Synthesis and antiviral evaluation of 3'-C-trifluoromethyl nucleoside derivatives bearing adenine as the base

Nucleosides Nucleotides Nucleic Acids. 2001 Apr-Jul;20(4-7):755-8. doi: 10.1081/NCN-100002423.

Abstract

3'-deoxy-3'-C-trifluoromethyl- (3), 2',3'-dideoxy-3'-C-trifluoromethyl- (5) and 2',3'-dideoxy-2',3'-didehydro-3'-C-trifluoromethyladenosine (6) derivatives have been synthesized and their antiviral properties examined. All these derivatives were stereospecifically prepared by glycosylation of adenine with a trifluoromethyl sugar precursor (1), followed by appropriate chemical modifications. The prepared compounds were tested for their activity against HIV, but they did not show an antiviral effect.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Anti-HIV Agents / chemical synthesis*
  • Anti-HIV Agents / pharmacology
  • Cell Line
  • Dideoxyadenosine / analogs & derivatives*
  • Dideoxyadenosine / chemical synthesis
  • Dideoxyadenosine / pharmacology
  • HIV-1 / drug effects
  • HIV-1 / physiology
  • Humans
  • Hydrocarbons, Fluorinated / chemical synthesis
  • Hydrocarbons, Fluorinated / pharmacology
  • Stereoisomerism
  • Virus Replication / drug effects

Substances

  • Anti-HIV Agents
  • Hydrocarbons, Fluorinated
  • Dideoxyadenosine