beta 1-selective adrenoceptor antagonists. 2. 4-ether-linked phenoxypropanolamines

J Med Chem. 1983 Nov;26(11):1570-6. doi: 10.1021/jm00365a005.

Abstract

A series of 4-substituted phenoxypropanolamines was prepared and examined for beta-adrenoceptor activity. Some of the compounds, especially the [4-[2-[[2-(4-fluorophenyl)ethyl] oxy]ethoxy]phenoxy]propanolamines (14, 15, and 24), showed potent beta 1-blockade with virtually no beta 2-blockade at doses over a 1000 times greater. The compounds also possessed partial agonist activity. Structure-activity relationships are discussed, and conclusions are drawn about the binding sites on beta-adrenoceptors.

MeSH terms

  • Adrenergic beta-Agonists / metabolism
  • Adrenergic beta-Agonists / pharmacology*
  • Animals
  • Biological Assay
  • Blood Pressure / drug effects
  • Heart Rate / drug effects
  • Indicators and Reagents
  • Isoproterenol / pharmacology
  • Magnetic Resonance Spectroscopy
  • Phenyl Ethers / chemical synthesis
  • Phenyl Ethers / pharmacology
  • Propanolamines / chemical synthesis*
  • Propanolamines / pharmacology
  • Rats
  • Structure-Activity Relationship

Substances

  • Adrenergic beta-Agonists
  • Indicators and Reagents
  • Phenyl Ethers
  • Propanolamines
  • Isoproterenol