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New Haloterpenes from the Marine Red Alga Laurencia papillosa: Structure Elucidation and Biological Activity

Analysis of the air-dried marine red alga Laurencia papillosa, collected near Ras-Bakr at the Suez gulf (Red Sea) in Egypt delivered five new halogenated terpene derivatives: aplysiolic acid (1), 7-acetyl-aplysiol (2), aplysiol-7-one (3), 11,14-dihydroaplysia-5,11,14,15-tetrol (5a), and a new maneon...

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Autores principales: Shaaban, Mohamed, Abou-El-Wafa, Ghada S. E., Golz, Christopher, Laatsch, Hartmut
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7830550/
https://www.ncbi.nlm.nih.gov/pubmed/33466896
http://dx.doi.org/10.3390/md19010035
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author Shaaban, Mohamed
Abou-El-Wafa, Ghada S. E.
Golz, Christopher
Laatsch, Hartmut
author_facet Shaaban, Mohamed
Abou-El-Wafa, Ghada S. E.
Golz, Christopher
Laatsch, Hartmut
author_sort Shaaban, Mohamed
collection PubMed
description Analysis of the air-dried marine red alga Laurencia papillosa, collected near Ras-Bakr at the Suez gulf (Red Sea) in Egypt delivered five new halogenated terpene derivatives: aplysiolic acid (1), 7-acetyl-aplysiol (2), aplysiol-7-one (3), 11,14-dihydroaplysia-5,11,14,15-tetrol (5a), and a new maneonene derivative 6, named 5-epi-maneolactone. The chemical structures of these metabolites were characterized employing spectroscopic methods, and the relative and absolute configurations were determined by comparison of experimental and ab initio-calculated NMR, NOE, ECD, and ORD data, and by X-ray diffraction of 2 and 6. The antimicrobial activities of the crude extract and compounds 1–3, 5a and 6 were studied.
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spelling pubmed-78305502021-01-26 New Haloterpenes from the Marine Red Alga Laurencia papillosa: Structure Elucidation and Biological Activity Shaaban, Mohamed Abou-El-Wafa, Ghada S. E. Golz, Christopher Laatsch, Hartmut Mar Drugs Article Analysis of the air-dried marine red alga Laurencia papillosa, collected near Ras-Bakr at the Suez gulf (Red Sea) in Egypt delivered five new halogenated terpene derivatives: aplysiolic acid (1), 7-acetyl-aplysiol (2), aplysiol-7-one (3), 11,14-dihydroaplysia-5,11,14,15-tetrol (5a), and a new maneonene derivative 6, named 5-epi-maneolactone. The chemical structures of these metabolites were characterized employing spectroscopic methods, and the relative and absolute configurations were determined by comparison of experimental and ab initio-calculated NMR, NOE, ECD, and ORD data, and by X-ray diffraction of 2 and 6. The antimicrobial activities of the crude extract and compounds 1–3, 5a and 6 were studied. MDPI 2021-01-14 /pmc/articles/PMC7830550/ /pubmed/33466896 http://dx.doi.org/10.3390/md19010035 Text en © 2021 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 (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Shaaban, Mohamed
Abou-El-Wafa, Ghada S. E.
Golz, Christopher
Laatsch, Hartmut
New Haloterpenes from the Marine Red Alga Laurencia papillosa: Structure Elucidation and Biological Activity
title New Haloterpenes from the Marine Red Alga Laurencia papillosa: Structure Elucidation and Biological Activity
title_full New Haloterpenes from the Marine Red Alga Laurencia papillosa: Structure Elucidation and Biological Activity
title_fullStr New Haloterpenes from the Marine Red Alga Laurencia papillosa: Structure Elucidation and Biological Activity
title_full_unstemmed New Haloterpenes from the Marine Red Alga Laurencia papillosa: Structure Elucidation and Biological Activity
title_short New Haloterpenes from the Marine Red Alga Laurencia papillosa: Structure Elucidation and Biological Activity
title_sort new haloterpenes from the marine red alga laurencia papillosa: structure elucidation and biological activity
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7830550/
https://www.ncbi.nlm.nih.gov/pubmed/33466896
http://dx.doi.org/10.3390/md19010035
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