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滇重楼的抗肿瘤活性成分研究
引用本文:王羽,张彦军,高文远,颜璐璐.滇重楼的抗肿瘤活性成分研究[J].中国中药杂志,2007,32(14):1425-1428.
作者姓名:王羽  张彦军  高文远  颜璐璐
作者单位:1. 天津大学,药物科学与技术学院,天津,300072
2. 天津中医药大学,天津,300193
摘    要:目的:研究滇重楼Paris polyphylla Smith var. yunnanensis根茎中具有抗肿瘤作用的活性成分。方法:利用硅胶柱色谱,Sephadex LH-20,反相制备HPLC等手段进行分离纯化,并通过波谱技术进行结构鉴定。采用MTT法对分离到的化合物进行抗肿瘤活性筛选。结果:从醋酸乙酯和正丁醇层中分离得到了6个化合物,鉴定为薯蓣皂苷元-3-O-α-L-呋喃阿拉伯糖基(1→4)-β-D-葡萄糖苷(1)、偏诺皂苷元-3-O-α-L-呋喃阿拉伯糖基(1→4)-β-D-葡萄糖苷(2)、异鼠李素-3-O-β-D-葡萄糖苷(3)、乙基-α-D-呋喃果糖苷(4)、偏诺皂苷元-3-O-α-L-吡喃鼠李糖基(1→4)-[α-L-吡喃鼠李糖基(1→2)]-β-D-葡萄糖苷(5)、偏诺皂苷元-3-O-α-L-吡喃鼠李糖基(1→4)-α-L-吡喃鼠李糖基(1→4)-[α-L-吡喃鼠李糖基(1→2)]-β-D-葡萄糖苷(6)。结论:化合物1~4为首次从滇重楼中分离得到,化合物3和4为首次从重楼属植物中分离得到,化合物5为首次从滇重楼的根茎中分离得到。药理实验表明,化合物1~3,5和6对小鼠肺腺癌细胞LA795都显示出一定的抑制作用,其中化合物5和6最显著。

关 键 词:滇重楼  异鼠李素-3-O-β-D-葡萄糖苷  乙基-α-D-呋喃果糖苷  甾体皂苷  抗肿瘤活性
文章编号:1001-5302(2007)14-1425-04
收稿时间:9/5/2006 12:00:00 AM
修稿时间:2006-09-05

Anti-tumor constituents from Paris polyphylla var. yunnanensis
WANG Yu; ZHANG Yan-jun; GAO Wen-yuan; YAN Lu-lu.Anti-tumor constituents from Paris polyphylla var. yunnanensis[J].China Journal of Chinese Materia Medica,2007,32(14):1425-1428.
Authors:WANG Yu; ZHANG Yan-jun; GAO Wen-yuan; YAN Lu-lu
Institution:1. College of Pharmaceuticals and Biotechnology, Tianjin University, Tianjin 300072, China; 2. Tianjin University of Traditional Chinese Medicine, Tianjin 300193, China
Abstract:OBJECTIVE: To study the anti-tumor active constituents from the rhizome of Paris polyphylla var. yunnanensis. METHOD: The compounds were isolated by column chromatography with silica gel, and purified by Sephadex LH-20 columu chromafography and reverse-phase preparative, HPLC. The structures were identified by spectroscopic methods. The anti-tumor experiment in vitro, the MTT, was used to screen constituents of P. polyphalla var. yunnanensis. RESULT: Six compounds were obtained and their structures were identified as diosgenin-3-O-alpha-L-arabinofuranosyl (1-->4) -beta-D-glycopyranoside (1), pennogenin-3-O-alpha-L-arabino-furanosyl (1-->4)-beta-D-glycopyranoside (2), isorhamn etin-3-O-beta-D-glycopyranoside (3), ethyl-alpha-D-fructofuranoside (4), pennogenin-3-O-alpha-L-rhamnopyranosyl (1-->4)-alpha-L-rhamnopyranosyl (1-->2)]-beta-D-glycopyranoside (5) and pennogenin-3-O-alpha-L-rhamnopyranosyl (1-->4)-alpha-L-rhamnopyranosyl (1-->4)-alpha-L-rhamnopyranosyl (1-->2)]-beta-D-glycopyranoside (6). CONCLUSION: Compounds 1-4 were isolated from this plant for the first time, compounds 3 and 4 was firstly isolated from genus Paris, compound 5 was firstly isolated from the rhizome of this plant. The pharmacological results showed that compounds 1-3, 5 and 6 showed certain inhibition, especially, the activities of compound 5 and 6 were the most significant.
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