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NG25 是TAK1(IC50:149 nM)和MAP4K2(IC50:21.7 nM)的双抑制剂。

NG25 是TAK1(IC50:149 nM)和MAP4K2(IC50:21.7 nM)的双抑制剂。
| 规格 | 价格 | 库存 | 数量 |
|---|---|---|---|
| 1 mg | ¥ 186 | 现货 | |
| 5 mg | ¥ 413 | 现货 | |
| 10 mg | ¥ 728 | 现货 | |
| 25 mg | ¥ 1,530 | 现货 | |
| 50 mg | ¥ 2,680 | 现货 | |
| 100 mg | ¥ 4,680 | 现货 | |
| 200 mg | ¥ 6,530 | 现货 | |
| 1 mL x 10 mM (in DMSO) | ¥ 489 | 现货 |
NG25 相关产品
| 产品描述 | NG25 is a potent dual TAK1 and MAP4K2 inhibitor, with IC50s of 149 nM and 21.7 nM, respectively. |
| 靶点活性 | GSK:56.4 nM, SRC:113 nM, Raf-1:7590 nM, MAP4K2:21.7 nM, ZAK:698 nM, TAK1:149 nM, EphB2:672 nM, ZC1/HGK:3250 nM, Abl/Arg:75.2 nM, EphB4:999 nM, FER:82.3 nM, EphA2:773 nM, Lyn:12.9 nM |
| 体外活性 | NG25能够增强体外乳腺癌细胞对Dox治疗的敏感性。这种组合有可能成为一种有效且可行的治疗方案,既能最大化Dox的疗效,同时又能最小化Dox在治疗乳腺癌时的副作用[1]。 |
| 细胞实验 | Breast cancer cells were seeded in 12-well plates at 2?×?10^3 cells per well, then incubated with Dox alone or Dox with NG25 at indicated concentrations after 72?h and then were cultured in fresh medium without drug.?Two weeks later, cells were fixed and stained with methanol/crystal violet for 10?min, and photographed.?Each experiment was performed in triplicates[1]. |
| 分子量 | 537.58 |
| 分子式 | C29H30F3N5O2 |
| CAS No. | 1315355-93-1 |
| Smiles | CCN1CCN(Cc2ccc(NC(=O)c3ccc(C)c(Oc4ccnc5[nH]ccc45)c3)cc2C(F)(F)F)CC1 |
| 密度 | 1.313 g/cm3 (Predicted) |
| 存储 | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature. | |||||||||||||||||||||||||
| 溶解度信息 | DMSO: 16.67 mg/mL (31.01 mM), Sonication is recommended. | |||||||||||||||||||||||||
| 体内实验配方 | 10% DMSO+40% PEG300+5% Tween 80+45% Saline: 2 mg/mL (3.72 mM), Sonication is recommended. 请按顺序添加溶剂,在添加下一种溶剂之前,尽可能使溶液澄清。如有必要,可通过加热、超声、涡旋处理进行溶解。工作液建议现配现用。以上配方仅供参考,体内配方并不是绝对的,请根据不同情况进行调整。 | |||||||||||||||||||||||||
溶液配制表 | ||||||||||||||||||||||||||
DMSO
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