Serveur d'exploration Chloroquine

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The antimalarial ferroquine: from bench to clinic.

Identifieur interne : 001462 ( Main/Exploration ); précédent : 001461; suivant : 001463

The antimalarial ferroquine: from bench to clinic.

Auteurs : Christophe Biot [France] ; F. Nosten [Royaume-Uni] ; L. Fraisse [France] ; D. Ter-Minassian [France] ; Jamal Khalife [France] ; Daniel Dive [France]

Source :

RBID : Hal:hal-00642112

Descripteurs français

English descriptors

Abstract

Ferroquine (FQ, SSR97193) is currently the most advanced organometallic drug candidate and about to complete phase II clinical trials as a treatment for uncomplicated malaria. This ferrocenecontaining compound is active against both chloroquine-susceptible and chloroquine-resistant Plasmodium falciparum and P. vivax strains and/or isolates. This article focuses on the discovery of FQ, its antimalarial activity, the hypothesis of its mode of action, the current absence of resistance in vitro and recent clinical trials.


Url:
DOI: 10.1051/parasite/2011183207


Affiliations:


Links toward previous steps (curation, corpus...)


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<name sortKey="Dive, Daniel" sort="Dive, Daniel" uniqKey="Dive D" first="Daniel" last="Dive">Daniel Dive</name>
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<orgName>Centre d’Infection et d’Immunité de Lille (CIIL) - U1019 - UMR 8204</orgName>
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<addrLine>1 Rue du Professeur Calmette - Lille Cedex - 59019 - BP 245</addrLine>
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<addrLine>25, rue du Dr Roux 75724 Paris Cedex 15</addrLine>
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</address>
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<addrLine>101, rue de Tolbiac, 75013 Paris </addrLine>
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<addrLine>Lille</addrLine>
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<orgName type="acronym">CNRS</orgName>
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</hal:affiliation>
<country>France</country>
</affiliation>
</author>
</analytic>
<idno type="DOI">10.1051/parasite/2011183207</idno>
<series>
<title level="j">Parasite</title>
<idno type="ISSN">1252-607X</idno>
<imprint>
<date type="datePub">2011</date>
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<keywords scheme="mix" xml:lang="en">
<term>bioorganometallics</term>
<term>drug candidate</term>
<term>ferroquine</term>
<term>malaria</term>
<term>mechanism of action</term>
<term>resistance</term>
</keywords>
<keywords scheme="mix" xml:lang="fr">
<term>bio-organométallique</term>
<term>candidat médicament</term>
<term>ferroquine</term>
<term>mécanisme d’action</term>
<term>paludisme</term>
<term>résistance</term>
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<front>
<div type="abstract" xml:lang="en">
<p>Ferroquine (FQ, SSR97193) is currently the most advanced organometallic drug candidate and about to complete phase II clinical trials as a treatment for uncomplicated malaria. This ferrocenecontaining compound is active against both chloroquine-susceptible and chloroquine-resistant Plasmodium falciparum and P. vivax strains and/or isolates. This article focuses on the discovery of FQ, its antimalarial activity, the hypothesis of its mode of action, the current absence of resistance in vitro and recent clinical trials.</p>
</div>
</front>
</TEI>
<affiliations>
<list>
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<li>France</li>
<li>Royaume-Uni</li>
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<name sortKey="Biot, Christophe" sort="Biot, Christophe" uniqKey="Biot C" first="Christophe" last="Biot">Christophe Biot</name>
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<name sortKey="Dive, Daniel" sort="Dive, Daniel" uniqKey="Dive D" first="Daniel" last="Dive">Daniel Dive</name>
<name sortKey="Fraisse, L" sort="Fraisse, L" uniqKey="Fraisse L" first="L." last="Fraisse">L. Fraisse</name>
<name sortKey="Khalife, Jamal" sort="Khalife, Jamal" uniqKey="Khalife J" first="Jamal" last="Khalife">Jamal Khalife</name>
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<name sortKey="Nosten, F" sort="Nosten, F" uniqKey="Nosten F" first="F." last="Nosten">F. Nosten</name>
</noRegion>
</country>
</tree>
</affiliations>
</record>

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