Please use this identifier to cite or link to this item: http://doi.org/10.25358/openscience-6020
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dc.contributor.authorHäseli, Sascha-
dc.contributor.authorHoly, Marion-
dc.contributor.authorJoksch, Markus-
dc.contributor.authorBergner, Carina-
dc.contributor.authorWree, Andreas-
dc.contributor.authorKurth, Jens-
dc.contributor.authorCankaya, Aylin-
dc.contributor.authorPiel, Markus-
dc.contributor.authorKrause, Bernd J.-
dc.contributor.authorSitte, Harald H.-
dc.contributor.authorRösch, Frank-
dc.date.accessioned2021-06-25T09:16:40Z-
dc.date.available2021-06-25T09:16:40Z-
dc.date.issued2021-
dc.identifier.urihttps://openscience.ub.uni-mainz.de/handle/20.500.12030/6029-
dc.description.abstractThe development of radiometal-labelled pharmaceuticals for neuroimaging could offer great potential due to easier handling during labelling and availability through radionuclide generator systems. Nonetheless, to date, no such tracers are available for positron emission tomography, primarily owing to the challenge of crossing the blood–brain barrier (BBB) and loss of affinity through chelator attachment. We have prepared a variety of 68Ga-labelled phenyltropanes showing that, through a simple hydrocarbon-linker, it is possible to introduce a chelator onto the lead structure while maintaining its high affinity for hDAT (human dopamine transporter) and simultaneously achieving adequate lipophilicity. One of the candidates, [68Ga]Ga-HBED-hexadiyne-tropane, showed an IC50 value of 66 nM, together with a log D7.4 of 0.96. A μPET study in a hemi-parkinsonian rat model showed a fast wash-out of the tracer, and no specific uptake in the brain, thus implying an inability to penetrate the BBB.en_GB
dc.language.isoengde
dc.rightsCC BY-NC-ND*
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subject.ddc540 Chemiede_DE
dc.subject.ddc540 Chemistry and allied sciencesen_GB
dc.title68Ga-labelled tropane analogues for the visualization of the dopaminergic systemen_GB
dc.typeZeitschriftenaufsatzde
dc.identifier.doihttp://doi.org/10.25358/openscience-6020-
jgu.type.dinitypearticleen_GB
jgu.type.versionPublished versionde
jgu.type.resourceTextde
jgu.organisation.departmentFB 09 Chemie, Pharmazie u. Geowissensch.de
jgu.organisation.number7950-
jgu.organisation.nameJohannes Gutenberg-Universität Mainz-
jgu.rights.accessrightsopenAccess-
jgu.journal.titleChemMedChemde
jgu.journal.volume16de
jgu.journal.issue5de
jgu.pages.start804de
jgu.pages.end808de
jgu.publisher.year2021-
jgu.publisher.nameWiley-VCHde
jgu.publisher.placeWeinheim u.a.-
jgu.publisher.urihttps://doi.org/10.1002/cmdc.202000820de
jgu.publisher.issn1860-7187de
jgu.organisation.placeMainz-
jgu.subject.ddccode540de
jgu.publisher.doi10.1002/cmdc.202000820
jgu.organisation.rorhttps://ror.org/023b0x485
Appears in collections:JGU-Publikationen

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