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Isolation and Potential Biological Applications of Haloaryl Secondary Metabolites from Macroalgae

Macroalgae have been reported as an important source of halogenated aromatic secondary metabolites, being the majority of these derivatives isolated from red algae. Halophenols and haloindoles are the most common haloaryl secondary metabolites isolated from these marine organisms. Nevertheless, some...

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Autores principales: Jesus, Ana, Correia-da-Silva, Marta, Afonso, Carlos, Pinto, Madalena, Cidade, Honorina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6409842/
https://www.ncbi.nlm.nih.gov/pubmed/30678253
http://dx.doi.org/10.3390/md17020073
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author Jesus, Ana
Correia-da-Silva, Marta
Afonso, Carlos
Pinto, Madalena
Cidade, Honorina
author_facet Jesus, Ana
Correia-da-Silva, Marta
Afonso, Carlos
Pinto, Madalena
Cidade, Honorina
author_sort Jesus, Ana
collection PubMed
description Macroalgae have been reported as an important source of halogenated aromatic secondary metabolites, being the majority of these derivatives isolated from red algae. Halophenols and haloindoles are the most common haloaryl secondary metabolites isolated from these marine organisms. Nevertheless, some halogenated aromatic sesquiterpenes and naphthalene derivatives have also been isolated. Most of these secondary metabolites showed interesting biological activities, such as antitumor, antimicrobial, antidiabetic, and antioxidant. This review describes in a systematic way the distribution and natural occurrence of halogenated aromatic secondary metabolites from extracts of red, brown, and green algae, as well as biological activities reported for these compounds.
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spelling pubmed-64098422019-03-29 Isolation and Potential Biological Applications of Haloaryl Secondary Metabolites from Macroalgae Jesus, Ana Correia-da-Silva, Marta Afonso, Carlos Pinto, Madalena Cidade, Honorina Mar Drugs Review Macroalgae have been reported as an important source of halogenated aromatic secondary metabolites, being the majority of these derivatives isolated from red algae. Halophenols and haloindoles are the most common haloaryl secondary metabolites isolated from these marine organisms. Nevertheless, some halogenated aromatic sesquiterpenes and naphthalene derivatives have also been isolated. Most of these secondary metabolites showed interesting biological activities, such as antitumor, antimicrobial, antidiabetic, and antioxidant. This review describes in a systematic way the distribution and natural occurrence of halogenated aromatic secondary metabolites from extracts of red, brown, and green algae, as well as biological activities reported for these compounds. MDPI 2019-01-22 /pmc/articles/PMC6409842/ /pubmed/30678253 http://dx.doi.org/10.3390/md17020073 Text en © 2019 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 Review
Jesus, Ana
Correia-da-Silva, Marta
Afonso, Carlos
Pinto, Madalena
Cidade, Honorina
Isolation and Potential Biological Applications of Haloaryl Secondary Metabolites from Macroalgae
title Isolation and Potential Biological Applications of Haloaryl Secondary Metabolites from Macroalgae
title_full Isolation and Potential Biological Applications of Haloaryl Secondary Metabolites from Macroalgae
title_fullStr Isolation and Potential Biological Applications of Haloaryl Secondary Metabolites from Macroalgae
title_full_unstemmed Isolation and Potential Biological Applications of Haloaryl Secondary Metabolites from Macroalgae
title_short Isolation and Potential Biological Applications of Haloaryl Secondary Metabolites from Macroalgae
title_sort isolation and potential biological applications of haloaryl secondary metabolites from macroalgae
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6409842/
https://www.ncbi.nlm.nih.gov/pubmed/30678253
http://dx.doi.org/10.3390/md17020073
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