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| 包装规格: | 10mg 25mg 100mg in glass bottle |
| 产品描述: | 基本信息 产品编号: F50005 产品名称: Fluvoxamine CAS: 54739-18-3 储存条件 粉末 -20℃ 四年 分子式: C15H21F3N2O2 溶于液体 -80℃ 6个月 分子量 318.33 -20℃ 1个月 化学名: (E)-5-Methoxy-1-(4-(trifluoromethyl)phenyl)pentan-1-one o-(2-aminoethyl) oxime Solubility (25°C): 体外: DMSO 160 mg/mL (502.62mM; Need ultrasonic) Ethanol Water 体内(现配现用): 1.请依序添加每种溶剂:10% DMSO→40% PEG300→5% Tween-80→45% saline Solubility: ≥ 2.08 mg/mL (6.53mM); Clear solution 此方案可获得 ≥ 2.08 mg/mL (6.53mM,饱和度未知) 的澄清溶液。 以 1mL 工作液为例,取 100μL 20.8 mg/mL 的澄清 DMSO 储备液加到 400μL PEG300 中,混合均匀;向上述体系中加入50μL Tween-80,混合均匀;然后继续加入 450 μL生理盐水定容至 1mL。 2.请依序添加每种溶剂: 10% DMSO→90% (20% SBE-β-CD in saline) Solubility: 2.08 mg/mL (6.53mM); Clear solution; Need ultrasonic 此方案可获得 2.08 mg/mL (6.53mM) 的澄清溶液。 以 1mL 工作液为例,取 100μL 20.8 mg/mL 的澄清 DMSO 储备液加到 900μL 20% 的 SBE-β-CD 生理盐水水溶液中,混合均匀。 3.请依序添加每种溶剂: 10% DMSO→90% corn oil Solubility: ≥ 2.08 mg/mL (6.53mM); Clear solution 此方案可获得 ≥ 2.08 mg/mL (6.53mM,饱和度未知) 的澄清溶液,此方案不适用于实验周期在半个月以上的实验。以 1mL 工作液为例,取 100μL 20.8 mg/mL 的澄清 DMSO 储备液加到 900μL玉米油中,混合均匀。 <1mg/ml表示微溶或不溶。 普西唐提供的所有化合物浓度为内部测试所得,实际溶液度可能与公布值有所偏差,属于正常的批间细微差异现象。 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。 制备储备液 浓度 溶液体积 质量 1mg 5mg 10mg 1mM 3.1414mL 15.7070mL 31.4139mL 5mM 0.6283mL 3.1414mL 6.2828mL 10mM 0.3141mL 1.5707mL 3.1414mL 生物活性 产品描述 一种5-羟色胺再吸收抑制剂,有抗抑郁活性。 靶点 SSRIs 体内研究 Fluvoxamine (DU-23000) is effective in inhibiting 5-ht uptake by blood platelets and brain synaptosomes. The antagonism by fluvoxamine of the reserpine-induced lowering of the pentamethylenetetrazole convulsive threshold can be regarded as due to an effect upon 5-HT uptake. In contrast to the effects of desmethylimipramine and imipramine, no stimulatory effects are found in rats when rapidly acting reserpine-like compounds are given following a dose of fluvoxamine. Fluvoxamine (DU23000) appears to improve combat-related PTSD symptoms but not depressive symptoms. The high attrition rate and lack of a placebo group limits the conclusions of our study. Controlled studies of fluvoxamine in the treatment of PTSD are warranted[2]. Fluvoxamine (DU-23000) was less potent at decreasing ethanol self-administration when food was available concurrently versus when ethanol was available in isolation [ED50: 4.0 (2.7-5.9) and 5.1 (4.3-6.0)]. Effects on food were similar under each condition in which food was available. The results demonstrate that the potency of fluvoxamine in reducing ethanol-maintained behavior depends on whether ethanol is available in isolation or in the context of concurrently scheduled food reinforcement. |
| 保存条件: | -20℃ 充氮保存 |
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