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首页|期刊导航|重庆医学|6,7,4′-三羟基异黄酮(T2)水溶性衍生物的合成及其对宫颈癌细胞抑制作用的研究

6,7,4′-三羟基异黄酮(T2)水溶性衍生物的合成及其对宫颈癌细胞抑制作用的研究

袁少隆 李蓉

重庆医学2017,Vol.46Issue(1):33-35,39,4.
重庆医学2017,Vol.46Issue(1):33-35,39,4.DOI:10.3969/j.issn.1671-8348.2017.01.005

6,7,4′-三羟基异黄酮(T2)水溶性衍生物的合成及其对宫颈癌细胞抑制作用的研究

Synthesize of water-solubility derivant of 6,7,4′-trihydroxyisoflavone (T2)and study of its inhibition effect on human breast cancer cell proliferation

袁少隆 1李蓉1

作者信息

  • 1. 第三军医大学军事预防医学院防原医学教研室/全军复合伤研究所/创伤、烧伤与复合伤国家重点实验室,重庆 400030
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摘要

Abstract

Objective To synthesize of water-solubility derivant of 6,7,4′- trihydroxyisoflavone(T2 ),to characterize its structure and to evaluate its anti-tumor activity.Methods The sulfonic group(-SO3 H)was grafted to 3'position in loop B of T2 through sulfonation reaction,then strong aqua was added to above production,and obtained a water-solubility elevated compound named T2-SO3 (NH4 )2 through ammoniation.The construction of T2-SO3 (NH4 )2 was characterized by 1 H-NMR,13 C NMR,MS and element analysis.Its activity for killing human breast cancer cells (Hela)was analyzed by CCK-8 assay and flow cytometry.Re-sults The two kinds of water-solubility derivant of T2-SO3 H·2H2 O and T2-SO3 (NH4 )2 were obtained through above methods, and their yield rates were 96% and 75% respectively.The biological experiments showed that the anti-tumor activity of T2-SO3 (NH4 )2 was significantly enhanced.Conclusion Compared to T2,T2-SO3 (NH4 )2 exhibit higher biocompatibility and anti-tumor activity with vast biological application prospect.

关键词

异黄酮类/宫颈肿瘤/异黄酮衍生物/水溶性/磺化反应/抗肿瘤

Key words

isoflavones/uterine cervical neoplasms/derivant of trihydroxyisoflavone/water-solubility/sulfonation reaction/anti-tumor

分类

医药卫生

引用本文复制引用

袁少隆,李蓉..6,7,4′-三羟基异黄酮(T2)水溶性衍生物的合成及其对宫颈癌细胞抑制作用的研究[J].重庆医学,2017,46(1):33-35,39,4.

基金项目

国家自然科学基金资助项目(81172601)。 ()

重庆医学

1671-8348

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