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Am J Physiol Endocrinol Metab 293(3):743753

To provide a tool for direct assessment of occupancy at the GCGR we recently developed the Positron Emission Tomography (PET) radioligand [ 68 Ga]Ga-DO3A-Tuna-2 (also known as [ 68 Ga]Ga-DO3A-S01-GCG) 7 that displayed suitable affinity and selectivity for the GCGR in rat, non-human and human liver, in combination and with negligible cross-activity on the GLP1R

Moreover, every batch follows pharmaceutical-grade standards

Mechanistically, the peptide perturbs the FOXO4 interaction with p53, which selectively causes p53 nuclear exclusion and cell-intrinsic apoptosis (Figure 2, this novel senolytic did remove cells from the PDL9 chondrocytes, which was accompanied by significantly reduced levels of SA--gal staining