@article{oai:tsukuba.repo.nii.ac.jp:00027890,
 author = {早川, 一郎 and 臼井, 健郎 and 木越, 英夫 and Hayakawa, Ichiro and Ikedo, Akiyuki and Chinen, Takumi and Usui, Takeo and 木越, 英夫},
 issue = {19},
 journal = {Bioorganic & medicinal chemistry},
 month = {Oct},
 note = {Various analogues of glaziovianin A, an antitumor isoflavone, were synthesized, and their biological activities were evaluated. O7-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.},
 pages = {5745--5756},
 title = {Design, synthesis, and biological evaluation of the analogues of glaziovianin A, a potent antitumor isoflavone},
 volume = {20},
 year = {2012},
 yomi = {キゴシ, ヒデオ}
}