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Structure via PubChem · Public domain (PubChem)
eterobarb
Sign in to saveEterobarb (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.
In the Vinony graph
Vinony's link graph records 492 inbound references to eterobarb, and connects out to benzodiazepine drug, allopregnanolone and isovaleric acid.
It sits within the topics Barbiturates, Chemical pages without DrugBank identifier and Drugboxes which contain changes to verified fields.
Vinony links it to 7 Wikipedia language editions.
Chemical data
- Formula
- C16H20N2O5
- Molecular weight
- 320.34 g/mol
- IUPAC name
- 5-ethyl-1,3-bis(methoxymethyl)-5-phenyl-1,3-diazinane-2,4,6-trione
- SMILES
- CCC1(C(=O)N(C(=O)N(C1=O)COC)COC)C2=CC=CC=C2
- InChIKey
- DACOQFZGGLCXMA-UHFFFAOYSA-N
- XLogP
- 1.5
- Polar surface area
- 76.2 Ų
- H-bond donors
- 0
- H-bond acceptors
- 5
- Formal charge
- 0
via PubChem
Drug data · ChEMBL
- Max clinical phase
- Phase 2
- Molecule type
- Small molecule
via ChEMBL · EBI
Wikidata facts
- Subclass of
- chemical compound
- Mass
- 320.137
Show 3 more facts
- chemical formula
- C₁₆H₂₀N₂O₅
- canonical SMILES
- CCC1(C(=O)N(C(=O)N(C1=O)COC)COC)C2=CC=CC=C2
- Commons category
- Eterobarb
Sources (2)
via Wikidata · CC0
~1 min read
Encyclopedic overview
2 sectionsContents
- Synthesis
- References
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.
==Synthesis== Eterobarb can be synthesized by reacting phenobarbital with chloromethyl methyl ether in presence of a base.
Excerpted from Wikipedia’s “eterobarb” article, available under the CC BY-SA 4.0 licence.
Available in 7 languages
via Wikidata sitelinks · CC0