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Bazedoxifene hydrochloride

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产品编号 T6404Cas号 198480-56-7
别名 WAY 140424 hydrochloride, TSE-424 hydrochloride, TSE424 hydrochloride, TSE 424 hydrochloride

Bazedoxifene hydrochloride (TSE 424 hydrochloride) 是一种能透过血脑屏障且具有口服活性、选择性和高效性的雌激素受体调节剂 (SERM),也是 IL-6/GP130 蛋白相互作用抑制剂,对 ERα 和 ERβ 具有很高的亲和力,可用于研究绝经后骨质疏松症和血管舒缩相关疾病。

Bazedoxifene hydrochloride

Bazedoxifene hydrochloride

Rating icon 很棒
纯度: 98.74%
产品编号 T6404 别名 WAY 140424 hydrochloride, TSE-424 hydrochloride, TSE424 hydrochloride, TSE 424 hydrochlorideCas号 198480-56-7

Bazedoxifene hydrochloride (TSE 424 hydrochloride) 是一种能透过血脑屏障且具有口服活性、选择性和高效性的雌激素受体调节剂 (SERM),也是 IL-6/GP130 蛋白相互作用抑制剂,对 ERα 和 ERβ 具有很高的亲和力,可用于研究绝经后骨质疏松症和血管舒缩相关疾病。

规格价格库存数量
1 mg¥ 492现货
5 mg¥ 1,270现货
10 mg¥ 2,300现货
25 mg¥ 3,590现货
50 mg¥ 5,680现货
100 mg¥ 7,690现货
500 mg¥ 15,300现货
1 mL x 10 mM (in DMSO)¥ 1,980现货
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"Bazedoxifene hydrochloride"的相关化合物库

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纯度:98.74%
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产品介绍

生物活性
产品描述
Bazedoxifene hydrochloride (TSE 424 hydrochloride) is an orally active, selective, and potent estrogen receptor modulator (SERM) that crosses the blood-brain barrier and is an inhibitor of IL-6/GP130 protein interactions with high affinity for ERα and ERβ. It has a high affinity for ERα and ERβ and can be used to study postmenopausal osteoporosis and vasodilator-related diseases.
靶点活性
ERβ (rat):99 nM, ERα:26 nM, ERα:23 nM, ERβ:89 nM
体外活性
在 AsPC-1 细胞中,Bazedoxifene hydrochloride(10 μM-20 μM;2 小时)能够抑制由 IL-6、IL-11 或 OSM(各50 ng/mL)诱导的 STAT3 磷酸化[2]。
体内活性
在 6 周龄的雌性无胸腺裸鼠中,Bazedoxifene hydrochloride(剂量为5 mg/kg;通过口服灌胃,每日一次,持续 18 天)被用于抑制胰腺癌异种移植瘤的生长,并在肿瘤细胞中诱导凋亡[2]。
激酶实验
Ligand binding competition experiments: Test compounds are initially solubilized in DMSO and the final concentration of DMSO in the binding assay is ≤ 1%. Eight dilutions of each test compound are used as an unlabelled competitor for [3H]17β-estradiol. Typically, a set of compound dilutions would be tested simultaneously on human, rat and mouse ER-α and ER-β. The results are plotted as measured DPM vs. concentration of test compound. For dose-response curve fitting, a four parameter logistic model on the transformed, weighted data are fit and the IC50 is defined as the concentration of compound decreasing maximum [3H]estradiol binding by 50%. For active compounds, the IC50 is determined at least three times. It should be noted that IC50 values are not direct measures of a ligand's affinity for the receptor. Rather, they can only be compared as relative values, in this case to 17β-estradiol.
细胞实验
For the proliferation assay, cells are plated at 20,000 cells/well in a 24-well plate in DMEM/F12 (50:50) (phenol red-free) with 10% charcoal/dextran-treated FBS and 1 × GlutaMAX-1. After overnight incubation, the medium is aspirated and treatments in DMEM/F12 (50:50) (phenol red-free) with 2% charcoal/dextran-treated FBS and 1 × GlutaMAX-1 are added to the wells. Each plate has a vehicle (baseline proliferation) and treatments. Treatments included 10 pM 17β-estradiol determined to be the EC80 for 17β-estradiol and 17β-estradiol in combination with six concentrations of BZA. Treatments from d 1 are renewed on d 3 and d 6 by aspirating medium from wells and replacing with fresh medium and treatments. On d 7, cells are detached from the plate using trypsin-EDTA and counted using a Multisizer II.(Only for Reference)
别名WAY 140424 hydrochloride, TSE-424 hydrochloride, TSE424 hydrochloride, TSE 424 hydrochloride
化学信息
分子量507.06
分子式C30H35ClN2O3
CAS No.198480-56-7
SmilesCl.OC=1C=CC(=CC1)C2=C(C3=CC(O)=CC=C3N2CC4=CC=C(OCCN5CCCCCC5)C=C4)C
密度no data available
储存&溶解度
存储store at low temperature,keep away from direct sunlight | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.
溶解度信息
H2O: <1 mg/mL
Ethanol: <1 mg/mL
DMSO: 93 mg/mL (183.4 mM)
溶液配制表
1mg5mg10mg50mg
1 mM1.9722 mL9.8608 mL19.7215 mL98.6077 mL
5 mM0.3944 mL1.9722 mL3.9443 mL19.7215 mL
10 mM0.1972 mL0.9861 mL1.9722 mL9.8608 mL
20 mM0.0986 mL0.4930 mL0.9861 mL4.9304 mL
50 mM0.0394 mL0.1972 mL0.3944 mL1.9722 mL
100 mM0.0197 mL0.0986 mL0.1972 mL0.9861 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

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