Human HDAC isoform selectivity achieved via exploitation of the acetate release channel with structurally unique small molecule inhibitors

Human HDAC isoform selectivity achieved via exploitation of the acetate release channel with structurally unique small molecule inhibitors Structural basis for the design and synthesis of selective HDAC inhibitors Novel HDAC6 isoform selective chiral small molecule histone deacetylase inhibitors Development of a Potent and Selective HDAC8 Inhibitor Discovery of the First Histone Deacetylase 6/8 Dual Inhibitors On the inhibition of histone deacetylase 8 Potent Histone Deacetylase Inhibitors Derived from 4-(Aminomethyl)-N-hydroxybenzamide with High Selectivity for the HDAC6 Isoform Discovery of meta-sulfamoyl N-hydroxybenzamides as HDAC8 selective inhibitors Inside HDAC with HDAC inhibitors Chemical phylogenetics of histone deacetylases