Dimiracetam

Dimiracetam
Names
	IUPAC name (RS)-3,6,7,7a-Tetrahydro-1H-pyrrolo[1,2-a]imidazole-2,5-dione
Identifiers
CAS Number	126100-97-8 ;
3D model (JSmol)	Interactive image; Interactive image;
ChEMBL	ChEMBL337612 ;
ChemSpider	59358 ;
PubChem CID	65955;
UNII	4AW7F70MZO ;
	InChI InChI=1S/C6H8N2O2/c9-5-3-8-4(7-5)1-2-6(8)10/h4H,1-3H2,(H,7,9) Key: XTXXOHPHLNROBN-UHFFFAOYSA-N ; InChI=1/C6H8N2O2/c9-5-3-8-4(7-5)1-2-6(8)10/h4H,1-3H2,(H,7,9) Key: XTXXOHPHLNROBN-UHFFFAOYAX;
	SMILES C1CC(=O)N2C1NC(=O)C2; O=C2NC1N(C(=O)CC1)C2;
Properties
Chemical formula	C6H8N2O2
Molar mass	140.142 g·mol−1
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). verify (what is ?) Infobox references

Dimiracetam is a nootropic drug of the racetam family,^[1] derivatives of which may have application in the treatment of neuropathic pain.^[2]

References

^ Pinza, M; Farina, C; Cerri, A; Pfeiffer, U; Riccaboni, MT; Banfi, S; Biagetti, R; Pozzi, O; et al. (1993). "Synthesis and pharmacological activity of a series of dihydro-1H-pyrrolo1,2-aimidazole-2,5(3H,6H)-diones, a novel class of potent cognition enhancers". Journal of Medicinal Chemistry. 36 (26): 4214–20. doi:10.1021/jm00078a011. PMID 8277504.
^ Farina, C; Gagliardi, S; Ghelardini, C; Martinelli, M; Norcini, M; Parini, C; Petrillo, P; Ronzoni, S (2008). "Synthesis and biological evaluation of novel dimiracetam derivatives useful for the treatment of neuropathic pain". Bioorganic & Medicinal Chemistry. 16 (6): 3224–32. doi:10.1016/j.bmc.2007.12.015. PMID 18171618.

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