Cyclic tetrapeptides with thioacetate tails or intramolecular disulfide bridge as potent inhibitors of histone deacetylases

Cyclic tetrapeptides with thioacetate tails or intramolecular disulfide bridge as potent inhibitors of histone deacetylases RETRACTED: Design and synthesis of CHAP31, trapoxin B and HC-toxin based bicyclic tetrapeptides disulfide as potent histone deacetylase inhibitors Interaction of aliphatic cap group in inhibition of histone deacetylases by cyclic tetrapeptides Bicyclic peptides as potent inhibitors of histone deacetylases: Optimization of alkyl loop length Molecular design of histone deacetylase inhibitors by aromatic ring shifting in chlamydocin framework Synthesis and histone deacetylase inhibitory activity of cyclic tetrapeptides containing a retrohydroxamate as zinc ligand Novel histone deacetylase inhibitors: cyclic tetrapeptide with trifluoromethyl and pentafluoroethyl ketones Design and Synthesis of a Potent Histone Deacetylase Inhibitor Discovery and activity profiling of thailandepsins A through F, potent histone deacetylase inhibitors, from Burkholderia thailandensis E264 Design and synthesis of novel hybrid benzamide–peptide histone deacetylase inhibitors