1. Membrane Transporter/Ion Channel
  2. Sodium Channel
  3. PF-05186462

PF-05186462 是一种有效和选择性的人 Nav1.7 电压依赖性钠通道抑制剂,IC50 值为 21 nM。PF-05186462 对 Nav1.7 与其他钠通道 (Nav 1.1、1.2、1.3、1.4、1.5、1.6 和 1.8) 相比显示出显着的选择性。PF-05186462 可用于急性或慢性疼痛的研究。

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PF-05186462 Chemical Structure

PF-05186462 Chemical Structure

CAS No. : 1235406-03-7

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规格 价格 是否有货 数量
1 mg ¥2210
1 周
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  • 生物活性

  • 纯度 & 产品资料

  • 参考文献

生物活性

PF-05186462 is a potent and selective inhibitor of human Nav1.7 voltage-dependent sodium channel, with an IC50 of 21 nM. PF-05186462 shows significant selectivity for Nav1.7 versus other sodium channels (Nav 1.1, 1.2, 1.3, 1.4, 1.5, 1.6, and 1.8). PF-05186462 can be used for the research of acute or chronic pain[1].

IC50 & Target

IC50: 21 nM (human Nav1.7)[1]

体外研究
(In Vitro)

PF-05186462 inhibits human Nav1.7 channels (IC50=21 nM) in HEK293 cells[1].
PF-05186462 exhibits a high plasma protein binding rate[1].

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

Clinical Trial
分子量

531.89

Formula

C19H10ClF4N5O3S2

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
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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:
PF-05186462
目录号:
HY-122001
需求量: