Butallylonal

Chemical compound
  • none
Legal statusLegal status Identifiers
  • 5-sec-Butyl-5-(beta-bromoallyl)barbituric acid
CAS Number
  • 1142-70-7 checkY
PubChem CID
  • 14362
ChemSpider
  • 13723 checkY
UNII
  • H223WHY93B
ChEMBL
  • ChEMBL469253 checkY
ECHA InfoCard100.013.215 Edit this at WikidataChemical and physical dataFormulaC11H15BrN2O3Molar mass303.156 g·mol−13D model (JSmol)
  • Interactive image
  • O=C1NC(=O)NC(=O)C1(C(C)CC)CC(\Br)=C
InChI
  • InChI=1S/C11H15BrN2O3/c1-4-6(2)11(5-7(3)12)8(15)13-10(17)14-9(11)16/h6H,3-5H2,1-2H3,(H2,13,14,15,16,17) checkY
  • Key:FWZMBTIUIQUJFF-UHFFFAOYSA-N checkY
  (verify)

Butallylonal is a barbiturate derivative invented in the 1920s.[1] It has sedative properties, and was used primarily as an anaesthetic in veterinary medicine.[2] Butallylonal is considered similar in effects to pentobarbital but is longer in action, being considered an intermediate-acting barbiturate rather than short-acting.

References

  1. ^ US 1739662 
  2. ^ Mittmann U, Schmidt HD, Schmier J, Wirth RH (1976). "Hemorrhagic shock with fixed hypotension and with spontaneous recovery of blood pressure. A comparison of two shock models". Basic Research in Cardiology. 71 (1): 47–59. doi:10.1007/BF01907782. PMID 1259685. S2CID 5567045.
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GABAA receptor positive modulators
Alcohols
BarbituratesBenzodiazepines
CarbamatesFlavonoidsImidazolesKava constituents
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MonoureidesNeuroactive steroidsNonbenzodiazepinesPhenolsPiperidinedionesPyrazolopyridinesQuinazolinonesVolatiles/gasesOthers/unsorted
  • Unsorted benzodiazepine site positive modulators: α-Pinene
  • MRK-409 (MK-0343)
  • TCS-1105
  • TCS-1205
See also: Receptor/signaling modulators • GABA receptor modulators • GABA metabolism/transport modulators
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