Reboxetine mesylate

Pricing Availability   Qty
说明: Potent and selective noradrenalin uptake inhibitor; orally active
化学名: (2R*)-2-[(R*)-(2-Ethoxyphenoxy)phenylmethyl]morpholine mesylate
纯度: ≥99% (HPLC)
说明书
引用文献 (9)
评论 (1)

生物活性 for Reboxetine mesylate

Reboxetine mesylate is a potent and selective inhibitor of noradrenalin uptake (Ki values are 1.1, 129 and > 10000 nM for rat NET, SERT and DAT respectively). Displays > 1000-fold selectivity over α-adrenoceptors, 5-HT, dopamine and muscarinic ACh receptors. Orally active antidepressant.

化合物库 for Reboxetine mesylate

Reboxetine mesylate is also offered as part of the Tocriscreen 2.0 Max. 了解 Tocris 化合物库的更多信息。

技术数据 for Reboxetine mesylate

分子量 409.5
公式 C19H23NO3.CH3SO3H
储存 Store at +4°C
纯度 ≥99% (HPLC)
CAS Number 98769-84-7
PubChem ID 76970698
InChI Key OEQQXKDUXVTKMH-BGLVZNNJSA-N
Smiles [H][C@]2(OCCNC2)[C@@H]([C@]3=CC=CC=C3)OC1=C(OCC)C=CC=C1.[H][C@@]5(OCCNC5)[C@H]([C@]6=CC=CC=C6)OC4=C(OCC)C=CC=C4.CS(=O)(O)=O.CS(=O)(O)=O

上方提供的技术数据仅供参考。批次相关数据请参见分析证书。

Tocris products are intended for laboratory research use only, unless stated otherwise.

溶解性数据 for Reboxetine mesylate

溶剂 最高浓度 mg/mL 最高浓度 mM
溶解性
water 20.48 50
DMSO 20.48 50

制备储备液 for Reboxetine mesylate

以下数据基于产品分子量 409.5。 Batch specific molecular weights may vary from batch to batch due to the degree of hydration, which will affect the solvent volumes required to prepare stock solutions.

选择批次从而根据批次分子量重新计算:
浓度/溶剂体积/质量 1 mg 5 mg 10 mg
0.5 mM 4.88 mL 24.42 mL 48.84 mL
2.5 mM 0.98 mL 4.88 mL 9.77 mL
5 mM 0.49 mL 2.44 mL 4.88 mL
25 mM 0.1 mL 0.49 mL 0.98 mL

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产品说明书 for Reboxetine mesylate

分析证书/产品说明书
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参考文献 for Reboxetine mesylate

参考文献是支持产品生物活性的出版物。

Sacchetti et al (1999) Studies on the acute and chronic effects of reboxetine on extracellular noradrenaline and other monoamines in the rat brain. Br.J.Pharmacol. 128 1332 PMID: 10578149

Wong et al (2000) Reboxetine: a pharmacologically potent, selective, and specific NE reuptake inhibitor. Biol.Psychiatry. 47 818 PMID: 10812041

Millan et al (2001) S33005, a novel ligand at both serotonin and NE transporters: I Receptor binding, electrophysiological, and neurochemical profile in comparison with venlafaxine, reboxetine, citalopram, and clomipramine. J.Pharmacol.Exp.Ther. 298 565 PMID: 11454918

Owen and Whitton (2003) Reboxetine modulates NE efflux in the frontal cortex of the freely moving rat: the involvement of α2 and 5-HT1A receptors. Neurosci.Lett. 348 171 PMID: 12932821


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关键词: Reboxetine mesylate, Reboxetine mesylate supplier, Potent, selective, noradrenalin, noradrenaline, reuptake, inhibitors, inhibits, orally, active, Transporters, NET, Adrenergic, adrenaline, adrenalin, Monoamine, Neurotransmitter, 1982, Tocris Bioscience

9 篇 Reboxetine mesylate 的引用文献

引用文献是使用了 Tocris 产品的出版物。 Reboxetine mesylate 的部分引用包括:

Munari et al (2015) Brain Histamine Is Crucial for Selective Serotonin Reuptake Inhibitors' Behavioral and Neurochemical Effects. Neurochem Int 18 pyv045 PMID: 25899065

Suto et al (2014) Peripheral nerve injury and gabapentin, but not their combination, impair attentional behavior via direct effects on noradrenergic signaling in the brain. Pain 155 1935 PMID: 24837843

Hutchinson et al (2012) Differential regulation of MeCP2 phosphorylation in the CNS by DA and serotonin. Pain 37 321 PMID: 21956448

Ferreira et al (2012) Presynaptic CB(1) cannabinoid receptors control frontocortical serotonin and glutamate release--species differences. Theriogenology 61 219 PMID: 22609378


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Reboxetine mesysate effect in mice. Brain MCP-1..
By Anonymous on 01/10/2018
分析类型: In Vivo
种属: Mouse

Reboxetine mesylate was dissolved in saline serum and 20 mg/kg (100 μL) were administered intraperitoneally to mice. After 24h, brain samples were taken and MCP-1 synthesis was analyzed by immunohistochemistry. This way, we confirmed that reboxetine treatment induces MCP-1 synthesis in cortical astrocytes.

In the figure, MCP-1 is labeled in red and GFAP in green.

review image