Rolicyclidine

Rolicyclidine
Clinical data
ATC code	none;
Legal status
Legal status	AU: S9 (Prohibited substance); BR: Class F2 (Prohibited psychotropics); CA: Schedule III; DE: Anlage I (Authorized scientific use only); UK: Class A; US: Schedule I; UN: Psychotropic Schedule I;
Identifiers
	IUPAC name 1-(1-phenylcyclohexyl)pyrrolidine;
CAS Number	2201-39-0;
PubChem CID	62436;
DrugBank	DB01549 ;
ChemSpider	56218 ;
UNII	183O9O9JE3;
KEGG	D12706 ;
ChEBI	CHEBI:60805 ;
CompTox Dashboard (EPA)	DTXSID8046167 ;
Chemical and physical data
Formula	C16H23N
Molar mass	229.367 g·mol−1
3D model (JSmol)	Interactive image;
	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 ; Key:FYOWWXMGDATDQY-UHFFFAOYSA-N ;
	(verify)

Rolicyclidine (PCPy) is a dissociative anesthetic that is similar in effects to phencyclidine, but is slightly less potent and has fewer stimulant effects.^[2] It instead produces a sedative effect described as being somewhat similar to a barbiturate, 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.