Acridine derivatives as anti-BVDV agents

Antiviral Res. 2011 Aug;91(2):133-41. doi: 10.1016/j.antiviral.2011.05.005. Epub 2011 May 14.

Abstract

Twenty-six 9-aminoacridine derivatives were evaluated in cell-based assays for cytotoxicity and antiviral activity against a panel of 10 RNA and DNA viruses. While seven compounds (9, 10, 14, 19, 21, 22, 24) did not affect any virus and two (6, 11) were moderately active against CVB-5 or Reo-1, 17 compounds exhibited a marked specific activity against BVDV, prototype of pestiviruses which are responsible for severe diseases of livestock. Most anti-BVDV agents showed EC(50) values in the range 0.1-8 μM, thus comparing favorably with the reference drugs ribavirine and NM 108. Some compounds, particularly those bearing a quinolizidinylalkyl side chain, displayed pronounced cytotoxicity. Further studies are warranted in order to achieve still better anti-BVDV agents, and to explore the potential antiproliferative activity of this kind of compounds.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acridines / chemical synthesis
  • Acridines / chemistry
  • Acridines / pharmacology*
  • Aminoacridines / chemistry
  • Aminoacridines / pharmacology*
  • Animals
  • Antiviral Agents / chemical synthesis
  • Antiviral Agents / chemistry
  • Antiviral Agents / pharmacology*
  • Cell Line
  • DNA Viruses / drug effects*
  • Diarrhea Viruses, Bovine Viral / drug effects*
  • Dimethyl Sulfoxide / chemistry
  • Humans
  • Linear Models
  • Microbial Sensitivity Tests
  • Molecular Structure
  • RNA Viruses / drug effects

Substances

  • Acridines
  • Aminoacridines
  • Antiviral Agents
  • 9-amino-6-chloro-2-methoxyacridine
  • Dimethyl Sulfoxide