Design and synthesis of 1H-1,2,3-triazoles derived from econazole as antitubercular agents

Bioorg Med Chem Lett. 2012 Nov 15;22(22):6844-7. doi: 10.1016/j.bmcl.2012.09.041. Epub 2012 Sep 23.

Abstract

Econazole has been known to be active against Mycobacterium tuberculosis. We have designed and synthesized 1H-1,2,3-triazoles derived from econazole as antitubercular agents. The majority of triazole derivatives have been prepared by microwave-assisted click chemistry. It turned out that all of the prepared triazoles had no antifungal activities. However, most of the hydroxy-triazoles (6a and 10) apparently turned out to have antitubercular activities. Overall, hydroxy-triazoles 10 were more active than their corresponding ether-triazoles 11. While the MIC value of hydroxy-triazole 10d was as good as econazole (16 μg/mL), the MIC value of 10a was two-fold more active than econazole, suggesting that this 1H-1,2,3-triazole scaffold (3) could be further optimized to develop Mtb specific agents.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antitubercular Agents / chemical synthesis*
  • Antitubercular Agents / pharmacology
  • Antitubercular Agents / toxicity
  • Cell Survival / drug effects
  • Chlorocebus aethiops
  • Click Chemistry
  • Drug Design*
  • Econazole / chemistry*
  • Microbial Sensitivity Tests
  • Microwaves
  • Mycobacterium tuberculosis / drug effects
  • Structure-Activity Relationship
  • Triazoles / chemistry*
  • Triazoles / pharmacology
  • Triazoles / toxicity
  • Vero Cells

Substances

  • Antitubercular Agents
  • Triazoles
  • Econazole