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A Flexible Synthesis of 68Ga-Labeled Carbonic Anhydrase IX (CAIX)-Targeted Molecules via CBT/1,2-Aminothiol Click Reaction.


ABSTRACT: We herein describe a flexible synthesis of a small library of 68Ga-labeled CAIX-targeted molecules via an orthogonal 2-cyanobenzothiazole (CBT)/1,2-aminothiol click reaction. Three novel CBT-functionalized chelators (1?3) were successfully synthesized and labeled with the positron emitter gallium-68. Cross-ligation between the pre-labeled bifunctional chelators (BFCs) and the 1,2-aminothiol-acetazolamide derivatives (8 and 9) yielded six new 68Ga-labeled CAIX ligands with high radiochemical yields. The click reaction conditions were optimized to improve the reaction rate for applications with short half-life radionuclides. Overall, our methodology allows for a simple and efficient radiosynthetic route to produce a variety of 68Ga-labeled imaging agents for tumor hypoxia.

SUBMITTER: Chen KT 

PROVIDER: S-EPMC6337199 | biostudies-literature | 2018 Dec

REPOSITORIES: biostudies-literature

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A Flexible Synthesis of <sup>68</sup>Ga-Labeled Carbonic Anhydrase IX (CAIX)-Targeted Molecules via CBT/1,2-Aminothiol Click Reaction.

Chen Kuo-Ting KT   Nguyen Kevin K   Ieritano Christian C   Gao Feng F   Seimbille Yann Y  

Molecules (Basel, Switzerland) 20181221 1


We herein describe a flexible synthesis of a small library of <sup>68</sup>Ga-labeled CAIX-targeted molecules via an orthogonal 2-cyanobenzothiazole (CBT)/1,2-aminothiol click reaction. Three novel CBT-functionalized chelators (<b>1</b>⁻<b>3</b>) were successfully synthesized and labeled with the positron emitter gallium-68. Cross-ligation between the pre-labeled bifunctional chelators (BFCs) and the 1,2-aminothiol-acetazolamide derivatives (<b>8</b> and <b>9</b>) yielded six new <sup>68</sup>Ga  ...[more]

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