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Napabucasin (BBI608) 是一种口服的 Stat3 和 Y 干细胞活性抑制剂。
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Napabucasin (BBI608) 是一种口服的 Stat3 和 Y 干细胞活性抑制剂。
规格 | 价格 | 库存 | 数量 |
---|---|---|---|
1 mg | ¥ 269 | 现货 | |
5 mg | ¥ 496 | 现货 | |
10 mg | ¥ 768 | 现货 | |
25 mg | ¥ 1,460 | 现货 | |
50 mg | ¥ 2,380 | 现货 | |
100 mg | ¥ 3,270 | 现货 | |
200 mg | ¥ 4,280 | 现货 | |
1 mL x 10 mM (in DMSO) | ¥ 546 | 现货 |
产品描述 | Napabucasin (BBI608) is an orally available Stat3 and Y cell stemness inhibitor. |
体外活性 | Napabucasin 通过 Stat3 降调干细胞性基因表达及癌干细胞特性,并高效抑制高干细胞性癌细胞的自我更新,IC50 范围为 0.291~1.19 μM,对正常干细胞的抑制作用。[1] |
体内活性 | 在携带PaCa-2异种移植瘤的小鼠中,Napabucasin(20 mg/kg,i.p.)显著抑制了肿瘤生长、复发和转移。[1] |
细胞实验 | For cancer stem cells, spheres are dissociated and plated under cancer stem cell culture conditions on coated 96-well plates. After 72 h of culture, wells are dosed with the indicated compounds. Seventy-two hours or 24 h after dosing, CellTiter-Glo 2.0 is added to each well, and the luminescence is measured as described by the manufacturer. IC50 values are calculated by fitting a four parameter dose–response curve to normalized data using GraphPad Prism software. For bulk cells, cells are plated at 5,000 cells per well on 96-well plates. Twenty-four hours after plating, cells are treated with the indicated compounds. Viability is determined at 72 h as described above.(Only for Reference) |
别名 | BBI608 |
分子量 | 240.21 |
分子式 | C14H8O4 |
CAS No. | 83280-65-3 |
存储 | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice. | ||||||||||||||||||||||||||||||
溶解度信息 | H2O: < 1 mg/mL (insoluble or slightly soluble) DMSO: 6.88 mg/mL (28.62 mM) acetonitrile: 0.799 mg/ml (3.3278 mM) Ethanol: < 1 mg/mL (insoluble or slightly soluble) | ||||||||||||||||||||||||||||||
溶液配制表 | |||||||||||||||||||||||||||||||
acetonitrile/DMSO
DMSO
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