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- W2174392433 abstract "Activation of various interacting stress kinases, particularly the c-Jun N-terminal kinases (JNK), and a concomitant phosphorylation of insulin receptor substrate 1 (IRS-1) at serine 307 play a central role both in insulin resistance and in β-cell dysfunction. IRS-1 phosphorylation is stimulated by elevated free fatty acid levels through different pathways in obesity. A series of novel pyrido[2,3-d]pyrimidin-7-one derivatives were synthesized as potential antidiabetic agents, preventing IRS-1 phosphorylation at serine 307 in a cellular model of lipotoxicity and type 2 diabetes." @default.
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- W2174392433 date "2016-01-01" @default.
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- W2174392433 title "Novel compounds reducing IRS-1 serine phosphorylation for treatment of diabetes" @default.
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- W2174392433 doi "https://doi.org/10.1016/j.bmcl.2015.11.099" @default.
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