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Nemiralisib (GSK2269557)

    
≥99%

GSK2269557 (free base)

源叶(MedMol)
S80228 一键复制产品信息
1254036-71-9
C26H28N6O
440.5401
2-(6-(1H-indol-4-yl)-1H-indazol-4-yl)-5-((4-isopropylpiperazin-1-yl)methyl)oxazole; 6-(1H-lndol-4-yl)-4-(5-{[4-(1-methylethyl)-1-piperazinyl]methyl}-1,3-oxazol-2-yl)-1H-indazole;;GSK2269557 (free base)
货号 规格 价格 上海 北京 珠海 重庆 武汉 购买数量
S80228-5mg促销
≥99%

¥950.00 ¥760.00

6 - - - -
S80228-10mg促销
≥99%

¥1540.00 ¥1230.00

4 - - - -
S80228-25mg促销
≥99%

¥3280.00 ¥2620.00

2 - - - -
S80228-50mg促销
≥99%

¥5760.00 ¥4600.00

1 - - - -
S80228-100mg促销
≥99%

¥9730.00 ¥7780.00

2 - - - -
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: Nemiralisib (GSK2269557 free base) is a potent and highly selective PI3Kδ inhibitor with a pKi of 9.9.
靶点: PI3Kδ:9.9 (pKi);PI3Kγ:5.2 (pIC50);PI3Kα:5.3 (pIC50);PI3Kβ:5.8 (pIC50);PI3K
体内研究: To assess the suitability of the series for inhaled delivery clearance data in rat microsomes and subsequently in vivo pharmacokinetic data from Sprague Dawley male rats is obtained. Compounds (e.g., Nemiralisib) are administered by the oral or intravenous routes, at a dose level of 3 and 1mg/kg respectively (n=2 rats/route). Nemiralisib free base is active in a disease relevant brown norway rat acute OVA model of Type 2 helper T-cells (Th2)-driven lung inflammation
参考文献: 1. Down K et al. Optimization of Novel Indazoles as Highly Potent and Selective Inhibitors of Phosphoinositide 3-Kinase δ for the Treatment of Respiratory Disease. J Med Chem. 2015 Sep 24;58(18):7381-99.
溶解性: Soluble  in  DMSO
保存条件: -20℃
配置溶液浓度参考:
1mg 5mg 10mg
1 mM 2.27 ml 11.35 ml 22.699 ml
5 mM 0.454 ml 2.27 ml 4.54 ml
10 mM 0.227 ml 1.135 ml 2.27 ml
50 mM 0.045 ml 0.227 ml 0.454 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

质检证书(COA)

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摩尔浓度计算器

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