氨基酸
拟肽
蛋白酶
洛比那韦
肽
生物
化学
人类免疫缺陷病毒(HIV)
生物化学
病毒学
酶
抗逆转录病毒疗法
病毒载量
作者
Andrzej S. Skwarecki,Michał G. Nowak,M.J. Milewska
出处
期刊:ChemMedChem
[Wiley]
日期:2021-07-13
卷期号:16 (20): 3106-3135
被引量:24
标识
DOI:10.1002/cmdc.202100397
摘要
Abstract A significant number of antiviral agents used in clinical practice are amino acids, short peptides, or peptidomimetics. Among them, several HIV protease inhibitors (e. g. lopinavir, atazanavir), HCV protease inhibitors (e. g. grazoprevir, glecaprevir), and HCV NS5A protein inhibitors have contributed to a significant decrease in mortality from AIDS and hepatitis. However, there is an ongoing need for the discovery of new antiviral agents and the development of existing drugs; amino acids, both proteinogenic and non‐proteinogenic in nature, serve as convenient building blocks for this purpose. The synthesis of non‐proteinogenic amino acid components of antiviral agents could be challenging due to the need for enantiomerically or diastereomerically pure products. Herein, we present a concise review of antiviral agents whose structures are based on amino acids of both natural and unnatural origin. Special attention is paid to the synthetic aspects of non‐proteinogenic amino acid components of those agents.
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