Movatterモバイル変換


[0]ホーム

URL:


Jump to content
WikipediaThe Free Encyclopedia
Search

Pentedrone

From Wikipedia, the free encyclopedia
Stimulant designer drug of the cathinone class
Pharmaceutical compound
Pentedrone
Clinical data
Other namesα-Methylaminovalerophenone; α-Propyl-β-keto-N-methylphenethylamine; α-Desmethyl-α-propyl-N-methylcathinone; α-Desmethyl-α-propylmethcathinone; α-Desmethyl-α-propyl-β-keto-N-methylamphetamine; α-Desmethyl-α-propyl-β-ketomethamphetamine
ATC code
  • none
Legal status
Legal status
Identifiers
  • (±)-1-phenyl-2-(methylamino)pentan-1-one
CAS Number
PubChemCID
ChemSpider
UNII
KEGG
CompTox Dashboard(EPA)
ECHA InfoCard100.231.338Edit this at Wikidata
Chemical and physical data
FormulaC12H17NO
Molar mass191.274 g·mol−1
3D model (JSmol)
  • O=C(C(CCC)NC)C1=CC=CC=C1
  • InChI=1S/C12H17NO/c1-3-7-11(13-2)12(14)10-8-5-4-6-9-10/h4-6,8-9,11,13H,3,7H2,1-2H3 checkY
  • Key:WLIWIUNEJRETFX-UHFFFAOYSA-N checkY
 ☒NcheckY (what is this?)  (verify)

Pentedrone (also known asα-methylaminovalerophenone) is astimulant of thecathinone class that has been sold as adesigner drug and has been found since 2010 as an ingredient in a number of "bath salt" mixes sold as legal highs.[3][4][5][6][7][8][9]

Pharmacology

[edit]

Pentedrone acts as anorepinephrine-dopamine reuptake inhibitor (NDRI) without inducingmonoamine release, a similarmechanism of action tomethylphenidate.[10][11] ItsIC50Tooltip half-maximal inhibitory concentration values forinhibition of monoamine reuptake have been reported to be 610 nM fornorepinephrine, 2,500 μM fordopamine, and 135,000 μM forserotonin.[10] In rodents, pentedrone has been found to produceconditioned place preference (CPP), to beself-administered, and todose-dependentlystimulate locomotor activity.[11] Hence, pentedrone showspsychostimulant-like andreinforcing effects in animals.[11]

Side effects

[edit]

Pentedrone has been linked to at least one death where it was combined withα-PVP and caused heart failure.[12]

Detection

[edit]

A forensic standard of pentedrone is available, and the compound has been posted on the Forendex website of potential drugs of abuse.[13]

Legal status

[edit]

On January 28, 2014, the DEA listed it, along with nine other synthetic cathinones, on the Schedule 1 with a temporary ban, effective February 27, 2014.[14]

Pentedrone is anAnlage II controlled drug in Germany.

As of October 2015 Pentedrone is a controlled substance in China.[15]

Pentedrone is banned in the Czech Republic.[16]

Pentedrone is banned in the Slovak Republic.[17]

See also

[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. Retrieved2023-08-27.
  2. ^"Substance Details Pentedrone". Retrieved2024-01-22.
  3. ^"EMCDDA Annual Report 2010"(PDF). Archived fromthe original(PDF) on 2012-03-14. Retrieved2011-10-15.
  4. ^Research on Head Shop drugs in Dublin: Part 2
  5. ^An overview of new psychoactive substances and the outlets supplying them
  6. ^Westphal F, Junge T, Girreser U, Greibl W, Doering C (April 2012)."Mass, NMR and IR spectroscopic characterization of pentedrone and pentylone and identification of their isocathinone by-products".Forensic Science International.217 (1–3):157–67.doi:10.1016/j.forsciint.2011.10.045.PMID 22115724.
  7. ^Maheux CR, Copeland CR (January 2012). "Chemical analysis of two new designer drugs: buphedrone and pentedrone".Drug Testing and Analysis.4 (1):17–23.doi:10.1002/dta.385.PMID 22113925.S2CID 3250022.
  8. ^Poklis JL, Wolf CE, ElJordi OI, Liu K, Zhang S, Poklis A (January 2015). "Analysis of the first- and second-generation Raving Dragon Novelty Bath Salts containing methylone and pentedrone".Journal of Forensic Sciences. 60 Suppl 1 (11): S234–40.doi:10.1111/1556-4029.12629.PMID 25470207.S2CID 38295463.
  9. ^Zancajo VM, Brito J, Carrasco MP, Bronze MR, Moreira R, Lopes A (November 2014)."Analytical profiles of "legal highs" containing cathinones available in the area of Lisbon, Portugal".Forensic Science International.244:102–10.doi:10.1016/j.forsciint.2014.08.010.hdl:10400.26/7695.PMID 25240621.
  10. ^abSimmler LD, Rickli A, Hoener MC, Liechti ME (April 2014)."Monoamine transporter and receptor interaction profiles of a new series of designer cathinones".Neuropharmacology.79:152–160.doi:10.1016/j.neuropharm.2013.11.008.PMID 24275046.S2CID 25259854.
  11. ^abcHwang JY, Kim JS, Oh JH, Hong SI, Ma SX, Jung YH, Ko YH, Lee SY, Kim HC, Jang CG (January 2017). "The new stimulant designer compound pentedrone exhibits rewarding properties and affects dopaminergic activity".Addiction Biology.22 (1):117–128.doi:10.1111/adb.12299.PMID 26290055.S2CID 23807079.
  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. ^"Pentedrone". Southern Association of Forensic Scientists. Retrieved8 September 2015.
  14. ^"Temporary Placement of 10 Synthetic Cathinones into Schedule I". 28 January 2014. Archived fromthe original on 17 October 2016. Retrieved16 February 2014.
  15. ^"关于印发《非药用类麻醉药品和精神药品列管办法》的通知" (in Chinese). China Food and Drug Administration. 27 September 2015. Archived fromthe original on 1 October 2015. Retrieved1 October 2015.
  16. ^"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 fromthe original(PDF) on 2016-03-09. Retrieved2016-02-06.
  17. ^"Zoznam omamných látok a psychotropných látok zaradených do I., II. A III. skupiny (ochrana pred omamnými látkami) | Lewik".www.lewik.org. Retrieved2024-06-19.
Adamantanes
Adenosine antagonists
Alkylamines
Ampakines
Arylcyclohexylamines
Benzazepines
Cathinones
Cholinergics
Convulsants
Eugeroics
Oxazolines
Phenethylamines
Phenylmorpholines
Piperazines
Piperidines
Phenethylpyrrolidines
Racetams
Psychedelics
Tropanes
Tryptamines
Others
DATTooltip Dopamine transporter
(DRIsTooltip Dopamine reuptake inhibitors)
NETTooltip Norepinephrine transporter
(NRIsTooltip Norepinephrine reuptake inhibitors)
SERTTooltip Serotonin transporter
(SRIsTooltip Serotonin reuptake inhibitors)
VMATsTooltip Vesicular monoamine transporters
Others
Phenethylamines
Amphetamines
Phentermines
Cathinones
Phenylisobutylamines
(and further-extended)
Catecholamines
(and close relatives)
Cyclized
phenethylamines
Phenylalkylpyrrolidines
2-Benzylpiperidines
(phenidates)
Phenylmorpholines
(phenmetrazines)
Phenyloxazolamines
(aminorexes)
Isoquinolines and
tetrahydroisoquinolines
2-Aminoindanes
2-Aminotetralins
Others / unsorted
Related compounds
Retrieved from "https://en.wikipedia.org/w/index.php?title=Pentedrone&oldid=1292225620"
Categories:
Hidden categories:

[8]ページ先頭

©2009-2025 Movatter.jp