Labeling and Glycosylation of Peptides Using Click Chemistry: A General Approach to 18F-Glycopeptides as Effective Imaging Probes for Positron Emission Tomography

被引:105
作者
Maschauer, Simone [1 ]
Einsiedel, Juergen [4 ]
Haubner, Roland [4 ]
Hocke, Carsten [1 ]
Ocker, Matthias [2 ]
Huebner, Harald [3 ]
Kuwert, Torsten [1 ]
Gmeiner, Peter [4 ]
Prante, Olaf [1 ]
机构
[1] Univ Erlangen Nurnberg, Nukl Med Klin, Lab Mol Bildgebung, D-91054 Erlangen, Germany
[2] Univ Klinikum Erlangen, Erlangen, Germany
[3] Med Univ Innsbruck, Innsbruck, Austria
[4] Univ Erlangen Nurnberg, Emil Fischer Ctr, D-91054 Erlangen, Germany
关键词
click chemistry; glycosylation; peptides; positron emission tomography; radiopharmaceuticals; CYCLIC PENTAPEPTIDES; PARALLEL SYNTHESIS; RECEPTOR LIGANDS; RGD PEPTIDES; EXPRESSION; PET; F-18-GLYCOSYLATION; F-18; RADIOSYNTHESIS; CYCLOADDITION;
D O I
10.1002/anie.200904137
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
(Figure Presented) Click for PET: An efficient strategy based on click chemistry has been developed for 18F-labeling alkyne-bearing peptides with concomitant glycosylation. The mild conditions and general applicability of this reliable reaction gives access to a new class of 18F- glycopeptide radiopharmaceuticals with improved biological properties for in vivo imaging studies by positron emission tomography (PET). © 2010 Wiley-VCH Verlag GmbH & Co. KGaA.
引用
收藏
页码:976 / 979
页数:4
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