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Derived from a naturally occurring gastric peptide sequence, BPC-157 has attracted significant scientific interest for its role in cell signaling, tissue integrity, and recovery-related pathways
(1992) described the IGF-1 LR3 analog and documented its dramatically reduced IGFBP binding compared to native IGF-1, establishing the pharmacokinetic rationale for its use as a research tool (PMID 1601853)
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