Powder: -20°C for 3 years | In solvent: -80°C for 1 year
H2-Gamendazole 是一种抑制精子发生和癌症治疗的新型化合物,可作为热休克蛋白和/或延伸因子1 α的抑制剂,是 Hsp90调节剂。
规格 | 价格/CNY | 货期 | 数量 | |
---|---|---|---|---|
1 mg | ¥ 828 | 现货 | ||
5 mg | ¥ 2,320 | 现货 | ||
10 mg | ¥ 3,490 | 现货 | ||
25 mg | ¥ 6,320 | 现货 | ||
50 mg | ¥ 8,520 | 现货 | ||
100 mg | ¥ 11,500 | 现货 | ||
1 mL * 10 mM (in DMSO) | ¥ 2,630 | 现货 |
产品描述 | H2-Gamendazole is a novel compound for spermatogenesis inhibition and cancer therapy as an inhibitor of heat shock proteins and/or elongation factor 1 alpha, and is an Hsp90 regulator. |
靶点活性 | MCF-7 cells:∼100 μM, ADPKD cells:5–10 μM, ErbB2:50 μM |
体外活性 |
H2-Gamendazole (H2-GMZ ; 0-100 μM) was effective in rapidly blocking forskolin-induced, Cl-mediated short-circuit currents in human ADPKD cells, and it significantly inhibited both cAMP- and epidermal growth factor-induced proliferation of ADPKD cells.[1] H2-GMZ (50 μM)-treated ADPKD cells showed decreased phosphorylated ERK and decreased hyperphosphorylated retinoblastoma levels through western blot analysis.[1] H2-GMZ (50 μM ; 24、48、72 h) treatment also decreased ErbB2, Akt, and cyclin-dependent kinase 4 and it decreased levels of the cystic fibrosis transmembrane conductance regulator Cl channel protein.[1] |
体内活性 | H2-Gamendazole (20 mg/kg ; intraperitoneal injections) was effective in slowing postnatal cyst formation and kidney enlargement in the ---Pkd1flox/flox: Pkhd1-Cre mouse model.[1] |
分子量 | 417.21 |
分子式 | C18H13Cl2F3N2O2 |
CAS No. | 877768-84-8 |
Powder: -20°C for 3 years | In solvent: -80°C for 1 year
DMSO: 30 mg/mL (71.91 mM)
可选溶剂 | 浓度 体积 质量 | 1 mg | 5 mg | 10 mg | 25 mg |
DMSO | 1 mM | 2.3969 mL | 11.9844 mL | 23.9687 mL | 59.9219 mL |
5 mM | 0.4794 mL | 2.3969 mL | 4.7937 mL | 11.9844 mL | |
10 mM | 0.2397 mL | 1.1984 mL | 2.3969 mL | 5.9922 mL | |
20 mM | 0.1198 mL | 0.5992 mL | 1.1984 mL | 2.9961 mL | |
50 mM | 0.0479 mL | 0.2397 mL | 0.4794 mL | 1.1984 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。
H2-Gamendazole 877768-84-8 Cytoskeletal Signaling Metabolism HSP Inhibitor inhibitor inhibit