Design, synthesis, and biological evaluation of novel histone deacetylase 1 inhibitors through click chemistry

Design, synthesis, and biological evaluation of novel histone deacetylase 1 inhibitors through click chemistry Histone Deacetylase Inhibitors through Click Chemistry Design, synthesis and activity evaluation of indole-based double – Branched HDAC1 inhibitors Development of N-Hydroxycinnamamide-Based Histone Deacetylase Inhibitors with an Indole-Containing Cap Group Design, synthesis and preliminary bioactivity studies of 1,2-dihydrobenzo[d]isothiazol-3-one-1,1-dioxide hydroxamic acid derivatives as novel histone deacetylase inhibitors Design, synthesis, and biological evaluation of 1, 3-disubstituted-pyrazole derivatives as new class I and IIb histone deacetylase inhibitors Navigating into the chemical space between MGCD0103 and SAHA: novel histone deacetylase inhibitors as a promising lead Novel Inhibitors of Human Histone Deacetylases:  Design, Synthesis, Enzyme Inhibition, and Cancer Cell Growth Inhibition of SAHA-Based Non-hydroxamates Rapid Discovery of Highly Potent and Selective Inhibitors of Histone Deacetylase 8 Using Click Chemistry to Generate Candidate Libraries Design, synthesis and preliminary bioactivity evaluations of substituted quinoline hydroxamic acid derivatives as novel histone deacetylase (HDAC) inhibitors