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Α-Pyrrolidinopentiophenone
Chemical compound
Chemical compound
| Field | Value | |||
|---|---|---|---|---|
| Verifiedfields | changed | |||
| Watchedfields | changed | |||
| verifiedrevid | 413315866 | |||
| drug_name | α-Pyrrolidinopentiophenone | |||
| image | Alpha-Pyrrolidinopentiophenone.svg | |||
| image_class | skin-invert-image | |||
| image2 | Alpha-PVP molecule ball.png | |||
| image_class2 | bg-transparent | |||
| alt2 | Ball-and-stick model of the alpha-PVP molecule | |||
| addiction_liability | Very high | |||
| routes_of_administration | By mouth, intranasal, inhalation, sublingual, intravenous | |||
| class | Stimulant; Norepinephrine–dopamine reuptake inhibitor (NDRI) | |||
| ATC_prefix | None | |||
| legal_AU | S9 | |||
| legal_BR | F2 | |||
| legal_BR_comment | ||||
| legal_CA | Unscheduled | |||
| legal_UK | Class B | |||
| legal_US | Schedule I | |||
| legal_DE | Anlage II | |||
| legal_NZ | Class C | |||
| legal_UN | P II | |||
| elimination_half-life | 2 hours | |||
| duration_of_action | 3–5 hours | |||
| excretion | ||||
| CAS_number_Ref | ||||
| CAS_number | 14530-33-7 | |||
| KEGG_Ref | ||||
| KEGG | C22754 | |||
| PubChem | 11148955 | |||
| DrugBank_Ref | ||||
| ChEBI | 234463 | |||
| ChemSpiderID_Ref | ||||
| ChemSpiderID | 9324063 | |||
| ChEMBL_Ref | ||||
| ChEMBL | 205082 | |||
| UNII_Ref | ||||
| UNII | 767K3AWA4R | |||
| synonyms | α-Pyrrolidinovalerophenone; α-PVP; O-2387; β-Keto-prolintane; Prolintanone; Desmethylpyrovalerone | |||
| IUPAC_name | (RS)-1-Phenyl-2-(pyrrolidin-1-yl)pentan-1-one | |||
| C | 15 | H=21 | N=1 | O=1 |
| SMILES | CCCC(C(C1=CC=CC=C1)=O)N2CCCC2 | |||
| StdInChI_Ref | ||||
| StdInChI | 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 | |||
| StdInChIKey_Ref | ||||
| StdInChIKey | YDIIDRWHPFMLGR-UHFFFAOYSA-N |
the drug substance α-PVP
| elimination_half-life = 2 hours
α-Pyrrolidinovalerophenone (α-PVP), also known as α-pyrrolidinopentiophenone , O-2387, β-keto-prolintane, prolintanone, or desmethylpyrovalerone, or colloquially as flakka or gravel, 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. α-PVP is chemically related to pyrovalerone and is the ketone analog of prolintane.
Use and effects
α-PVP is used by a variety of different routes of administration, including oral, insufflation, injection, vaporization, sublingual, and rectal. The dose range of α-PVP for therapeutic purposes was originally defined as 10 to 50mg, with a most-suitable dose of 20mg, whereas the recreational dose range is typically between 10 and 300mg. The effects of α-PVP onset after 10minutes, peak after 10 to 40minutes, and last 2 to 3hours.
The effects of α-PVP include cocaine-like psychostimulant effects, euphoria, elevated mood, alertness, pleasurable rush, feeling "sped up", mania-like symptoms, enhanced energy, motivation and productivity, enhanced music enjoyment, mild sexual stimulation, insomnia, paranoia, hallucinations, and increased aggression and violence. In emergency settings, commonly observed effects have included psychosis-like state, agitation, aggression, hallucinations, abnormal heart rate, and vomiting. It also produces sympathomimetic effects, such as increased heart rate and blood pressure.
Adverse effects
α-PVP, like other stimulants, can cause hyperstimulation, paranoia, and hallucinations. 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. α-PVP has also been linked to at least one death with pulmonary edema and moderately advanced atherosclerotic coronary artery disease when it was combined with pentedrone.
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 stimulants.
Pharmacology
Pharmacodynamics
α-PVP acts as a potent norepinephrine–dopamine reuptake inhibitor (NDRI), similarly to other NDRIs like methylphenidate, cocaine, and methylenedioxypyrovalerone (MDPV). Its values have been found to be 14 to 70nM for norepinephrine reuptake inhibition and 13 to 80nM for dopamine reuptake inhibition in rat brain synaptosomes and human embryonic kidney 293 (HEK293) cells expressing the monoamine transporters (MATs). In contrast to its effects on catecholamine reuptake, α-PVP has negligible effects on serotonin reuptake.
The drug is much more potent than amphetamine as an NDRI in in vitro, with 46-fold greater potency in terms of dopamine reuptake inhibition and 7-fold greater potency in terms of norepinephrine reuptake inhibition in HEK293 cells. It is one of the most potent dopamine reuptake inhibitors in vitro known.
Similarly to other cathinone, α-PVP has been shown to have stimulant-like effects (i.e., hyperlocomotion), reinforcing effects, and sympathomimetic effects in rodents.
Pharmacokinetics
The absorption of α-PVP is very rapid. In humans, the effects of the drug onset after 10minutes, peak between 10 and 40minutes, and last 2 to 3hours.
α-PVP is said to be highly lipophilic due to its pyrrolidine ring, which in turn is said to markedly enhance its ability to permeate the blood–brain barrier relative to other cathinones.
The distribution, metabolism, and elimination of α-PVP have been studied.
Chemistry
α-PVP gives no reaction with the Marquis reagent. It gives a grey/black reaction with the Mecke reagent.
Detection in body fluids
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.
History
α-PVP was first described in the literature in 1963.
Society and culture
Legal status
α-PVP is banned in Estonia, Finland, France, Germany, Hungary, Russia, Ireland, Latvia, Lithuania, Netherlands, Poland, Romania, Slovenia, Sweden, the United Kingdom, Turkey, Norway, as well as the Czech Republic.
Australia
α-PVP is a Schedule 9 prohibited substance under the Poisons Standard (July 2016). 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. 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.
China
As of October 2015, α-PVP is a controlled substance in China.
European Union
α-PVP was required to be banned by EU member states by 3 July 2017.
Italy
Cathinone and all structurally derived analogues (including pyrovalerone analogues) were classified as narcotics in January 2012.
United States
On January 28, 2014, the U.S. Drug Enforcement Agency (DEA) listed α-PVP, along with nine other synthetic cathinones, as a Schedule I controlled substance with a temporary ban, effective February 27, 2014. The temporary ban was then extended.
Economics
α-PVP is sometimes the active ingredient in recreational drugs sold as "bath salts". 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.
References
References
- Anvisa. (2023-07-24). "RDC Nº 804 - Listas de Substâncias Entorpecentes, Psicotrópicas, Precursoras e Outras sob Controle Especial". [[Diário Oficial da União]].
- (May 9, 2023). "PubChem Substance Record for SID 481087126, alpha-PVP". [[National Center for Biotechnology Information]].
- (March 3, 2023). "PubChem Substance Record for SID 172113243, alpha-Pyrrolidinovalerophenone". [[National Center for Biotechnology Information]].
- (November 2, 2017). "'Zombie drug' flakka may have hit Winnipeg streets: police". [[CBC News]].
- (August 17, 2016). "Flakka: What is the 'zombie drug' blamed for face-eating attacks?". [[The Independent]].
- (January 2019). "DARK Classics in Chemical Neuroscience: α-Pyrrolidinovalerophenone ("Flakka")". ACS Chem Neurosci.
- "α-Pyrrolidinovalerophenones".
- (September 13, 2013). "SOFT Designer Drug Committee Monographs: Alpha-PVP". Society of Forensic Toxicologists.
- (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.
- (6 April 2015). "Drugs of Abuse Emerging Trends". National Institute on Drug Abuse.
- (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.
- (2013). "t". AAFS Proceedings.
- "Cheap, synthetic 'flakka' dethroning cocaine on Florida drug scene".
- (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.
- (May 2015). "A Fatal Case of Pentedrone and α-Pyrrolidinovalerophenone Poisoning". Journal of Analytical Toxicology.
- (June 22, 2016). "Flakka-Induced Prolonged Psychosis". Wiley.
- (April 2020). "Designer drugs: mechanism of action and adverse effects". Arch Toxicol.
- (September 2015). "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).
- (December 2014). "Pharmacology of novel synthetic stimulants structurally related to the "bath salts" constituent 3,4-methylenedioxypyrovalerone (MDPV)". Neuropharmacology.
- (March 2015). "Monoamine transporter and receptor interaction profiles of novel psychoactive substances: para-halogenated amphetamines and pyrovalerone cathinones". European Neuropsychopharmacology.
- (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.
- (December 2017). "Measuring inhibition of monoamine reuptake transporters by new psychoactive substances (NPS) in real-time using a high-throughput, fluorescence-based assay". Toxicol in Vitro.
- (May 2018). "Relative reinforcing effects of second-generation synthetic cathinones: Acquisition of self-administration and fixed ratio dose-response curves in rats". Neuropharmacology.
- (October 2017). "Reinforcing effects of abused 'bath salts' constituents 3,4-methylenedioxypyrovalerone and α-pyrrolidinopentiophenone and their enantiomers". Behavioural Pharmacology.
- (November 2020). "Stereoselective neurochemical, behavioral, and cardiovascular effects of α-pyrrolidinovalerophenone enantiomers in male rats". Addict Biol.
- "Reactions table". Reagent Base.
- (November 2013). "Toxicity and death following recreational use of 2-pyrrolidino valerophenone". Clinical Toxicology.
- (2014). "Disposition of toxic drugs and chemicals in man". Biomedical Publications.
- "Látky, o které byl doplněn seznam č. 4 psychotropních látek (příloha č. 4 k nařízení vlády č. 463/2013 Sb.)". Ministerstvo zdravotnictví.
- Poisons Standard July 2016 [https://www.comlaw.gov.au/Details/F2015L01534 Comlaw.gov.au]
- "'Bath salts' death: lethal drug was a top seller". The Sydney Morning Herald.
- (30 Apr 2015). "Flakka, synthetic drug behind increasingly bizarre crimes". AP.
- link. (27 September 2015)
- {{CELEX
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- "Rules - 2014".
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: Scheduling Actions, Controlled Substances, Regulated Chemicals"](https://www.deadiversion.usdoj.gov/schedules/orangebook/orangebook.pdf). - (November 8, 2015). "Flakka: The New Illegal Drug You Need to Know About". Inc..
- (April 2, 2015). "Flakka: Rampant designer drug dubbed '$5 insanity'". [[Sun-Sentinel]].
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