponins, foegraecumosides A-K, and eight known ones, were isolated from the aerial parts of Lysimachia foenum-graecum. Their structures were elucidated by spectro-scopic data analyses and chemical methods. All isolated saponins were evaluated for their cytotoxicity against four human cancer cell lines (NCI-H460, MGC-803, HepG2, and T24). Seven saponins containing the aglycone cyclamiretin A exhibited moderate cytotoxicity against all tested human cancer cell lines, with IC50 values of 9.3-24.5 mu M. Simultaneously, the cytotoxic activities of foegraecumosides A and B, lysichriside A, ardisiacrispins A and B, cyclaminorin, and 3-O-alpha-L-rhamnopyranosyl-(1 -> 2)-beta-D-glucopyranosyl-(1 -> 4)-alpha-L-arabinopyranosyl-cyclamiretin A were tested on drug-resistant lung cancer cell lines (A549 and A549/CDDP, respectively). Ardisiacrispin B displayed moderate cytotoxicity against A549/CDDP, with an IC50 value of 8.7 mu M and a resistant factor (RF) of 0.9. (C) 2017 Elsevier Ltd. All rights reserved.
引用
收藏
页码:165 / 174
页数:10
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