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Brallobarbital
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Brallobarbital

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Brallobarbital
Brallobarbital.svg
Brallobarbital ball-and-stick animation.gif
Clinical data
Other names Brallobarbital
ATC code
  • none
Identifiers
  • 3,5 Bromo,4 Acitamido,2 Hydroxy Benzoic Acid Methyl Ester
CAS Number
PubChem CID
ChemSpider
UNII
ChEMBL
CompTox Dashboard (EPA)
ECHA InfoCard 100.008.387
Chemical and physical data
Formula C10H11BrN2O3
Molar mass 287.113 g·mol−1
3D model (JSmol)
  • O=C1NC(=O)NC(=O)C1(CC(\Br)=C)C\C=C
  • InChI=1S/C10H11BrN2O3/c1-3-4-10(5-6(2)11)7(14)12-9(16)13-8(10)15/h3H,1-2,4-5H2,(H2,12,13,14,15,16) checkY
  • Key:DYODAJAEQDVYFX-UHFFFAOYSA-N checkY
 ☒NcheckY (what is this?)  (verify)

Brallobarbital was a barbiturate developed in the 1920s. It has sedative and hypnotic properties, and was used for the treatment of insomnia. Brallobarbital was primarily sold as part of a combination product called Vesparax, composed of 150 mg secobarbital, 50 mg brallobarbital and 50 mg hydroxyzine. The long half-life of this combination of drugs tended to cause a hangover effect the next day, and Vesparax fell into disuse once newer drugs with lesser side effects had been developed. Vesparax reportedly was the drug that musician Jimi Hendrix supposedly overdosed on and led to his untimely death. It is no longer made.



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