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Structure–activity relationship study of glaziovianin A against cell cycle progression and spindle formation of HeLa S3 cells

✍ Scribed by Akiyuki Ikedo; Ichiro Hayakawa; Takeo Usui; Sayaka Kazami; Hiroyuki Osada; Hideo Kigoshi


Book ID
104004709
Publisher
Elsevier Science
Year
2010
Tongue
English
Weight
488 KB
Volume
20
Category
Article
ISSN
0960-894X

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✦ Synopsis


Various derivatives of glaziovianin A, an antitumor isoflavone, were synthesized, and the cytotoxicity of each against HeLa S 3 cells was investigated. Compared to glaziovianin A, the O 7 -allyl derivative was found to be more cytotoxic against HeLa S 3 cells and a more potent M-phase inhibitor.


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