Powder: -20°C for 3 years | In solvent: -80°C for 1 year
Ipenoxazone is an effective and centrally acting muscle relaxant.
规格 | 价格/CNY | 货期 | 数量 | |
---|---|---|---|---|
25 mg | ¥ 10,600 | 6-8周 | ||
50 mg | ¥ 13,800 | 6-8周 | ||
100 mg | ¥ 17,500 | 6-8周 |
产品描述 | Ipenoxazone is an effective and centrally acting muscle relaxant. |
体内活性 | An intravenous injection of 2 mg/kg Ipenoxazone causes a reduction of electromyographic activity which reaches a maximum within 3 min after the injection. High doses (greater than 30 mg/kg i.p.) of Ipenoxazone produce transient and dose-dependent sedation in almost all mice about 5 min after its administration. After the injection of Ipenoxazone at a dose of 4 mg/kg within 1 min, the blood pressure changes from a control level of 138±9 mmHg to a minimum level of 98±9 mmHg (n=6) but it rapidly returns to the control level within 1 to 2 min, while the rigidity is still reduced significantly at that time [2]. |
别名 | NC-1200, MLV-6976, 伊培沙宗 |
分子量 | 358.52 |
分子式 | C22H34N2O2 |
CAS No. | 104454-71-9 |
Powder: -20°C for 3 years | In solvent: -80°C for 1 year
对于不同动物的给药剂量换算,您也可以参考 更多...
请在以下方框中输入您的动物实验信息后点击计算,可以得到母液配置方法和体内配方的制备方法: 比如您的给药剂量是10 mg/kg,每只动物体重20 g,给药体积100 μL,一共给药动物10 只,您使用的配方为5% DMSO+30% PEG300+5% Tween 80+60% ddH2O。那么您的工作液浓度为2 mg/mL。
母液配置方法:2 mg 药物溶于 50 μL DMSO (母液浓度为 40 mg/mL), 如您需要配置的浓度超过该产品的溶解度,请先与我们联系。
体内配方的制备方法:取 50 μL DMSO 主液,加入 300 μL PEG300, 混匀澄清,再加 50 μL Tween 80,混匀澄清,再加 600 μL ddH2O, 混匀澄清。
您可能有的问题的答案可以在抑制剂处理说明中找到,包括如何准备库存溶液,如何存储产品,以及基于细胞的分析和动物实验需要特别注意的问题。
Ipenoxazone 104454-71-9 Others NC 1200 NC-1200 MLV-6976 伊培沙宗 MLV6976 NC1200 MLV 6976 Inhibitor inhibitor inhibit