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DYRK

DYRK inhibitors act on dual-specificity tyrosine phosphorylation-regulated kinases (DYRKs) in cell growth. The first family member, Dyrk, was described in 1996 as a kinase whose activity depends on tyrosine residues in its activation loop. DYRK1A lies in the Down syndrome critical region of chromosome 21, and DYRK1B is studied in cell quiescence. The beta-carboline alkaloid harmine inhibits DYRK1A, as shown in a 2007 kinase selectivity screen. AZ191 preferentially inhibits DYRK1B, LDN-192960 targets DYRK2, and GSK-626616 is listed as a DYRK3 inhibitor. The set also contains inhibitors of related targets such as homeodomain-interacting protein kinase 2 (HIPK2) and mitotic kinesin-like protein 2 (MKLP-2).

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  • Woodtide
    Cat. No.
    A35087
    CAS No.
    634592-23-7

    Woodtide

    Woodtide is a specific substrate for the DYRK family of kinases, derived from the phosphorylation site sequence of FKHR. This reagent is utilized in biochemical assays to investigate DYRK kinase activity and regulation, facilitating studies on cellular signaling pathways and developmental processes. Its application is crucial for researchers exploring the roles of DYRK kinases in various biological contexts, including cancer and neurodegenerative diseases.

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