Advances in the Development of SARS-CoV-2 Mpro Inhibitors

被引:44
|
作者
Agost-Beltran, Laura [1 ]
de la Hoz-Rodriguez, Sergio [1 ]
Bou-Iserte, Lledo [1 ]
Rodriguez, Santiago [1 ]
Fernandez-de-la-Pradilla, Adrian [2 ]
Gonzalez, Florenci V. [1 ]
机构
[1] Univ Jaume 1, Dept Quim Inorgan & Organ, Castellon de La Plana 12080, Spain
[2] Univ Jaume 1, Dept Quim Fis & Analit, Castellon de La Plana 12080, Spain
来源
MOLECULES | 2022年 / 27卷 / 08期
关键词
COVID-19; main protease; Mpro; inhibitors;
D O I
10.3390/molecules27082523
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Since the outbreak of COVID-19, one of the strategies used to search for new drugs has been to find inhibitors of the main protease (Mpro) of the virus SARS-CoV-2. Initially, previously reported inhibitors of related proteases such as the main proteases of SARS-CoV and MERS-CoV were tested. A huge effort was then carried out by the scientific community to design, synthesize and test new small molecules acting as inactivators of SARS-CoV-2 Mpro. From the chemical structure view, these compounds can be classified into two main groups: one corresponds to modified peptides displaying an adequate sequence for high affinity and a reactive warhead; and the second is a diverse group including chemical compounds that do not have a peptide framework. Although a drug including a SARS-CoV-2 main protease inhibitor has already been commercialized, denoting the importance of this field, more compounds have been demonstrated to be promising potent inhibitors as potential antiviral drugs.
引用
收藏
页数:15
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