Jump to content

Litoxetine

From Wikipedia, the free encyclopedia
Litoxetine
Clinical data
Other namesSL 81-0385; IXA-001
ATC code
  • None
Identifiers
  • 4-(naphthalen-2-ylmethoxy)piperidine
CAS Number
PubChem CID
ChemSpider
UNII
ChEMBL
CompTox Dashboard (EPA)
Chemical and physical data
FormulaC16H19NO
Molar mass241.334 g·mol−1
3D model (JSmol)
  • C3CNCCC3OCc2cc1ccccc1cc2

Litoxetine (developmental code names SL 81-0385, IXA-001) is an antidepressant which was under clinical development for the treatment of depression in the early 1990s but was never marketed.[1][2] It acts as a potent serotonin reuptake inhibitor (Ki for SERTTooltip serotonin transporter = 7 nM) and modest 5-HT3 receptor antagonist (Ki = 315 nM).[3][4] It has antiemetic activity, and unlike the selective serotonin reuptake inhibitors (SSRIs), appears to have a negligible incidence of nausea and vomiting.[5] The drug is structurally related to indalpine.[4] Development of litoxetine for depression was apparently ceased in the late 1990s.[1] However, as of March 2017, development of litoxetine has been reinitiated and the drug is now in the phase II stage for the treatment of urinary incontinence.[1]

References

[edit]
  1. ^ a b c "Litoxetine - IXALTIS". AdisInsight. Springer Nature Switzerland AG. Retrieved 2018-08-25.
  2. ^ Fairweather DB, Patat A, Rosenzweig P, Curson VH, Dunmore C, Dubruc C, Hindmarch I (August 1995). "The psychomotor and cognitive effects of litoxetine in young and middle aged volunteers". British Journal of Clinical Pharmacology. 40 (2): 119–125. doi:10.1111/j.1365-2125.1995.tb05767.x. PMC 1365170. PMID 8562293.
  3. ^ Gallagher PT (8 October 2012). "Beyond SSRIs: Second-generation Reuptake Inhibitors for the Treatment of Depression". In Rankovic Z, Hargreaves R, Bingham M (eds.). Drug Discovery for Psychiatric Disorders. Royal Society of Chemistry. pp. 195–. ISBN 978-1-84973-494-3.
  4. ^ a b Olivier B, Soudijn W, van Wijngaarden I (6 December 2012). "Serotonin, dopamine, and norepinephrine transporters". In Jucker E (ed.). Progress in Drug Research. Birkhäuser. pp. 80–. ISBN 978-3-0348-8391-7.
  5. ^ Angel I, Schoemaker H, Prouteau M, Garreau M, Langer SZ (March 1993). "Litoxetine: a selective 5-HT uptake inhibitor with concomitant 5-HT3 receptor antagonist and antiemetic properties". European Journal of Pharmacology. 232 (2–3): 139–145. doi:10.1016/0014-2999(93)90767-C. PMID 8385615.
[edit]
  • "Litoxetine". Drug Information Portal. U.S. National Library of Medicine.