An ongoing journey of chalcone analogues as single and multi-target ligands in the field of Alzheimer's disease: A review with structural aspects

被引:15
作者
Sharma, Pratibha [1 ]
Singh, Manjinder [1 ]
机构
[1] Chitkara Univ, Chitkara Coll Pharm, Rajpura, Punjab, India
关键词
Alzheimer's disease; Chalcone; AChE; MAO; -B; Amyloid beta; BACE-1; Antioxidants; AGEs; MONOAMINE-OXIDASE-B; GLYCATION END-PRODUCTS; MANNICH BASE DERIVATIVES; BETA-AMYLOID AGGREGATION; BIOLOGICAL EVALUATION; INHIBITORY-ACTIVITY; MULTIFUNCTIONAL AGENTS; ACETYLCHOLINESTERASE INHIBITORS; TAU-PROTEIN; PHARMACOLOGICAL EVALUATION;
D O I
10.1016/j.lfs.2023.121568
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Alzheimer's disease (AD) is a chronic and irreversible neurodegenerative disorder with progressive dementia and cognitive impairment. AD poses severe health challenge in elderly people and become one of the leading causes of death worldwide. It possesses complex pathophysiology with several hypotheses (cholinergic hypothesis, amyloid hypothesis, tau hypothesis, oxidative stress, mitochondrial dysfunction etc.). Several attempts have been made for the management of multifactorial AD. Acetylcholinesterase is the only target has been widely explored in the management of AD to the date. The current review set forth the chalcone based natural, semi-synthetic and synthetic compounds in the search of potential anti-Alzheimer's agents. The main highlights of current review emphasizes on chalcone target different enzymes and pathways like Acetylcholinesterase, beta-secretase (BACE1), tau proteins, MAO, free radicals, Advanced glycation end Products (AGEs) etc. and their structure activity relationships contributing in the inhibition of above mentioned various targets of AD.
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页数:21
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