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BPC-157

Body Protection Compound-157

The tissue-healing workhorse — accelerates repair of tendons, ligaments, gut lining, and nerves via VEGF-driven angiogenesis.

Tier C — Early or Mixed: Limited human trials; effect size uncertain. How our tiers work →
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Research facts

Half-life~4h SubQ / ~8h oral
RouteSubQ / IM / Oral
Typical dose250–500 mcg/day
FrequencyOnce or twice daily
SolventBacteriostatic water
pH5.5–7.0
Stability30 days at +4°C

Mechanism of action

BPC-157 is a synthetic 15-amino acid pentadecapeptide derived from a protective protein found in human gastric juice (BPC). It acts primarily through upregulation of VEGF and its receptor expression, driving angiogenesis — the formation of new blood vessels — in damaged tissue. This vascular response underpins its broad healing effects across disparate tissue types.

It also modulates the nitric oxide (NO) synthase pathway, enhancing vasodilation and endothelial repair. BPC-157 activates the growth hormone receptor signalling cascade locally, accelerating fibroblast activation and improving tendon/ligament cell survival under oxidative stress. Its gut-protective effects involve upregulation of mucosal integrity genes and suppression of TNF-α and NF-κB inflammatory cascades — explaining its documented efficacy in inflammatory bowel models.

Over 150 peer-reviewed animal studies demonstrate BPC-157's comprehensive tissue-protective properties. Human pharmacokinetic data is limited: early-phase trials in IBD used oral formulations. The compound has never progressed to Phase III trials despite decades of preclinical promise, which is why it remains C-tier despite widespread use.

Documented effects (research-model)

  • Accelerates tendon and ligament healing (Achilles, rotator cuff, MCL models)
  • Protects and heals GI mucosal lining (IBD, NSAID damage, leaky gut)
  • CNS neuroprotection and dopaminergic system support
  • Angiogenesis-driven wound healing
  • Bone fracture recovery acceleration
  • Liver protection and hepatotoxicity reversal
  • Anti-ulcer effects via mucosal prostaglandin upregulation

Research protocols

ProtocolDoseFrequencyCycleVial
Standard 250 mcg Once daily SubQ 8–12 weeks 2mg / 2mL BAC water
Advanced 500 mcg Twice daily 8 weeks 5mg / 2mL BAC water

Research context only. Not medical advice. Consult a qualified healthcare professional before any protocol decision.

Synergies

  • TB-500 HIGH
    The Wolverine Stack — BPC-157 drives localised angiogenesis and nerve repair; TB-500 provides systemic actin upregulation and cell migration. Complementary local + systemic healing.
  • GHK-Cu HIGH
    BPC-157 builds the vascular infrastructure; GHK-Cu synthesises the collagen matrix. Angiogenesis + matrix reconstruction.
  • Ipamorelin MODERATE
    Local tissue repair (BPC) + systemic GH pulse for amplified recovery.

Myths & misconceptions

Myth BPC-157 is just a peptide supplement — it's the same as collagen powder.
Reality BPC-157 is a sequence-specific signalling peptide with documented receptor-level activity (VEGF-R, GH-R, NO-synthase). Collagen powder is a bulk protein source. The mechanisms are entirely different.
Myth More BPC-157 = faster healing.
Reality Published animal data suggests a bell-shaped dose-response. Doses beyond 500 mcg/day show no additional benefit in most models. Excessive dosing may alter NO-mediated blood pressure regulation.
Myth BPC-157 has FDA human approval.
Reality It does not. All human use is off-label research. Early IBD trials existed but no Phase III data. The FDA placed it on the Category 2 restricted list in 2023, which was updated in 2026.

Evidence gaps

  • No completed randomised controlled trials in humans. All efficacy data is animal-derived.
  • Long-term safety profile in humans is entirely unknown — no study has followed subjects beyond a few months.
  • Optimal route of administration for specific injuries remains unresolved (SubQ vs. IM vs. oral).
  • Interaction with oncological processes: BPC-157 upregulates VEGF, which could theoretically accelerate tumour angiogenesis. No human data exists on this risk.

Safety notes

Well-tolerated in animal models across hundreds of studies. No significant toxicity at research doses. Injection site reactions possible. VEGF upregulation — theoretical concern in individuals with active malignancy.

Biomarkers to monitor

hs-CRPALTGGTVEGFIGF-1

Primary-source citations

  • PMID 9100337 — Stable gastric pentadecapeptide BPC 157 in trials for IBD (PL-10) (Curr Pharm Des. 2011)
  • PMID 10906069 — BPC 157 accelerates healing of transected rat Achilles tendon (J Orthop Res. 2000)
  • PMID 24165960 — BPC-157 in central nervous system disorders (Curr Neuropharmacol. 2014)

Frequently asked

What is BPC-157?

BPC-157 (Body Protection Compound-157) is a research compound classified in our library as Tier C — Limited human trials; effect size uncertain.. The tissue-healing workhorse — accelerates repair of tendons, ligaments, gut lining, and nerves via VEGF-driven angiogenesis.

What is the evidence tier for BPC-157?

We classify BPC-157 as Tier C: Limited human trials; effect size uncertain. See our full peptide evidence tiers explainer for how we assign S/A/B/C/D.

What is the research dose of BPC-157?

For BPC-157, typical research dose is 250–500 mcg/day, route is SubQ / IM / Oral, half-life is ~4h SubQ / ~8h oral. Protocols vary by research goal — see the protocols section on this page for standard and advanced dosing schedules. Research use only, not medical advice.

What does BPC-157 stack well with?

BPC-157 stacks well with TB-500. The Wolverine Stack — BPC-157 drives localised angiogenesis and nerve repair; TB-500 provides systemic actin upregulation and cell migration. Complementary local + systemic healing.

Is BPC-157 safe?

Well-tolerated in animal models across hundreds of studies. No significant toxicity at research doses. Research context only — no compound on this site is approved for human therapeutic use unless explicitly noted.

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