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SARS-CoV-2 3CLpro 抑制剂的进展:来自 SARS-CoV 3CLpro 肽模拟物和小分子抗炎化合物的启示
Authors Zhu J , Zhang H, Lin Q, Lyu J, Lu Lu, Chen H, Zhang X , Zhang Y, Chen K
Received 19 January 2022
Accepted for publication 26 March 2022
Published 8 April 2022 Volume 2022:16 Pages 1067—1082
DOI https://doi.org/10.2147/DDDT.S359009
Checked for plagiarism Yes
Review by Single anonymous peer review
Peer reviewer comments 2
Editor who approved publication: Dr Tuo Deng
Abstract: Coronavirus disease 2019 (COVID-19) caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) currently poses a threat to human health. 3C-like proteinase (3CLpro) plays an important role in the viral life cycle. Hence, it is considered an attractive antiviral target protein. Whole-genome sequencing showed that the sequence homology between SARS-CoV-2 3CLpro and SARS-CoV 3CLpro is 96.08%, with high similarity in the substrate-binding region. Thus, assessing peptidomimetic inhibitors of SARS-CoV 3CLpro could accelerate the development of peptidomimetic inhibitors for SARS-CoV-2 3CLpro. Accordingly, we herein discuss progress on SARS-CoV-2 3CLpro peptidomimetic inhibitors. Inflammation plays a major role in the pathophysiological process of COVID-19. Small-molecule compounds targeting 3CLpro with both antiviral and anti-inflammatory effects are also briefly discussed in this paper.
Keywords: SARS-CoV, SARS-CoV-2, 3CLpro, peptidomimetics, anti-inflammatory agents, small-molecule inhibitors, protease inhibitors