Open Access
Open access
volume Volume 16 pages 1067-1082

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

Jiajie Zhu 1
Haiyan Zhang 2
Qinghong Lin 1
Jingting Lyu 1
Lu Lu 1
Hanxi Chen 1
Xu-ning Zhang 1
Yanjun Zhang 3
Ke-Da Chen 1
1
 
Shulan International Medical College, Zhejiang Shuren University, Hangzhou, People's Republic of China.
3
 
Zhejiang Provincial Center for Disease Control and Prevention, Hangzhou, People's Republic of China.
Publication typeJournal Article
Publication date2022-04-08
scimago Q1
wos Q1
SJR1.190
CiteScore8.6
Impact factor5.1
ISSN11778881
PubMed ID:  35450403
Drug Discovery
Pharmacology
Pharmaceutical Science
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.
Found 
Found 

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GOST Copy
Zhu J. et al. Progress on SARS-CoV-2 3CLpro Inhibitors: Inspiration from SARS-CoV 3CLpro Peptidomimetics and Small-Molecule Anti-Inflammatory Compounds // Drug Design, Development and Therapy. 2022. Vol. Volume 16. pp. 1067-1082.
GOST all authors (up to 50) Copy
Zhu J., Zhang H., Lin Q., Lyu J., Lu L., Chen H., Zhang X., Zhang Y., Chen K. Progress on SARS-CoV-2 3CLpro Inhibitors: Inspiration from SARS-CoV 3CLpro Peptidomimetics and Small-Molecule Anti-Inflammatory Compounds // Drug Design, Development and Therapy. 2022. Vol. Volume 16. pp. 1067-1082.
RIS |
Cite this
RIS Copy
TY - JOUR
DO - 10.2147/dddt.s359009
UR - https://doi.org/10.2147/dddt.s359009
TI - Progress on SARS-CoV-2 3CLpro Inhibitors: Inspiration from SARS-CoV 3CLpro Peptidomimetics and Small-Molecule Anti-Inflammatory Compounds
T2 - Drug Design, Development and Therapy
AU - Zhu, Jiajie
AU - Zhang, Haiyan
AU - Lin, Qinghong
AU - Lyu, Jingting
AU - Lu, Lu
AU - Chen, Hanxi
AU - Zhang, Xu-ning
AU - Zhang, Yanjun
AU - Chen, Ke-Da
PY - 2022
DA - 2022/04/08
PB - Taylor & Francis
SP - 1067-1082
VL - Volume 16
PMID - 35450403
SN - 1177-8881
ER -
BibTex
Cite this
BibTex (up to 50 authors) Copy
@article{2022_Zhu,
author = {Jiajie Zhu and Haiyan Zhang and Qinghong Lin and Jingting Lyu and Lu Lu and Hanxi Chen and Xu-ning Zhang and Yanjun Zhang and Ke-Da Chen},
title = {Progress on SARS-CoV-2 3CLpro Inhibitors: Inspiration from SARS-CoV 3CLpro Peptidomimetics and Small-Molecule Anti-Inflammatory Compounds},
journal = {Drug Design, Development and Therapy},
year = {2022},
volume = {Volume 16},
publisher = {Taylor & Francis},
month = {apr},
url = {https://doi.org/10.2147/dddt.s359009},
pages = {1067--1082},
doi = {10.2147/dddt.s359009}
}