肽的主链N-甲基化:合成进展及其在药物开发中的应用。

IF 4.5 2区 医学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Xuefei Li , Ningchao Wang , Yuhang Liu , Weipiao Li , Xinyu Bai , Ping Liu , Chun-Yang He
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引用次数: 0

摘要

近年来,肽类药物在治疗各种疾病方面发挥着越来越重要的作用,引起了人们的广泛关注。然而,肽有限的药代动力学特性阻碍了它们的全部潜力。增强肽可药用性的一个突出策略是N-甲基化,它涉及在肽骨架的氮原子上添加甲基。这种修饰显著提高了候选肽药物的稳定性、生物利用度、受体结合亲和力和选择性。在这篇综述中,我们全面概述了N-甲基化肽合成方法的进展,以及相关的局限性。此外,我们还探讨了N-甲基化对肽性质各个方面的多功能影响。此外,我们强调致力于N-甲基化肽药物的努力,这些药物已成功获得上市批准。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Backbone N-methylation of peptides: Advances in synthesis and applications in pharmaceutical drug development

Backbone N-methylation of peptides: Advances in synthesis and applications in pharmaceutical drug development

Peptide-based drugs have garnered considerable attention in recent years owing to their increasingly crucial role in the treatment of diverse diseases. However, the limited pharmacokinetic properties of peptides have hindered their full potential. One prominent strategy for enhancing the druggability of peptides is N-methylation, which involves the addition of a methyl group to the nitrogen atom of the peptide backbone. This modification significantly improves the stability, bioavailability, receptor binding affinity and selectivity of peptide drug candidates. In this review, we provide a comprehensive overview of the advancements in synthetic methods for N-methylated peptide synthesis, as well as the associated limitations. Moreover, we explore the versatile effects of N-methylation on various aspects of peptide properties. Furthermore, we emphasize the efforts dedicated to N-methylated peptide pharmaceuticals that have successfully obtained marketing approval.

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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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