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Applications of fluorine-containing amino acids for drug design

机译:含氟氨基酸用于药物设计的应用

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Fluorine-containing amino acids are becoming increasingly prominent in new drugs due to two general trends in the modern pharmaceutical industry. Firstly, the growing acceptance of peptides and modified peptides as drugs; and secondly, fluorine editing has become a prevalent protocol in drug-candidate optimization. Accordingly, fluorine-containing amino acids represent one of the more promising and rapidly developing areas of research in organic, bio-organic and medicinal chemistry. The goal of this Review article is to highlight the current state-of-the-art in this area by profiling 42 selected compounds that combine fluorine and amino acid structural elements. The compounds under discussion represent pharmaceutical drugs currently on the market, or in clinical trials as well as examples of drug-candidates that although withdrawn from development had a significant impact on the progress of medicinal chemistry and/or provided a deeper understanding of the nature and mechanism of biological action. For each compound, we present features of biological activity, a brief history of the design principles and the development of the synthetic approach, focusing on the source of tailor-made amino acid structures and fluorination methods. General aspects of the medicinal chemistry of fluorine-containing amino acids and synthetic methodology are briefly discussed. (C) 2019 Elsevier Masson SAS. All rights reserved.
机译:由于现代制药行业的两种普遍趋势,含氟氨基酸在新药方面变得越来越突出。首先,养老肽的养老金和改性肽作为药物的养成越来越多;其次,氟编辑已成为药物候选优化中的普遍存在方案。因此,含氟氨基酸代表了有机,生物有机和药物化学的研究进程越来越快。本综述文章的目标是通过分析结合氟和氨基酸结构元素的42种所选化合物来突出该区域的当前现实最先进的。讨论的化合物代表目前市场上的药物,或在临床试验中以及诸如毒品 - 候选人的例子,虽然从发育中取出对药用化学的进展和/或提供了对自然的更深入了解的重大影响生物学作用机制。对于每种化合物,我们提出了生物活动的特征,设计原则的简要历史和合成方法的发展,重点是量身定制的氨基酸结构和氟化方法。简要讨论了含氟氨基酸的药物化学的一般方面。 (c)2019年Elsevier Masson SAS。版权所有。

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