<?xml version="1.0"?>
<oai_dc:dc xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
  <dc:title>Bioactive bromotyrosine derivatives from the Pacific marine sponge Suberea clavata (Pulitzer-Finali, 1982)</dc:title>
  <dc:creator>Moriou, C.</dc:creator>
  <dc:creator>Lacroix, D.</dc:creator>
  <dc:creator>/Petek, Sylvain</dc:creator>
  <dc:creator>El-Demerdash, A.</dc:creator>
  <dc:creator>Trepos, R.</dc:creator>
  <dc:creator>Leu, T. M.</dc:creator>
  <dc:creator>Florean, C.</dc:creator>
  <dc:creator>Diederich, M.</dc:creator>
  <dc:creator>Hellio, C.</dc:creator>
  <dc:creator>/Debitus, C&#xE9;cile</dc:creator>
  <dc:creator>Al-Mourabit, A.</dc:creator>
  <dc:subject>sponge</dc:subject>
  <dc:subject>Verongiida</dc:subject>
  <dc:subject>Suberea clavata</dc:subject>
  <dc:subject>bromotyrosine</dc:subject>
  <dc:subject>fistularin-3</dc:subject>
  <dc:subject>acetylcholinesterase inhibition</dc:subject>
  <dc:subject>antifouling</dc:subject>
  <dc:description>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.</dc:description>
  <dc:date>2021</dc:date>
  <dc:type>text</dc:type>
  <dc:identifier>https://www.documentation.ird.fr/hor/fdi:010081163</dc:identifier>
  <dc:identifier>fdi:010081163</dc:identifier>
  <dc:identifier>Moriou C., Lacroix D., Petek Sylvain, El-Demerdash A., Trepos R., Leu T. M., Florean C., Diederich M., Hellio C., Debitus C&#xE9;cile, Al-Mourabit A.. Bioactive bromotyrosine derivatives from the Pacific marine sponge Suberea clavata (Pulitzer-Finali, 1982). 2021, 19 (3), 143 [22 ]</dc:identifier>
  <dc:language>EN</dc:language>
  <dc:coverage>PACIFIQUE</dc:coverage>
</oai_dc:dc>
