Literature DB >> 33872675

Discovery of Chebulagic Acid and Punicalagin as Novel Allosteric Inhibitors of SARS-CoV-2 3CLpro.

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.
Copyright © 2021 Elsevier B.V. All rights reserved.

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


  9 in total

Review 1.  The SARS-CoV-2 main protease (Mpro): Structure, function, and emerging therapies for COVID-19.

Authors:  Qing Hu; Yuan Xiong; Guang-Hao Zhu; Ya-Ni Zhang; Yi-Wen Zhang; Ping Huang; Guang-Bo Ge
Journal:  MedComm (2020)       Date:  2022-07-14

2.  Perspectives on SARS-CoV-2 Main Protease Inhibitors.

Authors:  Kaifu Gao; Rui Wang; Jiahui Chen; Jetze J Tepe; Faqing Huang; Guo-Wei Wei
Journal:  J Med Chem       Date:  2021-11-19       Impact factor: 8.039

Review 3.  A Review of the Current Landscape of SARS-CoV-2 Main Protease Inhibitors: Have We Hit the Bullseye Yet?

Authors:  Guillem Macip; Pol Garcia-Segura; Júlia Mestres-Truyol; Bryan Saldivar-Espinoza; Gerard Pujadas; Santiago Garcia-Vallvé
Journal:  Int J Mol Sci       Date:  2021-12-27       Impact factor: 5.923

4.  Use of hyphenated analytical techniques to identify the bioactive constituents of Gunnera perpensa L., a South African medicinal plant, which potently inhibit SARS-CoV-2 spike glycoprotein-host ACE2 binding.

Authors:  Luke Invernizzi; Phanankosi Moyo; Joel Cassel; Freddie J Isaacs; Joseph M Salvino; Luis J Montaner; Ian Tietjen; Vinesh Maharaj
Journal:  Anal Bioanal Chem       Date:  2022-04-14       Impact factor: 4.142

5.  Punicalagin as an allosteric NSP13 helicase inhibitor potently suppresses SARS-CoV-2 replication in vitro.

Authors:  Lian Lu; Yun Peng; Huiqiao Yao; Yanqun Wang; Jinyu Li; Yang Yang; Zhonghui Lin
Journal:  Antiviral Res       Date:  2022-08-17       Impact factor: 10.103

Review 6.  Mayaro Virus: The State-of-the-Art for Antiviral Drug Development.

Authors:  Ana Paula Andreolla; Alessandra Abel Borges; Juliano Bordignon; Claudia Nunes Duarte Dos Santos
Journal:  Viruses       Date:  2022-08-16       Impact factor: 5.818

Review 7.  Allosteric Binding Sites of the SARS-CoV-2 Main Protease: Potential Targets for Broad-Spectrum Anti-Coronavirus Agents.

Authors:  Lara Alzyoud; Mohammad A Ghattas; Noor Atatreh
Journal:  Drug Des Devel Ther       Date:  2022-08-02       Impact factor: 4.319

Review 8.  Bioactive natural products in COVID-19 therapy.

Authors:  Zhonglei Wang; Ning Wang; Liyan Yang; Xian-Qing Song
Journal:  Front Pharmacol       Date:  2022-08-19       Impact factor: 5.988

9.  Identification of the SARS-CoV-2 Entry Receptor ACE2 as a Direct Target for Transcriptional Repression by Miz1.

Authors:  Jing Yang; Edith A Perez; Changchun Hou; Pin Zhang; Michelle Van Scoyk; Robert A Winn; Lijun Rong; Jing Liu
Journal:  Front Immunol       Date:  2021-07-07       Impact factor: 7.561

  9 in total

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