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Discovery of a Novel Series of Thienopyrimidine as Highly Potent and Selective PI3K Inhibitors.
분류 ADME 조회 1296
발행년도 2015 등록일 2015-09-20
출처 ACS Med Chem Lett. (바로가기)
Inhibition of the phosphoinositide 3-kinase (PI3K)/AKT/mammalian target of rapamycin (mTOR) signaling pathway provides a promising new approach for cancer therapy. Through a rational design, a novel series of thienopyrimidine was discovered as highly potent and selective PI3K inhibitors.
 
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