Recent Progress on Synthesis and Aritioance Activity of 4-Th azolidinone

被引：4

作者：

Senkardes, Sevil ^{[1
]}

Kucukguzel, S. G. Guniz ^{[1
]}

机构：

[1] Marmara Univ, Dept Pharmaceut Chem, Fac Pharm, TR-34668 Istanbul, Turkey

来源：

MINI-REVIEWS IN ORGANIC CHEMISTRY | 2016年 / 13卷 / 05期

关键词：

4-Thiazolidinone; anticancer activity; cytotoxic; diflunisal; etodolac; flurbiprofen; synthesis; ONE-POT SYNTHESIS; MICROWAVE-ASSISTED SYNTHESIS; BIOLOGICAL-ACTIVITIES; THIAZOLIDINONE DERIVATIVES; NONNUCLEOSIDE INHIBITORS; HYDRAZIDE DERIVATIVES; ANTIOXIDANT ACTIVITY; MOLECULAR DOCKING; ANTICANCER; 4-THIAZOLIDINONES;

D O I：

10.2174/1570193X13666160826154159

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

4-Thiazolidinones are sulphur analogues of oxazolidines. They are heterocyclic ring systems which have been explored for their antimicrobial, anticancer, anti-HCV, antifungal, anticonvulsant, antituberculosis, and other activities. While some earlier reviews on the biological activities of this ring system have been reported, the present review describes more recent synthetic strategies and medicinal aspects of 4-thiazolidinones as anticancer agents reported during the past few years (2010-2016).

引用

页码：377 / 388

页数：12

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