1. GPCR/G Protein Neuronal Signaling
  2. 5-HT Receptor
  3. 5-HT6R antagonist 3

5-HT6R antagonist 3 (compound 15) 是一种有效的、选择性的、可穿过血脑屏障的 5-HT6R 拮抗剂,对 5-HT6、5-HT1A、5-HT2A、5-HT7 的 Ki 值分别为 14 nM、3533 nM、35 nM、1449 nM。5-HT6R antagonist 3 显示出抗焦虑样作用,并具有神经保护和促认知样作用。5-HT6R antagonist 3 具有研究阿尔茨海默病的潜力。

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5-HT6R antagonist 3 Chemical Structure

5-HT6R antagonist 3 Chemical Structure

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  • 生物活性

  • 纯度 & 产品资料

  • 参考文献

生物活性

5-HT6R antagonist 3 (compound 15) is a potent, selective and brain-penetrant 5-HT6R antagonist with Ki values of 14 nM, 3533 nM, 35 nM, 1449 nM for 5-HT6, 5-HT1A, 5-HT2A, 5-HT7, respectively. 5-HT6R antagonist 3 shows anxiolytic-like and properties neuroprotective and procognitive-like effects. 5-HT6R antagonist 3 has the potential for the research of Alzheimer’s Disease[1].

IC50 & Target[1]

5-HT6 Receptor

14 nM (Ki)

5-HT1A Receptor

3533 nM (Ki)

5-HT2A Receptor

35 nM (Ki)

5-HT7 Receptor

1449 nM (Ki)

分子量

441.43

Formula

C21H26N6Se

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

5-HT6R antagonist 3 相关分类

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  • 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:
5-HT6R antagonist 3
目录号:
HY-163150
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