Design and synthesis of 1,2-annulated adamantane piperidines with anti-influenza virus activity

Bioorg Med Chem. 2009 Feb 15;17(4):1534-41. doi: 10.1016/j.bmc.2009.01.009. Epub 2009 Jan 15.

Abstract

1-2 Annulated adamantane piperidines 4, 6, 16, 17, 19, 23 and 25 were synthesized and evaluated for anti-influenza A virus activity. The stereoelectronic requirements for optimal antiviral potency were investigated. Piperidine 23 proved to be the most active of the compounds tested against influenza A virus, being 3.5-fold more active than amantadine, equipotent to rimantadine and 15-fold more potent than ribavirin. It is noteworthy that piperidine 23 displayed one of the highest selectivity indexes (SI>732) among aminoadamantanes or other cage structure amines tested till now.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adamantane / chemical synthesis*
  • Adamantane / chemistry
  • Adamantane / pharmacology*
  • Animals
  • Antiviral Agents / chemical synthesis
  • Antiviral Agents / chemistry
  • Antiviral Agents / pharmacology
  • Dogs
  • Humans
  • Influenza A Virus, H3N2 Subtype / drug effects*
  • Magnetic Resonance Spectroscopy
  • Molecular Structure
  • Piperidines / chemical synthesis
  • Piperidines / chemistry*
  • Piperidines / pharmacology*
  • Rimantadine / chemical synthesis
  • Rimantadine / pharmacology
  • Structure-Activity Relationship

Substances

  • Antiviral Agents
  • Piperidines
  • Rimantadine
  • Adamantane