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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...

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Autores principales: Cen-Pacheco, Francisco, Pérez Manríquez, Claudia, Luisa Souto, María, Norte, Manuel, Fernández, José Javier, Hernández Daranas, Antonio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
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.
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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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