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Nomifensine

Group of stereoisomers

Nomifensine

Group of stereoisomers

FieldValue
Verifiedfieldschanged
Watchedfieldschanged
verifiedrevid462262394
IUPAC_name(±)-2-Methyl-4-phenyl-1,2,3,4-tetrahydroisoquinolin-8-amine
imageNomifensine.svg
image_classskin-invert-image
width200
captionAbove: molecular structure of nomifensine
image2Nomifensine 3D.png
image_class2bg-transparent
tradenameMerital, Alival
legal_AU
legal_BRC1
legal_BR_comment
legal_CA
legal_DE
legal_NZ
legal_UK
legal_US
legal_UN
legal_statusWithdrawn
routes_of_administrationBy mouth
elimination_half-life1.5–4 hours
excretionKidney (88%) within 24 hours
<!--Identifiers-->IUPHAR_ligand4792
CAS_number_Ref
CAS_number24526-64-5
ATC_prefixN06
ATC_suffixAX04
PubChem4528
DrugBank_Ref
DrugBankDB04821
ChemSpiderID_Ref
ChemSpiderID4371
UNII_Ref
UNII1LGS5JRP31
ChEBI_Ref
ChEBI116225
ChEMBL_Ref
ChEMBL273575
KEGG_Ref
KEGGD05200
<!--Chemical data-->C16
H18
N2
smilesCN1Cc2c(N)cccc2C(c2ccccc2)C1
StdInChI_Ref
StdInChI1S/C16H18N2/c1-18-10-14(12-6-3-2-4-7-12)13-8-5-9-16(17)15(13)11-18/h2-9,14H,10-11,17H2,1H3
StdInChIKey_Ref
StdInChIKeyXXPANQJNYNUNES-UHFFFAOYSA-N

Below: 3D representation of a nomifensine molecule

| elimination_half-life = 1.5–4 hours

Nomifensine, formerly sold under the brand names Merital and Alival, is a norepinephrine–dopamine reuptake inhibitor (NDRI) drug that was developed in the 1960s by Hoechst AG (now Sanofi-Aventis), who then test marketed it in the United States.

Nomifensine was considered an effective antidepressant that lacked sedative effects. It did not interact significantly with alcohol and lacked anticholinergic effects. No withdrawal symptoms were seen after 6 months treatment. The drug was, however, considered not suitable for agitated patients as it presumably made agitation worse. In January 1986 the drug was withdrawn by its manufacturers for safety reasons.

Some case reports in the 1980s suggested that there was potential for psychological dependence on nomifensine, typically in patients with a history of stimulant addiction, or when the drug was used in very high doses (400–600 mg per day).

In a 1989 study it was investigated for use in treating attention deficit hyperactivity disorder (ADHD) in adults and was proven to be effective. In a 1977 study it was not proven of benefit in advanced parkinsonism, except for depression associated with the parkinsonism.

Medical uses

Nomifensine was investigated for use as an antidepressant in the 1970s, and was found to be a useful antidepressant at doses of 50–225 mg per day, both motivating and anxiolytic.

Adverse effects

During treatment with nomifensine there were relatively few adverse effects, mainly renal failure, paranoid symptoms, drowsiness or insomnia, headache, and dry mouth. Side effects affecting the cardiovascular system included tachycardia and palpitations, but nomifensine was significantly less cardiotoxic than the standard tricyclic antidepressants.

Withdrawal from market

Due to a risk of haemolytic anaemia, the U.S. Food and Drug Administration (FDA) withdrew approval for nomifensine on March 20, 1992. Nomifensine was subsequently withdrawn from the Canadian and UK markets as well. Some deaths were linked to immunohaemolytic anemia caused by this compound, although the mechanism remained unclear.

Synthesis

Nomifensine was a progenitor to Gastrophenzine.

doi = 10.1021/jm00157a012 }}</ref>

Radiolabelled:; Improved method:; Analogs: Enantiomers:]] The alkylation between N-methyl-2-nitrobenzylamine [56222-08-3] (1) and phenacyl bromide (2) gives CID:15326127 (3). Catalytic hydrogenation over Raney Nickel reduces the nitro group to give CID:15113381 (4). The reduction of the ketone group with sodium borohydride to alcohol gives [65514-97-8] (5). Acid catalysed ring closure completes the formation of nomifensine (6).

Research

Motivational disorders

Nomifensine has been found to reverse tetrabenazine-induced motivational deficits in animals. It shares these pro-motivational effects with other NDRIs like bupropion and methylphenidate and with selective dopamine reuptake inhibitors like modafinil and its analogues. Conversely, selective norepinephrine reuptake inhibitors like desipramine and atomoxetine and selective serotonin reuptake inhibitors like fluoxetine and citalopram have not shown pro-motivational effects in animals.

Wakefulness

Nomifensine shows wakefulness-promoting effects in animals and might be useful in the treatment of narcolepsy.

References

References

  1. Anvisa. (2023-03-31). "RDC Nº 784 - Listas de Substâncias Entorpecentes, Psicotrópicas, Precursoras e Outras sob Controle Especial". [[Diário Oficial da União]].
  2. (April 1984). "Kinetics and metabolism of nomifensine". The Journal of Clinical Psychiatry.
  3. (July 1979). "Nomifensine: A review of its pharmacological properties and therapeutic efficacy in depressive illness". Drugs.
  4. "4-Phenyl-8-Amino Tetrahydroisoquinolines".
  5. (1977). "A review of controlled studies with nomifensine, performed outside the UK". British Journal of Clinical Pharmacology.
  6. (April 1984). "An overview of side effects and long-term experience with nomifensine from United States clinical trials". The Journal of Clinical Psychiatry.
  7. (July 1986). "CSM Update: Withdrawal of nomifensine". British Medical Journal.
  8. (September 1986). "Nomifensine and psychological dependence--a case report". Pharmacopsychiatry.
  9. (May 1989). "Nomifensine maleate in adult attention deficit disorder". The Journal of Nervous and Mental Disease.
  10. (1977). "Nomifensine in Parkinson's disease". British Journal of Clinical Pharmacology.
  11. (1977). "A profile of nomifensine". British Journal of Clinical Pharmacology.
  12. "Nomifensine DB04821". Drugbank.ca.
  13. (1988). "[Hematologic toxicity of antidepressive agents]". L'Encéphale.
  14. "Pyridoindole derivatives, compositions and use".
  15. (July 1971). "[8-amino-4-phenyl-1,2,3,4-tetrahydroisoquinolines, a new group of antidepressive psycholeptic drugs]". Arzneimittel-Forschung.
  16. (July 1986). "Synthesis and pharmacological evaluation of some new tetrahydroisoquinoline derivatives inhibiting dopamine uptake and/or possessing a dopaminomimetic property". Journal of Medicinal Chemistry.
  17. (1989). "Synthesis of racemic (+) and (-) N-[methyl-11C]nomifensine, a ligand for evaluation of monoamine re-uptake sites by use of positron emission tomography". International Journal of Radiation Applications and Instrumentation, Part A.
  18. (1989). "Verbesserte Synthese von 8-Amino-2-methyl-4-phenyl-1, 2, 3, 4-Tetrahydroisochinolin.". Journal für Praktische Chemie.
  19. (1990). "A New Synthesis of 1, 2, 3, 4-Tetrahydro-2-methyl-4-phenylisoquinolines.". Synthesis.
  20. (December 2012). "4-Phenyl tetrahydroisoquinolines as dual norepinephrine and dopamine reuptake inhibitors". Bioorganic & Medicinal Chemistry Letters.
  21. (May 1987). "Resolution, absolute stereochemistry, and enantioselective activity of nomifensine and hexahydro-1H-indeno[1,2-b]pyridines". Journal of Medicinal Chemistry.
  22. (2023). "The Role of Dopamine in Effort- Based Decisions: Insights from Bupropion, Nomifensine, and Atomoxetine".
  23. (January 2024). "The Neurobiology of Activational Aspects of Motivation: Exertion of Effort, Effort-Based Decision Making, and the Role of Dopamine". Annu Rev Psychol.
  24. (October 2018). "The Psychopharmacology of Effort-Related Decision Making: Dopamine, Adenosine, and Insights into the Neurochemistry of Motivation". Pharmacol Rev.
  25. (February 2016). "Not All Antidepressants Are Created Equal: Differential Effects of Monoamine Uptake Inhibitors on Effort-Related Choice Behavior". Neuropsychopharmacology.
  26. (2016). "Narcolepsy". Springer International Publishing.
  27. (2007). "Narcolepsy: pathophysiology and pharmacology". J Clin Psychiatry.
  28. (October 2012). "A practical guide to the therapy of narcolepsy and hypersomnia syndromes". Neurotherapeutics.
  29. (1998). "Increased dopaminergic transmission mediates the wake-promoting effects of CNS stimulants". Sleep Res Online.
  30. Jellinger K, Koeppen D, Rössner M. Langzeitbehandlung depressiver Syndrome mit Psyton [Long-term treatment of depressive syndromes with Psyton (author's transl)]. Wien Med Wochenschr. 1982 Apr 30;132(8):183-8. German. PMID 6125057.
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