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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

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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.


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Synthesis of (E)-N-(3-bromoprop-2-enyl)-
✍ J. Helfenbein; P. Emond; C. Loc'h; M. Bottlaender; M. Ottaviani; D. Guilloteau; 📂 Article 📅 1999 🏛 John Wiley and Sons 🌐 French ⚖ 281 KB 👁 1 views

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