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Anticancer agent 47

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产品编号 T61412Cas号 2461795-23-1

Anticancer agent 47 (compound 4j) exhibits potent anticancer properties, demonstrating antiproliferative activities and inducing apoptosis as well as cell cycle arrest at G0/G1 phase. Moreover, Anticancer agent 47 has exhibited significant in vivo antitumor activities [1].

Anticancer agent 47

Anticancer agent 47

Rating icon 还可以
产品编号 T61412Cas号 2461795-23-1

Anticancer agent 47 (compound 4j) exhibits potent anticancer properties, demonstrating antiproliferative activities and inducing apoptosis as well as cell cycle arrest at G0/G1 phase. Moreover, Anticancer agent 47 has exhibited significant in vivo antitumor activities [1].

规格价格库存数量
25 mg
¥ 10,600
6-8周
50 mg
¥ 13,800
6-8周
100 mg
¥ 17,500
6-8周
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产品介绍

生物活性
产品描述
Anticancer agent 47 (compound 4j) exhibits potent anticancer properties, demonstrating antiproliferative activities and inducing apoptosis as well as cell cycle arrest at G0/G1 phase. Moreover, Anticancer agent 47 has exhibited significant in vivo antitumor activities [1].
体外活性
Anticancer agent 47 (compound 4j) shows antiproliferative activities with IC 50 s of 1.6, 0.72, 7.07 μM for HepG2, A549, H596 cells, respectively [1]. Anticancer agent 47 (0.8, 1.6, 3.2 μM; 24 h) induces apoptosis and cell cycle arrest at G0/G1 phase [1]. Anticancer agent 47 (5 μM; 5h) significantly increases ROS production [1]. Apoptosis Analysis [1] Cell Line: HepG2, H596 cells Concentration: 0.8, 1.6, 3.2 μM Incubation Time: 24 h Result: Induced apoptosis with the apoptotic cell rates were 14.23, 20.47 and 27.66% at 0.8, 1.6, 3.2 μM in HepG2 cell, respectively. Cell Cycle Analysis [1] Cell Line: HepG2 cells Concentration: 0.8, 1.6, 3.2 μM Incubation Time: 24 h Result: Showed 48.54%, 49.60% and 53.00% cells were at G0/G1 phase at 0.6, 1.2 and 2.4 μM, respectively.
体内活性
Anticancer agent 47 (20 mg/kg; i.v.; once every 2 days for 19 days) shows antitumor activities [1]. Animal Model: BALB/c nude mice (HepG2 xenografts) [1] Dosage: 20 mg/kg Administration: I.v.; once every 2 days for 19 days Result: Effectively inhibited tumor growth with the 58.7% tumor inhibition rate.
化学信息
分子量366.39
分子式C19H14N2O4S
CAS No.2461795-23-1
储存&溶解度
存储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
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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