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Published on: January 22, 2019
3,5-diarylazoles as novel and selective inhibitors of protein kinase D
Gabriel G Gamber1, Erik Meredith, Qingming Zhu
1Novartis Institutes for BioMedical Research, Cambridge, MA 02139, USA. gabriel.gamber@novartis.com
Abstract:
The synthesis and preliminary studies of the SAR of novel 3,5-diarylazole inhibitors of Protein Kinase D (PKD) are reported. Notably, optimized compounds in this class have been found to be active in cellular assays of phosphorylation-dependant HDAC5 nuclear export, orally bioavailable, and highly selective versus a panel of additional putative histone deacetylase (HDAC) kinases. Therefore these compounds could provide attractive tools for the further study of PKD/HDAC5 signaling.
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