
Dasotraline hydrochloride
CAS No. 675126-08-6
Dasotraline hydrochloride ( SEP-225289 hydrochloride )
产品货号. M17565 CAS No. 675126-08-6
Dasotraline Hydrochloride (SEP-225289 HydroHClide) 是一种三重再摄取抑制剂,可抑制多巴胺、去甲肾上腺素和血清素转运蛋白,IC50 值分别为 4、6 和 11 nM。
纯度: >98% (HPLC)






规格 | 价格/人民币 | 库存 | 数量 |
5MG | ¥332 | 有现货 |
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10MG | ¥535 | 有现货 |
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25MG | ¥794 | 有现货 |
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50MG | ¥1199 | 有现货 |
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100MG | 获取报价 | 有现货 |
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200MG | 获取报价 | 有现货 |
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500MG | 获取报价 | 有现货 |
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1G | 获取报价 | 有现货 |
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生物学信息
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产品名称Dasotraline hydrochloride
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注意事项本公司产品仅用于科研实验,不得用于人体或动物的临床与诊断
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产品简述Dasotraline Hydrochloride (SEP-225289 HydroHClide) 是一种三重再摄取抑制剂,可抑制多巴胺、去甲肾上腺素和血清素转运蛋白,IC50 值分别为 4、6 和 11 nM。
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产品描述Dasotraline hydrochloride (SEP-225289 hydrochloride) is a triple reuptake inhibitor? that inhibits dopamine, norepinephrine, and serotonin transporters with IC50 values of 4, 6, and 11 nM, respectively.(In Vivo):Acute administration of dasotraline dose-dependently decreases the spontaneous firing rate of LC NE, VTA DA and DR 5-HT neurons through the activation of α2, D2 and 5-HT1A autoreceptors, respectively. Dasotraline predominantly inhibits the firing rate of LC NE neurons while producing only a partial decrease in VTA DA and DR 5-HT neuronal discharge. SEP-225289 is equipotent at inhibiting 5-HT and NE transporters since it prolongs to the same extent the time required for a 50% recovery of the firing activity of dorsal hippocampus CA3 pyramidal neurons from the inhibition induced by microiontophoretic application of 5-HT and NE. Average dopamine and serotonin transporter occupancies increase with increasing doses of SEP-225289. Mean dopamine and serotonin transporter occupancies are 33%±11% and 2%±13%, respectively, for 8 mg; 44%±4% and 9%±10%, respectively, for 12 mg; and 49%±7% and 14%±15%, respectively, for 16 mg.
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体外实验——
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体内实验Acute administration of dasotraline dose-dependently decreases the spontaneous firing rate of LC NE, VTA DA and DR 5-HT neurons through the activation of α2, D2 and 5-HT1A autoreceptors, respectively. Dasotraline predominantly inhibits the firing rate of LC NE neurons while producing only a partial decrease in VTA DA and DR 5-HT neuronal discharge. SEP-225289 is equipotent at inhibiting 5-HT and NE transporters since it prolongs to the same extent the time required for a 50% recovery of the firing activity of dorsal hippocampus CA3 pyramidal neurons from the inhibition induced by microiontophoretic application of 5-HT and NE. Average dopamine and serotonin transporter occupancies increase with increasing doses of SEP-225289. Mean dopamine and serotonin transporter occupancies are 33%±11% and 2%±13%, respectively, for 8 mg; 44%±4% and 9%±10%, respectively, for 12 mg; and 49%±7% and 14%±15%, respectively, for 16 mg.
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同义词SEP-225289 hydrochloride
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通路Angiogenesis
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靶点Adrenergic Receptor
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受体5-HT| Dopamine| Norepinephrine (NE)
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研究领域——
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适应症——
化学信息
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CAS Number675126-08-6
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分子量328.66
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分子式C16H16Cl3N
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纯度>98% (HPLC)
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溶解度DMSO : ≥ 31 mg/mL. 94.32 mM
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SMILES[C@H]1(CC[C@H](c2ccccc12)c1cc(c(cc1)Cl)Cl)N.Cl
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化学全称——
运输与储存
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储存条件(-20℃)
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运输条件With Ice Pack
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稳定性≥ 2 years
参考文献
1. Guiard BP, et al. Int J Neuropsychopharmacol. 2011 Mar;14(2):211-23.