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Histone deacetylase (HDAC) is an attractive target for antitumor therapy. Therefore, the development of novel HDAC inhibitors is warranted. A series of HDAC inhibitors based on -hydroxycinnamamide fragment was designed as the clinically used belinostat analog using amide as the connecting unit. All target compounds were evaluated for their HDAC inhibitory activities and some selected compounds were tested for their antiproliferative activities. Among them, compound showed an IC value of 11.5 nM in inhibiting the HDAC in a pan-HDAC assay, being the most active compound of the series.
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| http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7607388 | PMC |
| http://dx.doi.org/10.4155/fmc-2018-0587 | DOI Listing |
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