Anti-influenza activity of monoterpene-derived substituted hexahydro-2H-chromenes

Bioorg Med Chem. 2016 Nov 1;24(21):5158-5161. doi: 10.1016/j.bmc.2016.08.037. Epub 2016 Aug 22.

Abstract

The antiviral activity of 4-hydroxy-hexahydro-2H-chromenes and 4-fluorine-hexahydro-2H-chromenes with an aromatic substituent, synthesized from monoterpene (-)-verbenone, was studied for the first time. Five of 11 (45 per cent) of 4-hydroxy-hexahydro-2H-chromene-type compounds have been found to exhibit antiviral activity against influenza A virus of subtype H1N1pdm09. Although a portion of active compounds among 4-fluorine-containing series was fewer, just compound 5i that contains a fluorine substituent exhibited more potent anti-influenza activity along with low cytotoxicity. Thus two new promising types of antiviral compounds were identified.

Keywords: Antiviral; Chromene; Influenza; Monoterpene.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antiviral Agents / chemical synthesis
  • Antiviral Agents / chemistry
  • Antiviral Agents / pharmacology*
  • Benzopyrans / chemistry
  • Benzopyrans / pharmacology*
  • Dose-Response Relationship, Drug
  • Humans
  • Influenza A virus / drug effects*
  • Microbial Sensitivity Tests
  • Molecular Structure
  • Monoterpenes / chemical synthesis
  • Monoterpenes / chemistry
  • Monoterpenes / pharmacology*
  • Structure-Activity Relationship

Substances

  • Antiviral Agents
  • Benzopyrans
  • Monoterpenes