The short answer
BPC-157 is Gly-Glu-Pro-Pro-Pro-Gly-Lys-Pro-Ala-Asp-Asp-Ala-Gly-Leu-Val: fifteen residues at 1419.5 Da for formula C62H98N16O22. Four prolines and three glycines dominate its backbone behaviour, and it carries no cysteine, methionine or aromatic residue, which makes it chemically robust and analytically awkward in equal measure.
Key facts
- Sequence
- GEPPPGKPADDAGLV
- Residues
- 15
- Prolines
- Four (positions 3, 4, 5, 8)
- Glycines
- Three (positions 1, 6, 13)
- Acidic
- Glu2, Asp10, Asp11
- Basic
- Lys7
- Cys / Met / aromatic
- None of any
The proline run
Positions 3, 4 and 5 are three consecutive prolines, with a fourth at position 8. A run of three prolines forms a polyproline helix, a distinctive extended, rigid conformation quite unlike an alpha helix. That segment is structurally locked, and it dominates the peptide's shape in a way no other feature does.
The glycines that answer it
Glycine has no side chain and is the most flexible residue available. Three of them sit at positions 1, 6 and 13: immediately after the proline run at 6, and near each terminus. The result is an alternating architecture, with rigid proline segments hinged by flexible glycines, rather than a uniformly stiff or uniformly floppy chain.
Research material referenced
BPC-157 5mg, third-party HPLC tested
Charge distribution
Glutamate at 2 and two aspartates at 10 and 11 give three negative charges; lysine at 7 gives one positive. Net negative at physiological pH, with the acidic residues clustered toward the C-terminal half. That asymmetry means the two ends of the molecule have quite different electrostatic character.
What is absent
No cysteine, so no disulfide chemistry and no reducing agent needed. No methionine, so no thioether oxidation and no +16 Da satellite. No tryptophan, tyrosine or phenylalanine, so no usable absorbance at 280 nm and no spectrophotometric quantification. This is the same profile as Selank and TB-500: chemically robust, analytically awkward.
Why the composition may explain the stability claim
The literature calls it the stable gastric pentadecapeptide. Proline-adjacent peptide bonds are poor substrates for most peptidases because proline constrains the backbone geometry those enzymes require. A peptide with four prolines, three of them consecutive, has a lot of protease-resistant bonds, which is a structural reason the stability claim is at least plausible rather than merely asserted.
Frequently asked questions
- What does GEPPPGKPADDAGLV mean?
- It is the single-letter sequence: glycine, glutamate, proline, proline, proline, glycine, lysine, proline, alanine, aspartate, aspartate, alanine, glycine, leucine, valine.
- Why do three consecutive prolines matter?
- They form a polyproline helix, an extended, rigid conformation that dominates the peptide's shape and resists most peptidases.
- Can BPC-157 be quantified at 280 nm?
- No. There is no tryptophan, tyrosine or phenylalanine, so it has no usable absorbance there.
Extended research context
The BPC-157 (Pentadecapeptide) deep dive
Deep dive: the pentadecapeptide sequence
BPC-157 is a synthetic pentadecapeptide with the sequence Gly-Glu-Pro-Pro-Pro-Gly-Lys-Pro-Ala-Asp-Asp-Ala-Gly-Leu-Val. It is derived from a fragment identified in human gastric juice by the Zagreb research group (Sikirić and colleagues), whose body of published work spans three decades and covers models ranging from tendon repair to gut integrity. The 'BPC' initials stand for 'body protection compound', the group's original characterisation term.
Two forms: acetate salt vs arginate
BPC-157 is supplied most commonly as an acetate salt; a small subset of suppliers offer the arginate form, which has slightly different solubility and stability properties. For research reproducibility, keep the salt form consistent across a study and confirm which form the CoA specifies (mass ± counterion changes the reading).
Reading a BPC-157 CoA
A trustworthy BPC-157 CoA lists HPLC purity (target ≥98% area), mass-spec confirmation (~1,419 Da for the free peptide), water content (Karl Fischer), acetate content, and residual solvents. Some batches also include endotoxin data. Any missing category is a red flag for a compromised supply chain.
Research applications
- ▸Cell-culture models of gut epithelial integrity
- ▸Tendon fibroblast migration and collagen-synthesis assays
- ▸Angiogenesis models involving VEGF and NO signalling
- ▸Stability studies comparing acetate vs arginate salt forms
- ▸Analytical reference for pentadecapeptide HPLC methods
Handling checklist
- ✓Store lyophilised vial at −20 °C long-term (2–8 °C short-term)
- ✓Reconstitute with bacteriostatic water; a 5 mg vial dissolves cleanly
- ✓Aliquot reconstituted solution; keep refrigerated 2–8 °C, use within 28 days
- ✓Protect from light and repeated warming
- ✓Verify CoA: HPLC ≥98%, mass ~1,419 Da, salt form declared
Common research-handling mistakes
Learnt from thousands of researcher orders across our UK labs.
✗ Mixing acetate and arginate BPC-157 across a study
Fix: Choose one salt form and stay with it. Different masses and solubility.
✗ Assuming stability at room temperature
Fix: Refrigerate reconstituted solution; discard after 28 days.
✗ Buying without a CoA
Fix: Only source from suppliers that publish batch HPLC + mass-spec data.
Continue researching
Peer-reviewed guides, comparators and matched reference materials.
Related questions researchers ask
- What does BPC-157 stand for?
- Is BPC-157 the same as pentadecapeptide?
- Who discovered BPC-157?
- What is the difference between BPC-157 acetate and arginate?
- How is BPC-157 reconstituted for research?
Primary sources & clinical trials
Peer-reviewed research and registered trials from PubMed, ClinicalTrials.gov, PubChem, FDA and NIH. All links open in a new tab and point to the primary source, so every claim can be verified at origin.
- PubChemPubChem · BPC-157 (CID 9941957)pubchem.ncbi.nlm.nih.gov
- PubMedSikiric P et al., Stable gastric pentadecapeptide BPC 157. Curr Pharm Des 2011 (PMID 21548867)pubmed.ncbi.nlm.nih.gov
- PubMedSikiric P et al., Fistulas Healing: Stable Gastric Pentadecapeptide BPC 157 Therapy. Curr Pharm Des 2020 (PMID 32329684)pubmed.ncbi.nlm.nih.gov
- PubMedKrivic A et al., Achilles detachment in rat and stable gastric pentadecapeptide BPC 157. J Orthop Res 2006 (PMID 16583442)pubmed.ncbi.nlm.nih.gov
- PubMedCerovecki T et al., Pentadecapeptide BPC 157 improves ligament healing in the rat. J Orthop Res 2010 (PMID 20225319)pubmed.ncbi.nlm.nih.gov
- PubMedSeiwerth S et al., BPC 157 and blood vessels. Curr Pharm Des 2014 (PMID 23782145)pubmed.ncbi.nlm.nih.gov
- PubMedNIH PubMed: Complete BPC-157 literature (Sikiric group)pubmed.ncbi.nlm.nih.gov
- GuidelineGoogle: Creating helpful, reliable, people-first contentdevelopers.google.com
Written and reviewed by
The UK Peptides Editorial Team · Research library, UK Peptides
The editorial team is responsible for supplier selection, batch release decisions and the content published in this research library. Every article here is sourced to primary literature and every product page to a signed third-party certificate. Corrections are made in place and the review date updated.
More BPC-157 (Pentadecapeptide) articles
- The Proline Problem in BPC-157 SynthesisFour prolines, three consecutive, make solid-phase synthesis meaningfully harder. Why proline coupling is a recognised difficult step, and what it costs purity.
- BPC-157 Molecular Structure and Physical Properties1419.5 Da, net negatively charged, highly water-soluble, conformationally mixed. The physical consequences of a proline- and glycine-rich fifteen-mer.
- Pentadecapeptide: The Word and What It Tells YouPenta-deca-peptide is fifteen. Where BPC-157 sits on the spectrum from short peptide to protein, and why fifteen residues is a useful size.
- What Does BPC-157 Stand For?BPC is body protection compound; 157 is a series designation with no chemical meaning. Why the name is a claim and where it came from.
- Body Protection Compound: A Name That Is a HypothesisThe name records what the Zagreb group believed they had found. What that framing asserts, and how to read a compound named for a proposed function.
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