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The Discovery of Novel 10,11-Dihydro-5H-dibenz[b,f]azepine SIRT2 Inhibitors.


ABSTRACT: Isoform selective inhibitors of the sirtuins (NAD+-dependent histone deacetylases) should enable an in depth study of the molecular biology underpinning these targets and how they are deregulated in diseases such as cancer and neurodegeneration. Herein, we present the discovery of structurally novel SIRT2 inhibitors. Hit molecule 8 was discovered through the chemical synthesis and biological characterization of a small-molecule compound library based around the 10,11-dihydro-5H-dibenz[b,f]azepine scaffold. In vitro screening assays revealed compound 8 to have an IC50 of 18 ?M against SIRT2 and to exhibit more than 30-fold selectivity compared to SIRT1. Cellular assays, performed on MCF-7 cells, confirmed the in vitro selectivity and showed hit 8 to have antiproliferative activity at a concentration of 30 ?M. Computational studies were performed to predict the SIRT2 binding mode and to rationalise the observed selectivity.

SUBMITTER: Di Fruscia P 

PROVIDER: S-EPMC3856871 | biostudies-literature | 2012 Mar

REPOSITORIES: biostudies-literature

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Isoform selective inhibitors of the sirtuins (NAD<sup>+</sup>-dependent histone deacetylases) should enable an in depth study of the molecular biology underpinning these targets and how they are deregulated in diseases such as cancer and neurodegeneration. Herein, we present the discovery of structurally novel SIRT2 inhibitors. Hit molecule <b>8</b> was discovered through the chemical synthesis and biological characterization of a small-molecule compound library based around the 10,11-dihydro-5H  ...[more]

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