## Abstract Synthesis of 2′‐deoxy‐2′‐[^18^F]fluoro‐5‐methyl‐1‐__β__‐D‐arabinofuranosyluracil ([^18^F]‐FMAU) is reported. 2‐Deoxy‐2‐[^18^F]fluoro‐1,3,5‐tri‐O‐benzoyl‐__α__‐D‐arabinofuranose **2** was prepared by the reaction of the respective triflate **1** with tetrabutylammonium[^18^F]fluoride. Th
Enzymatic synthesis and biodistribution in mice of β-O-D-galactopyranosyl-(1,4′)-2′-[18F]fluoro-2′-deoxy-D-glucopyranose (2′-[18F]fluorodeoxylactose]
✍ Scribed by G. Bormans; A. Verbruggen
- Publisher
- John Wiley and Sons
- Year
- 2001
- Tongue
- French
- Weight
- 100 KB
- Volume
- 44
- Category
- Article
- ISSN
- 0022-2135
- DOI
- 10.1002/jlcr.471
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
We have synthesized β‐O‐D‐galactopyranosyl‐(1,4′)‐2′‐[^18^F]fluoro‐2′‐deoxy‐D‐glucopyranose (2′‐[^18^F]fluorodeoxylactose, ^18^FDL) using an enzymatic method starting from ^18^FDG in order to evaluate this compound with regard to its usefulness for in vivo visualization of the expression of the LacZ gene. Incubation of ^18^FDL with β‐galactosidase results in the formation of ^18^FDG. Biodistribution studies in normal mice showed that ^18^FDL is cleared by urinary excretion and is not retained in any tissue. Biodistribution in Rosa‐26 mice is identical to the biodistribution in normal mice, suggesting that ^18^FDL is not able to cross the cell membrane. Copyright © 2001 John Wiley & Sons, Ltd.
📜 SIMILAR VOLUMES
## Abstract Several 2′‐deoxy‐2′‐[^18^F]fluoro‐1‐__β__‐D‐arabinofuranosyluracil derivatives have been synthesized. Coupling of 1‐bromo‐2‐deoxy‐2‐[^18^F]fluoro‐3,5‐di‐O‐benzoyl‐__α__‐D‐arabinofuranose **2** with protected uracil derivatives **3a–e** followed by hydrolysis and high‐performance liquid
## Abstract The mechanisms‐based glycosidase inhibitor 2‐deoxy‐2‐[^18^F]‐fluoro‐β‐mannosyl [^18^F]‐fluoride was synthesized and its covalent binding to __Agrobacterium__ β‐glucosidase was demonstrated __in vitro__.
## Abstract The development of ^18^F‐labelling methods adopted to proteins and bioactive peptides is of great interest in radiopharmaceutical sciences. In order to provide ^18^F‐labelled sugars as a polar prosthetic group for an enzymatic ^18^F‐labelling procedure, an appropriate nucleotide activat
## Abstract For Abstract see ChemInform Abstract in Full Text.