Design, Synthesis and Antifungal Activity of Novel Benzofuran-Triazole Hybrids

Molecules. 2016 Jun 7;21(6):732. doi: 10.3390/molecules21060732.

Abstract

A series of novel benzofuran-triazole hybrids was designed and synthesized by click chemistry, and their structures were characterized by HRMS, FTIR and NMR. The in vitro antifungal activity of target compounds was evaluated using the microdilution broth method against five strains of pathogenic fungi. The result indicated that the target compounds exhibited moderate to satisfactory activity. Furthermore, molecular docking was performed to investigate the binding affinities and interaction modes between the target compound and N-myristoyltransferase. Based on the results, preliminary structure activity relationships (SARs) were summarized to serve as a foundation for further investigation.

Keywords: 1,2,3-triazole; N-myristoyltransferase; antifungal activity; benzofuran; click chemistry; molecule hybrid.

MeSH terms

  • Benzofurans / chemical synthesis
  • Benzofurans / chemistry*
  • Benzofurans / pharmacology
  • Click Chemistry
  • Drug Design*
  • Fungi / drug effects*
  • Fungi / pathogenicity
  • Molecular Docking Simulation
  • Molecular Structure
  • Structure-Activity Relationship
  • Triazoles / chemical synthesis
  • Triazoles / chemistry*
  • Triazoles / pharmacology

Substances

  • Benzofurans
  • Triazoles
  • benzofuran