Noxiptiline

Noxiptiline
Systematic (IUPAC) name
10,11-dihydro-5H-dibenzo[a,d]cyclohepten-5-one O-[2-dimethylamino)ethyl]oxime
Clinical data
Pregnancy cat.  ?
Legal status Prescription only
Routes Oral
Identifiers
CAS number 4985-15-3
ATC code None
PubChem CID 21087
ChemSpider 19832 YesY
UNII DF7D3NY7EL YesY
Chemical data
Formula C19H22N2O 
Mol. mass 294.39 g/mol
SMILES eMolecules & PubChem
 YesY(what is this?)  (verify)

Noxiptiline (Agedal, Elronon, Nogedal), also known as noxiptyline and dibenzoxine, is a tricyclic antidepressant (TCA) that was introduced in Europe in the 1970s for the treatment of depression.[1][2][3] It has imipramine-like effects,[4] acting as a serotonin and norepinephrine reuptake inhibitor, among other properties.[5][6] Of the TCAs, noxiptiline has been shown to be one of the most effective, rivaling amitriptyline in clinical efficacy.[7][8]

See also

References

  1. ^ Swiss Pharmaceutical Society (2000). Index Nominum 2000: International Drug Directory (Book with CD-ROM). Boca Raton: Medpharm Scientific Publishers. p. 753. ISBN 3-88763-075-0. http://books.google.com/?id=5GpcTQD_L2oC&lpg=PA753&dq=noxiptiline&pg=PA753#v=onepage&q=&f=false. 
  2. ^ Aronson, Jeffrey Kenneth (2008). Meyler's Side Effects of Psychiatric Drugs (Meylers Side Effects). Amsterdam: Elsevier Science. p. 34. ISBN 0-444-53266-8. http://books.google.com/?id=s0XYvuPVgaAC&lpg=PP1&dq=noxiptiline&pg=PA34#v=onepage&q=&f=false. 
  3. ^ Dictionary of organic compounds. London: Chapman & Hall. 1996. p. 4868. ISBN 0-412-54090-8. http://books.google.com/?id=5S_uhYzKWisC&lpg=PA4868&dq=noxiptiline&pg=PA4868#v=onepage&q=&f=false. 
  4. ^ Mutschler, Ernst (1995). Drug actions: basic principles and theraputic aspects. Stuttgart, German: Medpharm Scientific Pub. p. 127. ISBN 0-8493-7774-9. http://books.google.com/?id=IvN4mZxraMkC&lpg=PA723&dq=noxiptiline&pg=PA127#v=onepage&q=&f=false. 
  5. ^ Ernst Jucker; S. Ren; Soudijn, W.; Wijngaarden, I. van; M. Kumari; D. Poyner; M. Bushfield; H. Horikoshi; Fujiwara, Tamenari (2000). Progress in Drug Research, Volume 54 (Progress in Drug Research). Boston: Birkhauser. p. 81. ISBN 3-7643-6113-1. http://books.google.com/?id=gwhdUGoO6KwC&lpg=PA80&dq=noxiptiline%20fluvoxamine&pg=PA81#v=onepage&q=&f=false. 
  6. ^ 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 Archives of Pharmacology 288 (2-3): 215–31. doi:10.1007/BF00500528. PMID 1161046. 
  7. ^ 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)]" (in Polish). Psychiatria Polska 25 (3-4): 13–8. PMID 1687987. 
  8. ^ Lingjaerde O, Asker T, Bugge A, et al. (January 1975). "Noxiptilin (Agedal)--a new tricyclic antidepressant with a faster onset of action? A double-blind, multicentre comparison with amitriptyline". Pharmakopsychiatrie, Neuro-Psychopharmakologie 8 (1): 26–35. PMID 788000.