Discovery of novel class 1 phosphatidylinositide 3-kinases (PI3K) fragment inhibitors through structure-based virtual screening.

Bioorganic & Medicinal Chemistry Letters（2011）

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摘要

The identification of novel class 1 phosphatidylinositide 3-kinases (PI3K) inhibitors by fragment-based virtual screening is described.

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关键词

Docking,Fragment-based,Phosphatidylinositide 3-kinase,PI3K,p110β inhibitor,Virtual screening

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