Progress in the study of anti-Alzheimer's disease activity of pyrimidine-containing bioactive molecules

IF 6 2区 医学 Q1 CHEMISTRY, MEDICINAL
Yu-Lin Liu, Qian Zhang, Bing-Qian Li, Di Zhang, Rui-Hao Chui, Lin-Lin Zhang, Qi Zhang, Li-Ying Ma
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引用次数: 0

Abstract

Pyrimidines are aromatic, heterocyclic organic compounds characterized by a six-membered ring that contains four carbon atoms and two nitrogen atoms. They have been reported to exhibit a variety of biological activities such as antifungal, antiviral, and anti-Parkinsonian effects. Recently, there has been an increased focus on their potential anti-Alzheimer's properties. Several pyrimidine-based drugs and their analogues are currently undergoing various phases of clinical trials, indicating pyrimidine as a promising chemical structure for drug development. Notably, modifications to the pyrimidine structure significantly influence their activity against Alzheimer's disease. For instance, the introduction of heteroatoms into the pyrimidine ring or alternations in the length of the linkage region have been shown to enhance therapeutic efficacy. This review provides a comprehensive overview of pyrimidine derivatives as potential therapeutics for Alzheimer's disease, with a focus on structure-activity relationship (SAR) studies, design strategies, and binding mechanisms. These insights could pave the way for the development of more effective anti-Alzheimer's medications.

Abstract Image

含嘧啶生物活性分子抗阿尔茨海默病活性的研究进展
嘧啶是芳香的杂环有机化合物,其特征是六元环包含四个碳原子和两个氮原子。据报道,它们具有多种生物活性,如抗真菌、抗病毒和抗帕金森病作用。最近,人们越来越关注它们潜在的抗阿尔茨海默氏症的特性。一些基于嘧啶的药物及其类似物目前正在进行不同阶段的临床试验,表明嘧啶是一种有前景的药物开发化学结构。值得注意的是,嘧啶结构的修饰显著影响其抗阿尔茨海默病的活性。例如,在嘧啶环中引入杂原子或改变连接区域的长度已被证明可以提高治疗效果。本文综述了嘧啶衍生物作为阿尔茨海默病的潜在治疗药物的全面概述,重点介绍了结构-活性关系(SAR)研究、设计策略和结合机制。这些发现可能为开发更有效的抗阿尔茨海默病药物铺平道路。
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来源期刊
CiteScore
11.70
自引率
9.00%
发文量
863
审稿时长
29 days
期刊介绍: The European Journal of Medicinal Chemistry is a global journal that publishes studies on all aspects of medicinal chemistry. It provides a medium for publication of original papers and also welcomes critical review papers. A typical paper would report on the organic synthesis, characterization and pharmacological evaluation of compounds. Other topics of interest are drug design, QSAR, molecular modeling, drug-receptor interactions, molecular aspects of drug metabolism, prodrug synthesis and drug targeting. The journal expects manuscripts to present the rational for a study, provide insight into the design of compounds or understanding of mechanism, or clarify the targets.
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