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Synthesis of (S)-2-Ethoxy-3-Phenylpropanoic Acid Derivatives and Their Insulin-Sensitizing Activity
引用本文:吴英华 夏彬. Synthesis of (S)-2-Ethoxy-3-Phenylpropanoic Acid Derivatives and Their Insulin-Sensitizing Activity[J]. 中国化学, 2007, 25(3): 265-267. DOI: 10.1002/cjoc.200790052
作者姓名:吴英华 夏彬
作者单位:[1]Department of Pharmaceuticals, Huaihua Medical College, Huaihua, Hunan 418000, China [2]College of Chemistry and Environmental Science, Guizhou University for Nationalities, Guiyang, Guizhou 550025, China
基金项目:Project supported by the National Natural Science Foundation of China (No. 30500390) and the Science Foundation of the Hunan Education Department (No. 06B075).
摘    要:A series of (S)-2-ethoxy-3-phenylpropanoic acid derivatives were synthesized and their insulin-sensitizing activities were evaluated in 3T3-L1 cells. Compounds 1b, 1d, 1e and 1f exhibited more potent insulin-sensitizing activity than rosiglitazone.

关 键 词:(S)-2-乙氧基-3-苯基丙酸衍生物 合成 胰岛素敏化活性 2型糖尿病
修稿时间:2006-06-122006-12-05

Synthesis of (S)‐2‐Ethoxy‐3‐Phenylpropanoic Acid Derivatives and Their Insulin‐Sensitizing Activity
WU Ying-Hua, XIA Bing. Synthesis of (S)‐2‐Ethoxy‐3‐Phenylpropanoic Acid Derivatives and Their Insulin‐Sensitizing Activity[J]. Chinese Journal of Chemistry, 2007, 25(3): 265-267. DOI: 10.1002/cjoc.200790052
Authors:WU Ying-Hua   XIA Bing
Affiliation:a.Department of Pharmaceuticals, Huaihua Medical College, Huaihua, Hunan 418000, China ; b. College of Chemistry and Environmental Science, Guizhou University for Nationalities, Guiyang, Guizhou 550025, China
Abstract:A series of (S)‐2‐ethoxy‐3‐phenylpropanoic acid derivatives were synthesized and their insulin‐sensitizing activities were evaluated in 3T3‐L1 cells. Compounds 1b , 1d , 1e and 1f exhibited more potent insulin‐sensitizing activity than rosiglitazone.
Keywords:(S)‐2‐ethoxy‐3‐phenylpropanoic acid derivative  type 2 diabetes  insulin‐sensitizing agent
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