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Short description : Chemical compound
Vinbarbital Clinical data Routes of administration Oral ATC code Legal status Legal status
Identifiers
5-ethyl-5-[(1E )-1-methylbut-1-en-1-yl]pyrimidine-2,4,6(1H ,3H ,5H )-trione
CAS Number PubChem CID ChemSpider UNII KEGG ChEMBL Chemical and physical data Formula C 11 H 16 N 2 O 3 Molar mass 224.260 g·mol−1 3D model (JSmol )
O=C1NC(=O)NC(=O)C1(/C(=C/CC)C)CC
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+
Y Key:RAFOHKSPUDGZPR-VOTSOKGWSA-N
Y
N Y (what is this?) (verify)
Vinbarbital is a hypnotic drug which is a barbiturate derivative.[1] It was developed by Sharp and Dohme in 1939.[2]
References
Alcohols Barbiturates Benzodiazepines Carbamates Flavonoids Imidazoles Kava constituentsMonoureides Neuroactive steroids Nonbenzodiazepines Phenols Piperidinediones Pyrazolopyridines Quinazolinones Volatiles /gases Others/unsorted
3-Hydroxybutanal
α-EMTBL
AA-29504
Avermectins (e.g., ivermectin )
Bromide compounds (e.g., lithium bromide , potassium bromide , sodium bromide)
Carbamazepine
Chloralose
Chlormezanone
Clomethiazole
DEABL
Dihydroergolines (e.g., dihydroergocryptine , dihydroergosine , dihydroergotamine , ergoloid (dihydroergotoxine) )
DS2
Efavirenz
Etazepine
Etifoxine
Fenamates (e.g., flufenamic acid , mefenamic acid , niflumic acid , tolfenamic acid )
Fluoxetine
Flupirtine
Hopantenic acid
Lanthanum
Lavender oil
Lignans (e.g., 4-O-methylhonokiol , honokiol , magnolol , obovatol )
Loreclezole
Menthyl isovalerate (validolum)
Monastrol
Niacin
Nicotinamide (niacinamide)
Org 25,435
Phenytoin
Propanidid
Retigabine (ezogabine)
Safranal
Seproxetine
Stiripentol
Sulfonylalkanes (e.g., sulfonmethane (sulfonal) , tetronal , trional )
Terpenoids (e.g., borneol )
Topiramate
Valerian constituents (e.g., isovaleric acid , isovaleramide , valerenic acid , valerenol )
Original source: https://en.wikipedia.org/wiki/Vinbarbital. Read more