A novel fluoro-chromogenic click reaction for the labelling of proteins and nanoparticles with near-IR theranostic agents

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Abstract

Reaction of porphycene isothiocyanates with primary and secondary amines leads to the formation of thiazolo[4,5-c]porphycenes, with a substantial shift in the absorption and fluorescence spectra. The conjugates show fluorescence in the near-infrared and are capable of photosensitizing the production of the cytotoxic species singlet oxygen. This journal is

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Planas, O., Gallavardin, T., & Nonell, S. (2015). A novel fluoro-chromogenic click reaction for the labelling of proteins and nanoparticles with near-IR theranostic agents. Chemical Communications, 51(26), 5586–5589. https://doi.org/10.1039/c4cc09070e

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