Synthesis and In Vitro Anti Leishmania amazonensis Biological Screening of Morita-Baylis-Hillman Adducts Prepared from Eugenol, Thymol and Carvacrol

Molecules. 2016 Nov 8;21(11):1483. doi: 10.3390/molecules21111483.

Abstract

Leishmaniasis represents a series of severe neglected tropical diseases caused by protozoa of the genus Leishmania and is widely distributed around the world. Here, we present the syntheses of Morita-Baylis-Hillman adducts (MBHAs) prepared from eugenol, thymol and carvacrol, and their bioevaluation against promastigotes of Leishmania amazonensis. The new MBHAs are prepared in two steps from essential oils in moderate to good yields and present IC50 values in the range of 22.30-4.71 μM. Moreover, the selectivity index to the most potent compound is very high (SIrb > 84.92), far better than that of Glucantime® (SIrb 1.39) and amphotericin B (SIrb = 22.34). Conformational analysis were carried out at the M062X//6-31+G(d,p) level of theory to corroborate a hypothesis about the nitroaromatic bioreduction mechanism.

Keywords: Leishmania amazonensis; Morita-Baylis-Hillman adducts; carvacrol; eugenol; thymol.

MeSH terms

  • Acrylates / chemical synthesis*
  • Acrylates / chemistry
  • Acrylates / pharmacology
  • Antiprotozoal Agents / chemical synthesis*
  • Antiprotozoal Agents / chemistry
  • Antiprotozoal Agents / pharmacology
  • Cymenes
  • Drug Evaluation, Preclinical
  • Eugenol / chemistry*
  • Green Chemistry Technology / methods
  • In Vitro Techniques
  • Leishmania / drug effects*
  • Molecular Structure
  • Monoterpenes / chemistry*
  • Oils, Volatile / chemistry
  • Structure-Activity Relationship
  • Thymol / chemistry*

Substances

  • Acrylates
  • Antiprotozoal Agents
  • Cymenes
  • Monoterpenes
  • Oils, Volatile
  • Thymol
  • Eugenol
  • carvacrol