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Oxiracetam information


Oxiracetam
Clinical data
Routes of
administration
Oral
ATC code
  • N06BX07 (WHO)
Legal status
Legal status
  • AU: S4 (Prescription only)
  • US: Unscheduled
Pharmacokinetic data
Bioavailability56-82%
Onset of action30-90 Minutes
Elimination half-life8 hours
ExcretionRenal
Identifiers
IUPAC name
  • (RS)-2-(4-hydroxy-2-oxopyrrolidin-1-yl)acetamide
CAS Number
  • 62613-82-5 ☒N
PubChem CID
  • 4626
ChemSpider
  • 4465 checkY
UNII
  • P7U817352G
KEGG
  • D07346 checkY
ChEMBL
  • ChEMBL36633 checkY
CompTox Dashboard (EPA)
  • DTXSID9045180 Edit this at Wikidata
ECHA InfoCard100.164.173 Edit this at Wikidata
Chemical and physical data
FormulaC6H10N2O3
Molar mass158.157 g·mol−1
3D model (JSmol)
  • Interactive image
ChiralityRacemic mixture
SMILES
  • O=C(N)CN1C(=O)CC(O)C1
InChI
  • InChI=1S/C6H10N2O3/c7-5(10)3-8-2-4(9)1-6(8)11/h4,9H,1-3H2,(H2,7,10) checkY
  • Key:IHLAQQPQKRMGSS-UHFFFAOYSA-N checkY
 ☒NcheckY (what is this?)  (verify)

Oxiracetam (developmental code name ISF 2522) is a nootropic drug of the racetam family and a very mild stimulant.[1][2] Several studies suggest that the substance is safe even when high doses are consumed for a long period of time.[3][4][5] However, the mechanism of action of the racetam drug family is still a matter of research. Oxiracetam is not approved by Food and Drug Administration for any medical use in the United States.

  1. ^ Malykh AG, Sadaie MR (February 2010). "Piracetam and piracetam-like drugs: from basic science to novel clinical applications to CNS disorders". Drugs. 70 (3): 287–312. doi:10.2165/11319230-000000000-00000. PMID 20166767. S2CID 12176745.
  2. ^ Valzelli L, Baiguerra G, Giraud O (June 1986). "Difference in learning and retention by Albino Swiss mice. Part III. Effect of some brain stimulants". Methods and Findings in Experimental and Clinical Pharmacology. 8 (6): 337–41. PMID 3736279.
  3. ^ Parnetti L, Mecocci P, Petrini A, Longo A, Buccolieri A, Senin U (1989). "Neuropsychological results of long-term therapy with oxiracetam in patients with dementia of Alzheimer type and multi-infarct dementia in comparison with a control group". Neuropsychobiology. 22 (2): 97–100. doi:10.1159/000118599. PMID 2518332.
  4. ^ Itil TM, Menon GN, Songar A, Itil KZ (1986). "CNS pharmacology and clinical therapeutic effects of oxiracetam". Clinical Neuropharmacology. 9 (Suppl 3): S70-2. doi:10.1097/00002826-198609003-00011. PMID 3594458.
  5. ^ Perucca E, Parini J, Albrici A, Visconti M, Ferrero E (1987). "Oxiracetam pharmacokinetics following single and multiple dose administration in the elderly". European Journal of Drug Metabolism and Pharmacokinetics. 12 (2): 145–8. doi:10.1007/bf03189889. PMID 3691580. S2CID 11415210.

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industry affiliations, often undisclosed. Racetams, such as piracetam, oxiracetam, phenylpiracetam, and aniracetam, are often marketed as cognitive enhancers...

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