基本信息
文件名称:EGFR-HER2-IN-17-生命科学试剂-MCE.pdf
文件大小:462.39 KB
总页数:1 页
更新时间:2025-06-12
总字数:约2.17千字
文档摘要

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Inhibitors?ScreeningLibraries?Proteins

www.MedChemE

EGFR/HER2-IN-17

Cat.No.:HY-172623

分?式:C??H??N?O?

分?量:517.57

作?靶点:EGFR;Caspase;Apoptosis;Bcl-2Family

作?通路:JAK/STATSignaling;ProteinTyrosineKinase/RTK;Apoptosis

储存?式:Pleasestoretheproductundertherecommendedconditionsin

theCertificateofAnalysis.

BIOLOGICALACTIVITY

?物活性EGFR/HER2-IN-17(Compound7h)是表??长因?受体(EGFR)和?表??长因?受体2(HER2)的双重抑制剂

。EGFR/HER2-IN-17抑制癌细胞增殖。EGFR/HER2-IN-17与EGFR和HER2的结合?袋相互作?,激活

Caspase-3和Caspase-8,降低Bcl-2的表达,从?诱导凋亡(apoptosis)。EGFR/HER2-IN-17有望?于癌症的

研究[1]。

IC50TargetCaspase-3Caspase-8

REFERENCES

[1].Al-WahaibiLH,etal.Design,Synthesis,andComputationalStudiesofNovelPyrazoline-BasedDualEGFR/HER2Inhibitorswith

ApoptoticAntiproliferativeActivity[J].JournalofMolecularStructure,2025:142364.

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