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- 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
- 规格:
10 mM * 1 mL/5 mg/10 mg/50 mg/100 mg
| 规格: | 10 mM * 1 mL | 产品价格: | ¥291.0 |
|---|---|---|---|
| 规格: | 5 mg | 产品价格: | ¥237.0 |
| 规格: | 10 mg | 产品价格: | ¥380.0 |
| 规格: | 50 mg | 产品价格: | ¥700.0 |
| 规格: | 100 mg | 产品价格: | ¥1045.0 |
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Atorvastatin
CAS No. : 134523-00-5
MCE 国际站:Atorvastatin
产品活性:Atorvastatin 是一种具有口服活性的 HMG-CoA 还原酶抑制剂,具有有效降低血脂的能力。Atorvastatin 以 IC50 值分别为 0.39 μM 和 2.39 μM 来抑制人 SV-SMC 细胞的增殖和侵袭。
研究领域:Metabolic Enzyme/Protease | Autophagy
作用靶点:HMG-CoA Reductase (HMGCR) | Autophagy
In Vitro: Atorvastatin treatment decreases apoptosis of myocardial cells by down-regulating GRP78, caspase-12 and CHOP expression in myocardial cells after myocardial infarction, and the endoplasmic reticulum (ER) stress is activated in response to heart failure and angiotensin II (Ang II) stimulation.
In Vivo: Atorvastatin (20-30 mg/kg; oral gavage; once a day; for 28 days; ApoE−/− mice) treatment significantly reduces endoplasmic reticulum (ER) stress signaling proteins, the number of apoptotic cells, and the activation of Caspase12 and Bax in the Ang II-induced ApoE-/- mice. Proinflammatory cytokines such as IL-6, IL-8, IL-1β are all remarkably inhibited after Atorvastatin treatment.
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