Synthesis and histone deacetylase inhibitory activity of cyclic tetrapeptides containing a retrohydroxamate as zinc ligand

Synthesis and histone deacetylase inhibitory activity of cyclic tetrapeptides containing a retrohydroxamate as zinc ligand Bicyclic peptides as potent inhibitors of histone deacetylases: Optimization of alkyl loop length Novel histone deacetylase inhibitors: cyclic tetrapeptide with trifluoromethyl and pentafluoroethyl ketones Interaction of aliphatic cap group in inhibition of histone deacetylases by cyclic tetrapeptides A series of novel, potent, and selective histone deacetylase inhibitors Discovery of Potent and Selective Histone Deacetylase Inhibitors via Focused Combinatorial Libraries of Cyclic α₃β-Tetrapeptides Design and Synthesis of a Potent Histone Deacetylase Inhibitor Discovery of HDAC Inhibitors That Lack an Active Site Zn²⁺-Binding Functional Group RETRACTED: Design and synthesis of CHAP31, trapoxin B and HC-toxin based bicyclic tetrapeptides disulfide as potent histone deacetylase inhibitors Design, synthesis and preliminary biological evaluation of new hydroxamate histone deacetylase inhibitors as potential antileukemic agents