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d-alanine2-glucagon-like peptide-1 is a synthetic peptide analog of the human incretin hormone glucagon-like peptide-1 (GLP-1). It is specifically engineered with a D-alanine substitution at the second amino acid position (replacing the naturally occurring L-alanine), which confers resistance to rapid degradation by the enzyme dipeptidyl peptidase-4 (DPP-4). This modification significantly extends the peptide's biological half-life while maintaining its potency as an agonist for the glucagon-like peptide-1 receptor (GLP1R). The drug functions by stimulating glucose-dependent insulin secretion from pancreatic beta cells, inhibiting glucagon release, and slowing gastric emptying. Research has primarily focused on its potential for treating Type 2 diabetes mellitus, including the development of oral delivery systems using polymer-based microspheres to improve bioavailability and patient compliance.
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