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Research-onlyVendors pendingFacts verified · 2026-05-25

BPC-157

Also known as bepecin, pl 14736, body protection compound 157, gastric pentadecapeptide, bpc · Wikipedia

BPC-157 (Body Protection Compound-157, also designated PL 14736 in the Pliva clinical program) is a synthetic 15-amino-acid pentadecapeptide originally derived from a putative cytoprotective fragment of human gastric juice protein. It is widely marketed as a 'healing peptide' associated with injury recovery, tendon/ligament repair, gut protection, and joint health. The overwhelming majority of efficacy evidence derives from rodent models, predominantly from a single research group led by Predrag Sikirić at the University of Zagreb, who have published several hundred preclinical papers describing protective effects on the gastrointestinal tract, musculoskeletal system, and central nervous system. A small early-2000s human IBD program by Pliva (PL-14736) reached Phase II but was never advanced to approval, and BPC-157 remains a research chemical without any FDA-approved indication. WADA prohibits its use in athletic competition (Category S0).

4–8 wk

typical

cycle

250 µg

daily

dose

Sub-Q

primary

route

Animal

studies

only

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Mechanism of action

BPC-157 has no single defined receptor and instead appears to act through multiple repair-related pathways characterized almost entirely in rodent models. The most reproducible mechanism is upregulation of VEGFR2-Akt-eNOS signalling, producing pro-angiogenic effects in muscle, tendon, ligament, and gut models (Hsieh et al.

BPC-157 has no single defined receptor and instead appears to act through multiple repair-related pathways characterized almost entirely in rodent models. The most reproducible mechanism is upregulation of VEGFR2-Akt-eNOS signalling, producing pro-angiogenic effects in muscle, tendon, ligament, and gut models (Hsieh et al., 2017, https://pubmed.ncbi.nlm.nih.gov/27847966/; Brcic et al., https://pubmed.ncbi.nlm.nih.gov/20388964/). Additional preclinical observations include modulation of the nitric oxide (NO) system, activation of growth-factor and focal-adhesion signaling (FAK-paxillin, EGR-1) in fibroblasts and tendon cells, induction of collagen synthesis, and stabilizing effects on the dopaminergic and serotonergic systems within the gut-brain axis. Recent reviews summarize a broad effect profile spanning wound healing, tendon-to-bone reattachment, and cytoprotection of the gastrointestinal mucosa (Józwiak et al., Pharmaceuticals 2025, https://pmc.ncbi.nlm.nih.gov/articles/PMC11859134/; Sikirić et al. commentary, https://pmc.ncbi.nlm.nih.gov/articles/PMC12567428/). Independent reviewers caution that >80% of records originate from one group and that single-dose study designs limit dose-response interpretation (https://pmc.ncbi.nlm.nih.gov/articles/PMC12446177/). Manufacturer claims of oral 'gastric stability' are extrapolated from rat oral dosing; rigorous human PK/oral-bioavailability data are essentially absent.

Pharmacokinetic properties

Half-life

Approximately 4–6 hours after subcutaneous administration in rodent models; systemic exposure after oral dosing is poorly characterized in humans.

Routes

subcutaneous · intramuscular · oral · topical · intranasal

Bioavailability

Manufacturer and vendor literature describe BPC-157 as 'gastric-stable,' and rodent oral studies demonstrate pharmacological activity by that route, but no rigorous human oral PK or bioavailability data exist. Most published efficacy data are from rodent intraperitoneal or intramuscular dosing; commercial human use is overwhelmingly subcutaneous.

Amino-acid sequence

Gly-Glu-Pro-Pro-Pro-Gly-Lys-Pro-Ala-Asp-Asp-Ala-Gly-Leu-Val

Use & research dosing

There is no FDA-approved human dose. Commonly reported in research and self-experimentation protocols at roughly 200–500 mcg subcutaneously once or twice daily, frequently administered near the site of injury, in cycles of 4–8 weeks with washout. These figures are extrapolated by allometric scaling from rodent studies (typically 10 µg/kg or 10 ng/kg in Sikirić-group experiments) and are not derived from validated human pharmacokinetic or dose-finding work. Oral protocols in the 250–500 µg/day range are also reported; intestinal absorption in humans has not been formally measured, despite manufacturer 'gastric-stable' marketing. Topical and intranasal routes are described anecdotally with no PK validation. All dosing should be considered exploratory.

Research-use framing only. SavePeptides sells nothing for human consumption. Doses above reflect reported research / self-experimentation ranges, not clinical recommendations.

Editorial perspective

Despite enormous popular use, virtually all efficacy data for BPC-157 are preclinical (rodent) and over 80% of records derive from the Sikirić group in Zagreb (https://pmc.ncbi.nlm.nih.gov/articles/PMC12446177/). The single human program of record — Pliva's PL-14736 for inflammatory bowel disease — established tolerability but was never advanced to Phase III, and Pliva later dropped the program (https://pubmed.ncbi.nlm.nih.gov/17186181/). FDA classified BPC-157 as a Category 2 (significant safety risk) bulk drug substance for 503A compounding in 2023, with PCAC review of additional bulk-substance nominations scheduled for 2026. The 'stomach-stable' marketing claim for oral BPC-157 has not been validated in humans.

— SavePeptides editorial desk · last updated 2026-05-25

Cautions & contraindications

Before researching this compound, note:

  • No completed human safety pharmacology trials; long-term toxicology unknown
  • Pro-angiogenic activity raises a theoretical concern in active malignancy
  • WADA-prohibited in athletic competition (S0 non-approved substances)
  • Not approved by FDA for any indication; placed on the 503A Category 2 bulks list in 2023 (significant safety risk for compounding)
  • Unknown immunogenicity, reproductive, and developmental effects
  • Avoid in pregnancy and lactation due to absent safety data
  • Vast majority of efficacy data come from a single research group, limiting independent replication
  • Oral 'gastric stability' is a manufacturer claim, not a validated human PK finding
  • Injection-site irritation reported anecdotally
  • Quality and purity of research-grade material varies widely between vendors
  • Potential drug-interaction profile undefined

Facts verified

2026-05-25

Confidence

medium

What this means

  • preclinical-only evidence (rodent-dominant; >80% of records from a single research group)
  • no completed Phase III human trials
  • FDA 503A Category 2 (significant safety risk) bulk substance
  • oral 'gastric stability' claim not validated in humans

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BPC-157 · SavePeptides