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PD173955

    
10mM in DMSO

PD173955

源叶(MedMol)
T93764 一键复制产品信息
260415-63-2
C21H16Cl2N4OS
443.35
6-(2,6-dichlorophenyl)-8-methyl-2-((3-(methylthio)phenyl)amino)pyrido[2,3-d]pyrimidin-7(8H)-one
货号 规格 价格 上海 北京 珠海 重庆 武汉 购买数量
T93764-1ml促销
10mM in DMSO

¥982.00 ¥884.00

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: Bcr-Abl 抑制剂;Bcr-Abl Inhibitors;产品介绍PD173955是Src激酶家族选择性抑制剂,对Src、Yes和Abl激酶IC50值约为22nM,对FGFR_alpha_抑制性弱,对InsR和PKC无活性。;InformationPD173955 PD173955 is a potent Bcr-Abl inhibitor with IC50 of 1-2 nM, also inhibiting Src activity with IC50 of 22 nM.TargetsBcr-Abl ; Src 1 nM-2 nM; 22 nMIn vitroPD173955 potently inhibits Bcr-Abl-dependent cell growth with IC50 of 2-35 nM in Bcr-Abl-positive cell lines, about 100- to 200-fold more sensitive than in Bcr-Abl-negative cell lines. PD173955 also inhibits kit ligand-dependent proliferation of M07e cells with IC50 of 40 nM, by inhibition of kit ligand-dependent c-kit autophosphorylation. In addition, PD173955, as a Src inhibitor, potently inhibits mitotic progression during early mitosis in cells of all types and induces varying degrees of apoptotic cell death.Cell Research(from reference)Cell lines:Bcr-Abl-positive cell lines (R10(+), R10(−), K562, and RWLeu4); Bcr-Abl-negative cell lines (HL-60, SK-N-ER, SK-N-MC, U138MG, and HS-16) Concentrations:10 μM Incubation Time:48 hours 
靶点: IC50: 22 nM (Src).
保存条件: -80℃(运输条件:冰袋低温运输)
配置溶液浓度参考:
1mg 5mg 10mg
1 mM 2.256 ml 11.278 ml 22.556 ml
5 mM 0.451 ml 2.256 ml 4.511 ml
10 mM 0.226 ml 1.128 ml 2.256 ml
50 mM 0.045 ml 0.226 ml 0.451 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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