Cyclobarbital

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Cyclobarbital
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Clinical data
AHFS/Drugs.comInternational Drug Names
Routes of
administration
Oral (tablets)
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Legal status
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Pharmacokinetic data
MetabolismHepatic
ExcretionRenal
Identifiers
  • 5-(1-cyclohexenyl)-5-ethyl-1,3-diazinane-2,4,6-trione
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Chemical and physical data
FormulaC12H16N2O3
Molar mass236.271 g·mol−1
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  • 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
Data page
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Cyclobarbital, cyclobarbitol or cyclobarbitone is a barbiturate derivative developed in the early 1970s in the Soviet Union.[2]

It was available in Russia until 2019, marketed and distributed as Reladorm, a fixed-dose combination pairing 100 mg cyclobarbital and 10 mg diazepam (a benzodiazepine anxiolytic, muscle relaxant, and anticonvulsant) indicated for treating insomnia before it was discontinued in 2019.

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. ^ Page Module:Citation/CS1/styles.css has no content.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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