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TB-500 is a synthetic peptide fragment corresponding to the active region of Thymosin Beta-4 (TB4) a 43-amino acid G-actin sequestering protein that is one of the most abundant intracellular peptides in mammalian cells

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

The mechanism work mapping the VEGFR2 pathway was reported by the Chang research group at Chang Gung University, Taiwan, the only non-Zagreb laboratory to have published substantive original mechanism research on BPC-157 [2]

BPC-157 is an experimental peptide, and it has not been approved by the FDA to diagnose, treat, cure, or prevent any disease