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. 2023 Mar;75(2):263–308. doi: 10.1124/pharmrev.122.000654

Fig. 4.

Fig. 4

Fluorescence titration of CLR01 with Lys or Arg derivatives. All the reactions were carried out in 10 mM phosphate buffer, pH 7.6, and were monitored using λex = 285 nm, λem = 336 nm. (A) Schematic structure of Ac-Lys-OMe. (B) Schematic structure of Ac-Arg-OMe. (C) Fluorescence spectra of CLR01 in the absence or presence of increasing concentrations of Ac-Lys-OMe. (D) Change in fluorescence intensity as a function of increasing Ac-Lys-OMe concentration. (E) Fluorescence spectra of CLR01 in the absence or presence of increasing concentrations of Ac-Arg-OMe. (F) Change in fluorescence intensity as a function of increasing Ac-Arg-OMe concentration.