Recovery & RepairResearch OnlyNot For Human Consumption

BPC-157

Body Protection Compound 157 · PL 14736

Gastric pentadecapeptide with broad cytoprotective properties across tendon, ligament, and GI repair models.

MECHANISM OF ACTION

BPC-157 is a synthetic 15-amino acid peptide derived from a cytoprotective protein found in human gastric juice. Research indicates it promotes angiogenesis via upregulation of VEGFR2 signalling, modulates nitric oxide (NO) synthesis, and activates the FAK-paxillin pathway - critical for cytoskeletal reorganisation and cellular migration. Preclinical models demonstrate dose-dependent acceleration of tendon, ligament, and bone healing. It also exhibits GABAergic activity in rodent models, suggesting CNS involvement, and shows anti-inflammatory properties via NF-κB pathway downregulation.

RESEARCH APPLICATIONS

  • Tendon and ligament healing (Achilles, rotator cuff, MCL models)
  • Gastrointestinal mucosal protection and fistula models
  • Angiogenesis and wound-closure research
  • CNS protection models (TBI, inflammatory bowel disease)
  • Bone fracture repair and cartilage regeneration

RESEARCH HIGHLIGHTS

Tendon-to-Bone Healing Acceleration

2018

Multiple rodent studies demonstrate significant acceleration of Achilles tendon healing vs. controls, with histological evidence of improved collagen organisation at 14 and 28 days.

Ref: Sikiric et al., J Physiol Pharmacol

GI Mucosal Cytoprotection

2009

BPC-157 showed protective effects against NSAID-induced gastric ulceration in animal models, with proposed mechanism via NO pathway modulation.

Ref: Ilic et al., World J Gastroenterol

Angiogenic Activity via VEGFR2

2005

In vitro and in vivo data confirm upregulation of VEGFR2, with consequent endothelial proliferation and capillary formation - relevant for wound-bed vascularisation.

Ref: Hsieh et al., Regul Pept

RESEARCH PROTOCOL NOTES

Research concentration250–500 mcg per administration in rodent models
Route (preclinical)Intraperitoneal (IP) or subcutaneous (SC)
ReconstitutionBacteriostatic water; swirl gently, avoid agitation
Available formatsVial (5–10mg), Pen, Tablet (oral bioavailability debated)

Chemical Identity

Molecular FormulaC62H98N16O22
Molecular Weight1419.5 g/mol
CAS Number137525-51-0
Half-Life (t½)~4–6 hours in rodent models
SolubilitySoluble in water and physiological saline

Sequence

Gly-Glu-Pro-Pro-Pro-Gly-Lys-Pro-Ala-Asp-Asp-Ala-Gly-Leu-Val

Storage & Stability

Lyophilised: -20°C, protected from light. Reconstituted: use within 28 days at 2–8°C. Avoid repeated freeze-thaw cycles.

Regulatory Status

No FDA, EMA, or SAHPRA approval for human use. Research compound. WADA: not explicitly prohibited as of 2024.