CAS NO: | 58-28-6 |
包装 | 价格(元) |
10 mM * 1 mL in DMSO | 电议 |
100mg | 电议 |
500mg | 电议 |
1 g | 电议 |
5 g | 电议 |
生物活性 | Desipramine hydrochloride is an inhibitor ofnorepinephrine transporter(NET),5-HT transporter(SERT) anddopamine transporter(DAT) withKis of 4, 61 and 78,720 nM, respectively. | ||||||||||||||||
IC50& Target | Ki: 4 nM (NET), 61 nM (SERT), 78720 nM (DAT)[1] | ||||||||||||||||
体内研究 (In Vivo) | Treatment of rats with Desipramine hydrochloride for 14 days reduces norepinephrine transporter (NET) expression in a dose-dependent manner, as indicated by a reduction of the specific binding of3H-nisoxetine to the NET in preparations of cerebral cortex (F(3,16)=4.33, p<0.05) and hippocampus (F(3,16)=4.34, p<0.05). This NET down regulation is observed 2 days after discontinuation of chronic Desipramine hydrochloride treatment, a time when plasma and brain concentrations of Desipramine hydrochloride and desmethyldesipramine are undetectable (ie below the 25 ng detection limit of the assay)[2]. | ||||||||||||||||
分子量 | 302.84 | ||||||||||||||||
性状 | Solid | ||||||||||||||||
Formula | C18H23ClN2 | ||||||||||||||||
CAS 号 | 58-28-6 | ||||||||||||||||
中文名称 | 盐酸去甲咪嗪;盐酸地昔帕明 | ||||||||||||||||
运输条件 | Room temperature in continental US; may vary elsewhere. | ||||||||||||||||
储存方式 | 4°C, sealed storage, away from moisture *In solvent : -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture) | ||||||||||||||||
溶解性数据 | In Vitro: DMSO : ≥ 100 mg/mL(330.21 mM) H2O : 100 mg/mL(330.21 mM;Need ultrasonic) *"≥" means soluble, but saturation unknown. 配制储备液
* 请根据产品在不同溶剂中的溶解度选择合适的溶剂配制储备液;一旦配成溶液,请分装保存,避免反复冻融造成的产品失效。 In Vivo: 请根据您的实验动物和给药方式选择适当的溶解方案。以下溶解方案都请先按照In Vitro方式配制澄清的储备液,再依次添加助溶剂: ——为保证实验结果的可靠性,澄清的储备液可以根据储存条件,适当保存;体内实验的工作液,建议您现用现配,当天使用;
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