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Dupracetam

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Dupracetam
220px
Systematic (IUPAC) name
2-(2-oxopyrrolidin-1-yl)-N'-[2-(2-oxopyrrolidin-1-yl)acetyl]acetohydrazide
Clinical data
  • Unscheduled
Identifiers
59776-90-8 7pxY
None
PubChem CID 68793
ChemSpider 62033 7pxN
UNII BVM2UGN450 7pxY
Chemical data
Formula C12H18N4O4
282.296 g/mol
 14pxN (what is this?)  (verify)

Dupracetam is a nootropic drug from the racetam family.[1][2]

One of its metabolites, 1-Methylhydantoin, displays renal toxicity in high doses. [3]

See also

References

  1. Dell HD, Jacobi H, Kamp R, Kurz J, Wünsche C (August 1981). "[1-Methylhydantoin, an unexpected metabolite of the intelligence-affecting substance dupracetam (author's transl)]". Archiv Der Pharmazie (in German) 314 (8): 697–702. PMID 7294979. 
  2. Hall ED, Von Voigtlander PF (November 1987). "Facilitatory effects of piracetam on excitability of motor nerve terminals and neuromuscular transmission". Neuropharmacology 26 (11): 1573–9. PMID 2829047. doi:10.1016/0028-3908(87)90003-7. 
  3. Yang, B.; Liu, D.; Li, C.; Liu, F.; Peng, Y.; Jiang, Y. (2007). "1-Methylhydantoin Cytotoxicity on Renal Proximal Tubular Cells in Vitro". Renal Failure 29 (8): 1025–1029. PMID 18067051. doi:10.1080/08860220701641272.  edit


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