Centanafadine hydrochloride (Synonyms: EB-1020 hydrochloride)
目录号: PL09188 纯度: ≥99%
CAS No. :923981-14-0
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中文名称
Centanafadine hydrochloride
英文名称
Centanafadine hydrochloride
英文别名
Centanafadine hydrochloride;Centanafadine (hydrochloride);265DN9X85W;Centanafadine hydrochloride [USAN];Centanafadine hydrochloride (USAN);DOV 216,419;D10698;(5S,1R)-1-(2-naphthyl)-3-azabicyclo[3.1.0]hexane HCl;(1R,5S)-1-(naphthalen-2-yl)-3-azabicyclo(3.1.0)hexane hydrochloride;3-Azabicyclo(3.1.0)hexane, 1-(2-;EB-1020 hydrochloride;(1R,5S)-1-(Naphthalen-2-yl)-3-azabicyclo[3.1.0]hexane hydrochloride;DOV 216419 hydrochloride;EB 1020 hydrochloride
Cas No.
923981-14-0
分子式
C15H16ClN
分子量
245.75
包装储存
4°C, sealed storage, away from moistur In solvent : -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture)
产品详情
Centanafadine (hydrochloride) 是去甲肾上腺素 (NE)/多巴胺 (DA) 转运的双抑制剂,还能抑制5-羟色胺 (serotonin) 转运体,其对人 NE,DA 和5-羟色胺转运体的IC50 值分别为6 nM,38 nM 和 83 nM。
生物活性
Centanafadine (hydrochloride) is dual norepinephrine (NE)/dopamine (DA) transporter inhibitor, also inhibits serotonin transporter, with IC 50 s of 6 nM, 38 nM and 83 nM for human NE, DA and serotonin transporter , respectively.
性状
Solid
IC50 & Target[1][2]
IC50: 6 nM (human NE), 38 nM (human DA), 83 nM (human serotonin).
体外研究(In Vitro)
Centanafadine (EB-1020) preferentially inhibits monoamine reuptake in cloned cell lines transfected with human transporters with IC50 values of 6 and 38 nM, respectively, for NE and DA transporters, Centanafadine has lesser effects on 5-HT transporter as it inhibits the reuptake of 5-HT with an IC50 value of 83 nM . has not independently confirmed the accuracy of these methods. They are for reference only.
体内研究(In Vivo)
In microdialysis studies, Centanafadine markedly increases NE, and DA concentrations levels in rat prefrontal cortex in vivo with peak increases of 375 and 300%, respectively with the greatest effects on NE, and also increases DA extracellular concentrations in the striatum to 400% of baseline concentrations. Behavioral studies demonstrate that Centanafadine dose-dependently decreases immobility in the mouse tail suspension test of depression to 13% of control levels, and do not stimulate locomotor activity in adult rats in the optimal dose range. Centanafadine dose-dependently inhibits locomotor hyperactivity in juvenile rats lesioned with the neurotoxin 6-hydroxydopamine (100 μg intracisternally) as neonates; a well-established animal model for attention-deficit hyperactivity disorder (ADHD). has not independently con
运输条件
Room temperature in continental US; may vary elsewhere.
储存方式
4°C, sealed storage, away from moistur In solvent : -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture)
ClinicalTrial
参考文献
[1]. Bymaster FP, et al. Pharmacological characterization of the norepinephrine and dopamine reuptake inhibitor EB-1020: implications for treatment of attention-deficit hyperactivity disorder. Synapse. 2012 Jun;66(6):522-32.
溶解度数据
In Vitro: DMSO : 125 mg/mL (508.65 mM; Need ultrasonic)配制储备液
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1:一般建议:溶解度为Medlife测试数据,可能与文献描述存在差异。这是由于生产工艺和批次不同产生的正常现象。为了使其更好的溶解,请用37℃加热试管并在超声波水浴中震动片刻。不同批次产品溶解度各有差异,仅做参考,具体以实验方案为准。

2:储存条件:粉末-20°C一般情况可以保存3年,溶于溶剂-80°C一般情况可以保存1年。不同产品及不同批次产品可能存在差异,请细致阅读产品信息,并辅助参考相关文献描述。

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