Nitrogen analogues of phencyclidine: 1-alkyl-4-phenyl-4-(1-piperidinyl)piperidines

Farmaco Sci. 1984 Jul;39(7):599-611.

Abstract

In order to investigate the effect of the introduction of a nitrogen atom in the alicyclic moiety of phencyclidine (PCP) a series of 1-alkyl-4-phenyl-4-(1-piperidinyl)piperidines were synthesized. The in vivo assays in mice and EEG in rabbits indicated that the presence of a second basic center in the molecule resulted in a loss of PCP-like activity. The new compounds were devoid of analgesic activity.

MeSH terms

  • Animals
  • Anticonvulsants / chemical synthesis
  • Brain / physiology
  • Chemical Phenomena
  • Chemistry
  • Electroencephalography
  • Electrophysiology
  • Lethal Dose 50
  • Male
  • Mice
  • Molecular Conformation
  • Motor Activity / drug effects
  • Phencyclidine / analogs & derivatives*
  • Phencyclidine / chemical synthesis
  • Phencyclidine / pharmacology
  • Potentiometry
  • Rabbits
  • Structure-Activity Relationship

Substances

  • Anticonvulsants
  • Phencyclidine