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| 包装规格: | 500g in glass bottle |
| 溶解性: | 溶于DMSO(≥100mg/mL) |
| 产品描述: | 基本信息 产品编号: P11137 产品名称: Phenacetin CAS: 62-44-2 储存条件 粉末 室温 四年 分子式: C10H13NO2 溶于液体 -80℃ 6个月 分子量: 179.22 -20℃ 1个月 化学名: Phenacetin melting point standard,Pharmaceutical Secondary Standard;Certified Reference Material Solubility (25°C): 体外: DMSO 36mg/mL (200.87mM) Ethanol 36mg/mL (200.87mM) Water Insoluble 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 5.5797mL 27.8987mL 55.7973mL 5mM 1.1159mL 5.5797mL 11.1595mL 10mM 0.5580mL 2.7899mL 5.5797mL 50mM 0.1116mL 0.5580mL 1.1159mL 生物活性 产品描述 一种非阿片类镇痛/解热化合物。 靶点 COX-3 102μM (IC50) 体外研究 Phenacetin shows inhibitory activity for COX-3 with an IC50 value of 102μM in insect cells.Phenacetin is a substrate widely used as an in vitro and in vivo probe to measure the activity of CYP1A2,because the metabolism of phenacetin to acetaminophen is thought to be a selective CYP1A2-mediated reaction. 体内研究 Phenacetin exhibits elimination half-life (rat 2.06h) and Cmax (6,728.3μg/L) following oral administration (rat 20mg/kg). Animal Model: Male Sprague-Dawley rats (180-200g) Dosage: 20mg/kg Administration: Oral administration (Pharmacokinetic Analysis) Result: T1/2 (2.06 hours),Cmax(6,728.3μg/L). |
| 保存条件: | 室温 |
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