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Rosuvastatin

SKU: orb1225424

描述

A potent, competitive inhibitor of HMG-CoA reductase (HMGCR) with IC50 of 11 nM; potently inhibits cholesterol biosynthesis (IC50=1.12 nM) in rat isolated hepatocytes, 100 times more potent than pravastatin; also exerts important anti-inflammatory effects via inhibition of endothelial cell adhesion molecule expression.Dyslipidemia Approved(In Vivo):Rosuvastatin Calcium (10 mg/kg, intraperitoneal) prolonges QTc in conscious and unrestraines guinea pigs from 201±1 to 210±2 ms.Rosuvastatin (20 mg/kg/day, for 2 weeks) significantly reduces very low-density lipoproteins Calcium (VLDL) in diabetes mellitus rats induced by Streptozocin.

研究领域

Pharmacology & Drug Discovery

图片与验证

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关键属性

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CAS 号287714-41-4
MW481.5376
纯度>98% (HPLC)
分子式C22H28FN3O6S
SMILESCC(C)C1=NC(=NC(=C1/C=C/[C@H](C[C@H](CC(=O)O)O)O)C2=CC=C(C=C2)F)N(C)S(=O)(=O)C
靶点HMGCR
溶解性10 mM in DMSO

生物活性

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体内
Rosuvastatin (10 mg/kg, intraperitoneal) prolonges QTc in conscious and unrestraines guinea pigs from 201±1 to 210±2 ms. Rosuvastatin (20 mg/kg/day, for 2 weeks) significantly reduces very low-density lipoproteins (VLDL) in diabetes mellitus rats induced by Streptozocin.

储存与操作

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储存Storage temperature: -20°C. Stability: ≥ 2 years
有效期12 months from date of receipt.
免责声明For research use only

别名

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ZD-4522

相似产品

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    greater than or equal to 98% (HPLC)

    147098-20-2

    480.6 . 20.0

    C22H27FN3O6S . 1/2Ca

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  • Rosuvastatin impurity 40 calcium [orb3216952]

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  • Rosuvastatin impurity 33 [orb3217089]

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    C26H34FN3O6S

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  • Rosuvastatin impurity 34 [orb3217159]

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  • Rosuvastatin impurity 41 [orb3217165]

    1283766-30-2

    523.62

    C25H34FN3O6S

    50 mg, 10 mg
质量保证

质量保证

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实验方案信息

可选规格

请在下方选择规格

500 mg
5 mg
¥ 1,170.00
10 mg
¥ 1,690.00
25 mg
¥ 2,730.00
50 mg
¥ 3,640.00
100 mg
¥ 5,850.00
200 mg
¥ 8,060.00