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Marine Longilenes, Oxasqualenoids with Ser-Thr Protein Phosphatase 2A Inhibition Activity
The red seaweed Laurencia viridis is a rich source of oxygenated secondary metabolites that were derived from squalene. We report here the structures of three novel compounds, (+)-longilene peroxide (1), longilene (2), and (+)-prelongilene (3) that were isolated from this alga, in addition to other...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5923418/ https://www.ncbi.nlm.nih.gov/pubmed/29673138 http://dx.doi.org/10.3390/md16040131 |
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author | Cen-Pacheco, Francisco Pérez Manríquez, Claudia Luisa Souto, María Norte, Manuel Fernández, José Javier Hernández Daranas, Antonio |
author_facet | Cen-Pacheco, Francisco Pérez Manríquez, Claudia Luisa Souto, María Norte, Manuel Fernández, José Javier Hernández Daranas, Antonio |
author_sort | Cen-Pacheco, Francisco |
collection | PubMed |
description | The red seaweed Laurencia viridis is a rich source of oxygenated secondary metabolites that were derived from squalene. We report here the structures of three novel compounds, (+)-longilene peroxide (1), longilene (2), and (+)-prelongilene (3) that were isolated from this alga, in addition to other substances, 4 and 5, resulting from their acid-mediated degradation. The effect of compounds 1 and 3 against Ser-Thr protein phosphatase type 2A (PP2A) was evaluated, showing that (+)-longilene peroxide (1) inhibited PP2A (IC(50) 11.3 μM). In order to explain the interaction between PP2A and compounds 1 and 3, molecular docking simulations onto the PP2A enzyme-binding region were used. |
format | Online Article Text |
id | pubmed-5923418 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-59234182018-05-03 Marine Longilenes, Oxasqualenoids with Ser-Thr Protein Phosphatase 2A Inhibition Activity Cen-Pacheco, Francisco Pérez Manríquez, Claudia Luisa Souto, María Norte, Manuel Fernández, José Javier Hernández Daranas, Antonio Mar Drugs Article The red seaweed Laurencia viridis is a rich source of oxygenated secondary metabolites that were derived from squalene. We report here the structures of three novel compounds, (+)-longilene peroxide (1), longilene (2), and (+)-prelongilene (3) that were isolated from this alga, in addition to other substances, 4 and 5, resulting from their acid-mediated degradation. The effect of compounds 1 and 3 against Ser-Thr protein phosphatase type 2A (PP2A) was evaluated, showing that (+)-longilene peroxide (1) inhibited PP2A (IC(50) 11.3 μM). In order to explain the interaction between PP2A and compounds 1 and 3, molecular docking simulations onto the PP2A enzyme-binding region were used. MDPI 2018-04-17 /pmc/articles/PMC5923418/ /pubmed/29673138 http://dx.doi.org/10.3390/md16040131 Text en © 2018 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 Cen-Pacheco, Francisco Pérez Manríquez, Claudia Luisa Souto, María Norte, Manuel Fernández, José Javier Hernández Daranas, Antonio Marine Longilenes, Oxasqualenoids with Ser-Thr Protein Phosphatase 2A Inhibition Activity |
title | Marine Longilenes, Oxasqualenoids with Ser-Thr Protein Phosphatase 2A Inhibition Activity |
title_full | Marine Longilenes, Oxasqualenoids with Ser-Thr Protein Phosphatase 2A Inhibition Activity |
title_fullStr | Marine Longilenes, Oxasqualenoids with Ser-Thr Protein Phosphatase 2A Inhibition Activity |
title_full_unstemmed | Marine Longilenes, Oxasqualenoids with Ser-Thr Protein Phosphatase 2A Inhibition Activity |
title_short | Marine Longilenes, Oxasqualenoids with Ser-Thr Protein Phosphatase 2A Inhibition Activity |
title_sort | marine longilenes, oxasqualenoids with ser-thr protein phosphatase 2a inhibition activity |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5923418/ https://www.ncbi.nlm.nih.gov/pubmed/29673138 http://dx.doi.org/10.3390/md16040131 |
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