Imipraminoxide

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Imipraminoxide
Imipraminoxide skeletal.svg
Imipraminoxide-3D-balls.png
Clinical data
Trade names Imiprex, Elepsin
Routes of
administration
Oral
ATC code
Legal status
Legal status
  • In general: ℞ (Prescription only)
Pharmacokinetic data
Elimination half-life Intravenous: 1.8 hours [1]
Identifiers
  • 3-(5,6-dihydrobenzo[b][f]benzazepin- 11-yl)- N,N-dimethyl- propan- 1-amine N-oxide
CAS Number
PubChem CID
ChemSpider
UNII
KEGG
ChEMBL
CompTox Dashboard (EPA)
ECHA InfoCard 100.027.188 OOjs UI icon edit-ltr-progressive.svg
Chemical and physical data
Formula C19H24N2O
Molar mass 296.414 g·mol−1

Imipraminoxide (brand names Imiprex, Elepsin), or imipramine N-oxide, is a tricyclic antidepressant (TCA) that was introduced in Europe in the 1960s for the treatment of depression. [2] [3] [4] [5]

Imipraminoxide is both an analogue and a metabolite of imipramine, and has similar effects. [6] [7] [8] [9] However, in clinical trials, imipraminoxide was found to have a faster onset of action, slightly higher efficacy, and fewer and less marked side effects, including diminished orthostatic hypotension and anticholinergic effects like dry mouth, sweating, dizziness, and fatigue. [6] [7] [8] [9] [10] [11]

Imipraminoxide's pharmacology has not been well elucidated, but based on its very close relationship with imipramine, it likely acts as a serotonin and norepinephrine reuptake inhibitor and serotonin, adrenenaline, histamine, and muscarinic acetylcholine receptor antagonist, though with weaker antiadrenergic and anticholinergic actions. [10] [11]

Imipraminoxide has been said to be a prodrug of imipramine. [12]

See also

Related Research Articles

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<span class="mw-page-title-main">Moclobemide</span> Antidepressant

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<span class="mw-page-title-main">Dimetacrine</span>

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<span class="mw-page-title-main">Metapramine</span>

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The psychopharmacology revolution covers the introduction of various psychiatric drugs into clinical practice as well as their continued development. Although not exclusively limited to the 1950s period, the literature tends to suggest that this decade was a particularly fruitful time for CNS drug discovery and it has been referred to as a "golden era".

References

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