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Article ; Online: Characterization of an

Lee, Daniel / Latour, Simon / Emblem, Michael / Clark, Hunter J / Santos, Jobette T / Jang, Jaewan / McGuigan, Alison P / Nitz, Mark

Bioconjugate chemistry

2023  Volume 34, Issue 12, Page(s) 2358–2365

Abstract: Aldehydes are attractive bioorthogonal coupling partners. The ease of manipulation of aldehydes and their orthogonality to other classes of bioorthogonal reactions have inspired the exploration of chemistries, which generate irreversible conjugates. ... ...

Abstract Aldehydes are attractive bioorthogonal coupling partners. The ease of manipulation of aldehydes and their orthogonality to other classes of bioorthogonal reactions have inspired the exploration of chemistries, which generate irreversible conjugates. Similarly, nitrones have been shown to be potent 1,3-dipoles in bioorthogonal reactions when paired with strained alkynes. Here, we combine the reactivity of nitrones with the simplicity of aldehydes using an
MeSH term(s) Humans ; HEK293 Cells ; Proteins/chemistry ; Nitrogen Oxides/chemistry ; Alkynes/chemistry ; Aldehydes ; Azides/chemistry ; Cycloaddition Reaction
Chemical Substances nitrones ; Proteins ; Nitrogen Oxides ; Alkynes ; Aldehydes ; Azides
Language English
Publishing date 2023-12-05
Publishing country United States
Document type Journal Article ; Research Support, Non-U.S. Gov't
ZDB-ID 1024041-x
ISSN 1520-4812 ; 1043-1802
ISSN (online) 1520-4812
ISSN 1043-1802
DOI 10.1021/acs.bioconjchem.3c00463
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