Discovery of Potent and Selective Histone Deacetylase Inhibitors via Focused Combinatorial Libraries of Cyclic α<sub>3</sub>β-Tetrapeptides
作者:Christian A. Olsen、M. Reza Ghadiri
DOI:10.1021/jm900850t
日期:2009.12.10
libraries to the discovery of potent HDAC ligands using a convenient screening platform. Our studies led to the first HDAC6-selective cyclictetrapeptide analogue, which extends the use of cyclictetrapeptides to the class II HDAC isoforms. These findings highlight the persistent potential of cyclictetrapeptides as epigenetic modulators and possible anticancer drug lead compounds.