Article ID Journal Published Year Pages File Type
7802805 European Journal of Medicinal Chemistry 2011 9 Pages PDF
Abstract
► Forty five novel 2-arylamino-3-(arylsulfonyl)quinoxalines were synthesized. ► Most compounds exhibited potent in vitro cytotoxicities against tested cell lines. ► Compounds were tested as PI3Kα inhibitors. ► Compound 17 (PI3Kα IC50: 0.07 μM) showed the most potent cellular activities.
Related Topics
Physical Sciences and Engineering Chemistry Organic Chemistry
Authors
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