AS-041164CAS号: 6318-41-8;1146702-72-8分子式: C11H7NO4S分子量: 249.2描述纯度储存/保存方法别名可溶性/溶解性参考文献
产品描述 | |
描述 |
The phosphatidylinositol 3-kinases (PI3Ks) are lipid and protein kinases involved in diverse biological processes, including cell growth, migration, and metabolism. AS-041164 is a potent inhibitor of PI3K with selectivity for the class IB isoform PI3Kγ (IC50 = 70 nM), compared to PI3Kα (IC50 = 240 nM), PI3Kβ (IC50 = 1.45 μM), and PI3Kδ (IC50 =1.70 μM). When tested at 1.0 μM, it shows little or no activity against 38 other common kinases. When given orally to mice, AS-041164 shows a pharmacokinetic profile that is similar to the general PI3K inhibitor LY294002 but is three times more potent (ED50 = 27.4 mg/kg for AS-041164 versus 81.6 mg/kg for LY294002) in blocking neutrophil recruitment induced by RANTES. |
纯度 |
≥98%
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储存/保存方法 |
Store at -20℃ for one year(Powder);Store at 2-4℃ for two weeks;Store at -20℃ for six months after dissolution.
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基本信息 | |
别名 |
S 041164
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可溶性/溶解性 |
Soluble in DMSO (~25 mg/ml), dimethyl formamide (~25 mg/ml), and 1:9 ethanol:PBS(pH 7.2) (~0.1 mg/ml).
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参考文献 | |
参考文献 |
1.Hirsch, E.,Ciraolo, E.,Ghigo, A., et al. Taming the PI3K team to hold inflammation and cancer at bay. Pharmacology & Therapeutics 118, 192-205 (2008).
2.Ferrandi, C.,Ardissone, V.,Ferro, P., et al. Phosphoinositide 3-kinase γ inhibition plays a crucial role in early steps of inflammation by blocking neutrophil recruitment. Journal of Pharmacology and Experimental Therapeutics 322, 923-930 (2007). |
分子结构图