Drug repurposing: small molecules against Cu(II)-amyloid-β and free radicals

被引:5
|
作者
Nam, Geewoo [1 ]
Suh, Jong-Min [1 ]
Yi, Yelim [1 ]
Lim, Mi Hee [1 ]
机构
[1] Korea Adv Inst Sci & Technol KAIST, Dept Chem, Daejeon 34141, South Korea
基金
新加坡国家研究基金会;
关键词
Drug repurposing; Chemical reagents; Metal ions; Amyloid-beta; Free radicals; Alzheimer's disease; AMYLOID-BETA; ALZHEIMERS-DISEASE; A-BETA; MONOAMINE-OXIDASE; CHEMICAL TOOLS; METAL-IONS; IN-VITRO; AGGREGATION; DEPRESSION; PEPTIDES;
D O I
10.1016/j.jinorgbio.2021.111592
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) presents a complex pathology entangling numerous pathological factors, including amyloid-beta (A beta), metal ions, and reactive oxygen species (ROS). Increasing evidence reveals pathological connections among these distinct components in AD. For instance, the association between the amyloid cascade and metal ion hypotheses has introduced a novel pathogenic target: metal-bound A beta. Investigation of such interconnections requires substantial research and can be expedited by chemical reagents that are able to modify multiple pathogenic factors in AD. Drug repurposing is an efficient approach for rediscovering previously utilized molecules with desirable biological and pharmaceutical properties as chemical reagents. Herein, we report the evaluation of three pre-approved drug molecules, selected based on their chemical structure and properties, as chemical reagents that can be used for elucidating the complicated pathology of AD.
引用
收藏
页数:10
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