alpha-Pyrrolidinopentiophenone

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This article is about the drug substance α-PVP. For the pharmaceutical excipient called PVP, see polyvinylpyrrolidone.
alpha-Pyrrolidinopentiophenone
Ball-and-stick model of the alpha-PVP molecule
Clinical data
Routes of
administration		By mouth, intranasal, vaporization, intravenous, sublingual
Legal status
Legal status
Identifiers
  • (RS)-1-Phenyl-2-(pyrrolidin-1-yl)pentan-1-one
CAS Number
PubChem CID
ChemSpider
UNII
KEGG
ChEMBL
CompTox Dashboard (EPA)
Chemical and physical data
FormulaC15H21NO
Molar mass231.339 g·mol−1
3D model (JSmol)
  • CCCC(C(C1=CC=CC=C1)=O)N2CCCC2
  • InChI=1S/C15H21NO/c1-2-8-14(16-11-6-7-12-16)15(17)13-9-4-3-5-10-13/h3-5,9-10,14H,2,6-8,11-12H2,1H3 checkY
  • Key:YDIIDRWHPFMLGR-UHFFFAOYSA-N checkY
 ☒NcheckY (what is this?)  (verify)

α-Pyrrolidinopentiophenone (also known as α-pyrrolidinovalerophenone, α-PVP, O-2387, β-keto-prolintane, prolintanone,[citation needed] or desmethylpyrovalerone) is a synthetic stimulant of the cathinone class developed in the 1960s that has been sold as a designer drug and often consumed for recreational reasons.[2][3] α-PVP is chemically related to pyrovalerone and is the ketone analog of prolintane.[4]

Colloquially, it is sometimes called flakka, gravel and the zombie drug.[5][6]

Adverse effects[edit]

α-PVP, like other psychostimulants, can cause hyperstimulation, paranoia, and hallucinations.[7] α-PVP has been reported to be the cause, or a significant contributory cause of death in suicides and overdoses caused by combinations of drugs.[8][9][10][11] α-PVP has also been linked to at least one death with pulmonary edema and moderately advanced atherosclerotic coronary disease when it was combined with pentedrone.[12]

According to Craig Crespi in the journal Case Reports in Psychiatry, "symptoms are known to easily escalate into frightening delusions, paranoid psychosis, extreme agitation, and a multitude of other altered mental states." These common adverse effects of α-PVP are in line with other psychostimulants.

In addition, agitated delirium has been named as an adverse effect of α-PVP.[13]

Pharmacology[edit]

α-PVP acts as a norepinephrine-dopamine reuptake inhibitor with IC50 values of 14.2 and 12.8 nM, respectively, similar to its methylenedioxy derivative MDPV.[14][15][16][17] Similar to other cathinones, α-PVP has been shown to have reinforcing effects in rats.[18][19]

Chemistry[edit]

α-PVP gives no reaction with the Marquis reagent. It gives a grey/black reaction with the Mecke reagent.[20]

Detection in body fluids[edit]

α-PVP may be quantified in blood, plasma or urine by liquid chromatography-mass spectrometry to confirm a diagnosis of poisoning in hospitalized patients or to provide evidence in a medicolegal death investigation. Blood or plasma α-PVP concentrations are expected to be in a range of 10–50 μg/L in persons using the drug recreationally, >100 μg/L in intoxicated patients and >300 μg/L in victims of acute overdosage.[21][22]

Society and culture[edit]

Legal status[edit]

α-PVP is banned in Estonia, Finland, France, Germany, Hungary, Russia, Ireland, Latvia, Lithuania, Netherlands, Poland, Romania, Slovenia, Sweden, United Kingdom, Turkey, Norway,[14] as well as the Czech Republic.[23]

Australia[edit]

α-PVP is a Schedule 9 prohibited substance under the Poisons Standard (July 2016).[24] A Schedule 9 substance is a substance which may be abused or misused, the manufacture, possession, sale or use of which should be prohibited by law except when required for medical or scientific research, or for analytical, teaching or training purposes with approval of Commonwealth and/or State or Territory Health Authorities.[24] The drug was explicitly made illegal in New South Wales after it was illegally marketed with the imprimatur of erroneous legal advice that it was not encompassed by analog provisions of the relevant act. It is encompassed by those provisions, and therefore has been illegal for many years in New South Wales. The legislative action followed the death of two individuals from using it; one jumping off a balcony, another having a heart attack after a state of delirium.[25][26]

EU[edit]

α-PVP was required to be banned by EU member states by 3 July 2017[27] and appears in Schedule II of the UN Convention on Psychotropic Substances.

China[edit]

As of October 2015, α-PVP is a controlled substance in China.[28]

Italy[edit]

Cathinone and all structurally derived analogues (including pyrovalerone analogues) were classified as narcotics in January 2012.[29][14]

US[edit]

On 28 January 2014, the DEA listed α-PVP, along with nine other synthetic cathinones, on the Schedule 1 with a temporary ban, effective February 27, 2014.[30] The temporary ban was then extended.[31]

Economics[edit]

α-PVP is sometimes the active ingredient in recreational drugs sold as "bath salts".[25] It may also be distinguished from "bath salts" and sold under a different name: "flakka", a name used in Florida, or "gravel" in other parts of the U.S. It is reportedly available as cheaply as US$5 per dose.[32] A laboratory for one county in Florida reported a steady rise in α-PVP detections in seized drugs from none in January–February 2014 to 84 in September 2014.[33]

See also[edit]

Notes[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. Retrieved 2023-08-27.
  2. ^ GB 927475, "α-Pyrrolidinovalerophenones", published May 29, 1963 
  3. ^ Logan BK (September 13, 2013). "SOFT Designer Drug Committee Monographs: Alpha-PVP" (PDF). Society of Forensic Toxicologists. Archived from the original (PDF) on April 6, 2015.
  4. ^ Sauer C, Peters FT, Haas C, Meyer MR, Fritschi G, Maurer HH (June 2009). "New designer drug alpha-pyrrolidinovalerophenone (PVP): studies on its metabolism and toxicological detection in rat urine using gas chromatographic/mass spectrometric techniques". Journal of Mass Spectrometry. 44 (6): 952–64. Bibcode:2009JMSp...44..952S. doi:10.1002/jms.1571. PMID 19241365.
  5. ^ Coubrough J (November 2, 2017). "'Zombie drug' flakka may have hit Winnipeg streets: police". CBC News.
  6. ^ England C, Garcia F (August 17, 2016). "Flakka: What is the 'zombie drug' blamed for face-eating attacks?". The Independent. Archived from the original on 2016-08-18.
  7. ^ "Drugs of Abuse Emerging Trends". National Institute on Drug Abuse. 6 April 2015.
  8. ^ Marinetti LJ, Antonides HM (April 2013). "Analysis of synthetic cathinones commonly found in bath salts in human performance and postmortem toxicology: method development, drug distribution and interpretation of results". Journal of Analytical Toxicology. 37 (3): 135–46. doi:10.1093/jat/bks136. PMID 23361867.
  9. ^ Richards-Waugh LL, Bailey KM, Clay DJ, Gebhardt MA, Newsome-Sparks CL, Majmoud HE, Venuti SE, Kraner JC (2013). "t" (PDF). AAFS Proceedings. Abstract K16. Archived from the original (PDF) on 2016-11-08. Retrieved 2015-04-03.
  10. ^ "Cheap, synthetic 'flakka' dethroning cocaine on Florida drug scene". 27 people have died from flakka-related overdoses in the last eight months in Broward County
  11. ^ Klavž J, Gorenjak M, Marinšek M (August 2016). "Suicide attempt with a mix of synthetic cannabinoids and synthetic cathinones: Case report of non-fatal intoxication with AB-CHMINACA, AB-FUBINACA, alpha-PHP, alpha-PVP and 4-CMC". Forensic Science International. 265: 121–4. doi:10.1016/j.forsciint.2016.01.018. PMID 26890319.
  12. ^ Sykutera M, Cychowska M, Bloch-Boguslawska E (May 2015). "A Fatal Case of Pentedrone and α-Pyrrolidinovalerophenone Poisoning". Journal of Analytical Toxicology. 39 (4): 324–9. doi:10.1093/jat/bkv011. PMID 25737339.
  13. ^ Mash DC (2016). "Excited Delirium and Sudden Death: A Syndromal Disorder at the Extreme End of the Neuropsychiatric Continuum". Frontiers in Physiology. 7: 435. doi:10.3389/fphys.2016.00435. PMC 5061757. PMID 27790150.
  14. ^ a b c "EMCDDA–Europol Joint Report on a new psychoactive substance: 1-phenyl-2-(1-pyrrolidinyl)-1-pentanone (α-PVP)". European Monitoring Centre for Drugs and Drug Addiction (EMCDDA). September 2015.
  15. ^ Marusich JA, Antonazzo KR, Wiley JL, Blough BE, Partilla JS, Baumann MH (December 2014). "Pharmacology of novel synthetic stimulants structurally related to the "bath salts" constituent 3,4-methylenedioxypyrovalerone (MDPV)". Neuropharmacology. 87: 206–13. doi:10.1016/j.neuropharm.2014.02.016. PMC 4152390. PMID 24594476.
  16. ^ Rickli A, Hoener MC, Liechti ME (March 2015). "Monoamine transporter and receptor interaction profiles of novel psychoactive substances: para-halogenated amphetamines and pyrovalerone cathinones" (PDF). European Neuropsychopharmacology. 25 (3): 365–76. doi:10.1016/j.euroneuro.2014.12.012. PMID 25624004. S2CID 5511568.
  17. ^ Meltzer PC, Butler D, Deschamps JR, Madras BK (February 2006). "1-(4-Methylphenyl)-2-pyrrolidin-1-yl-pentan-1-one (Pyrovalerone) analogues: a promising class of monoamine uptake inhibitors". Journal of Medicinal Chemistry. 49 (4): 1420–32. doi:10.1021/jm050797a. PMC 2602954. PMID 16480278.
  18. ^ Gannon BM, Galindo KI, Mesmin MP, Sulima A, Rice KC, Collins GT (May 2018). "Relative reinforcing effects of second-generation synthetic cathinones: Acquisition of self-administration and fixed ratio dose-response curves in rats". Neuropharmacology. 134 (Pt A): 28–35. doi:10.1016/j.neuropharm.2017.08.018. PMC 5809320. PMID 28811192.
  19. ^ Gannon BM, Rice KC, Collins GT (October 2017). "Reinforcing effects of abused 'bath salts' constituents 3,4-methylenedioxypyrovalerone and α-pyrrolidinopentiophenone and their enantiomers". Behavioural Pharmacology. 28 (7): 578–581. doi:10.1097/FBP.0000000000000315. PMC 5599337. PMID 28570297.
  20. ^ "Reactions table". Reagent Base. Archived from the original on 2015-12-08. Retrieved 3 December 2015.
  21. ^ Eiden C, Mathieu O, Cathala P, Debruyne D, Baccino E, Petit P, Peyriere H (November 2013). "Toxicity and death following recreational use of 2-pyrrolidino valerophenone". Clinical Toxicology. 51 (9): 899–903. doi:10.3109/15563650.2013.847187. PMID 24111554. S2CID 22826544.
  22. ^ Baselt RC (2014). Disposition of toxic drugs and chemicals in man. Seal Beach, Ca.: Biomedical Publications. p. 1751. ISBN 978-0-9626523-9-4.
  23. ^ "Látky, o které byl doplněn seznam č. 4 psychotropních látek (příloha č. 4 k nařízení vlády č. 463/2013 Sb.)" (PDF) (in Czech). Ministerstvo zdravotnictví. Archived from the original (PDF) on 2020-05-15.
  24. ^ a b Poisons Standard July 2016 Comlaw.gov.au
  25. ^ a b Olding R. "'Bath salts' death: lethal drug was a top seller". The Sydney Morning Herald.
  26. ^ "Flakka, synthetic drug behind increasingly bizarre crimes". AP. 30 Apr 2015. Archived from the original on 2 May 2015. Retrieved 30 April 2015.
  27. ^ "Council Implementing Decision (EU) 2016/1070 of 27 June 2016 on subjecting α-PVP to control measures". eur-lex.europa.eu. Retrieved 2021-08-13.
  28. ^ 关于印发《非药用类麻醉药品和精神药品列管办法》的通知. China Food and Drug Administration (in Chinese). 27 September 2015. Archived from the original on 1 October 2015. Retrieved 1 October 2015.
  29. ^ "Decreto 29 dicembre 2011 (12A00013) (G.U. Serie Generale n. 3 del 4 gennaio 2012)" (PDF). Archived from the original (PDF) on 2016-07-01. Retrieved 2016-05-28.
  30. ^ "Rules - 2014". DEA/DOJ Diversion Control. Archived from the original on 2016-10-17. Retrieved 2014-02-01.
  31. ^ "Lists of:Scheduling Actions, Controlled Substances, Regulated Chemicals" (PDF). US Department of Justice. August 2016. Retrieved September 29, 2016.
  32. ^ Steinberg J (November 8, 2015). "Flakka: The New Illegal Drug You Need to Know About". Inc. Retrieved November 11, 2015.
  33. ^ Alvarez T (April 2, 2015). "Flakka: Rampant designer drug dubbed '$5 insanity'". Sun-Sentinel. Fort Lauderdale, Fla.
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