1-(alkylamino)isochromans: hypotensives with peripheral and central activities

J Med Chem. 1982 Jan;25(1):75-81. doi: 10.1021/jm00343a015.

Abstract

A series of 1-[1-(3,4-dimethoxy-1H-2-benzopyran-1-yl)alkyl]-4-arylpiperazines that shows hypotensive activity in the conscious rat has been investigated. Structure-activity relationships are described. A typical example that was investigated in greater detail is 1-[2-(3,4-dihydro-6,7-dimethoxy-1H-2-benzopyran-1-yl)ethyl]-4-(4-fluorophenyl)piperazine. This compound decreases sympathetic nerve activity recorded from the external carotid and splanchnic nerves of baroreceptor-denervated cats and, therefore, has a central component to its mechanism of action. It also blocks pressor effects of norepinephrine and phenylephrine and is thus an alpha-adrenergic antagonist. Binding data characterize this as alpha 1-adrenergic receptor blockade.

MeSH terms

  • Adrenergic alpha-Antagonists / pharmacology
  • Animals
  • Antihypertensive Agents / chemical synthesis
  • Antihypertensive Agents / pharmacology*
  • Benzopyrans / pharmacology*
  • Blood Pressure / drug effects
  • Brain / drug effects
  • Cats
  • Chromans / chemical synthesis
  • Chromans / pharmacology*
  • Female
  • Heart Rate / drug effects
  • Male
  • Rats
  • Rats, Inbred Strains
  • Receptors, Adrenergic, alpha / metabolism
  • Structure-Activity Relationship
  • Sympathetic Nervous System / drug effects

Substances

  • Adrenergic alpha-Antagonists
  • Antihypertensive Agents
  • Benzopyrans
  • Chromans
  • Receptors, Adrenergic, alpha