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A straightforward synthesis of phenyl boronic acid (PBA) containing BODIPY dyes: new functional and modular fluorescent tools for the tethering of the glycan domain of antibodies

We report here on the efficient and straightforward synthesis of a series of modular and functional PBA-BODIPY dyes 1–4. They are an outstanding example of the efficient merge of the versatility of the 3,5-dichloro-BODIPY derivatives and the receptor-like ability of the PBA moiety. The potential bio...

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Detalles Bibliográficos
Autores principales: Giacomazzo, Gina Elena, Palladino, Pasquale, Gellini, Cristina, Salerno, Gianluca, Baldoneschi, Veronica, Feis, Alessandro, Scarano, Simona, Minunni, Maria, Richichi, Barbara
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9072199/
https://www.ncbi.nlm.nih.gov/pubmed/35529362
http://dx.doi.org/10.1039/c9ra07608e
Descripción
Sumario:We report here on the efficient and straightforward synthesis of a series of modular and functional PBA-BODIPY dyes 1–4. They are an outstanding example of the efficient merge of the versatility of the 3,5-dichloro-BODIPY derivatives and the receptor-like ability of the PBA moiety. The potential bioanalytical applicability of these tools was assessed by measuring the binding to glycan chains of antibodies by a Quartz Crystal Microbalance (QCM).