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| 包装规格: | 100mg in glass bottle |
| 产品描述: | 基本信息 产品编号: F10324 产品名称: Fabesetron CAS: 129300-27-2 储存条件 粉末 -20℃ 四年 分子式: C18H19N3O 溶于液体 -80℃ 6个月 分子量 293.36 -20℃ 1个月 化学名: (+)-(R)-8,9-Dihydro-10-methyl-7-((5-methylimidazol-4-yl)methyl)pyrido(1,2-a)indol-6(7H)-one Solubility (25°C): 体外: DMSO Ethanol Water 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。 生物活性 产品描述 一种具有口服活性的 5-HT3 和 5-HT4 受体的拮抗剂。 靶点 5-HT3 Receptor 5-HT4 Receptor 体内研究 Fabesetron (FK1052) (0.1 mg/kg p.o.) inhibits completely the increases in the colonic transit. FK1052 (100 µg/kg) completely prevents emesis induced by cisplatin (18 mg/kg, i.p.) in Suncus murinus. Animal Model: Male Sprague-Dawley rats weighing 220 to 330 g and male ddy mice weighing 25 to 35 g were used. Dosage: 0.1 mg/kg. Administration: P.O. Result: Significantly caused delay and its degree of inhibition was 33.8 ± 4.8% by 0.1 mg/kg p.o.. Animal Model: Suncus murinus of either sex (>10-week-old; 30-70 g body weight). Dosage: 1, 10, and 100 µg/kg. Administration: Orally administered 30 min before the injection of cisplatin. Result: Inhibited cisplatininduced emesis in a dose-dependent manner, and no emesis was observed in three animals given the compound at 100 µg/kg. |
| 保存条件: | -20℃ |
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