Suppr超能文献

杂环同前列腺素衍生物的抗氧化、抗炎和抗高血糖活性。

Antioxidant, anti-inflammatory and anti-hyperglycaemic activities of heterocyclic homoprostanoid derivatives.

机构信息

Department of Pharmacology, Manipal College of Pharmaceutical Sciences, Manipal University, Madhav Nagar, Manipal 576 104, Karnataka, India.

出版信息

Bioorg Med Chem. 2011 Jan 1;19(1):384-92. doi: 10.1016/j.bmc.2010.11.016. Epub 2010 Nov 11.

Abstract

A series of 19 heterocyclic homoprostanoids were synthesized from easily available oleic and ricinoleic acids and evaluated for their possible antioxidant, anti-inflammatory and anti-hyperlipidaemic activities. Compounds with thioxo- and oxoimidazole ring (1) and (2) have shown potent antioxidant activity with IC(50) values 0.23±0.09 and 0.41±0.01mM comparable with standard ascorbic acid. Compound (3) with a quinoxaline ring showed maximum inhibition of BSA denaturation at 1mM concentration and comparable with standard diclofenac. Incorporation of electron withdrawing substitutions like chloro- and nitro-groups in the quinoxaline ring has resulted in an increase anti-inflammatory activity. Test compounds (3), (3a) and (3c) showed modest inhibition of DPP-IV in vitro. However, the unsubstituted quinoxaline (3) and substituted quinoxalines (3b and 3c) reduced plasma glucose levels indicating the presence of hypoglycemic activity.

摘要

从易得的油酸和蓖麻油酸合成了一系列 19 种杂环同系前列腺素,并对其可能的抗氧化、抗炎和抗高血脂活性进行了评估。具有硫代和氧代咪唑环的化合物 (1) 和 (2) 表现出很强的抗氧化活性,IC(50) 值分别为 0.23±0.09 和 0.41±0.01mM,与标准抗坏血酸相当。具有喹喔啉环的化合物 (3) 在 1mM 浓度下显示出对 BSA 变性的最大抑制作用,与标准双氯芬酸相当。在喹喔啉环中引入吸电子取代基如氯和硝基,会导致抗炎活性增加。测试化合物 (3)、(3a) 和 (3c) 在体外对 DPP-IV 表现出适度的抑制作用。然而,未取代的喹喔啉 (3) 和取代的喹喔啉 (3b 和 3c) 降低了血浆葡萄糖水平,表明存在降血糖活性。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验