Recent progress of small-molecule-based theranostic agents in Alzheimer's disease

被引:5
作者
Gao, Furong [1 ]
Chen, Jiefang [1 ]
Zhou, Yuancun [1 ]
Cheng, Letong [1 ]
Hu, Ming [1 ]
Wang, Xiaohui [1 ]
机构
[1] Nanjing Tech Univ, Sch Chem & Mol Engn, State Key Lab Mat Oriented Chem Engn, Inst Chem Biol & Funct Mol, Nanjing 211816, Peoples R China
来源
RSC MEDICINAL CHEMISTRY | 2023年 / 14卷 / 11期
基金
中国国家自然科学基金;
关键词
BETA-AMYLOID AGGREGATION; IN-VIVO; ALZHEIMERS-DISEASE; A-BETA; CROSS-LINKING; INHIBITION; PLAQUES; CYANINE; PROBE; BIOMARKERS;
D O I
10.1039/d3md00330b
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) is the most common form of neurodegenerative dementia. As a multifactorial disease, AD involves several etiopathogenic mechanisms, in which multiple pathological factors are interconnected with each other. This complicated and unclear pathogenesis makes AD lack effective diagnosis and treatment. Theranostics, exerting the synergistic effect of diagnostic and therapeutic functions, would provide a promising strategy for exploring AD pathogenesis and developing drugs for combating AD. With the efforts in small drug-like molecules for both diagnosis and treatment of AD, small-molecule-based theranostic agents have attracted significant attention owing to their facile synthesis, high biocompatibility and reproducibility, and easy clearance from the body through the excretion systems. In this review, the small-molecule-based theranostic agents reported in the literature for anti-AD are classified into four groups according to their diagnostic modalities. Their design rationales, chemical structures, and working mechanisms for theranostics are summarized. Finally, the opportunities for small-molecule-based theranostic agents in AD are also proposed. This review discusses the developments of small-molecule-based theranostic agents in terms of design rationales, chemical structures, and theranostic performances in Alzheimer's disease.
引用
收藏
页码:2231 / 2245
页数:15
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