Antiplasmodial activities of gold(I) complexes involving functionalized N-heterocyclic carbenes

Bioorg Med Chem. 2016 Jul 1;24(13):3075-3082. doi: 10.1016/j.bmc.2016.05.023. Epub 2016 May 17.

Abstract

A series of twenty five molecules, including imidazolium salts functionalized by N-, O- or S-containing groups and their corresponding cationic, neutral or anionic gold(I) complexes were evaluated on Plasmodium falciparum in vitro and then on Vero cells to determine their selectivity. Among them, eight new compounds were synthesized and fully characterized by spectroscopic methods. The X-ray structures of three gold(I) complexes are presented. Except one complex (18), all the cationic gold(I) complexes show potent antiplasmodial activity with IC50 in the micro- and submicromolar range, correlated with their lipophilicity. Structure-activity relationships enable to evidence a lead-complex (21) displaying a good activity (IC50=210nM) close to the value obtained with chloroquine (IC50=514nM) and a weak cytotoxicity.

Keywords: Antiplasmodial drugs; Gold; N-Heterocyclic carbene; Organometallic complexes.

MeSH terms

  • Animals
  • Antimalarials / chemical synthesis
  • Antimalarials / chemistry
  • Antimalarials / pharmacology*
  • Antimalarials / toxicity
  • Cell Survival / drug effects
  • Chlorocebus aethiops
  • Chloroquine / chemistry
  • Chloroquine / pharmacology
  • Crystallography, X-Ray
  • Gold / chemistry
  • Gold / pharmacology*
  • Inhibitory Concentration 50
  • Methane / analogs & derivatives*
  • Methane / chemistry
  • Methane / pharmacology
  • Molecular Structure
  • Organometallic Compounds / chemical synthesis*
  • Organometallic Compounds / chemistry
  • Organometallic Compounds / pharmacology
  • Organometallic Compounds / toxicity
  • Plasmodium falciparum / drug effects*
  • Structure-Activity Relationship
  • Vero Cells

Substances

  • Antimalarials
  • Organometallic Compounds
  • carbene
  • Gold
  • Chloroquine
  • Methane