Synthesis and Positive Inotropic Activity of [1,2,4]Triazolo[4,3-a] Quinoxaline Derivatives Bearing Substituted Benzylpiperazine and Benzoylpiperazine Moieties

Molecules. 2017 Feb 11;22(2):273. doi: 10.3390/molecules22020273.

Abstract

In an attempt to search for more potent positive inotropic agents, two series of [1,2,4]triazolo[4,3-a] quinoxaline derivatives bearing substituted benzylpiperazine and benzoylpiperazine moieties were synthesized and their positive inotropic activities evaluated by measuring left atrial stroke volume in isolated rabbit heart preparations. Several compounds showed favorable activities compared with the standard drug, milrinone. Compound 6c was the most potent agent, with an increased stroke volume of 12.53% ± 0.30% (milrinone: 2.46% ± 0.07%) at 3 × 10-5 M. The chronotropic effects of compounds having considerable inotropic effects were also evaluated.

Keywords: [1,2,4]triazolo[4,3-a] quinoxaline; atrium; milrinone; positive inotropic activity; stroke volume.

MeSH terms

  • Animals
  • Cardiotonic Agents / chemical synthesis*
  • Cardiotonic Agents / pharmacology*
  • Dose-Response Relationship, Drug
  • Heart Atria / drug effects
  • Heart Failure / drug therapy
  • Heart Failure / etiology
  • Heart Failure / physiopathology
  • Milrinone / pharmacology
  • Molecular Structure
  • Myocardial Contraction / drug effects
  • Piperazines / chemistry*
  • Quinoxalines / chemical synthesis*
  • Quinoxalines / pharmacology*
  • Rabbits
  • Stroke Volume / drug effects

Substances

  • Cardiotonic Agents
  • Piperazines
  • Quinoxalines
  • Milrinone