Rolicyclidine

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Not to be confused with α-PCyP.
Rolicyclidine
Rolicyclidine.svg
Clinical data
ATC code
  • none
Legal status
Legal status
  • AU: S9 (Prohibited substance)
  • CA: Schedule III
  • DE: Anlage I (Authorized scientific use only)
  • UK: Class A
  • US: Schedule I
Identifiers
IUPAC name
  • 1-(1-phenylcyclohexyl)pyrrolidine
CAS Number
PubChem CID
DrugBank
ChemSpider
UNII
ChEBI
CompTox Dashboard (EPA)
Chemical and physical data
FormulaC16H23N
Molar mass229.367 g·mol−1
3D model (JSmol)
SMILES
  • c1ccccc1C3(N2CCCC2)CCCCC3
InChI
  • InChI=1S/C16H23N/c1-3-9-15(10-4-1)16(11-5-2-6-12-16)17-13-7-8-14-17/h1,3-4,9-10H,2,5-8,11-14H2 checkY
  • Key:FYOWWXMGDATDQY-UHFFFAOYSA-N checkY
  

Rolicyclidine (PCPy) is a dissociative anesthetic drug with hallucinogenic and sedative effects. It is similar in effects to phencyclidine but is slightly less potent and has less stimulant effects[1] instead producing a sedative effect described as being somewhat similar to a barbiturate, but with additional PCP-like dissociative, anaesthetic and hallucinogenic effects.[2] 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

References[]

  1. ^ Kalir A, Edery H, Pelah Z, Balderman D, Porath G (May 1969). "1-Phenycycloalkylamine derivatives. II. Synthesis and pharmacological activity". Journal of Medicinal Chemistry. 12 (3): 473–7. doi:10.1021/jm00303a030. PMID 4977945.
  2. ^ DEA Microgram Bulletin, 8, 143, 1975


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