Histone deacetylase enzymes (HDACs) are responsible for the global silencing of tumour-suppressor genes. Treatment with a histone deacetylase inhibitor (HDACi) can reverse this process and restore normal cell function. Herein, we report a small series of boron-based (boronic acid, boronate ester and closo-1,2-carborane) HDAC2 inhibitors with IC values in the nanomolar range. The boronate ester 4 b was the most potent compound assessed in this study (IC =40.6±1.5 nM), followed closely by the 1,2-closo-carborane (IC =42.9±1.5 nM). Compound 4 b exceeds the potency of the related gold-standard HDAC pan-inhibitor vorinostat (1) toward this particular HDAC isoform.
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http://dx.doi.org/10.1002/cbic.202000131 | DOI Listing |
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