Design and synthesis of novel histone deacetylase inhibitor derived from nuclear localization signal peptide

Design and synthesis of novel histone deacetylase inhibitor derived from nuclear localization signal peptide Novel histone deacetylase inhibitors: design, synthesis, enzyme inhibition, and binding mode study of SAHA-Based non-hydroxamates Thiol-based SAHA analogues as potent histone deacetylase inhibitors Biological and Biophysical Properties of the Histone Deacetylase Inhibitor Suberoylanilide Hydroxamic Acid Are Affected by the Presence of Short Alkyl Groups on the Phenyl Ring Structural requirements of HDAC inhibitors: SAHA analogs functionalized adjacent to the hydroxamic acid Design and synthesis of novel hybrid benzamide–peptide histone deacetylase inhibitors Novel Inhibitors of Human Histone Deacetylases:  Design, Synthesis, Enzyme Inhibition, and Cancer Cell Growth Inhibition of SAHA-Based Non-hydroxamates Design and synthesis of a novel class of histone deacetylase inhibitors Design, synthesis and biological evaluation of saccharin-based N -hydroxybenzamides as histone deacetylases (HDACs) inhibitors The structural requirements of histone deacetylase inhibitors: Suberoylanilide hydroxamic acid analogs modified at the C6 position