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| Type |
Poster Presentation |
| Area |
Organic Chemistry |
| Room No. |
Event Hall |
| Time |
4월 19일 (목요일) 11:00~12:30 |
| Code |
ORGN.P-347 |
| Subject |
Synthesis and photophysical study of 2-fluorenyl-1,2,3-triazole-labeled 2’-deoxyuridine and its oligonucleotide |
| Authors |
SeungWoo Hong, Gil Tae Hwang*
Department of Chemistry, Kyungpook National University, Korea
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| Abstract |
Fluorene is being regarded as one of the most important fluorophores, because it has a good quantum yield and is less bulky than other commonly used fluorophores. We attached fluorene to 2’-deoxyuridine through ethynyl linker and observed good solvent-dependent photophysical properties. In this study, we tried to synthesize another fluorene-labeled 2’-deoxyuridine linked by triazole group via copper-catalyzed azide-alkyne cycloaddition (CuAAC). here we prepared 2-fluorenyl-1,2,3-triazol-4-yl-2’-deoxyuridine (UFT) and inserted it at the central position of an oligodeoxynucleotide (ODN). UFT displays different fluorescence intensities and emission maxima in different solvents, indicating its potential for application as an environmentally sensitive probe.However ODN containing UFT did not exhibit selective thermal stability and fluorescence changes upon duplex formation with matched and single-base mismatched targets. This highlighted the importance of selecting the appropriate linker to connect the fluorophore to the nucleobase when developing such DNA probes |
| E-mail |
tmddnzkf1@naver.com |
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121st General Meeting of the KCS