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dc.contributor.authorSENGE, MATHIASen
dc.contributor.authorSERGEEVA, NATALIAen
dc.contributor.authorDAVIES, ANTHONYen
dc.date.accessioned2011-08-15T13:53:52Z
dc.date.available2011-08-15T13:53:52Z
dc.date.issued2011en
dc.date.submitted2011en
dc.identifier.citationNatalia N. Sergeeva, Marion Donnier-Marechal, Gisela M. Vaz, Anthony M. Davies, Mathias O. Senge, Simple but powerful: Phenanthroline-based small molecules for cellular imaging and cancer screening, Bioorganic & Medicinal Chemistry Letters, 21, 15, 2011, 4385-4388en
dc.identifier.otherYen
dc.descriptionPUBLISHEDen
dc.description.abstractA two-step synthetic procedure gives highly fluorescent phenanthroline molecular probes. The compounds localize in the endoplasmic reticulum and their potential as bioactive probes was evaluated. The materials are quickly taken up by living cells within 5 min. Preliminary in vitro studies have shown that these compounds are selective to esophageal cancer cells and can be used as selective markers in intracellular cancer diagnostics. The materials show a remarkable cytotoxicity towards cancer cells vs. normal as 7 to 1.en
dc.format.extent4385-4388en
dc.language.isoenen
dc.relation.ispartofseriesBioorganic & Medicinal Chemistry Lettersen
dc.relation.ispartofseries21en
dc.relation.ispartofseries15en
dc.rightsYen
dc.subjectOncologyen
dc.subjectEsophageal canceren
dc.titleSimple but powerful: Phenanthroline-based small molecules for cellular imaging and cancer screeningen
dc.typeJournal Articleen
dc.type.supercollectionscholarly_publicationsen
dc.type.supercollectionrefereed_publicationsen
dc.identifier.peoplefinderurlhttp://people.tcd.ie/sengemen
dc.identifier.peoplefinderurlhttp://people.tcd.ie/amitcheen
dc.identifier.rssinternalid73708en
dc.subject.TCDThemeCanceren
dc.identifier.rssurihttp://dx.doi.org/10.1016/j.bmcl.2011.06.051en
dc.contributor.sponsorHealth Research Board (HRB)en
dc.contributor.sponsorGrantNumberTRA/2007/11en
dc.contributor.sponsorScience Foundation Ireland (SFI)en
dc.contributor.sponsorGrantNumber09/IN.1/B2650en
dc.identifier.urihttp://hdl.handle.net/2262/58662


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