植物化学
化学
皂甙
草本植物
二维核磁共振波谱
传统医学
质谱法
立体化学
化学结构
色谱法
生物化学
草药
有机化学
医学
病理
替代医学
作者
Victoria L. Challinor,Peter G. Parsons,Sonet Chap,Eve F. White,Joanne T. Blanchfield,R. Lehmann,James J. De Voss
出处
期刊:Steroids
[Elsevier BV]
日期:2012-04-01
卷期号:77 (5): 504-511
被引量:33
标识
DOI:10.1016/j.steroids.2012.01.009
摘要
Phytochemical characterization of a commercial herb sample supplied as Smilax ornata Lem. (sarsaparilla) led to the isolation of five steroidal saponins, including two new furostanol saponins sarsaparilloside B (1) and sarsaparilloside C (2), whose structures were elucidated via a combination of multistage mass spectrometry (MSn), 1D and 2D NMR experiments, and chemical degradation. The previously unreported spectroscopic characterization of sarsaparilloside (3), Δ20(22)-sarsaparilloside (4), and parillin (5) is also provided. The antiproliferative activity of the isolated saponins was compared in six human cell lines derived from different tumor types and one of the structures (2) was particularly active against the HT29 colon tumor cell line.
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