1. GPCR/G Protein Neuronal Signaling
  2. Adrenergic Receptor
  3. Atomoxetine-d3 hydrochloride

Atomoxetine-d3 hydrochloride 是氘代标记的Atomoxetine hydrochloride。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5,77和1451 nM。

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Atomoxetine-d3 hydrochloride Chemical Structure

Atomoxetine-d3 hydrochloride Chemical Structure

CAS No. : 1217776-38-9

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Other Forms of Atomoxetine-d3 hydrochloride:

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生物活性

Atomoxetine-d3 hydrochloride is the deuterium labeled Atomoxetine hydrochloride. Atomoxetine hydrochloride is a potent and selective noradrenalin re-uptake inhibitor (Ki values are 5, 77 and 1451 nM for inhibition of radioligand binding to human NET, SERT and DAT respectively)[1][2].

体外研究
(In Vitro)

Stable heavy isotopes of hydrogen, carbon, and other elements have been incorporated into drug molecules, largely as tracers for quantitation during the drug development process. Deuteration has gained attention because of its potential to affect the pharmacokinetic and metabolic profiles of drugs[3].

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

分子量

294.83

Formula

C17H19D3ClNO

CAS 号
性状

固体

颜色

White to off-white

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

Atomoxetine-d3 hydrochloride 相关分类

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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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产品名称:
Atomoxetine-d3 hydrochloride
目录号:
HY-110223
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