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通过在膦酸酯前体上的 F 的自发位点特异性亲核取代对生物分子进行直接 F-标记。

Direct F-Labeling of Biomolecules via Spontaneous Site-Specific Nucleophilic Substitution by F on Phosphonate Prostheses.

机构信息

Centre for Molecular Imaging and Translational Medicine, State Key Laboratory of Molecular Vaccinology and Molecular Diagnostics, School of Public Health, Xiamen University, Xiamen, Fujian 361102, P.R. China.

Tianjin Engineering Technology Centre of Chemical Wastewater Source Reduction and Recycling, School of Science, Tianjin Chengjian University, Tianjin 300384, P.R. China.

出版信息

Org Lett. 2021 Jun 4;23(11):4261-4266. doi: 10.1021/acs.orglett.1c01211. Epub 2021 May 4.

Abstract

We describe a high radiochemical yield late-stage direct F-labeling of bare biomolecules containing common active groups. Spontaneity and site-selectivity are attributed to the remarkably higher rates of nucleophilic substitution reactions on phosphonates than on other electrophiles by F at various hydrogen bond forms. Rapid access to many medicinally significant F-labeled biomolecules is achieved at 21-68% radiochemical yields and 35.9-55.1 GBq μmol molar activities both manually or automatically.

摘要

我们描述了一种高放射化学产率的晚期直接 F 标记裸生物分子的方法,这些生物分子包含常见的活性基团。这种自发性和位点选择性归因于 F 在各种氢键形式下对膦酸盐的亲核取代反应速率明显高于其他亲电试剂。通过手动或自动方法,以 21-68%的放射化学产率和 35.9-55.1GBqμmol摩尔活度,快速获得了许多具有医学意义的 F 标记生物分子。

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