Synthesis and evaluation of 1-arylsulfonyl-3-piperazinone derivatives as a factor Xa inhibitor II. Substituent effect on biological activities

Chem Pharm Bull (Tokyo). 2002 Sep;50(9):1187-94. doi: 10.1248/cpb.50.1187.

Abstract

Intravascular clot formation is an important event in a number of cardiovascular diseases. The prevention of blood coagulation has become a major target for new therapeutic agents. Factor Xa (FXa) is a trypsin-like serine protease that plays a key role in the blood coagulation cascade and represents an attractive target for anticoagulant drug development. We have investigated substituents in the central part of a lead compound (3: M55113), and discovered that compound M55551 (34: (R)-4-[(6-Chloro-2-naphthalenyl)sulfonyl]-6-oxo-1-[[1-(4-pyridinyl)-4-piperidinyl]methyl]-2-piperazinecarboxylic acid) is a potent inhibitor of FXa (IC(50)=0.006 microM), with high selectivity for FXa over trypsin and thrombin. The activity of this compound is ten times more powerful than the lead compound.

MeSH terms

  • Arylsulfonates / chemical synthesis
  • Arylsulfonates / pharmacology
  • Crystallization
  • Factor Xa Inhibitors*
  • Hydrogen Bonding
  • Indicators and Reagents
  • Oxidation-Reduction
  • Piperazines / chemical synthesis
  • Piperazines / pharmacology
  • Piperidines / chemical synthesis
  • Piperidines / pharmacology
  • Structure-Activity Relationship
  • Thrombin / antagonists & inhibitors
  • Trypsin Inhibitors / chemical synthesis
  • Trypsin Inhibitors / pharmacology

Substances

  • Arylsulfonates
  • Factor Xa Inhibitors
  • Indicators and Reagents
  • Piperazines
  • Piperidines
  • Trypsin Inhibitors
  • Thrombin