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Submit ReviewReboxetine 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.
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。
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.
溶剂 | 最高浓度 mg/mL | 最高浓度 mM | |
---|---|---|---|
溶解性 | |||
water | 20.48 | 50 | |
DMSO | 20.48 | 50 |
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.
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 |
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
If you know of a relevant reference for Reboxetine mesylate, please let us know.
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
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
Zhu et al (2018) Cortical bone is an extraneuronal site of norepinephrine uptake in adult mice. Bone Rep 9 188 PMID: 30581894
Hughes et al (2013) Endogenous analgesic action of the pontospinal noradrenergic system spatially restricts and temporally delays the progression of neuropathic pain following tibial nerve injury. Int J Neuropsychopharmacol 154 1680 PMID: 23707289
Kreiner et al (2019) Stimulation of noradrenergic transmission by reboxetine is beneficial for a mouse model of progressive parkinsonism. Sci Rep 9 5262 PMID: 30918302
Stuart et al (2013) A translational rodent assay of affective biases in depression and antidepressant therapy. Neuropsychopharmacology 38 1625 PMID: 23503126
Kobayashi et al (2010) Inhibition of G-protein-activated inwardly rectifying K+ channels by the selective NE reuptake inhibitors atomox. and reboxetine. Neuropsychopharmacology 35 1560 PMID: 20393461
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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.