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in Current Pharmaceutical Design documented BPC-157s multi-organ protective effects across more than two decades of preclinical research, with particular focus on its remarkable stability in gastric acid a property that distinguishes it from most biologically active peptides and enables oral delivery studies in animal models [1]
Esophagogastric anastomosis in rats: improved healing by BPC 157 and L-arginine, aggravated by L-NAME
Cu(II) is held in a square-planar coordination sphere by the N-terminal amine, the deprotonated glycyl amide nitrogen and the histidine imidazole, at a stability constant (log K approximately 16.4) close to that of the copper transport site on human serum albumin
