Statements in which the resource exists.
SubjectPredicateObjectContext
pubmed-article:19762125rdf:typepubmed:Citationlld:pubmed
pubmed-article:19762125lifeskim:mentionsumls-concept:C1257890lld:lifeskim
pubmed-article:19762125lifeskim:mentionsumls-concept:C0031603lld:lifeskim
pubmed-article:19762125lifeskim:mentionsumls-concept:C0006222lld:lifeskim
pubmed-article:19762125lifeskim:mentionsumls-concept:C0007447lld:lifeskim
pubmed-article:19762125lifeskim:mentionsumls-concept:C0028158lld:lifeskim
pubmed-article:19762125lifeskim:mentionsumls-concept:C0014406lld:lifeskim
pubmed-article:19762125lifeskim:mentionsumls-concept:C0441655lld:lifeskim
pubmed-article:19762125lifeskim:mentionsumls-concept:C1280500lld:lifeskim
pubmed-article:19762125lifeskim:mentionsumls-concept:C0002611lld:lifeskim
pubmed-article:19762125lifeskim:mentionsumls-concept:C0243071lld:lifeskim
pubmed-article:19762125lifeskim:mentionsumls-concept:C0068006lld:lifeskim
pubmed-article:19762125lifeskim:mentionsumls-concept:C0205460lld:lifeskim
pubmed-article:19762125pubmed:issue12lld:pubmed
pubmed-article:19762125pubmed:dateCreated2009-11-25lld:pubmed
pubmed-article:19762125pubmed:abstractTextA series of dialkylamino and nitrogen heterocyclic analogues of hexadecylphosphocholine and cetyltrimethylammonium bromide have been synthesized. The prepared compounds exhibit significant cytotoxic, antifungal and antiprotozoal activities. Alkylphosphocholines possess higher antifungal activity against Candida albicans in comparison with quaternary ammonium compounds. However, quaternary ammonium compounds exhibit significant higher activity against human tumor cells and Acanthamoeba lugdunensis compared to alkylphosphocholines. In addition, their haemolytic toxicity has been investigated. The relationship between structure and biological activity of the tested compounds is discussed.lld:pubmed
pubmed-article:19762125pubmed:languageenglld:pubmed
pubmed-article:19762125pubmed:journalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:19762125pubmed:citationSubsetIMlld:pubmed
pubmed-article:19762125pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:19762125pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:19762125pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:19762125pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:19762125pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:19762125pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:19762125pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:19762125pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:19762125pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:19762125pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:19762125pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:19762125pubmed:statusMEDLINElld:pubmed
pubmed-article:19762125pubmed:monthDeclld:pubmed
pubmed-article:19762125pubmed:issn1768-3254lld:pubmed
pubmed-article:19762125pubmed:authorpubmed-author:KarlovskáJank...lld:pubmed
pubmed-article:19762125pubmed:authorpubmed-author:LackoIvanIlld:pubmed
pubmed-article:19762125pubmed:authorpubmed-author:DevínskyFerdi...lld:pubmed
pubmed-article:19762125pubmed:authorpubmed-author:OndriskaFrant...lld:pubmed
pubmed-article:19762125pubmed:authorpubmed-author:MrvaMartinMlld:pubmed
pubmed-article:19762125pubmed:authorpubmed-author:ValentováJind...lld:pubmed
pubmed-article:19762125pubmed:authorpubmed-author:MojzisJánJlld:pubmed
pubmed-article:19762125pubmed:authorpubmed-author:MojzisováGabr...lld:pubmed
pubmed-article:19762125pubmed:authorpubmed-author:LukácMilosMlld:pubmed
pubmed-article:19762125pubmed:authorpubmed-author:BukovskýMariá...lld:pubmed
pubmed-article:19762125pubmed:issnTypeElectroniclld:pubmed
pubmed-article:19762125pubmed:volume44lld:pubmed
pubmed-article:19762125pubmed:ownerNLMlld:pubmed
pubmed-article:19762125pubmed:authorsCompleteYlld:pubmed
pubmed-article:19762125pubmed:pagination4970-7lld:pubmed
pubmed-article:19762125pubmed:meshHeadingpubmed-meshheading:19762125...lld:pubmed
pubmed-article:19762125pubmed:meshHeadingpubmed-meshheading:19762125...lld:pubmed
pubmed-article:19762125pubmed:meshHeadingpubmed-meshheading:19762125...lld:pubmed
pubmed-article:19762125pubmed:meshHeadingpubmed-meshheading:19762125...lld:pubmed
pubmed-article:19762125pubmed:meshHeadingpubmed-meshheading:19762125...lld:pubmed
pubmed-article:19762125pubmed:meshHeadingpubmed-meshheading:19762125...lld:pubmed
pubmed-article:19762125pubmed:meshHeadingpubmed-meshheading:19762125...lld:pubmed
pubmed-article:19762125pubmed:meshHeadingpubmed-meshheading:19762125...lld:pubmed
pubmed-article:19762125pubmed:meshHeadingpubmed-meshheading:19762125...lld:pubmed
pubmed-article:19762125pubmed:meshHeadingpubmed-meshheading:19762125...lld:pubmed
pubmed-article:19762125pubmed:meshHeadingpubmed-meshheading:19762125...lld:pubmed
pubmed-article:19762125pubmed:meshHeadingpubmed-meshheading:19762125...lld:pubmed
pubmed-article:19762125pubmed:meshHeadingpubmed-meshheading:19762125...lld:pubmed
pubmed-article:19762125pubmed:year2009lld:pubmed
pubmed-article:19762125pubmed:articleTitleDialkylamino and nitrogen heterocyclic analogues of hexadecylphosphocholine and cetyltrimetylammonium bromide: effect of phosphate group and environment of the ammonium cation on their biological activity.lld:pubmed
pubmed-article:19762125pubmed:affiliationDepartment of Chemical Theory of Drugs, Faculty of Pharmacy, Comenius University, Kalinciakova 8, 832 32 Bratislava, Slovakia. lukac@fpharm.uniba.sklld:pubmed
pubmed-article:19762125pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:19762125pubmed:publicationTypeResearch Support, Non-U.S. Gov'tlld:pubmed
http://linkedlifedata.com/r...http://linkedlifedata.com/r...pubmed-article:19762125lld:chembl