1. GPCR/G Protein
  2. Prostaglandin Receptor
  3. S-5751

S-5751 是一种具有口服活性的前列腺素 DP 受体拮抗剂。S-5751 可抑制 PGD2 诱导的富血小板血浆 cAMP 生成,IC50 为 0.12 μM。S-5751 具有抗炎活性。S-5751 可用于哮喘的研究。

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S-5751 Chemical Structure

S-5751 Chemical Structure

CAS No. : 209268-36-0

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查看 Prostaglandin Receptor 亚型特异性产品:

  • 生物活性

  • 纯度 & 产品资料

  • 参考文献

生物活性

S-5751 is an orally active prostaglandin DP receptor antagonist. S-5751 inhibits cAMP generation in platelet-rich plasma induced by PGD2 with IC50 0.12 μM. S-5751 has anti-inflammatory activity. S-5751 can be used in asthma research[1].

分子量

441.58

Formula

C25H31NO4S

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
  • 摩尔计算器

  • 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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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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产品名称:
S-5751
目录号:
HY-19755
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