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Its working mechanism is allosteric facilitation of HGF/c-Met signaling: Dihexa binds HGF with high affinity (reported K d ~65 pM in the original work) and is proposed to potentiate HGF dimerization and c-Met phosphorylation at subthreshold endogenous HGF concentrations

Compounds such as semaglutide and retatrutide are frequently used in metabolic research systems to investigate how different peptide receptor agonists interact with overlapping or complementary endocrine signaling networks

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