Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1364772 | Bioorganic & Medicinal Chemistry Letters | 2008 | 5 Pages |
Abstract
Histone deacetylase (HDAC) inhibitors offer a promising strategy for cancer therapy and the first generation HDAC inhibitors are currently in the clinic. Herein we describe the optimization of a series of ketone small molecule HDAC inhibitors leading to potent and selective class I HDAC inhibitors with good dog PK.
Graphical abstractThe optimization of a series of ketone small molecule HDAC inhibitors leading to potent and selective class I HDAC inhibitors with good dog PK is reported.Figure optionsDownload full-size imageDownload as PowerPoint slide
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Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Giovanna Pescatore, Olaf Kinzel, Barbara Attenni, Ottavia Cecchetti, Fabrizio Fiore, Massimiliano Fonsi, Michael Rowley, Carsten Schultz-Fademrecht, Sergio Serafini, Christian Steinkühler, Philip Jones,