Short description : Chemical compound
Piperidione Clinical data Trade names Ascron, Dihyprylon, Dihyprylone, Sedulon, Tusseval ATC code Identifiers
IUPAC name
3,3-diethylpiperidine-2,4-dione
CAS Number 77-03-2 N PubChem CID ChemSpider 6222 Y UNII Chemical and physical data Formula C 9 H 15 N O 2 Molar mass 169.224 g·mol−1 3D model (JSmol)
InChI
InChI=1S/C9H15NO2/c1-3-9(4-2)7(11)5-6-10-8(9)12/h3-6H2,1-2H3,(H,10,12)
Y Key:RGEVWUKXWFOAID-UHFFFAOYSA-N
Y
N Y (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 After Roche failed to submit evidence of efficacy to the Drug Efficacy Study Implementation program in 1972, it was withdrawn from the US market.[4]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
References
↑ "On pethidine and methadone derivatives". Bulletin of the World Health Organization 2 (2): 193–204. 1949. PMID 15409516.
↑ "The use of piperidione as a cough sedative". Medical Times 76 (10): 445–7. October 1948. PMID 18102053.
↑ "[Use of an antitussive drug in pulmonary pathology]". Bollettino Chimico Farmaceutico 124 (2): 1S–6S. February 1985. PMID 3839404.
↑ "Certain Preparations Containing Dihyprylone or Pipazethate Hydrochloride; Notice of Withdrawal of Approval of New-Drug Applications ". Federal Register 37 (152): 15887. August 5, 1972. FDC–D–458. https://www.govinfo.gov/content/pkg/FR-1972-08-05/pdf/FR-1972-08-05.pdf .
Cough and cold preparations (R05)
Expectorants
Althea root
Antimony pentasulfide
Creosote
Guaiacolsulfonate
Guaifenesin (+ oxomemazine)
Ipecacuanha (Syrup of ipecac)
Levoverbenone
Potassium iodide
Senega
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Acetylcysteine#
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Codeine#
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Zipeprol
# WHO-EM
‡ Withdrawn from market
Clinical trials:
† Phase III
§ Never to phase III
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CGS-8216
CGS-9896
CGS-13767
CGS-20625
CL-218,872
CP-615,003
CTP-354
ELB-139
GBLD-345
Imepitoin
JM-1232
L-838,417
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NS-2664
NS-2710
NS-11394
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ROD-188
RWJ-51204
SB-205,384
SX-3228
TGSC01AA
TP-003
TPA-023
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U-89843A
U-90042
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Y-23684
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Piperidione
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ICI-190,622
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Propane
Propylene
Roflurane
Sevoflurane
Synthane
Teflurane
Toluene
Trichloroethane (methyl chloroform)
Trichloroethylene
Vinyl ether
Others/unsorted
3-Hydroxybutanal
α-EMTBL
AA-29504
Avermectins (e.g., ivermectin)
Bromide compounds (e.g., lithium bromide, potassium bromide, sodium bromide)
Carbamazepine
Chloralose
Chlormezanone
Clomethiazole
DEABL
Dihydroergolines (e.g., dihydroergocryptine, dihydroergosine, dihydroergotamine, ergoloid (dihydroergotoxine))
DS2
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Fenamates (e.g., flufenamic acid, mefenamic acid, niflumic acid, tolfenamic acid)
Fluoxetine
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Hopantenic acid
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Lignans (e.g., 4-O-methylhonokiol, honokiol, magnolol, obovatol)
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Org 25,435
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Terpenoids (e.g., borneol)
Topiramate
Valerian constituents (e.g., isovaleric acid, isovaleramide, valerenic acid, valerenol)
Unsorted benzodiazepine site positive modulators: α-Pinene
MRK-409 (MK-0343)
TCS-1105
TCS-1205
See also: Receptor/signaling modulators • GABA receptor modulators • GABA metabolism/transport modulators
Original source: https://en.wikipedia.org/wiki/Piperidione. Read more