Radiosynthesis of [123I]N-(3-iodoprop-(2E)-enyl)-2α-(imino-methyl)-3β-(3′,4′-dichlorophenyl) nortropane as a potential SPET tracer for dopamine transporter
✍ Scribed by Meixiang Yu; Anu J. Airaksinen; Antony D. Gee; Simo Lötjönen; Jyrki T. Kuikka; Jouko J. Vepsäläinen; Jukka Hiltunen; Kim A. Bergström
- Publisher
- John Wiley and Sons
- Year
- 2002
- Tongue
- French
- Weight
- 93 KB
- Volume
- 45
- Category
- Article
- ISSN
- 0022-2135
- DOI
- 10.1002/jlcr.619
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✦ Synopsis
Abstract
The radiosynthesis of a novel tropane derivative [^123^I]KUC‐25019, [[^123^I];N‐(3‐iodoprop‐(2__E__)‐enyl)‐2α‐(imino‐methyl)‐3β‐(3′,4′‐dichlorophenyl)nortropane], a potential inhibitor of the dopamine transporter is reported. The synthetic routes include the preparation of standard reference, the stannyl precursor and the ^123^I‐labeling synthesis. The no‐carrier‐added ^123^I‐labeling has about 20% yield, the specific activity of [^123^I]KUC‐25019 is > 107 GBq/µmol and the radiochemical purity of [^123^I] KUC‐25019 is >95%. Copyright © 2002 John Wiley & Sons, Ltd.
📜 SIMILAR VOLUMES
SUMMARY In order to study the dopamine transporter by \(\mathrm{PET}\), we prepared ( \(E\) )-N-(3-bromoprop-2-enyl)\(2 \beta\)-carbomethoxy-3 \(\beta\)-(4'-tolyl) nortropane (PE2Br) and its radiobrominated analogue. PE2Br and \(\left[{ }^{76} \mathrm{Br}\right] \mathrm{PE} 2 \mathrm{Br}\) were synt