Simvastatin hydroxy acid sodium(Synonyms: Tenivastatin sodium; Simvastatin Impurity A sodium)

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Simvastatin hydroxy acid sodium (Synonyms: Tenivastatin sodium; Simvastatin Impurity A sodium)

Simvastatin hydroxy acid sodium (Tenivastatin sodium; Simvastatin Impurity A sodium) 是辛伐他汀 (HY-17502) 活性水解代谢物。Simvastatin 是一种竞争性的 HMG-CoA 还原酶抑制剂, Ki 值为 0.2 nM。

Simvastatin hydroxy acid sodium(Synonyms: Tenivastatin sodium; Simvastatin Impurity A sodium)

Simvastatin hydroxy acid sodium Chemical Structure

CAS No. : 101314-97-0

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生物活性

Simvastatin hydroxy acid sodium (Tenivastatin sodium; Simvastatin Impurity A sodium) is an active hydrolytic metabolite of Simvastatin (HY-17502)[1]. Simvastatin shows a inhibition of HMG-CoA reductase with a Ki value of 0.12 nM[2].

体外研究
(In Vitro)

Simvastatin sodium shows a inhibition of HMG-CoA reductase in human lymphoblasts and SV40 transformed MRCS fibroblasts[1].
Simvastatin sodium (100 μM) inhibits the Na+/H+ antiport activity leading to a fall of intracellular pH and to a reduced cell proliferation.And the inhibitory effect is prevented by mevalonate but not dolichol or squalene[1].

Shanghai Jinpan Biotech Co Ltd has not independently confirmed the accuracy of these methods. They are for reference only.

体内研究
(In Vivo)

Simvastatin sodium (oral administration; 8 mg/kg; 18 days) reduces plasma cholesterol levels 33%, simvastatin can be used in combination with ezetimibe to treat dyslipidemia[1].

Shanghai Jinpan Biotech Co Ltd has not independently confirmed the accuracy of these methods. They are for reference only.

分子量

458.56

Formula

C25H39NaO6

CAS 号

101314-97-0

中文名称

辛伐他汀羟基酸

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.

参考文献
  • [1]. Corsini A, et al. Pharmacology of competitive inhibitors of HMG-CoA reductase.Pharmacol Res. 1995 Jan;31(1):9-27.

    [2]. Andrew Marsh, et al. Simvastatin Sodium Salt and Fluvastatin Interact with Human Gap Junction Gamma-3 Protein. PLoS One. 2016 Feb 10;11(2):e0148266.

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