PMID

Data

Article Title

Organization

Discovery of uracil-based histone deacetylase inhibitors able to reduce acquired antifungal resistance and trailing growth in Candida albicans.

Sapienza University of Rome

Histone deacetylase inhibitors: from bench to clinic.

Menarini Ricerche

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

Institute of Technology

Synthesis and biological properties of novel, uracil-containing histone deacetylase inhibitors.

Sapienza University of Rome

On the function of the 14 A long internal cavity of histone deacetylase-like protein: implications for the design of histone deacetylase inhibitors.

University of Notre Dame

Antiproliferative and phenotype-transforming antitumor agents derived from cysteine.

University of Queensland

3-(4-Aroyl-1-methyl-1H-pyrrol-2-yl)-N-hydroxy-2-propenamides as a new class of synthetic histone deacetylase inhibitors. 3. Discovery of novel lead compounds through structure-based drug design and docking studies.

Sapienza University of Rome

Binding mode analysis of 3-(4-benzoyl-1-methyl-1H-2-pyrrolyl)-N-hydroxy-2-propenamide: a new synthetic histone deacetylase inhibitor inducing histone hyperacetylation, growth inhibition, and terminal cell differentiation.

Sapienza University of Rome

Structural and in Vivo Characterization of Tubastatin A, a Widely Used Histone Deacetylase 6 Inhibitor.

University of Illinois At Chicago

Histone deacetylase inhibitors

Orchid Chemicals & Pharmaceuticals