Cyclobarbital
Barbiturate
- N05CA10 (WHO)
- BR: Class B1 (Psychoactive drugs)[1]
- CA: Schedule IV
- DE: Anlage II (Authorized trade only, not prescriptible)
- UK: Class B
- UN: Psychotropic Schedule III
- 5-(1-cyclohexenyl)-5-ethyl-1,3-diazinane-2,4,6-trione
- 52-31-3 Y
- calcium: 143-76-0 Y
- 5838
- 5632 Y
- 0M8A98AD9H
- calcium: 0HZN7FV25R Y
- D07323 N
- ChEMBL268164 Y
- DTXSID9022865
- Interactive image
- 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) Y
- Key:WTYGAUXICFETTC-UHFFFAOYSA-N Y
Cyclobarbital, also known as cyclobarbitol or cyclobarbitone, is a barbiturate derivative.[2] It was available in Russia as a fixed-dose combination with diazepam (100 mg cyclobarbital + 10 mg diazepam; brand name Reladorm) for the treatment of insomnia but was discontinued in 2019.
References
- ^ 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. Retrieved 2023-08-16.
- ^ 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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