dc.creatorEstébanez, Sandra
dc.creatorThomas, Andrés Héctor
dc.creatorLorente, Carolina
dc.date.accessioned2018-11-06T19:07:42Z
dc.date.accessioned2022-10-15T15:45:33Z
dc.date.available2018-11-06T19:07:42Z
dc.date.available2022-10-15T15:45:33Z
dc.date.created2018-11-06T19:07:42Z
dc.date.issued2017-11
dc.identifierEstébanez, Sandra; Thomas, Andrés Héctor; Lorente, Carolina; Deoxythymidine–Pterin Fluorescent Adduct Formation through a Photosensitized Process; Wiley VCH Verlag; Chemphyschem; 19; 3; 11-2017; 300-306
dc.identifier1439-4235
dc.identifierhttp://hdl.handle.net/11336/63805
dc.identifierCONICET Digital
dc.identifierCONICET
dc.identifier.urihttps://repositorioslatinoamericanos.uchile.cl/handle/2250/4404713
dc.description.abstractA new fluorescent compound was isolated from UVA-irradiated aqueous solutions containing pterin (Ptr) and 2′deoxythymidine (dT) in anaerobic conditions. Pterins are widespread in living systems in small amounts, but they are accumulated in some pathological situations. Under UVA radiation, pterins are photochemically active, fluorescent, and photosensitize the generation of singlet oxygen [1O2(1Δg)]. The isolated compound was structurally characterized by using liquid chromatography coupled to tandem mass spectrometry, and its photophysical properties were studied with the time-correlated single-photon-counting technique. The molecular weight and the analysis of the fragmentation correspond to a molecule where the pterinic moiety is attached to the thymine nucleobase. The product exhibits photophysical properties similar to those of Ptr, including relatively high fluorescence and 1O2 production quantum yields.
dc.languageeng
dc.publisherWiley VCH Verlag
dc.relationinfo:eu-repo/semantics/altIdentifier/doi/http://dx.doi.org/10.1002/cphc.201701101
dc.relationinfo:eu-repo/semantics/altIdentifier/url/https://onlinelibrary.wiley.com/doi/abs/10.1002/cphc.201701101
dc.rightshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subject2′-DEOXYTHYMIDINE
dc.subjectELECTRON TRANSFER
dc.subjectPHOTOSENSITIZATION
dc.subjectPTERINS
dc.subjectRADICALS
dc.titleDeoxythymidine–Pterin Fluorescent Adduct Formation through a Photosensitized Process
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:ar-repo/semantics/artículo
dc.typeinfo:eu-repo/semantics/publishedVersion


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