SB 239063 (p38 MAPK inhibitor)

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品牌: Gene Operation
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更新: 2021-05-29
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货号: IMA1015-0005MG
保存条件: -20℃
CAS号: 193551-21-2
供应商: 上海伟进生物科技有限公司
数量: 50
英文名: SB 239063
保质期: 2 years
规格: 5mg

Biological Activity

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SB 239063 is a highly potent and selective inhibitor of p38 MAP kinase with IC50 value of 44 nM.The compound exibits equipotent inhibitory activity against α- and β- isoform, and no activity (up to 100 μM) against the γ- and δ-kinase isoforms. In LPS-stimulated human PBMCs, SB 239063 suppresses IL-1 and TNF-α production (IC50 = 0.12 and 0.35 μM, respectively).SB 239063 acts as a potent inhibitor of inflammatory cytokine production, inhibits eosinophil recruitment, in addition to enhancing apoptosis of these cells. SB 239063 may be a potential therapeutic for the treatment of asthma and other inflammatory disorders [1].As a second-generation p38 MAPK inhibitor, SB 239063 displays improved kinase selectivity and increased cellular (3-fold) and in vivo (3- to 10-fold) activity over the first-generation inhibitors such as SB 203580. SB 239063 dosed through different routes reduces brain injury and neurological deficits in cerebral focal ischemia [2].

 

Chemical Properties

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Cas No.: 193551-21-2

M. Wt.: 368.41

Formula: C20H21FN4O2

Purity: 98% (HPLC)

Chemical Name: trans-1-(4-hydroxycyclohexyl) -4-(4-fluorophenyl)-5-(2-methoxypyridimidin-4-yl)imidazole

Appearance: White solid

SolubilitySoluble to 10 mM in DMSO with slight warming to achieve full solubilization.

StorageStore desiccated at -20 ºC for the stability up to two years, prevent from light.

 

Application Concentration (Just for reference) 

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The appropriate working concentration of SB 239063 depends on cell types, cell culture properties and specific applications. It is recommended that researchers start with optimal experiments for first use.

 

温馨提示:不可用于临床治疗。