MAZ51 ≥98%
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| 包装规格: | 5mg 10mg 25mg 50mg 100mg in glass bottle |
| 溶解性: | 溶于DMSO(7.69 mg/mL 超声) |
| 产品描述: | 基本信息 产品编号:M10792 产品名称:MAZ51 CAS: 163655-37-6 储存条件 粉末 -20℃ 四年 分子式: C21H18N2O 溶于液体 -80℃ 六个月 分子量 314.38 -20℃ 一个月 化学名: 3-[[4-(Dimethylamino)-1-naphthalenyl]methylidene]-1H-indol-2-one Solubility (25°C) 体外 DMSO 8.33mg/mL (26.50mM) Ethanol Insoluble 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 3.1809mL 15.9043mL 31.8086mL 5mM 0.6362mL 3.1809mL 6.3617mL 10mM 0.3181mL 1.5904mL 3.1809mL 生物活性 产品描述 VEGFR-3 酪氨酸激酶的选择性抑制剂。MAZ51 抑制 VEGF-C 诱导的 VEGFR-3 激活,而没有阻断 VEGF-C 介导的VEGFR2 刺激。 靶点/IC50 VEGFR3 体外研究 MAZ51 (2.5-10μM; 24 hours) blocks proliferation and induces apoptosis in a wide variety of tumor cells.MAZ51 (0.5-50μM; 25 minutes) has no effect on ligand-induced autophosphorylation of EGFR, IGF-1R and PDGFRβ in A431 cells, HEK-293 cells, and PAE cells, respectively . Cell Proliferation Assay Cell Line: MT450, 1AS, ASM, G, AT6.1, MTLN3, MTLY, NM-081 cells Concentration: 2.5, 10 μM Incubation Time: 24 hours Result: Induced apoptosis in a wide variety of tumor cells. Apoptosis Analysis Cell Line: MT450, 1AS, ASM, G, AT6.1, MTLN3, MTLY, NM-081 cells Concentration: 2.5, 10μM Incubation Time: 24 hours Result: Blocked proliferation in a wide variety of tumor cells. 体内研究 Animal Model: Wistar Furth rats (bearing MT450 cells) Dosage: 8mg/kg Administration: Intraperitoneal injection; daily for 15 day Result: Significantly suppressed the growth of MT450 tumors. |
| 保存条件: | -20℃ |
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