Dapoxetine hydrochloride ≥98%
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| 包装规格: | 1g 5g 25g 100g in glass bottle |
| 溶解性: | 溶于DMSO(≥32mg/mL) |
| 产品描述: | 基本信息 产品编号: D70306 产品名称: Dapoxetine hydrochloride CAS: 129938-20-1 储存条件 粉末 -20℃ 四年 分子式: C21H23NO.HCl 溶于液体 -80℃ 6个月 分子量 341.87 -20℃ 1个月 化学名: (S)-N,N-Dimethyl-3-(naphthalen-1-yloxy)-1-phenylpropan-1-amine hydrochloride Solubility (25°C): 体外: DMSO 68 mg/mL (198.9mM) Water 68 mg/mL (198.9mM) Ethanol 68 mg/mL (198.9mM) 体内(现配现用): <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 2.9251mL 14.6254mL 29.2509mL 5mM 0.5850mL 2.9251mL 5.8502mL 10mM 0.2925mL 1.4625mL 2.9251mL 50mM 0.0585mL 0.2925mL 0.5850mL 生物活性 产品描述 一种具有口服活性的选择性血清素再摄取 (serotonin reuptake) 抑制剂 (SSRI)。Dapoxetine hydrochloride 可用于早泄 (PE) 的相关研究。 靶点 5-HT 体外研究 Dapoxetine hydrochloride binds to 5-HT, norepinephrine, and dopamine reuptake transporters and inhibits 5-HT, norepinephrine, and dopamine uptake with an order of potency: 5-HT >norepinephrine≫dopamine. Dapoxetine hydrochloride inhibits the uptake of [3H]5-HT by the 5-HT reuptake transporter with a value of 1.12nM, and Dapoxetine inhibits the uptake of [3H]norepinephrine into cells utilizing the norepinephrine reuptake transporter and uptake of [3H]dopamine by the dopamine reuptake transporter with IC50 values of 202nM and 1720nM, respectively. 体内研究 Dapoxetine hydrochloride (oral gavage; 1-10 mg/kg; once daily) significantly inhibits testosterone mediated increase in the prostate weight and relative prostate weight and attenuates testosterone-induced prostatic hyperplasia in rats . Animal Model: Adult male Wistar rats Dosage: 1 mg/kg, 5 mg/kg, 10 mg/kg Administration: Oral gavage; 1-10 mg/kg; once daily Result: Reverted most of the changes made by testosterone injection |
| 保存条件: | 2-8℃ |
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