(-)-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%
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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.
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基本信息 | |
别名 |
MK 801; MK801; C13737
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外观 |
Powder
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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
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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.
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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
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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