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Title: A novel versatile precursor suitable for 18 F-radiolabeling via "click chemistry". Author: Lugato B, Stucchi S, Ciceri S, Iannone MN, Turolla EA, Giuliano L, Chinello C, Todde S, Ferraboschi P. Journal: J Labelled Comp Radiopharm; 2017 Aug; 60(10):466-480. PubMed ID: 28600889. Abstract: As an effort to improve 18 F-radiolabeling of biomolecules in method robustness and versatility, we report the synthesis and radiolabeling of a new azido precursor potentially useful for the so-called "click reaction," in particular the ligand-free version of the copper(I)-catalyzed alkyne-azide cycloaddition. The new azido precursor may help to overcome problems sometimes exhibited by most of the currently used analogues, as it is safe to handle and it displays long-term chemical stability, thus facilitating the development of new radiolabeling procedures. Moreover, the formed 18 F-labeled 1,2,3-triazole is potentially metabolically stable and could enhance the in vivo circulation time. The above azido precursor was successfully radiolabeled with 18 F, with 51% radiochemical yield (nondecay-corrected). As a proof of concept, the 18 F-labeled azide was then tested with a suitable alkyne functionalized aminoacid (l-propargylglycine), showing 94% of conversion, and a final radiochemical yield of 27% (>99% radiochemical purity), nondecay-corrected, with a total preparation time of 104 minutes.[Abstract] [Full Text] [Related] [New Search]