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Rolicyclidine

From Wikipedia, the free encyclopedia
Chemical compound
Not to be confused withα-PCyP.
Pharmaceutical compound
Rolicyclidine
Clinical data
ATC code
  • none
Legal status
Legal status
Identifiers
  • 1-(1-phenylcyclohexyl)pyrrolidine
CAS Number
PubChemCID
DrugBank
ChemSpider
UNII
KEGG
ChEBI
CompTox Dashboard(EPA)
Chemical and physical data
FormulaC16H23N
Molar mass229.367 g·mol−1
3D model (JSmol)
  • c1ccccc1C3(N2CCCC2)CCCCC3
  • 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
  (verify)

Rolicyclidine (PCPy) is adissociativeanesthetic that is similar in effects tophencyclidine, but is slightly less potent and has fewer stimulant effects.[2] It instead produces a sedative effect described as being somewhat similar to abarbiturate, but with additional PCP-like dissociative, anaesthetic and hallucinogenic effects.[3] 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

[edit]

References

[edit]
  1. ^Anvisa (2023-07-24)."RDC Nº 804 - Listas de Substâncias Entorpecentes, Psicotrópicas, Precursoras e Outras sob Controle Especial" [Collegiate Board Resolution No. 804 - Lists of Narcotic, Psychotropic, Precursor, and Other Substances under Special Control] (in Brazilian Portuguese).Diário Oficial da União (published 2023-07-25).Archived from the original on 2023-08-27. Retrieved2023-08-27.
  2. ^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.
  3. ^DEA Microgram Bulletin, 8, 143, 1975
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