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(±)-Norcantharidin

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产品编号 T5656Cas号 29745-04-8
别名 去甲斑蝥素, Norcantharidin, Endothall anhydride

(±)-Norcantharidin (Endothall anhydride) 是一种人类结肠癌中 c-Met 和 EGFR 的双重抑制剂,可研究抗癌,具有抗血管生成活性。

(±)-Norcantharidin

(±)-Norcantharidin

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纯度: 99.43%
产品编号 T5656 别名 去甲斑蝥素, Norcantharidin, Endothall anhydrideCas号 29745-04-8

(±)-Norcantharidin (Endothall anhydride) 是一种人类结肠癌中 c-Met 和 EGFR 的双重抑制剂,可研究抗癌,具有抗血管生成活性。

规格价格库存数量
5 mg¥ 269现货
10 mg¥ 382现货
25 mg¥ 659现货
50 mg¥ 979现货
100 mg¥ 1,450现货
500 mg¥ 3,630现货
1 g¥ 5,250现货
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产品介绍

生物活性
产品描述
(±)-Norcantharidin (Endothall anhydride) is a synthetic anticancer compound which is a dual inhibitor for c-Met and EGFR in human colon cancers.
体内活性
NCTD可能是一种实惠且有效的候选化合物,以替代gefitinib来满足癌症患者的治疗需求[1]。通过诱导凋亡和阻断细胞周期,NCTD在体内抑制裸鼠人类胆囊癌异种移植瘤的生长[2]。
细胞实验
Two human colon cancer cell lines, HCT116 and HT29, were used as model systems to investigate the anti-cancer molecular mechanism of NCTD. Cell cycle arrest and early/late apoptosis were analyzed by flow cytometry. The levels of EGFR, phospho-EGFR, c-Met, phospho-c-Met and other related proteins were quantified by western blot analysis[1]
动物实验
The tumor xenograft model of human gallbladder carcinoma in nude mice in vivo was established with subcutaneous GBC-SD cells. The experimental mice were randomly divided into control, 5-FU, NCTD, and NCTD+5-FU groups which were given different treatments. Tumor growth in terms of size, growth curve, and inhibitory rate was evaluated. Cell cycle, apoptosis, and morphological changes of the xenografted tumors were assessed by flow cytometry and light/electron microscopy. The expression of the cell cycle-related proteins cyclin-D1 and p27 as well as the apoptosis-related proteins Bcl-2, Bax, and survivin were determined by the streptavidin-biotin complex (SABC) method and RT-PCR[2].
别名去甲斑蝥素, Norcantharidin, Endothall anhydride
化学信息
分子量168.15
分子式C8H8O4
CAS No.29745-04-8
SmilesO=C1OC(=O)C2C3CCC(O3)C12
密度1.468g/cm3
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: 60 mg/mL (356.82 mM), Sonication is recommended.
溶液配制表
1mg5mg10mg50mg
1 mM5.9471 mL29.7354 mL59.4707 mL297.3536 mL
5 mM1.1894 mL5.9471 mL11.8941 mL59.4707 mL
10 mM0.5947 mL2.9735 mL5.9471 mL29.7354 mL
20 mM0.2974 mL1.4868 mL2.9735 mL14.8677 mL
50 mM0.1189 mL0.5947 mL1.1894 mL5.9471 mL
100 mM0.0595 mL0.2974 mL0.5947 mL2.9735 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

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