Keçeci Sarıkaya Meryem, Yıldırım Şuheda, Kocyigit Umit M, Ceylan Mustafa, Yırtıcı Ümit, Eyüpoğlu Volkan
Faculty of Arts and Science, Tokat Gaziosmanpaşa University, Tokat, Turkey.
Faculty of Pharmacy, Department of Biochemistry, Sivas Cumhuriyet University, Sivas, Turkey.
Chem Biodivers. 2025 May;22(5):e202402777. doi: 10.1002/cbdv.202402777. Epub 2025 Jan 5.
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.
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。