1. Epigenetics PI3K/Akt/mTOR Protein Tyrosine Kinase/RTK MAPK/ERK Pathway
  2. AMPK FLT3 Src VEGFR Ephrin Receptor MNK Ribosomal S6 Kinase (RSK)
  3. Multi-kinase-IN-12

Multi-kinase-IN-12 是一种非选择性的多靶点抑制剂,对人源靶点的 IC50 值分别为:Flt3 < 0.001 μM、c-Src 0.002 μM、KDR 0.004 μM、Eph-A2MNK-1Flt1 0.011 μM、Lck 0.016 μM、Rsk1 0.21 μM、AMPK α2 亚基 0.041 μM。Multi-kinase-IN-12 可用于实体瘤的相关研究。

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Multi-kinase-IN-12

Multi-kinase-IN-12 Chemical Structure

CAS No. : 597544-21-3

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  • 生物活性

  • 纯度 & 产品资料

  • 参考文献

生物活性

Multi-kinase-IN-12 is a non-selective multi-target inhibitor, with IC50 values against human targets as follows: Flt3 < 0.001 μM, c-Src 0.002 μM, KDR 0.004 μM, Eph-A2, MNK-1 and Flt1 0.011 μM, Lck 0.016 μM, Rsk1 0.21 μM, and α2 subunit of AMPK 0.041 μM. Multi-kinase-IN-12 can be used in research related to solid tumors[1].

体外研究
(In Vitro)

Multi-kinase-IN-12 可强效抑制重组人源 AMPK α2/β1/γ1 异源三聚体,其 IC50 为 0.04 μM[1]
Multi-kinase-IN-12 (1-10 μM; 6 h) 可抑制 MEF 细胞中的细胞 AMPK 活性 (通过 ACC 磷酸化水平检测),在 10 μM 处理 6 小时时可观察到显著抑制作用[1]

MCE has not independently confirmed the accuracy of these methods. They are for reference only.

Western Blot Analysis[1]

Cell Line: Mouse embryonic fibroblast (MEF) cells
Concentration: 1, 5 and 10 μM
Incubation Time: 6 h
Result: Reduced ACC phosphorylation to ~1.2-fold of untreated control at 1 μM.
Reduced ACC phosphorylation to ~1.1-fold of untreated control at 5 μM.
Significantly reduced ACC phosphorylation to ~0.5-fold of untreated control at 10 μM.
分子量

401.47

Formula

C23H23N5O2

CAS 号
运输条件

Room temperature in continental US; may vary elsewhere.

储存方式

Please store the product under the recommended conditions in the Certificate of Analysis.

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参考文献
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  • Do most proteins show cross-species activity?

    Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

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