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PCPEP

From Wikipedia, the free encyclopedia

PCPEP
Identifiers
  • 1-(1-phenylcyclopentyl)piperidine
CAS Number
PubChem CID
CompTox Dashboard (EPA)
Chemical and physical data
FormulaC16H23N
Molar mass229.367 g·mol−1
3D model (JSmol)
  • C1CCN(CC1)C2(CCCC2)C3=CC=CC=C3
  • InChI=1S/C16H23N/c1-3-9-15(10-4-1)16(11-5-6-12-16)17-13-7-2-8-14-17/h1,3-4,9-10H,2,5-8,11-14H2
  • Key:KNZVHCGBSJFKIX-UHFFFAOYSA-N

PCPEP (1-phenyl-1-piperidinylcyclopentane) is a designer drug from the arylcyclohexylamine family, which has dissociative effects. It is the ring-contracted cyclopentyl homologue of PCP and has around 1/10th the potency of PCP, making it a similar potency to ketamine.[1][2] It has been sold as an illicit drug in Japan.

See also

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References

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  1. Shulgin AT, Mac Lean DE (1976). "Illicit synthesis of phencyclidine (PCP) and several of its analogs". Clinical Toxicology. 9 (4): 553–560. doi:10.3109/15563657608988157. PMID 975751.
  2. Shannon HE, McQuinn RL, Vaupel DB, Cone EJ (February 1983). "Effects of cycloalkyl ring analogs of phencyclidine on behavior in rodents". The Journal of Pharmacology and Experimental Therapeutics. 224 (2): 327–333. doi:10.1016/S0022-3565(25)33474-9. PMID 6822958.