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PreclinicalVendors pendingFacts verified · 2026-05-25

PEG-MGF

Also known as pegylated igf-1ec e-peptide, peg-mgf · Wikipedia

PEG-MGF is the pegylated form of Mechano Growth Factor, the C-terminal E-peptide of the IGF-1Ec splice variant produced in mechanically loaded skeletal muscle. PEGylation extends the very short native half-life and allows systemic (subcutaneous) dosing, in contrast to unpegylated MGF which is typically used by local intramuscular injection post-exercise. It is marketed in the research-chemical channel for muscle repair and hypertrophy support, but no published human clinical trials exist for PEG-MGF specifically, and the underlying MGF biology itself remains debated, with some studies failing to replicate the satellite-cell effects.

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Mechanism of action

PEG-MGF is the polyethylene-glycol-conjugated form of Mechano Growth Factor (MGF), the C-terminal E-domain peptide of the IGF-1Ec splice variant. The E-peptide is hypothesized to act independently of the IGF-1 receptor on quiescent muscle satellite cells, promoting their proliferation and delaying differentiation, thereby expanding the local myogenic stem-cell pool available for repair (Mills et al.

PEG-MGF is the polyethylene-glycol-conjugated form of Mechano Growth Factor (MGF), the C-terminal E-domain peptide of the IGF-1Ec splice variant. The E-peptide is hypothesized to act independently of the IGF-1 receptor on quiescent muscle satellite cells, promoting their proliferation and delaying differentiation, thereby expanding the local myogenic stem-cell pool available for repair (Mills et al., PubMed 21354439). PEGylation extends the otherwise very short plasma half-life (native MGF ~5-7 min) by reducing renal clearance and proteolytic degradation, enabling systemic dosing. The precise E-peptide receptor remains undefined, and independent groups have failed to reproduce satellite-cell proliferation effects with synthetic MGF peptide (Fornaro et al., PubMed 24253050), so the mechanism is contested.

Pharmacokinetic properties

Half-life

Several hours to ~48-72 hours (estimates vary; uncharacterized in peer-reviewed human PK studies)

Routes

subcutaneous · intramuscular

Bioavailability

PEG conjugation extends native MGF's ~5-7 minute plasma half-life dramatically. Systemic dosing 1-2x weekly typical; native (unpegylated) MGF requires local intramuscular dosing post-workout.

Amino-acid sequence

(PEGylated MGF E-peptide; see IGF-1Ec literature)

Use & research dosing

No FDA-approved indication and no published human clinical trials with PEG-MGF specifically. Self-experimentation protocols circulating in the research-chemical channel commonly report 200-500 mcg subcutaneously or intramuscularly 1-3 times per week, sometimes timed post-workout. By contrast, native (unpegylated) MGF is typically used by local intramuscular injection immediately post-workout because of its very short plasma half-life of approximately 5-7 minutes. Research framing only.

Research-use framing only. SavePeptides sells nothing for human consumption. Doses above reflect reported research / self-experimentation ranges, not clinical recommendations.

Editorial perspective

Mechanistically distinct from systemic IGF-1: claimed to act on the local muscle stem-cell pool rather than the IGF-1 receptor. PEGylation is essential for systemic dosing because native MGF is cleared in minutes. The underlying biology is contested - some groups reproduce satellite-cell proliferation effects, others do not, and the receptor target has not been definitively identified. No human clinical trial data with PEG-MGF exist.

— SavePeptides editorial desk · last updated 2026-05-25

Cautions & contraindications

Before researching this compound, note:

  • Not FDA-approved; no published human clinical trials for PEG-MGF specifically
  • Avoid in active or suspected malignancy - satellite-cell proliferative signaling
  • Avoid in pregnancy and breastfeeding
  • Rare anaphylactoid reactions to PEG have been reported with other PEG-conjugated drugs
  • Injection-site reactions possible
  • Vendor quality, actual PEG conjugation status, and identity assurance are highly variable in the gray market
  • Mechanism contested - independent groups have failed to reproduce satellite-cell effects of synthetic MGF E-peptide
  • Long-term safety in humans is undefined

Facts verified

2026-05-25

Confidence

low

What this means

  • no human clinical trials with PEG-MGF
  • mechanism contested in independent replication studies
  • PEG conjugation quality in gray market unverifiable

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PEG-MGF · SavePeptides