Improved antiproliferative activity of 1,3,4-thiadiazole-containing histone deacetylase (HDAC) inhibitors by introduction of the heteroaromatic surface recognition motif

Improved antiproliferative activity of 1,3,4-thiadiazole-containing histone deacetylase (HDAC) inhibitors by introduction of the heteroaromatic surface recognition motif 2,5-Disubstituted-1,3,4-oxadiazoles/thiadiazole as surface recognition moiety: Design and synthesis of novel hydroxamic acid based histone deacetylase inhibitors Thiol-based SAHA analogues as potent histone deacetylase inhibitors Benzothiazole-containing hydroxamic acids as histone deacetylase inhibitors and antitumor agents 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 Novel thiol-based histone deacetylase inhibitors bearing 3-phenyl-1 H -pyrazole-5-carboxamide scaffold as surface recognition motif: Design, synthesis and SAR study Design and synthesis of a new generation of substituted purine hydroxamate analogs as histone deacetylase inhibitors 1,3,4-Oxadiazole-Containing Histone Deacetylase Inhibitors: Anticancer Activities in Cancer Cells Synthesis and structure–activity relationship of histone deacetylase (HDAC) inhibitors with triazole-linked cap group Trithiocarbonates—Exploration of a new head group for HDAC inhibitors