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芒果苷的结构修饰
引用本文:廖洪利,吴秋业,胡宏岗,臧志和,宋丽,杨倩.芒果苷的结构修饰[J].华西药学杂志,2008,23(4).
作者姓名:廖洪利  吴秋业  胡宏岗  臧志和  宋丽  杨倩
作者单位:1. 成都医学院药学院,四川,成都,610083;第二军医大学药学院,上海,200433
2. 第二军医大学药学院,上海,200433
3. 成都医学院药学院,四川,成都,610083
摘    要:目的对芒果苷进行结构修饰,寻求新的抗糖尿病化合物。方法以芒果苷为原料,经烷基化得到一系列3,6,7-O-三取代芒果苷衍生物,并以芒果苷为对照进行体外抗糖尿病活性测试。结果共合成了11个目标化合物,结构均经核磁共振氢谱确证。结论化合物5和11显示出比芒果苷更强的抗糖尿病活性。

关 键 词:芒果苷  结构修饰  抗糖尿病活性

Structure modification of mangiferin
LIAO Hong-li,WU Qiu-ye,HU Hong-gang,ZANG Zhi-he,SONG Li,YANG Qian.Structure modification of mangiferin[J].West China Journal of Pharmaceutical Sciences,2008,23(4).
Authors:LIAO Hong-li  WU Qiu-ye  HU Hong-gang  ZANG Zhi-he  SONG Li  YANG Qian
Abstract:OBJECTIVE In order to look for new antidiabetic compounds,the structure of mangiferin is modified.METHODS Using mangiferin as starting material,a series of 3,6,7-O-trisubstituted derivatives of mangiferin were synthesized,and then their antidiabetic activities were tested in vitro with mangiferin as the control.RESULTS A total of 11 target compounds were synthesized,and their structures were all confirmed by 1HNMR.CONCLUSION Compounds 5 and 11 were shown to have better antidiabetic activities than mangiferin.
Keywords:mangiferin  structure modification  antidiabetic activity
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