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enallylpropymal
Sign in to saveEnallylpropymal (Narconumal) is a barbiturate derivative developed by Hoffman la Roche in the 1930s. It has sedative and hypnotic effects and is considered to have a moderate abuse potential.
In the Vinony graph
Vinony's link graph records 492 inbound references to enallylpropymal, and connects out to benzodiazepine drug, allopregnanolone and isovaleric acid.
It sits within the topics Allyl compounds, Barbiturates and Chemical pages without DrugBank identifier.
Vinony links it to 8 Wikipedia language editions.
Chemical data
- Formula
- C11H16N2O3
- Molecular weight
- 224.26 g/mol
- IUPAC name
- 1-methyl-5-propan-2-yl-5-prop-2-enyl-1,3-diazinane-2,4,6-trione
- SMILES
- CC(C)C1(C(=O)NC(=O)N(C1=O)C)CC=C
- InChIKey
- AXJXURWWUFZZKN-UHFFFAOYSA-N
- XLogP
- 1.8
- Polar surface area
- 66.5 Ų
- H-bond donors
- 1
- H-bond acceptors
- 3
- Formal charge
- 0
via PubChem
Wikidata facts
- Subclass of
- chemical compound
- Mass
- 224.116
Show 3 more facts
- canonical SMILES
- CC(C)C1(C(=O)NC(=O)N(C1=O)C)CC=C
- chemical formula
- C₁₁H₁₆N₂O₃
- Commons category
- Enallylpropymal
Sources (2)
via Wikidata · CC0
~1 min read
Encyclopedic overview
1 sectionsContents
- References
Enallylpropymal (Narconumal) is a barbiturate derivative developed by Hoffman la Roche in the 1930s. It has sedative and hypnotic effects and is considered to have a moderate abuse potential.
== References ==
Excerpted from Wikipedia’s “enallylpropymal” article, available under the CC BY-SA 4.0 licence.
Available in 8 languages
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