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The mean (+SD) plasma concentration of BPC157 versus time curves following administration of various BPC157 doses in rats are shown in Figures 1AC, and the corresponding pharmacokinetic parameters are presented in Tables 1Tables 3

Sperry, J., & Brse, S

For these regions, the side chains were stubbed in the final PDB models if no robust density was present in the EM maps

doi:10.1097/CRD.0000000000000143 Chan JH, Lim S, Wong WS

Unlike most peptides which degrade rapidly in stomach acid (pH 1.5-3.5), BPC-157 demonstrates remarkable acid stability, consistent with its derivation from a protein naturally active in gastric juice