Progress of SARS‐CoV‐2 Main protease peptide‐like inhibitors

Author:

Liu Xiaoyong1,Ren Xiaoli1,Hua Miao2,Liu Fang3,Ren Xiaoping1,Sui Chaoya1,Li Qing1,Luo Fen1,Jiang Zhiyong1,Xia Ziqiao1,Chen Jingxia1,Yang Bing1

Affiliation:

1. College of Environment and Quality Inspection Chongqing Chemical Industry Vocational College Chongqing China

2. Chongqing Experimental School Chongqing China

3. Biomedical Analysis and Testing Center, College of Basic Medicine Third Military Medical University Chongqing China

Abstract

AbstractThe pneumonia outbreak caused by Severe Acute Respiratory Syndrome 2 (SARS‐CoV‐2) infection poses a serious threat to people worldwide. Although vaccines have been developed, antiviral drugs are still needed to combat SARS‐CoV‐2 infection due to the high mutability of the virus. SARS‐CoV‐2 main protein (Mpro) is a special cysteine protease that is a key enzyme for SARS‐CoV‐2 replication. It is encoded by peptides and is responsible for processing peptides into functional proteins, making it an important drug target. The paper reviews the structure and peptide‐like inhibitors of SARS‐CoV‐2 Mpro, also the binding mode and structure–activity relationship between the inhibitors and Mpro are introduced in detail. It is hoped that this review can provide ideas and help for the development of anti‐coronavirus drugs such as COVID‐19, and help to develop broad‐spectrum antiviral drug for the treatment of coronavirus diseases as soon as possible.

Publisher

Wiley

Subject

Molecular Medicine,Biochemistry,Drug Discovery,Pharmacology,Organic Chemistry

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