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- AS-252424 900515-16-4

- AS-252424 900515-16-4
AS-252424 900515-16-4
产品描述 描述 AS-252424 is a potent and selective inhibitor of PI3Kγ with IC50 of 33 nM; >10 fold selectivity for PI3Kγ versus PI3Kα.
纯度 98%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.基本信息 别名 AS252424;AS 252424外观 Yellow to brown crystalline solid.可溶性/溶解性 DMSO : 30.5 mg/mL (100 mM)生物活性 靶点 Casein Kinase 2 ,PI3Kγ ,PI3KαIn vitro(体外研究) AS-252424 is a furan-2-ylmethylene thiazolidinedione as a selective ATP-competitive PI3Kγ inhibitor with IC50 with 33 nM. AS-252424 shows reduced potency on PI3Kα with an IC50 with 935 nM. When screening against 80 different Ser/Thr and Tyr kinases, AS-252424 doesn't show significant inhibit towards any of them at 10 μM except for CK2. AS-252424 inhibits C5a-mediated PKB/Akt phosphorylation in a concentration- dependent manner with submicromolar or low-micromolarIC50 value. AS-252424 inhibits MCP-1-mediated chemotaxis in wild-type primary monocytes in a concentration-dependent manner with an IC50 value of 52 μM, as well as in the monocytic cell line THP-1 with an IC50 value of 53 μM. AS252424 specifically blocks proliferation in the pancreatic cancer cell lines HPAF and Capan1, as assessed by cell counting. A recent research indicates 100 nM of AS-252424 significantly reduces i, ICa and Ca2+ transients in HL-1 cardiomyocytes.In vivo(体内研究) Oral administration of AS-252424 at 10 mg/kg results in moderate reduction of neutrophil recruitment (35%), almost matching the result observed in PI3Kγ-deficient mice.研究领域 研究领域 CancerTumor biomarkersDrug DiscoverySmall Molecule DrugLead Compound DiscoveryAS-252424 900515-16-4温馨提示:本产品仅作科研实验使用,不支持临床等研究
