Structure via PubChem · Public domain (PubChem)
rolicyclidine
Sign in to saveAlso known as 1-(1-phenylcyclohexyl)pyrrolidine, PCPy, Pyrrolidine analog of phencyclidine, Roliciclidina, Rolicyclidinum
Rolicyclidine (PCPy) is a dissociative anesthetic that is similar in effects to phencyclidine, but is slightly less potent and has fewer stimulant effects. It instead produces a sedative effect described as being somewhat similar to a barbiturate, but with additional PCP-like dissociative, anaesthetic and hallucinogenic effects. Due to its similarity in effects to PCP, PCPy was placed into the Schedule I list of illegal drugs in the 1970s, although it has never been widely abused and is now little known.
Chemical data
- Formula
- C16H23N
- Molecular weight
- 229.36 g/mol
- IUPAC name
- 1-(1-phenylcyclohexyl)pyrrolidine
- SMILES
- C1CCC(CC1)(C2=CC=CC=C2)N3CCCC3
- InChIKey
- FYOWWXMGDATDQY-UHFFFAOYSA-N
- XLogP
- 3.3
- Polar surface area
- 3.2 Ų
- H-bond donors
- 0
- H-bond acceptors
- 1
- Formal charge
- 0
via PubChem
Drug data · ChEMBL
- Max clinical phase
- Phase 2
- Molecule type
- Small molecule
via ChEMBL · EBI
Wikidata facts
- Subclass of
- chemical compound
- Mass
- 229.18305
Show 3 more facts
- chemical formula
- C₁₆H₂₃N
- canonical SMILES
- C1CCC(CC1)(C2=CC=CC=C2)N3CCCC3
- World Health Organisation international non-proprietary name
- rolicyclidine
Sources (2)
via Wikidata · CC0
~1 min read
Encyclopedic overview
2 sectionsContents
- See also
- References
Rolicyclidine (PCPy) is a dissociative anesthetic that is similar in effects to phencyclidine, but is slightly less potent and has fewer stimulant effects. It instead produces a sedative effect described as being somewhat similar to a barbiturate, but with additional PCP-like dissociative, anaesthetic and hallucinogenic effects. Due to its similarity in effects to PCP, PCPy was placed into the Schedule I list of illegal drugs in the 1970s, although it has never been widely abused and is now little known.
==See also== PCP Arylcyclohexylamine Picilorex α-PHP
Excerpted from Wikipedia’s “rolicyclidine” article, available under the CC BY-SA 4.0 licence.