Statements in which the resource exists.
SubjectPredicateObjectContext
pubmed-article:12197394rdf:typepubmed:Citationlld:pubmed
pubmed-article:12197394lifeskim:mentionsumls-concept:C0027388lld:lifeskim
pubmed-article:12197394lifeskim:mentionsumls-concept:C0301713lld:lifeskim
pubmed-article:12197394lifeskim:mentionsumls-concept:C0220781lld:lifeskim
pubmed-article:12197394lifeskim:mentionsumls-concept:C1883254lld:lifeskim
pubmed-article:12197394lifeskim:mentionsumls-concept:C0057582lld:lifeskim
pubmed-article:12197394lifeskim:mentionsumls-concept:C1705938lld:lifeskim
pubmed-article:12197394lifeskim:mentionsumls-concept:C1527178lld:lifeskim
pubmed-article:12197394lifeskim:mentionsumls-concept:C0740230lld:lifeskim
pubmed-article:12197394pubmed:issue4lld:pubmed
pubmed-article:12197394pubmed:dateCreated2002-8-28lld:pubmed
pubmed-article:12197394pubmed:abstractTextTwo triad systems were synthesized from deuteroporphyrin IX by tethering 1,4-naphthoquinone derivatives and aromatic amino acids to its propionic groups using the method of mixed anhydrides. Physicochemical characteristics of the triads were studied, and the pi-electron systems of their chromophores were shown to interact. The English version of the paper: Russian Journal of Bioorganic Chemistry, 2002, vol. 28, no. 4; see also http://www.maik.ru.lld:pubmed
pubmed-article:12197394pubmed:languageruslld:pubmed
pubmed-article:12197394pubmed:journalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:12197394pubmed:citationSubsetIMlld:pubmed
pubmed-article:12197394pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:12197394pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:12197394pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:12197394pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:12197394pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:12197394pubmed:statusMEDLINElld:pubmed
pubmed-article:12197394pubmed:issn0132-3423lld:pubmed
pubmed-article:12197394pubmed:authorpubmed-author:EvstigneevaR...lld:pubmed
pubmed-article:12197394pubmed:authorpubmed-author:LuzginaV NVNlld:pubmed
pubmed-article:12197394pubmed:authorpubmed-author:LarkinaE AEAlld:pubmed
pubmed-article:12197394pubmed:issnTypePrintlld:pubmed
pubmed-article:12197394pubmed:volume28lld:pubmed
pubmed-article:12197394pubmed:ownerNLMlld:pubmed
pubmed-article:12197394pubmed:authorsCompleteYlld:pubmed
pubmed-article:12197394pubmed:pagination357-61lld:pubmed
pubmed-article:12197394pubmed:dateRevised2006-11-15lld:pubmed
pubmed-article:12197394pubmed:meshHeadingpubmed-meshheading:12197394...lld:pubmed
pubmed-article:12197394pubmed:meshHeadingpubmed-meshheading:12197394...lld:pubmed
pubmed-article:12197394pubmed:meshHeadingpubmed-meshheading:12197394...lld:pubmed
pubmed-article:12197394pubmed:meshHeadingpubmed-meshheading:12197394...lld:pubmed
pubmed-article:12197394pubmed:meshHeadingpubmed-meshheading:12197394...lld:pubmed
pubmed-article:12197394pubmed:meshHeadingpubmed-meshheading:12197394...lld:pubmed
pubmed-article:12197394pubmed:articleTitle[Synthesis of triads based on deuteroporphyrin IX, naphthoquinone, and aromatic amino acids].lld:pubmed
pubmed-article:12197394pubmed:affiliationLomonosov State Academy of Fine Chemical Technology, pr. Vernadskogo 86, Moscow, 117571 Russia.lld:pubmed
pubmed-article:12197394pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:12197394pubmed:publicationTypeEnglish Abstractlld:pubmed