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顶部相关产品产品介绍化学信息储存和溶解信息计算器

Flutamide-D7

货号 T69758Cas号 223134-72-3 一键复制产品信息
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Flutamide-D7 is intended for use as an internal standard for the quantification of flutamide by GC- or LC-MS. Flutamide (T0489) is an androgen receptor antagonist and prodrug form of 2-hydroxy flutamide. Flutamide (T0489) is converted to 2-hydroxy flutamide by the cytochrome P450 (CYP) isoform CYP1A2 in human liver microsomes. It is cytotoxic to PC3 and LNCaP prostate cancer cells with IC50 values of 98.8 and 81.8 µM,respectively. Flutamide (T0489) (50 mg/kg per day)reduces tumor growth in a PC-82 mouse xenograft model. Formulations containing flutamide have been used in the treatment of prostate cancer.

Flutamide-D7

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货号 T69758Cas号 223134-72-3

Flutamide-D7 is intended for use as an internal standard for the quantification of flutamide by GC- or LC-MS. Flutamide (T0489) is an androgen receptor antagonist and prodrug form of 2-hydroxy flutamide. Flutamide (T0489) is converted to 2-hydroxy flutamide by the cytochrome P450 (CYP) isoform CYP1A2 in human liver microsomes. It is cytotoxic to PC3 and LNCaP prostate cancer cells with IC50 values of 98.8 and 81.8 µM,respectively. Flutamide (T0489) (50 mg/kg per day)reduces tumor growth in a PC-82 mouse xenograft model. Formulations containing flutamide have been used in the treatment of prostate cancer.

Flutamide-D7
其他形式的 “Flutamide-D7”:
FlutamideT048913311-84-7
现货
规格价格库存数量
500 μg
¥ 2,680
35日内发货
1 mg
¥ 4,730
35日内发货
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产品介绍

生物活性
产品描述
Flutamide-D7 is intended for use as an internal standard for the quantification of flutamide by GC- or LC-MS. Flutamide (T0489) is an androgen receptor antagonist and prodrug form of 2-hydroxy flutamide. Flutamide (T0489) is converted to 2-hydroxy flutamide by the cytochrome P450 (CYP) isoform CYP1A2 in human liver microsomes. It is cytotoxic to PC3 and LNCaP prostate cancer cells with IC50 values of 98.8 and 81.8 µM, respectively. Flutamide (T0489) (50 mg/kg per day) reduces tumor growth in a PC-82 mouse xenograft model. Formulations containing flutamide have been used in the treatment of prostate cancer.
化学信息
分子量283.26
分子式C11H4D7F3N2O3
CAS No.223134-72-3
SmilesC(F)(F)(F)C1=C(N(=O)=O)C=CC(NC(C(C([2H])([2H])[2H])(C([2H])([2H])[2H])[2H])=O)=C1
储存&溶解度
存储

Powder: -20°C for 3 years | In solvent: -80°C for 1 year Shipping with blue ice/Shipping at ambient temperature.

实际储存温度请以COA为准

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：
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 10% DMSO + 40% PEG300 + 5% Tween 80 + 45% Saline / PBS / 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 100 μL DMSO （ 母液浓度为 20 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 100 μL DMSO 母液， 添加 400 μL PEG300 混匀澄清， 再加 50 μL Tween 80, 混匀澄清, 再加 450 μL Saline / PBS / ddH2O 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。
方案所需的各类助溶剂如： DMSO， PEG300， PEG400， Tween 80， SBE-β-CD， 玉米油等， 均可在TargetMol网站点击购买。
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
% Saline/PBS/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

IACS9439IACS 9439Flutamide-d713311-84-7
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