Design, synthesis and evaluation of phenethylaminoheterocycles as K(v)1.5 inhibitors

Bioorg Med Chem Lett. 2014 Jul 15;24(14):3018-22. doi: 10.1016/j.bmcl.2014.05.035. Epub 2014 May 20.

Abstract

Phenethylaminoheterocycles have been prepared and assayed for inhibition of the Kv1.5 potassium ion channel as a potential approach to the treatment of atrial fibrillation. A diverse set of heterocycles were identified as potent Kv1.5 inhibitors and were advanced to pharmacodynamic evaluation based on selectivity and pharmacokinetic profile. Heterocycle optimization and template modification lead to the identification of compound 24 which demonstrated increased atrial effective refractory period in the rabbit pharmacodynamic model with mild effects on blood pressure and heart rate.

Keywords: AERP; Aminoheterocycle; Atrial fibrillation; I(Kur); K(v)1.5.

MeSH terms

  • Animals
  • Carbamates / chemical synthesis
  • Carbamates / chemistry
  • Carbamates / pharmacology*
  • Dose-Response Relationship, Drug
  • Drug Design*
  • Heart Atria / drug effects
  • Heart Rate / drug effects
  • Humans
  • Indazoles / chemical synthesis
  • Indazoles / chemistry
  • Indazoles / pharmacology*
  • Kv1.5 Potassium Channel / antagonists & inhibitors*
  • Models, Molecular
  • Molecular Structure
  • Potassium Channel Blockers / chemical synthesis
  • Potassium Channel Blockers / chemistry
  • Potassium Channel Blockers / pharmacology*
  • Rabbits
  • Rats
  • Structure-Activity Relationship

Substances

  • Carbamates
  • Indazoles
  • Kv1.5 Potassium Channel
  • Potassium Channel Blockers