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While it is less potent than natural ligands at the glucagon and GLP‑1 receptors (0.3 and 0.4 times as active, respectively), it is significantly more potent at the GIP receptor, with activity approximately 8.9 times higher than that of the endogenous ligand
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doi: 10.3748/wjg.v20.i40.14821 [DOI] [PMC free article] [PubMed] [Google Scholar] 54
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