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Pivagabine

From Wikipedia, the free encyclopedia
Pivagabine
Seletal formula of pivagabine with some implicit hydrogens shown
Seletal formula of pivagabine with some implicit hydrogens shown
Names
Preferred IUPAC name
4-(2,2-Dimethylpropanamido)butanoic acid
Identifiers
3D model (JSmol)
ChemSpider
ECHA InfoCard100.067.287Edit this at Wikidata
EC Number
  • 274-038-3
KEGG
MeSHN-trimethylacetyl-4-aminobutyric+acid
UNII
  • InChI=1S/C9H17NO3/c1-9(2,3)8(13)10-6-4-5-7(11)12/h4-6H2,1-3H3,(H,10,13)(H,11,12) checkY
    Key: SRPNQDXRVRCTNK-UHFFFAOYSA-N checkY
  • CC(C)(C)C(=O)NCCCC(O)=O
Properties
C9H17NO3
Molar mass187.239 g·mol−1
Pharmacology
N06AX15 (WHO)
Oral
Pharmacokinetics:
6.4 hours
Legal status
  • In general: ℞ (Prescription only)
Related compounds
Related alkanoic acids
Except where otherwise noted, data are given for materials in theirstandard state (at 25 °C [77 °F], 100 kPa).
Chemical compound

Pivagabine (INN; brand nameTonerg), also known asN-pivaloyl-γ-aminobutyric acid orN-pivaloyl-GABA, is anantidepressant andanxiolyticdrug which was introduced inItaly in 1997 for the treatment ofdepressive andmaladaptivesyndromes. But it was discontinued in Italy (according toMartindale). Originally believed to function as aprodrug toGABA,[1] pivagabine is now believed to act somehow via modulation ofcorticotropin-releasing factor (CRF).[2][3][4][5][6]

See also

[edit]

References

[edit]
  1. ^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.
  2. ^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.
  3. ^Esposito G, Luparini MR (November 1997). "Pivagabine: a novel psychoactive drug".Arzneimittelforschung.47 (11A):1306–9.PMID 9450153.
  4. ^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.
  5. ^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.
  6. ^George I. Papakostas; Maurizio Fava (2010).Pharmacotherapy for Depression and Treatment-resistant Depression. World Scientific. pp. 370–.ISBN 978-981-4287-59-3.
SSRIsTooltip Selective serotonin reuptake inhibitors
SNRIsTooltip Serotonin–norepinephrine reuptake inhibitors
NRIsTooltip Norepinephrine reuptake inhibitors
NDRIsTooltip Norepinephrine–dopamine reuptake inhibitors
NaSSAsTooltip Noradrenergic and specific serotonergic antidepressants
SARIsTooltip Serotonin antagonist and reuptake inhibitors
SMSTooltip Serotonin modulator and stimulators
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TCAsTooltip Tricyclic antidepressants
TeCAsTooltip Tetracyclic antidepressants
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Non-selective
MAOATooltip Monoamine oxidase A-selective
MAOBTooltip Monoamine oxidase B-selective
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5-HT1ARTooltip 5-HT1A receptoragonists
GABAARTooltip GABAA receptorPAMsTooltip positive allosteric modulators
Hypnotics
Gabapentinoids
(α2δVDCCblockers)
Antidepressants
Antipsychotics
Sympatholytics
(Antiadrenergics)
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