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Chemically, Sitagliptin (2R)-4-Oxo-4-(3-(trifluoromethyl)-5,6-dihydro(1,2,4)triazolo(4,3-a)pyrazin-7(8H)-yl)-1-(2,4,5-trifluorophenyl) Butan-2-amine exhibits a significant degree of DPP-4 selectivity

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(Montreal, Canada) and first described in peer-reviewed literature in the context of dipeptidylpeptidase-4 (DPP-4) resistance: native GHRH is rapidly cleaved in circulation by DPP-4 at the TyrAla bond, and the N-terminal hexenoyl modification was structurally characterized as blocking this cleavage site, preserving the intact GHRH(144) sequence for hypothalamic-pituitary receptor interaction in preclinical models