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ERK5-IN-2

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Chemical Structure| 1888305-96-1 同义名 : -
CAS号 : 1888305-96-1
货号 : A1164824
分子式 : C17H11BrFN3O2
纯度 : 99%+
分子量 : 388.191
MDL号 : MFCD32174287
存储条件:

粉末 Inert atmosphere,Room Temperature

液体 -20°C:3-6个月-80°C:12个月

溶解度 :

DMSO: 250 mg/mL(644.01 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:
生物活性
描述 Extracellular signal-regulated kinase 5 (ERK5), a member of the mitogen-activated protein kinase (MAPK) family, is ubiquitously expressed in mammalian tissues and cell types, where it is activated by extracellular stimuli, including several growth factors and cellular stresses[1]. ERK5-IN-2 is an orally active, sub-micromolar, selective ERK5 inhibitor with IC50s of 0.82 μM, 3 μM for ERK5 and ERK5 MEF2D, respectively[2]. An anti-angiogenic effect was apparent with Matrigel plugs from mice treated with ERK5-IN-2 (100 mg/kg, p.o.) twice daily for 7 days[2]. In a human tumour xenograft model (A2780 cells), ERK5-IN-2 (100 mg/kg, p.o.) treatment twice-daily for 10 days led to significant tumour volume reduction by 57% when compared to the control group[2].
作用机制 ERK5-IN-2 binds in the ERK5 ATP-binding site.
实验方案
1mg 5mg 10mg

1 mM

5 mM

10 mM

2.58mL

0.52mL

0.26mL

12.88mL

2.58mL

1.29mL

25.76mL

5.15mL

2.58mL

参考文献

[1]Stecca B, Rovida E. Impact of ERK5 on the Hallmarks of Cancer. Int J Mol Sci. 2019 Mar 21;20(6):1426. doi: 10.3390/ijms20061426. PMID: 30901834; PMCID: PMC6471124.

[2]Myers SM, Miller DC, Molyneux L, Arasta M, Bawn RH, Blackburn TJ, Cook SJ, Edwards N, Endicott JA, Golding BT, Griffin RJ, Hammonds T, Hardcastle IR, Harnor SJ, Heptinstall AB, Lochhead PA, Martin MP, Martin NC, Newell DR, Owen PJ, Pang LC, Reuillon T, Rigoreau LJM, Thomas HD, Tucker JA, Wang LZ, Wong AC, Noble MEM, Wedge SR, Cano C. Identification of a novel orally bioavailable ERK5 inhibitor with selectivity over p38α and BRD4. Eur J Med Chem. 2019 Sep 15;178:530-543. doi: 10.1016/j.ejmech.2019.05.057. Epub 2019 May 25. PMID: 31212132.