Powder: -20°C for 3 years | In solvent: -80°C for 1 year
Imidacloprid-urea 是吡虫啉的次级代谢产物。吡虫啉是一种有效且广泛使用的新烟碱类化合物,对谷物,蔬菜,茶叶和棉花的害虫具有抑制作用。Imidacloprid-urea 可以占据或阻断吡虫啉在土壤上的吸附位点,从而可能影响吡虫啉在环境中的去向、转运和生物利用度。
规格 | 价格/CNY | 货期 | 数量 | |
---|---|---|---|---|
5 mg | ¥ 193 | 现货 | ||
10 mg | ¥ 265 | 现货 | ||
25 mg | ¥ 563 | 现货 | ||
50 mg | ¥ 895 | 现货 | ||
100 mg | ¥ 1,350 | 现货 |
产品描述 | Imidacloprid-urea is a secondary metabolite of imidacloprid. Imidacloprid is a potent and widely used neonicotinoid with inhibitory effects on pests of cereals, vegetables, tea and cotton. imidacloprid-urea can occupy or block the adsorption sites of imidacloprid on the soil, which may affect the fate, transport and bioavailability of imidacloprid in the environment. |
体外活性 | Imidacloprid (0, 10, and 20 μM ; 4-6 days) can reduce insulin-stimulated glucose uptake in adipocytes (3T3-L1), hepatocytes (HepG2), and myotubes (C2C12) cell culture models. Treatment with imidacloprid inhibits phosphorylation of protein kinase B (AKT) and ribosomal S6 kinase (S6K).[3] |
体内活性 | Imidacloprid(0, 5, 10, 20 mg/kg/day ; oral ; female rats) shows mild pathological changes in the brain, liver, and kidneys of rats.[4] |
分子量 | 211.65 |
分子式 | C9H10ClN3O |
CAS No. | 120868-66-8 |
Powder: -20°C for 3 years | In solvent: -80°C for 1 year
H2O: 11.2 mg/mL (53.2 mM ), Sonication is recommended.
DMSO: 112.5 mg/mL (531.5 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 | 4.7248 mL | 23.6239 mL | 47.2478 mL | 118.1195 mL |
5 mM | 0.945 mL | 4.7248 mL | 9.4496 mL | 23.6239 mL | |
10 mM | 0.4725 mL | 2.3624 mL | 4.7248 mL | 11.812 mL | |
20 mM | 0.2362 mL | 1.1812 mL | 2.3624 mL | 5.906 mL | |
50 mM | 0.0945 mL | 0.4725 mL | 0.945 mL | 2.3624 mL | |
DMSO | 100 mM | 0.0472 mL | 0.2362 mL | 0.4725 mL | 1.1812 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。
Imidacloprid-urea 120868-66-8 Inhibitor inhibitor inhibit