<?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>Unguiculins A-C : cytotoxic bis-guanidine alkaloids from the French Polynesian sponge, Monanchora n. sp.</dc:title>
  <dc:creator>El-Demerdash, A.</dc:creator>
  <dc:creator>Moriou, C.</dc:creator>
  <dc:creator>Martin, M. T.</dc:creator>
  <dc:creator>/Petek, Sylvain</dc:creator>
  <dc:creator>/Debitus, C&#xE9;cile</dc:creator>
  <dc:creator>Al-Mourabit, A.</dc:creator>
  <dc:subject>Monanchora</dc:subject>
  <dc:subject>Crambeidae</dc:subject>
  <dc:subject>unguiculin</dc:subject>
  <dc:subject>guanidine</dc:subject>
  <dc:subject>spermidine alkaloid</dc:subject>
  <dc:description>Two new acyclic bis-guanidine alkaloids, unguiculins B-C (2-3), were isolated from a French Polynesian sponge Monanchora n. sp. together with the known compound unguiculin A (1). Their structures were established by spectroscopic data interpretation and comparison with the literature. Unguiculins A-C displayed antiproliferative and cytotoxic efficacy against several human cancer cells with IC50 values in the micromolar range. [GRAPHICS] .</dc:description>
  <dc:date>2018</dc:date>
  <dc:type>text</dc:type>
  <dc:identifier>https://www.documentation.ird.fr/hor/fdi:010073062</dc:identifier>
  <dc:identifier>fdi:010073062</dc:identifier>
  <dc:identifier>El-Demerdash A., Moriou C., Martin M. T., Petek Sylvain, Debitus C&#xE9;cile, Al-Mourabit A.. Unguiculins A-C : cytotoxic bis-guanidine alkaloids from the French Polynesian sponge, Monanchora n. sp.. 2018, 32 (13),  1512-1517</dc:identifier>
  <dc:language>EN</dc:language>
  <dc:coverage>PACIFIQUE</dc:coverage>
  <dc:coverage>POLYNESIE FRANCAISE</dc:coverage>
</oai_dc:dc>
