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Piperidione

From Wikipedia, the free encyclopedia
Chemical compound
Pharmaceutical compound
Piperidione
Clinical data
Trade namesAscron, Dihyprylon, Dihyprylone, Sedulon, Tusseval
ATC code
Identifiers
  • 3,3-diethylpiperidine-2,4-dione
CAS Number
PubChemCID
ChemSpider
UNII
CompTox Dashboard(EPA)
ECHA InfoCard100.000.909Edit this at Wikidata
Chemical and physical data
FormulaC9H15NO2
Molar mass169.224 g·mol−1
3D model (JSmol)
  • O=C1C(C(=O)NCC1)(CC)CC
  • InChI=1S/C9H15NO2/c1-3-9(4-2)7(11)5-6-10-8(9)12/h3-6H2,1-2H3,(H,10,12) checkY
  • Key:RGEVWUKXWFOAID-UHFFFAOYSA-N checkY
 ☒NcheckY (what is this?)  (verify)

Piperidione (trade nameSedulon) is asedative drug, structurally related tomethyprylon andpyrithyldione.It used to be marketed byRoche as acough medicine available in liquid form.[1][2][3] In the US, it was approved by the FDA on grounds of safety alone in 1947. After Roche failed to submit evidence of efficacy to theDrug Efficacy Study Implementation program in 1972, it was withdrawn from the US market.[4]

See also

[edit]

References

[edit]
  1. ^Wolff PO (1949)."On pethidine and methadone derivatives".Bulletin of the World Health Organization.2 (2):193–204.PMC 2553950.PMID 15409516.
  2. ^Jacobs S (October 1948). "The use of piperidione as a cough sedative".Medical Times.76 (10):445–7.PMID 18102053.
  3. ^Rimoldi R, Fioretti M, Bandella M (February 1985). "[Use of an antitussive drug in pulmonary pathology]".Bollettino Chimico Farmaceutico.124 (2):1S –6S.PMID 3839404.
  4. ^Certain Preparations Containing Dihyprylone or Pipazethate Hydrochloride; Notice of Withdrawal of Approval of New-Drug Applications(PDF).Federal Register (Report). Vol. 37. August 5, 1972. p. 15887. FDC–D–458.
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