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Abstract Glucagon-like peptide 1 receptor agonists (GLP-1 RAs) have emerged as a transformative class of therapies initially developed for glycemic control in type 2 diabetes mellitus

Both employ fatty acid acylation of lysine 26 to facilitate serum albumin noncovalent binding to prolong their plasma half-lives (95)

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In the same study, Z-VAD-FMK, a PANoptosis inhibitor targeting the entire caspase family, demonstrated synergistic enhancement of the hepatoprotective effects of Si-Wu-Tang [181]