| CAS NO: | 1195765-45-7 |
| 包装 | 价格(元) |
| 10 mM * 1 mL in DMSO | 电议 |
| 5mg | 电议 |
| 10mg | 电议 |
| 50mg | 电议 |
| 100mg | 电议 |
| 200mg | 电议 |
| 500mg | 电议 |
| 1 g | 电议 |
| 生物活性 | Dabrafenib (GSK2118436A) is an ATP-competitive inhibitor ofRafwithIC50s of 5 nM and 0.6 nM forC-RafandB-RafV600E, respectively[4]. | ||||||||||||||||
| IC50& Target[4] |
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| 体外研究 (In Vitro) | Dabrafenib (GSK2118436, 1 μM) with 0.01 μM GSK1120212 inhibits more than 90% of cell growth in the NRAS mutant clones. GSK2118436 is sufficient to reduce S6P phosphorylation in A375[1]. Dabrafenib suppresses the PolyP-mediated vascular barrier permeability, upregulation of inflammatory biomarkers, adhesion/migration of leukocytes, and activation and/or production of nuclear factor-κB, tumor necrosis factor-α, and interleukin-6[2]. Dabrafenib inhibits the release of HMGB1 and downregulates HMGB1-dependent inflammatory responses by enhancing the expressions of cell adhesion molecules (CAMs) in human endothelial cells[3]. | ||||||||||||||||
| 体内研究 (In Vivo) | Dabrafenib-treated females have mostly immature reproductive tracts with no evidence of ovulation, similar to age-matched controls; however, DAB-treated females have keratinized and histologically open vaginas[5]. | ||||||||||||||||
| Clinical Trial | |||||||||||||||||
| 分子量 | 519.56 | ||||||||||||||||
| 性状 | Solid | ||||||||||||||||
| Formula | C23H20F3N5O2S2 | ||||||||||||||||
| CAS 号 | 1195765-45-7 | ||||||||||||||||
| 中文名称 | 达拉非尼 | ||||||||||||||||
| 运输条件 | Room temperature in continental US; may vary elsewhere. | ||||||||||||||||
| 储存方式 |
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| 溶解性数据 | In Vitro: DMSO : ≥ 33 mg/mL(63.52 mM) *"≥" means soluble, but saturation unknown. 配制储备液
* 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。 In Vivo: 请根据您的实验动物和给药方式选择适当的溶解方案。以下溶解方案都请先按照In Vitro方式配制澄清的储备液,再依次添加助溶剂: ——为保证实验结果的可靠性,澄清的储备液可以根据储存条件,适当保存;体内实验的工作液,建议您现用现配,当天使用;
以下溶剂前显示的百
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