包装 | 价格(元) |
500 µg | 电议 |
1mg | 电议 |
5mg | 电议 |
别名 | UCB-6215-d6 |
Canonical SMILES | NC(CN1C(C([2H])([2H])C([2H])([2H])C1([2H])[2H])=O)=O |
分子式 | C6H4D6N2O2 |
分子量 | 148.2 |
溶解度 | DMSO: soluble,Methanol: soluble,Water: soluble |
储存条件 | -20°C |
General tips | For obtaining a higher solubility , please warm the tube at 37 ℃ and shake it in the ultrasonic bath for a while. |
Shipping Condition | Evaluation sample solution : ship with blue ice All other available size: ship with RT , or blue ice upon request |
产品描述 | Piracetam-d6is intended for use as an internal standard for the quantification of piracetam by GC- or LC-MS. Piracetam is a nootropic cyclic GABA derivative.1It is a positive allosteric modulator of AMPA receptors and enhances binding of the NMDA antagonist MK-801 to rat forebrain membranes.2,3Piracetam (1 mM) protects against amyloid-β-induced decreases in the mitochondrial membrane potential, as well as decreases in neurite outgrowth in the presence of NGF, in PC12 rat adrenal medulla cells.4It prevents scopolamine-induced amnesia in a passive avoidance test in mice when administered at a dose of 30 mg/kg.5Formulations containing piracetam have been used in the treatment of myoclonus. 1.Winnicka, K., Tomasiak, M., and Bielawska, A.Piracetam - An old drug with novel properties•Acta Pol. Pharm.62(5)405-409(2005) 2.Copani, A., Genassani, A.A., Aleppo, G., et al.Nootropic drugs positively modulate α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid-sensitive glutamate receptors in neuronal culturesJ. Neurochem.58(4)1199-1204(1992) 3.Hamelin, S.M., and Lehmann, J.C.Effects of putative cognition enhancers on the NMDA receptor by [3H]MK801 bindingEur. J. Pharmacol.281(3)R11-R13(1995) 4.Kurz, C., Ungerer, I., Lipka, U., et al.The metabolic enhancer piracetam ameliorates the impairment of mitochondrial function and neurite outgrowth induced by β-amyloid peptideBr. J. Pharmacol.160(2)246-257(2010) 5.Ghelardini, C., Galeotti, N., Gualtieri, F., et al.The novel nootropic compound DM232 (unifiram) ameliorates memory impairment in mice and ratsDrug Develop. Res.56(1)23-32(2002) |