| Literature DB >> 34798775 |
Kaifu Gao1, Rui Wang1, Jiahui Chen1, Jetze J Tepe2, Faqing Huang3, Guo-Wei Wei1,4,5.
Abstract
The main protease (Mpro) plays a crucial role in severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) replication and is highly conserved, rendering it one of the most attractive therapeutic targets for SARS-CoV-2 inhibition. Currently, although two drug candidates targeting SARS-CoV-2 Mpro designed by Pfizer are under clinical trials, no SARS-CoV-2 medication is approved due to the long period of drug development. Here, we collect a comprehensive list of 817 available SARS-CoV-2 and SARS-CoV Mpro inhibitors from the literature or databases and analyze their molecular mechanisms of action. The structure-activity relationships (SARs) among each series of inhibitors are discussed. Additionally, we broadly examine available antiviral activity, ADMET (absorption, distribution, metabolism, excretion, and toxicity), and animal tests of these inhibitors. We comment on their druggability or drawbacks that prevent them from becoming drugs. This Perspective sheds light on the future development of Mpro inhibitors for SARS-CoV-2 and future coronavirus diseases.Entities:
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Year: 2021 PMID: 34798775 PMCID: PMC9357291 DOI: 10.1021/acs.jmedchem.1c00409
Source DB: PubMed Journal: J Med Chem ISSN: 0022-2623 Impact factor: 8.039