Evidence map›Paper›PMID 19020475›Full record

ArticleMolecules (Basel, Switzerland)2008

Ferroquine, an ingenious antimalarial drug: thoughts on the mechanism of action.

Faustine Dubar, Jamal Khalife, Jacques Brocard, Daniel Dive, Christophe Biot

Open access · goldAbstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
4.7field-weighted citation impact, top 5% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

31 citing papers in PubMed, 161 citations in OpenAlex.

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  13. ACS infectious diseases · 2020
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  20. Ferroquine and its derivatives: new generation of antimalarial agents.European journal of medicinal chemistry · 2015
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors at 2 institutions in 1 country.

Faustine DubarUniversité des Sciences et Technologies de Lille, Unité de Catalyse et Chimie du Solide, UMR CNRS 8181, Ecole Nationale Supérieure de Chimie de Lille, Bâtiment C7, Villeneuve d'Ascq Cedex, France. faustine.dubar@free.fr
Jamal Khalife
Jacques Brocard
Daniel Dive
Christophe Biot
École Nationale Supérieure de Chimie de Lille · FRInserm · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

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.

Indexed as

AminoquinolinesAnimalsAntimalarialsDrug ResistanceFerrous CompoundsHeminLipidsMetallocenesPlasmodium falciparumReactive Oxygen SpeciesAminoquinolinesAntimalarialsferroquineFerrous CompoundsHeminLipidsMetallocenesReactive Oxygen Species

Identifiers

PMID19020475
PMCPMC6245066
OpenAlexW2098220218

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.