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美金刚衍生物作为阿尔茨海默病的多靶标药物。

Memantine Derivatives as Multitarget Agents in Alzheimer's Disease.

机构信息

Department of Pharmacy and Biotechnology, Alma Mater Studiorum-University of Bologna, Via Belmeloro 6, 40126 Bologna, Italy.

出版信息

Molecules. 2020 Sep 2;25(17):4005. doi: 10.3390/molecules25174005.

Abstract

Memantine (3,5-dimethyladamantan-1-amine) is an orally active, noncompetitive N-methyl-D-aspartate receptor (NMDAR) antagonist approved for treatment of moderate-to-severe Alzheimer's disease (AD), a neurodegenerative condition characterized by a progressive cognitive decline. Unfortunately, memantine as well as the other class of drugs licensed for AD treatment acting as acetylcholinesterase inhibitors (AChEIs), provide only symptomatic relief. Thus, the urgent need in AD drug development is for disease-modifying therapies that may require approaching targets from more than one path at once or multiple targets simultaneously. Indeed, increasing evidence suggests that the modulation of a single neurotransmitter system represents a reductive approach to face the complexity of AD. Memantine is viewed as a privileged NMDAR-directed structure, and therefore, represents the driving motif in the design of a variety of multi-target directed ligands (MTDLs). In this review, we present selected examples of small molecules recently designed as MTDLs to contrast AD, by combining in a single entity the amantadine core of memantine with the pharmacophoric features of known neuroprotectants, such as antioxidant agents, AChEIs and Aβ-aggregation inhibitors.

摘要

盐酸美金刚(3,5-二甲基金刚烷-1-胺)是一种具有口服活性的、非竞争性的 N-甲基-D-天冬氨酸受体(NMDAR)拮抗剂,已被批准用于治疗中重度阿尔茨海默病(AD),这是一种以进行性认知能力下降为特征的神经退行性疾病。不幸的是,盐酸美金刚以及其他获准用于 AD 治疗的作为乙酰胆碱酯酶抑制剂(AChEIs)的药物类别,仅提供对症缓解。因此,AD 药物开发的当务之急是需要采用疾病修饰疗法,这些疗法可能需要同时从多个途径或多个靶点入手。事实上,越来越多的证据表明,单一神经递质系统的调节代表了一种简化方法,难以应对 AD 的复杂性。盐酸美金刚被视为一种受优待的 NMDAR 靶向结构,因此,它是设计各种多靶标导向配体(MTDL)的主要驱动力。在这篇综述中,我们介绍了最近设计的一些小分子作为 MTDL 的例子,这些小分子通过将盐酸美金刚的金刚烷核心与已知的神经保护剂(如抗氧化剂、AChEIs 和 Aβ 聚集抑制剂)的药效团特征结合在单个实体中,用于对比 AD。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a0f5/7504780/dbf13c364e2e/molecules-25-04005-g001.jpg

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