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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 | 98+% | ||||||||||||||||
FR 180204 |
+
ERK1, Ki: 0.31 μM |
++
ERK2, Ki: 0.14 μM |
98% | ||||||||||||||||
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。 |
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]. |
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 |
CAS号 | 2035509-96-5 |
分子式 | C32H40N8O5S |
分子量 | 648.776 |
别名 | |
运输 | 蓝冰 |
存储条件 |
液体 -20°C:3-6个月-80°C:12个月 粉末 Sealed in dry,2-8°C |
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 |