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Antimicrobial Agents and Chemotherapy, April 2008, p. 1215-1220, Vol. 52, No. 4
0066-4804/08/$08.00+0 doi:10.1128/AAC.01043-07
Copyright © 2008, American Society for Microbiology. All Rights Reserved.
New Active Drugs against Liver Stages of Plasmodium Predicted by Molecular Topology
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Nassira Mahmoudi,1,2*
Ramon Garcia-Domenech,3
Jorge Galvez,3
Khemais Farhati,1,2
Jean-François Franetich,1,2
Robert Sauerwein,4
Laurent Hannoun,5
Francis Derouin,6
Martin Danis,1,2,7 and
Dominique Mazier1,2,7*
Université Pierre et Marie Curie-Paris 6, UMR S511, Paris F-75013, France,1 INSERM, U511, Paris F-75013, France,2 Unidad de Investigación de Diseño de Fármacos y Conectividad Molecular, Dep. Química Física, Facultad de Farmacia, Universitat de València, Burjassot, Valencia, Spain,3 Department of Medical Microbiology, University of Nijmengen, Nijmengen, The Netherlands,4 AP-HP, Groupe Hospitalier Pitié-Salpêtrière, Service de Chirurgie Digestive Hépato-Bilio-Pancréatique et de Transplantation Hépatique, Paris F-75013, France,5 Laboratoire de Parasitologie-Mycologie, and Hôpital Saint-Louis, Assistance Publique-Hôpitaux de Paris 1, Avenue Claude Vellefaux, 75010 Paris, France,6 AP-HP, Groupe Hospitalier Pitié-Salpêtrière, Service Parasitologie-Mycologie, Paris F-75013, France7
Received 8 August 2007/ Returned for modification 31 October 2007/ Accepted 13 January 2008
We conducted a quantitative structure-activity relationship (QSAR) study based on a database of 127 compounds previously tested against the liver stage of Plasmodium yoelii in order to develop a model capable of predicting the in vitro antimalarial activities of new compounds. Topological indices were used as structural descriptors, and their relation to antimalarial activity was determined by using linear discriminant analysis. A topological model consisting of two discriminant functions was created. The first function discriminated between active and inactive compounds, and the second identified the most active among the active compounds. The model was then applied sequentially to a large database of compounds with unknown activity against liver stages of Plasmodium. Seventeen drugs that were predicted to be active or inactive were selected for testing against the hepatic stage of P. yoelii in vitro. Antiretroviral, antifungal, and cardiotonic drugs were found to be highly active (nanomolar 50% inhibitory concentration values), and two ionophores completely inhibited parasite development. The 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay was performed on hepatocyte cultures for all compounds, and none of these compounds were toxic in vitro. For both ionophores, the same in vitro assay as those for P. yoelii has confirmed their in vitro activities on Plasmodium falciparum. A similar topological model was used to estimate the octanol/water partition of each compound. These results demonstrate the utility of the QSAR and molecular topology approaches for identifying new drugs that are active against the hepatic stage of malaria parasites. We also show the remarkable efficacy of some drugs that were not previously reported to have antiparasitic activity.
* Corresponding author. Mailing address: Université Pierre et Marie Curie-Paris 6, UMR S511, Paris F-75013, France. Phone: 33140779736. Fax: 33145838858. E-mail for Nassira Mahmoudi: nassira{at}netcourrier.com. E-mail for Dominique Mazier: mazier{at}chups.jussieu.fr
Published ahead of print on 22 January 2008.
Supplemental material for this article may be found at http://aac.asm.org/.
Antimicrobial Agents and Chemotherapy, April 2008, p. 1215-1220, Vol. 52, No. 4
0066-4804/08/$08.00+0 doi:10.1128/AAC.01043-07
Copyright © 2008, American Society for Microbiology. All Rights Reserved.
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