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Osteogenic Growth Peptide (OGP)

A 14-aa C-terminal histone H4 fragment circulating naturally in serum; the active short fragment OGP(10-14) (Tyr-Gly-Phe-Gly-Gly) stimulates osteoblast proliferation and bone formation in rodents a… | Compound

Aliases (5)
OGP · OGP(10-14) · histone H4 fragment 90-103 · sOGP · synthetic OGP
TYPICAL DOSE
Rodent doses typically 1-50 µg/kg SC or IP, 5×/…
ROUTE
CYCLE
STORAGE
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Overview TL;DR

A 14-aa C-terminal histone H4 fragment circulating naturally in serum; the active short fragment OGP(10-14) (Tyr-Gly-Phe-Gly-Gly) stimulates osteoblast proliferation and bone formation in rodents and accelerates marrow recovery after irradiation/chemotherapy. Promising bench/preclinical profile, almost no human data. NOT-RELEVANT for Dylan.

Mechanism of action

Discovered in 1989 by Bab et al. as the bone-marrow regenerative factor in post-ablation rat marrow. Sequence corresponds to histone H4 residues 90-103. Circulates bound to α2-macroglobulin in inactive complex; released → activated.

Active C-terminal pentapeptide OGP(10-14) [Tyr-Gly-Phe-Gly-Gly] retains all biological activity. Mechanism involves:

  • Gi/o-coupled receptor on osteoblasts (receptor identity not fully resolved)
  • Downstream activation of MAPK/ERK and PI3K/Akt
  • ↑ osteoblast proliferation, alkaline phosphatase, type I collagen, osteocalcin
  • Hematopoietic stimulation in marrow stroma — synergistic with G-CSF in animal models
  • Antagonizes glucocorticoid-induced bone loss in some models
Pharmacokinetics No data
Pharmacokinetics data not available for this compound.
No half-life mentions found in the source notes.
What to expect Generic
  1. 1
    Week 1
    Tolerability and dose-response.
  2. 2
    Week 2-4
    Early effect window.
  3. 3
    Week 4-8
    Peak benefit assessment.
  4. 4
    Week 8+
    Cycle decision point.
Side effects + safety
  • Common (>10% users): Unknown — no real safety data
  • Less common: Injection-site reactions
  • Rare-serious (<1% but worth knowing):
    • Theoretical concern: peptide also affects hematopoiesis — could in principle alter blood counts
    • Theoretical concern: any growth factor with mitogenic activity carries hypothetical neoplasia risk if subclinical malignancy present
    • Unknown immunogenicity
  • Specific watch periods: No clinical guidance exists
Interactions2 compounds
  • In bench/animal studies:Synergistic
    G-CSF (hematopoietic synergy), BMPs (additive osteogenic)
  • Forum-claimed (low evidence):Synergistic
    BPC-157, TB-500 for "complete recovery stack" — no rigorous data
References4 sources
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