Propallylonal
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| Propallylonal
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| Systematic (IUPAC) name | |
| 5-(2-bromoprop-2-enyl)-5-propan-2-yl-1,3-diazinane-2,4,6-trione | |
| Identifiers | |
| CAS number | |
| ATC code | ? |
| PubChem | |
| Chemical data | |
| Formula | C10H13BrN2O3 |
| Mol. mass | 289.126 g/mol |
| Synonyms | Propallylonal, Nostal, Quietal, Ibomal, 5-isopropyl-5-(β-bromoallyl)barbituric acid |
| Pharmacokinetic data | |
| Bioavailability | ? |
| Metabolism | ? |
| Half life | ? |
| Excretion | ? |
| Therapeutic considerations | |
| Pregnancy cat. |
? |
| Legal status | |
| Routes | ? |
Propallylonal (trade names Nostal, Quietal, Ibomal) is a barbiturate derivative invented in the 1920s[1]. It has sedative, hypnotic and anticonvulsant properties,[2] and is still rarely prescribed as a sleeping medication in some European countries.
References
Barbiturates (N01AF, N03AA, N05CA) |
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Allobarbital • Alphenal • Amobarbital • Aprobarbital • Barbexaclone • Barbital • Brallobarbital • Butabarbital • Butalbital • Butobarbital • Butallylonal • Crotylbarbital • Cyclobarbital • Cyclopal • Ethallobarbital • Febarbamate • Heptabarbital • Hexethal • Hexobarbital • Mephobarbital • Metharbital • Methohexital • Methylphenobarbital • Narcobarbital • Nealbarbital • Pentobarbital • Phenobarbital • Probarbital • Propallylonal • Proxibarbal • Proxibarbital • Reposal • Secbutabarbital • Secobarbital • Sigmodal • Talbutal • Thialbarbital • Thiamylal • Thiobarbital • Thiobutabarbital • Thiopental • Valofane • Vinbarbital • Vinylbital |
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