Design, synthesis and trypanocidal evaluation of novel 1,2,4-triazoles-3-thiones derived from natural piperine

Molecules. 2013 May 29;18(6):6366-82. doi: 10.3390/molecules18066366.

Abstract

The work reported herein describes the synthesis and the assessment of the trypanocidal activity of thirteen new 1,2,4-triazole-3-thiones obtained from natural piperine, the main constituent of the dry fruits of Piper nigrum. It is part of a research program aiming to use abundant and easily available natural products as starting materials for the design and synthesis of new molecules potentially useful as antiparasitic drugs. The variously substituted triazole derivatives were synthesized from the natural amide in four steps with the use of microwave irradiation on overall yields ranging from 32% to 51%. The cyclohexyl substituted derivative showed the best trypanocidal profile on proliferative forms of Trypanosoma cruzi (Y strain), with IC₅₀s = 18.3 and 8.87 mM against epimastigotes and amastigotes, respectively.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alkaloids / chemistry*
  • Benzodioxoles / chemistry*
  • Drug Design
  • Inhibitory Concentration 50
  • Molecular Structure
  • Parasitic Sensitivity Tests
  • Piperidines / chemistry*
  • Polyunsaturated Alkamides / chemistry*
  • Thiones / chemical synthesis
  • Thiones / chemistry*
  • Triazoles / chemical synthesis
  • Triazoles / chemistry*
  • Trypanocidal Agents / chemical synthesis
  • Trypanocidal Agents / chemistry*
  • Trypanocidal Agents / pharmacology*
  • Trypanosoma cruzi / drug effects

Substances

  • Alkaloids
  • Benzodioxoles
  • Piperidines
  • Polyunsaturated Alkamides
  • Thiones
  • Triazoles
  • Trypanocidal Agents
  • 1,2,4-triazole
  • piperine