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Conjugation reactions usually involve metabolite activation by a highenergy intermediate and have been classified into two general types: type I (e.g., glucuronidation and sulfonation), in which an activated conjugating agent combines with substrate to yield the conjugated product, and type II (e.g., amino acid conjugation), in which the substrate is activated and then combined with an amino acid to yield a conjugated product (Hodgson, 2004)
More recently, dual and triple agonists targeting additional incretin and metabolic hormone receptors have demonstrated enhanced therapeutic potential, revolutionizing the landscape of MASLD treatment [11,12]
