Piperidione

Chemical compound
  • R05DB23 (WHO)
Identifiers
  • 3,3-diethylpiperidine-2,4-dione
CAS Number
  • 77-03-2 ☒N
PubChem CID
  • 6465
ChemSpider
  • 6222 checkY
UNII
  • BZ6KL0Q8UD
CompTox Dashboard (EPA)
  • DTXSID30227804 Edit this at Wikidata
ECHA InfoCard100.000.909 Edit this at WikidataChemical and physical dataFormulaC9H15NO2Molar mass169.224 g·mol−13D model (JSmol)
  • Interactive image
  • O=C1C(C(=O)NCC1)(CC)CC
InChI
  • 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 name Sedulon) is a sedative drug, structurally related to methyprylon and pyrithyldione. It used to be marketed by Roche as a cough 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 After Roche failed to submit evidence of efficacy to the Drug Efficacy Study Implementation program in 1972, it was withdrawn from the US market.[4]

See also

  • Glutethimide

References

  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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