Pyrovalerone

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Pyrovalerone
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Clinical data
Routes of
administration		By mouth
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  • none
Legal status
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Identifiers
  • (RS)-1-(4-methylphenyl)-2-(1-pyrrolidinyl)pentan-1-one
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Chemical and physical data
FormulaC16H23NO
Molar mass245.366 g·mol−1
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ChiralityRacemic mixture
  • O=C(C(CCC)N1CCCC1)C2=CC=C(C)C=C2
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Pyrovalerone (Centroton, 4-Methyl-β-keto-prolintane, Thymergix, O-2371)[2] is a central nervous system (CNS) stimulant that acts as a norepinephrine–dopamine reuptake inhibitor (NDRI). It was developed in the 1980s and had briefly been approved in Spain and France for chronic fatigue or lethargy[3] and as an appetite suppressant, but was withdrawn from both markets around 2001 due to safety concerns including problems with abuse and dependence.[4] It is closely related on a structural level to a number of other cathinone stimulants, such as α-PVP, MDPV and prolintane.

Side effects of pyrovalerone include decreased appetite, anxiety, fragmented sleep or insomnia, and trembling, shaking, or muscle tremors. Withdrawal symptoms following abuse upon discontinuation often results in depression.

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

See also

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Look up pyrovalerone in Wiktionary, the free dictionary.

References

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  1. ^ Page Module:Citation/CS1/styles.css has no content.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 português do Brasil). Diário Oficial da União (published 2023-04-04). Archived from the original on 2023-08-03. Retrieved 2023-08-16.
  2. ^ US Patent 3314970
  3. ^ Page Module:Citation/CS1/styles.css has no content.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. ^ Page Module:Citation/CS1/styles.css has no content.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. ^ Page Module:Citation/CS1/styles.css has no content.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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