Synthesis and in vitro evaluation of antibacterial and antibiofilm activities of novel triphenylphosphonium-functionalized substituted pyrimidines

Chem Biol Drug Des. 2024 Feb;103(2):e14483. doi: 10.1111/cbdd.14483.

Abstract

The increase in the prevalence of antibiotic-resistant pathogens leads to a decrease in the number of antimicrobial agents for the treatment of infections and prompts researchers to search for new effective antimicrobial drugs. This study reports the synthesis of novel triphenylphosphonium-functionalized substituted pyrimidines and in vitro evaluation of their antibacterial and antibiofilm activity. Most of the synthesized derivatives showed high antibacterial activity (MIC = 0.39-1.56 μg/mL) against the methicillin-resistant strain of S. aureus 222. Compounds 2a and 11 exhibited a high level of antibiofilm activity against S. aureus 222 and E. coli 311. The triphenylphosphonium-containing pyrimidines 11 and 2a reduced S. aureus 222 biofilm formation by 99.1% and 95.8%, respectively. In addition, compound 2a was the most active against E. coli 311 biofilm formation (the biomass decreased by 98.4%).

Keywords: (pyrimidin-5-yl)triphenylphosphonium; antibacterial; antibiofilm activity; pyrimidines; triphenylphosphonium.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Anti-Bacterial Agents / pharmacology
  • Anti-Infective Agents* / pharmacology
  • Biofilms
  • Escherichia coli
  • Methicillin-Resistant Staphylococcus aureus*
  • Microbial Sensitivity Tests
  • Organophosphorus Compounds*
  • Pyrimidines / pharmacology
  • Staphylococcus aureus
  • Structure-Activity Relationship

Substances

  • Pyrimidines
  • triphenylphosphonium
  • Anti-Bacterial Agents
  • Anti-Infective Agents
  • Organophosphorus Compounds