store at low temperature,keep away from direct sunlight | Powder: -20°C for 3 years | In solvent: -80°C for 1 year
Y-33075 dihydrochloride 是一种选择性ROCK 抑制剂,IC50为 3.6 nM。
规格 | 价格/CNY | 货期 | 数量 | |
---|---|---|---|---|
1 mg | ¥ 259 | 现货 | ||
2 mg | ¥ 369 | 现货 | ||
5 mg | ¥ 591 | 现货 | ||
10 mg | ¥ 978 | 现货 | ||
25 mg | ¥ 2,380 | 现货 | ||
50 mg | ¥ 3,820 | 现货 | ||
100 mg | ¥ 5,530 | 现货 | ||
500 mg | ¥ 11,500 | 现货 | ||
1 mL * 10 mM (in DMSO) | ¥ 830 | 现货 |
产品描述 | Y-33075 dihydrochloride is a selective inhibitor of ROCK(IC50 of 3.6 nM). |
靶点活性 | PKC:420 nM, ROCK:3.6 nM, CaMK II:810 nM |
体外活性 | Y-33075 (Y-39983) is a potent inhibitor of ROCK(IC50 of 3.6 nM). Y-33075 also inhibits PKC and CaMKII more potently than Y-27632(IC50s of Y-27632 and Y-33075 for PKC are 9.0 μM and 0.42 μM, respectively), whereas the IC50s of Y-27632 and Y-33075 for CaMKII are 26 μM and 0.81 μM, respectively. The IC50s of Y-27632 and Y-33075 for PKC is 82 and 117 times those for ROCK, respectively, whereas the IC50s of Y-27632 and Y-33075 for CaMKII is 236 and 225 times those for ROCK, respectively[1]. Y-33075 (Y-39983, 10 μM) extends neurites in the retinal ganglion cells (RGCs) compared with those in RGCs treated without Y-39983[2]. Y-33075 (Y-39983, 1 μM) inhibits the contraction of rabbit ciliary artery segments evoked by histamine in Ca2+-free solutions[3]. |
体内活性 | Y-39983 (≥0.01%) significantly lowers intraocular pressure (IOP) at 2 hours after topical administration in rabbits. Y-39983 (0.05%)-treated eyes show significant reduction of IOP between 2 and 7 hours after topical administration in monkeys[1]. Y-39983 (100 μM) increases the regenerating axons of retinal ganglion cells (RGCs) in the eyes of the rats[2]. |
分子量 | 353.25 |
分子式 | C16H18Cl2N4O |
CAS No. | 173897-44-4 |
store at low temperature,keep away from direct sunlight | Powder: -20°C for 3 years | In solvent: -80°C for 1 year
DMSO: 100 mg/mL (283.09 mM), Sonification is recommended.
H2O: 50 mg/mL (141.54 mM), Sonification is recommended.
可选溶剂 | 浓度 体积 质量 | 1 mg | 5 mg | 10 mg | 25 mg |
DMSO / H2O | 1 mM | 2.8309 mL | 14.1543 mL | 28.3086 mL | 70.7714 mL |
5 mM | 0.5662 mL | 2.8309 mL | 5.6617 mL | 14.1543 mL | |
10 mM | 0.2831 mL | 1.4154 mL | 2.8309 mL | 7.0771 mL | |
20 mM | 0.1415 mL | 0.7077 mL | 1.4154 mL | 3.5386 mL | |
50 mM | 0.0566 mL | 0.2831 mL | 0.5662 mL | 1.4154 mL | |
100 mM | 0.0283 mL | 0.1415 mL | 0.2831 mL | 0.7077 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。
Y-33075 dihydrochloride 173897-44-4 Cell Cycle/Checkpoint Chromatin/Epigenetic Cytoskeletal Signaling Neuroscience Stem Cells CaMK ROCK PKC Y33075 dihydrochloride Y33075 Y 33075 Dihydrochloride ROK Rho-associated kinase Y-33075 Y-33075 Dihydrochloride Y33075 Dihydrochloride Inhibitor Rho-associated protein kinase Y 33075 dihydrochloride Rho-kinase inhibit Y 33075 inhibitor