Department of Pharmaceutical Chemistry, School of Pharmacy, Faculty of Health Sciences, Aristotle University of Thessaloniki, 54124 Thessaloniki, Greece.
Molecules. 2023 Jan 21;28(3):1084. doi: 10.3390/molecules28031084.
Alzheimer's disease (AD), a neurodegenerative brain disorder that affects millions of people worldwide, is characterized by memory loss and cognitive decline. Low levels of acetylcholine and abnormal levels of beta-amyloid, T protein aggregation, inflammation, and oxidative stress, have been associated with AD, and therefore, research has been oriented towards the cholinergic system and primarily on acetylcholinesterase (AChE) inhibitors. In this review, we are focusing on the discovery of AChE inhibitors using computer-based modeling and simulation techniques, covering the recent literature from 2018-2022. More specifically, the review discusses the structures of novel, potent acetylcholinesterase inhibitors and their binding mode to AChE, as well as the physicochemical requirements for the design of potential AChE inhibitors.
阿尔茨海默病(AD)是一种神经退行性脑疾病,影响着全球数以百万计的人,其特征是记忆丧失和认知能力下降。乙酰胆碱水平低和β-淀粉样蛋白、T 蛋白聚集、炎症和氧化应激水平异常与 AD 有关,因此,研究方向一直针对胆碱能系统,主要是乙酰胆碱酯酶(AChE)抑制剂。在这篇综述中,我们专注于使用基于计算机的建模和模拟技术发现 AChE 抑制剂,涵盖了 2018-2022 年的最新文献。更具体地说,该综述讨论了新型强效乙酰胆碱酯酶抑制剂的结构及其与 AChE 的结合模式,以及设计潜在 AChE 抑制剂的物理化学要求。