Kareem Rzgar Tawfeeq, Abedinifar Fahimeh, Mahmood Evan Abdolkareem, Ebadi Abdol Ghaffar, Rajabi Fatemeh, Vessally Esmail
Department of Chemistry, College of Science, University of Bu Ali Sina Hamadan Iran.
School of Chemistry, College of Science, University of Tehran Tehran Iran.
RSC Adv. 2021 Sep 16;11(49):30781-30797. doi: 10.1039/d1ra03718h. eCollection 2021 Sep 14.
Dementia is a term used to define different brain disorders that affect memory, thinking, behavior, and emotion. Alzheimer's disease (AD) is the second cause of dementia that is generated by the death of cholinergic neurons (especially acetylcholine (ACh)), which have a vital role in cognition. Acetylcholinesterase inhibitors (AChEI) affect acetylcholine levels in the brain and are broadly used to treat Alzheimer's. Donepezil, rivastigmine, and galantamine, which are FDA-approved drugs for AD, are cholinesterase inhibitors. In addition, scientists are attempting to develop hybrid molecules and multi-target-directed ligands (MTDLs) that can simultaneously modulate multiple biological targets. This review highlights recent examples of MTDLs and fragment-based strategy in the rational design of new potential AD medications from 2010 onwards.
痴呆症是一个用于定义影响记忆、思维、行为和情感的不同脑部疾病的术语。阿尔茨海默病(AD)是痴呆症的第二大病因,它由胆碱能神经元(尤其是乙酰胆碱(ACh))死亡所致,这些神经元在认知中起着至关重要的作用。乙酰胆碱酯酶抑制剂(AChEI)会影响大脑中的乙酰胆碱水平,被广泛用于治疗阿尔茨海默病。多奈哌齐、卡巴拉汀和加兰他敏是美国食品药品监督管理局(FDA)批准用于治疗AD的药物,它们都是胆碱酯酶抑制剂。此外,科学家们正在尝试开发能够同时调节多个生物靶点的杂合分子和多靶点导向配体(MTDL)。本综述重点介绍了自2010年以来,MTDL和基于片段的策略在合理设计新型潜在AD药物方面的最新实例。