論文

査読有り 国際誌
2022年7月1日

Synthesis and Cytotoxic Activities of 8- and 6-Demethyleucalyptins.

Bioscience, biotechnology, and biochemistry
  • Ryuki Asakawa
  • Kanta Fuchiyama
  • Yunosuke Ishii
  • Keisuke Hosaka
  • Atsushi Kobayashi
  • Kei Shimazaki
  • Junki Nagasawa
  • Sayaka Tsuchida
  • Kazunari Ushida
  • Makoto Matsubayashi
  • Yuuki Furuyama
  • Kenji Ohgane
  • Kouji Kuramochi
  • 全て表示

記述言語
英語
掲載種別
研究論文(学術雑誌)
DOI
10.1093/bbb/zbac105

Secondary metabolites in plants influence the health of herbivores such as Japanese rock ptarmigans that feed on the leaves and fruits of alpine plants. Thus, it is important to understand the secondary metabolites of alpine plants and their biological activities for conserving Japanese rock ptarmigans. We isolated C-methylflavone from the leaves of Kalmia procumbens, on which Japanese rock ptarmigans feed. Although its structure was deduced to be 8-demethyleucalyptin by comparing its NMR data with the reported ones, the possibility that the isolated compound is 6-demethyleucalyptin cannot be ruled out. Thus, both isomers were synthesized. The isolated compound was unambiguously determined to be 8-demethyleucalyptin by comparing its NMR data with those of the synthetic ones. Cytotoxic evaluation of 8- and 6-demethyleucalyptins revealed that only the former showed cytotoxicity against HCT116 and MRC-5 cells. The present study provides not only easy access to 8- and 6-demethyleucalyptins, but also their biological information.

リンク情報
DOI
https://doi.org/10.1093/bbb/zbac105
PubMed
https://www.ncbi.nlm.nih.gov/pubmed/35776954
ID情報
  • DOI : 10.1093/bbb/zbac105
  • PubMed ID : 35776954

エクスポート
BibTeX RIS