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Oxetorone

From Wikipedia, the free encyclopedia
Chemical compound

Pharmaceutical compound
Oxetorone
Skeletal formula of oxetorone
Space-filling model of the oxetorone molecule
Clinical data
AHFS/Drugs.comInternational Drug Names
ATC code
Identifiers
  • (3Z)-3-[1]benzofuro[3,2-c][1]benzoxepin-6(12H)-ylidene-N,N-dimethylpropan-1-amine
CAS Number
PubChemCID
ChemSpider
UNII
KEGG
CompTox Dashboard(EPA)
ECHA InfoCard100.043.086Edit this at Wikidata
Chemical and physical data
FormulaC21H21NO2
Molar mass319.404 g·mol−1
3D model (JSmol)
  • CN(C)CCC=C1C2=CC=CC=C2OCC3=C1OC4=CC=CC=C34
  • InChI=1S/C21H21NO2/c1-22(2)13-7-10-17-15-8-3-5-11-19(15)23-14-18-16-9-4-6-12-20(16)24-21(17)18/h3-6,8-12H,7,13-14H2,1-2H3
  • Key:VZVRZTZPHOHSCK-UHFFFAOYSA-N
  (verify)

Oxetorone (INNTooltip International Nonproprietary Name), asoxetorone fumarate (USANTooltip United States Adopted Name) (brand namesNocertone,Oxedix), is aserotonin antagonist,antihistamine, andalpha blocker used as anantimigraine drug.[1][2][3][4] Association withhyperprolactinemia has been described[5] andantidopaminergic actions are also suspected.[6]

References

[edit]
  1. ^Ganellin CR, Triggle DJ (21 November 1996).Dictionary of Pharmacological Agents. CRC Press. pp. 1493–.ISBN 978-0-412-46630-4.
  2. ^William Andrew Publishing (22 October 2013).Pharmaceutical Manufacturing Encyclopedia (3rd ed.). Elsevier. pp. 2935–.ISBN 978-0-8155-1856-3.
  3. ^van Boxtel CJ, Santoso B, Edwards IR (6 August 2008).Drug Benefits and Risks: International Textbook of Clinical Pharmacology (Revised 2nd ed.). IOS Press. pp. 699–.ISBN 978-1-60750-345-3.
  4. ^Massiou H (2000)."[Prophylactic treatments of migraine]".Revue Neurologique (in French).156 (Suppl 4): 4S79–86.PMID 11139754.
  5. ^Pradalier A (December 1996). "Hyperprolactinaemia and depression induced by oxetorone".Cephalalgia.16 (8):560–1.doi:10.1046/j.1468-2982.1996.1608560.x.PMID 8980859.S2CID 43533753.
  6. ^Deguigne M, Bruneau C, Touré A, Turcant A, Le Roux G (February 2017). "New evidence for oxetorone toxicity".Clin Toxicol (Phila).55 (2):142–146.doi:10.1080/15563650.2016.1267358.PMID 27967233.S2CID 2137489.


Analgesic/abortive
Serotonergics
Ergolines
5-HT1 agonists
Triptans
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CGRP-R antagonists
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Prophylactic
Calcium channel blockers
Progestogens
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α1
Agonists
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5-HT37
5-HT3
5-HT4
5-HT5A
5-HT6
5-HT7
Classes
Antidepressants
(Tricyclic antidepressants(TCAs))
Antihistamines
Antipsychotics
Anticonvulsants
Anticholinergics
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