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