Potent histone deacetylase inhibitors: N-hydroxybenzamides with antitumor activities.

Bioorg Med Chem

Department of Biotechnology, Faculty of Engineering, Kansai University, Suita, Osaka 564-8680, Japan.

Published: August 2004

The screening tests of N-hydroxybenzamides for their HDAC-inhibitory activities led to the discovery of the promising compounds with a 2-naphthylcarbonyl group and with a 1,4-biphenylcarbonyl group. These compounds were further modified to optimize their physico-chemical profile. As a result, the inhibitor with a 6-amino-2-naphthylcarbonyl was obtained, which showed not only promising growth inhibitions against a panel of tumor cells, but also an improved water solubility. It exhibited the maximal 185% of survival rate (%T/C) in a in vivo experiment with P388 cell-inoculated mice.

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http://dx.doi.org/10.1016/j.bmc.2004.06.020DOI Listing

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