This title appears in the Scientific Report :
2007
Please use the identifier:
http://dx.doi.org/10.1002/jlcr.1161 in citations.
Chemoenzymatic n.c.a synthesis of the coenzyme UDP-2-deoxy-2-(18F)fluoro-alpha-D-glucopyranose as substrate of glycosyltransferases
Chemoenzymatic n.c.a synthesis of the coenzyme UDP-2-deoxy-2-(18F)fluoro-alpha-D-glucopyranose as substrate of glycosyltransferases
The development of F-18-labelling methods adopted to proteins and bioactive peptides is of great interest in radiopharmaceutical sciences. In order to provide F-18-labelled sugars as a polar prosthetic group for an enzymatic 18 F-labelling procedure, an appropriate nucleotide activated sugar is need...
Saved in:
Personal Name(s): | Prante, O. |
---|---|
Hamacher, K. / Coenen, H. H. | |
Contributing Institute: |
Nuklearchemie; INB-4 |
Published in: | Journal of labelled compounds and radiopharmaceuticals, 50 (2007) 1, S. 55 - 63 |
Imprint: |
New York, NY [u.a.]
Wiley
2007
|
Physical Description: |
55 - 63 |
DOI: |
10.1002/jlcr.1161 |
Document Type: |
Journal Article |
Research Program: |
Funktion und Dysfunktion des Nervensystems |
Series Title: |
Journal of Labelled Compounds and Radiopharmaceuticals
50 |
Subject (ZB): | |
Publikationsportal JuSER |
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520 | |a The development of F-18-labelling methods adopted to proteins and bioactive peptides is of great interest in radiopharmaceutical sciences. In order to provide F-18-labelled sugars as a polar prosthetic group for an enzymatic 18 F-labelling procedure, an appropriate nucleotide activated sugar is needed. Here, we present the radiosynthesis of n.c.a. UDP-2-deoxy-2-[F-18]fluoro-alpha-D-glucopyranose (UDP-[F-18]FDG) as a substrate for glycosyltransferases. The MacDonald synthesis of [F-18]FDG-1-phosphate was successfully combined with an enzymatic activation to obtain UDP-[F-18]FDG directly in an aqueous medium located in the void volume of a solid phase cartridge. The radiochemical yield of UDP-[F-18]FDG was 20% (based on [F-18] fluoride) after a total synthesis time of 110 min. Thus, an intermediate was provided for the enzymatic transfer of [F-18]FDG using UDP-[ 18 F]FDG as glycosyl donor making use of a suitable glycosyltransferase. This would represent a highly selective and mild F-18-labelling method for glycosylated biomolecules. Copyright (c) 2007 John Wiley & Sons, Ltd. | ||
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