DNA Oligomers Having a Diazapyrenium Dication (DAP^<2+>); Synthesis and DNA Cleavage Activities
スポンサーリンク
概要
- 論文の詳細を見る
Aiming at the creation of functionalized antisense DNA oligomers possessing site-selective DNA cleaving activity, viologen and a related compound, diazapyrenium dication (DAP^<2+>), were selected and introduced into oligodeoxyribonucleotides as a functionalized molecule. The conjugation of these functionalized molecules with DNA proceeded smoothly by using standard H-phosphonate chemistry. A part of the DAP^<2+> -tethered DNA oligomers was synthesized by a combination of solid support method and liquid phase technique. Viologen-tethered DNA oligomers showed no significant activity toward DNA cleavage in spite of their characteristic ESR spectra. On the other hand, it was observed that the DAP^<2+>-tethered DNA oligomers formed more stable duplexes with their complementary strands than the corresponding wild type, and these molecules effectively cleaved the complementary strands at the specific site of 2-3 bases away from the modified phosphoramidate linkage. The effect of position and length of the linker arm on the selectivity in the cleavage reaction was also investigated, and it was found that introduction at the 3'- or 5'-end phosphate site is more favorable, probably due to duplex stabilization.
- 公益社団法人日本薬学会の論文
- 1999-10-15
著者
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Yoneda Fumio
Faculty of Pharmaceutical Sciences, Kyoto University
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FUJI KAORU
Institute for Chemical Research, Kyoto University
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Fuji Kaoru
Institute For Chemical Research Kyoto University
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Yoneda F
Faculty Of Pharmaceutical Sciences Kyoto University
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Yoneda Fumio
Faculty Of Pharmaceutical Sciences Kyoto University
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IKEDA Hisafumi
Institute for Chemical Research, Kyoto University
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TANAKA Kiyoshi
Institute for Chemical Research, Kyoto University
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ISO Yasuyoshi
Faculty of Pharmaceutical Sciences, Kyoto University
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Iso Yasuyoshi
Faculty Of Pharmaceutical Sciences Kyoto University
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Tanaka Kiyoshi
Institute For Chemical Research Kyoto University
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Ikeda Hisafumi
Institute For Chemical Research Kyoto University
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