Multicomponent reactions as a privileged tool for multitarget-directed ligand strategies in Alzheimer's disease therapy

被引:3
|
作者
Grosjean, Sylvain [1 ]
Pachon-Angona, Irene [1 ,2 ]
Dawra, Michella [1 ]
Refouvelet, Bernard [1 ]
Ismaili, Lhassane [1 ]
机构
[1] Univ Bourgogne Franche Comte, Lab Rech Integrat Neurosci & Psychol Cognit UR LI, UFR Sante, Grp Chim Medicinale, 19 Rue Ambroise Pare, F-25000 Besancon, France
[2] Swiss Fed Inst Technol, Inst Pharmaceut Sci Comp Assisted Drug Design, Vladimir Prelog Weg 1-5-10, CH-8093 Zurich, Switzerland
关键词
Alzheimer's disease; multicomponent reactions; multitarget-directed ligand strategy; ONE-POT SYNTHESIS; BIGINELLI REACTION; BIOLOGICAL-ACTIVITY; EFFICIENT SYNTHESIS; OXIDATIVE STRESS; AMYLOID PEPTIDE; INHIBITORS; DERIVATIVES; ACETYLCHOLINESTERASE; MELATONIN;
D O I
10.4155/fmc-2022-0170
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Among neurodegenerative pathologies affecting the older population, Alzheimer's disease is the most common type of dementia and leads to neurocognitive and behavioral disorders. It is a complex and progressive age-related multifactorial disease characterized by a series of highly interconnected pathophysiological processes. Within the last decade, the multitarget-directed ligand strategy has emerged as a viable approach to developing complex molecules that exhibit several pharmacophores which can target the different enzymes and receptors involved in the pathogenesis of the disease. Herein, we focus on using multicomponent reactions such as Hantzsch, Biginelli and Ugi to develop these biologically active multitopic ligands.
引用
收藏
页码:1583 / 1606
页数:24
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