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      <ref-type name="Journal Article">17</ref-type>
      <work-type>ACL : Articles dans des revues avec comité de lecture répertoriées par l'AERES</work-type>
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        <authors>
          <author>
            <style face="normal" font="default" size="100%">Cachet, N.</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Hoakwie, F.</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Bertani, S.</style>
          </author>
          <author>
            <style face="bold" font="default" size="100%">Bourdy, Geneviève</style>
          </author>
          <author>
            <style face="bold" font="default" size="100%">Deharo, Eric</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Stien, D.</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Houel, E.</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Gornitzka, H.</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Fillaux, J.</style>
          </author>
          <author>
            <style face="bold" font="default" size="100%">Chevalley, Séverine</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Valentin, A.</style>
          </author>
          <author>
            <style face="bold" font="default" size="100%">Jullian, Valérie</style>
          </author>
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      <titles>
        <title>Antimalarial activity of simalikalactone E, a new quassinoid from Quassia amara L. (Simaroubaceae)</title>
        <secondary-title>Antimicrobial Agents and Chemotherapy</secondary-title>
      </titles>
      <pages>4393-4398</pages>
      <dates>
        <year>2009</year>
      </dates>
      <call-num>PAR00004140</call-num>
      <language>ENG</language>
      <periodical>
        <full-title>Antimicrobial Agents and Chemotherapy</full-title>
      </periodical>
      <isbn>0066-4804</isbn>
      <accession-num>ISI:000270020600047</accession-num>
      <number>10</number>
      <electronic-resource-num>10.1128/aac.00951-09</electronic-resource-num>
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          <url>https://www.documentation.ird.fr/intranet/publi/2024-01/010086178.pdf</url>
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      <volume>53</volume>
      <remote-database-provider>Horizon (IRD)</remote-database-provider>
      <abstract>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.</abstract>
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