Yang Wen-Chao, Sun Qi, Yu Ning-Xi, Zhu Xiao-Lei, Yang Guang-Fu
Key Laboratory of Pesticide & Chemical Biology, Ministry of Education, College of Chemistry, Central China Normal University, Wuhan 430079, China.
Yao Xue Xue Bao. 2012 Mar;47(3):313-21.
Alzheimer's disease (AD) is a complex neurodegenerative disorder which seriously causes the dementia in elderly people and afflicts millions of people worldwide. Drug discovery for Alzheimer's disease therapy has been a hot research area and a big challenge, in which development of acetylcholinesterase (AChE) inhibitors design was the most active and some AChE inhibitors are commercially available for AD medication already. However, practical using of commercial AChE inhibitors showed their limited usefulness and related adverse effects. Thus, it is extremely urgent to find novel AChE inhibitors with higher potency and less adverse effects. Based on the accurate crystallographic studies about AChE, strategies for multi-binding site AChE inhibitors have been formed, followed by design of the multi-target directed ligands. In this review, the structures and binding modes of commercial AChE inhibitors were briefly discussed, together with the development of AChE inhibitor design for AD therapy: from multi-binding site inhibitors to multi-target directed ligands.
阿尔茨海默病(AD)是一种复杂的神经退行性疾病,严重导致老年人痴呆,困扰着全球数百万人。用于阿尔茨海默病治疗的药物研发一直是一个热门研究领域且极具挑战性,其中乙酰胆碱酯酶(AChE)抑制剂的设计发展最为活跃,一些AChE抑制剂已在市场上用于AD药物治疗。然而,商业AChE抑制剂的实际应用显示出其效用有限且存在相关不良反应。因此,寻找具有更高效力和更少不良反应的新型AChE抑制剂迫在眉睫。基于对AChE的精确晶体学研究,已形成了多结合位点AChE抑制剂的策略,随后设计了多靶点导向配体。在本综述中,简要讨论了商业AChE抑制剂的结构和结合模式,以及用于AD治疗的AChE抑制剂设计的发展:从多结合位点抑制剂到多靶点导向配体。