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Biol Trace Elem Res (2010) 138:10715
The breadth of documented activity reflects what the original investigators have described as systems-level pharmacology: rather than acting through a single high-affinity receptor, BPC-157 appears to modulate multiple intersecting cellular pathways including nitric oxide signalling, growth-factor receptor expression, dopamine and serotonin metabolism, and angiogenic vessel formation
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Specifically, it represents the C-terminal fragment of HGH (residues 176-191), the precise portion of the molecule that handles fat metabolism, with an added disulfide bridge for stability
