Synthesis and structure-activity relationships of new 9-N-alkyl derivatives of 9(S)-erythromycylamine

J Med Chem. 1990 Nov;33(11):3086-94. doi: 10.1021/jm00173a028.

Abstract

A series of new 9-N-alkyl derivatives of 9(S)-erythromycylamine has been synthesized by reductive alkylation of erythromycylamine with aliphatic aldehydes and sodium cyanoborohydride. Alternative syntheses employing hydrogenation methods have also been developed. These new 9-N-alkyl derivatives possess excellent antimicrobial activity in vitro and in vivo, especially when administered orally to treat experimental infections in mice. From structure-activity studies, 9-N-(1-propyl)erythromycylamine (LY281389) was selected as the most efficacious derivative. These methods have also been extended to the synthesis of some 9-N,N-dialkyl derivatives of erythromycylamine.

Publication types

  • Comparative Study

MeSH terms

  • Alkylation
  • Animals
  • Bacterial Infections / drug therapy
  • Chemical Phenomena
  • Chemistry
  • Erythromycin / analogs & derivatives*
  • Erythromycin / chemical synthesis
  • Erythromycin / chemistry
  • Erythromycin / therapeutic use
  • Magnetic Resonance Spectroscopy
  • Mice
  • Molecular Structure
  • Rats
  • Staphylococcal Infections / drug therapy
  • Streptococcal Infections / drug therapy
  • Structure-Activity Relationship

Substances

  • 9-N-(1-propyl)erythromyclamine
  • erythromyclamine
  • Erythromycin