

ab120882 · 5 mg
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Description
MW 469.5 Da, Purity >98 %. Potent, ATP-competitive Phosphatidylinositol 3-kinase PI3K inhibitor IC50 = 4, 5, 7 and 75 nM for PI3Kalpha, -gamma, -delta, and -beta respectively and mTOR inhibitor. Able to directly induce G1 arrest and inhibit angiogenesis in vitro and potentiate the efficacy of other anticancer agents in vivo.






