Statements in which the resource exists.
SubjectPredicateObjectContext
pubmed-article:15203135rdf:typepubmed:Citationlld:pubmed
pubmed-article:15203135lifeskim:mentionsumls-concept:C1333201lld:lifeskim
pubmed-article:15203135lifeskim:mentionsumls-concept:C0220781lld:lifeskim
pubmed-article:15203135lifeskim:mentionsumls-concept:C0220825lld:lifeskim
pubmed-article:15203135lifeskim:mentionsumls-concept:C1524075lld:lifeskim
pubmed-article:15203135lifeskim:mentionsumls-concept:C1883254lld:lifeskim
pubmed-article:15203135lifeskim:mentionsumls-concept:C0598631lld:lifeskim
pubmed-article:15203135lifeskim:mentionsumls-concept:C0337112lld:lifeskim
pubmed-article:15203135pubmed:issue14lld:pubmed
pubmed-article:15203135pubmed:dateCreated2004-6-18lld:pubmed
pubmed-article:15203135pubmed:abstractTextThe high lipophilicity of a series of cytosolic phospholipase A(2) inhibitors has been reduced by the modification of a decyloxyphenyl chain designed to mimic the arachidonyl group of the natural substrate. These changes have resulted in an improvement in the whole cell potency of the inhibitors.lld:pubmed
pubmed-article:15203135pubmed:languageenglld:pubmed
pubmed-article:15203135pubmed:journalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:15203135pubmed:citationSubsetIMlld:pubmed
pubmed-article:15203135pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:15203135pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:15203135pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:15203135pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:15203135pubmed:statusMEDLINElld:pubmed
pubmed-article:15203135pubmed:monthJullld:pubmed
pubmed-article:15203135pubmed:issn0960-894Xlld:pubmed
pubmed-article:15203135pubmed:authorpubmed-author:MurrayDavidDlld:pubmed
pubmed-article:15203135pubmed:authorpubmed-author:ConnollySteph...lld:pubmed
pubmed-article:15203135pubmed:authorpubmed-author:BennionColinClld:pubmed
pubmed-article:15203135pubmed:authorpubmed-author:CroshawPamela...lld:pubmed
pubmed-article:15203135pubmed:authorpubmed-author:HardyKimKlld:pubmed
pubmed-article:15203135pubmed:authorpubmed-author:HartoppPaulPlld:pubmed
pubmed-article:15203135pubmed:authorpubmed-author:JacksonClive...lld:pubmed
pubmed-article:15203135pubmed:authorpubmed-author:KingSarah JSJlld:pubmed
pubmed-article:15203135pubmed:authorpubmed-author:LawrenceLouis...lld:pubmed
pubmed-article:15203135pubmed:authorpubmed-author:MeteAntonioAlld:pubmed
pubmed-article:15203135pubmed:authorpubmed-author:RobinsonDavid...lld:pubmed
pubmed-article:15203135pubmed:authorpubmed-author:SteinLindaLlld:pubmed
pubmed-article:15203135pubmed:authorpubmed-author:WaltersIainIlld:pubmed
pubmed-article:15203135pubmed:authorpubmed-author:WellsEdwardElld:pubmed
pubmed-article:15203135pubmed:authorpubmed-author:John...lld:pubmed
pubmed-article:15203135pubmed:issnTypePrintlld:pubmed
pubmed-article:15203135pubmed:day16lld:pubmed
pubmed-article:15203135pubmed:volume14lld:pubmed
pubmed-article:15203135pubmed:ownerNLMlld:pubmed
pubmed-article:15203135pubmed:authorsCompleteYlld:pubmed
pubmed-article:15203135pubmed:pagination3645-9lld:pubmed
pubmed-article:15203135pubmed:dateRevised2007-11-15lld:pubmed
pubmed-article:15203135pubmed:meshHeadingpubmed-meshheading:15203135...lld:pubmed
pubmed-article:15203135pubmed:meshHeadingpubmed-meshheading:15203135...lld:pubmed
pubmed-article:15203135pubmed:meshHeadingpubmed-meshheading:15203135...lld:pubmed
pubmed-article:15203135pubmed:meshHeadingpubmed-meshheading:15203135...lld:pubmed
pubmed-article:15203135pubmed:meshHeadingpubmed-meshheading:15203135...lld:pubmed
pubmed-article:15203135pubmed:meshHeadingpubmed-meshheading:15203135...lld:pubmed
pubmed-article:15203135pubmed:meshHeadingpubmed-meshheading:15203135...lld:pubmed
pubmed-article:15203135pubmed:meshHeadingpubmed-meshheading:15203135...lld:pubmed
pubmed-article:15203135pubmed:meshHeadingpubmed-meshheading:15203135...lld:pubmed
pubmed-article:15203135pubmed:meshHeadingpubmed-meshheading:15203135...lld:pubmed
pubmed-article:15203135pubmed:year2004lld:pubmed
pubmed-article:15203135pubmed:articleTitleSynthesis and evaluation of substrate-mimicking cytosolic phospholipase A2 inhibitors--reducing the lipophilicity of the arachidonyl chain isostere.lld:pubmed
pubmed-article:15203135pubmed:affiliationDepartments of Medicinal Chemistry, Molecular Biology, and Discovery BioScience, AstraZeneca R&D Charnwood, Bakewell Road, Loughborough, Leicestershire LE11 5RH, United Kingdom. iain.walters@astrazeneca.comlld:pubmed
pubmed-article:15203135pubmed:publicationTypeJournal Articlelld:pubmed
http://linkedlifedata.com/r...http://linkedlifedata.com/r...pubmed-article:15203135lld:chembl