Statements in which the resource exists.
SubjectPredicateObjectContext
pubmed-article:18444231rdf:typepubmed:Citationlld:pubmed
pubmed-article:18444231lifeskim:mentionsumls-concept:C0009263lld:lifeskim
pubmed-article:18444231lifeskim:mentionsumls-concept:C0009262lld:lifeskim
pubmed-article:18444231lifeskim:mentionsumls-concept:C0439849lld:lifeskim
pubmed-article:18444231lifeskim:mentionsumls-concept:C0679199lld:lifeskim
pubmed-article:18444231lifeskim:mentionsumls-concept:C0445223lld:lifeskim
pubmed-article:18444231lifeskim:mentionsumls-concept:C0449851lld:lifeskim
pubmed-article:18444231lifeskim:mentionsumls-concept:C0085973lld:lifeskim
pubmed-article:18444231lifeskim:mentionsumls-concept:C0243071lld:lifeskim
pubmed-article:18444231lifeskim:mentionsumls-concept:C1552599lld:lifeskim
pubmed-article:18444231lifeskim:mentionsumls-concept:C1704787lld:lifeskim
pubmed-article:18444231pubmed:issue5lld:pubmed
pubmed-article:18444231pubmed:dateCreated2008-9-2lld:pubmed
pubmed-article:18444231pubmed:abstractTextAs a part of a project designed to investigate Colchicum species in Jordan, the chemical constituents of Colchicum crocifolium Boiss. (Colchicaceae) were investigated using LC-MS and LC-UV/Vis PDA. A decision tree for working with colchicinods has been developed by incorporating data from LC-UV/PDA and LC-MS. This dereplication strategy draws upon the UV/PDA spectra to classify compounds into one of four structural groups and combines this with retention time and mass spectra/molecular weight to identify the compounds. This strategy was applied on a small amount of extract (2 mg) of Colchicum crocifolium to dereplicate 10 known compounds from four different structural groups, namely (-)-demecolcine, 2-demethyl-(-)-colchicine or 3-demethyl-(-)-colchicine, N-deacetyl-(-)-colchicine, (-)-colchiciline, (-)-colchicine, beta-lumidemecolcine, 2-demethyl-beta-lumicolchicine or 3-demethyl-beta-lumicolchicine, N,N-dimethyl-N-deacetyl-beta-lumicornigerine, (-)-isoandrocymbine and (-)-autumnaline. Furthermore, a new compound was identi?ed as N,N-dimethyl-N-deacetyl-(-)-cornigerine. Three compounds, which had molecular ions at m/z 325, 340 and 374, could not be dereplicated into any obvious structural classes that have been isolated in our laboratories previously or reported in the literature.lld:pubmed
pubmed-article:18444231pubmed:languageenglld:pubmed
pubmed-article:18444231pubmed:journalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:18444231pubmed:citationSubsetIMlld:pubmed
pubmed-article:18444231pubmed:chemicalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:18444231pubmed:statusMEDLINElld:pubmed
pubmed-article:18444231pubmed:monthSeplld:pubmed
pubmed-article:18444231pubmed:issn1099-1565lld:pubmed
pubmed-article:18444231pubmed:authorpubmed-author:OberliesNicho...lld:pubmed
pubmed-article:18444231pubmed:authorpubmed-author:AlaliFeras...lld:pubmed
pubmed-article:18444231pubmed:authorpubmed-author:TawahaKhaledKlld:pubmed
pubmed-article:18444231pubmed:authorpubmed-author:GharaibehAhma...lld:pubmed
pubmed-article:18444231pubmed:authorpubmed-author:GhawanmehAbdu...lld:pubmed
pubmed-article:18444231pubmed:issnTypeElectroniclld:pubmed
pubmed-article:18444231pubmed:volume19lld:pubmed
pubmed-article:18444231pubmed:ownerNLMlld:pubmed
pubmed-article:18444231pubmed:authorsCompleteYlld:pubmed
pubmed-article:18444231pubmed:pagination385-94lld:pubmed
pubmed-article:18444231pubmed:meshHeadingpubmed-meshheading:18444231...lld:pubmed
pubmed-article:18444231pubmed:meshHeadingpubmed-meshheading:18444231...lld:pubmed
pubmed-article:18444231pubmed:meshHeadingpubmed-meshheading:18444231...lld:pubmed
pubmed-article:18444231pubmed:meshHeadingpubmed-meshheading:18444231...lld:pubmed
pubmed-article:18444231pubmed:meshHeadingpubmed-meshheading:18444231...lld:pubmed
pubmed-article:18444231pubmed:meshHeadingpubmed-meshheading:18444231...lld:pubmed
pubmed-article:18444231pubmed:year2008lld:pubmed
pubmed-article:18444231pubmed:articleTitleColchicinoids from Colchicum crocifolium Boiss.: a case study in dereplication strategies for (-)-colchicine and related analogues using LC-MS and LC-PDA techniques.lld:pubmed
pubmed-article:18444231pubmed:affiliationDepartment of Medicinal Chemistry and Pharmacognosy, Faculty of Pharmacy, Jordan University of Science and Technology, PO Box 3030, Irbid 22110, Jordan. falali@just.edu.jolld:pubmed
pubmed-article:18444231pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:18444231pubmed:publicationTypeResearch Support, Non-U.S. Gov'tlld:pubmed
http://linkedlifedata.com/r...pubmed:referesTopubmed-article:18444231lld:pubmed