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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%">Moriou, C.</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Lacroix, D.</style>
          </author>
          <author>
            <style face="bold" font="default" size="100%">Petek, Sylvain</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">El-Demerdash, A.</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Trepos, R.</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Leu, T. M.</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Florean, C.</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Diederich, M.</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Hellio, C.</style>
          </author>
          <author>
            <style face="bold" font="default" size="100%">Debitus, Cécile</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Al-Mourabit, A.</style>
          </author>
        </authors>
      </contributors>
      <titles>
        <title>Bioactive bromotyrosine derivatives from the Pacific marine sponge Suberea clavata (Pulitzer-Finali, 1982)</title>
        <secondary-title>Marine Drugs</secondary-title>
      </titles>
      <pages>143 [22 ]</pages>
      <keywords>
        <keyword>sponge</keyword>
        <keyword>Verongiida</keyword>
        <keyword>Suberea clavata</keyword>
        <keyword>bromotyrosine</keyword>
        <keyword>fistularin-3</keyword>
        <keyword>acetylcholinesterase inhibition</keyword>
        <keyword>antifouling</keyword>
        <keyword>PACIFIQUE</keyword>
        <keyword>SALOMON ILES</keyword>
      </keywords>
      <dates>
        <year>2021</year>
      </dates>
      <call-num>fdi:010081163</call-num>
      <language>ENG</language>
      <periodical>
        <full-title>Marine Drugs</full-title>
      </periodical>
      <accession-num>ISI:000633826900001</accession-num>
      <number>3</number>
      <electronic-resource-num>10.3390/md19030143</electronic-resource-num>
      <urls>
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          <url>https://www.documentation.ird.fr/hor/fdi:010081163</url>
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          <url>https://horizon.documentation.ird.fr/exl-doc/pleins_textes/2021-05/010081163.pdf</url>
        </pdf-urls>
      </urls>
      <volume>19</volume>
      <remote-database-provider>Horizon (IRD)</remote-database-provider>
      <abstract>Chemical investigation of the South-Pacific marine sponge Suberea clavata led to the isolation of eight new bromotyrosine metabolites named subereins 1-8 (2-9) along with twelve known co-isolated congeners. The detailed configuration determination of the first representative major compound of this family 11-epi-fistularin-3 (11R,17S) (1) is described. Their chemical characterization was achieved by HRMS and integrated 1D and 2D NMR (nuclear magnetic resonance) spectroscopic studies and extensive comparison with literature data. For the first time, a complete assignment of the absolute configurations for stereogenic centers C-11/17 of the known members (11R,17S) 11-epi-fistularin-3 (1) and 17-deoxyfistularin-3 (10) was determined by a combination of chemical modifications, Mosher's technology, and ECD spectroscopy. Consequently, the absolute configurations of all our new isolated compounds 2-9 were determined by the combination of NMR, Mosher's method, ECD comparison, and chemical modifications. Interestingly, compounds 2-7 were obtained by chemical transformation of the major compound 11-epi-fistularin-3 (1). Evaluation for acetylcholinesterase inhibition (AChE), DNA methyltransferase 1 (DNMT1) modulating activity and antifouling activities using marine bacterial strains are also presented.</abstract>
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