Drug intelligence / Profile preview

rolicyclidine

Development stage
Unknown
Modality
Allosteric Modulators → Classical Binding Small Molecules → Small Molecules
Administration
Oral, Inhalation (smoked), Intravenous (rare/research Context)
01

Overview

Rolicyclidine is a dissociative anesthetic drug belonging to the arylcyclohexylamine class. It exhibits hallucinogenic and sedative properties similar to phencyclidine (PCP), but is slightly less potent and has fewer stimulant effects. Its pharmacological profile includes inducing sedation reminiscent of barbiturates while retaining dissociative and hallucinogenic characteristics typical of PCP-like substances. The primary mechanism of action is antagonism at the N-methyl-D-aspartate (NMDA) receptor, leading to altered sensory perception and a sense of detachment from the environment. Additional interactions with dopamine receptors have been reported, contributing further to its psychoactive effects. Due to its similarity with PCP in both structure and effect profile, rolicyclidine was classified as a Schedule I controlled substance in several jurisdictions during the 1970s; however, it was never widely abused or used clinically[1][2][3][5][6][8].

Other names
1-(1-phenylcyclohexyl)pyrrolidineRoliciclidinaRolicyclidinumRolicyclidine [INN]
02

Targets

NMDAR (Glutamate receptor ionotropic, NMDA)DRD2 (Dopamine D2 Receptor)

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