Triterpenoid-Mediated Inhibition of Virus-Host Interaction: Is Now the Time for Discovering Viral Entry/Release Inhibitors from Nature?

J Med Chem. 2020 Dec 24;63(24):15371-15388. doi: 10.1021/acs.jmedchem.0c01348. Epub 2020 Nov 17.

Abstract

Fatal infectious diseases caused by HIV-1, influenza A virus, Ebola virus, and currently pandemic coronavirus highlight the great need for the discovery of antiviral agents in mechanisms different from current viral replication-targeted approaches. Given the critical role of virus-host interactions in the viral life cycle, the development of entry or shedding inhibitors may expand the current repertoire of antiviral agents; the combination of antireplication inhibitors and entry or shedding inhibitors would create a multifaceted drug cocktail with a tandem antiviral mechanism. Therefore, we provide critical information about triterpenoids as potential antiviral agents targeting entry and release, focusing specifically on the emerging aspect of triterpenoid-mediated inhibition of a variety of virus-host membrane fusion mechanisms via a trimer-of-hairpin motif. These properties of triterpenoids supply their host an evolutionary advantage for chemical defense and may protect against an increasingly diverse array of viruses infecting mammals, providing a direction for antiviral drug discovery.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Animals
  • Antiviral Agents / therapeutic use*
  • Cell Line, Tumor
  • Humans
  • Molecular Structure
  • RNA Viruses / drug effects*
  • SARS-CoV-2 / drug effects
  • Structure-Activity Relationship
  • Triterpenes / therapeutic use*
  • Virus Internalization / drug effects*
  • Virus Release / drug effects*
  • Virus Shedding / drug effects

Substances

  • Antiviral Agents
  • Triterpenes