1. Others Vitamin D Related/Nuclear Receptor
  2. Isotope-Labeled Compounds Estrogen Receptor/ERR
  3. 17-Epiestriol-d5-1

17-Epiestriol-d5-1 是 17-Epiestriol (HY-163712) 的氘代物。17-Epiestriol 是一种雌激素代谢产物,同时也是一种选择性雌激素受体 (ER) β激动剂。17-epiestriol 可抑制肿瘤坏死因子 α (TNFα) 诱导的血管细胞黏附分子 VCAM-1 的 mRNA 和蛋白表达。17-epiestriol 还抑制 TNFα 诱导的 VCAM-1 表达,并阻止 NF-κB 迁移到细胞核。17-Epiestriol 也诱导内皮型一氧化氮合酶的 mRNA 和蛋白表达。

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17-Epiestriol-d<sub>5</sub>-1 Chemical Structure

17-Epiestriol-d5-1 Chemical Structure

CAS No. : 2734919-65-2

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查看 Estrogen Receptor/ERR 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

17-Epiestriol-d5-1 is the deuterium labeled 17-Epiestriol (HY-163712). 17-Epiestriol is an estrogen metabolite and a selective estrogen receptor (ER) β agonist. 17-epiestriol inhibits the mRNA and protein expression of the vascular cell adhesion molecule VCAM-1 induced by tumor necrosis factor α (TNFα). 17-epiestriol also inhibits TNFα-induced VCAM-1 expression and prevents NF-κB migration to the nucleus. 17-Epiestriol also induces the mRNA and protein expression of endothelial nitric oxide synthase[1].

体外研究
(In Vitro)

氢、碳和其他元素的稳定重同位素已被掺入药物分子中,主要用作药物开发过程中定量的示踪剂。氘化因其可能影响药物的药代动力学和代谢特征而受到关注。

MCE has not independently confirmed the accuracy of these methods. They are for reference only.

分子量

293.41

Formula

C18H19D5O3

CAS 号
非标记 CAS
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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    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:
17-Epiestriol-d5-1
目录号:
HY-163712S
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