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旱莲皂苷的溶血活性及构效关系研究

The Study on Hemolytic Activities and Structure-Activity Relationships of Eclalbasaponins from Eclipta alba

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【作者】 刘怀叶向荣过七根张炳火

【Author】 LIU Huai;YE Xiangrong;GUO Qigen;ZHANG Binghuo;Affiliated Hospital, Jiujiang University;College of Pharmacy and Life Sciences, Jiujiang University;

【通讯作者】 张炳火;

【机构】 九江学院附属医院九江学院药学与生命科学学院

【摘要】 从旱莲草中分离到7个单体化合物,经波谱数据分析,鉴定为旱莲皂苷eclalbasaponinsⅠ~Ⅵ(缩写为E-Ⅰ~E-Ⅵ)和β-香树素,其中E-Ⅰ~E-Ⅴ有溶血活性,活性强弱依次为E-Ⅱ>E-Ⅳ>E-Ⅴ>E-Ⅰ>E-Ⅲ.构效关系分析结果表明:C-28位的游离羧基对旱莲皂苷的溶血活性强弱至关重要,C-3位葡萄糖基的数量或硫酸酯化对其溶血活性也有影响.

【Abstract】 Seven compounds are isolated from Eclipta alba.These compounds are identified as eclalbasaponins Ⅰ~Ⅵ(abbreviated for E-Ⅰ~E-Ⅵ) and β-amyrin based on the spectral data.Five compounds, namely E-Ⅰ~E-Ⅴ,show hemolytic activities that the decreasing order is E-Ⅱ>E-Ⅳ>E-Ⅴ>E-Ⅰ>E-Ⅲ.Analysis of structure-activity relationships indicates that free carboxyl at C-28 plays a crucial role in the hemolytic activities of eclalbasaponins.Both the amount and the sulfation of the glucosyl at C-3 also influence the hemolytic activities of eclalbasaponins.

【基金】 国家自然科学基金(31660096)资助项目
  • 【文献出处】 江西师范大学学报(自然科学版) ,Journal of Jiangxi Normal University(Natural Science Edition) , 编辑部邮箱 ,2023年06期
  • 【分类号】R285
  • 【下载频次】28
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