OSIP-486823 ≥98%
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| 包装规格: | 1mg 5mg 10mg 25mg 50mg in glass bottle |
| 产品描述: | 基本信息 产品编号:O10229 产品名称:OSIP-486823 CAS: 200803-37-8 储存条件 粉末 -20℃ 四年 分子式: C29H28FNO4 溶于液体 -80℃ 六个月 分子量: 473.54 -20℃ 一个月 化学名: 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 一种新型的微管干扰剂,对蛋白激酶 G (PKG) 和微管均具有生物学作用。 靶点/IC50 Microtubule 体外研究 OSIP486823 inhibits growth and induce apoptosis in SW480 human colon cancer cells, with IC50 of 0.1μM. OSIP-486823 (OSIP486823) causes depolymerization of microtubules in interphase cells, inhibit spindle formation in mitotic cells, and induce multinucleated cells. Exisulind and the potent synthetic derivative OSIP-486823 are members of a new class of drugs known as selective apoptotic antineoplastic drugs that target cyclic guanosine 3′,5′-monophosphate phosphodiesterases (cGMP-PDE). OSIP-486823 also disrupts microtubule polymerization, perturbs mitotic spindle function, and arrests cells in mitosis in human glioma cells. 推荐实验方法(仅供参考) 细胞实验: The SW480 human colon adenocarcinoma and NIH3T3 mouse fibroblast cell lines are seeded in six-well plates at a density of 3×104 per well, grown for 36 to 48 hours, and then exposed to increasing concentrations of each compound (e.g., OSIP486823; 1, 2 and 4μM) for 48 hours. Cell numbers are determined using a Coulter counter and results are expressed as a percentage of the control culture. All assays are done in triplicate. Data are analyzed in Excel and the IC50s are determined graphically from cell survival curves. |
| 保存条件: | -20℃ |
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