The high-throughput screening (HTS) of several novel conventional small molecule inhibitors and phytochemicals targeting FN3K is highly significant and contributes to the development of novel inhibitors for targeting oncogenic Nrf2-driven cancers.
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The Taming of Nuclear Factor Erythroid-2-Related Factor-2 (Nrf2) Deglycation by Fructosamine-3-Kinase (FN3K)-Inhibitors-A Novel Strategy to Combat Cancers.
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