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Therapeutic efficacy of CEP-33779, a novel selective JAK2 inhibitor, in a mouse model of colitis-induced colorectal cancer
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Identification of inhibitors of the leishmania cdc2-related protein kinase CRK3
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Signalling through Class I PI3Ks in mammalian cells
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PI3Kd and PI3Kg as targets for autoimmune and inflammatory diseases
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SAR studies around a series of triazolopyridines as potent and selective PI3Kg inhibitors
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A selective inhibitor reveals PI3Kg dependence of TH17 cell differentiation
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Discovery of novel PI3Kg/d inhibitors as potential agents for inflammation
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Novel antifungal agents: Triazolopyridines as inhibitors of b -1,6-glucan synthesis
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DNA gyrase (GyrB)/topoisomerase IV (ParE) inhibitors: Synthesis and antibacterial activity
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(2S,3S)-3-amino-4-(3,3-difluoropyrrolidin-1-yl)-N,N-dimethyl-4-oxo-2-(4- [1, 2,4]triazolo[1,5-a]-pyridin-6-ylphenyl)butanamide: A selective a-amino amide dipeptidyl peptidase IV inhibitor for the treatment of type 2 diabetes
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The evolution of phosphatidylinositol 3-kinases as regulators of growth and metabolism
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Discovery of GSK2126458, a highly potent inhibitor of PI3K and the mammalian target of rapamycin
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Phospshoinositide 3-kinase (PI3K)/mammalian target of rapamycin (mTOR) dual inhibitors: Discovery and structureeactivity relationships of a series of quinoline and quinoxaline derivatives
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Discovery and optimization of a series of benzothiazole phosphoinositide 3-kinase (PI3K)/mammalian target of rapamycin (mTOR) dual inhibitors
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