噻唑烷:治疗中枢神经系统疾病的有效候选药物

Radhe Shyam Bahare, Swastika Ganguly, Ritesh Agrawal, Subodh Narayan Dikshit
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引用次数: 0

摘要

噻唑烷类是多元分子,具有多种生物活性,还具有抗惊厥和抗抑郁活性。它是一类多样化的杂环化合物。噻唑烷二酮类化合物(TZD)对多种中枢神经系统疾病都有益处。噻唑烷二酮类化合物诱导神经保护作用的重要机制在于防止小胶质细胞活化和细胞因子(导致炎症和趋化因子表达)。在分子水平上,TZDs 还能防止促炎转录因子的激活,并促进受损中枢神经系统的抗氧化机制。本文讨论了重要的 SAR、分子机制和强效生物活性,并特别提到了中枢神经系统。各种研究表明,该分子为设计和发现新的候选药物铺平了道路。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Thiazolidine: A Potent Candidate for Central Nervous Systems Diseases.

Thiazolidines are multifaceted molecules and exhibit varied types of biological activities, and also showed anticonvulsants and antidepressants activity. It is the diversified class of heterocyclic compounds. Thiazolidinediones (TZD) has been shown beneficial action in various CNS diseases. The significant mechanism of TZD-induced neuroprotection useful in prevention of microglial activation and cytokine that is responsible for inflammatory condition and chemokine expression. At the molecular level TZDs were also responsible to prevent the activation of pro-inflammatory transcription factors as well as promoting the anti-oxidant mechanisms in the injured CNS. Important SAR, molecular mechanism and potent biological activities with special references to central nervous system are discussed in this article. Various investigations suggest that this moiety pave the way for design and discovery of new drug candidates.

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