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- 详细信息
- 文献和实验
- 技术资料
- 保存条件：
Powder: -20°C, 3 years; 4°C, 2 years.In solvent: -80°C, 6 months; -20°C, 1 month.
- 库存：
货期：1-2天
- 供应商：
MedChemExpress LLC
- CAS号：
23749-58-8
- 规格：
10 mM * 1 mL/5 mg/10 mg/25 mg/50 mg/100 mg
| 规格： | 10 mM * 1 mL | 产品价格： | ￥550.0 |
|---|---|---|---|
| 规格： | 5 mg | 产品价格： | ￥500.0 |
| 规格： | 10 mg | 产品价格： | ￥800.0 |
| 规格： | 25 mg | 产品价格： | ￥1600.0 |
| 规格： | 50 mg | 产品价格： | ￥2600.0 |
| 规格： | 100 mg | 产品价格： | ￥4200.0 |
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AHR agonist 3
CAS No. : 23749-58-8
MCE 国际站：AHR agonist 3
产品活性：AHR agonist 3 是一种芳香烃受体 (AhR) 激动剂，可通过激活肿瘤抑制转录程序诱导细胞周期停滞或细胞凋亡 (apoptosis)。AHR agonist 3 通过 AhR 抑制三阴性乳腺癌 (TNBC) 干细胞生长，同时对正常人原代细胞毒性极小，可用于癌症研究。
研究领域：Apoptosis | Immunology/Inflammation
作用靶点：Apoptosis | Aryl Hydrocarbon Receptor
In Vitro: AHR agonist 3 (Analog 523) (10 nΜ; 24 hour or 2-3 weeks) induces cell cycle arrest and inhibits clonogenicity in AhR WT and AhR KO MDA-MB-468 cells .
AHR agonist 3 (0-10 μΜ; 48-72 hours) drives AhR-dependent apoptosis and growth inhibition in breast cancerous cells, but not normal breast epithelial cells or on-tumorigenic cells and inhibits TNBC stem cell growth via AhR..
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文献和实验Cell-Based Assays for Identification of Aryl Hydrocarbon Receptor (AhR) Activators
and potency of the inducing chemical. The AhR agonist activity of positive test chemicals can be confirmed by demonstrating their ability to stimulate expression of CYP1A1, an endogenous AhR-responsive gene, using quantitative real-time PCR. The detailed
. GRA of the aryl hydrocarbon receptor (AhR) relies on the in vitro ability of the cytosolic AhR protein complex to convert into its high affinity DNA binding form following its interaction with and activation by an AhR agonist and, as such, the GRA
Overview of Receptor Allosterism
assessment of relative agonist efficacy. Biochem. Pharmacol. 58:735‐748. Colquhoun, D. 1973. The relation between classical and cooperative models for drug action. In Drug
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