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Exploring marine toxins: comparative analysis of chemical reactivity properties and potential for drug discovery
Marine toxins, produced by various marine microorganisms, pose significant risks to both marine ecosystems and human health. Understanding their diverse structures and properties is crucial for effective mitigation and exploration of their potential as therapeutic agents. This study presents a compa...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10646282/ https://www.ncbi.nlm.nih.gov/pubmed/38025068 http://dx.doi.org/10.3389/fchem.2023.1286804 |
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author | Flores-Holguín, Norma Salas-Leiva, Joan S. Núñez-Vázquez, Erick J. Tovar-Ramírez, Dariel Glossman-Mitnik, Daniel |
author_facet | Flores-Holguín, Norma Salas-Leiva, Joan S. Núñez-Vázquez, Erick J. Tovar-Ramírez, Dariel Glossman-Mitnik, Daniel |
author_sort | Flores-Holguín, Norma |
collection | PubMed |
description | Marine toxins, produced by various marine microorganisms, pose significant risks to both marine ecosystems and human health. Understanding their diverse structures and properties is crucial for effective mitigation and exploration of their potential as therapeutic agents. This study presents a comparative analysis of two hydrophilic and two lipophilic marine toxins, examining their reactivity properties and bioavailability scores. By investigating similarities among these structurally diverse toxins, valuable insights into their potential as precursors for novel drug development can be gained. The exploration of lipophilic and hydrophilic properties in drug design is essential due to their distinct implications on drug distribution, elimination, and target interaction. By elucidating shared molecular properties among toxins, this research aims to identify patterns and trends that may guide future drug discovery efforts and contribute to the field of molecular toxinology. The findings from this study have the potential to expand knowledge on toxins, facilitate a deeper understanding of their bioactivities, and unlock new therapeutic possibilities to address unmet biomedical needs. The results showcased similarities among the studied systems, while also highlighting the exceptional attributes of Domoic Acid (DA) in terms of its interaction capabilities and stability. |
format | Online Article Text |
id | pubmed-10646282 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-106462822023-01-01 Exploring marine toxins: comparative analysis of chemical reactivity properties and potential for drug discovery Flores-Holguín, Norma Salas-Leiva, Joan S. Núñez-Vázquez, Erick J. Tovar-Ramírez, Dariel Glossman-Mitnik, Daniel Front Chem Chemistry Marine toxins, produced by various marine microorganisms, pose significant risks to both marine ecosystems and human health. Understanding their diverse structures and properties is crucial for effective mitigation and exploration of their potential as therapeutic agents. This study presents a comparative analysis of two hydrophilic and two lipophilic marine toxins, examining their reactivity properties and bioavailability scores. By investigating similarities among these structurally diverse toxins, valuable insights into their potential as precursors for novel drug development can be gained. The exploration of lipophilic and hydrophilic properties in drug design is essential due to their distinct implications on drug distribution, elimination, and target interaction. By elucidating shared molecular properties among toxins, this research aims to identify patterns and trends that may guide future drug discovery efforts and contribute to the field of molecular toxinology. The findings from this study have the potential to expand knowledge on toxins, facilitate a deeper understanding of their bioactivities, and unlock new therapeutic possibilities to address unmet biomedical needs. The results showcased similarities among the studied systems, while also highlighting the exceptional attributes of Domoic Acid (DA) in terms of its interaction capabilities and stability. Frontiers Media S.A. 2023-11-01 /pmc/articles/PMC10646282/ /pubmed/38025068 http://dx.doi.org/10.3389/fchem.2023.1286804 Text en Copyright © 2023 Flores-Holguín, Salas-Leiva, Núñez-Vázquez, Tovar-Ramírez and Glossman-Mitnik. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Chemistry Flores-Holguín, Norma Salas-Leiva, Joan S. Núñez-Vázquez, Erick J. Tovar-Ramírez, Dariel Glossman-Mitnik, Daniel Exploring marine toxins: comparative analysis of chemical reactivity properties and potential for drug discovery |
title | Exploring marine toxins: comparative analysis of chemical reactivity properties and potential for drug discovery |
title_full | Exploring marine toxins: comparative analysis of chemical reactivity properties and potential for drug discovery |
title_fullStr | Exploring marine toxins: comparative analysis of chemical reactivity properties and potential for drug discovery |
title_full_unstemmed | Exploring marine toxins: comparative analysis of chemical reactivity properties and potential for drug discovery |
title_short | Exploring marine toxins: comparative analysis of chemical reactivity properties and potential for drug discovery |
title_sort | exploring marine toxins: comparative analysis of chemical reactivity properties and potential for drug discovery |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10646282/ https://www.ncbi.nlm.nih.gov/pubmed/38025068 http://dx.doi.org/10.3389/fchem.2023.1286804 |
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