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

Akiyuki Ikedo, Ichiro Hayakawa, Takeo Usui, Sayaka Kazami, Hiroyuki Osada, Hideo Kigoshi

Research output: Contribution to journalArticle

16 Citations (Scopus)

Abstract

Various derivatives of glaziovianin A, an antitumor isoflavone, were synthesized, and the cytotoxicity of each against HeLa S3 cells was investigated. Compared to glaziovianin A, the O7-allyl derivative was found to be more cytotoxic against HeLa S3 cells and a more potent M-phase inhibitor.

Original languageEnglish
Pages (from-to)5402-5404
Number of pages3
JournalBioorganic and Medicinal Chemistry Letters
Volume20
Issue number18
DOIs
Publication statusPublished - Sep 15 2010

Keywords

  • Antitumor activity
  • Glaziovianin A
  • Isoflavone
  • Structure-activity relationship study

ASJC Scopus subject areas

  • Biochemistry
  • Molecular Medicine
  • Molecular Biology
  • Pharmaceutical Science
  • Drug Discovery
  • Clinical Biochemistry
  • Organic Chemistry

Fingerprint Dive into the research topics of 'Structure-activity relationship study of glaziovianin A against cell cycle progression and spindle formation of HeLa S<sub>3</sub> cells'. Together they form a unique fingerprint.

  • Cite this