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Febarbamate

From Wikipedia, the free encyclopedia
Chemical compound
Pharmaceutical compound
Febarbamate
Clinical data
Other namesMS-543
ATC code
Identifiers
  • [1-butoxy-3-(5-ethyl-2,4,6-trioxo-5-phenyl-1,3-
    diazinan-1-yl)propan-2-yl] carbamate
CAS Number
PubChemCID
ChemSpider
UNII
KEGG
ChEMBL
CompTox Dashboard(EPA)
ECHA InfoCard100.032.919Edit this at Wikidata
Chemical and physical data
FormulaC20H27N3O6
Molar mass405.451 g·mol−1
3D model (JSmol)
  • C1(=O)NC(C(C(=O)N1CC(OC(=O)N)COCCCC)(C2=CC=CC=C2)CC)=O
  • InChI=1S/C20H27N3O6/c1-3-5-11-28-13-15(29-18(21)26)12-23-17(25)20(4-2,16(24)22-19(23)27)14-9-7-6-8-10-14/h6-10,15H,3-5,11-13H2,1-2H3,(H2,21,26)(H,22,24,27) checkY
  • Key:QHZQILHUJDRDAI-UHFFFAOYSA-N checkY
 ☒NcheckY (what is this?)  (verify)

Febarbamate (INN;Solium,Tymium), also known asphenobamate, is ananxiolytic andtranquilizer of thebarbiturate andcarbamate families which is used in Europe by itself and as part of acombination drugformulation calledtetrabamate.[1][2][3][4]

See also

[edit]

References

[edit]
  1. ^World Health Organization (2004)."The use of stems in the selection of International Nonproprietary Names (INN) for pharmaceutical substance"(PDF).
  2. ^Index nominum 2000: international drug directory. Taylor & Francis US. 2000. p. 427.ISBN 978-3-88763-075-1. Retrieved26 November 2011.
  3. ^Gentili E (March 1972). "[Therapeutic effects of a new psycholeptic agent (febarbamate, Solium) in pediatrics]".Minerva Medica (in Italian).63 (18):1058–60.PMID 5016064.
  4. ^Morton I, Hall JM (1999).Concise dictionary of pharmacological agents: properties and synonyms. Springer. p. 118.ISBN 978-0-7514-0499-9. Retrieved26 November 2011.
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