Click Chemistry and Radiochemistry: An Update.

Click Chemistry and Radiochemistry: An Update.
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点击化学和放射化学:更新。

DOI:
10.1021/acs.bioconjchem.3c00286
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发表时间:
2023-11-15
影响因子:
4.7
通讯作者:
Zeglis, Brian M.
Zeglis, Brian M.
中科院分区:
化学2区
文献类型:
--
作者:
Bauer, David;Cornejo, Mike A.;Hoang, Tran T.;Lewis, Jason S.;Zeglis, Brian M.

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“点击化学”一词描述了一类有机转化,其开发是为了使化学合成更简单、更容易,本质上允许化学家将分子亚基组合起来,就像它们是拼图一样。在过去的 25 年里,点击化学工具箱已经从经典的铜催化叠氮-炔环加成扩展到涵盖一系列连接,包括生物正交变体,例如应变促进的叠氮-炔环加成和逆电子需求 Diels-Alder 反应。毫无疑问,点击化学的兴起影响了化学和生物科学的所有领域。然而,放射性药物化学的独特特征使其成为该技术特别肥沃的土壤。在本次更新中,我们力求为点击化学和放射性药物化学交叉点的最新发展提供全面的指南,并阐明该领域的几个令人兴奋的趋势,包括放射合成中紧急点击转化的使用、使用点击化学合成的新型探针的临床转化以及基于点击的体内预靶向的出现。
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.
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发表时间: 2016-02
影响因子: 3.1
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