論文

査読有り
2011年2月

Design and synthesis of highly solvatochromic fluorescent 2 '-deoxyguanosine and 2 '-deoxyadenosine analogs

BIOORGANIC & MEDICINAL CHEMISTRY LETTERS
  • Katsuhiko Matsumoto
  • ,
  • Naoya Takahashi
  • ,
  • Azusa Suzuki
  • ,
  • Takashi Morii
  • ,
  • Yoshio Saito
  • ,
  • Isao Saito

21
4
開始ページ
1275
終了ページ
1278
記述言語
英語
掲載種別
研究論文(学術雑誌)
DOI
10.1016/j.bmcl.2010.11.129
出版者・発行元
PERGAMON-ELSEVIER SCIENCE LTD

We synthesized various substituted 8-styryl-2'-deoxyguanosine and 8-styryl-2'-deoxyadenosine derivatives. Among them only acetyl substituted 8-styryl-2'-deoxyguanosine analog 5b showed a remarkable solvatochromicity (Delta lambda(em)(max) = 91 nm), that is, strong fluorescence at 477 nm in 1,4-dioxane, but in methanol the fluorescence was red shifted to 558 nm with very low intensity. Such environmentally sensitive solvatochromic fluorescent guanosine analogs may be useful as a sensor for investigating interactions of DNA with DNA binding proteins. (C) 2010 Elsevier Ltd. All rights reserved.

リンク情報
DOI
https://doi.org/10.1016/j.bmcl.2010.11.129
PubMed
https://www.ncbi.nlm.nih.gov/pubmed/21273064
Web of Science
https://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=JSTA_CEL&SrcApp=J_Gate_JST&DestLinkType=FullRecord&KeyUT=WOS:000286972400040&DestApp=WOS_CPL
ID情報
  • DOI : 10.1016/j.bmcl.2010.11.129
  • ISSN : 0960-894X
  • PubMed ID : 21273064
  • Web of Science ID : WOS:000286972400040

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