4.7 Article

Design, Synthesis, and Structure-Activity Relationship of 7-Propanamide Benzoxaboroles as Potent Anticancer Agents

Journal

JOURNAL OF MEDICINAL CHEMISTRY
Volume 62, Issue 14, Pages 6765-6784

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.jmedchem.9b00736

Keywords

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Funding

  1. National Key Research and Development Program of China [2017YFA0505200]
  2. National Science Foundation of China [81222042, 81573264]
  3. E-Institutes of Shanghai Universities (EISU) Chemical Biology Division

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Benzoxaboroles, as a novel class of bioactive molecules with unique physicochemical properties, have been shown to possess excellent antimicrobial activities with tavaborole approved in 2014 as an antifungal drug. Although urgently needed, the investigation of benzoxaboroles as anticancer agents has been lacking so far. In this study, we report the design, synthesis, and anticancer structure activity relationship of a series of 7-propanamide benzoxaboroles. Compounds 103 and 115 showed potent activity against ovarian cancer cells with IC50 values of 33 and 21 nM, respectively. Apoptosis was induced by these compounds and colony formation was effectively inhibited. Furthermore, they also showed excellent efficacy in ovarian tumor xenograft mouse model.

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