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Development of hydroxamate-based histone deacetylase inhibitors of bis-substituted aromatic amides with antitumor activities.


ABSTRACT: Previously, we designed and synthesized a series of bis-substituted aromatic amide-based histone deacetylase (HDAC) inhibitors. In this study, we report the replacement of a bromine atom by different amides on the phenyl ring of the CAP region. Representative compounds 9d and 10k exhibited low nanomolar IC50 values against HDAC1, which were ten times lower than that of the positive control SAHA. The IC50 of 9d against the human A549 cancer cell line was 2.13 ?M. Furthermore, 9d increased the acetylation of histones H3 and H4 in a dose-dependent manner. Moreover, 9d significantly arrested A549 cells at the G2/M phase and induced A549 cell apoptosis. Finally, molecular docking investigation rationalized the high potency of compound 9d.

SUBMITTER: Ge D 

PROVIDER: S-EPMC7053699 | biostudies-literature | 2019 Oct

REPOSITORIES: biostudies-literature

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Development of hydroxamate-based histone deacetylase inhibitors of bis-substituted aromatic amides with antitumor activities.

Ge Di D   Han Lina L   Yang Feifei F   Zhao Na N   Yang Yang Y   Zhang Hua H   Chen Yihua Y  

MedChemComm 20190820 10


Previously, we designed and synthesized a series of bis-substituted aromatic amide-based histone deacetylase (HDAC) inhibitors. In this study, we report the replacement of a bromine atom by different amides on the phenyl ring of the CAP region. Representative compounds <b>9d</b> and <b>10k</b> exhibited low nanomolar IC<sub>50</sub> values against HDAC1, which were ten times lower than that of the positive control SAHA. The IC<sub>50</sub> of <b>9d</b> against the human A549 cancer cell line was  ...[more]

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