Potent and selective inhibitors of the proteasome: Dipeptidyl boronic acids

Potent and selective inhibitors of the proteasome: Dipeptidyl boronic acids Structurally Novel Highly Potent Proteasome Inhibitors Created by the Structure-Based Hybridization of Nonpeptidic Belactosin Derivatives and Peptide Boronates Design, synthesis and biological evaluation of novel non-peptide boronic acid derivatives as proteasome inhibitors Synthesis and biological evaluation of boron peptide analogues of Belactosin C as proteasome inhibitors Peptido Sulfonyl Fluorides as New Powerful Proteasome Inhibitors Preliminary Studies of New Proteasome Inhibitors in the Tumor Targeting Approach: Synthesis and in Vitro Cytotoxicity α,β-Unsaturated N-Acylpyrrole Peptidyl Derivatives: New Proteasome Inhibitors Synthesis and Biological Activity of Peptide α-Ketoamide Derivatives as Proteasome Inhibitors New betulinic acid derivatives as potent proteasome inhibitors N-Terminal-prolonged vinyl ester-based peptides as selective proteasome β1 subunit inhibitors