Synthesis and antimicrobial activity of N-alkyl and N-aryl piperazine derivatives

Bioorg Med Chem. 2006 Mar 15;14(6):1819-26. doi: 10.1016/j.bmc.2005.10.032. Epub 2005 Nov 9.

Abstract

A series of substituted piperazine derivatives have been synthesized and tested for antimicrobial activity. The antibacterial activity was tested against Staphylococcus aureus (MTCCB 737), Pseudomonas aeruginosa (MTCCB 741), Streptomyces epidermidis (MTCCB 1824) and Escherichia coli (MTCCB 1652), and antifungal activity against Aspergillus fumigatus, Aspergillus flavus and Aspergillus niger. All synthesized compounds showed significant activity against bacterial strains but were found to be less active against tested fungi. In vitro toxicity tests demonstrated that compounds 4d and 6a showed very less toxicity against human erythrocytes.

MeSH terms

  • Anti-Infective Agents / chemical synthesis
  • Anti-Infective Agents / chemistry*
  • Anti-Infective Agents / pharmacology*
  • Bacteria / drug effects
  • Erythrocytes / drug effects
  • Fungi / drug effects
  • Humans
  • Microbial Sensitivity Tests
  • Molecular Structure
  • Piperazines / chemical synthesis
  • Piperazines / chemistry
  • Piperazines / pharmacology*

Substances

  • Anti-Infective Agents
  • Piperazines