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Solwaric Acids A and B, Antibacterial Aromatic Acids from a Marine Solwaraspora sp.
Two novel trialkyl-substituted aromatic acids, solwaric acids A and B, were isolated from a marine Solwaraspora sp. cultivated from the ascidian Trididemnum orbiculatum. Solwaric acids A and B were isotopically labeled with U-(13)C glucose, and analysis of a (13)C–(13)C COSY allowed for unambiguous...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2014
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3944528/ https://www.ncbi.nlm.nih.gov/pubmed/24534844 http://dx.doi.org/10.3390/md12021013 |
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author | Ellis, Gregory A. Wyche, Thomas P. Fry, Charles G. Braun, Doug R. Bugni, Tim S. |
author_facet | Ellis, Gregory A. Wyche, Thomas P. Fry, Charles G. Braun, Doug R. Bugni, Tim S. |
author_sort | Ellis, Gregory A. |
collection | PubMed |
description | Two novel trialkyl-substituted aromatic acids, solwaric acids A and B, were isolated from a marine Solwaraspora sp. cultivated from the ascidian Trididemnum orbiculatum. Solwaric acids A and B were isotopically labeled with U-(13)C glucose, and analysis of a (13)C–(13)C COSY allowed for unambiguous determination of the location of the phenyl methyl group. The two novel compounds demonstrated antibacterial activity against methicillin-resistant Staphylococcus aureus (MRSA) and methicillin-sensitive Staphylococcus aureus (MSSA). |
format | Online Article Text |
id | pubmed-3944528 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-39445282014-03-07 Solwaric Acids A and B, Antibacterial Aromatic Acids from a Marine Solwaraspora sp. Ellis, Gregory A. Wyche, Thomas P. Fry, Charles G. Braun, Doug R. Bugni, Tim S. Mar Drugs Two novel trialkyl-substituted aromatic acids, solwaric acids A and B, were isolated from a marine Solwaraspora sp. cultivated from the ascidian Trididemnum orbiculatum. Solwaric acids A and B were isotopically labeled with U-(13)C glucose, and analysis of a (13)C–(13)C COSY allowed for unambiguous determination of the location of the phenyl methyl group. The two novel compounds demonstrated antibacterial activity against methicillin-resistant Staphylococcus aureus (MRSA) and methicillin-sensitive Staphylococcus aureus (MSSA). MDPI 2014-02-14 /pmc/articles/PMC3944528/ /pubmed/24534844 http://dx.doi.org/10.3390/md12021013 Text en © 2014 by the authors; licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/). |
spellingShingle | Ellis, Gregory A. Wyche, Thomas P. Fry, Charles G. Braun, Doug R. Bugni, Tim S. Solwaric Acids A and B, Antibacterial Aromatic Acids from a Marine Solwaraspora sp. |
title | Solwaric Acids A and B, Antibacterial Aromatic Acids from a Marine Solwaraspora sp. |
title_full | Solwaric Acids A and B, Antibacterial Aromatic Acids from a Marine Solwaraspora sp. |
title_fullStr | Solwaric Acids A and B, Antibacterial Aromatic Acids from a Marine Solwaraspora sp. |
title_full_unstemmed | Solwaric Acids A and B, Antibacterial Aromatic Acids from a Marine Solwaraspora sp. |
title_short | Solwaric Acids A and B, Antibacterial Aromatic Acids from a Marine Solwaraspora sp. |
title_sort | solwaric acids a and b, antibacterial aromatic acids from a marine solwaraspora sp. |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3944528/ https://www.ncbi.nlm.nih.gov/pubmed/24534844 http://dx.doi.org/10.3390/md12021013 |
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