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HIF-1/2α-IN-1

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产品编号 T61442

HIF-1/2α-IN-1, an orally active compound, functions as an inhibitor of HIF-2α. Its inhibitory effect on HIF-2α activity is significant, with an IC 50 value of 0.92 μM. Furthermore, HIF-1/2α-IN-1 has the ability to decrease HIF-1α levels. This compound is particularly valuable for research on clear cell renal cell carcinoma (ccRCC) [1].

HIF-1/2α-IN-1

HIF-1/2α-IN-1

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产品编号 T61442

HIF-1/2α-IN-1, an orally active compound, functions as an inhibitor of HIF-2α. Its inhibitory effect on HIF-2α activity is significant, with an IC 50 value of 0.92 μM. Furthermore, HIF-1/2α-IN-1 has the ability to decrease HIF-1α levels. This compound is particularly valuable for research on clear cell renal cell carcinoma (ccRCC) [1].

规格价格库存数量
25 mg
¥ 10,600
10-14周
50 mg
¥ 13,800
10-14周
100 mg
¥ 17,500
10-14周
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产品介绍

生物活性
产品描述
HIF-1/2α-IN-1, an orally active compound, functions as an inhibitor of HIF-2α. Its inhibitory effect on HIF-2α activity is significant, with an IC 50 value of 0.92 μM. Furthermore, HIF-1/2α-IN-1 has the ability to decrease HIF-1α levels. This compound is particularly valuable for research on clear cell renal cell carcinoma (ccRCC) [1].
体外活性
HIF-1/2α-IN-1 (compound #25) (0.01-100 μM) inhibits HIF-2α activity with an IC 50 value of 0.92 μM [1]. HIF-1/2α-IN-1 (0-10 μM, 24 h) decrease HIF-2α by inhibiting IRE-dependent translation and also inhibit HIF-1α at higher concentrations,which effects mediates by inhibiting the function of iron sulfur cluster assembly 2 (ISCA2) [1]. HIF-1/2α-IN-1 (1 μM, 24 h) targets ISCA2 and trigger the iron starvation response [1]. HIF-1/2α-IN-1 (0-100 μM, 24 h) decreased cell viability in 786-0 cells (IC 50 =1.7 μM (786-0), 10.6 μM (786-0 VHL)) and RCC4 cells (IC 50 =4.8 μM (RCC4), 71.0 μM (RCC4 VHL)) [1]. Cell Viability Assay [1] Cell Line: 786-0 cells and RCC4 cells Concentration: 0.01-100 μM Incubation Time: 24 h Result: Decreased cell viability in 786-0 cells and RCC4 cells. Western Blot Analysis [1] Cell Line: 786-0 cells and RCC10 cells Concentration: 0, 0.5, 1, 2.5, 10 μM Incubation Time: 24 h Result: Decreased HIF-2α activity and protein levels. Decreased HIF-1α levels at higher concentrations or treatment durations, but do not promote proteasomal degradation of HIF-1/2α. Inhibited the production of luciferase driven by the HIF-2α IRE (IRE-Luc). Increasesed IRP2, TFRC in dose-dependent and decreased FTH. RT-PCR [1] Cell Line: 786-0 cells Concentration: 0, 0.5, 1, 5 μM Incubation Time: 24 h Result: Resulted in a dose-dependent decrease in the transcription of HIF-2α target genes VEGFA and POU5F1, but not inhibited HIF-2α transcription.
体内活性
HIF-1/2α-IN-1 (compound #25) (p.o.; 30, 60 mg/kg; daily) significantly reduced ccRCC xenograft growth in vivo [1]. Animal Model: NRG or Balb/c mice [1] (6-8 week old, male, 10 per group) Dosage: 30, 60 mg/kg Administration: p.o., daily Result: Significantly inhibited tumor growth. Had well tolerated with no significant weight loss.
化学信息
分子量368.35
分子式C17H16N6O4
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
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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

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