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环维黄杨星D的结构改造及抗脂质氧化活性研究
引用本文:邓兰,黄衡,徐鸣夏. 环维黄杨星D的结构改造及抗脂质氧化活性研究[J]. 药学学报, 2006, 41(2): 121-124
作者姓名:邓兰  黄衡  徐鸣夏
作者单位:四川大学,华西药学院,四川,成都,610041
摘    要:目的以20或21-氨基甾体化合物为先导化合物,对植物活性单体——环维黄杨星D进行结构改造,以寻求抗脂质氧化活性更强的心脑血管药物。方法根据合理药物设计原理,设计合成目标化合物,并研究其抗脂质氧化活性。结果获得4个环维黄杨星D新衍生物,并经光谱证明了结构。结论采用硫代巴比妥酸(TBA)法测定脂质过氧化物(MDA),结果表明,部分化合物药理效果优于环维黄杨星D。

关 键 词:环维黄杨星D  结构改造  抗脂质氧化
文章编号:0513-4870(2006)02-0121-04
收稿时间:2005-06-01
修稿时间:2005-06-01

Structural modification of cyclovirobuxine D and their inhibition activity on lipid peroxidation
DENG Lan,HUANG Heng,XU Ming-xia. Structural modification of cyclovirobuxine D and their inhibition activity on lipid peroxidation[J]. Acta pharmaceutica Sinica, 2006, 41(2): 121-124
Authors:DENG Lan  HUANG Heng  XU Ming-xia
Affiliation:West China School of Pharmacy, Sichuan University, Chengdu 610041, China
Abstract:Aim To search for compounds through structural modification of cyclovirobuxine D, using 20 or 21-aminosteroids as lead compound for the treatment of cerebrovascular diseases with better lipid peroxidation inhibitory activity. Methods According to rational drug design principle, a series of cyclovirobuxine D analogues were prepared, and their bioactivities were tested. Results Four new compounds were obtained and confirmed by spectra. Conclusion Lipid peroxidation inhibitory effects of cyclovirobuxine D analogues were tested by using TBA method. Some compounds showed better activity than that of cyclovirobuxine D.
Keywords:cyclovirobuxine D   structural modification   lipid peroxidation inhibition
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