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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>
      <contributors>
        <authors>
          <author>
            <style face="normal" font="default" size="100%">Boufridi, A.</style>
          </author>
          <author>
            <style face="bold" font="default" size="100%">Petek, Sylvain</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Evanno, L.</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Beniddir, M.A.</style>
          </author>
          <author>
            <style face="bold" font="default" size="100%">Debitus, Cécile</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Buisson, D.</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Poupon, E.</style>
          </author>
        </authors>
      </contributors>
      <titles>
        <title>Biotransformations versus chemical modifications : new cytotoxic analogs of marine sesquiterpene ilimaquinone [plus Supporting information]</title>
        <secondary-title>Tetrahedron Letters</secondary-title>
      </titles>
      <pages>4922-4925 [+ 12 ]</pages>
      <dates>
        <year>2016</year>
      </dates>
      <call-num>fdi:010068406</call-num>
      <language>ENG</language>
      <periodical>
        <full-title>Tetrahedron Letters</full-title>
      </periodical>
      <isbn>0040-4039</isbn>
      <accession-num>ISI:000386415300011</accession-num>
      <number>44</number>
      <electronic-resource-num>10.1016/j.tetlet.2016.09.075</electronic-resource-num>
      <urls>
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          <url>https://www.documentation.ird.fr/hor/fdi:010068406</url>
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        <pdf-urls>
          <url>https://www.documentation.ird.fr/intranet/publi/depot/2016-10-19/010068406.pdf</url>
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      <volume>57</volume>
      <remote-database-provider>Horizon (IRD)</remote-database-provider>
      <abstract>Highly biologically active marine sesquiterpene ilimaquinone was selected for chemical modifications. Its biotransformation was investigated using a combinatorial approach as an original way to screen different strains of microorganisms. Mucor circinelloides ATCC 8541 was able to structurally modify ilimaquinone into three different compounds. A stereospecific epoxidation was observed and compared to chemical epoxidation. A hydroxylation of the decalin ring was also observed as well as an unexpected substitution on the quinone ring by ethanolamine. Compounds were evaluated against several cell lines.</abstract>
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