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Structures, Activities and Drug-Likeness of Anti-Infective Xanthone Derivatives Isolated from the Marine Environment: A Review
Marine organisms represent almost half of total biodiversity and are a very important source of new bioactive substances. Within the varied biological activities found in marine products, their antimicrobial activity is one of the most relevant. Infectious diseases are responsible for high levels of...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6359551/ https://www.ncbi.nlm.nih.gov/pubmed/30634698 http://dx.doi.org/10.3390/molecules24020243 |
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author | Loureiro, Daniela R. P. Soares, José X. Costa, Joana C. Magalhães, Álvaro F. Azevedo, Carlos M. G. Pinto, Madalena M. M. Afonso, Carlos M. M. |
author_facet | Loureiro, Daniela R. P. Soares, José X. Costa, Joana C. Magalhães, Álvaro F. Azevedo, Carlos M. G. Pinto, Madalena M. M. Afonso, Carlos M. M. |
author_sort | Loureiro, Daniela R. P. |
collection | PubMed |
description | Marine organisms represent almost half of total biodiversity and are a very important source of new bioactive substances. Within the varied biological activities found in marine products, their antimicrobial activity is one of the most relevant. Infectious diseases are responsible for high levels of morbidity and mortality and many antimicrobials lose their effectiveness with time due to the development of resistance. These facts justify the high importance of finding new, effective and safe anti-infective agents. Among the variety of biological activities of marine xanthone derivatives, one that must be highlighted is their anti-infective properties. In this work, a literature review of marine xanthones with anti-infective activity, namely antibacterial, antifungal, antiparasitic and antiviral, is presented. Their structures, biological activity, sources and the methods used for bioactivity evaluation are described. The xanthone derivatives are grouped in three sets: xanthones, hydroxanthones and glycosylated derivatives. Moreover, molecular descriptors, biophysico-chemical properties, and pharmacokinetic parameters were calculated, and the chemical space occupied by marine xanthone derivatives is recognized. The chemical space was compared with marketed drugs and framed accordingly to the drug-likeness concept in order to profile the pharmacokinetic of anti-infective marine xanthone derivatives. |
format | Online Article Text |
id | pubmed-6359551 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-63595512019-02-06 Structures, Activities and Drug-Likeness of Anti-Infective Xanthone Derivatives Isolated from the Marine Environment: A Review Loureiro, Daniela R. P. Soares, José X. Costa, Joana C. Magalhães, Álvaro F. Azevedo, Carlos M. G. Pinto, Madalena M. M. Afonso, Carlos M. M. Molecules Review Marine organisms represent almost half of total biodiversity and are a very important source of new bioactive substances. Within the varied biological activities found in marine products, their antimicrobial activity is one of the most relevant. Infectious diseases are responsible for high levels of morbidity and mortality and many antimicrobials lose their effectiveness with time due to the development of resistance. These facts justify the high importance of finding new, effective and safe anti-infective agents. Among the variety of biological activities of marine xanthone derivatives, one that must be highlighted is their anti-infective properties. In this work, a literature review of marine xanthones with anti-infective activity, namely antibacterial, antifungal, antiparasitic and antiviral, is presented. Their structures, biological activity, sources and the methods used for bioactivity evaluation are described. The xanthone derivatives are grouped in three sets: xanthones, hydroxanthones and glycosylated derivatives. Moreover, molecular descriptors, biophysico-chemical properties, and pharmacokinetic parameters were calculated, and the chemical space occupied by marine xanthone derivatives is recognized. The chemical space was compared with marketed drugs and framed accordingly to the drug-likeness concept in order to profile the pharmacokinetic of anti-infective marine xanthone derivatives. MDPI 2019-01-10 /pmc/articles/PMC6359551/ /pubmed/30634698 http://dx.doi.org/10.3390/molecules24020243 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 Loureiro, Daniela R. P. Soares, José X. Costa, Joana C. Magalhães, Álvaro F. Azevedo, Carlos M. G. Pinto, Madalena M. M. Afonso, Carlos M. M. Structures, Activities and Drug-Likeness of Anti-Infective Xanthone Derivatives Isolated from the Marine Environment: A Review |
title | Structures, Activities and Drug-Likeness of Anti-Infective Xanthone Derivatives Isolated from the Marine Environment: A Review |
title_full | Structures, Activities and Drug-Likeness of Anti-Infective Xanthone Derivatives Isolated from the Marine Environment: A Review |
title_fullStr | Structures, Activities and Drug-Likeness of Anti-Infective Xanthone Derivatives Isolated from the Marine Environment: A Review |
title_full_unstemmed | Structures, Activities and Drug-Likeness of Anti-Infective Xanthone Derivatives Isolated from the Marine Environment: A Review |
title_short | Structures, Activities and Drug-Likeness of Anti-Infective Xanthone Derivatives Isolated from the Marine Environment: A Review |
title_sort | structures, activities and drug-likeness of anti-infective xanthone derivatives isolated from the marine environment: a review |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6359551/ https://www.ncbi.nlm.nih.gov/pubmed/30634698 http://dx.doi.org/10.3390/molecules24020243 |
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