A systematic study of medicinal chemistry aimed at identifying a new generation of HDAC inhibitors, through the introduction of a thiol zinc-binding group (ZBG) and of an amide-lactam in the ω-position of the polyethylene chain of the vorinostat scaffold
Giuseppe Giannini*†, Loredana Vesci†, Gianfranco Battistuzzi†, Davide Vignola†, Ferdinando M. Milazzo†, Mario Berardino Guglielmi, et al. (2014). ST7612AA1, a Thioacetate-ω(γ-lactam carboxamide) Derivative Selected from a Novel Generation of Oral HDAC Inhibitors. JOURNAL OF MEDICINAL CHEMISTRY, 57(20), 8358-8377 [10.1021/jm5008209].
ST7612AA1, a Thioacetate-ω(γ-lactam carboxamide) Derivative Selected from a Novel Generation of Oral HDAC Inhibitors
Cabri W
2014
Abstract
A systematic study of medicinal chemistry aimed at identifying a new generation of HDAC inhibitors, through the introduction of a thiol zinc-binding group (ZBG) and of an amide-lactam in the ω-position of the polyethylene chain of the vorinostat scaffoldFile in questo prodotto:
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