Arylaminopropanone Derivatives as Potential Cholinesterase Inhibitors: Synthesis, Docking Study and Biological Evaluation
作者:Anna Hudcová、Aleš Kroutil、Renata Kubínová、Adriana D. Garro、Lucas J. Gutierrez、Daniel Enriz、Michal Oravec、Jozef Csöllei
DOI:10.3390/molecules25071751
日期:——
acetylcholine is observed are growing worldwide. In the present study, a series of new arylaminopropanone derivatives with N-phenylcarbamate moiety (1–16) were prepared as potential acetylcholinesterase and butyrylcholinesterase inhibitors. In vitro enzyme assays were performed; the results are expressed as a percentage of inhibition and the IC50 values. The inhibitory activities were compared with
观察到乙酰胆碱减少的神经退行性疾病正在世界范围内增加。在本研究中,制备了一系列具有 N-苯基氨基甲酸酯部分 (1-16) 的新型芳基氨基丙酮衍生物作为潜在的乙酰胆碱酯酶和丁酰胆碱酯酶抑制剂。进行了体外酶分析;结果表示为抑制百分比和 IC50 值。将抑制活性与参考药物加兰他敏和卡巴拉汀进行比较,显示哌啶衍生物 (1-3) 是最有效的。通过使用对接、分子动力学模拟和量子力学计算的组合技术,从分子建模研究中确定了这些化合物的可能作用机制。