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Dibenzepin

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Dibenzepin
Skeletal formula of dibenzepin
Space-filling model of the dibenzepin molecule
Clinical data
Trade namesNoveril, Anslopax, Deprex, Ecatril, Neodit, Victoril
AHFS/Drugs.comInternational Drug Names
Routes of
administration		Oral
ATC code
Legal status
Legal status
  • BR: Class C1 (Other controlled substances)[1]
  • In general: ℞ (Prescription only)
Pharmacokinetic data
Bioavailability25%
Protein binding80%
MetabolismHepatic
Elimination half-life5 hours
ExcretionUrine (80%), feces (20%)
Identifiers
  • 10-(2-(dimethylamino)ethyl)-5-methyl-5H-dibenzo[b,e][1,4]diazepin-11(10H)-one
CAS Number
PubChem CID
ChemSpider
UNII
KEGG
ChEMBL
CompTox Dashboard (EPA)
Chemical and physical data
FormulaC18H21N3O
Molar mass295.386 g·mol−1
3D model (JSmol)
  • O=C2c1c(cccc1)N(c3c(N2CCN(C)C)cccc3)C
  • InChI=1S/C18H21N3O/c1-19(2)12-13-21-17-11-7-6-10-16(17)20(3)15-9-5-4-8-14(15)18(21)22/h4-11H,12-13H2,1-3H3 checkY
  • Key:QPGGEKPRGVJKQB-UHFFFAOYSA-N checkY
 ☒NcheckY (what is this?)  (verify)

Dibenzepin, sold under the brand name Noveril among others, is a tricyclic antidepressant (TCA) used widely throughout Europe for the treatment of depression.[2][3][4] It has similar efficacy and effects relative to other TCAs like imipramine but with fewer side effects.[5][6][7][8]

Medical uses

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Dibenzepin is used mainly in the treatment of major depressive disorder.

Like other TCAs, dibenzepin may have potential use in the treatment of chronic neuropathic pain.

Overdose

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Main article: Tricyclic antidepressant overdose

As TCAs have a relatively narrow therapeutic index, the likelihood of overdose (both accidental and intentional) is fairly high and should be considered carefully by the prescribing physician prior to patient use. Symptoms of overdose are similar to those of other TCAs, with cardiac toxicity (due to inhibition of sodium and calcium channels) generally occurring before the threshold for serotonin syndrome is reached. Due to this risk, TCAs are rarely selected as the first-line treatment for depression.

Pharmacology

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Pharmacodynamics

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See also: Pharmacology of antidepressants and Tricyclic antidepressant § Binding profiles
Dibenzepin[9]
Site Ki (nM) Species Ref
SERTTooltip Serotonin transporter ND ND ND
NETTooltip Norepinephrine transporter ND ND [10]
DATTooltip Dopamine transporter >100,000 Rat [11]
5-HT1A >10,000 Rat [12]
5-HT2A ≥1,500 Rat [12]
5-HT2C ND ND ND
α1 >10,000 Rat [12]
α2 >10,000 Rat [12]
DA >10,000 Bovine [12]
H1 23 Human [13]
H2 1,950 Human [13]
H3 >100,000 Human [13]
H4 >100,000 Human [13]
mAChTooltip Muscarinic acetylcholine receptor 1,750 Rat [12][14]
Values are Ki (nM). The smaller the value, the more strongly the drug binds to the site.

Dibenzepin acts as a selective norepinephrine reuptake inhibitor (NRI), with similar potency to that of imipramine.[10] It is also a potent antihistamine.[12][13] The drug has weak or negligible effects on serotonin and dopamine reuptake.[15][11] Unlike many other TCAs, dibenzepin has no antiadrenergic (α1, α2), antiserotonergic (5-HT1A, 5-HT2A), or antidopaminergic effects and has few or no anticholinergic (mAChTooltip muscarinic acetylcholine receptor) effects.[12][14]

Pharmacokinetics

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Therapeutic levels of dibenzepin are approximately 85 to 850 nM.[13] Its plasma protein binding is approximately 80%.[16]

History

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Dibenzepin was first introduced, in Switzerland and West Germany, in 1965.[3] It was introduced in France in 1967, in Italy in 1968, in the United Kingdom in 1970, and in Japan in 1975.[3] It was also marketed in a number of other countries, including Portugal and Israel.[3]

Society and culture

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Brand names

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Dibenzepin is or was marketed mainly under the brand name Noveril.[3] It has also been marketed under a number of other brand names, including Ansiopax, Deprex, Ecatril, Neodit, and Victoril.[3]

References

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  1. ^ Anvisa (2023-03-31). "RDC Nº 784 - Listas de Substâncias Entorpecentes, Psicotrópicas, Precursoras e Outras sob Controle Especial" [Collegiate Board Resolution No. 784 - Lists of Narcotic, Psychotropic, Precursor, and Other Substances under Special Control] (in Brazilian Portuguese). Diário Oficial da União (published 2023-04-04). Archived from the original on 2023-08-03. Retrieved 2023-08-16.
  2. ^ Swiss Pharmaceutical Society (2000). Index Nominum 2000: International Drug Directory (Book with CD-ROM). Boca Raton: Medpharm Scientific Publishers. ISBN 3-88763-075-0.
  3. ^ a b c d e f Sittig M (1988). Pharmaceutical manufacturing encyclopedia. Park Ridge, N.J., U.S.A: Noyes Publications. ISBN 0-8155-1144-2.
  4. ^ Beresewicz M, Bidzińska E, Koszewska I, Puzyński S (1991). "[Results of using tricyclic antidepressive drugs in the treatment of endogenous depression (comparative analysis of 7 drugs)]". Psychiatria Polska (in Polish). 25 (3–4): 13–8. PMID 1687987.
  5. ^ "Novartis (dibenzepin) - Prescribing Information" (PDF).
  6. ^ Paloucek FP, Leikin JB (2007). Poisoning and Toxicology Handbook, Fourth Edition (Poisoning and Toxicology Handbook (Leiken & Paloucek's)). Informa Healthcare. ISBN 978-1-4200-4479-9.
  7. ^ Gowardman M, Brown RA (March 1976). "Dibenzepin and amitriptyline in depressive states: comparative double-blind trial". The New Zealand Medical Journal. 83 (560): 194–7. PMID 6928.
  8. ^ Baron DP, Unger HR, Williams HE, Knight RG (April 1976). "A double blind study of the antidepressants dibenzepin (Noveril) and amitriptyline". The New Zealand Medical Journal. 83 (562): 273–4. PMID 8749.
  9. ^ Roth BL, Driscol J. "PDSP Ki Database". Psychoactive Drug Screening Program (PDSP). University of North Carolina at Chapel Hill and the United States National Institute of Mental Health. Retrieved 14 August 2017.
  10. ^ a b Barth N, Manns M, Muscholl E (1975). "Arrhythmias and inhibition of noradrenaline uptake caused by tricyclic antidepressants and chlorpromazine on the isolated perfused rabbit heart". Naunyn-Schmiedeberg's Arch. Pharmacol. 288 (2–3): 215–31. doi:10.1007/bf00500528. PMID 1161046. S2CID 11641400.
  11. ^ a b Hyttel J (1978). "Inhibition of [3H]dopamine accumulation in rat striatal synaptosomes by psychotropic drugs". Biochem. Pharmacol. 27 (7): 1063–8. doi:10.1016/0006-2952(78)90159-4. PMID 656154.
  12. ^ a b c d e f g h Closse A, Jaton AL (1984). "Investigation of the influence of lithium upon the down-regulation of serotonin2 receptors in rat frontal cortex induced by long-term treatment with dibenzepin, an antidepressant without appreciable affinity to serotonin2 receptors". Naunyn-Schmiedeberg's Arch. Pharmacol. 326 (4): 291–3. doi:10.1007/bf00501432. PMID 6148707. S2CID 24925602.
  13. ^ a b c d e f Appl H, Holzammer T, Dove S, Haen E, Strasser A, Seifert R (2012). "Interactions of recombinant human histamine H1R, H2R, H3R, and H4R receptors with 34 antidepressants and antipsychotics". Naunyn-Schmiedeberg's Arch. Pharmacol. 385 (2): 145–70. doi:10.1007/s00210-011-0704-0. PMID 22033803. S2CID 14274150.
  14. ^ a b Rehavi M, Maayani S, Goldstein L, Assael M, Sokolovsky M (1977). "Antimuscarinic properties of antidepressants: dibenzepin (Noveril)". Psychopharmacology. 54 (1): 35–8. doi:10.1007/bf00426538. PMID 20647. S2CID 27031652.
  15. ^ Rao ML, Frahnert C, Zagorski O (2002). "Initial serotonin transport into viable platelets and imipramine binding to platelet membranes". J Neural Transm (Vienna). 109 (5–6): 547–56. doi:10.1007/s007020200045. PMID 12111448. S2CID 9703461.
  16. ^ Aldenhoff J (2007). "Medikamente und andere Behandlungsverfahren". Psychiatrische Therapie. Schattauer Verlag. pp. 270–. ISBN 978-3-7945-2189-0.
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