Eterobarb
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Systematic (IUPAC) name | |
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5-ethyl-1,3-bis(methoxymethyl)-5-phenyl-1,3-diazinane-2,4,6-trione
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Clinical data | |
Routes of administration |
Oral |
Identifiers | |
CAS Number | 27511-99-5 Y |
ATC code | none |
PubChem | CID: 33925 |
ChemSpider | 31271 N |
UNII | 432SI047GA Y |
KEGG | D04077 Y |
Chemical data | |
Formula | C16H20N2O5 |
Molecular mass | 320.340 g/mol |
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NY (what is this?) (verify) |
Eterobarb (Antilon) is a barbiturate derivative. It has mainly anticonvulsant action with less sedative effects than the closely related compound phenobarbital. It saw reasonable success in clinical trials, but is not in widespread medical use.[1][2]
Synthesis
Eterobarb can be synthesized by reacting phenobarbital with chloromethyl methyl ether in presence of a base.[3]
References
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Categories:
- Chemical articles having calculated molecular weight overwritten
- Articles with changed InChI identifier
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- Articles without EBI source
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- Drugs not assigned an ATC code
- Drugs with no legal status
- Barbiturates
- Ethers
- GABAA receptor positive allosteric modulators
- Nervous system drug stubs