Activity of selenazofurin against influenza A and B viruses in vitro

Antimicrob Agents Chemother. 1985 Sep;28(3):375-7. doi: 10.1128/AAC.28.3.375.

Abstract

Activity of the new antiviral compound selenazofurin was compared with the known active compounds ribavirin and amantadine against influenza A and B viruses. In experiments with Madin Darby canine kidney cells, selenazofurin inhibited the cytopathic effect and yield of influenza A/NWS/33 virus, with 50% effective dose ranges of 0.7 to 1.4 micrograms/ml (virus rating [VR], 1.3 to 1.4). The 50% effective dose range for ribavirin was 1.2 to 1.6 micrograms/ml (VR, 1.0 to 1.3), and for amantadine it was 9 micrograms/ml (VR, 0.9). Selenazofurin and ribavirin were similarly inhibitory to influenza B/Lee/40 virus, whereas amantadine was inactive. Selenazofurin appeared somewhat cytotoxic in these studies at concentrations as low as 1 micrograms/ml.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amantadine / pharmacology
  • Animals
  • Cell Division / drug effects
  • Cells, Cultured
  • Cytopathogenic Effect, Viral / drug effects
  • Dogs
  • In Vitro Techniques
  • Influenza A virus / drug effects*
  • Influenza B virus / drug effects*
  • Organoselenium Compounds*
  • Ribavirin / pharmacology
  • Ribonucleosides / pharmacology*
  • Selenium / pharmacology*
  • Virus Replication / drug effects

Substances

  • Organoselenium Compounds
  • Ribonucleosides
  • Ribavirin
  • Amantadine
  • Selenium
  • selenazofurin