Powder: -20°C for 3 years | In solvent: -80°C for 1 year
(S)-Mapracorat is a selective and less active agonist of glucocorticoid receptor.
产品描述 | (S)-Mapracorat is a selective and less active agonist of glucocorticoid receptor. |
体内活性 | During the 60-minute observation period, intradermal injection of compound 48/80 (50 μg in 50 μL saline) resulted in a significant wheal and flare reaction. Topical pre-treatment with (S)-Mapracorat (0.1%) leads to significant reduction in the wheal and flare responses compared to vehicle (acetone) treated areas. |
别名 | (S)-ZK-245186, (S)-BOL-303242X |
分子量 | 462.48 |
分子式 | C25H26F4N2O2 |
CAS No. | 887375-15-7 |
Powder: -20°C for 3 years | In solvent: -80°C for 1 year
DMSO: 50.6 mg/mL (109.41 mM)
可选溶剂 | 浓度 体积 质量 | 1 mg | 5 mg | 10 mg | 25 mg |
DMSO | 1 mM | 2.1623 mL | 10.8113 mL | 21.6226 mL | 54.0564 mL |
5 mM | 0.4325 mL | 2.1623 mL | 4.3245 mL | 10.8113 mL | |
10 mM | 0.2162 mL | 1.0811 mL | 2.1623 mL | 5.4056 mL | |
20 mM | 0.1081 mL | 0.5406 mL | 1.0811 mL | 2.7028 mL | |
50 mM | 0.0432 mL | 0.2162 mL | 0.4325 mL | 1.0811 mL | |
100 mM | 0.0216 mL | 0.1081 mL | 0.2162 mL | 0.5406 mL |
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。
(S)-Mapracorat 887375-15-7 Others ZK-245186 BOL-303242X ZK245186 (S)-ZK-245186 Mapracorat (S)-BOL-303242X ZK 245186 (S)Mapracorat (S) Mapracorat Inhibitor inhibitor inhibit