| Literature DB >> 33872675 |
Ruikun Du1, Laura Cooper2, Zinuo Chen3, Hyun Lee4, Lijun Rong5, Qinghua Cui6.
Abstract
The emerging SARS-CoV-2 infection is the cause of the global COVID-19 pandemic. To date, there are limited therapeutic options available to fight this disease. Here we examined the inhibitory abilities of two broad-spectrum antiviral natural products chebulagic acid (CHLA) and punicalagin (PUG) against SARS-CoV-2 viral replication. Both CHLA and PUG reduced virus-induced plaque formation in Vero-E6 monolayer at noncytotoxic concentrations, by targeting the enzymatic activity of viral 3-chymotrypsin-like cysteine protease (3CLpro) as allosteric regulators. Our study demonstrates the potential use of CHLA and PUG as novel COVID-19 therapies.Entities:
Keywords: 3CLpro; SARS-CoV-2; allosteric inhibitor; chebulagic acid; punicalagin
Year: 2021 PMID: 33872675 DOI: 10.1016/j.antiviral.2021.105075
Source DB: PubMed Journal: Antiviral Res ISSN: 0166-3542 Impact factor: 5.970