“…Molecules containing the azobenzene group can change their geometry from trans (E form, thermodynamically more stable) to cis (Z form) when irradiated by UV light (λ ~365 nm) and switch back to their original form via thermal relaxation or if irradiated with blue (λ ~465 nm) or visible light, as shown in Figure 1a. So far, azobenzene moieties have been successfully integrated into (i) receptors and ion channels [23,24], (ii) transporters and ion pumps [25], (iii) enzymatic ligands and inhibitors [25], (iv) DNA [26], (v) antimicrobics [27], (vi) prodrugs and drug delivery systems [28], allowing for their remote photoactivation and/or photomodulation with high spatial and temporal resolutions. Despite the biomedical applications of synthetic photoswitches still being in their preliminary stages, their efficacy has been demonstrated at the cellular level and, in some cases, on animal models, for the treatment of microbial infection, diabetes, cancer, pain, and blindness, providing evidence of their biocompatibility and for promising therapeutical applications in the near future [25].…”