Development of a Potent and Selective HDAC8 Inhibitor

Development of a Potent and Selective HDAC8 Inhibitor Discovery of meta-sulfamoyl N-hydroxybenzamides as HDAC8 selective inhibitors Design, Synthesis, and Biological Evaluation of Tetrahydroisoquinoline-Based Histone Deacetylase 8 Selective Inhibitors Rapid Discovery of Highly Potent and Selective Inhibitors of Histone Deacetylase 8 Using Click Chemistry to Generate Candidate Libraries Discovery of histone deacetylase 8 selective inhibitors Histone deacetylase 8 (HDAC8) and its inhibitors with selectivity to other isoforms: An overview On the inhibition of histone deacetylase 8 Discovery of the First Histone Deacetylase 6/8 Dual Inhibitors Structure-Based Design and Biological Characterization of Selective Histone Deacetylase 8 (HDAC8) Inhibitors with Anti-Neuroblastoma Activity Human HDAC isoform selectivity achieved via exploitation of the acetate release channel with structurally unique small molecule inhibitors