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Marine-Derived Xanthone from 2010 to 2021: Isolation, Bioactivities and Total Synthesis

Marine life has proved to be an invaluable source of new compounds with significant bioactivities, such as xanthones. This review summarizes the advances made in the study of marine-derived xanthones from 2010 to 2021, from isolation towards synthesis, highlighting their biological activities. Most...

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Autores principales: Veríssimo, Ana C. S., Pinto, Diana C. G. A., Silva, Artur M. S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9225453/
https://www.ncbi.nlm.nih.gov/pubmed/35736150
http://dx.doi.org/10.3390/md20060347
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author Veríssimo, Ana C. S.
Pinto, Diana C. G. A.
Silva, Artur M. S.
author_facet Veríssimo, Ana C. S.
Pinto, Diana C. G. A.
Silva, Artur M. S.
author_sort Veríssimo, Ana C. S.
collection PubMed
description Marine life has proved to be an invaluable source of new compounds with significant bioactivities, such as xanthones. This review summarizes the advances made in the study of marine-derived xanthones from 2010 to 2021, from isolation towards synthesis, highlighting their biological activities. Most of these compounds were isolated from marine-derived fungi, found in marine sediments, and associated with other aquatic organisms (sponge and jellyfish). Once isolated, xanthones have been assessed for different bioactivities, such as antibacterial, antifungal, and cytotoxic properties. In the latter case, promising results have been demonstrated. Considering the significant bioactivities showed by xanthones, efforts have been made to synthesize these compounds, like yicathins B and C and the secalonic acid D, through total synthesis.
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spelling pubmed-92254532022-06-24 Marine-Derived Xanthone from 2010 to 2021: Isolation, Bioactivities and Total Synthesis Veríssimo, Ana C. S. Pinto, Diana C. G. A. Silva, Artur M. S. Mar Drugs Review Marine life has proved to be an invaluable source of new compounds with significant bioactivities, such as xanthones. This review summarizes the advances made in the study of marine-derived xanthones from 2010 to 2021, from isolation towards synthesis, highlighting their biological activities. Most of these compounds were isolated from marine-derived fungi, found in marine sediments, and associated with other aquatic organisms (sponge and jellyfish). Once isolated, xanthones have been assessed for different bioactivities, such as antibacterial, antifungal, and cytotoxic properties. In the latter case, promising results have been demonstrated. Considering the significant bioactivities showed by xanthones, efforts have been made to synthesize these compounds, like yicathins B and C and the secalonic acid D, through total synthesis. MDPI 2022-05-25 /pmc/articles/PMC9225453/ /pubmed/35736150 http://dx.doi.org/10.3390/md20060347 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Veríssimo, Ana C. S.
Pinto, Diana C. G. A.
Silva, Artur M. S.
Marine-Derived Xanthone from 2010 to 2021: Isolation, Bioactivities and Total Synthesis
title Marine-Derived Xanthone from 2010 to 2021: Isolation, Bioactivities and Total Synthesis
title_full Marine-Derived Xanthone from 2010 to 2021: Isolation, Bioactivities and Total Synthesis
title_fullStr Marine-Derived Xanthone from 2010 to 2021: Isolation, Bioactivities and Total Synthesis
title_full_unstemmed Marine-Derived Xanthone from 2010 to 2021: Isolation, Bioactivities and Total Synthesis
title_short Marine-Derived Xanthone from 2010 to 2021: Isolation, Bioactivities and Total Synthesis
title_sort marine-derived xanthone from 2010 to 2021: isolation, bioactivities and total synthesis
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9225453/
https://www.ncbi.nlm.nih.gov/pubmed/35736150
http://dx.doi.org/10.3390/md20060347
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