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Berglundh T, Armitage G, Araujo MG, et al

Its activity is not as potent as we expected, whereas its derivatives such as curcumin and chlorogenic acid have potent activity for HDAC inhibition, which suggests that caffeic acid may be considered a promising lead structure for HDAC inhibitors that have the potential to provide new therapeutics for cancer (Bora-Tatar et al., 2009)

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This labelling method allows selective tracking of the bacterial cell consumption and specific visualization of glycan units of PG upon macrophage infection, which can be used in future studies towards the identification and characterization of naturally occurring immunostimulatory NAM-containing PG fragments