重新调整用途
肌萎缩侧索硬化
药物发现
药物重新定位
疾病
药品
小分子
痴呆
蛋白质聚集
医学
药理学
计算生物学
神经科学
生物
生物信息学
生物化学
细胞生物学
病理
生态学
作者
Wei Liu,Gang Wang,Zhiwen Wang,Guan Wang,Jianping Huang,Bo Liu
标识
DOI:10.1016/j.drudis.2022.04.003
摘要
Neurodegenerative diseases (NDs) are often age-related disorders that can cause dementia in people, usually over 65 years old, are still lacking effective therapies. Some NDs have recently been linked to toxic protein aggregates, for example Alzheimer’s disease, Parkinson’s disease, Amyotrophic lateral sclerosis and Huntington disease; therefore, mulating toxic protein aggregates would be a promising therapeutic strategy. Moreover, drug repurposing, in other words exploiting drugs that are already in use for another indication, has been attracting mounting attention for potential therapeutic purposes in NDs. Thus, in this review, we focus on summarizing a series of repurposed small-molecule drugs for eliminating or inhibiting toxic protein aggregates and further discuss their intricate molecular mechanisms to improve the current ND treatment. Taken together, these findings will shed new light on exploiting more repurposed small-molecule drugs targeting different types of toxic proteins to fight NDs in the future.
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