4-Amino-6-chloro-2-piperazinopyrimidines with selective affinity for alpha 2-adrenoceptors

J Med Chem. 1986 Aug;29(8):1394-8. doi: 10.1021/jm00158a013.

Abstract

A series of 4-amino-6-chloro-2-piperazinopyrimidines were synthesized and evaluated for their ability to interact with alpha 1- and alpha 2-adrenoceptors in vitro in binding assays using [3H]WB-4101, [3H]clonidine, and [3H]idazoxan as radioligands. Some compounds were also tested as inhibitors of [3H]spiroperidol binding. Several members of this series showed high and selective affinity for alpha 2-adrenoceptors. The nature of the 4-amino substituent seems to be the most critical factor in determining the potency at these receptors.

MeSH terms

  • Animals
  • Binding, Competitive
  • Cerebral Cortex / metabolism
  • Clonidine / metabolism
  • Corpus Striatum / metabolism
  • Dioxanes / metabolism
  • Idazoxan
  • Piperazines / metabolism*
  • Pyrimidines / metabolism*
  • Rats
  • Receptors, Adrenergic, alpha / metabolism*
  • Spiperone / metabolism
  • Structure-Activity Relationship

Substances

  • Dioxanes
  • Piperazines
  • Pyrimidines
  • Receptors, Adrenergic, alpha
  • Spiperone
  • (2-(2',6'-dimethoxy)phenoxyethylamino)methylbenzo-1,4-dioxane
  • Clonidine
  • Idazoxan