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<OAI-PMH schemaLocation=http://www.openarchives.org/OAI/2.0/ http://www.openarchives.org/OAI/2.0/OAI-PMH.xsd> <responseDate>2018-01-15T18:29:47Z</responseDate> <request identifier=oai:HAL:hal-01032126v1 verb=GetRecord metadataPrefix=oai_dc>http://api.archives-ouvertes.fr/oai/hal/</request> <GetRecord> <record> <header> <identifier>oai:HAL:hal-01032126v1</identifier> <datestamp>2018-01-11</datestamp> <setSpec>type:ART</setSpec> <setSpec>subject:sdv</setSpec> <setSpec>collection:CNRS</setSpec> <setSpec>collection:UNIV-AG</setSpec> <setSpec>collection:CIRAD</setSpec> <setSpec>collection:MNHN</setSpec> <setSpec>collection:AGROPARISTECH</setSpec> <setSpec>collection:INRA</setSpec> <setSpec>collection:ECOFOG</setSpec> </header> <metadata><dc> <publisher>HAL CCSD</publisher> <title lang=en>Antimalarial activity of simalikalactone E, a new quassinoid from quassia amara L (simaroubaceae)</title> <creator>Cachet, N.</creator> <creator>Hoakwie, Franciane</creator> <creator>Bertani, Stéphanie</creator> <creator>Bourdy, Geneviève</creator> <creator>Deharo, Eric</creator> <creator>Stien, Didier</creator> <creator>Houel, Emeline</creator> <creator>Gornitzka, Heinz</creator> <creator>Fillaux, Judith</creator> <creator>Chevalley, S.</creator> <creator>Valentin, Alexis</creator> <creator>Jullian, V.</creator> <contributor>UMR 152, UPS, Laboratoire de Pharmacochimie des Substances Naturelles et Pharmacophores Redox ; Université de Toulouse</contributor> <contributor>UMR 152 ; Institut de Recherche pour le Développement (IRD)</contributor> <contributor>USM 0307, Laboratoire de Parasitologie Comparée et Modèles Expérimentaux ; Muséum National d'Histoire Naturelle (MNHN)</contributor> <contributor>Ecologie des forêts de Guyane (ECOFOG) ; Centre de Coopération Internationale en Recherche Agronomique pour le Développement (CIRAD) - Institut National de la Recherche Agronomique (INRA) - Université des Antilles et de la Guyane (UAG) - AgroParisTech - Centre National de la Recherche Scientifique (CNRS)</contributor> <contributor>LCC, UPR 8241 ; Centre National de la Recherche Scientifique (CNRS)</contributor> <contributor>Service de Parasitologie-Mycologie, CHU Rangueil ; Centre Hospitalier Universitaire de Toulouse</contributor> <description> </description> <source>ISSN: 0066-4804</source> <source>EISSN: 1098-6596</source> <source>Antimicrobial Agents and Chemotherapy</source> <publisher>American Society for Microbiology</publisher> <identifier>hal-01032126</identifier> <identifier>https://hal.archives-ouvertes.fr/hal-01032126</identifier> <source>https://hal.archives-ouvertes.fr/hal-01032126</source> <source>Antimicrobial Agents and Chemotherapy, American Society for Microbiology, 2009, 53 (10), pp.4393-4398. 〈10.1128/AAC.00951-09〉</source> <identifier>DOI : 10.1128/AAC.00951-09</identifier> <relation>info:eu-repo/semantics/altIdentifier/doi/10.1128/AAC.00951-09</relation> <language>en</language> <subject lang=en> </subject> <subject>[SDV.SA] Life Sciences [q-bio]/Agricultural sciences</subject> <type>info:eu-repo/semantics/article</type> <type>Journal articles</type> <description lang=en>We report the isolation and identification of a new quassinoid named simalikalactone E (SkE), extracted from a widely used Amazonian antimalarial remedy made out of Quassia amara L. (Simaroubaceae) leaves. This new molecule inhibited the growth of Plasmodium falciparum cultured in vitro by 50%, in the concentration range from 24 to 68 nM, independently of the strain sensitivity to chloroquine. We also showed that this compound was able to decrease gametocytemia with a 50% inhibitory concentration sevenfold lower than that of primaquine. SkE was found to be less toxic than simalikalactone D (SkD), another antimalarial quassinoid from Q. amara, and its cytotoxicity on mammalian cells was dependent on the cell line, displaying a good selectivity index when tested on nontumorogenic cells. In vivo, SkE inhibited murine malaria growth of Plasmodium vinckei petteri by 50% at 1 and 0.5 mg/kg of body weight/day, by the oral or intraperitoneal routes, respectively. The contribution of quassinoids as a source of antimalarial molecules needs therefore to be reconsidered.</description> <date>2009</date> </dc> </metadata> </record> </GetRecord> </OAI-PMH>