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α-Glucosidase-IN-18

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产品编号 T61519

α-Glucosidase-IN-18 (7B) is an orally active inhibitor of α-glucosidase, displaying an IC 50 value of 3.96 μM. This compound exhibits antidiabetic properties [1].

α-Glucosidase-IN-18

α-Glucosidase-IN-18

Rating icon 还可以
产品编号 T61519

α-Glucosidase-IN-18 (7B) is an orally active inhibitor of α-glucosidase, displaying an IC 50 value of 3.96 μM. This compound exhibits antidiabetic properties [1].

规格价格库存数量
25 mg
¥ 10,600
10-14周
50 mg
¥ 13,800
10-14周
100 mg
¥ 17,500
10-14周
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产品介绍

生物活性
产品描述
α-Glucosidase-IN-18 (7B) is an orally active inhibitor of α-glucosidase, displaying an IC 50 value of 3.96 μM. This compound exhibits antidiabetic properties [1].
体内活性
α-Glucosidase-IN-18 (7B) (p.o., 10 or 20 mg/kg) has antidiabetic activity and significantly reduces blood glucose levels, from 392.16 mg/dL of diabetic control to 112.97 mg/dL at a concentration of 20 mg/kg after 28 days, while effectively slowing weight loss due to diabetes in male Wistar albino rats with streptozotocin-induced diabetes [1]. α-Glucosidase-IN-18 (7B) (p.o., 10 or 20 mg/kg) had an anti-hyperlipidemic effect with total CH levels from 226.03 mg/dL in the diabetic control to 136.4 mg/dL, LDL levels from 183.3 mg/dL to 114.18 mg/dL and TG levels from 189.35 mg/dL to 118.61 mg/dL in male Wistar albino rats with streptozotocin-induced diabetes [1]. α-Glucosidase-IN-18 (7B) decreases ALP levels from 3.01 mg/dL to 0.85 mg/dL and 0.79 mg/dL, SGPT levels from 59.43 mg/dL to 27.07 mg/dL and 23.91 mg/dL, SGOT levels from 49.67 mg/dL to 26.71 mg/dL and 23.08 mg/dL, serum creatinine from 3.01 mg/dL to 0.85 mg/dL and 0.79 mg/dL, and insulin levels from 0.369 mg/dL to 0.621 mg/dL and 0.639 mg/dL, respectively at doses of 10 and 20 mg/kg in male Wistar albino rats with streptozotocin-induced diabetes [1].
化学信息
分子量373.47
分子式C23H19NO2S
储存&溶解度
存储Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.

SCI 文献

计算器

  • 摩尔浓度 计算器
  • 稀释 计算器
  • 配液 计算器
  • 分子量 计算器

体内实验配液计算器

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:
TargetMol | Animal experiments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 μLTargetMol | Animal experiments 一共给药动物 10 只 ,您使用的配方为 5% TargetMol | reagent 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 μLDMSOTargetMol | reagent ( 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:50μLDMSOTargetMol | reagent 母液,添加 300 μLPEG300TargetMol | reagent 混匀澄清,再加 50μLTween 80, 混匀澄清,再加 600μLddH2OTargetMol | reagent 混匀澄清

以上为“体内实验配液计算器”的使用方法举例,并不是具体某个化合物的推荐配制方式,请根据您的实验动物和给药方式选择适当的溶解方案。

1 请输入动物实验的基本信息
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g
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2 请输入动物体内配方组成,不同的产品配方组成不同,如有配方需求,可先联系我们提供正确的体内配方。
% DMSO
%
%Tween 80
%ddH2O

剂量转换

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