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dc.contributor.authorSCANLAN, EOINen
dc.contributor.authorSENGE, MATHIASen
dc.date.accessioned2015-05-06T14:27:15Z
dc.date.available2015-05-06T14:27:15Z
dc.date.issued2012en
dc.date.submitted2012en
dc.identifier.citationDaly R, Vaz G, Davies AM, Senge MO, Scanlan EM, Synthesis and biological evaluation of a library of glycoporphyrin compounds., Chemistry (Weinheim an der Bergstrasse, Germany), 18, 46, 2012, 14671-9en
dc.identifier.otherYen
dc.identifier.urihttp://hdl.handle.net/2262/73859
dc.descriptionPUBLISHEDen
dc.descriptionPubMed ID: 23018896en
dc.description.abstractA library of glycosylated porphyrins (Glycoporphyrins) was prepared and evaluated for their PDT activity against oesophageal squamous cell carcinoma cell line OE21 in vitro. Synthetic methodology was developed to allow incorporation of biologically active carbohydrates including the histo blood group antigen trisaccharide, Lewis x onto the porphyrin backbone. The effect of the carbohydrate group and substitution pattern on the PDT activity, cell uptake and subcellular localisation of the glycoporphyrin compounds is reported.en
dc.description.sponsorshipThis work was supported by grants from the School of Chemistry (TCD), the Health Research Board (translational research award 2007 TRA/2007/11), Science Foundation Ireland (SFI P.I. 09/IN.1/B2650) Fundac?o da Ciencia e Tecnologia (SFRH / BD / 62364 / 2009) and IRCSET.en
dc.format.extent14671-9en
dc.language.isoenen
dc.relation.ispartofseriesChemistry (Weinheim an der Bergstrasse, Germany)en
dc.relation.ispartofseries18en
dc.relation.ispartofseries46en
dc.rightsYen
dc.titleSynthesis and biological evaluation of a library of glycoporphyrin compounds.en
dc.typeJournal Articleen
dc.type.supercollectionscholarly_publicationsen
dc.type.supercollectionrefereed_publicationsen
dc.identifier.peoplefinderurlhttp://people.tcd.ie/scanlaeen
dc.identifier.peoplefinderurlhttp://people.tcd.ie/sengemen
dc.identifier.rssinternalid83167en
dc.identifier.doihttp://dx.doi.org/10.1002/chem.201202064en
dc.rights.ecaccessrightsOpenAccess
dc.subject.TCDThemeCanceren


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