Kaur Manjal Sundeep, Kaur Ramandeep, Bhatia Rohit, Kumar Kapil, Singh Virender, Shankar Ravi, Kaur Rupinder, Rawal Ravindra K
Department of Pharmaceutical Chemistry, Indo-Soviet Friendship College of Pharmacy (ISFCP), Moga Punjab-142001, India.
Department of Chemistry, National Institute of Technology (NIT) Jalandhar, 144011 Punjab, India.
Bioorg Chem. 2017 Dec;75:406-423. doi: 10.1016/j.bioorg.2017.10.014. Epub 2017 Oct 23.
In the modern scenario, thiazolidinone scaffold has emerged as a very potent scaffold as per its clinical significance concerned. It has attracted the keen interest of the researchers due to its great diversity in biological activities. Thiazolidinones are the saturated form of thiazole, called thiazolidine with a carbonyl group. The 1,3-thiazolidin-4-ones possess wide range of pharmacological activities such as anti-cancer, anti-diabetic, anti-microbial, anti-viral, anti-inflammatory and anti-convulsant. In the past few years, various newer synthetic approaches have been designed to synthesize diverse scaffolds to explore the various types of biological activities. In this review, an attempt has been made by the authors to summarize various synthetic strategies for thiazolidinone derivatives as well as their biological significance.
在现代情况下,就其临床意义而言,噻唑烷酮骨架已成为一种非常有效的骨架。由于其在生物活性方面具有极大的多样性,它引起了研究人员的浓厚兴趣。噻唑烷酮是噻唑的饱和形式,称为带有羰基的噻唑烷。1,3-噻唑烷-4-酮具有广泛的药理活性,如抗癌、抗糖尿病、抗微生物、抗病毒、抗炎和抗惊厥。在过去几年中,人们设计了各种更新的合成方法来合成不同的骨架,以探索各种类型的生物活性。在这篇综述中,作者试图总结噻唑烷酮衍生物的各种合成策略及其生物学意义。