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Stillwater BioLabs
Tissue Repair & Regeneration

Pentadecarginine

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$52

A BPC-157 analog with arginine salt form studied for enhanced stability and bioavailability.

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In-vitro research only — not for human use

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Pentadecarginine

How pentadecarginine works in research

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Characteristics

Characteristics of Pentadecarginine
PropertyValue
Molecular FormulaC₆₂H₉₈N₁₆O₂₂ (peptide) + C₆H₁₄N₄O₂ (arginine salt)
CAS NumberNot yet assigned (novel arginine salt form)
Molar Mass~1593.7 g/mol (peptide + arginine counter-ion)
Amino Acid SequenceGly-Glu-Pro-Pro-Pro-Gly-Lys-Pro-Ala-Asp-Asp-Ala-Gly-Leu-Val (BPC-157 core)
SynonymsBPC-157 Arginine Salt, BPC-157-Arg, Pentadecarginine
Physical FormLyophilized powder
SolubilityFreely soluble in water; enhanced solubility compared to acetate salt
Organoleptic ProfileWhite to off-white lyophilized powder; odorless
Storage ConditionsStore lyophilized at -20°C; reconstituted solution stable at 2-8°C for up to 14 days
CompositionLyophilized BPC-157 with L-arginine counter-ion

How is Pentadecarginine Used in Research?

Pentadecarginine is an arginine salt formulation of BPC-157, the well-studied body protection compound pentadecapeptide. By pairing the BPC-157 peptide with an L-arginine counter-ion rather than the traditional acetate salt, this formulation is designed to enhance aqueous solubility and potentially improve bioavailability. L-arginine itself serves as a precursor to nitric oxide (NO) via the nitric oxide synthase pathway, and since BPC-157's mechanism of action is known to involve NO system modulation, the arginine salt form may offer complementary activity through enhanced NO substrate availability.

The core peptide retains the same 15-amino acid sequence as standard BPC-157, and therefore the extensive preclinical literature supporting BPC-157's activity in wound healing, gastrointestinal cytoprotection, and tissue repair is directly applicable. Research on BPC-157 has demonstrated its effects on angiogenesis via VEGF upregulation, tendon and ligament healing through improved collagen fiber organization, and neuroprotective activity through modulation of dopaminergic pathways. The arginine salt formulation represents a pharmaceutical chemistry optimization rather than a novel peptide entity.

The rationale for arginine salt formulation draws on research demonstrating that counter-ion selection can significantly influence peptide stability, solubility, and absorption characteristics. Arginine-based salt forms have been explored across pharmaceutical chemistry for their favorable pH buffering properties and their role in NO-mediated vasodilation, which may facilitate tissue distribution of the active peptide.

This product is supplied in a lyophilized form and requires reconstitution prior to laboratory handling. For research and laboratory use only. Not for human or veterinary consumption.

Areas of Study

Enhanced Bioavailability Research

Investigated as an alternative salt form to improve aqueous solubility, stability, and potential absorption characteristics compared to the standard acetate salt.

Nitric Oxide System Modulation

The arginine counter-ion provides additional NO precursor substrate, potentially complementing BPC-157's known NO pathway interactions.

Tissue Repair & Wound Healing

Retains the full BPC-157 peptide sequence, with applicable preclinical evidence for accelerated healing of musculoskeletal and soft tissue injuries.

Gastrointestinal Protection

The core BPC-157 peptide is extensively studied for cytoprotective effects against NSAID-, alcohol-, and cytotoxin-induced GI lesions.

Pharmaceutical Formulation Science

Studied in the context of counter-ion optimization for peptide drugs, where salt form selection affects stability, solubility, and shelf life.

References

  1. [1]Sikiric P, Seiwerth S, Rucman R, et al. (2018). Stable gastric pentadecapeptide BPC 157: novel therapy in gastrointestinal tract. Current Pharmaceutical Design, 24(18), 1990-2001.
  2. [2]Sikiric P, Seiwerth S, Rucman R, et al. (2014). Stable gastric pentadecapeptide BPC 157-NO-system relation. Current Pharmaceutical Design, 20(7), 1126-1135.
  3. [3]Stout E, McKessor A. (2012). Glycine-arginine salt effects on peptide solubility and stability in pharmaceutical formulations. International Journal of Pharmaceutics, 438(1-2), 16-23.
  4. [4]Cerovecki T, Bojanic I, Brcic L, et al. (2010). Pentadecapeptide BPC 157 (PL 14736) improves ligament healing in the rat. Journal of Orthopaedic Research, 28(9), 1155-1161.

Disclaimer: The information provided is for research reference only and does not constitute medical advice. Products are sold strictly for in-vitro research use.

Certificate of Analysis (COA)

Third-Party Verified Quality

Every batch of Pentadecarginineis independently tested by an accredited third-party laboratory. Our COAs include HPLC purity analysis, mass spectrometry identity confirmation, and batch-specific lot numbers. We publish these results publicly so you can verify exactly what you're getting.

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