Recovery & RepairResearch OnlyNot For Human Consumption

BPC-157

Body Protection Compound 157 · PL 14736

Studied for its role in faster tissue recovery, tendons, ligaments, and the gut lining. One of the most studied recovery compounds available.

MECHANISM OF ACTION

BPC-157 is a small chain of 15 building blocks (amino acids) originally found in the stomach's protective lining. Research shows it helps grow new blood vessels in injured areas, improves blood flow, and kick-starts the repair process in damaged cells. It is also studied for its role in managing inflammation signalling. Studies have looked at tendon injuries, ligament tears, gut damage, bone fractures, and even brain protection. It's one of the most well-researched peptides in the recovery space.

RESEARCH APPLICATIONS

  • Tendon and ligament recovery (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 preclinical studies demonstrate significant acceleration of Achilles tendon recovery 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 , 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
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
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.