1. Others Membrane Transporter/Ion Channel Neuronal Signaling
  2. Isotope-Labeled Compounds iGluR Sodium Channel Calcium Channel Potassium Channel
  3. Bupivacaine-d9

Bupivacaine-d9  (Synonyms: 布比卡因-d9)

目录号: HY-B0405S
产品使用指南

Bupivacaine-d99是 Bupivacaine 的氘代化合物。Bupivacaine 是一种 NMDA 受体抑制剂。Bupivacaine 可以阻断钠、L-钙和钾通道。Bupivacaine 有效阻断 SCN5A 通道,IC50 为 69.5 μM。Bupivacaine 可用于慢性疼痛的研究。

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Bupivacaine-d<sub>9</sub> Chemical Structure

Bupivacaine-d9 Chemical Structure

CAS No. : 474668-57-0

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5 mg
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1 mg ¥1035
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Other Forms of Bupivacaine-d9:

  • 生物活性

  • 纯度 & 产品资料

  • 参考文献

生物活性

Bupivacaine-d99 is a deuterium labeled Bupivacaine. Bupivacaine is a NMDA receptor inhibitor.Bupivacaine can block sodium, L-calcium, and potassium channels.Bupivacaine potently blocks SCN5A channels with the IC50 of 69.5 μM. Bupivacaine can be used for the research of chronic pain[1][2][3].

IC50 & Target

NMDA Receptor

 

分子量

297.48

Formula

C18H19D9N2O

CAS 号
Unlabeled CAS

38396-39-3

中文名称

布比卡因-d9

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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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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Bupivacaine-d9
目录号:
HY-B0405S
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