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Zhang, Xiaohui and Xu, Yao-Zhong
(2011).
DOI: https://doi.org/10.3390/molecules16075655
Abstract
5-Substituted-4-thio-2’-deoxyuridine nucleosides have been chemically synthesized and studied by NMR and UV spectroscopy. The results have been analyzed and discussed in connection with the previous data. The imino proton signal and the carbon signal of the thiocarbonyl group in the 5-substituted-4-thio-2’-deoxyuridines were found to be at much lower field, offering a potential for monitoring these modified bases at the DNA level. All 4-thionucleosides have strong absorptions at around 340 nm and consequently would be useful as potential UVA-induced anticancer agents.
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About
- Item ORO ID
- 29051
- Item Type
- Journal Item
- ISSN
- 1420-3049
- Project Funding Details
-
Funded Project Name Project ID Funding Body Not Set Not Set The Open University, UK Not Set Not Set the Scientific Research Foundation for the Returned Overseas Chinese Scholars, State Education Ministry, China - Keywords
- NMR; UV; 4-thiothymidine; DNA
- Academic Unit or School
-
Faculty of Science, Technology, Engineering and Mathematics (STEM) > Life, Health and Chemical Sciences
Faculty of Science, Technology, Engineering and Mathematics (STEM) - Copyright Holders
- © 2011 The Authors
- Depositing User
- Yao Xu