SDZ 220-581铵盐

SDZ 220-581铵盐是NMDA谷氨酸受体竞争性拮抗剂。

信号通路 >> 跨膜转运 >> iGluR

信号通路 >> 神经信号通路 >> iGluR

研究领域 >> 神经疾病

[1]. Gilmour G, Broad LM, Wafford KA, In vitro characterisation of the novel positive allosteric modulators of the mGlu5 receptor, LSN2463359 and LSN2814617, and their effects on sleep architecture and operant responding in the rat. Neuropharmacology. 2013 Jan;64:224-39.

[2]. Urwyler S, Campbell E, Fricker G, Biphenyl-derivatives of 2-amino-7-phosphono-heptanoic acid, a novel class of potent competitive N-methyl-D-aspartate receptor antagonists--II. Pharmacological characterization in vivo. Neuropharmacology. 1996 Jun;35(6):655-69.

[3]. Bakshi VP, Tricklebank M, Neijt HC, Disruption of prepulse inhibition and increases in locomotor activity by competitive N-methyl-D-aspartate receptor antagonists in rats. J Pharmacol Exp Ther. 1999 Feb;288(2):643-52.

[4]. Linderholm K, Powell S, Olsson E, Role of the NMDA-receptor in Prepulse Inhibition in the Rat. Int J Tryptophan Res. 2010;3:1-12.

(+)-MK 801 马来酸盐(马来酸地佐环平)(mM/ml) | 6-氰基-7-硝基喹喔啉-2,3-二酮 | N-甲基-D-天冬氨酸水合物 | 酒石酸艾芬地尔 | (R)-(-)-2-氨基-5-膦酰戊酸 | 1,4-二氢-6,7-二硝基-2,3-喹喔啉二酮 | Ro 25-6981马来酸盐 | 马来酸氟吡汀 | Mibampator | 苯并二氧六环-6-(1-哌啶基)甲酰胺 | Naspm | (8R)-7-乙酰基-5-(4-氨基苯基)-8,9-二氢-8-甲基-7H-1,3-二氧杂环戊烯并[4,5-H][2,3]苯并二氮杂卓 | 盐酸甲氯芬酯 | 24羟基胆固醇