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PIP-199

    
≥98%

PIP-199

源叶(MedMol)
S89260 一键复制产品信息
622795-76-0
C27H28N4O3
456.54
PIP-199; PIP199; PIP 199; 4-[(1-Hydroxy-2-phenyl-1H-indol-3-yl)-pyridin-2-yl-methyl]-piperazine-1-carboxylic acid ethyl ester
货号 规格 价格 上海 北京 珠海 重庆 武汉 购买数量
S89260-5mg
≥98%

¥2500.00

货期:3-5天 - - - -
S89260-10mg
≥98%

¥4500.00

货期:3-5天 - - - -
S89260-25mg
≥98%

¥9000.00

货期:3-5天 - - - -
S89260-100mg
≥98%

¥27000.00

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: PIP-199 is a selective inhibitor of RMI (RecQ-mediated genome instability protein) core complex/MM2 interaction, with an IC50 of 36 μM. PIP-199 can be used for the research of sensitizing resistant tumors to DNA crosslinking chemotherapeutics
靶点: IC50: 36 μM (RMI core complex/MM2 interaction)
体外研究: MM2 is the binding site of RMI complex on Fanconi anemia complementation group M protein (FANCM).
Induction of the Fanconi anemia (FA) DNA repair pathway is a common mechanism by which tumors evolve resistance to DNA crosslinking chemotherapies.
Proper execution of the FA pathway requires interaction between the FANCM and the RMI complex, and mutations that disrupt FANCM/RMI interactions sensitize cells to DNA crosslinking agents.
参考文献: 1. Andrew F. Voter, et al. A high throughput screening strategy to identify protein-protein interaction inhibitors that block the Fanconi anemia DNA repair pathway. J Biomol Screen. 2016 Jul; 21(6): 626–633.
溶解性: Soluble  in  DMSO
保存条件: -20℃
配置溶液浓度参考:
1mg 5mg 10mg
1 mM 2.19 ml 10.952 ml 21.904 ml
5 mM 0.438 ml 2.19 ml 4.381 ml
10 mM 0.219 ml 1.095 ml 2.19 ml
50 mM 0.044 ml 0.219 ml 0.438 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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