Synthesis of conjugates between oxazolidinone antibiotics and a pyochelin analogue

Bioorg Med Chem Lett. 2017 Nov 1;27(21):4867-4870. doi: 10.1016/j.bmcl.2017.09.039. Epub 2017 Sep 18.

Abstract

Pseudomonas aeruginosa is a Gram-negative pathogenic bacterium responsible for severe infections, and it is naturally resistant to many clinically approved antibiotic families. Oxazolidinone antibiotics are active against many Gram-positive bacteria, but are inactive against P. aeruginosa. Increasing the uptake of oxazolidinones through the bacterial envelope could lead to an increased antibiotic effect. Pyochelin is a siderophore of P. aeruginosa which delivers external iron to the bacterial cytoplasm and is a potential vector for the development of Trojan Horse oxazolidinone conjugates. Novel pyochelin-oxazolidinone conjugates were synthesized using an unexpectedly regioselective peptide coupling between an amine functionalized pyochelin and oxazolidinones functionalized with a terminal carboxylate.

Keywords: Linezolid; Oxazolidinone antibiotic; Pyochelin; Siderophore; Trojan Horse strategy.

MeSH terms

  • Anti-Bacterial Agents / chemical synthesis*
  • Anti-Bacterial Agents / chemistry
  • Anti-Bacterial Agents / pharmacology
  • Drug Design
  • Oxazolidinones / chemistry*
  • Phenols / chemistry*
  • Pseudomonas aeruginosa / drug effects
  • Siderophores / chemical synthesis
  • Siderophores / chemistry
  • Siderophores / pharmacology
  • Thiazoles / chemistry*

Substances

  • Anti-Bacterial Agents
  • Oxazolidinones
  • Phenols
  • Siderophores
  • Thiazoles
  • pyochelin