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Salvadenosine, a 5′-Deoxy-5′-(methylthio) Nucleoside from the Bahamian Tunicate Didemnum sp.
[Image: see text] Salvadenosine, (1) a rare 5′-deoxy-5′-(methylthio) nucleoside, was isolated from the deep-water Bahaman tunicate Didemnum sp. The structure was solved by integrated analysis of MS and 1D and 2D NMR data. We revise the structure of the known natural product, hamiguanosinol, which is...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical
Society
2014
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4227578/ https://www.ncbi.nlm.nih.gov/pubmed/25284474 http://dx.doi.org/10.1021/jo501486p |
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author | Jamison, Matthew T. Boddy, Christopher N. Molinski, Tadeusz F. |
author_facet | Jamison, Matthew T. Boddy, Christopher N. Molinski, Tadeusz F. |
author_sort | Jamison, Matthew T. |
collection | PubMed |
description | [Image: see text] Salvadenosine, (1) a rare 5′-deoxy-5′-(methylthio) nucleoside, was isolated from the deep-water Bahaman tunicate Didemnum sp. The structure was solved by integrated analysis of MS and 1D and 2D NMR data. We revise the structure of the known natural product, hamiguanosinol, which is a constitutional isomer of 1, to 5 by interpretation of the spectroscopic data and comparison with synthesized nucleosides. |
format | Online Article Text |
id | pubmed-4227578 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | American Chemical
Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-42275782015-10-03 Salvadenosine, a 5′-Deoxy-5′-(methylthio) Nucleoside from the Bahamian Tunicate Didemnum sp. Jamison, Matthew T. Boddy, Christopher N. Molinski, Tadeusz F. J Org Chem [Image: see text] Salvadenosine, (1) a rare 5′-deoxy-5′-(methylthio) nucleoside, was isolated from the deep-water Bahaman tunicate Didemnum sp. The structure was solved by integrated analysis of MS and 1D and 2D NMR data. We revise the structure of the known natural product, hamiguanosinol, which is a constitutional isomer of 1, to 5 by interpretation of the spectroscopic data and comparison with synthesized nucleosides. American Chemical Society 2014-10-03 2014-11-07 /pmc/articles/PMC4227578/ /pubmed/25284474 http://dx.doi.org/10.1021/jo501486p Text en Copyright © 2014 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes. |
spellingShingle | Jamison, Matthew T. Boddy, Christopher N. Molinski, Tadeusz F. Salvadenosine, a 5′-Deoxy-5′-(methylthio) Nucleoside from the Bahamian Tunicate Didemnum sp. |
title | Salvadenosine, a 5′-Deoxy-5′-(methylthio)
Nucleoside from the Bahamian Tunicate Didemnum sp. |
title_full | Salvadenosine, a 5′-Deoxy-5′-(methylthio)
Nucleoside from the Bahamian Tunicate Didemnum sp. |
title_fullStr | Salvadenosine, a 5′-Deoxy-5′-(methylthio)
Nucleoside from the Bahamian Tunicate Didemnum sp. |
title_full_unstemmed | Salvadenosine, a 5′-Deoxy-5′-(methylthio)
Nucleoside from the Bahamian Tunicate Didemnum sp. |
title_short | Salvadenosine, a 5′-Deoxy-5′-(methylthio)
Nucleoside from the Bahamian Tunicate Didemnum sp. |
title_sort | salvadenosine, a 5′-deoxy-5′-(methylthio)
nucleoside from the bahamian tunicate didemnum sp. |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4227578/ https://www.ncbi.nlm.nih.gov/pubmed/25284474 http://dx.doi.org/10.1021/jo501486p |
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