<?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>Homophymines B-E and A1-E1, a family of bioactive cyclodepsipeptides from the sponge Homophymia sp.</dc:title>
  <dc:creator>Zampella, A.</dc:creator>
  <dc:creator>Sepe, V.</dc:creator>
  <dc:creator>Bellotta, F.</dc:creator>
  <dc:creator>Luciano, P.</dc:creator>
  <dc:creator>D'Auria, M. V.</dc:creator>
  <dc:creator>Cresteil, T.</dc:creator>
  <dc:creator>/Debitus, C&#xE9;cile</dc:creator>
  <dc:creator>/Petek, Sylvain</dc:creator>
  <dc:creator>Poupat, C.</dc:creator>
  <dc:creator>Ahond, A.</dc:creator>
  <dc:description>Nine new cyclodepsipeptides, homophymines B-E (2-5) and A1-E1 (1a-5a), were isolated from the polar extracts of the sponge Homophymia sp. The new structures, featuring new polyketide-derived end groups, were determined by interpretation of NMR and MS data. The configurations of the new end groups was secured by the application of J-based configurational analysis. Homophymines displayed very potent antiproliferative activity (IC50 in the nM range) against a panel of human cancer cell lines.</dc:description>
  <dc:date>2009</dc:date>
  <dc:type>text</dc:type>
  <dc:identifier>https://www.documentation.ird.fr/hor/fdi:010056917</dc:identifier>
  <dc:identifier>fdi:010056917</dc:identifier>
  <dc:identifier>Zampella A., Sepe V., Bellotta F., Luciano P., D'Auria M. V., Cresteil T., Debitus C&#xE9;cile, Petek Sylvain, Poupat C., Ahond A.. Homophymines B-E and A1-E1, a family of bioactive cyclodepsipeptides from the sponge Homophymia sp.. 2009, 7 (19),  4037-4044</dc:identifier>
  <dc:language>EN</dc:language>
</oai_dc:dc>
