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Dupracetam

January 01, 1970

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

Dupracetam
Clinical data
ATC code
  • none
Legal status
Legal status
  • In general: unscheduled
Identifiers
  • 2-(2-oxopyrrolidin-1-yl)-N'-[2-(2-oxopyrrolidin-1-yl)acetyl]acetohydrazide
CAS Number
  • 59776-90-8 Y
PubChem CID
  • 68793
ChemSpider
  • 62033 N
UNII
  • BVM2UGN450
ChEMBL
  • ChEMBL2104359 N
CompTox Dashboard (EPA)
  • DTXSID40975187
ECHA InfoCard100.056.279
Chemical and physical data
FormulaC12H18N4O4
Molar mass282.300 g·mol−1
3D model (JSmol)
  • Interactive image
  • C1CC(=O)N(C1)CC(=O)NNC(=O)CN2CCCC2=O
  • InChI=1S/C12H18N4O4/c17-9(7-15-5-1-3-11(15)19)13-14-10(18)8-16-6-2-4-12(16)20/h1-8H2,(H,13,17)(H,14,18) N
  • Key:YPUPYVWSTBYCBY-UHFFFAOYSA-N N
 NY (what is this?)  (verify)

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

See also edit

References edit

  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. doi:10.1002/ardp.19813140808. PMID 7294979. S2CID 95603731.
  2. ^ Hall ED, Von Voigtlander PF (November 1987). "Facilitatory effects of piracetam on excitability of motor nerve terminals and neuromuscular transmission". Neuropharmacology. 26 (11): 1573–1579. doi:10.1016/0028-3908(87)90003-7. PMID 2829047. S2CID 7759558.
  3. ^ Yang B, Liu D, Li CZ, Liu FY, Peng YM, Jiang YS (2007). "1-Methylhydantoin cytotoxicity on renal proximal tubular cells in vitro". Renal Failure. 29 (8): 1025–1029. doi:10.1080/08860220701641272. PMID 18067051. S2CID 26843776.
 

This drug article relating to the nervous system is a stub. You can help Wikipedia by expanding it.

January 01, 1970
dupracetam, nootropic, drug, from, racetam, family, clinical, dataatc, codenonelegal, statuslegal, statusin, general, unscheduledidentifiersiupac, name, oxopyrrolidin, oxopyrrolidin, acetyl, acetohydrazidecas, number59776, ypubchem, cid68793chemspider62033, nu. Dupracetam is a nootropic drug from the racetam family 1 2 DupracetamClinical dataATC codenoneLegal statusLegal statusIn general unscheduledIdentifiersIUPAC name 2 2 oxopyrrolidin 1 yl N 2 2 oxopyrrolidin 1 yl acetyl acetohydrazideCAS Number59776 90 8 YPubChem CID68793ChemSpider62033 NUNIIBVM2UGN450ChEMBLChEMBL2104359 NCompTox Dashboard EPA DTXSID40975187ECHA InfoCard100 056 279Chemical and physical dataFormulaC 12H 18N 4O 4Molar mass282 300 g mol 13D model JSmol Interactive imageSMILES C1CC O N C1 CC O NNC O CN2CCCC2 OInChI InChI 1S C12H18N4O4 c17 9 7 15 5 1 3 11 15 19 13 14 10 18 8 16 6 2 4 12 16 20 h1 8H2 H 13 17 H 14 18 NKey YPUPYVWSTBYCBY UHFFFAOYSA N N N Y what is this verify One of its metabolites 1 Methylhydantoin displays renal toxicity in high doses 3 See also editPiracetamReferences edit Dell HD Jacobi H Kamp R Kurz J Wunsche 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 doi 10 1002 ardp 19813140808 PMID 7294979 S2CID 95603731 Hall ED Von Voigtlander PF November 1987 Facilitatory effects of piracetam on excitability of motor nerve terminals and neuromuscular transmission Neuropharmacology 26 11 1573 1579 doi 10 1016 0028 3908 87 90003 7 PMID 2829047 S2CID 7759558 Yang B Liu D Li CZ Liu FY Peng YM Jiang YS 2007 1 Methylhydantoin cytotoxicity on renal proximal tubular cells in vitro Renal Failure 29 8 1025 1029 doi 10 1080 08860220701641272 PMID 18067051 S2CID 26843776 nbsp This drug article relating to the nervous system is a stub You can help Wikipedia by expanding it vte Retrieved from https en wikipedia org w index php title Dupracetam amp oldid 1186029410, wikipedia, wiki, book, books, library,

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