货号:A860936 同义名: TYRPHOSTINAG126
AG 126 selectively inhibits the phosphorylation of ERK1 and ERK2 at 25-50 μM.
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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 | AS-8351 is a histone demethylase inhibitor used to induce the reprogramming of fibroblasts into functional cardiomyocytes. Combination of AS8351 with CHIR99021, A83-01, BIX01294, SC1, Y27632 and OAC2 could efficiently induce cardiac reprogramming. |
作用机制 | AS8351 affects epigenetic modifications by competing with α-ketoglutarate for chelating iron/Fe(II) required by JmjC-KDMs.[1] |
Dose | Rat[2] (i.p.): 1 mg/kg - 10 mg/kg; Mice[3] (s.c.): 15 mg/kg |
Administration | i.p., s.c. |
计算器 | ||||
存储液制备 | 1mg | 5mg | 10mg | |
1 mM 5 mM 10 mM |
4.65mL 0.93mL 0.46mL |
23.24mL 4.65mL 2.32mL |
46.48mL 9.30mL 4.65mL |
CAS号 | 118409-62-4 |
分子式 | C10H5N3O3 |
分子量 | 215.165 |
别名 | TYRPHOSTINAG126 |
运输 | 蓝冰 |
存储条件 |
液体 -20°C:3-6个月-80°C:12个月 粉末 Keep in dark place,Inert atmosphere,Store in freezer, under -20°C |
溶解度 |
DMSO: 105 mg/mL(488 mM),配合低频超声,并水浴加热至45℃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 |