Powder: -20°C for 3 years | In solvent: -80°C for 1 year
DJ-V-159 (DJ-V159) 是一种G 蛋白偶联受体家族C 组6 A 的激动剂。
规格 | 价格/CNY | 货期 | 数量 | |
---|---|---|---|---|
1 mg | ¥ 159 | 现货 | ||
2 mg | ¥ 219 | 现货 | ||
5 mg | ¥ 347 | 现货 | ||
10 mg | ¥ 567 | 现货 | ||
25 mg | ¥ 1,150 | 现货 | ||
50 mg | ¥ 1,960 | 现货 | ||
100 mg | ¥ 3,190 | 现货 | ||
500 mg | ¥ 6,910 | 现货 | ||
1 mL * 10 mM (in DMSO) | ¥ 383 | 现货 |
产品描述 | DJ-V-159 is a GPRC6A agonist, targeting the G protein-coupled receptor family C group 6 member A (GPRC6A). |
体外活性 | DJ-V159 activates ERK in HEK-293 transfected with GPRC6A but not in non-transfected HEK-293 cells, with potency similar to L-Arg. In addition, DJ-V159 dose-dependently stimulates cAMP production in GPRC6A expressing HEK-293 cells, achieving a response a 0.2 nM concentrations in the media. DJ-V159 stimulates insulin secretion in mouse beta-cell MIN-6 cells. The DJ-V159 increased insulin stimulation index (SI) in MIN-6 cells similar to the effects of Ocn, known ligand of GPRC6A [1]. |
体内活性 | DJ-V-159 (10 mg/kg, i.p.) reduces blood glucose levels in wild-type mice at 60 and 90 minutes, whereas the vehicle (95% PEG + 5% DMSO) has no effect on blood glucose. DJ-V-159 (10 mg/kg, i.p.) reduces blood glucose levels in wild-type mice by 43.6% and 41.9% at 60 and 90 minutes, respectively. The mice tolerated this short-term exposure to DJ-V-159 without any overt side-effects. DJ-V-159, however, is almost in or on the boundary of the Lipinski's Rule of Five [1]. |
别名 | DJ-V159 |
分子量 | 502.37 |
分子式 | C24H12F6N4O2 |
CAS No. | 2253744-53-3 |
Powder: -20°C for 3 years | In solvent: -80°C for 1 year
DMSO: 5.02 mg/mL (10 mM)
可选溶剂 | 浓度 体积 质量 | 1 mg | 5 mg | 10 mg | 25 mg |
DMSO | 1 mM | 1.9906 mL | 9.9528 mL | 19.9056 mL | 49.7641 mL |
5 mM | 0.3981 mL | 1.9906 mL | 3.9811 mL | 9.9528 mL | |
10 mM | 0.1991 mL | 0.9953 mL | 1.9906 mL | 4.9764 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。
DJ-V-159 2253744-53-3 Endocrinology/Hormones GPCR/G Protein GPR Androgen Receptor DJV159 Inhibitor inhibit DJ-V159 DJ V 159 DJ-V 159 inhibitor