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bucolome

Structure via PubChem · Public domain (PubChem)

EntityQ4983624· pop 7· linked from 2 articles

Also known as 5-Butyl-1-cyclohexylbarbituric acid, 5-butyl-1-cyclohexyl-2,4,6(1H,3H,5H)-pyrimidinetrione

Bucolome (Paramidine) is a barbiturate derivative. Unlike most barbiturates it does not have any significant sedative or hypnotic effects, but instead acts as an analgesic and antiinflammatory. It also acts as a CYP2C9 inhibitor and reduces the metabolism of several commonly used drugs, which makes it useful for potentiating or extending the duration of action of those drugs, or reducing the production of unwanted metabolites.

In the Vinony graph

Within Vinony's link graph, bucolome is referenced by 2 other articles, and connects out to fenamic acid, cocaine and cannabis.

It is catalogued under topics including Barbiturates, Chemical pages without DrugBank identifier and Cyclohexyl compounds.

Its subject is documented across 6 Wikipedia language editions.

Chemical data

Formula
C14H22N2O3
Molecular weight
266.34 g/mol
IUPAC name
5-butyl-1-cyclohexyl-1,3-diazinane-2,4,6-trione
SMILES
CCCCC1C(=O)NC(=O)N(C1=O)C2CCCCC2
InChIKey
DVEQCIBLXRSYPH-UHFFFAOYSA-N
XLogP
2.9
Polar surface area
66.5 Ų
H-bond donors
1
H-bond acceptors
3
Formal charge
0

via PubChem

Drug data · ChEMBL

Max clinical phase
Phase 2
Molecule type
Small molecule

via ChEMBL · EBI

Wikidata facts

Mass
266.163
Show 3 more facts
chemical formula
C₁₄H₂₂N₂O₃
canonical SMILES
CCCCC1C(=O)NC(=O)N(C1=O)C2CCCCC2
Commons category
Bucolome
Sources (2)

via Wikidata · CC0

~1 min read

Encyclopedic overview

1 sections
Contents
  • References

Bucolome (Paramidine) is a barbiturate derivative. Unlike most barbiturates it does not have any significant sedative or hypnotic effects, but instead acts as an analgesic and antiinflammatory. It also acts as a CYP2C9 inhibitor and reduces the metabolism of several commonly used drugs, which makes it useful for potentiating or extending the duration of action of those drugs, or reducing the production of unwanted metabolites.

== References ==

Excerpted from Wikipedia’s “bucolome” article, available under the CC BY-SA 4.0 licence.

Available in 6 languages

via Wikidata sitelinks · CC0

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