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RYZENBPC-1575 mgRYZ-BPC1-2608199.3% RP-HPLCRESEARCH USE ONLY

Most recent release

99.4%

Batch RYZ-BPC1-26081 · released 12 Aug 2026

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Tissue Repair & RegenerativeMost ordered

BPC-157

Body protection compound 157 · PL 14736

Fifteen-residue gastric pentadecapeptide fragment studied in angiogenesis and repair models.

Fill weight

Total, ex VAT

£36.00

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  • Released at ≥ 99.0% (RP-HPLC, area %)
  • Identity confirmed by ESI-MS against theoretical mass
  • Batch certificate matched to the vial, verifiable online
  • Same working day dispatch before 14:00, tracked

For laboratory research use only. Not for human or veterinary use, and not a medicine, food or cosmetic. Sold to qualified researchers and institutions who accept responsibility for safe handling and lawful use.

Compound data

What is in the vial

Indicative values for this line. The certificate issued with your batch is the authoritative record and reports the measured figures for the material you receive.

CAS number
137525-51-0
Molecular formula
C62H98N16O22
Average mass
1419.53 g/mol
Sequence
Gly-Glu-Pro-Pro-Pro-Gly-Lys-Pro-Ala-Asp-Asp-Ala-Gly-Leu-Val
Residues
15
Class
Gastric pentadecapeptide fragment
Form as supplied
Lyophilised powder
Appearance
White to off-white lyophilised powder
Purity specification
≥ 99.0% (RP-HPLC, area %)
Solubility
Soluble in sterile or bacteriostatic water.
Storage
Lyophilised: −20 °C, desiccated and dark. Reconstituted: 2–8 °C.

Targets and pathways

  • VEGFR2 signalling and angiogenesis
  • Nitric oxide system
  • Focal adhesion / FAK-paxillin pathways

Overview

About BPC-157

BPC-157 is a fifteen-residue sequence derived from a protein found in gastric juice. It is unusually stable for an unmodified peptide — it survives in gastric acid, which is what drew attention to it — and that stability comes from its proline-rich composition rather than from any synthetic modification.

The research literature centres on angiogenesis and tissue repair, with proposed mechanisms including VEGFR2 pathway activation, nitric oxide system interaction and effects on focal adhesion complexes. Much of the primary work comes from a small number of groups, which is worth knowing when weighing the evidence base.

In short

  • Fifteen residues, proline-rich, unusually acid-stable without modification
  • Studied in angiogenesis, tendon, ligament and gastrointestinal repair models
  • Released at ≥ 99.0% area-percent by RP-HPLC
  • Available in a five-vial pack for extended study programmes

Where it is used

Research applications

Angiogenesis

VEGFR2 pathway involvement is the most-studied proposed mechanism, examined in endothelial cell and vessel formation assays.

Tendon and ligament models

Fibroblast outgrowth and collagen organisation are common endpoints in the musculoskeletal literature.

Gastrointestinal repair

Given its origin in gastric juice, mucosal integrity models remain a significant strand of work.

Handling

Reconstitution and stability

Reconstitution

Reconstitute with sterile or bacteriostatic water added slowly against the inner wall of the vial. Allow the cake to dissolve without agitation, swirling gently if required. Do not vortex or shake.

Stability

Lyophilised at −20 °C, desiccated and protected from light, stable for at least 24 months. Reconstituted and held at 2–8 °C, use within 28 days. Avoid repeated freeze-thaw.

Notes

  • Bring the vial to room temperature before opening so atmospheric moisture does not condense onto cold powder.
  • Record the reconstitution date on the vial; concentration drift between runs is usually evaporation, not synthesis variance.
  • Aliquot at first reconstitution where the working programme needs more than a few withdrawals.

Laboratory reference

Reconstitution calculator

Enter the fill weight on the vial and the diluent volume you intend to add. The calculator returns the resulting solution concentration and the volume that contains a given mass.

Concentration
2.500 mg/mL · 2500 µg/mL
Volume containing target mass
100.0 µL · 0.1000 mL

Figures are mass-to-volume arithmetic for laboratory preparation of BPC-157 and take no account of net peptide content, which is stated on the batch certificate and should be applied to the fill weight before calculating. Nothing here constitutes dosing, administration or clinical guidance of any kind.

Published work

What the literature reports

Summaries of published findings, provided as research reference. These describe work done by others in preclinical and clinical settings; they are not claims about this material or outcomes for any reader.

  1. Angiogenic mechanism

    Work implicating VEGFR2 signalling in the compound's effects on endothelial cells and vessel formation.

    Hsieh et al., Journal of Molecular Medicine, 2017

  2. Tendon fibroblast studies

    Reported effects on tendon fibroblast outgrowth, migration and survival in culture.

    Chang et al., Journal of Applied Physiology, 2011

Questions

BPC-157 — asked and answered

Something not covered here? Ask us directly — technical questions reach someone who runs the assays.

Which salt form is supplied?
Acetate. Residual acetate is reported on the certificate, which matters when calculating net peptide content from gross weight.
Is it stable in acidic conditions?
Notably so for an unmodified peptide, which is what made it of interest. For laboratory storage the usual conditions still apply: −20 °C lyophilised, 2–8 °C in solution.
How strong is the evidence base?
Much of the primary literature comes from a limited number of groups. We supply material to specification; assessing the literature is the researcher's judgement.

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Important

BPC-157 is supplied strictly for laboratory research and analytical use. It is not a medicine, food, cosmetic or veterinary product; it is not for human or animal consumption; and it is not intended to diagnose, treat, cure or prevent any condition. It is not manufactured, tested or released to any standard that would support administration to humans or animals. Information on this page is compiled for research reference and is not medical advice. No dosing, administration or therapeutic guidance is given or implied. By ordering you confirm you are a qualified researcher or institution and accept responsibility for safe handling and lawful use.