Design, synthesis, and biological evaluation of the analogues of glaziovianin A, a potent antitumor isoflavone

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Abstract

Various analogues of glaziovianin A, an antitumor isoflavone, were synthesized, and their biological activities were evaluated. O 7-modified glaziovianin A showed strong cytotoxicity against HeLa S3 cells. Compared to glaziovianin A, the O7-benzyl and O7-propargyl analogues were more cytotoxic against HeLa S3 cells and more potent M-phase inhibitors. Furthermore, O7-modified molecular probes of glaziovianin A were synthesized for biological studies. © 2012 Elsevier Ltd. All rights reserved.

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Hayakawa, I., Ikedo, A., Chinen, T., Usui, T., & Kigoshi, H. (2012). Design, synthesis, and biological evaluation of the analogues of glaziovianin A, a potent antitumor isoflavone. Bioorganic and Medicinal Chemistry, 20(19), 5745–5756. https://doi.org/10.1016/j.bmc.2012.08.005

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