Development of 2,2-dimethylchromanol cysteinyl LT1 receptor antagonists

Bioorg Med Chem Lett. 1998 Dec 15;8(24):3577-82. doi: 10.1016/s0960-894x(98)00654-4.

Abstract

A new series of cysLT1 receptor antagonists represented by CP-288,886 (7) and CP-265,298 (8) were developed which are equipotent to clinical cysLT1 receptor antagonists Zafirlukast (1) and Pranlukast (2).

MeSH terms

  • Animals
  • Anti-Asthmatic Agents / chemical synthesis*
  • Anti-Asthmatic Agents / pharmacokinetics
  • Anti-Asthmatic Agents / pharmacology
  • Biological Availability
  • Guinea Pigs
  • Humans
  • Leukotriene Antagonists*
  • Magnetic Resonance Spectroscopy
  • Membrane Proteins*
  • Quinolines / chemical synthesis*
  • Quinolines / pharmacokinetics
  • Quinolines / pharmacology
  • Rats
  • Receptors, Leukotriene*
  • Stereoisomerism
  • Thiazoles / chemical synthesis*
  • Thiazoles / pharmacokinetics
  • Thiazoles / pharmacology
  • U937 Cells

Substances

  • Anti-Asthmatic Agents
  • CP 265298
  • Leukotriene Antagonists
  • Membrane Proteins
  • Quinolines
  • Receptors, Leukotriene
  • Thiazoles
  • CP 288886
  • cysteinyl leukotriene receptor 2
  • leukotriene D4 receptor