Natural Product-Inspired Synthesis of Thiazolidine and Thiazolidinone Compounds and their Anticancer Activities

被引:66
|
作者
Zhang, Qiu [2 ]
Zhou, Hongyu
Zhai, Shumei [2 ]
Yan, Bing [1 ,2 ]
机构
[1] St Jude Childrens Res Hosp, Dept Chem Biol & Therapeut, Memphis, TN 38105 USA
[2] Shandong Univ, Sch Chem & Chem Engn, Jinan 250100, Shandong, Peoples R China
基金
美国国家科学基金会;
关键词
Thiazolidine; thiazolidinone; natural products; anticancer; combinatorial library approach; ACTIVATED-RECEPTOR-GAMMA; PROSTATE-CANCER CELLS; SENSITIZES TUMOR-CELLS; HUMAN GASTRIC-CANCER; HUMAN BREAST-CANCER; BIOLOGICAL EVALUATION; COLON-CANCER; LUNG-CANCER; IN-VITRO; ANTIPROLIFERATIVE ACTIVITY;
D O I
10.2174/138161210791208983
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Nature makes many pharmacologically active compounds containing thiazolidine and thiazolidinone scaffolds. These privileged structures have been identified in many random screening assays. Molecules containing these core structures have been designed and synthesized, and they show a broad range of anticancer activities in vitro and in vivo. The combinatorial library approach has been demonstrated to be effective in lead discovery and optimization in order to improve the potency and toxicity of these compounds.
引用
收藏
页码:1826 / 1842
页数:17
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