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Ferroquine, an Ingenious Antimalarial Drug –Thoughts on the Mechanism of Action
Ferroquine (FQ or SR97193) is a novel antimalarial drug candidate, currently in development at Sanofi-Aventis. In contrast to conventional drugs, FQ is the first organometallic drug: a ferrocenyl group covalently flanked by a 4-aminoquinoline and a basic alkylamine. FQ is able to overcome the CQ res...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2008
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6245066/ https://www.ncbi.nlm.nih.gov/pubmed/19020475 http://dx.doi.org/10.3390/molecules13112900 |
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author | Dubar, Faustine Khalife, Jamal Brocard, Jacques Dive, Daniel Biot, Christophe |
author_facet | Dubar, Faustine Khalife, Jamal Brocard, Jacques Dive, Daniel Biot, Christophe |
author_sort | Dubar, Faustine |
collection | PubMed |
description | Ferroquine (FQ or SR97193) is a novel antimalarial drug candidate, currently in development at Sanofi-Aventis. In contrast to conventional drugs, FQ is the first organometallic drug: a ferrocenyl group covalently flanked by a 4-aminoquinoline and a basic alkylamine. FQ is able to overcome the CQ resistance problem, an important limit to the control of Plasmodium falciparum, the principal causative agent of malaria. After fifteen years of effort, it is now possible to propose a multifactorial mechanism of action of FQ by its capacity to target lipids, to inhibit the formation of hemozoin and to generate reactive oxygen species. |
format | Online Article Text |
id | pubmed-6245066 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-62450662018-11-30 Ferroquine, an Ingenious Antimalarial Drug –Thoughts on the Mechanism of Action Dubar, Faustine Khalife, Jamal Brocard, Jacques Dive, Daniel Biot, Christophe Molecules Review Ferroquine (FQ or SR97193) is a novel antimalarial drug candidate, currently in development at Sanofi-Aventis. In contrast to conventional drugs, FQ is the first organometallic drug: a ferrocenyl group covalently flanked by a 4-aminoquinoline and a basic alkylamine. FQ is able to overcome the CQ resistance problem, an important limit to the control of Plasmodium falciparum, the principal causative agent of malaria. After fifteen years of effort, it is now possible to propose a multifactorial mechanism of action of FQ by its capacity to target lipids, to inhibit the formation of hemozoin and to generate reactive oxygen species. MDPI 2008-11-20 /pmc/articles/PMC6245066/ /pubmed/19020475 http://dx.doi.org/10.3390/molecules13112900 Text en © 2008 by the authors. Licensee Molecular Diversity Preservation International, Basel, Switzerland. This article is an open-access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/). |
spellingShingle | Review Dubar, Faustine Khalife, Jamal Brocard, Jacques Dive, Daniel Biot, Christophe Ferroquine, an Ingenious Antimalarial Drug –Thoughts on the Mechanism of Action |
title | Ferroquine, an Ingenious Antimalarial Drug –Thoughts on the Mechanism of Action |
title_full | Ferroquine, an Ingenious Antimalarial Drug –Thoughts on the Mechanism of Action |
title_fullStr | Ferroquine, an Ingenious Antimalarial Drug –Thoughts on the Mechanism of Action |
title_full_unstemmed | Ferroquine, an Ingenious Antimalarial Drug –Thoughts on the Mechanism of Action |
title_short | Ferroquine, an Ingenious Antimalarial Drug –Thoughts on the Mechanism of Action |
title_sort | ferroquine, an ingenious antimalarial drug –thoughts on the mechanism of action |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6245066/ https://www.ncbi.nlm.nih.gov/pubmed/19020475 http://dx.doi.org/10.3390/molecules13112900 |
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