2,2-Dialkylnaphthalen-1-ones as new potassium channel activators

J Med Chem. 1993 Jul 23;36(15):2121-33. doi: 10.1021/jm00067a011.

Abstract

A new series of 2,2-dialkylnaphthalen-1-one potassium channel activators has been prepared, and their in vitro relaxant activities in isolated rat portal vein and guinea pig tracheal spirals as well as their oral antihypertensive effect in spontaneously hypertensive rats have been evaluated. The group of 1,2-dihydro-4-(1,2-dihydro-2-oxo-1-pyridyl)-2,2-dimethylnaphthalen -1- ones with an electron-withdrawing substituent at the 6-position contain the most active compounds and 1,2-dihydro-4-(1,2-dihydro-2-oxo-1-pyridyl)-2,2-dimethyl-1-oxonaphtha lene-6- carbonitrile, 17f (UR-8225), has been selected for further pharmacological development.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antihypertensive Agents / chemical synthesis*
  • Benzopyrans / chemical synthesis*
  • Benzopyrans / pharmacology
  • Blood Pressure / drug effects
  • Guinea Pigs
  • Male
  • Naphthalenes / chemical synthesis*
  • Naphthalenes / pharmacology
  • Potassium Channels / drug effects*
  • Pyridones / chemical synthesis*
  • Pyridones / pharmacology
  • Rats
  • Rats, Inbred SHR
  • Structure-Activity Relationship
  • Trachea / drug effects

Substances

  • Antihypertensive Agents
  • Benzopyrans
  • Naphthalenes
  • Potassium Channels
  • Pyridones
  • UR 8225