Deucravacitinib (BMS-986165) is an orally active allosteric inhibitor of tyrosine kinase 2 ( TYK2 ), with an IC 50 of 0.2 nM and a K i of 0.02 nM against the JH2 domain of TYK2 , and it exhibits selectivity over other JAK subtypes and most of the kinome. Deucravacitinib blocks IL-23 , IL-12 , p-STAT1/3 and Type I IFN signaling, and inhibits Th17/Th1-mediated psoriasis inflammation . Deucravacitinib can be used in research related to moderate-to-severe plaque psoriasis, inflammatory bowel disease and systemic lupus erythematosus.
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