2. Neuronal Signaling Others Membrane Transporter/Ion Channel
  3. Isotope-Labeled Compounds Sodium Channel Serotonin Transporter
  4. (Rac)-Atomoxetine-d7 hydrochloride

(Rac)-Atomoxetine-d7 hydrochloride  (Synonyms: (Rac)-Tomoxetine d7 (hydrochloride); (Rac)-LY 139603 d7)

目录号: HY-107370AS
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摩尔计算器

(Rac)-Atomoxetine-d7 (hydrochloride) 是 (Rac)-Atomoxetine hydrochloride 的氘代物。(Rac)-Atomoxetine hydrochloride 是 Atomoxetine hydrochloride 的外消旋形式，Atomoxetine hydrochloride 是去甲肾上腺素重吸收抑制剂，与人 NET，SERT 和 DAT 的放射性配体结合的 Ki 分别为 5 nM，77 nM 和 1451 nM。

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(Rac)-Atomoxetine-d<sub>7</sub> hydrochloride Chemical Structure

(Rac)-Atomoxetine-d7 hydrochloride Chemical Structure

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Other Forms of (Rac)-Atomoxetine-d7 hydrochloride:

(Rac)-Atomoxetine-d7 hydrochloride 相关抗体

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  • 生物活性

  • 纯度 & 产品资料

  • 参考文献

生物活性

(Rac)-Atomoxetine-d7 (hydrochloride) is a deuterium labeled (Rac)-Atomoxetine hydrochloride. (Rac)-Atomoxetine hydrochloride is a racemic form of Atomoxetine hydrochloride. Atomoxetine hydrochloride is a potent and selective noradrenalin re-uptake inhibitor (Ki values are 5 nM, 77 nM and 1451 nM for inhibition of radioligand binding to human NET, SERT and DAT respectively)[1].

分子量

298.86

Formula

C17H15D7ClNO
非标记 CAS

82857-40-7
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

(Rac)-Atomoxetine-d7 hydrochloride 相关分类

  • 摩尔计算器

  • 稀释计算器

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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.

Keywords:

(Rac)-Atomoxetine-d7(Rac)-Tomoxetine d7(Rac)-LY 139603 d7Isotope-Labeled CompoundsSodium ChannelSerotonin TransporterNa channelsNa+ channels5-HTTSERTSLC6A4Deuteriumlabeledracemicnoradrenalinre-uptakeNETDATInhibitorinhibitorinhibit

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