Powder: -20°C for 3 years | In solvent: -80°C for 1 year
ABT 724 trihydrochloride 是一种有效的选择性 D4 受体激动剂(EC50 = 12.4 nM,14.3 nM 和 23.2 nM,分别对人、大鼠和雪貂)。 ABT-724 trihydrochloride 可用于勃起功能障碍研究。
规格 | 价格/CNY | 货期 | 数量 | |
---|---|---|---|---|
1 mg | ¥ 477 | 现货 | ||
5 mg | ¥ 1,160 | 现货 | ||
10 mg | ¥ 1,850 | 现货 | ||
25 mg | ¥ 2,970 | 现货 | ||
50 mg | ¥ 4,390 | 现货 | ||
100 mg | ¥ 6,180 | 现货 | ||
500 mg | ¥ 12,300 | 现货 | ||
1 mL * 10 mM (in DMSO) | ¥ 1,270 | 现货 |
产品描述 | ABT 724 trihydrochloride is an effective and selective agonist of the D4 receptor (EC50 = 12.4 nM, 14.3 nM, and 23.2 nM for human, rat and ferret, respectively). ABT-724 trihydrochloride can be used in erectile dysfunction studies. |
靶点活性 | D4 receptor:12.4 nM(EC50,human), D4 receptor:14.3 nM(EC50, rat), D4 receptor:23.2(EC50, ferret) |
体外活性 | A weak affinity to 5-HT1A receptors (Ki = 2780 nM) is observed. ABT 724 trihydrochloride(10 μM) exhibits a selective biochemical profile, as indicated by a lack of binding affinity for >70 neurotransmitter/uptake/ion channels including D2, D3, or D5 receptors. ABT 724 trihydrochloride(10 μM) does not inhibit the PDE activity of PDE1, PDE5, or PDE6[1]. |
体内活性 | In male adult Wistar rats, ABT 724 trihydrochloride (8.8 μg/kg; s.c.) treatment facilitated penile erection in a dose-dependent manner[1]. |
分子量 | 402.75 |
分子式 | C17H22Cl3N5 |
CAS No. | 587870-77-7 |
Powder: -20°C for 3 years | In solvent: -80°C for 1 year
H2O: 100 mg/mL (248.29 mM)
DMSO: 15 mg/mL (37.24 mM), Sonication is recommended.
可选溶剂 | 浓度 体积 质量 | 1 mg | 5 mg | 10 mg | 25 mg |
H2O / DMSO | 1 mM | 2.4829 mL | 12.4146 mL | 24.8293 mL | 62.0732 mL |
5 mM | 0.4966 mL | 2.4829 mL | 4.9659 mL | 12.4146 mL | |
10 mM | 0.2483 mL | 1.2415 mL | 2.4829 mL | 6.2073 mL | |
20 mM | 0.1241 mL | 0.6207 mL | 1.2415 mL | 3.1037 mL | |
H2O | 50 mM | 0.0497 mL | 0.2483 mL | 0.4966 mL | 1.2415 mL |
100 mM | 0.0248 mL | 0.1241 mL | 0.2483 mL | 0.6207 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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