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Specimen Atlas of Research Peptides30 plates · MIT
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IIIPlate IIIReviewed 2026-04-25

BPC-157

Pentadecapeptide

also known as BPC 157, BPC157, Body Protection Compound, PL-14736

Synthetic 15-amino-acid pentadecapeptide derived from a protective sequence found in human gastric juice (BPC = Body Protection Compound). Stable in simulated gastric conditions and the most extensively studied healing peptide in animal literature. Demonstrates tendon, ligament, muscle, and gastrointestinal mucosa healing across 20+ rodent models. Clinically evaluated under designation PL-14736 in a Phase 2 ulcerative colitis trial.

§ I

At a glance

Daily dose
250–500 mcg
Evidence level
Phase 2
Half-life (est.)
~30 min
Route

SQ or IM · Local · Once or twice daily

§ II

Mechanism

Primary target — VEGFR2 / nitric oxide / FAK-paxillin axes (proposed) [chang-2014][sikiric-2018].

Pathway — Upregulates VEGFR2 → angiogenesis; modulates NO synthase; promotes fibroblast outgrowth via FAK-paxillin [chang-2014].

Downstream effect — Accelerated tissue repair, reduced inflammation, improved gut barrier integrity [sikiric-2018].

Origin — Synthetic pentadecapeptide derived from a sequence in human gastric juice; first characterised by Sikiric et al. [sikiric-2018].

Feedback intact — No known endogenous receptor; mechanism still under investigation.

§ III

Dosage

Protocols described in the cited literature; not medical advice.

ParameterValue
Standard dose250–500 mcg / day [hwang-2016]Anecdotal community range. Phase 2 trial used 1.0 mg PL-14736 IV/day.
FrequencyOnce or twice dailySplit dosing reported anecdotally for chronic injury.
Lower / starter dose200 mcg / dayConservative starter for new users.
Evidence basisAnimal-strong + Phase 2 clinical [sikiric-2018][hwang-2016]
Duration2–4 weeks (acute injury); 4–8 weeks (chronic)Anecdotal; no long-term human safety data.
ReconstitutionBacteriostatic water, 1–2 mL
TimingLocal SQ to injury site preferred (anecdotal)Systemic SQ also used; oral bioavailability shown in animal studies.
Half-life~30 min plasma (estimated)Tissue half-life longer; mechanism may explain durable effect.
§ III · b

Reconstitution

A pure mass-to-volume utility. Enter what you have in the vial; the atlas computes the volume per dose. No prescription information.

Inputs
The calculator does pure mass-to-volume math. It does not recommend a dose. Refer to BPC-157's cited literature for protocol specifics.
Volumetric outputFig. C — reconstitution math
Volume per dose
0.100mL
10.0 units on a U-100 insulin syringe
Concentration
2500
mcg per mL
Doses per vial
20
at this dose
§ V

Adverse events

Severities follow the FDA / CTCAE convention.

Injection site reactionmild
Mild irritation (anecdotal)
GI symptomsmild
None reported in PL-14736 Phase 2
Cardiovascularmild
Not reported
Cancer riskmoderate
Theoretical concern via VEGF angiogenesis pathway [sikiric-2018]
Antibody formationmild
No data (no long-term human trials)
Pregnancy / OBsevere
Avoid — insufficient safety data
Long-term safetymoderate
Unknown beyond Phase 2 trial duration
Drug interactionsmild
None established
Absolute contraindications
  • Pregnancy / breastfeeding
  • Known active malignancy (theoretical VEGF concern)
Relative contraindications
  • History of cancer
  • Concurrent VEGF inhibitor therapy (theoretical)
  • Acute thrombotic events
§ VI

Administration

  1. 01
    Reconstitution

    Add 1–2 mL bacteriostatic water to a 5 mg vial. Roll gently; do not shake. Solution should be clear and colourless.

  2. 02
    Injection site

    Subcutaneous near the injury site is the most common anecdotal route. Systemic SQ (abdomen) also used. Rotate sites.

  3. 03
    Timing

    No strict timing requirement. Most users dose once or twice daily, often morning + evening.

  4. 04
    Storage

    Lyophilised: room temp, light-protected. Reconstituted: refrigerate 2–8 °C, use within 30 days.

  5. 05
    Needle

    27–31G insulin syringe, 4–8 mm. Local injection allows finer 31G.

§ VII

Synergies

Appendix

Sources

17%

of 53 rendered claims carry a resolvable citation.

  1. [chang-2014]
    Chang 2014The promoting effect of pentadecapeptide BPC 157 on tendon healing involves tendon outgrowth, cell survival, and cell migration
    J Appl Physiol, 2014
  2. [hwang-2016]
    Hwang 2016BPC 157 (PL 14736) — Crohn's disease phase II clinical trial
    Inflamm Bowel Dis, 2016
  3. [sikiric-2018]
    Sikiric 2018Stable gastric pentadecapeptide BPC 157, an effective anti-inflammatory agent: a comprehensive review
    Curr Pharm Des, 2018
Plate composed 2026-04-25 · maturity reviewed · schema v1 · Contributors: peptidesdb-core · 44 fields uncited — open contributions