Synthesis and identification of chiral aminomethylpiperidine carboxamides as inhibitor of collagen induced platelet activation

Eur J Med Chem. 2014 Jun 23:81:456-72. doi: 10.1016/j.ejmech.2014.05.017. Epub 2014 May 10.

Abstract

A series of chiral lactam carboxamides of aminomethylpiperidine were synthesized and investigated for the collagen induced in vitro anti-platelet efficacy and collagen plus epinephrine induced in vivo pulmonary thromboembolism. The compound 31a (30 μM/kg) displayed a remarkable antithrombotic efficacy (60% protection) which was sustained for more than 24 h and points to its excellent bioavailability. The compounds 31a (IC50 = 6.6 μM) and 32a (IC50 = 37 μM), as well as their racemic mixture 28i (IC50 = 16 μM) significantly inhibited collagen-induced human platelet aggregation in vitro. Compound 34c displayed dual mechanism of action against both collagen (IC50 = 3.3 μM) and U46619 (IC50 = 2.7 μM) induced platelet aggregation. The pharmacokinetic study of 31a indicated very faster absorption, prolonged and constant systemic exposure and thereby exhibiting better therapeutic response.

Keywords: Aminomethylpiperidine; Antiplatelet; Collagen; Epinephrine; Pyroglutamic acid; Thrombosis.

MeSH terms

  • Acetamides / administration & dosage
  • Acetamides / chemical synthesis
  • Acetamides / pharmacology*
  • Animals
  • Blood Coagulation / drug effects
  • Blood Coagulation Tests
  • Collagen / antagonists & inhibitors*
  • Collagen / pharmacology
  • Dose-Response Relationship, Drug
  • Humans
  • Mice
  • Molecular Conformation
  • Piperidines / administration & dosage
  • Piperidines / chemical synthesis
  • Piperidines / pharmacology*
  • Platelet Activation / drug effects*
  • Platelet Aggregation Inhibitors / administration & dosage
  • Platelet Aggregation Inhibitors / chemical synthesis
  • Platelet Aggregation Inhibitors / pharmacology*
  • Structure-Activity Relationship

Substances

  • Acetamides
  • Piperidines
  • Platelet Aggregation Inhibitors
  • Collagen