French
DeutschPheniprazine
 | |
| Clinical data | |
|---|---|
| Trade names | Catron, Cavodil |
| Other names | Amphetamine hydrazide;[1] α-Methylphenethylhydrazine; JB-516; α-Methylphenelzine; N-Aminoamphetamine |
| Routes of administration | Oral |
| ATC code |
|
| Legal status | |
| Legal status | |
| Identifiers | |
| |
| CAS Number | |
| PubChem CID | |
| ChemSpider | |
| UNII | |
| ChEMBL | |
| CompTox Dashboard (EPA) | |
| ECHA InfoCard | 100.000.215 |
| Chemical and physical data | |
| Formula | C9H14N2 |
| Molar mass | 150.225 g·mol−1 |
| |
  (what is this?) (verify) | |
Pheniprazine, formerly sold under the brand names Catron and Cavodil, is an irreversible and non-selective monoamine oxidase inhibitor (MAOI) of the hydrazine group that was used as an antidepressant to treat depression in the 1960s.[3][4][5][6] It was also used in the treatment of angina pectoris and schizophrenia.[7][8] Pheniprazine has been largely discontinued due to toxicity concerns such as jaundice, amblyopia, and optic neuritis.[9][10][11]
Pharmacology
[edit]Pheniprazine is a monoamine oxidase inhibitor (MAOI).[3]
Amphetamine has been detected as an active metabolite of pheniprazine in animals.[12] Pheniprazine produces amphetamine- and psychostimulant-like effects at high doses in animals.[13] The same is true of certain other MAOIs, including iproniazid, phenelzine, tranylcypromine, and pargyline, but not nialamide.[13][14][15]
Chemistry
[edit]Pheniprazine, also known as α-methylphenethylhydrazine,[1] is a phenethylamine, amphetamine, and hydrazine derivative.
It is a close analogue of phenelzine (phenethylhydrazine) and amphetamine (α-methylphenethylamine) and can also be referred to by synonyms including amphetamine hydrazide,[1] α-methylphenelzine, and N-aminoamphetamine.
Metfendrazine (α,N-dimethylphenethylhydrazine; N-methylpheniprazine) is the corresponding methamphetamine (N-methylamphetamine) analogue.
Society and culture
[edit]Names
[edit]Pheniprazine is the generic name of the drug and its INN and BAN.[3] It is also known by the former developmental code name JB-516.[3]
References
[edit]- ^ a b c Sanan S, Vogt M (February 1962). "Effect of drugs on the noradrenaline content of brain and peripheral tissues and its significance". Br J Pharmacol Chemother. 18 (1): 109–127. doi:10.1111/j.1476-5381.1962.tb01155.x. PMC 1482167. PMID 14496718.
Pheniprazine (α-methylphenethylhydrazine; 1-phenyl-2-hydrazinopropane; amphetamine hydrazide) [...]
- ^ Anvisa (2023-03-31). "RDC Nº 784 - Listas de Substâncias Entorpecentes, Psicotrópicas, Precursoras e Outras sob Controle Especial" [Collegiate Board Resolution No. 784 - Lists of Narcotic, Psychotropic, Precursor, and Other Substances under Special Control] (in Brazilian Portuguese). Diário Oficial da União (published 2023-04-04). Archived from the original on 2023-08-03. Retrieved 2023-08-16.
- ^ a b c d Elks J (2014). The Dictionary of Drugs: Chemical Data: Chemical Data, Structures and Bibliographies. Springer US. p. 809. ISBN 978-1-4757-2085-3. Retrieved 12 August 2024.
- ^ Lear TE, Browne MW, Greeves JA (November 1962). "A controlled trial of cavodil (pheniprazine) in depression". The Journal of Mental Science. 108 (457): 856–858. doi:10.1192/bjp.108.457.856. PMID 13928843.
- ^ Fagervall I, Ross SB (April 1986). "Inhibition of monoamine oxidase in monoaminergic neurones in the rat brain by irreversible inhibitors". Biochemical Pharmacology. 35 (8): 1381–1387. doi:10.1016/0006-2952(86)90285-6. PMID 2870717.
- ^ Eberson LE, Persson K (July 1962). "Studies on Monoamine Oxidase Inhibitors. I. The Autoxidation of β-Phenylisopropylhydrazine as a Model Reaction for Irreversible Monoamine Oxidase Inhibition". Journal of Medicinal and Pharmaceutical Chemistry. 5 (4): 738–752. doi:10.1021/jm01239a006. PMID 14056405.
- ^ Sandler G (March 1961). "Clinical evaluation of pheniprazine in angina pectoris". British Medical Journal. 1 (5228): 792–794. doi:10.1136/bmj.1.5228.792. PMC 1953879. PMID 13746179.
- ^ Wickstrom L, Hahn N (September 1962). "[beta-Phenylisoprophlhydrazine (Catran) in schizophrenia]". Nordisk Medicin. 68: 1165–1167. PMID 14000469.
- ^ Fentem PH, Howitt G (December 1961). "Fatal jaundice after administration of pheniprazine". British Medical Journal. 2 (5267): 1616–1617. doi:10.1136/bmj.2.5267.1616. PMC 1970739. PMID 13892290.
- ^ Frandsen E (1962). "Toxic amblyopia during antidepressant treatment with pheniprazine (Catran)". Acta Psychiatrica Scandinavica. 38 (1): 1–14. doi:10.1111/j.1600-0447.1962.tb01780.x. PMID 13894598. S2CID 35152293.
- ^ Thomsen NJ (January 1963). "[Optic neuritis after treatment with Catran]". Ugeskrift for Laeger. 125: 138–139. PMID 13981222.
- ^ Baker GB, Coutts RT (1989). "Metabolism of monoamine oxidase inhibitors". Progress in Neuro-Psychopharmacology & Biological Psychiatry. 13 (3–4): 395–403. doi:10.1016/0278-5846(89)90128-0. PMID 2664891.
- ^ a b Spencer PS (1977). "Review of the pharmacology of existing antidepressants". British Journal of Clinical Pharmacology. 4 (Suppl 2): 57S – 68S. doi:10.1111/j.1365-2125.1977.tb05761.x. PMC 1429129. PMID 334231.
- ^ Kitanaka J, Kitanaka N, Takemura M (2006). "Modification of Monoaminergic Activity by MAO Inhibitors Influences Methamphetamine Actions". Drug Target Insights. 1: 19–28. doi:10.1177/117739280600100001. PMC 3155216. PMID 21901055.
- ^ Barbelivien A, Nyman L, Haapalinna A, Sirviö J (June 2001). "Inhibition of MAO-A activity enhances behavioural activity of rats assessed using water maze and open arena tasks". Pharmacology & Toxicology. 88 (6): 304–312. doi:10.1034/j.1600-0773.2001.880604.x. PMID 11453370.