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rel-Delequamine  (Synonyms: rel-RS-15385-197)

目录号: HY-106874B
产品使用指南

rel-Delequamine (rel-RS-15385-197) 是具有口服活性,脑渗透性的强效选择性 M2-肾上腺素受体 (M2-adrenoceptor) 拮抗剂和 α2-肾上腺素受体 (α2-adrenoceptor) 拮抗剂。rel-Delequamine 对大鼠皮层的 α2-adrenoceptorpKi 值为 9.45。rel-Delequamine 增强了 K+ 引发的去甲肾上腺素释放,其 pEC50 值为 1 nM。

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rel-Delequamine Chemical Structure

rel-Delequamine Chemical Structure

CAS No. : 119813-87-5

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  • 参考文献

生物活性

rel-Delequamine (rel-RS-15385-197) is an orally active, brain-penetrant, potent and selective M2-adrenoceptor antagonist and α2-adrenoceptor antagonist. rel-Delequamine has a pKi of 9.45 for α2-adrenoceptors in the rat cortex. rel-Delequamine augments K+-evoked release of noradrenaline with an EC50 of 1 nM[1].

分子量

350.48

Formula

C18H26N2O3S

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

rel-Delequamine 相关分类

  • 摩尔计算器

  • 稀释计算器

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

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浓度 (start) × 体积 (start) = 浓度 (final) × 体积 (final)
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  • 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:
rel-Delequamine
目录号:
HY-106874B
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