Synthesis and antibacterial activity of 6-O-(heteroaryl-isoxazolyl)propynyl 2-fluoro ketolides

Bioorg Med Chem Lett. 2012 Sep 1;22(17):5739-43. doi: 10.1016/j.bmcl.2012.06.092. Epub 2012 Jul 6.

Abstract

Macrolide antibiotics are widely prescribed for the treatment of respiratory tract infections; however, the increasing prevalence of macrolide-resistant pathogens is a public health concern. Therefore, the development of new macrolide derivatives with activities against resistant pathogens is urgently needed. A series of novel 6-O-(heteroaryl-isoxazolyl)propynyl 2-fluoro ketolides has been synthesized from erythromycin A. These compounds have shown very promising in vitro and in vivo antibacterial activities against key respiratory pathogens including erythromycin-susceptible/resistant strains.

MeSH terms

  • Anti-Bacterial Agents / chemical synthesis
  • Anti-Bacterial Agents / chemistry*
  • Anti-Bacterial Agents / pharmacology*
  • Crystallography, X-Ray
  • Drug Resistance, Bacterial
  • Erythromycin / analogs & derivatives
  • Erythromycin / chemical synthesis
  • Erythromycin / pharmacology
  • Haemophilus Infections / drug therapy
  • Haemophilus influenzae / drug effects*
  • Halogenation
  • Humans
  • Ketolides / chemical synthesis
  • Ketolides / chemistry*
  • Ketolides / pharmacology*
  • Microbial Sensitivity Tests
  • Models, Molecular
  • Respiratory Tract Infections / drug therapy
  • Respiratory Tract Infections / microbiology*
  • Staphylococcal Infections / drug therapy
  • Staphylococcus / drug effects*

Substances

  • Anti-Bacterial Agents
  • Ketolides
  • Erythromycin