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first-draw protocol] Travison TG et al

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We identified key regions in the p53 transactivation domain (TAD) involved in FOXO4 binding and designed an optimized peptide inhibitor (CPP-CAND) with improved cell permeability

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The metabolic pathway of BPC-157 involves rapid breakdown into various small peptide fragments in vivo, ultimately forming single amino acids that enter normal amino acid metabolism and excretion pathways