Isocarboxazid
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Non-proprietary name | Isocarboxazid | |||||||||||||||||||||
other names |
N ′ -Benzyl-5-methylisoxazole-3-carbohydrazide ( IUPAC ) |
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Molecular formula | C 12 H 13 N 3 O 2 | |||||||||||||||||||||
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Molar mass | 231.25 g mol −1 | |||||||||||||||||||||
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As far as possible and customary, SI units are used. Unless otherwise noted, the data given apply to standard conditions . |
Isocarboxazid is an irreversible, non-selective inhibitor of monoamine oxidase ( MAO inhibitor ) from the group of hydrazines , which is used as an antidepressant and anxiolytic . Along with phenelzine , it is one of the few hydrazine-based MAO inhibitors still in use.
Isocarboxazid is used to combat various health disorders, such as depression , social phobia or panic disorders, and is now also used to support the fight against Parkinson's disease and other dementia-related disorders. Although isocarboxazid is a helpful drug , it has numerous side effects.
Side effects
Side effects of isocarboxazid include:
- a headache
- Jaundice
- Chest pain
- rapid weight gain
- Faint
- Drowsiness
- Tremor (tremor)
Others
Isocarboxazid is not the drug of choice for depression and anxiety disorder because it interacts with various foods that contain tyramine . It inhibits the breakdown of this biogenic amine, which is contained in everyday foods, which, among other things, can lead to severe blood pressure crises. As a result, isocarboxazid and other MAOIs are often considered the last resort for depression.
literature
- Fiedorowicz JG, Swartz KL: The role of monoamine oxidase inhibitors in current psychiatric practice . In: Journal of Psychiatric Practice . 10, No. 4, July 2004, pp. 239-248. PMID 15552546 . PMC 2075358 (free full text).
Individual evidence
- ↑ harmonized classification for this substance . A labeling of isocarboxazid in the Classification and Labeling Inventory of the European Chemicals Agency (ECHA), which was accessed on February 11, 2020, is reproduced from a self-classification by the distributor . There is not yet a
- ↑ Fagervall I, Ross SB: Inhibition of monoamine oxidase in monoaminergic neurones in the rat brain by irreversible inhibitors . In: Biochemical pharmacology . 35, No. 8, April 1986, pp. 1381-7. doi : 10.1016 / 0006-2952 (86) 90285-6 . PMID 2870717 .
- ↑ Volz, Hanz-Peter. (November 1998) “Monoamine Oxidase Inhibitors A Perspective on Their Use in The Elderly” Biochemical pharmacology (5) 341-352.