(S)-MCPG ≥98%
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| 包装规格: | 5mg 10mg 25mg 50mg in glass bottle |
| 溶解性: | 溶于DMSO(1mg/mL超声) |
| 产品描述: | 基本信息 产品编号: S11184 产品名称: (S)-MCPG CAS: 150145-89-4 储存条件 粉末 -20℃ 四年 分子式: C10H11NO4 溶于液体 -80℃ 6个月 分子量: 209.20 -20℃ 1个月 化学名: 4-[(1S)-1-amino-1-carboxyethyl]benzoic acid Solubility (25°C): 体外: DMSO Ethanol Water 体内(现配现用): <1mg/ml表示微溶或不溶。 普西唐提供的所有化合物浓度为内部测试所得,实际溶液度可能与公布值有所偏差,属于正常的批间细微差异现象。 请根据产品在不同溶剂中的溶解度选择合适的溶剂配制储备液;⼀旦配成溶液,请分装保存,避免反复冻融造成的产品失效。 制备储备液 浓度 溶液体积 质量 1mg 5mg 10mg 1mM 4.7801mL 23.9006mL 47.8011mL 生物活性 产品描述 一种有效的 I/II 类代谢型谷氨酸受体 (mGluRs) 拮抗剂,是 (RS)-MCPG的活性异构体。(S)-MCPG 可用于 mGluRs 在空间学习中的作用研究。 靶点 mGluR 体外研究 (S)-MCPG (100μM) has no detectable effects on basal spine formation or elimination mechanisms in WT slice cultures.(S)-MCPG prevents the increase in spine turnover triggered by TBS and interferes with the mechanisms of activity-dependent spine stabilization in Hippocampal slice cultures. 体内研究 MCPG (intraventricular injection;20μg) treated rat are slower to learn the task and takes longer to reach the platform than vehicle injected animals.On days 2 and 3,MCPG rats has a significant longer escape latency and the measure of search error is significantly longer on each of the first 3 days.On day 4,MCPG-treated animals reaches the same level of performance as control animals in Morris water maze. Animal Model: Male Lister-Hooded rats in the learning of the Morris water maze Dosage: 20μg Administration: Intraventricular injection;20μg;4 days Result: Impaired the performance of rats in the spatial version of the Morris water maze,but 1/10 of this dose did not. |
| 保存条件: | -20℃ |
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