Structure-based optimization of phenylbutyrate-derived histone deacetylase inhibitors

Qiang Lu, Da Sheng Wang, Chang Shi Chen, Yuan Dong Hu, Ching Shih Chen

研究成果: Article同行評審

78 引文 斯高帕斯(Scopus)

摘要

Previously, we developed a strategy to develop a novel class of histone deacetylase (HDAC) inhibitors by tethering short-chain fatty acids with Zn 2+-chelating motifs, which led to N-hydroxy-4-(4-phenylbutyryl-amino) benzamide (HTPB), a hydroxamate-tethered phenylbutyrate derivative with sub-micromolar potency in inhibiting HDAC activity and cancer cell proliferation. In this study, we carried out structure-based optimization of HTPB by using the framework generated by the structure of histone deacetylase-like protein (HDLP)-trichostatin A (TSA) complexes. Docking of HTPB into the HDLP binding domain suggested that the hydrophobic microenvironment encompassed by Phe-198 and Phe-200 could be exploited for structural optimization. This premise was corroborated by the greater potency of (S)-(+)-N-hydroxy-4-(3-methyl-2-phenylbutyrylamino)-benzamide [(S)-11] (IC 50 in HDAC inhibition, 16 nM), of which the isopropyl moiety was favorable in interacting with this hydrophobic motif. (S)-11 at concentrations as low as 0.1 μM was effective in causing histone hyperacetylation and p21WAF/CIP1 overexpression and suppressing proliferation in cancer cells.

原文English
頁(從 - 到)5530-5535
頁數6
期刊Journal of Medicinal Chemistry
48
發行號17
DOIs
出版狀態Published - 2005 八月 25

All Science Journal Classification (ASJC) codes

  • Molecular Medicine
  • Drug Discovery

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