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The Tetrahydrofuran Motif in Marine Lipids and Terpenes
Heterocycles are particularly common moieties within marine natural products. Specifically, tetrahydrofuranyl rings are present in a variety of compounds which present complex structures and interesting biological activities. Focusing on terpenoids, a high number of tetrahydrofuran-containing metabo...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9605582/ https://www.ncbi.nlm.nih.gov/pubmed/36286465 http://dx.doi.org/10.3390/md20100642 |
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author | González-Andrés, Paula Fernández-Peña, Laura Díez-Poza, Carlos Barbero, Asunción |
author_facet | González-Andrés, Paula Fernández-Peña, Laura Díez-Poza, Carlos Barbero, Asunción |
author_sort | González-Andrés, Paula |
collection | PubMed |
description | Heterocycles are particularly common moieties within marine natural products. Specifically, tetrahydrofuranyl rings are present in a variety of compounds which present complex structures and interesting biological activities. Focusing on terpenoids, a high number of tetrahydrofuran-containing metabolites have been isolated during the last decades. They show promising biological activities, making them potential leads for novel antibiotics, antikinetoplastid drugs, amoebicidal substances, or anticancer drugs. Thus, they have attracted the attention of the synthetics community and numerous approaches to their total syntheses have appeared. Here, we offer the reader an overview of marine-derived terpenoids and related compounds, their isolation, structure determination, and a special focus on their total syntheses and biological profiles. |
format | Online Article Text |
id | pubmed-9605582 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-96055822022-10-27 The Tetrahydrofuran Motif in Marine Lipids and Terpenes González-Andrés, Paula Fernández-Peña, Laura Díez-Poza, Carlos Barbero, Asunción Mar Drugs Review Heterocycles are particularly common moieties within marine natural products. Specifically, tetrahydrofuranyl rings are present in a variety of compounds which present complex structures and interesting biological activities. Focusing on terpenoids, a high number of tetrahydrofuran-containing metabolites have been isolated during the last decades. They show promising biological activities, making them potential leads for novel antibiotics, antikinetoplastid drugs, amoebicidal substances, or anticancer drugs. Thus, they have attracted the attention of the synthetics community and numerous approaches to their total syntheses have appeared. Here, we offer the reader an overview of marine-derived terpenoids and related compounds, their isolation, structure determination, and a special focus on their total syntheses and biological profiles. MDPI 2022-10-15 /pmc/articles/PMC9605582/ /pubmed/36286465 http://dx.doi.org/10.3390/md20100642 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 González-Andrés, Paula Fernández-Peña, Laura Díez-Poza, Carlos Barbero, Asunción The Tetrahydrofuran Motif in Marine Lipids and Terpenes |
title | The Tetrahydrofuran Motif in Marine Lipids and Terpenes |
title_full | The Tetrahydrofuran Motif in Marine Lipids and Terpenes |
title_fullStr | The Tetrahydrofuran Motif in Marine Lipids and Terpenes |
title_full_unstemmed | The Tetrahydrofuran Motif in Marine Lipids and Terpenes |
title_short | The Tetrahydrofuran Motif in Marine Lipids and Terpenes |
title_sort | tetrahydrofuran motif in marine lipids and terpenes |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9605582/ https://www.ncbi.nlm.nih.gov/pubmed/36286465 http://dx.doi.org/10.3390/md20100642 |
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