Promising heterocycle-based scaffolds in recent (2019-2021) anti-Alzheimer's drug design and discovery

被引:23
作者
Dorababu, Atukuri [1 ]
机构
[1] SRMPP Govt First Grade Coll, Huvinahadagali 583219, India
关键词
Alzheimer's disease; Cholinesterase inhibitors; Monoaminase inhibitors; A beta-aggregation inhibitory activity; Structure-activity relationship; Cytotoxicity; BIOLOGICAL EVALUATION; ACETYLCHOLINESTERASE INHIBITORS; MOLECULAR DOCKING; PHARMACOLOGICAL EVALUATION; MULTIFUNCTIONAL AGENTS; GSK-3-BETA INHIBITORS; MELATONIN HYBRIDS; DUAL INHIBITORS; DERIVATIVES; POTENT;
D O I
10.1016/j.ejphar.2022.174847
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Alzheimer's disease (AD) is one of the neurodegenerative diseases that led to morbidity and mortality worldwide. It is a complex disease whose etiology is not completely known that leads to difficulty in prevention or cure of the AD. Also, there are only few approved drugs for AD treatment. Apart from deaths due to AD, expenditure of treatment and care of AD patients is higher than that of treatment of HIV and cancer diseases combined. Hence, it leads to an economic burden also. Although research is being carried out on designing drugs for AD, most of them have ended up in poor inhibitors with high toxicity. Hence, researchers should shoulder a great responsibility of discovery of efficient drugs for AD treatment. In the field of drug discovery, heterocycles played an important role. Also, most of the heterocyclic scaffolds have been used in design of potent anti-AD agents. In view of this, heterocyclic molecules reported recently are compiled and evaluated comprehensively. Especially, the molecules which exhibited pronounced activity are emphasized and described with respect to structure-activity relationship (SAR) in brief.
引用
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页数:22
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