Melitracen - Wikipedia, the free encyclopedia

Melitracen

From Wikipedia, the free encyclopedia
Jump to: navigation, search
Melitracen
Systematic (IUPAC) name
3-(10,10-dimethylanthracen-9(10H)-ylidene)-N,N-dimethylpropan-1-amine
Clinical data
AHFS/Drugs.com International Drug Names
Pregnancy cat.  ?
Legal status Prescription only
Routes Oral, IM
Identifiers
CAS number 5118-29-6 N
ATC code N06AA14
PubChem CID 25382
ChemSpider 23697 YesY
UNII Q7T0Y1109Z YesY
KEGG D08171 YesY
ChEMBL CHEMBL110094 YesY
Chemical data
Formula C21H25N 
Mol. mass 291.43 g/mol
SMILES eMolecules & PubChem
 N(what is this?)  (verify)

Melitracen (Adaptol, Adepril, Dixeran, Melixeran, Thymeol, Trausabun) is a tricyclic antidepressant (TCA) marketed in Europe and Japan by Lundbeck and Takeda, respectively, for the treatment of depression and anxiety.1234 In addition to single drug preparations, it is also available as Deanxit, a combination product containing both melitracen and flupentixol.5678

The pharmacology of melitracen has not been properly investigated and is largely unknown, but it is likely to act in a similar manner to other TCAs. Indeed, melitracen is reported to have imipramine and amitriptyline-like effects and efficacy against depression and anxiety, though with improved tolerability and a somewhat faster onset of action.910

See also

  • Fluotracen
  • Litracen

References

  1. ^ Swiss Pharmaceutical Society (2000). Index Nominum 2000: International Drug Directory (Book with CD-ROM). Boca Raton: Medpharm Scientific Publishers. ISBN 3-88763-075-0. http://books.google.com/?id=5GpcTQD_L2oC&lpg=PA643&dq=melitracen&pg=PA643#v=onepage&q=. 
  2. ^ Hall, Chapman and; Chemical Abstracts Service, American Chemical Society; Rhodes, P. H (1996). Dictionary of organic compounds. London: Chapman & Hall. ISBN 0-412-54090-8. http://books.google.com/?id=x2Su3GKCvtsC&lpg=PA4129&dq=melitracen&pg=PA4129#v=onepage&q=. 
  3. ^ O'Neil, Maryadele J. (2001). The Merck index: an encyclopedia of chemicals, drugs, and biologicals. Rahway, NJ: Merck Research Laboratories. ISBN 0-911910-13-1. 
  4. ^ José Miguel Vela; Helmut Buschmann; Jörg Holenz; Antonio Párraga; Antoni Torrens (2007). Antidepressants, Antipsychotics, Anxiolytics: From Chemistry and Pharmacology to Clinical Application. Weinheim: Wiley-VCH. ISBN 3-527-31058-4. http://books.google.com/?id=yXD4QA-Y_Z0C&lpg=PA248&dq=melitracen&pg=PA248#v=onepage&q=. 
  5. ^ Muller, Niels F; Dessing, Rudolf P; Pharmacy, European Society of Clinical (1998). European Drug Index, 4th Edition. Boca Raton: CRC Press. ISBN 3-7692-2114-1. http://books.google.com/?id=HiSdvzs2pPAC&lpg=PA380&dq=melitracen&pg=PA327#v=onepage&q=melitracen. 
  6. ^ Van Moffaert M, Dierick M, De Meulemeester F, Vereecken A (1983). "Treatment of depressive anxiety states associated with psychosomatic symptoms. A double-blind multicentre clinical study: mianserin versus melitracen-flupentixol". Acta Psychiatrica Belgica 83 (5): 525–39. PMID 6670581. 
  7. ^ Bin Yaacob H (April 1985). "Flupenthixol and Melitracen in the management of trigeminal neuralgia". Dental Journal of Malaysia 8 (2): 37–8. PMID 3917005. 
  8. ^ Hashash JG, Abdul-Baki H, Azar C et al. (June 2008). "Clinical trial: a randomized controlled cross-over study of flupenthixol + melitracen in functional dyspepsia". Alimentary Pharmacology & Therapeutics 27 (11): 1148–55. doi:10.1111/j.1365-2036.2008.03677.x. PMID 18331614. http://www3.interscience.wiley.com/resolve/openurl?genre=article&sid=nlm:pubmed&issn=0269-2813&date=2008&volume=27&issue=11&spage=1148. 
  9. ^ Aronson, Jeffrey Kenneth (2008). Meyler's Side Effects of Psychiatric Drugs (Meylers Side Effects). Amsterdam: Elsevier Science. ISBN 0-444-53266-8. http://books.google.com/?id=s0XYvuPVgaAC&lpg=PA34&dq=melitracen%20amitriptyline&pg=PA34#v=onepage&q=. 
  10. ^ Author Unknown (1970). Ann Reports Medicinal Chem V5 (v. 5). Boston: Academic Press. ISBN 0-12-040505-9. http://books.google.com/?id=JIdV5T356CQC&lpg=PA13&dq=melitracen%20amitriptyline&pg=PA13#v=onepage&q=melitracen.