
Atorvastatin
CAS No. 134523-00-5
Atorvastatin ( —— )
产品货号. M11381 CAS No. 134523-00-5
一种 HMG-CoA 还原酶的竞争性抑制剂,可作为降脂剂来预防与心血管疾病相关的事件。
纯度: >98% (HPLC)






规格 | 价格/人民币 | 库存 | 数量 |
100MG | 获取报价 | 有现货 |
![]() ![]() |
200MG | 获取报价 | 有现货 |
![]() ![]() |
500MG | 获取报价 | 有现货 |
![]() ![]() |
1G | 获取报价 | 有现货 |
![]() ![]() |
生物学信息
-
产品名称Atorvastatin
-
注意事项本公司产品仅用于科研实验,不得用于人体或动物的临床与诊断
-
产品简述一种 HMG-CoA 还原酶的竞争性抑制剂,可作为降脂剂来预防与心血管疾病相关的事件。
-
产品描述A competitive inhibitor of HMG-CoA reductase that acts as a lipid-lowering agent for prevention of events associated with cardiovascular disease.Dyslipidemia Approved(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.
-
体外实验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.
-
体内实验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. Animal Model:Forty 8-week-old ApoE?/? mice induced with angiotensin II (Ang II) Dosage:20 mg/kg, 30 mg/kg Administration:Oral gavage; once a day; for 28 days Result:Significantly reduced 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 were all remarkably inhibited.
-
同义词——
-
通路Metabolic Enzyme/Protease
-
靶点HMGCR
-
受体HMGCR
-
研究领域Cardiovascular Disease
-
适应症Dyslipidemia
化学信息
-
CAS Number134523-00-5
-
分子量558.6398
-
分子式C33H35FN2O5
-
纯度>98% (HPLC)
-
溶解度10 mM in DMSO
-
SMILESCC(C)C1=C(C(=C(N1CCC(CC(CC(=O)O)O)O)C2=CC=C(C=C2)F)C3=CC=CC=C3)C(=O)NC4=CC=CC=C4
-
化学全称1H-Pyrrole-1-heptanoic acid, 2-(4-fluorophenyl)-β,δ-dihydroxy-5-(1-methylethyl)-3-phenyl-4-[(phenylamino)carbonyl]-, (βR,δR)-
运输与储存
-
储存条件(-20℃)
-
运输条件With Ice Pack
-
稳定性≥ 2 years
参考文献
产品手册




关联产品
-
Atorvastatin lactone
阿托伐他汀内酯是阿托伐他汀的前药形式。它是一种口服活性 3-羟基-3-甲基戊二酰辅酶 A (HMG-CoA) 还原酶抑制剂。
-
Monacolin J
Monacolin J 是一种胆固醇生物合成抑制剂。
-
Anhydrosimvastatin
脱水辛伐他汀是辛伐他汀的杂质。辛伐他汀是一种 HMG-CoA 还原酶抑制剂。