Chemistry:Dupracetam

Dupracetam
Clinical data
ATC code	none;
Legal status
Legal status	In general: unscheduled;
Identifiers
	IUPAC name 2-(2-oxopyrrolidin-1-yl)-N'-[2-(2-oxopyrrolidin-1-yl)acetyl]acetohydrazide;
CAS Number	59776-90-8 ;
PubChem CID	68793;
ChemSpider	62033 ;
UNII	BVM2UGN450;
ChEMBL	ChEMBL2104359 ;
Chemical and physical data
Formula	C12H18N4O4
Molar mass	282.300 g·mol−1
3D model (JSmol)	Interactive image;
	SMILES C1CC(=O)N(C1)CC(=O)NNC(=O)CN2CCCC2=O;
	InChI 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) ; Key:YPUPYVWSTBYCBY-UHFFFAOYSA-N ;
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Short description: Chemical compound

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

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

References

↑ "[1-Methylhydantoin, an unexpected metabolite of the intelligence-affecting substance dupracetam (author's transl)]" (in de). Archiv der Pharmazie 314 (8): 697–702. August 1981. doi:10.1002/ardp.19813140808. PMID 7294979.
↑ "Facilitatory effects of piracetam on excitability of motor nerve terminals and neuromuscular transmission". Neuropharmacology 26 (11): 1573–1579. November 1987. doi:10.1016/0028-3908(87)90003-7. PMID 2829047.
↑ "1-Methylhydantoin cytotoxicity on renal proximal tubular cells in vitro". Renal Failure 29 (8): 1025–1029. 2007. doi:10.1080/08860220701641272. PMID 18067051.

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Clinical data

ATC code	none
Legal status
Legal status	In general: unscheduled
Identifiers
IUPAC name 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
Chemical and physical data
Formula	C₁₂H₁₈N₄O₄
Molar mass	282.300 g·mol⁻¹
3D model (JSmol)	Interactive image
SMILES C1CC(=O)N(C1)CC(=O)NNC(=O)CN2CCCC2=O
InChI 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)