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ZM-39923 is a small molecule experimental drug primarily known as a potent and selective inhibitor of Janus kinase 3 (JAK3), with additional inhibitory activity against JAK1, epidermal growth factor receptor (EGFR), cyclin-dependent kinase 4 (CDK4), and tissue transglutaminase (TGM2)[6][5][7]. It acts as a prodrug that breaks down in neutral buffer to form the active JAK3 inhibitor ZM449829[4][8]. The compound has been used extensively in research settings to study JAK/STAT signaling pathways and transglutaminase biology. It is not approved for clinical use and remains investigational[2]. In addition to its kinase inhibition profile, it has shown effects in disease models such as Machado-Joseph Disease in Drosophila melanogaster[4].
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