1. Membrane Transporter/Ion Channel
  2. Sodium Channel
  3. Nav1.7-IN-13

Nav1.7-IN-13 (compound 3g) 是钠离子通道抑制剂,可显著抑制 Veratridine (HY-N6691) 诱导的神经元活动。Nav1.7-IN-13 以浓度依赖性方式抑制 DRG 神经元的总 Na+ 电流;减缓了 Navs 的激活。Nav1.7-IN-13 显著缓解了神经损伤 (SNI) 大鼠模型的机械性疼痛行为,具有镇痛活性。

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Nav1.7-IN-13 Chemical Structure

Nav1.7-IN-13 Chemical Structure

CAS No. : 2776235-57-3

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  • 生物活性

  • 纯度 & 产品资料

  • 参考文献

生物活性

Nav1.7-IN-13 (compound 3g) is a sodium channel inhibitor that significantly inhibits Veratridine (HY-N6691)-induced neuronal activity. Nav1.7-IN-13 inhibits total Na+ current in DRG neurons in a concentration-dependent manner; slows down the activation of Navs. Nav1.7-IN-13 significantly alleviated mechanical pain behavior in a rat model of nerve injury (SNI) and had analgesic activity[1].

IC50 & Target

Nav1.7

 

体外研究
(In Vitro)

Nav1.7-IN-13 (compound 3g) 可阻断处于过度兴奋状态的开放状态。Nav1.7-IN-13 (50-150 μM; 16 h) 以剂量依赖性抑制大鼠的 DRG 神经元中钠离子通道激活,且在 150 μM 浓度下不会抑制 hERG 通道电流,具有安全性[1]

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

分子量

472.33

Formula

C23H22BrNO5

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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  • 稀释计算器

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Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

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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)
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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:
Nav1.7-IN-13
目录号:
HY-162347
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