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MK-801 (Dizocilpine)77086-21-6

更新时间:2024-02-02

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MK-801 (Dizocilpine)77086-21-6
上海一基实业有限公司是主要从事、配套试剂的生产和销售的企业,产品用途:科研实验,标准对照品研究中心代理的作为一种衡量标准。

MK-801 (Dizocilpine)77086-21-6

 MK801(Dizocilpine)
分子式:C16H15N   分子量:221.3
 
产品描述
Dizocilpine是有效的N-methyl-D-aspartate(NMDA)受体拮抗剂,Ki为30.5 nM。
靶点
NMDA
         
IC50
30.5 nM (Ki)
         
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 [3H] 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.
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 < .05) better neurological outcome and good recovery. Histopathology reveals severe neuronal necrosis in the lumbar gray matter of control rats, whereas dizocilpine–treated rats show mild injury. These results demonstrate that a single dose of dizocilpine given before ISCI provides significant neuroprotection. 
溶解性
DMSO 67 mg/mL,水 <1 mg/mL,乙醇 7 mg/mL
稳定性
2年 -20°C粉状,6月-80°C溶于DMSO

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