Amino Acid and Peptide-Based Antiviral Agents

被引:19
|
作者
Skwarecki, Andrzej S. [1 ,2 ]
Nowak, Michal G. [2 ,3 ]
Milewska, Maria J. [2 ,3 ]
机构
[1] Gdansk Univ Technol, Dept Pharmaceut Technol & Biochem, 11-12 Gabriela Narutowicza St, PL-80233 Gdansk, Poland
[2] Gdansk Univ Technol, BioTechMed Ctr, 11-12 Gabriela Narutowicza St, PL-80233 Gdansk, Poland
[3] Gdansk Univ Technol, Dept Organ Chem, 11-12 Gabriela Narutowicza St, PL-80233 Gdansk, Poland
关键词
amino acids; antiviral agents; synthesis; viruses; HIV-1 PROTEASE INHIBITORS; NS5B POLYMERASE INHIBITORS; DEPENDENT RNA-POLYMERASE; CHIRAL BUILDING-BLOCKS; L-TERT-LEUCINE; CRYSTAL-STRUCTURES; HCVNS5B POLYMERASE; BIOLOGICAL EVALUATION; ASYMMETRIC-SYNTHESIS; WILD-TYPE;
D O I
10.1002/cmdc.202100397
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
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.
引用
收藏
页码:3106 / 3135
页数:30
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