| Literature DB >> 22921744 |
Ichiro Hayakawa1, Akiyuki Ikedo, Takumi Chinen, Takeo Usui, Hideo Kigoshi.
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 S(3) cells. Compared to glaziovianin A, the O(7)-benzyl and O(7)-propargyl analogues were more cytotoxic against HeLa S(3) cells and more potent M-phase inhibitors. Furthermore, O(7)-modified molecular probes of glaziovianin A were synthesized for biological studies.Entities:
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Year: 2012 PMID: 22921744 DOI: 10.1016/j.bmc.2012.08.005
Source DB: PubMed Journal: Bioorg Med Chem ISSN: 0968-0896 Impact factor: 3.641