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Cidabenamine is a highly selective histone deacetylase (HDAC) inhibitor, with specificity for HDAC subtypes 1, 2, 3, and 10. HDAC inhibitors function by blocking the activity of histone deacetylases—enzymes that remove acetyl groups from lysine residues on histones and other proteins. This inhibition leads to increased acetylation of histones, resulting in altered gene expression and potential anti-tumor effects. Cidabenamine's selectivity distinguishes it from pan-HDAC inhibitors by targeting specific HDAC isoforms implicated in cancer biology[7].
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