Abstract:Selective histone deacetylase 6 (HDAC6) inhibitors are safe and well‐tolerated with less off‐target effect. However, most available HDAC6 inhibitors contain hydroxamate as a zinc‐binding group (ZBG), and their unfavorable pharmacokinetic properties along with potential genotoxicity limited wide application in diverse diseases. Therefore, we designed and synthesized a series of selective HDAC6 inhibitors utilizing thiol as the ZBG and discussed their structure‐activity relationship based on molecular docking. I… Show more
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