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Pyridoclax

    
≥98%

Pyridoclax

源叶(MedMol)
S83813 一键复制产品信息
1651890-44-6
C29H22N4
426.5118
货号 规格 价格 上海 北京 珠海 重庆 武汉 购买数量
S83813-2mg
≥98%

¥430.00

货期:3-5天 - - - -
S83813-5mg
≥98%

¥780.00

货期:3-5天 - - - -
S83813-10mg
≥98%

¥1180.00

货期:3-5天 - - - -
S83813-50mg
≥98%

¥4180.00

货期:3-5天 - - - -
S83813-100mg
≥98%

¥6700.00

货期:3-5天 - - - -
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: Pyridoclax is a potential Mcl-1 inhibitor.
靶点: Mcl-1;BCL
体外研究: Pyridoclax directly binds to Mcl-1. Without cytotoxic activity when administered as a single agent, Pyridoclax induces apoptosis in combination with Bcl-xL-targeting siRNA or with ABT-737 in ovarian, lung, and mesothelioma cancer cells. Pyridoclax directly binds to Mcl-1, and hence sensitizes ovarian carcinoma cells to Bcl-xL-targeting strategies. Pyridoclax induces apoptosis in ovarian, and also in lung, and mesothelioma cancer cells when it is administrated in combination with Bcl-xL-targeting siRNA or Bcl-xL targeting molecules such as ABT-737 or its orally available derivative ABT-263
参考文献: 1. Gloaguen C, et al. First evidence that oligopyridines, α-helix foldamers, inhibit Mcl-1 and sensitize ovarian carcinoma cells to Bcl-xL-targeting strategies. J Med Chem. 2015 Feb 26;58(4):1644-68. 2. Groo AC, et al. Comparison of 2 strategies to enhance Pyridoclax solubility: Nanoemulsion delivery system versus salt synthesis. Eur J Pharm Sci. 2017 Jan 15;97:218-226.
溶解性: soluble  in  DMSO
保存条件: -20℃
配置溶液浓度参考:
1mg 5mg 10mg
1 mM 2.345 ml 11.723 ml 23.446 ml
5 mM 0.469 ml 2.345 ml 4.689 ml
10 mM 0.234 ml 1.172 ml 2.345 ml
50 mM 0.047 ml 0.234 ml 0.469 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

质量 (mg) = 浓度 (mM) x 体积 (mL) x 分子摩尔量 (g/mol)

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