Pivagabine
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Names | |
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Preferred IUPAC name
4-(2,2-Dimethylpropanamido)butanoic acid | |
Identifiers | |
3D model (JSmol)
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ChemSpider | |
ECHA InfoCard | 100.067.287 |
EC Number |
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KEGG | |
MeSH | N-trimethylacetyl-4-aminobutyric+acid |
PubChem CID
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UNII | |
CompTox Dashboard (EPA)
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Properties | |
C9H17NO3 | |
Molar mass | 187.239 g·mol−1 |
Pharmacology | |
N06AX15 (WHO) | |
Oral | |
Pharmacokinetics: | |
6.4 hours | |
Legal status |
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Related compounds | |
Related alkanoic acids
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Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Pivagabine (INN; brand name Tonerg), also known as N-pivaloyl-γ-aminobutyric acid or N-pivaloyl-GABA, is an antidepressant and anxiolytic drug which was introduced in Italy in 1997 for the treatment of depressive and maladaptive syndromes. But it was discontinued in Italy (according to Martindale). Originally believed to function as a prodrug to GABA,[1] pivagabine is now believed to act somehow via modulation of corticotropin-releasing factor (CRF).[2][3][4][5][6]
See also
References
- ^ Bianchi M, Quadro G, Mourier G, Galzigna L (1983). "Pharmacokinetics and in vitro effects of a 4-aminobutyric acid derivative with anticonvulsant action". Pharmacology. 27 (4): 237–40. doi:10.1159/000137876. PMID 6634934.
- ^ Scapagnini U, Matera M (November 1997). "Effects of pivagabine on psychophysical performance and behavioural response in experimental models of stress". Arzneimittel-Forschung. 47 (11A): 1310–4. PMID 9450154.
- ^ Esposito G, Luparini MR (November 1997). "Pivagabine: a novel psychoactive drug". Arzneimittelforschung. 47 (11A): 1306–9. PMID 9450153.
- ^ Gerra G, Zaimovic A, Giusti F, et al. (July 2001). "Pivagabine effects on neuroendocrine responses to experimentally-induced psychological stress in humans". Behavioural Brain Research. 122 (1): 93–101. doi:10.1016/S0166-4328(01)00177-2. PMID 11287080. S2CID 23067609.
- ^ Serra M, Concas A, Mostallino MC, et al. (April 1999). "Antagonism by pivagabine of stress-induced changes in GABAA receptor function and corticotropin-releasing factor concentrations in rat brain". Psychoneuroendocrinology. 24 (3): 269–84. doi:10.1016/S0306-4530(98)00049-3. PMID 10101733. S2CID 11382166.
- ^ George I. Papakostas; Maurizio Fava (2010). Pharmacotherapy for Depression and Treatment-resistant Depression. World Scientific. pp. 370–. ISBN 978-981-4287-59-3.
Categories:
- Pages using the JsonConfig extension
- Articles without InChI source
- Articles without EBI source
- ECHA InfoCard ID from Wikidata
- Drugs with non-standard legal status
- Articles containing unverified chemical infoboxes
- Articles with short description
- Short description matches Wikidata
- Antidepressants
- Carboxamides
- Drugs with unknown mechanisms of action
- GABA analogues
- Gamma-Amino acids