biostudies-literatureUnknown9(53)Giacomazzo GEMinistero dell’Istruzione, dell’Università e della RicercaWe 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).RSC advances30773-30777https://www.ebi.ac.uk/biostudies/studies/S-EPMC9072199biostudies-literatureA 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.PMC9072199Gellini CBaldoneschi VPalladino PSalerno GMinunni MScarano SFeis AGiacomazzo GERichichi BfalseA 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 bioanalytical applicability of these tools was assessed by measuring the binding to glycan chains of antibodies by a Quartz Crystal Microbalance (QCM).2019-01-01T00:00:00Z2019 Sep2025-06-01T01:27:46.325Z2025-06-01T01:27:46.325ZS-EPMC90721993552936210.1039/c9ra07608e