Cargando…
N-Terminal Cysteine Bioconjugation with (2-Cyanamidophenyl)boronic Acids Enables the Direct Formation of Benzodiazaborines on Peptides
[Image: see text] Benzodiazaborines (BDABs) have emerged as a valuable tool to produce stable and functional bioconjugates via a click-type transformation. However, the current available methods to install them on peptides lack bioorthogonality, limiting their applications. Here, we report a strateg...
Autores principales: | Padanha, Rita, Cavadas, Rafaela A. N., Merino, Pedro, António, João P. M., Gois, Pedro M. P. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2023
|
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10391619/ https://www.ncbi.nlm.nih.gov/pubmed/37466099 http://dx.doi.org/10.1021/acs.orglett.3c01835 |
Ejemplares similares
-
Interactive Bioconjugation at N‐Terminal Cysteines by Using O‐Salicylaldehyde Esters towards Dual Site‐Selective Functionalization
por: Silva, Maria J. S. A., et al.
Publicado: (2022) -
Organometallic Palladium Reagents for Cysteine Bioconjugation
por: Vinogradova, Ekaterina V., et al.
Publicado: (2015) -
Cysteine specific bioconjugation with benzyl isothiocyanates
por: Petri, László, et al.
Publicado: (2020) -
Rapid and robust cysteine bioconjugation with vinylheteroarenes
por: Seki, Hikaru, et al.
Publicado: (2021) -
Development and Recent Advances in Lysine and N-Terminal Bioconjugation for Peptides and Proteins
por: Tantipanjaporn, Ajcharapan, et al.
Publicado: (2023)