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α-PCYP

From Wikipedia, the free encyclopedia
Stimulant drug
Not to be confused withPCPy.
Pharmaceutical compound
α-PCyP
Legal status
Legal status
Identifiers
  • 2-cyclohexyl-1-phenyl-2-(pyrrolidin-1-yl)ethanone
CAS Number
PubChemCID
UNII
CompTox Dashboard(EPA)
Chemical and physical data
FormulaC18H25NO
Molar mass271.404 g·mol−1
3D model (JSmol)
  • O=C(C(C1CCCCC1)N2CCCC2)c3ccccc3
  • InChI=1S/C18H25NO/c20-18(16-11-5-2-6-12-16)17(19-13-7-8-14-19)15-9-3-1-4-10-15/h2,5-6,11-12,15,17H,1,3-4,7-10,13-14H2
  • Key:FKEHRWJWTWDTDB-UHFFFAOYSA-N

α-PCyP (α-PyrrolidinoCyclohexanoPhenone) is astimulant drug of thecathinone class that has been sold online as adesigner drug. In a series of alpha-substituted pyrrolidinyl cathinone derivatives developed in 2015, the alpha-cyclopentyl derivative was found to have around the same potencyin vitro as aninhibitor of thedopamine transporter as the alpha-propyl derivativeα-PVP, while the alpha-cyclohexyl derivative α-PCyP was around twice as strong.[2][3][4]

See also

[edit]

References

[edit]
  1. ^"§ 54.1-3446. Schedule I."Virginia Law. Retrieved14 September 2023.
  2. ^Kolanos R, Sakloth F, Jain AD, Partilla JS, Baumann MH, Glennon RA (October 2015)."Structural Modification of the Designer Stimulant α-Pyrrolidinovalerophenone (α-PVP) Influences Potency at Dopamine Transporters".ACS Chemical Neuroscience.6 (10):1726–31.doi:10.1021/acschemneuro.5b00160.PMC 5349767.PMID 26217965.
  3. ^Glennon RA, Dukat M (2016). "Structure-Activity Relationships of Synthetic Cathinones".Neuropharmacology of New Psychoactive Substances (NPS). Current Topics in Behavioral Neurosciences. Vol. 32. pp. 19–47.doi:10.1007/7854_2016_41.ISBN 978-3-319-52442-9.PMC 5818155.PMID 27830576.
  4. ^Baumann MH, Walters HM, Niello M, Sitte HH (2018). "Neuropharmacology of Synthetic Cathinones".New Psychoactive Substances. Handbook of Experimental Pharmacology. Vol. 252. pp. 113–142.doi:10.1007/164_2018_178.ISBN 978-3-030-10560-0.PMC 7257813.PMID 30406443.
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