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GPi688 是一种有效且具有口服活性的糖原磷酸化酶 (GPa) 抑制剂,对人肝脏 GPa、小鼠肝脏 GPa、人骨骼肌 GPa 的 IC50 分别为 19 nM、61 nM 和 12 nM。GPi688 可在大鼠原代肝细胞中抑制胰高血糖素介导的葡萄糖输出。GPi688 可用于胰高血糖素介导的高血糖症的研究。

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GPi688 Chemical Structure

GPi688 Chemical Structure

CAS No. : 918902-32-6

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  • 生物活性

  • 纯度 & 产品资料

  • 参考文献

生物活性

GPi688 is a potent and orally active glycogen phosphorylase (GPa) inhibitor with IC50s of 19 nM, 61 nM and 12 nM for human liver GPa, rat liver GPa and human skeletal muscle GPa, respectively[1]. GPi688 can inhibit glucagons-mediated glucose output in rat primary hepatocytes. GPi688 can be used for researching glucagon-mediated hyperglycaemia[2].

IC50 & Target

IC50: 19 nM (human liver GPa), 61 nM (rat liver GPa), 12 nM (human skeletal muscle GPa)[1]

分子量

419.88

Formula

C19H18ClN3O4S

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

GPi688 相关分类

  • 摩尔计算器

  • 稀释计算器

The molarity calculator equation

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

质量   浓度   体积   分子量 *
= × ×

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)
× = ×
C1   V1   C2   V2
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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产品名称:
GPi688
目录号:
HY-108614
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