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Vinbarbital

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Chemical compound Pharmaceutical compound
Vinbarbital
Clinical data
Routes of
administration
Oral
ATC code
Legal status
Legal status
Identifiers
IUPAC name
  • 5-ethyl-5-pyrimidine-2,4,6(1H,3H,5H)-trione
CAS Number
PubChem CID
ChemSpider
UNII
KEGG
ChEMBL
CompTox Dashboard (EPA)
ECHA InfoCard100.004.309 Edit this at Wikidata
Chemical and physical data
FormulaC11H16N2O3
Molar mass224.260 g·mol
3D model (JSmol)
SMILES
  • O=C1NC(=O)NC(=O)C1(/C(=C/CC)C)CC
InChI
  • InChI=1S/C11H16N2O3/c1-4-6-7(3)11(5-2)8(14)12-10(16)13-9(11)15/h6H,4-5H2,1-3H3,(H2,12,13,14,15,16)/b7-6+
  • Key:RAFOHKSPUDGZPR-VOTSOKGWSA-N
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Vinbarbital is a hypnotic drug which is a barbiturate derivative. It was developed by Sharp and Dohme in 1939.

References

  1. Mueller VA (March 1950). "An analysis and evaluation of vinbarbital sodium for obstetric amnesia and analgesia". American Journal of Obstetrics and Gynecology. 59 (3): 679–84. doi:10.1016/0002-9378(50)90253-5. PMID 15405833.
  2. US 2187703 
Hypnotics/sedatives (N05C)
GABAA
Alcohols
Barbiturates
Benzodiazepines
Carbamates
Imidazoles
Monoureides
Neuroactive steroids
Nonbenzodiazepines
Phenols
Piperidinediones
Quinazolinones
Others
GABAB
H1
Antihistamines
Antidepressants
Antipsychotics
α2-Adrenergic
5-HT2A
Antidepressants
Antipsychotics
Others
Melatonin
Orexin
α2δ VDCC
Others
GABAA receptor positive modulators
Alcohols
Barbiturates
Benzodiazepines
Carbamates
Flavonoids
Imidazoles
Kava constituents
Monoureides
Neuroactive steroids
Nonbenzodiazepines
Phenols
Piperidinediones
Pyrazolopyridines
Quinazolinones
Volatiles/gases
Others/unsorted
See also: Receptor/signaling modulatorsGABA receptor modulatorsGABA metabolism/transport modulators
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