Your browser doesn't support javascript.
Ginkgolic acid and anacardic acid are specific covalent inhibitors of SARS-CoV-2 cysteine proteases.
Chen, Zinuo; Cui, Qinghua; Cooper, Laura; Zhang, Pin; Lee, Hyun; Chen, Zhaoyu; Wang, Yanyan; Liu, Xiaoyun; Rong, Lijun; Du, Ruikun.
  • Chen Z; College of Pharmacy, Shandong University of Traditional Chinese Medicine, Jinan, 250355, China.
  • Cui Q; College of Pharmacy, Shandong University of Traditional Chinese Medicine, Jinan, 250355, China.
  • Cooper L; Experimental Center, Shandong University of Traditional Chinese Medicine, Jinan, 250355, China.
  • Zhang P; Qingdao Academy of Chinese Medicinal Sciences, Shandong University of Traditional Chinese Medicine, Qingdao, 266122, China.
  • Lee H; Department of Microbiology and Immunology, College of Medicine, University of Illinois at Chicago, Chicago, IL, 60612, USA.
  • Chen Z; Chicago BioSolutions Inc, 2242 W Harrison Street, Chicago, Illinois, 60612, United States.
  • Wang Y; Department of Pharmaceutical Sciences, Center for Biomolecular Sciences, College of Pharmacy, Biophysics Core at Research Resources Center, University of Illinois at Chicago, Chicago, IL, 60607, USA.
  • Liu X; College of Pharmacy, Shandong University of Traditional Chinese Medicine, Jinan, 250355, China.
  • Rong L; College of Pharmacy, Shandong University of Traditional Chinese Medicine, Jinan, 250355, China.
  • Du R; Experimental Center, Shandong University of Traditional Chinese Medicine, Jinan, 250355, China.
Cell Biosci ; 11(1): 45, 2021 Feb 28.
Article in English | MEDLINE | ID: covidwho-1105737
ABSTRACT

BACKGROUND:

In the urgent campaign to develop therapeutics against SARS-CoV-2, natural products have been an important source of new lead compounds.

RESULTS:

We herein identified two natural products, ginkgolic acid and anacardic acid, as inhibitors using a high-throughput screen targeting the SARS-CoV-2 papain-like protease (PLpro). Moreover, our study demonstrated that the two hit compounds are dual inhibitors targeting the SARS-CoV-2 3-chymotrypsin-like protease (3CLpro) in addition to PLpro. A mechanism of action study using enzyme kinetics further characterized the two compounds as irreversible inhibitors against both 3CLpro and PLpro. Significantly, both identified compounds inhibit SARS-CoV-2 replication in vitro at nontoxic concentrations.

CONCLUSIONS:

Our finding provides two novel natural products as promising SARS-CoV-2 antivirals.
Keywords

Full text: Available Collection: International databases Database: MEDLINE Language: English Journal: Cell Biosci Year: 2021 Document Type: Article Affiliation country: S13578-021-00564-x

Similar

MEDLINE

...
LILACS

LIS


Full text: Available Collection: International databases Database: MEDLINE Language: English Journal: Cell Biosci Year: 2021 Document Type: Article Affiliation country: S13578-021-00564-x