治疗神经退行性疾病的天然类似物的最新进展

IF 4.5 2区 医学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
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引用次数: 0

摘要

神经退行性疾病(NDs)是众多令人丧失能力且无法治疗的疾病的标志,其发病率正在迅速上升,阿尔茨海默病和帕金森病就是其中的典型代表。为了治疗这些使人衰弱的疾病,迫切需要研制出疗效高、毒性小的药物。天然产物结构复杂,种类繁多,具有广泛的生物活性,因而在药物发现史上具有重要的贡献。然而,天然产物也给药物发现带来了挑战,包括耗时的分离过程、低含量、低生物利用度以及其他相关问题。为了应对这些挑战,人们合成了大量天然产物的类似物。这种方法可以快速合成天然产物的类似物,这些类似物有可能成为药物开发的先导化合物,从而为新型药物的发现铺平道路。本文概述了 127 种具有不同天然产物结构的合成类似物,包括黄酮类、生物碱类、香豆素类、苯丙类、萜类、多酚类和酰胺类。这些化合物根据其治疗各种疾病的功效进行了分类。此外,本文还深入探讨了某些类似物的结构-活性关系(SAR),为系统开发治疗神经退行性疾病的药物提供了全面的参考。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Recent advances in the natural product analogues for the treatment of neurodegenerative diseases

Recent advances in the natural product analogues for the treatment of neurodegenerative diseases

Neurodegenerative diseases (NDs) represent a hallmark of numerous incapacitating and untreatable conditions, the incidence of which is escalating swiftly, exemplified by Alzheimer’s disease and Parkinson’s disease. There is an urgent necessity to create pharmaceuticals that exhibit high efficacy and minimal toxicity in order to address these debilitating diseases. The structural complexity and diversity of natural products confer upon them a broad spectrum of biological activities, thereby significantly contributing to the history of drug discovery. Nevertheless, natural products present challenges in drug discovery, including time-consuming separation processes, low content, low bioavailability, and other related issues. To address these challenges, numerous analogs of natural products have been synthesized. This methodology enables the rapid synthesis of analogs of natural products with the potential to serve as lead compounds for drug development, thereby paving the way for the discovery of novel pharmaceuticals. This paper provides a summary of 127 synthetic analogues featuring various natural product structures, including flavonoids, alkaloids, coumarins, phenylpropanoids, terpenoids, polyphenols, and amides. The compounds are categorized based on their efficacy in treating various diseases. Furthermore, this article delves into the structure–activity relationship (SAR) of certain analogues, offering a thorough point of reference for the systematic development of pharmaceuticals aimed at addressing neurodegenerative conditions.

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来源期刊
Bioorganic Chemistry
Bioorganic Chemistry 生物-生化与分子生物学
CiteScore
9.70
自引率
3.90%
发文量
679
审稿时长
31 days
期刊介绍: Bioorganic Chemistry publishes research that addresses biological questions at the molecular level, using organic chemistry and principles of physical organic chemistry. The scope of the journal covers a range of topics at the organic chemistry-biology interface, including: enzyme catalysis, biotransformation and enzyme inhibition; nucleic acids chemistry; medicinal chemistry; natural product chemistry, natural product synthesis and natural product biosynthesis; antimicrobial agents; lipid and peptide chemistry; biophysical chemistry; biological probes; bio-orthogonal chemistry and biomimetic chemistry. For manuscripts dealing with synthetic bioactive compounds, the Journal requires that the molecular target of the compounds described must be known, and must be demonstrated experimentally in the manuscript. For studies involving natural products, if the molecular target is unknown, some data beyond simple cell-based toxicity studies to provide insight into the mechanism of action is required. Studies supported by molecular docking are welcome, but must be supported by experimental data. The Journal does not consider manuscripts that are purely theoretical or computational in nature. The Journal publishes regular articles, short communications and reviews. Reviews are normally invited by Editors or Editorial Board members. Authors of unsolicited reviews should first contact an Editor or Editorial Board member to determine whether the proposed article is within the scope of the Journal.
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