Progress on SARS-CoV-2 3CLpro Inhibitors: Inspiration from SARS-CoV 3CLpro Peptidomimetics and Small-Molecule Anti-Inflammatory Compounds

被引:30
|
作者
Zhu, Jiajie [1 ]
Zhang, Haiyan [2 ]
Lin, Qinghong [1 ]
Lyu, Jingting [1 ]
Lu, Lu [1 ]
Chen, Hanxi [1 ]
Zhang, Xuning [1 ]
Zhang, Yanjun [3 ]
Chen, Keda [1 ]
机构
[1] Zhejiang Shuren Univ, Shulan Int Med Coll, Hangzhou, Peoples R China
[2] Zhejiang Chinese Med Univ, Hangzhou, Peoples R China
[3] Zhejiang Prov Ctr Dis Control & Prevent, Hangzhou, Peoples R China
来源
关键词
SARS-CoV; SARS-CoV-2; 3CLpro; peptidomimetics; anti-inflammatory agents; small-molecule inhibitors; protease; inhibitors; CORONAVIRUS 3C-LIKE PROTEASE; MAIN PROTEASE; CRYSTAL-STRUCTURE; DIMER INTERFACE; PROTEINASE; MECHANISM; DESIGN; DISSOCIATION; DIMERIZATION; FLAVONOIDS;
D O I
10.2147/DDDT.S359009
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
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.
引用
收藏
页码:1067 / 1082
页数:16
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