Powder: -20°C for 3 years | In solvent: -80°C for 1 year
0990CL 是一种有效的异三聚体Gαi subunit 特异性抑制剂,可与纯化的Go±在gdp 结合状态下相互作用,能够阻断α2AR 介导的cAMP 调控。 在细胞模型中低浓度0990CL 能够部分恢复cAMP 水平,高浓度的0990CL (10 μM)下,开始对细胞活力产生负面影响。
规格 | 价格/CNY | 货期 | 数量 | |
---|---|---|---|---|
1 mg | ¥ 2,160 | 现货 | ||
5 mg | ¥ 5,270 | 现货 | ||
10 mg | ¥ 7,430 | 现货 | ||
25 mg | ¥ 10,800 | 现货 | ||
50 mg | ¥ 14,800 | 现货 | ||
100 mg | ¥ 19,600 | 现货 | ||
1 mL * 10 mM (in DMSO) | ¥ 5,580 | 现货 |
产品描述 | 0990CL is an effective heterotrimer Gαi subunit specific inhibitor, which can interact with purified Go± in GDP-bound state, and can block α2AR mediated cAMP regulation. In the cell model, low concentration of 0990CL could partially restore cAMP level, and high concentration of 0990CL (10μM) began to have negative effects on cell viability. |
体外活性 | 0990CL (at a concentration of 30 μM with a 30-minute pre-treatment) exhibits preferential binding to Gαi1 compared to Gαq. It displays selectivity towards Gαi and Gαq, resulting in a maximum reduction of endpoint fluorescence by 38±8% and 10%, respectively. Treatment with 0990CL (100 nM to 1 μM , 24 h) restores α2AR/Gαi-mediated cAMP levels induced by Fsk and UK14304 in HEK293 GloSensor cells. At a dosage of 100 nM, it reinstates 31% of the reduced cAMP levels[1]. |
分子量 | 343.42 |
分子式 | C21H21N5 |
CAS No. | 511514-03-7 |
Powder: -20°C for 3 years | In solvent: -80°C for 1 year
DMSO: 45.0 mg/mL (131.0 mM), Sonication is recommended.
可选溶剂 | 浓度 体积 质量 | 1 mg | 5 mg | 10 mg | 25 mg |
DMSO | 1 mM | 2.9119 mL | 14.5594 mL | 29.1189 mL | 72.7972 mL |
5 mM | 0.5824 mL | 2.9119 mL | 5.8238 mL | 14.5594 mL | |
10 mM | 0.2912 mL | 1.4559 mL | 2.9119 mL | 7.2797 mL | |
20 mM | 0.1456 mL | 0.728 mL | 1.4559 mL | 3.6399 mL | |
50 mM | 0.0582 mL | 0.2912 mL | 0.5824 mL | 1.4559 mL | |
100 mM | 0.0291 mL | 0.1456 mL | 0.2912 mL | 0.728 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。
0990CL 511514-03-7 GPCR/G Protein Others cAMP Inhibitor inhibitor inhibit