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Cyclobarbital

From Wikipedia, the free encyclopedia
(Redirected fromCyclobarbitone)
Barbiturate
Pharmaceutical compound
Cyclobarbital
Clinical data
AHFS/Drugs.comInternational Drug Names
Routes of
administration
Oral (tablets)
ATC code
Legal status
Legal status
Pharmacokinetic data
MetabolismHepatic
ExcretionRenal
Identifiers
  • 5-(1-cyclohexenyl)-5-ethyl-1,3-diazinane-2,4,6-trione
CAS Number
PubChemCID
ChemSpider
UNII
KEGG
ChEMBL
CompTox Dashboard(EPA)
ECHA InfoCard100.000.127Edit this at Wikidata
Chemical and physical data
FormulaC12H16N2O3
Molar mass236.271 g·mol−1
3D model (JSmol)
  • O=C1NC(=O)NC(=O)C1(/C2=C/CCCC2)CC
  • InChI=1S/C12H16N2O3/c1-2-12(8-6-4-3-5-7-8)9(15)13-11(17)14-10(12)16/h6H,2-5,7H2,1H3,(H2,13,14,15,16,17) checkY
  • Key:WTYGAUXICFETTC-UHFFFAOYSA-N checkY
 ☒NcheckY (what is this?)  (verify)

Cyclobarbital,cyclobarbitol orcyclobarbitone is abarbituratederivative developed in the early 1970s in theSoviet Union.[2]

It was available inRussia until 2019,marketed and distributed asReladorm, afixed-dose combination pairing 100 mg cyclobarbital and 10 mgdiazepam (abenzodiazepineanxiolytic,muscle relaxant, andanticonvulsant) indicated for treatinginsomnia before it was discontinued in 2019.

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. ^Breimer DD, Winten MA (March 1976). "Pharmacokinetics and relative bioavailability of cyclobarbital calcium in man after oral administration".European Journal of Clinical Pharmacology.09 (5–6):443–50.doi:10.1007/bf00606563.PMID 989475.S2CID 20271169.
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