125I-Labeled 2-O- and 3-O-m-iodobenzyl, and 6-O-m-iodophenyl derivatives of L-ascorbic acid: synthesis and preliminary tissue distribution
✍ Scribed by Fumihiko Yamamoto; Eri Kuwano; Tetsuo Kaneshiro; Shigeki Sasaki; Minoru Maeda
- Publisher
- John Wiley and Sons
- Year
- 2003
- Tongue
- French
- Weight
- 157 KB
- Volume
- 46
- Category
- Article
- ISSN
- 0022-2135
- DOI
- 10.1002/jlcr.714
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✦ Synopsis
Abstract
Three ^125^I‐labeled 2__‐O‐__ and 3__‐O‐m‐iodobenzyl, and 6‐O‐m‐__iodophenyl derivatives of L‐ascorbic acid were prepared by melt exchange procedures in isolated radiochemical yields of 12–60% after HPLC purification. Biodistribution studies in tumor‐bearing mice showed very different in vivo tissue uptake properties from previous results obtained with ^14^C‐labeled ascorbic acid and 6‐deoxy‐6‐[^18^F]fluoro‐L‐ascorbic acid. None of these seems to be suitable radioiodinated analogs of L‐ascorbic acid for imaging study of its in vivo biochemistry. Copyright © 2003 John Wiley & Sons, Ltd.
📜 SIMILAR VOLUMES
The title branched-trisaccharide derivatives (9 and 13) have been synthesised from methyl 2,3-O-(2-nitrobenzylidene)-a-L-rhamnopyranoside (2) using the 2nitrobenzylidene residue as a temporary blocking-group. Condensation of 2 with methyl (2,3,4-tri-O-acetyl-a-D-glucopyranosyl bromide)uronate afford