Donepezil-based multi-functional cholinesterase inhibitors for treatment of Alzheimer's disease

被引:166
作者
Li, Qi [1 ]
He, Siyu [1 ]
Chen, Yao [2 ]
Feng, Feng [3 ]
Qu, Wei [3 ]
Sun, Haopeng [1 ]
机构
[1] China Pharmaceut Univ, Dept Med Chem, Nanjing 210009, Jiangsu, Peoples R China
[2] Nanjing Univ Chinese Med, Sch Pharm, Nanjing 210023, Jiangsu, Peoples R China
[3] China Pharmaceut Univ, Dept Nat Med Chem, Nanjing 210009, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
Alzheimer's disease; Donepezil; Multi-target-directed ligands (MTDLs); TARGET-DIRECTED LIGANDS; MONOAMINE-OXIDASE-B; NICOTINIC ACETYLCHOLINE-RECEPTORS; BETA-AMYLOID AGGREGATION; FERULIC ACID HYBRIDS; BIOLOGICAL EVALUATION; BUTYRYLCHOLINESTERASE INHIBITORS; CAREGIVER BURDEN; IN-VITRO; ISOINDOLINE-1,3-DIONE DERIVATIVES;
D O I
10.1016/j.ejmech.2018.09.031
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Alzheimer's disease (AD) is one of the most common neurodegenerative disorders in elderly people. Considering the multifactorial nature of AD, the concept of multi-target-directed ligands (MTDLs) has recently emerged as a new strategy for designing therapeutic agents on AD. MTDLs are confirmed to simultaneously affect diverse targets which contribute to etiology of AD. As the most potent approved drug, donepezil affects various events of AD, like inhibiting cholinesterases activities, anti-A beta aggregation, anti-oxidative stress et al. Modifications of donepezil or hybrids with pharmacophores of donepezil in recent five years are summarized in this article. On the basis of case studies, our concerns and opinions about development of donepezil derivatives, designing of MTDLs, and perspectives for AD treatments are discussed in final part. (C) 2018 Elsevier Masson SAS. All rights reserved.
引用
收藏
页码:463 / 477
页数:15
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