Powder: -20°C for 3 years | In solvent: -80°C for 1 year
Temocapril hydrochloride (CS-622 HCl) 是血管紧张素转化酶 (ACE) 抑制剂。Temocapril HCl 能够用于充血性心力衰竭、急性心肌梗死、高血压、胰岛素抵抗和肾脏疾病的研究。
规格 | 价格/CNY | 货期 | 数量 | |
---|---|---|---|---|
5 mg | ¥ 252 | 现货 | ||
10 mg | ¥ 397 | 现货 | ||
25 mg | ¥ 743 | 现货 | ||
50 mg | ¥ 1,090 | 现货 | ||
100 mg | ¥ 1,620 | 现货 | ||
200 mg | ¥ 2,390 | 待询 | ||
1 mL * 10 mM (in DMSO) | ¥ 252 | 现货 |
产品描述 | Temocapril hydrochloride (CS-622 HCl), the hydrochloride of Temocapril, is a long-acting ACE inhibitor used for the therapy of hypertension. |
激酶实验 | C2C12 cells are seeded into 96-well plates at 2,000 cells per well in DMEM supplemented with 2% FBS. The wells are treated in quadruplicate with BMP ligands and LDN-193189 or vehicle. The cells are collected after 6 d in culture in 50 μL Tris-buffered saline and 1% Triton X-100. The lysates are added to p-nitro-phenylphosphate reagent in 96-well plates for 1 h and then evaluated alkaline phosphatase activity (absorbance at 405 nm). Cell viability are measured and quantity by Cell Titer Aqueous One (absorbance at 490 nm), using replicate wells treated identically to those used for alkaline phosphatase measurements[1]. |
别名 | CS-622 HCl, Acecol, Temocapril HCl, CS-622, 盐酸替莫普利 |
分子量 | 513.07 |
分子式 | C23H28N2O5S2·HCl |
CAS No. | 110221-44-8 |
Powder: -20°C for 3 years | In solvent: -80°C for 1 year
H2O: < 1 mg/mL (insoluble or slightly soluble)
Ethanol: 95 mg/mL (185.2 mM)
DMSO: 95 mg/mL (185.2 mM)
可选溶剂 | 浓度 体积 质量 | 1 mg | 5 mg | 10 mg | 25 mg |
Ethanol / DMSO | 1 mM | 1.9491 mL | 9.7453 mL | 19.4905 mL | 48.7263 mL |
5 mM | 0.3898 mL | 1.9491 mL | 3.8981 mL | 9.7453 mL | |
10 mM | 0.1949 mL | 0.9745 mL | 1.9491 mL | 4.8726 mL | |
20 mM | 0.0975 mL | 0.4873 mL | 0.9745 mL | 2.4363 mL | |
50 mM | 0.039 mL | 0.1949 mL | 0.3898 mL | 0.9745 mL | |
100 mM | 0.0195 mL | 0.0975 mL | 0.1949 mL | 0.4873 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。
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