化学
芳基
示踪剂
组合化学
体内
化学合成
有机化学
体外
烷基
生物化学
生物
物理
生物技术
核物理学
作者
Nils Walter,Jan Bertram,Birte Drewes,Victor Bahutski,Marco Timmer,Markus B. Schütz,Felicia Krämer,Felix Neumaier,Heike Endepols,Bernd Neumaier,Boris D. Zlatopolskiy
标识
DOI:10.1016/j.ejmech.2022.114383
摘要
Recently, a protocol for radiolabeling of aryl fluorosulfates ("SuFEx click radiolabeling") using ultrafast 18F/19F isotopic exchange has been reported. Although promising, the original procedure turned out to be rather inefficient. However, systematic optimization of the reaction parameters allowed for development of a robust method for SuFEx radiolabeling which obviates the need for azeotropic drying, base addition and HPLC purification. The developed protocol enabled efficient 18F-fluorination of low nanomolar amounts of aryl fluorosulfates in highly diluted solution (micromolar concentrations). It was successfully used to prepare a series of 29 18F-fluorosulfurylated phenols - including modified ezetimibe, α-tocopherol and etoposide, the two tyrosine derivatives Boc-Tyr([18F]FS)-OMe and H-Tyr([18F]FS)-OMe, the FAP-specific ligand [18F]FS-UAMC1110, and the DPA-714 analog [18F]FS-DPA - in fair to excellent yields. Preliminary evaluation demonstrated sufficient in vivo stability of radiofluorinated electron rich or neutral {Boc-Tyr([18F]FS)-OMe), H-Tyr([18F]FS)-OMe and [18F]FS-DPA} aryl fluorosulfates. Furthermore, [18F]FS-DPA was identified as a promising tracer for visualization of TSPO expression.
科研通智能强力驱动
Strongly Powered by AbleSci AI