Pargyline
| Clinical data | |
|---|---|
| Trade names | Eutonyl; Eutron |
| Other names | MO-911; A-19120; Lopac-P-8013; NSC-43798; N-Methyl-N-propargylbenzylamine |
| MedlinePlus | a682088 |
| Routes of administration | Oral[1][2] |
| ATC code | |
| Pharmacokinetic data | |
| Metabolites | • N-Methylbenzylamine[3] • N-Propargylbenzylamine[3] • N-Methylpropargylamine[3] • Benzylamine[3] • Propiolaldehyde[3] • Propargylamine[3] • Benzaldehyde[3] • Pargyline-N-oxide[3] |
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| CompTox Dashboard (EPA) | |
| ECHA InfoCard | 100.008.275 |
| Chemical and physical data | |
| Formula | C11H13N |
| Molar mass | 159.232 g·mol−1 |
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Pargyline, sold under the brand name Eutonyl among others, is a monoamine oxidase inhibitor (MAOI) medication which has been used to treat hypertension (high blood pressure) but is no longer marketed.[4][5][6] It has also been studied as an antidepressant, but was never licensed for use in the treatment of depression.[7][8] The drug is taken by mouth.[1][2]
Side effects of pargyline include orthostatic hypotension among others.[1] It has the potential for serious food and drug interactions with sympathomimetic agents like tyramine that can result in hypertensive crisis.[1] Pargyline acts as a non-selective and irreversible inhibitor of the monoamine oxidases MAO-A and MAO-B.[6] The exact mechanism of the hypotensive effects of pargyline and other MAOIs is unclear.[9][10][11][12] Structurally, pargyline is a benzylamine derivative and is related to selegiline and clorgyline.[13][14][15]
Pargyline was first described in 1960[9][16][17] and was introduced for medical use in 1963.[18] It was available in the United States and the United Kingdom.[18][2][5] The clinical use of pargyline was limited due to its side effects and interactions.[1] The drug remained available in the United States as late as 2000.[5] However, it was fully discontinued worldwide by 2007.[19]
- ^ a b c d e Hayes AH, Schneck DW (May 1976). "Antihypertensive pharmacotherapy". Postgraduate Medicine. 59 (5): 155–162. doi:10.1080/00325481.1976.11714363. PMID 57611.
- ^ a b c Cite error: The named reference
Drugs@FDAwas invoked but never defined (see the help page). - ^ a b c d e f g h Cite error: The named reference
KoppakaThompsonChen2012was invoked but never defined (see the help page). - ^ Elks J (2014). The Dictionary of Drugs: Chemical Data: Chemical Data, Structures and Bibliographies. Springer US. p. 934. ISBN 978-1-4757-2085-3. Retrieved 11 August 2024.
- ^ a b c Schweizerischer Apotheker-Verein (2000). Index Nominum 2000: International Drug Directory. Medpharm Scientific Publishers. p. 795. ISBN 978-3-88763-075-1. Retrieved 2024-08-11.
- ^ a b Finberg JP (August 2014). "Update on the pharmacology of selective inhibitors of MAO-A and MAO-B: focus on modulation of CNS monoamine neurotransmitter release". Pharmacology & Therapeutics. 143 (2): 133–152. doi:10.1016/j.pharmthera.2014.02.010. PMID 24607445.
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