Design and Synthesis of a Potent Histone Deacetylase Inhibitor

Design and Synthesis of a Potent Histone Deacetylase Inhibitor Design and synthesis of novel hybrid benzamide–peptide histone deacetylase inhibitors Novel amide derivatives as inhibitors of histone deacetylase: Design, synthesis and SAR Bicyclic peptides as potent inhibitors of histone deacetylases: Optimization of alkyl loop length Design, synthesis and activity evaluation of indole-based double – Branched HDAC1 inhibitors Design, synthesis and primary activity assay of tripeptidomimetics as histone deacetylase inhibitors with linear linker and branched cap group Design and synthesis of a new generation of substituted purine hydroxamate analogs as histone deacetylase inhibitors A series of novel, potent, and selective histone deacetylase inhibitors Synthesis and histone deacetylase inhibitory activity of cyclic tetrapeptides containing a retrohydroxamate as zinc ligand Design and synthesis of novel histone deacetylase inhibitor derived from nuclear localization signal peptide