Ethallobarbital

Ethallobarbital
Clinical data
Other namesAethallymal, Aethylal, Etallobarbital, Go 1067
Routes of
administration		Oral
ATC code
Legal status
Legal status
Pharmacokinetic data
MetabolismHepatic
ExcretionRenal
Identifiers
IUPAC name
  • 5-ethyl-5-prop-2-enyl-1,3-diazinane-2,4,6-trione
CAS Number
PubChem CID
ChemSpider
UNII
CompTox Dashboard (EPA)
ECHA InfoCard100.017.412
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Chemical and physical data
FormulaC9H12N2O3
Molar mass196.206 g·mol−1
3D model (JSmol)
SMILES
  • O=C1NC(=O)NC(=O)C1(CC)C\C=C
InChI
  • InChI=1S/C9H12N2O3/c1-3-5-9(4-2)6(12)10-8(14)11-7(9)13/h3H,1,4-5H2,2H3,(H2,10,11,12,13,14) checkY
  • Key:QPADNTZLUBYNEN-UHFFFAOYSA-N checkY
  (verify)

Ethallobarbital (brand names Dormin, Dumex, Dormitiv, Dorval), also known as ethallymal and 5-allyl-5-ethylbarbituric acid, is an allyl-substituted barbiturate described as a sedative/hypnotic.[1][2][3][4][5] It was first synthesized in 1927.[1]

See also

References

  1. 1 2 Ganellin CR, Triggle DJ (21 November 1996). Dictionary of Pharmacological Agents. CRC Press. pp. 51–. ISBN 978-0-412-46630-4.
  2. ↑ Negwer M (1978). Organic-chemical drugs and their synonyms: an international survey. Akademie-Verlag. ISBN 978-0-89573-100-5.
  3. ↑ Muller NF, Dessing RP (19 June 1998). European Drug Index: European Drug Registrations (Fourth ed.). CRC Press. pp. 1440–. ISBN 978-3-7692-2114-5.
  4. ↑ Frigerio A, McCamish M (1980). Recent Developments in Mass Spectrometry in Biochemistry and Medicine. Elsevier Scientific Publishing Company. ISBN 9780444418708.
  5. ↑ Goldhahn H, Barth H (November 1953). "[Barbituric acids. II]". Pharmazie. 8 (11): 913–8. PMID 13133697.



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