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AX-15836 99%+

货号:A798244 Ambeed 开学季,买赠积分,赢豪礼

AX 15836 is a potent and selective ERK5 inhibitor with IC50 of 8 nM.

AX-15836 化学结构 CAS号:2035509-96-5
AX-15836 化学结构
CAS号:2035509-96-5
AX-15836 3D分子结构
CAS号:2035509-96-5
AX-15836 化学结构 CAS号:2035509-96-5
AX-15836 3D分子结构 CAS号:2035509-96-5
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AX-15836 纯度/质量文件 产品仅供科研

货号:A798244 标准纯度: 99%+
批次查询: 批次纯度:

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产品名称 ERK ERK1 ERK2 ERK5 其他靶点 纯度
DEL-22379 +

ERK, IC50: 0.5 μM

+

ERK, IC50: 0.5 μM

98%
Pluripotin ++

ERK1, Kd: 98 nM

RasGAP 99%+
FR 180204 +

ERK1, Ki: 0.31 μM

++

ERK2, Ki: 0.14 μM

99%+
Ravoxertinib +++

ERK1, IC50: 1.1 nM

++++

ERK2, IC50: 0.3 nM

99%+
SCH772984 +++

ERK1, IC50: 4 nM

++++

ERK2, IC50: 1 nM

99%+
Temuterkib +++

ERK1, IC50: 5 nM

+++

ERK2, IC50: 5 nM

99%+
VX-11e +++

ERK2, Ki: <2 nM

99%+
Ulixertinib ++++

ERK2, IC50: <0.3 nM

99%+
XMD17-109 ++

ERK5, IC50: 162 nM

99%+
1. 鼠标悬停在“+”上可以显示相关IC50的具体数值。"+"越多,抑制作用越强。2. "✔"表示该化合物对相应的亚型有抑制作用,但抑制强度暂时没有相关数据。

AX-15836 生物活性

描述 AX-15836 is a highly selective inhibitor of ERK5, exhibiting over 1,000-fold selectivity against more than 200 other kinases. It also demonstrates greater selectivity over BRD4, with a Kd of 3,600 nM. AX-15836 shows similar intracellular potency (4–9 nM) across all tested cell types, including peripheral blood mononuclear cells (PBMCs), endothelial cells, and cancer cell lines. It is completely ineffective in inhibiting the inflammatory cytokine response (EC50 > 10 μM), indicating that the BRD inhibition component of the compound mediates the reduction in cytokines. In HUVEC and HeLa cell types, samples treated with AX-15836 exhibit few differentially expressed genes. AX15836 significantly inhibits the phosphorylated form of ERK5 stimulated by EGF in HeLa cells[1].

AX-15836 参考文献

[1]Lin EC, et al. ERK5 kinase activity is dispensable for cellular immune response and proliferation. Proc Natl Acad Sci U S A. 2016 Oct 18;113(42):11865-11870.

AX-15836 实验方案

计算器
存储液制备 1mg 5mg 10mg

1 mM

5 mM

10 mM

1.54mL

0.31mL

0.15mL

7.71mL

1.54mL

0.77mL

15.41mL

3.08mL

1.54mL

AX-15836 技术信息

CAS号2035509-96-5
分子式C32H40N8O5S
分子量 648.776
别名
运输蓝冰
存储条件

粉末 Sealed in dry,2-8°C

液体 -20°C:3-6个月-80°C:12个月

溶解度

DMSO: 105 mg/mL(161.84 mM),配合低频超声助溶,注意:DMSO长时间开封后,会吸水并导致溶解能力下降,请避免使用长期开封的DMSO

动物实验配方
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