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- 详细信息
- 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:
1613509-49-1
- 规格:
10 mM * 1 mL/1 mg/5 mg/10 mg/25 mg/50 mg
| 规格: | 10 mM * 1 mL | 产品价格: | ¥865.0 |
|---|---|---|---|
| 规格: | 1 mg | 产品价格: | ¥500.0 |
| 规格: | 5 mg | 产品价格: | ¥1100.0 |
| 规格: | 10 mg | 产品价格: | ¥1800.0 |
| 规格: | 25 mg | 产品价格: | ¥3600.0 |
| 规格: | 50 mg | 产品价格: | ¥5800.0 |
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SRI-41315
CAS No. : 1613509-49-1
MCE 国际站:SRI-41315
产品活性:SRI-41315 诱导终止密码子的长时间停顿,抑制与永久和初级人类支气管上皮细胞囊性纤维化相关的 PTCs (过早终止密码子),恢复 CFTR (囊性纤维化跨膜传导调节剂)的表达和功能。SRI-41315 通过减少终止因子 eRF1 的丰度来抑制 PTCs。SRI-41315 还增强了氨基糖苷介导的通读,导致 CFTR 活性的协同增加。
研究领域:Membrane Transporter/Ion Channel
作用靶点:CFTR
In Vitro: SRI-41315 exhibits target cell cytotoxicity (CC50) values >50 µM in both FRT and 16BE14o- cells.
SRI-41315 shows improved potency and efficacy in FRT cells that translated to 16HBE14o- cells.
SRI-41315 (5 µM, 20 h) depletes eRF1 levels through a proteasome-mediated degradation pathway.
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