PeptideDB

Atorvastatin sodium

CAS: 134523-01-6 F: C33H34FN2NaO5 W: 580.62

Atorvastatin sodium is an orally active HMG-CoA reductase inhibitor, has the ability to effectively decrease blood lipid
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Bioactivity 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].
Invitro 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[4]。
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]。
Name Atorvastatin sodium
CAS 134523-01-6
Formula C33H34FN2NaO5
Molar Mass 580.62
Transport Room temperature in continental US; may vary elsewhere.
Storage

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

Reference [1]. Br J Pharmacol. 2006 Sep;149(1):14-22. [2]. Turner NA, et al. Comparison of the efficacies of five different statins on inhibition of human saphenous vein smooth muscle cell proliferation and invasion. J Cardiovasc Pharmacol. 2007 Oct;50(4):458-61. [3]. Nawrocki, J.W., et al., Reduction of LDL cholesterol by 25% to 60% in patients with primary hypercholesterolemia by atorvastatin, a new HMG-CoA reductase inhibitor. Arterioscler Thromb Vasc Biol, 1995. 15(5): p. 678-82. [4]. Song XJ, et al. Atorvastatin inhibits myocardial cell apoptosis in a rat model with post-myocardial infarction heart failure by downregulating ER stress response. Int J Med Sci. 2011;8(7):564-72. [5]. Li Y, et al. Inhibition of endoplasmic reticulum stress signaling pathway: A new mechanism of statins to suppress the development of abdominal aortic aneurysm. PLoS One. 2017 Apr 3;12(4):e0174821. [6]. Ming-Bai Hu, et al. Atorvastatin induces autophagy in MDA-MB-231 breast cancer cells. Ultrastruct Pathol. Sep-Oct 2018;42(5):409-415.