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首页> 外文期刊>Bioorganic and Medicinal Chemistry Letters >Discovery of a novel tricyclic 4H-thiazolo[5 ',4 ':4,5]pyrano[2,3-c]pyridine-2-amino scaffold and its application in a PI3K alpha inhibitor with high PI3K isoform selectivity and potent cellular activity
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Discovery of a novel tricyclic 4H-thiazolo[5 ',4 ':4,5]pyrano[2,3-c]pyridine-2-amino scaffold and its application in a PI3K alpha inhibitor with high PI3K isoform selectivity and potent cellular activity

机译:新型三环4H-噻唑并[5',4':4,5]吡喃并[2,3-c]吡啶-2-氨基支架的发现及其在具有高PI3K同工型选择性和有效细胞活性的PI3Kα抑制剂中的应用

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摘要

A novel, previously undescribed 4H-thiazolo[5',4':4,5]pyrano[2,3-c]pyridine tricyclic scaffold has been discovered. The application of this novel chemotype leading to a potent and selective prototype PI3K alpha inhibitor with favorable physicochemical and PK-properties is described. (C) 2015 Elsevier Ltd. All rights reserved.
机译:已经发现了新颖的,以前未描述的4H-噻唑并[5',4':4,5]吡喃并[2,3-c]吡啶三环支架。描述了这种新颖的化学型的应用,其产生了具有良好的物理化学和PK性质的有效且选择性的原型PI3Kα抑制剂。 (C)2015 Elsevier Ltd.保留所有权利。

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