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Novel N-Arylaminophosphonates Bearing a Pyrrole Moiety and Their Ecotoxicological Properties

A wide range of biological activities of aminophosphonates predisposes them to find applications as anticancer, antiviral, antimicrobial, antifungal, or herbicidal agents. Despite a number of positive aspects of the use of aminophosphonates, their applications may cause a risk to the environment, wh...

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Autores principales: Lewkowski, Jarosław, Morawska, Marta, Kaczmarek, Anna, Rogacz, Diana, Rychter, Piotr
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6152063/
https://www.ncbi.nlm.nih.gov/pubmed/28686206
http://dx.doi.org/10.3390/molecules22071132
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author Lewkowski, Jarosław
Morawska, Marta
Kaczmarek, Anna
Rogacz, Diana
Rychter, Piotr
author_facet Lewkowski, Jarosław
Morawska, Marta
Kaczmarek, Anna
Rogacz, Diana
Rychter, Piotr
author_sort Lewkowski, Jarosław
collection PubMed
description A wide range of biological activities of aminophosphonates predisposes them to find applications as anticancer, antiviral, antimicrobial, antifungal, or herbicidal agents. Despite a number of positive aspects of the use of aminophosphonates, their applications may cause a risk to the environment, which is well exemplified by the case of glyphosate. Therefore, scientists see a pressing need to rate ecotoxicity of aminophosphonates. Nowadays, it is recommended to use comprehensive tools to carry out appropriate and effective risk assessments of toxic substances. For these purposes, tests based on the acute toxicity of the luminescent bacteria Aliivibrio fischeri, as well as the measurement of sub-chronic toxicity of the crustacean Heterocypris incongruens seem to be the most convenient. A series of five diphenyl N-arylamino(pyrrole-2-yl)methylphosphonates was synthesized and preliminary evaluation of their ecotoxicological properties was performed. In order to carry out such investigations, we applied the two biotests mentioned above. Results showed that the N-(4-nitrophenyl) derivative was the most toxic for bacteria in comparison to other tested compounds. As for crustaceans, N-phenyl and N-naphthyl derivatives were found to be the most harmful, simultaneously being relatively harmless for bacteria. Such a phenomenon are discussed in correlation with the literature, while its reason is discussed with respect to the aspect of structure of the tested compounds.
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spelling pubmed-61520632018-11-13 Novel N-Arylaminophosphonates Bearing a Pyrrole Moiety and Their Ecotoxicological Properties Lewkowski, Jarosław Morawska, Marta Kaczmarek, Anna Rogacz, Diana Rychter, Piotr Molecules Article A wide range of biological activities of aminophosphonates predisposes them to find applications as anticancer, antiviral, antimicrobial, antifungal, or herbicidal agents. Despite a number of positive aspects of the use of aminophosphonates, their applications may cause a risk to the environment, which is well exemplified by the case of glyphosate. Therefore, scientists see a pressing need to rate ecotoxicity of aminophosphonates. Nowadays, it is recommended to use comprehensive tools to carry out appropriate and effective risk assessments of toxic substances. For these purposes, tests based on the acute toxicity of the luminescent bacteria Aliivibrio fischeri, as well as the measurement of sub-chronic toxicity of the crustacean Heterocypris incongruens seem to be the most convenient. A series of five diphenyl N-arylamino(pyrrole-2-yl)methylphosphonates was synthesized and preliminary evaluation of their ecotoxicological properties was performed. In order to carry out such investigations, we applied the two biotests mentioned above. Results showed that the N-(4-nitrophenyl) derivative was the most toxic for bacteria in comparison to other tested compounds. As for crustaceans, N-phenyl and N-naphthyl derivatives were found to be the most harmful, simultaneously being relatively harmless for bacteria. Such a phenomenon are discussed in correlation with the literature, while its reason is discussed with respect to the aspect of structure of the tested compounds. MDPI 2017-07-07 /pmc/articles/PMC6152063/ /pubmed/28686206 http://dx.doi.org/10.3390/molecules22071132 Text en © 2017 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
Lewkowski, Jarosław
Morawska, Marta
Kaczmarek, Anna
Rogacz, Diana
Rychter, Piotr
Novel N-Arylaminophosphonates Bearing a Pyrrole Moiety and Their Ecotoxicological Properties
title Novel N-Arylaminophosphonates Bearing a Pyrrole Moiety and Their Ecotoxicological Properties
title_full Novel N-Arylaminophosphonates Bearing a Pyrrole Moiety and Their Ecotoxicological Properties
title_fullStr Novel N-Arylaminophosphonates Bearing a Pyrrole Moiety and Their Ecotoxicological Properties
title_full_unstemmed Novel N-Arylaminophosphonates Bearing a Pyrrole Moiety and Their Ecotoxicological Properties
title_short Novel N-Arylaminophosphonates Bearing a Pyrrole Moiety and Their Ecotoxicological Properties
title_sort novel n-arylaminophosphonates bearing a pyrrole moiety and their ecotoxicological properties
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6152063/
https://www.ncbi.nlm.nih.gov/pubmed/28686206
http://dx.doi.org/10.3390/molecules22071132
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