## Abstract __The__ syntheses of adenosine analogues, 2′‐deoxy‐2′‐[^18^F]fluoro‐9‐β‐D‐arabinofuranosyladenine ([^18^F]‐FAA) and 3′‐deoxy‐3′‐[^18^F]fluoro‐9‐β‐D‐xylofuranosyladenine ([^18^F]‐FXA) are reported. Adenosine (**1**) was converted to its methoxytrityl derivatives **2** and **3** as a mixt
Synthesis of 11C-labelled metomidate analogues as adrenocortical imaging agents
✍ Scribed by Farhad Karimi; Maria Erlandsson; Örjan Lindhe; Bengt Långström
- Publisher
- John Wiley and Sons
- Year
- 2008
- Tongue
- French
- Weight
- 154 KB
- Volume
- 51
- Category
- Article
- ISSN
- 0022-2135
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
Clinical findings using [^11^C]methyl 1‐[(1__R__)‐1‐phenylethyl]‐1__H__‐imidazole‐5‐carboxylate ([^11^C]MTO, 1) show high uptake in lesions of adrenocortical origin, including adenomas, but low uptake in lesions of non‐adrenocortical origin. In this paper the synthesis and preclinical evaluation of two new ^11^C‐labelled analogues of MTO, [^11^C]methyl 1‐[(1__R__)‐1‐(4‐chlorophenyl)ethyl]‐1__H__‐imidazole‐5‐carboxylate ([^11^C]CLM, 2) and [^11^C]methyl 1‐[(1__R__)‐1‐(4‐bromophenyl)ethyl]‐1__H__‐imidazole‐5‐carboxylate ([^11^C]BRM, 3), using frozen‐section autoradiography, organ distribution and a metabolic study are presented. Copyright © 2008 John Wiley & Sons, Ltd.
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