Hybrid Antibiotics Based on Azithromycin and Glycopeptides: Synthesis and Antibacterial Activity

Antibiot Khimioter. 2016;61(11-12):3-8.
[Article in English, Russian]

Abstract

A series of hybrid antibiotics on the basis of azithromycin and glycopeptides with the glycopeptide molecule attached via the aminoalkylcarbamoyl spacer to 11-position of the macrolide was synthesized. All the synthesized compounds demonstrated equal or superior to azithromycin and vancomycin antibacterial activity against 7 tested strains of grampositive bacteria. The new hybrid antibiotics were more active than azithromycin or vancomycin against S.pneumoniae ATCC 49619. Some of the compounds were active against E.faecium and E.faecalis strains resistant to vancomycin.

MeSH terms

  • Anti-Bacterial Agents* / chemical synthesis
  • Anti-Bacterial Agents* / chemistry
  • Anti-Bacterial Agents* / pharmacology
  • Azithromycin* / chemical synthesis
  • Azithromycin* / chemistry
  • Azithromycin* / pharmacology
  • Enterococcus faecalis / growth & development*
  • Enterococcus faecium / growth & development*
  • Glycopeptides* / chemical synthesis
  • Glycopeptides* / chemistry
  • Glycopeptides* / pharmacology
  • Streptococcus pneumoniae / growth & development*
  • Vancomycin Resistance / drug effects

Substances

  • Anti-Bacterial Agents
  • Glycopeptides
  • Azithromycin