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RAF265 (CHIR-265),Raf激酶和VEGFR-2抑制剂

    
≥98%

RAF265 (CHIR-265)

源叶(MedMol)
S81108 一键复制产品信息
927880-90-8
C24H16F6N6O
518.43
1-甲基-5-[[2-[5-(三氟甲基)-1H-咪唑-2-基]-4-吡啶基]氧基]-N-[4-(三氟甲基)苯基]-1H-苯并咪唑-2-胺;RAF265 (CHIR-265)
货号 规格 价格 上海 北京 珠海 重庆 武汉 购买数量
S81108-1mg
≥98%

¥298.00

10 - - - -
S81108-5mg
≥98%

¥740.00

10 - - - -
S81108-10mg
≥98%

¥1200.00

10 - - - -
S81108-50mg
≥98%

¥3240.00

10 - - - -
产品介绍 参考文献 质检证书(COA) 摩尔浓度计算器 相关产品
产品描述: RAF265 is a potent and orally active RAF/VEGFR2 inhibitor.
靶点: VEGFR2;RAF;Apoptosis; Raf; VEGFR; Autophagy
体内研究: In single-compound efficacy studies, optimal dosing of RAD001 and RAF265 is 5 to 12 mg/kg daily and 30 mg/kg every two days, respectively. However, combination tolerability studies in nontumor-bearing mice defin dose-limiting toxicity as a 10% weight loss with the combination of RAD001 at a dose of 12 mg/kg daily and RAF265 at a dose of 20 mg/kg every two days. Therefore, the combination of RAF265 at a dose of 12 mg/kg qd and RAD001 at a dose of 12 mg/kg qd seems to be the maximal tolerated dose. RAD001 and RAF265 are both given at a dose of 12 mg/kg qd, alone or concurrently, over 6 days. After a 2-day stop, the compounds are given for another 6 days, and the treatment is then stopped. To confirm the potential of the combination of RAF265 and RAD001, the antitumor effect of the combination is tested in HCT116 xenografts (KRAS mut, PIK3CA mut). In HCT116 xenografts, RAD001 or RAF265 given alone shows 60% to 65% and 71% to 72% TVI%, respectively
参考文献: 1. Mordant P, et al. Dependence on phosphoinositide 3-kinase and RAS-RAF pathways drive the activity of RAF265, a novel RAF/VEGFR2 inhibitor, and RAD001 (Everolimus) in combination. Mol Cancer Ther. 2010 Feb;9(2):358-68.
溶解性: Soluble  in  DMSO、Ethanol
保存条件: -20℃
配置溶液浓度参考:
1mg 5mg 10mg
1 mM 1.929 ml 9.645 ml 19.289 ml
5 mM 0.386 ml 1.929 ml 3.858 ml
10 mM 0.193 ml 0.964 ml 1.929 ml
50 mM 0.039 ml 0.193 ml 0.386 ml
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。

参考文献

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摩尔浓度计算器

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