Phosphonates as Modulators of Brain Chemistry

IF 13.6 1区 医学 Q1 CHEMISTRY, MEDICINAL
Medicinal Research Reviews Pub Date : 2026-10-05 Epub Date: 2026-06-14 DOI:10.1002/med.70070
Susana Santos Braga, Nádia E. Santos, Maria Almeida-Santos, Flávio F. Figueira, Filipe A. Almeida Paz
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引用次数: 0

Abstract

The present review describes the current knowledge on phosphonates designed for brain disease therapeutics, a less explored aspect of the studies on their medicinal chemistry. Because of their structural similarity with phosphates and of the ubiquitous presence of phosphate-dependent processes in the brain, phosphonate compounds are able to influence brain chemistry, interfering with neurotransmission and phosphorous-dependent bioprocesses. One of the main applications for phosphonates in the brain is Alzheimer's disease, for which they can be new drug candidates and/or afford innovative strategies for diagnostics. Such applications are described in the first section of this review, which includes a large number of reports on phosphonates with cholinesterase-inhibiting activity, some recent studies exploring phosphonates for inhibiting the interaction between amyloid-β protein and alcohol dehydrogenases, and phosphonate-based materials used in proteomics-based investigative and diagnosis platforms for the different stages of development of Alzheimer's disease. The second section of the review is dedicated to ischemic brain injury and to the development of phosphonates for active against NMDA and AMPA receptors with the purpose of reducing brain damage caused by glutamate excitotoxicity. Furthermore, agonists targeting the mGlu-4 receptor suggest potential for promoting neuroregeneration. The review concludes by emphasizing the relevance of phosphonate stability, versatility, and ability to mimic natural phosphate groups in the development of new therapeutic agents for brain disorders, weighing the advantages against the gaps in knowledge in order to set future directions of research in brain health.

磷酸盐作为脑化学调节剂。
目前的综述描述了目前的知识,磷酸盐设计用于脑病治疗,其药物化学研究的一个较少探索的方面。由于它们与磷酸盐的结构相似,以及大脑中普遍存在的磷酸盐依赖过程,膦酸盐化合物能够影响大脑化学,干扰神经传递和磷依赖的生物过程。磷酸盐在大脑中的主要应用之一是阿尔茨海默病,它们可以作为新的候选药物和/或提供创新的诊断策略。本综述的第一部分描述了这些应用,其中包括大量关于具有胆碱酯酶抑制活性的磷酸盐的报道,一些最近的研究探索磷酸盐抑制淀粉样蛋白-β蛋白和醇脱氢酶之间的相互作用,以及磷酸盐基材料用于基于蛋白质组学的阿尔茨海默病不同发展阶段的调查和诊断平台。第二部分综述了缺血性脑损伤和抗NMDA和AMPA受体的膦酸盐的开发,目的是减少谷氨酸兴奋毒性引起的脑损伤。此外,靶向mGlu-4受体的激动剂可能促进神经再生。综述最后强调了膦酸盐的稳定性、多功能性和模仿天然磷酸盐基团的能力在开发新的脑部疾病治疗剂中的相关性,并权衡了其优势和知识空白,以确定未来脑部健康研究的方向。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
29.30
自引率
0.00%
发文量
52
审稿时长
2 months
期刊介绍: Medicinal Research Reviews is dedicated to publishing timely and critical reviews, as well as opinion-based articles, covering a broad spectrum of topics related to medicinal research. These contributions are authored by individuals who have made significant advancements in the field. Encompassing a wide range of subjects, suitable topics include, but are not limited to, the underlying pathophysiology of crucial diseases and disease vectors, therapeutic approaches for diverse medical conditions, properties of molecular targets for therapeutic agents, innovative methodologies facilitating therapy discovery, genomics and proteomics, structure-activity correlations of drug series, development of new imaging and diagnostic tools, drug metabolism, drug delivery, and comprehensive examinations of the chemical, pharmacological, pharmacokinetic, pharmacodynamic, and clinical characteristics of significant drugs.
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