1. Metabolic Enzyme/Protease Autophagy
  2. HMG-CoA Reductase (HMGCR) Autophagy
  3. Atorvastatin sodium

Atorvastatin sodium 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 sodium 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。

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Atorvastatin sodium Chemical Structure

Atorvastatin sodium Chemical Structure

CAS No. : 134523-01-6

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10 mg ¥595
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  • 生物活性

  • 纯度 & 产品资料

  • 参考文献

生物活性

Atorvastatin sodium is an orally active HMG-CoA reductase inhibitor, has the ability to effectively decrease blood lipids. Atorvastatin sodium inhibits human SV-SMC proliferation and invasion with IC50s of 0.39 μM and 2.39 μM, respectively[1][2][3][4][5].

体外研究
(In Vitro)

Atorvastatin sodium 通过下调心肌梗死后心肌细胞中 GRP78、caspase-12 和 CHOP 的表达来减少心肌细胞凋亡,并响应心力衰竭和血管紧张素 II (Ang II) 刺激而激活内质网 (ER) 应激< sup>[4]。

MCE has not independently confirmed the accuracy of these methods. They are for reference only.

体内研究
(In Vivo)

Atorvastatin(20-30 mg/kg;口服灌胃;每天一次;持续 28 天;ApoE−/− 小鼠)sodium 显着降低内质网 (ER) 应激信号蛋白、凋亡细胞数量,以及 Ang II 诱导的 ApoE-/- 小鼠中 Caspase12 和 Bax 的激活。Atorvastatin sodium 治疗后,IL-6、IL-8、IL-1β 等促炎细胞因子均受到显着抑制[5]

MCE has not independently confirmed the accuracy of these methods. They are for reference only.

分子量

580.62

Formula

C33H34FN2NaO5

CAS 号
运输条件

Room temperature in continental US; may vary elsewhere.

储存方式

Please store the product under the recommended conditions in the Certificate of Analysis.

纯度 & 产品资料
参考文献
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  • 稀释计算器

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  • Do most proteins show cross-species activity?

    Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

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