| 货号 | 规格 | 价格 | 上海 | 北京 | 珠海 | 武汉 | 购买数量 |
|---|---|---|---|---|---|---|---|
S81055-5mg |
99.10% | ￥500.00 |
5 | - | - | - |
|
S81055-10mg |
99.10% | ￥800.00 |
7 | - | - | - |
|
S81055-25mg促销 |
99.10% | ￥1600.00 ￥1280.00 |
6 | - | - | - |
|
S81055-100mg促销 |
≥99% | ￥3950.00 ￥3160.00 |
货期：2-3天 | - | - | - |
|
| 产品描述： | AZ 628 is a pan-Raf kinase inhibitor with IC50s of 105, 34 and 29 nM for B-Raf, B-RafV600E, and c-Raf-1, respectively. | ||||||||||||||||||||
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| 靶点： | c-Raf-1:29 nM (IC50);B-RafV600E:34 nM (IC50);B-Raf:105 nM (IC50);Apoptosis; Raf | ||||||||||||||||||||
| 体外研究： | AZ 628 reduces activities of preactivated B-Raf, B-RafV600E, and c-Raf-1 in in vitro kinase assays, with IC50 values of 105, 34 and 29 nM, respectively. AZ 628 also inhibits activation of number of tyrosine protein kinases including VEGFR2, DDR2, Lyn, Flt1, FMS and others. AZ 628 inhibits anchorage-dependent and -independent growth, causes cell cycle arrest, and induces apoptosis in colon and melanoma cell lines harboring B-RafV600E mutation. AZ 628 suppresses growth in cells expressing K-RASG13D. Inhibition of RAF with AZ 628 suppresses MEK and ERK phosphorylation. AZ 628 selectively affects viability in K-RAS mutant cells. | ||||||||||||||||||||
| 参考文献： | 1. Khazak V, et al. Selective Raf inhibition in cancer therapy. Expert Opin Ther Targets. 2007 Dec;11(12):1587-609. 2. Lau KS, et al. BAY61-3606 affects the viability of colon cancer cells in a genotype-directed manner. PLoS One. 2012;7(7):e41343. | ||||||||||||||||||||
| 溶解性： | soluble in DMSO | ||||||||||||||||||||
| 保存条件： | -20℃ | ||||||||||||||||||||
| 配置溶液浓度参考： |
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| 注意： | 部分产品我司仅能提供部分信息，我司不保证所提供信息的权威性，仅供客户参考交流研究之用。 |
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