Fiboflapon-sodium-GSK2190915-sodium-salt-DataSheet-MedChemExpress

1、Hotline: 400-820-3792Inhibitors Agonists Screening Librarieswww.MedChemEFiboflapon sodiumCat. No.: HY-15874ACAS No.: 1196070-26-4Synonyms: GSK2190915 (sodium salt); AM-803 sodium分式: CHNNaOS分量: 659.81作靶點: FLAP作通路: Immunology/Inflammation儲存式: Powder -20C 3 years4C 2 yearsIn solvent -80C 6 months-20C 1

2、 month溶解性數(shù)據(jù)體外實驗 DMSO : 32 mg/mL (48.50 mM)* means soluble, but saturation unknown.Mass Solvent1 mg 5 mg 10 mg Concentration制備儲備液1 mM 1.5156 mL 7.5779 mL 15.1559 mL5 mM 0.3031 mL 1.5156 mL 3.0312 mL10 mM 0.1516 mL 0.7578 mL 1.5156 mL請根據(jù)產(chǎn)品在不同溶劑中的溶解度，選擇合適的溶劑配制儲備液，并請注意儲備液的保存式和期限。BIOLOGICAL ACTIVITY物活性 F

3、iboflapon sodium (GSK2190915 (sodium salt)FLAP 效選擇性抑制劑，binding IC50值為 2.9 nM。IC50 & Target IC50: 76 nM (inhibition of LTB4 in human blood 5 h incubation) 1.體外研究Fiboflapon (AM803) exhibits excellent preclinical toxicology and pharmacokinetics in rat and dog. Fiboflapon1/2 Master of Small Molecules 您邊

4、的抑制劑師www.MedChemE(AM803) also demonstrated an extended pharmacodynamic effect in a rodent bronchoalveolar lavage (BAL)model 1. Oral administration of Fiboflapon (AM803) (1 mg/kg) resulted in sustained inhibition of ex vivoionophore-challenged whole blood LTB4 biosynthesis with 90% inhibition for up

5、to 12 h and an EC50 ofapproximately 7 nM. When rat lungs were challenged in vivo with calcium-ionophore, Fiboflapon (AM803)inhibited LTB4 and cysteinyl leukotriene (CysLT) production with ED50s of 0.12 mg/kg and 0.37 mg/kg,respectively. The inhibition measured 16 h following a single oral dose of 3

6、mg/kg was 86% and 41% forLTB4 and CysLTs, respectively. In an acute inflammation setting, Fiboflapon (AM803) dose-dependentlyreduced LTB4, CysLTs, plasma protein extravasation and neutrophil influx induced by peritoneal zymosaninjection. Finally, AM803 increased survival time in mice exposed to a le

7、thal intravenous injection of plateletactivating factor (PAF) 2.REFERENCES1. Stock NS, et al. 5-Lipoxygenase-activating protein (FLAP) inhibitors. Part 4: development of 3-3-tert-butylsulfanyl-1-4-(6-ethoxypyridin-3-yl)benzyl-5-(5-methylpyridin-2-ylmethoxy)-1H-indol-2-yl-2,2-dimethylpropionic acid (

8、AM803), a potent, oral, once daily FLAP inhibitor. JMed Chem. 2011 Dec 8;54(23):8013-29.2. Lorrain DS, et al. Pharmacology of AM803, a novel selective five-lipoxygenase-activating protein (FLAP) inhibitor in rodent models ofacute inflammation. Eur J Pharmacol. 2010 Aug 25;640(1-3):211-8.McePdfHeightCaution: Product has not been fully validated for medical applications