<oai_dc:dc xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" 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:creator>Caron G</dc:creator>
  <dc:creator>Reymond F</dc:creator>
  <dc:creator>Carrupt PA</dc:creator>
  <dc:creator>Girault HH</dc:creator>
  <dc:creator>Testa B</dc:creator>
  <dc:date>1999</dc:date>
  <dc:description xmlns:ns0="xml" ns0:lang="en">Traditional lipophilicity parameters (log P and log D) are well-known physico-chemical descriptors largely used in QSAR studies. Besides their numerical value, log P data contain a variety of information about inter- and intramolecular forces affecting partitioning and its related biological phenomena. The deconvolution of information from log P can be accessed only by adequate interpretative tools, such as new lipophilic-combined descriptors, of which features and some applications are presented in this review.</dc:description>
  <dc:identifier>https://sonar.ch/global/documents/981</dc:identifier>
  <dc:language>eng</dc:language>
  <dc:relation>info:eu-repo/semantics/altIdentifier/doi/10.1016/s1461-5347(99)00180-7</dc:relation>
  <dc:relation>info:eu-repo/semantics/altIdentifier/pmid/10441277</dc:relation>
  <dc:source>Pharmaceutical science &amp; technology today. - 1999</dc:source>
  <dc:title xmlns:ns1="xml" ns1:lang="en">Combined molecular lipophilicity descriptors and their role in understanding intramolecular effects.</dc:title>
  <dc:type>http://purl.org/coar/resource_type/c_6501</dc:type>
</oai_dc:dc>