多肽钉接用多氟试剂

Wanzhen Lin , Xin Ding , Jun-Wei Han , Li-Shuang Yu , Fa-Jie Chen
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引用次数: 0

摘要

肽段钉接技术作为一种调节肽段结构和增强其功能特性的有价值的方法,在药物开发和生物分子工程中有着广泛的应用。在各种装订策略中,多氟试剂介导的方法因其独特的能力而脱颖而出,提供理想的物理化学性质,如改善的稳定性、亲脂性和结合亲和力。本文综述了用于天然肽钉接的多氟试剂的最新进展,重点介绍了三大类:芳基化、乙烯基化和酰胺化试剂。这些试剂通过利用氟取代基调节的反应性和选择性来实现精确的肽修饰,促进了天然肽和生物制剂的工程。
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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Polyfluorinated reagents for peptide stapling
Peptide stapling has emerged as a valuable approach for modulating peptide structures and enhancing their functional properties, with broad applications for drug discovery and biomolecular engineering. Among the diverse stapling strategies, polyfluorinated reagent-mediated approaches stand out due to their unique ability to provide desirable physicochemical properties such as improved stability, lipophilicity, and binding affinity. This review highlights recent advancements in polyfluorinated reagents for native peptide stapling, focusing on three major classes: arylation, vinylation, and amidation reagents. These reagents enable precise peptide modifications by leveraging the reactivity and selectivity modulated by fluorine substituents, facilitating the engineering of native peptides and biologics.
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