Synthesis, antiarrhythmic activity, and toxicological evaluation of mexiletine analogues

Eur J Med Chem. 2016 Oct 4:121:300-307. doi: 10.1016/j.ejmech.2016.05.046. Epub 2016 May 24.

Abstract

Four mexiletine analogues have been tested for their antiarrhythmic, inotropic, and chronotropic effects on isolated guinea pig heart tissues and to assess calcium antagonist activity, in comparison with the parent compound mexiletine. All analogues showed from moderate to high antiarrhythmic activity. In particular, three of them (1b,c,e) were more active and potent than the reference drug, while exhibiting only modest or no negative inotropic and chronotropic effects and vasorelaxant activity, thus showing high selectivity of action. All compounds showed no cytotoxicity and 1b,c,d did not impair motor coordination. All in, these new analogues exhibit an interesting cardiovascular profile and deserve further investigation.

Keywords: Antiarrhythmics; Inotropism; MW-assisted synthesis; Mexiletine; P-glycoprotein.

MeSH terms

  • Animals
  • Anti-Arrhythmia Agents / chemical synthesis
  • Anti-Arrhythmia Agents / chemistry
  • Anti-Arrhythmia Agents / pharmacology*
  • Anti-Arrhythmia Agents / toxicity*
  • Aorta / drug effects
  • Aorta / physiopathology
  • Cell Survival / drug effects
  • Chemistry Techniques, Synthetic
  • Dogs
  • Guinea Pigs
  • Heart Atria / drug effects
  • Heart Atria / physiopathology
  • Hep G2 Cells
  • Humans
  • Madin Darby Canine Kidney Cells
  • Mexiletine / chemical synthesis
  • Mexiletine / chemistry
  • Mexiletine / pharmacology*
  • Mexiletine / toxicity*
  • Muscle Relaxation / drug effects

Substances

  • Anti-Arrhythmia Agents
  • Mexiletine