Review on development of potential inhibitors of SARS-CoV-2 main protease (MPro)

被引:14
|
作者
Katre, Soumya Gulab [1 ]
Asnani, Alpana Jagdish [1 ]
Pratyush, Kumar [1 ]
Sakharkar, Nilima Gangadhar [1 ]
Bhope, Ashwini Gajanan [1 ]
Sawarkar, Kanchan Tekram [1 ]
Nimbekar, Vaibhav Santosh [1 ]
机构
[1] Priyadarshini JL Coll Pharm, Dept Pharmaceut Chem, Nagpur 440016, MH, India
关键词
SARS-CoV-2 (severe acute respiratory syndrome coronavirus 2); MERS-CoV (Middle East respiratory syndrome coronavirus); M-Pro inhibitor (main protease inhibitor); Virtual and in vitro screening; CRYSTAL-STRUCTURES; CORONAVIRUS; SARS; COMPLEX; DESIGN;
D O I
10.1186/s43094-022-00423-7
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Background: The etiological agent for the coronavirus illness outbreak in 2019-2020 is a novel coronavirus known as severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) (COVID-19), whereas coronavirus disease pandemic of 2019 (COVID-19) has compelled the implementation of novel therapeutic options. Main body of the abstract: There are currently no targeted therapeutic medicines for this condition, and effective treatment options are quite restricted; however, new therapeutic candidates targeting the viral replication cycle are being investigated. The primary protease of the severe acute respiratory syndrome coronavirus 2 virus is a major target for therapeutic development (M-Pro). Severe acute respiratory syndrome coronavirus 2, severe acute respiratory syndrome coronavirus, and Middle East respiratory syndrome coronavirus (MERS-CoV) all seem to have a structurally conserved substrate-binding domain that can be used to develop novel protease inhibitors. Short conclusion: With the recent publication of the X-ray crystal structure of the severe acute respiratory syndrome coronavirus 2 Mm, virtual and in vitro screening investigations to find M-Pro inhibitors are fast progressing. The focus of this review is on recent advancements in the quest for small-molecule inhibitors of the severe acute respiratory syndrome coronavirus 2 main protease.
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页数:9
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