Discovery of a Novel Series of Thienopyrimidine as Highly Potent and Selective PI3K Inhibitors. | |||
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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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