Synthesis and biological evaluation of quinones derived from natural product komaroviquinone as anti-Trypanosoma cruzi agents

Bioorg Med Chem Lett. 2015 Aug 1;25(15):2967-71. doi: 10.1016/j.bmcl.2015.05.022. Epub 2015 May 16.

Abstract

Current chemotherapy drugs for Chagas' disease are insufficient due to their limited efficacy; however, anti-trypanosomal agents have recently shown promise. As such, synthetic intermediates of komaroviquinone were evaluated for anti-trypanosomal activity. Based on the results, a series of novel quinone derivatives were screened for anti-trypanosomal activity and mammalian cytotoxicity. Several quinone derivatives displayed higher antiprotozoal activity against Trypanosoma cruzi trypomastigotes than the reference drug benznidazole, without concomitant toxicity toward the host cell.

Keywords: Chagas’ disease; Quinone; Trypanosoma cruzi.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 3T3 Cells
  • Animals
  • Chagas Disease / drug therapy*
  • Chagas Disease / parasitology
  • Diterpenes / chemical synthesis
  • Diterpenes / chemistry*
  • Diterpenes / pharmacology*
  • Humans
  • Mice
  • Quinones / chemical synthesis
  • Quinones / chemistry*
  • Quinones / pharmacology*
  • Trypanocidal Agents / chemical synthesis
  • Trypanocidal Agents / chemistry*
  • Trypanocidal Agents / pharmacology*
  • Trypanosoma cruzi / drug effects*

Substances

  • Diterpenes
  • Quinones
  • Trypanocidal Agents
  • komaroviquinone