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The interaction of heme with plakortin and a synthetic endoperoxide analogue: new insights into the heme-activated antimalarial mechanism
In the present work we performed a combined experimental and computational study on the interaction of the natural antimalarial endoperoxide plakortin and its synthetic analogue 4a with heme. Obtained results indicate that the studied compounds produce reactive carbon radical species after being red...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5382535/ https://www.ncbi.nlm.nih.gov/pubmed/28383076 http://dx.doi.org/10.1038/srep45485 |
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author | Persico, Marco Fattorusso, Roberto Taglialatela-Scafati, Orazio Chianese, Giuseppina de Paola, Ivan Zaccaro, Laura Rondinelli, Francesca Lombardo, Marco Quintavalla, Arianna Trombini, Claudio Fattorusso, Ernesto Fattorusso, Caterina Farina, Biancamaria |
author_facet | Persico, Marco Fattorusso, Roberto Taglialatela-Scafati, Orazio Chianese, Giuseppina de Paola, Ivan Zaccaro, Laura Rondinelli, Francesca Lombardo, Marco Quintavalla, Arianna Trombini, Claudio Fattorusso, Ernesto Fattorusso, Caterina Farina, Biancamaria |
author_sort | Persico, Marco |
collection | PubMed |
description | In the present work we performed a combined experimental and computational study on the interaction of the natural antimalarial endoperoxide plakortin and its synthetic analogue 4a with heme. Obtained results indicate that the studied compounds produce reactive carbon radical species after being reductively activated by heme. In particular, similarly to artemisinin, the formation of radicals prone to inter-molecular reactions should represent the key event responsible for Plasmodium death. To our knowledge this is the first experimental investigation on the reductive activation of simple antimalarial endoperoxides (1,2-dioxanes) by heme and results were compared to the ones previously obtained from the reaction with FeCl(2). The obtained experimental data and the calculated molecular interaction models represent crucial tools for the rational optimization of our promising class of low-cost synthetic antimalarial endoperoxides. |
format | Online Article Text |
id | pubmed-5382535 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-53825352017-04-10 The interaction of heme with plakortin and a synthetic endoperoxide analogue: new insights into the heme-activated antimalarial mechanism Persico, Marco Fattorusso, Roberto Taglialatela-Scafati, Orazio Chianese, Giuseppina de Paola, Ivan Zaccaro, Laura Rondinelli, Francesca Lombardo, Marco Quintavalla, Arianna Trombini, Claudio Fattorusso, Ernesto Fattorusso, Caterina Farina, Biancamaria Sci Rep Article In the present work we performed a combined experimental and computational study on the interaction of the natural antimalarial endoperoxide plakortin and its synthetic analogue 4a with heme. Obtained results indicate that the studied compounds produce reactive carbon radical species after being reductively activated by heme. In particular, similarly to artemisinin, the formation of radicals prone to inter-molecular reactions should represent the key event responsible for Plasmodium death. To our knowledge this is the first experimental investigation on the reductive activation of simple antimalarial endoperoxides (1,2-dioxanes) by heme and results were compared to the ones previously obtained from the reaction with FeCl(2). The obtained experimental data and the calculated molecular interaction models represent crucial tools for the rational optimization of our promising class of low-cost synthetic antimalarial endoperoxides. Nature Publishing Group 2017-04-06 /pmc/articles/PMC5382535/ /pubmed/28383076 http://dx.doi.org/10.1038/srep45485 Text en Copyright © 2017, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Persico, Marco Fattorusso, Roberto Taglialatela-Scafati, Orazio Chianese, Giuseppina de Paola, Ivan Zaccaro, Laura Rondinelli, Francesca Lombardo, Marco Quintavalla, Arianna Trombini, Claudio Fattorusso, Ernesto Fattorusso, Caterina Farina, Biancamaria The interaction of heme with plakortin and a synthetic endoperoxide analogue: new insights into the heme-activated antimalarial mechanism |
title | The interaction of heme with plakortin and a synthetic endoperoxide analogue: new insights into the heme-activated antimalarial mechanism |
title_full | The interaction of heme with plakortin and a synthetic endoperoxide analogue: new insights into the heme-activated antimalarial mechanism |
title_fullStr | The interaction of heme with plakortin and a synthetic endoperoxide analogue: new insights into the heme-activated antimalarial mechanism |
title_full_unstemmed | The interaction of heme with plakortin and a synthetic endoperoxide analogue: new insights into the heme-activated antimalarial mechanism |
title_short | The interaction of heme with plakortin and a synthetic endoperoxide analogue: new insights into the heme-activated antimalarial mechanism |
title_sort | interaction of heme with plakortin and a synthetic endoperoxide analogue: new insights into the heme-activated antimalarial mechanism |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5382535/ https://www.ncbi.nlm.nih.gov/pubmed/28383076 http://dx.doi.org/10.1038/srep45485 |
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