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MedChemExpress LLC
- CAS号:
2494010-63-6
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询盘
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ERK-IN-7
CAS No. : 2494010-63-6
MCE 国际站:ERK-IN-7
产品活性:RK-IN-7 (Example 10) 是 SHR2415 (HY-151367) 的类似物,是一种有效的 ERK 抑制剂,对 ERK1 和 ERK2 的 IC50 分别为 5 nM 和 7 nM。
研究领域:MAPK/ERK Pathway | Stem Cell/Wnt
作用靶点:ERK
In Vitro: ERK-IN-7 (Example 10; 24 h) inhibits Colo205 proliferation with an IC50 of 62 nM.
In Vivo: ERK-IN-7 (Example 10; 2 mg/kg; i.g.) shows good pharmacokinetic results.
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文献和实验Signal Transduction Inhibitors in Cellular Function
through membrane-bound Ras to the nucleus of the cell. In this chapter, detailed protocols for analyzing the kinase activities of the key components of the MAPKs pathway—MEK1, ERK1, JNK, and p38 MAPK—are described. A brief introduction to the chemical inhibitors
Using 3D Culture to Investigate the Role of Mechanical Signaling in Keratinocyte Stem Cells
in the reorganization of the cytoskeleton, integrating the cells within each aggregate. Within the aggregates, KSCs retain stem cell properties, such as p63 expression, despite the increased calcium concentration and show activation of the mitogen-activated protein
它。14 活化的PAK65能够结合MEKK,然后磷酸化Ser219和Ser223 ,从而激活SEK/JNKK。活化的SEK/JNKK磷酸化JNK/SAPK(TPY Motif结构),依次结合到c-Jun的N末端并磷酸化Ser63和Ser73。ERK和JNK的磷酸化位点保守,然而,这些位点定位在不同的特异性双重磷酸化Motif (JNK在TPY Motif,ERK在TEY Motif)。分子克隆研究表明在JNK/SAPK和典型的MAPK之间约有40-45%的序列同源性。 p38蛋白
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