Click chemistry and radiochemistry: An update Review
| Authors: | Bauer, D.; Cornejo, M. A.; Hoang, T. T.; Lewis, J. S.; Zeglis, B. M. |
| Review Title: | Click chemistry and radiochemistry: An update |
| Abstract: | The term "click chemistry" describes a class of organic transformations that were developed to make chemical synthesis simpler and easier, in essence allowing chemists to combine molecular subunits as if they were puzzle pieces. Over the last 25 years, the click chemistry toolbox has swelled from the canonical copper-catalyzed azide-alkyne cycloaddition to encompass an array of ligations, including bioorthogonal variants, such as the strain-promoted azide-alkyne cycloaddition and the inverse electron-demand Diels-Alder reaction. Without question, the rise of click chemistry has impacted all areas of chemical and biological science. Yet the unique traits of radiopharmaceutical chemistry have made it particularly fertile ground for this technology. In this update, we seek to provide a comprehensive guide to recent developments at the intersection of click chemistry and radiopharmaceutical chemistry and to illuminate several exciting trends in the field, including the use of emergent click transformations in radiosynthesis, the clinical translation of novel probes synthesized using click chemistry, and the advent of click-based in vivo pretargeting. |
| Keywords: | diels-alder reaction; biological evaluation; growing applications; tumor uptake; preclinical evaluation; tetrazine; bioorthogonal chemistry; trans-cyclooctene; pretargeted immuno-pet; psma-ligands |
| Journal Title: | Bioconjugate Chemistry |
| Volume: | 34 |
| Issue: | 11 |
| ISSN: | 1043-1802 |
| Publisher: | American Chemical Society |
| Date Published: | 2023-11-15 |
| Start Page: | 1925 |
| End Page: | 1950 |
| Language: | English |
| ACCESSION: | WOS:001071410700001 |
| DOI: | 10.1021/acs.bioconjchem.3c00286 |
| PROVIDER: | wos |
| PMCID: | PMC10655046 |
| PUBMED: | 37737084 |
| Notes: | Review -- Source: Wos |
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