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Tesofensine {[allProObj[0].p_purity_real_show]}

货号:A239666 同义名: NS-2330 Ambeed 开学季,买赠积分,赢豪礼

Tesofensine 化学结构 CAS号:195875-84-4
Tesofensine 化学结构
CAS号:195875-84-4
Tesofensine 3D分子结构
CAS号:195875-84-4
Tesofensine 化学结构 CAS号:195875-84-4
Tesofensine 3D分子结构 CAS号:195875-84-4
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Tesofensine 纯度/质量文件 产品仅供科研

货号:A239666 标准纯度: {[allProObj[0].p_purity_real_show]}
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Tesofensine 生物活性

描述 Tesofensine (NS-2330) is a powerful triple monoamine reuptake inhibitor that blocks the reuptake of dopamine (DA; IC50=6.5 nM), norepinephrine (NE; IC50=1.7 nM), and serotonin (5-HT; IC50=11 nM), and is investigated as a potential anti-obesity agent[1]. Tesofensine acts as a central nervous system (CNS) anti-obesity agent[2].
体内研究

Tesofensine, administered in a single dose ranging from 0.1 to 3 mg/kg subcutaneously, induces hypophagia in DIO rats. A single dose of Tesofensine robustly and dose-dependently reduces food intake in DIO rats throughout a 12-hour nocturnal observation period. Moreover, daily administration of Tesofensine at a moderate dose of 2.0 mg/kg subcutaneously for 16 days leads to a significant reduction in body weight starting from the fourth day of treatment compared to vehicle-treated controls[3].

Tesofensine 参考文献

[1]Lieuwe Appel, et al. Tesofensine, a novel triple monoamine re-uptake inhibitor with anti-obesity effects: dopamine transporter occupancy as measured by PET. Eur Neuropsychopharmacol. 2014 Feb;24(2):251-61.

[2]Ann A Coulter, et al. Centrally Acting Agents for Obesity: Past, Present, and Future. Drugs. 2018 Jul;78(11):1113-1132.

[3]Anne Marie D Axel, et al. Tesofensine, a novel triple monoamine reuptake inhibitor, induces appetite suppression by indirect stimulation of alpha1 adrenoceptor and dopamine D1 receptor pathways in the diet-induced obese rat.Neuropsychopharmacology. 2010 J

Tesofensine 实验方案

计算器
存储液制备 1mg 5mg 10mg

1 mM

5 mM

10 mM

3.05mL

0.61mL

0.30mL

15.23mL

3.05mL

1.52mL

30.46mL

6.09mL

3.05mL

Tesofensine 技术信息

CAS号195875-84-4
分子式C17H23Cl2NO
分子量 328.277
别名 NS-2330
运输蓝冰
存储条件

粉末 Keep in dark place,Sealed in dry,2-8°C

液体 -20°C:3-6个月-80°C:12个月

溶解度

DMSO: 2 mg/mL(6.09 mM),配合低频超声,并水浴加热至45℃助溶,注意:DMSO长时间开封后,会吸水并导致溶解能力下降,请避免使用长期开封的DMSO

动物实验配方
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