Synthesis and antibacterial activity of 3-O-carbamoyl derivatives of 6,11-di-O-methylerythromycin A: a novel class of acylides

Eur J Med Chem. 2010 Sep;45(9):3636-44. doi: 10.1016/j.ejmech.2010.05.009. Epub 2010 May 12.

Abstract

A novel series of acylides, 3-O-carbamoyl derivatives of 6,11-di-O-methylerythromycin A, were synthesized and evaluated for their antibacterial activity. These compounds have significant antibacterial activity against gram-positive pathogens, including erythromycin-resistant but methicillin-susceptible Staphylococcus aureus, erythromycin-resistant and methicillin-resistant S. aureus, erythromycin-resistant Streptococcus pneumoniae, and gram-negative pathogens, such as Haemophilus influenzae. Among the derivatives tested, compounds 4p, 4r, 4w, 4x and 4z were found to have potent activity against most susceptible and resistant bacteria. Compound 4p exhibited excellent antibacterial activity in comparison to the others.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Anti-Bacterial Agents / chemical synthesis*
  • Anti-Bacterial Agents / chemistry
  • Anti-Bacterial Agents / pharmacology*
  • Bacteria / drug effects*
  • Clarithromycin / analogs & derivatives*
  • Clarithromycin / chemical synthesis
  • Clarithromycin / chemistry
  • Clarithromycin / pharmacology
  • Drug Discovery
  • Microbial Sensitivity Tests

Substances

  • 6,11-di-O-methylerythromycin A
  • Anti-Bacterial Agents
  • Clarithromycin