4.7 Review

Research Progress on the Antiviral Activity of Glycyrrhizin and its Derivatives in Liquorice

Journal

FRONTIERS IN PHARMACOLOGY
Volume 12, Issue -, Pages -

Publisher

FRONTIERS MEDIA SA
DOI: 10.3389/fphar.2021.680674

Keywords

liquorice; triterpenoid; antiviral activity; glycyrrhizin; glycyrrhetinic acid

Funding

  1. National Natural Science Foundation of China [31902253]
  2. Natural Science Foundation of Jiangsu Province [BK20180921]
  3. individual technology research and development of modern agricultural industry of Jiangsu Province [CX(19)3024]
  4. China Postdoctoral Science Foundation [2018M632399]
  5. Priority Academic Program Development of Jiangsu Higher Education Institutions (PAPD)
  6. earmarked fund for Jiangsu Agricultural Industry Technology System

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Liquorice, a traditional medicine, contains triterpenoids such as glycyrrhizin and glycyrrhetinic acid which have inhibitory effects on various viruses, including SARS-CoV-2. These compounds work through mechanisms such as inhibition of virus replication, direct inactivation of viruses, and inhibition of inflammation. Further research on unknown antiviral mechanisms, structural modifications, and drug combinations is emphasized for future studies.
Liquorice is a traditional medicine. Triterpenoids such as glycyrrhizin and glycyrrhetinic acid are the main active constituents of liquorice. Studies have revealed that these compounds exert inhibitory effects on several viruses, including SARS-CoV-2. The main mechanisms of action of these compounds include inhibition of virus replication, direct inactivation of viruses, inhibition of inflammation mediated by HMGB1/TLR4, inhibition of beta-chemokines, reduction in the binding of HMGB1 to DNA to weaken the activity of viruses, and inhibition of reactive oxygen species formation. We herein review the research progress on the antiviral effects of glycyrrhizin and its derivatives. In addition, we emphasise the significance of exploring unknown antiviral mechanisms, structural modifications, and drug combinations in future studies.

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