1. Neuronal Signaling Membrane Transporter/Ion Channel
  2. Serotonin Transporter Sodium Channel
  3. Atomoxetine

Atomoxetine  (Synonyms: 托莫西汀; Tomoxetine; (R)-Tomoxetine)

目录号: HY-107370
产品使用指南

Atomoxetine (Tomoxetine) 是一种选择性去甲肾上腺素再摄取抑制剂 (noradrenaline reuptake),去甲肾上腺素 (NE)、5-羟色胺 (5-HT) 和多巴胺 (DA) 转运体的 Ki 值分别为 5、77 和 1451 nM。Atomoxetine (Tomoxetine) 可以增加 PFC 中 DAEX 和 NEEX,从而增强儿茶酚胺能神经传递。Atomoxetine (Tomoxetine) 是一种有效的Na+ 通道阻断剂 (VGSCs)。Atomoxetine (Tomoxetine) 可用于注意力缺陷多动障碍 (ADHD) 的研究。

在相同的摩尔浓度下,化合物盐形式与游离形式有相同的生物活性,但盐形式 Atomoxetine hydrochloride 通常具有更好的水溶性和稳定性。

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Atomoxetine Chemical Structure

Atomoxetine Chemical Structure

CAS No. : 83015-26-3

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  • 生物活性

  • 纯度 & 产品资料

  • 参考文献

生物活性

Atomoxetine (Tomoxetine) is a selective noradrenaline reuptake inhibitor with Ki values of 5, 77 and 1451 nM for norepinephrine (NE), serotonin (5-HT) and dopamine (DA) transporters, respectively. Atomoxetine (Tomoxetine) increases of DAEX and NEEX in the PFC and enhances catecholaminergic neurotransmission. Atomoxetine (Tomoxetine) is a potent Na+ channels (VGSCs) blocker. Atomoxetine (Tomoxetine) can be used for attention-deficit hyperactivity disorder (ADHD) research[1][2][3].

体外研究
(In Vitro)

Atomoxetine (Tomoxetine) (1-100 µM; 0.5-20 seconds; tsA201 cells) interacts with the human heart muscle sodium channel (hNav1.5) in a state and dose-dependent manner[2].

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

体内研究
(In Vivo)

Atomoxetine (Tomoxetine) (0.3-3 mg/kg; i.p.; 0-4 hours; male Sprague-Dawley rats) increases extracellular norepinephrine and dopamine by 3-fold and increases Fos expression in the rat prefrontal cortex[1].
Atomoxetine (Tomoxetine) (0.1-5 mg/kg; i.p. and p.o; for 14 days; spontaneously hypertensive rat) can improve behaviors associated with ADHD in rats[3].

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

Animal Model: Male Sprague-Dawley rats[1]
Dosage: 0.3, 1 and 3 mg/kg
Administration: Intraperitoneal injection; for 4 hours
Result: Increased the number of cells expressing Fos-like immunoreactivity in PFC 3.7-fold and increased extracellular norepinephrine and dopamine by 3-fold.
Animal Model: Spontaneously hypertensive rat (SHR)[3]
Dosage: 0.1, 0.3, 1.25 and 5.0 mg/kg
Administration: Intraperitoneal injection and oral administration; for 14 days
Result: Had non-impact on the measurement of motor activity.
Clinical Trial
分子量

255.35

Formula

C17H21NO

CAS 号
中文名称

托莫西汀

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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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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