1. Metabolic Enzyme/Protease
  2. Angiotensin-converting Enzyme (ACE)
  3. Moexiprilat

Moexiprilat  (Synonyms: RS 10029)

目录号: HY-A0114
产品使用指南

Moexiprilat (RS 10029)是一种血管紧张素转换酶 (ACE;IC50=2.1 nM) 抑制剂,也是前体药物莫昔普利 (HY-117281) 的活性代谢物。它由莫昔普利在体内通过侧链酯水解而形成。Moexiprilat (RS 10029) (10 nM) 可防止雌酮或血管紧张素 II 刺激的原代新生大鼠心脏成纤维细胞增殖。每天以 50 mg/kg 的剂量给药时,它可以降低卵巢切除小鼠的平均动脉血压,并增加心房利钠肽(高血压标志物)的水平。

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Moexiprilat Chemical Structure

Moexiprilat Chemical Structure

CAS No. : 103775-14-0

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Other Forms of Moexiprilat:

  • 生物活性

  • 纯度 & 产品资料

  • 参考文献

生物活性

Moexiprilat is an inhibitor of angiotensin-converting enzyme (ACE; IC50=2.1 nM) and an active metabolite of the prodrug Moexipril (HY-117281). It is formed from moexipril in vivo by side chain ester hydrolysis. Moexiprilat (10 nM) prevents the estrone- or angiotensin II-stimulated proliferation of primary neonatal rat cardiac fibroblasts. It reduces mean arterial blood pressure and increases the levels of atrial natriuretic peptide, a marker of hypertension, in ovariectomized mice when administered at a dose of 50 mg/kg per day.

分子量

470.51

Formula

C25H30N2O7

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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Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

质量   浓度   体积   分子量 *
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The dilution calculator equation

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

This equation is commonly abbreviated as: C1V1 = C2V2

浓度 (start) × 体积 (start) = 浓度 (final) × 体积 (final)
× = ×
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Help & FAQs
  • 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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