New Insights into the Development of Donepezil-Based Hybrid and Natural Molecules as Multi-Target Drug Agents for Alzheimer's Disease Treatment

被引:0
|
作者
Angelova, Violina T. [1 ]
Stoyanov, Boris P. [2 ]
Simeonova, Rumyana [2 ]
机构
[1] Med Univ Sofia, Fac Pharm, Dept Chem, Sofia 1000, Bulgaria
[2] Med Univ Sofia, Fac Pharm, Dept Pharmacol Pharmacotherapy & Toxicol, Sofia 1000, Bulgaria
来源
MOLECULES | 2024年 / 29卷 / 22期
关键词
Alzheimer's disease; antioxidation; beta-amyloid; benzylpiperidine hybrids; cholinergic; donepezil analogs; multi-target drugs; melatonin; tau hyperphosphorylation; neuroinflammation; natural molecules; ATTENUATES AMYLOID-BETA; NEURODEGENERATIVE DISEASES; OXIDATIVE STRESS; DIRECTED LIGANDS; TAU-PROTEIN; CANNABIDIOL; DESIGN; ANTIOXIDANT; PROLIFERATION; MECHANISMS;
D O I
10.3390/molecules29225314
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Alzheimer's disease (AD) involves a complex pathophysiology with multiple interconnected subpathologies, including protein aggregation, impaired neurotransmission, oxidative stress, and microglia-mediated neuroinflammation. Current treatments, which generally target a single subpathology, have failed to modify the disease's progression, providing only temporary symptom relief. Multi-target drugs (MTDs) address several subpathologies, including impaired aggregation of pathological proteins. In this review, we cover hybrid molecules published between 2014 and 2024. We offer an overview of the strategies employed in drug design and approaches that have led to notable improvements and reduced hepatotoxicity. Our aim is to offer insights into the potential development of new Alzheimer's disease drugs. This overview highlights the potential of multi-target drugs featuring heterocycles with N-benzylpiperidine fragments and natural compounds in improving Alzheimer's disease treatment.
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页数:30
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