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MK-886 sodium salt
CAS No. : 118427-55-7
MCE 国际站:MK-886 sodium salt
产品活性:MK-886 (L 663536) sodium salt 是一种有效的,细胞可渗透的且具有口服活性的 FLAP (IC50 为 30 nM) 和白三烯生物合成 (完整白细胞和人全血中的 IC50 分别为 3 nM 和 1.1μM) 的抑制剂。MK-886 sodium salt 也是一种非竞争性 PPARα 拮抗剂,可以诱导细胞凋亡。
研究领域:Cell Cycle/DNA Damage | Immunology/Inflammation | Vitamin D Related/Nuclear Receptor | GPCR/G Protein | Metabolic Enzyme/Protease | Apoptosis
作用靶点:PPAR | Leukotriene Receptor | Apoptosis | FLAP
In Vitro: MK-886 sodium salt (0.5-2 μM; 15?hours; primary keratinocytes) treatment reduces keratin-1 expression in a culture of mouse primary keratinocytes.
?Using a transient transfection system in monkey kidney fibroblast CV-1 cells, mouse keratinocyte 308 cells and human lung adenocarcinoma A549 cells, 10 μM MK-886 sodium salt is able to inhibit Wy-14643 activation of PPARα by ~80%. MK-886 sodium salt also decreases PPARα activation by fatty acids in the stable transfection system.
?Although Jurkat cells express all PPAR isoforms, various PPARα and PPARγ agonists are unable to prevent MK-886 sodium salt-induced apoptosis.
In Vivo: MK-886 sodium salt (L 663536; 5 mg/kg; oral administration; male Sprague-Dawley rats) treatment potently inhibits the antigen-induced dyspnea in inbred rats pretreated with methysergide.
?MK-886 sodium salt (L 663536) inhibits leukotriene biosynthesis in vivo in a rat pleurisy model (ED50, 0.2 mg/kg p.o.), an inflamed rat paw model (ED50, 0.8 mg/kg), a model of leukotriene excretion in rat bile following antigen provocation.
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