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Tirbanibulin dihydrochloride

产品编号 T15674Cas号 1038395-65-1
别名 KX-01 (dihydrochloride)|||KX2-391 (dihydrochloride)

Tirbanibulin is an inhibitor of Src that targets the peptide substrate site of Src (GI50: 9-60 nM in cancer cell lines).

Tirbanibulin dihydrochloride

Tirbanibulin dihydrochloride

产品编号 T15674别名 KX-01 (dihydrochloride), KX2-391 (dihydrochloride)Cas号 1038395-65-1

Tirbanibulin is an inhibitor of Src that targets the peptide substrate site of Src (GI50: 9-60 nM in cancer cell lines).

规格价格库存数量
2 mg¥ 3245日内发货
5 mg¥ 5385日内发货
1 mL x 10 mM (in DMSO)¥ 6865日内发货
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产品介绍

生物活性
产品描述
Tirbanibulin is an inhibitor of Src that targets the peptide substrate site of Src (GI50: 9-60 nM in cancer cell lines).
靶点活性
Src (HepG2):60 nM, Src (PLC/PRF/5):13 nM, Src (HuH-7):(GI50)9 nM, Src (Hep3B):26 nM
体外活性
Tirbanibulin (KX2-391) is found to inhibit certain leukemia cells that are resistant to current commercially available drugs, such as those derived from chronic leukemia cells with the T3151 mutation. KX2-391 displays steep dose-response curves against Huh7 (GI50=9 nM), PLC/PRF/5 (GI50=13 nM), Hep3B (GI50=26 nM), and HepG2 (GI50=60 nM), four hepatic cell cancer (HCC) cell lines[1]. Tirbanibulin is evaluated in engineered Src driven cell growth assays inNIH3T3/c-Src527F and SYF/c-Src527F cells and exhibits GI50 with 23 nM and 39 nM, respectively[2].
体内活性
In pre-clinical animal models of cancer, Tirbanibulin (p.o.) is shown to inhibit primary tumor growth and to suppress metastasis[2].
别名KX-01 (dihydrochloride), KX2-391 (dihydrochloride)
化学信息
分子量504.45
分子式C26H31Cl2N3O3
CAS No.1038395-65-1
储存&溶解度
存储Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.
溶解度信息
DMSO: 33.33 mg/mL (66.07 mM), Sonication is recommended.
溶液配制表
DMSO
1mg5mg10mg50mg
1 mM1.9824 mL9.9118 mL19.8236 mL99.1179 mL
5 mM0.3965 mL1.9824 mL3.9647 mL19.8236 mL
10 mM0.1982 mL0.9912 mL1.9824 mL9.9118 mL
20 mM0.0991 mL0.4956 mL0.9912 mL4.9559 mL
50 mM0.0396 mL0.1982 mL0.3965 mL1.9824 mL

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
mg/kg
g
μL
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

对于不同动物的给药剂量换算,您也可以参考 更多

关键词

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