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Sulfonadyn-47是一种dynamin抑制剂,能在无细胞测定中抑制dynamin的GTP酶活性(IC50 = 3.5 µM)。在U2OS细胞中,Sulfonadyn-47抑制clathrin介导的内吞作用(IC50 = 27.3 µM),同时在分离的大鼠脑突触体中抑制由去极化刺激的FM4-64摄取,后者是突触小泡内吞(SVE)的标志(IC50 = 12.3 µM)。在体内,Sulfonadyn-47(30和60 mg/kg)在6 Hz角膜电引发小鼠癫痫模型中具有抗惊厥活性。
Sulfonadyn-47是一种dynamin抑制剂,能在无细胞测定中抑制dynamin的GTP酶活性(IC50 = 3.5 µM)。在U2OS细胞中,Sulfonadyn-47抑制clathrin介导的内吞作用(IC50 = 27.3 µM),同时在分离的大鼠脑突触体中抑制由去极化刺激的FM4-64摄取,后者是突触小泡内吞(SVE)的标志(IC50 = 12.3 µM)。在体内,Sulfonadyn-47(30和60 mg/kg)在6 Hz角膜电引发小鼠癫痫模型中具有抗惊厥活性。
规格 | 价格 | 库存 | 数量 |
---|---|---|---|
500 μg | ¥ 455 | 35日内发货 | |
1 mg | ¥ 682 | 35日内发货 | |
5 mg | ¥ 2,240 | 35日内发货 | |
10 mg | ¥ 3,570 | 35日内发货 |
产品描述 | Sulfonadyn-47 is a dynamin inhibitor that effectively inhibits dynamin GTPase activity with an IC50 of 3.5 µM in cell-free assays. Additionally, it disrupts clathrin-mediated endocytosis in U2OS cells (IC50 = 27.3 µM) and impedes the depolarization-stimulated uptake of the synaptic vesicle endocytosis (SVE) marker FM4-64 in isolated rat brain synaptosomes (IC50 = 12.3 µM). Significantly, in vivo administration of sulfonadyn-47 at doses of 30 and 60 mg/kg demonstrates anticonvulsant properties in the 6 Hz corneal kindling mouse model of seizures. |
分子量 | 459.40 |
分子式 | C22H23BrN2O2S |
存储 | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice. |
溶解度信息 | DMF: 10 mg/ml DMSO: 10 mg/ml |
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