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Pyrovalerone

From Wikipedia, the free encyclopedia
Chemical compound
Pharmaceutical compound
Pyrovalerone
Clinical data
Routes of
administration
By mouth
ATC code
  • none
Legal status
Legal status
Identifiers
  • (RS)-1-(4-methylphenyl)-2-(1-pyrrolidinyl)pentan-1-one
CAS Number
PubChemCID
ChemSpider
UNII
KEGG
ChEMBL
CompTox Dashboard(EPA)
ECHA InfoCard100.230.426Edit this at Wikidata
Chemical and physical data
FormulaC16H23NO
Molar mass245.366 g·mol−1
3D model (JSmol)
ChiralityRacemic mixture
  • O=C(C(CCC)N1CCCC1)C2=CC=C(C)C=C2
  • InChI=1S/C16H23NO/c1-3-6-15(17-11-4-5-12-17)16(18)14-9-7-13(2)8-10-14/h7-10,15H,3-6,11-12H2,1-2H3 checkY
  • Key:SWUVZKWCOBGPTH-UHFFFAOYSA-N checkY
 ☒NcheckY (what is this?)  (verify)

Pyrovalerone (Centroton,4-Methyl-β-keto-prolintane,Thymergix,O-2371)[2] is acentral nervous system (CNS)stimulant thatacts as anorepinephrine–dopamine reuptake inhibitor (NDRI). It wasdeveloped in the 1980s and had briefly been approved in Spain and France forchronic fatigue orlethargy[3] and as anappetite suppressant, but was withdrawn from both markets around 2001 due to safety concerns including problems withabuse anddependence.[4] It is closely related on astructural level to a number of other cathinone stimulants, such asα-PVP,MDPV andprolintane.

Side effects of pyrovalerone includedecreased appetite,anxiety, fragmentedsleep orinsomnia, andtrembling,shaking, ormuscle tremors.Withdrawal symptoms following abuse upon discontinuation often results indepression.

TheR-enantiomer of pyrovalerone is devoid of pharmacologic activity.[5]

See also

[edit]
Look uppyrovalerone in Wiktionary, the free dictionary.

References

[edit]
  1. ^Anvisa (2023-03-31)."RDC Nº 784 - Listas de Substâncias Entorpecentes, Psicotrópicas, Precursoras e Outras sob Controle Especial" [Collegiate Board Resolution No. 784 - Lists of Narcotic, Psychotropic, Precursor, and Other Substances under Special Control] (in Brazilian Portuguese).Diário Oficial da União (published 2023-04-04).Archived from the original on 2023-08-03. Retrieved2023-08-16.
  2. ^US Patent 3314970
  3. ^Gardos G, Cole JO (October 1971). "Evaluation of pyrovalerone in chronically fatigued volunteers".Current Therapeutic Research, Clinical and Experimental.13 (10):631–5.PMID 4402508.
  4. ^Deniker P, Lôo H, Cuche H, Roux JM (November 1975). "[Abuse of pyrovalerone by drug addicts]".Annales médico-psychologiques.2 (4):745–8.PMID 9895.
  5. ^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.
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