(-)-MK 801 maleate

(-)-MK 801 maleateCAS号: 121917-57-5分子式: C20H19NO4分子量: 337.37描述纯度储存/保存方法别名外观可溶性/溶解性靶点In vitro(体外研究)In vivo(体内研究)参考文献

产品描述
描述

(-)-MK 801 Maleate is the enantiomer of (+)-MK-801; (+)-MK-801 is a highly potent and selective non-competitive NMDA glutamate receptor antagonist .

纯度
>98%
储存/保存方法
Store at -20℃ for one year(Powder);Store at 2-4℃ for two weeks;Store at -20℃ for six months after dissolution.
基本信息
别名
MK 801; MK801; C13737
外观
Powder
可溶性/溶解性
DMSO:67 mg/mL (198.59 mM)

Ethanol:7 mg/mL (20.74 mM)

生物活性
靶点
NMDA receptor
In vitro(体外研究)
Neurophysiological studies in vitro, using a rat cortical-slice preparation, demonstrates a potent, selective, and noncompetitive antagonistic action of dizocilpine on depolarizing responses to N-Me-D-Asp but not to kainate or quisqualate. The potencies of phencyclidine, ketamine, SKF 10047, and the enantiomers of dizocilpine as N-Me-D-Asp antagonists correlate closely (r = 0.99) with their potencies as inhibitors of dizocilpine binding. This suggests that the dizocilpine binding sites are associated with N-Me-D-Asp receptors and provides an explanation for the mechanism of action of dizocilpine as an anticonvulsant.
In vivo(体内研究)
All the control rats have severe permanent neurological deficits after ischemic spinal cord injury (ISCI), whereas the dizocilpine–treated rats have statistically (P
参考文献
参考文献
[1] Wong EH et al., Proc Natl Acad Sci U S A, 1986, 83(18), 7104-7108.
[2] Wise-Faberowski L et al., J Neurosurg Anesthesiol, 2006, 18(4), 240-246.
[3] Kocaeli H et al., Surg Neurol, 2005, 64 Suppl 2, S22-S26.

分子结构图

(-)-MK 801 maleate