What semaglutide is
Semaglutide is a 31-residue acylated analog of human GLP-1, described in its discovery paper by Lau et al. (2015).[4] Three modifications carry the design: an Aib substitution at position 8 that blocks DPP-4 cleavage, an Arg substitution at position 34, and a C18 fatty diacid attached through a spacer at Lys26 that drives albumin binding. Together they take the half-life from minutes to roughly a week.
It is a single-receptor agonist. Every published effect runs through the GLP-1 receptor, which is what distinguishes it from tirzepatide and retatrutide and what makes it the cleanest available tool compound for isolating GLP-1 receptor pharmacology.

