Suppr超能文献

新型氨基噻唑-查尔酮类似物:合成、乙酰胆碱酯酶活性评估及计算机模拟分析

Novel Aminothiazole-Chalcone Analogs: Synthesis, Evaluation Acetylcholinesterase Activity, In Silico Analysis.

作者信息

Keçeci Sarıkaya Meryem, Yıldırım Şuheda, Kocyigit Umit M, Ceylan Mustafa, Yırtıcı Ümit, Eyüpoğlu Volkan

机构信息

Faculty of Arts and Science, Tokat Gaziosmanpaşa University, Tokat, Turkey.

Faculty of Pharmacy, Department of Biochemistry, Sivas Cumhuriyet University, Sivas, Turkey.

出版信息

Chem Biodivers. 2025 May;22(5):e202402777. doi: 10.1002/cbdv.202402777. Epub 2025 Jan 5.

Abstract

In this study, novel thiazole-chalcone analogs were synthesized, and their inhibitory effects on acetylcholinesterase (AChE) were examined. In vitro enzyme activity studies were conducted to calculate IC values, which were found to range between 2.55 and 72.78 µM (tacrine IC = 53.31 µM). The K values of the compounds showing the best inhibition (6g and 6e) were calculated and compared to those of the standard substance tacrine. All compounds reduced the AChE activity. Additionally, predictions made with SwissADME indicated that all compounds complied with Lipinski's rules and possessed good oral bioavailability properties, and the inhibitory effects of compounds 6e and 6g on AChE were evaluated using molecular docking and molecular dynamics simulations (100 ns). The results showed that compounds 6e and 6g had strong and stable interactions with AChE.

摘要

在本研究中,合成了新型噻唑-查尔酮类似物,并检测了它们对乙酰胆碱酯酶(AChE)的抑制作用。进行了体外酶活性研究以计算IC值,发现其范围在2.55至72.78 μM之间(他克林IC = 53.31 μM)。计算了表现出最佳抑制作用的化合物(6g和6e)的K值,并与标准物质他克林的K值进行比较。所有化合物均降低了AChE活性。此外,使用SwissADME进行的预测表明,所有化合物均符合Lipinski规则并具有良好的口服生物利用度特性,并且使用分子对接和分子动力学模拟(100 ns)评估了化合物6e和6g对AChE的抑制作用。结果表明,化合物6e和6g与AChE具有强而稳定的相互作用。

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