Development of 18F-Labeled Radiotracers for PET Imaging of the Adenosine A2A Receptor: Synthesis, Radiolabeling and Preliminary Biological Evaluation (original ) (raw )Development of a Radiofluorinated Adenosine A2B Receptor Antagonist as Potential Ligand for PET Imaging
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International Journal of Molecular Sciences, 2020
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Development of [ 18 F]-Labeled Pyrazolo[4,3- e ]-1,2,4- triazolo[1,5- c ]pyrimidine (SCH442416) Analogs for the Imaging of Cerebral Adenosine A 2A Receptors with Positron Emission Tomography
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Journal of Medicinal Chemistry, 2014
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{"__content__"=>"Preclinical evaluation of the first adenosine A receptor partial agonist radioligand for positron emission tomography (PET) imaging.", "sub"=>{"__content__"=>"1"}}
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Journal of medicinal chemistry, 2018
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Journal of medicinal chemistry, 2014
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Automatisation and First Evaluation of [18F]FE@SUPPY:2, an Alternative PET-Tracer for the Adenosine A3 Receptor: A Comparison with [18F]FE@SUPPY
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The Open Nuclear Medicine Journal, 2009
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The use of [18F]4-fluorobenzyl iodide (FBI) in PET radiotracer synthesis: Model alkylation studies and its application in the design of dopamine D1 and D2 receptor-based imaging agents
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Nuclear Medicine and Biology, 1993
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Current Medicinal Chemistry, 2013
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European Journal of Medicinal Chemistry, 2019
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Nuclear Medicine and Biology, 2009
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Molecules, 2020
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Molecules, 2019
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2020
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Bioorganic & Medicinal Chemistry, 2009
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Pyrazoles as Key Scaffolds for the Development of Fluorine-18-Labeled Radiotracers for Positron Emission Tomography (PET)
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Molecules
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[18F]FE@SUPPY: a suitable PET tracer for the adenosine A3 receptor? An in vivo study in rodents
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European Journal of Nuclear Medicine and Molecular Imaging, 2015
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The use of [18F] 4-fluorobenzyl iodide (FBI) in PET radiotracer synthesis: model alkylation studies and its application in the design of dopamine D1 and D2 receptor- …
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Nuclear medicine and …, 1993
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International Journal of Radiation Applications and Instrumentation. Part A. Applied Radiation and Isotopes, 1992
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