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IGF-1 LR3

Long R3 IGF-1, LR3IGF-1

A modified form of IGF-1 with enhanced potency and extended half-life. Modifications prevent binding protein sequestration, increasing bioavailability approximately 2-3 fold.

What is IGF-1 LR3?

IGF-1 LR3 (Long R3 Insulin-like Growth Factor-1) is a modified form of IGF-1 with enhanced potency and extended half-life. The modifications include an arginine substitution at position 3 and a 13-amino acid N-terminal extension, making it approximately 2-3 times more potent than native IGF-1.

These modifications prevent binding to IGF binding proteins (IGFBPs), resulting in greater bioavailability and longer duration of action compared to regular IGF-1.


Structural Modifications

Key Changes from IGF-1

  1. Position 3: Glutamic acid → Arginine (R3)
  2. N-terminus: 13 amino acid extension added
  3. Total length: 83 amino acids (vs 70 for IGF-1)

Result of Modifications

  • Reduced IGFBP binding (~1000x less)
  • Increased half-life
  • Greater bioavailability
  • Enhanced potency

Molecular Profile

PropertyIGF-1 LR3Native IGF-1
Amino Acids8370
Molecular Weight~9200 Da~7649 Da
Half-life20-30 hours10-20 minutes
IGFBP BindingVery lowHigh

Mechanism of Action

IGF-1 Receptor Activation

  • Binds IGF-1 receptors
  • Activates PI3K/Akt pathway
  • Stimulates protein synthesis
  • Promotes cell proliferation

Effects

Anabolic:

  • Enhanced protein synthesis
  • Muscle hypertrophy
  • Cell proliferation

Metabolic:

  • Glucose uptake
  • Amino acid transport
  • Lipid metabolism

Research Interest

Body Composition Studies

  • Muscle growth research
  • Fat metabolism
  • Performance studies
  • Regenerative research

Considerations

Potential Risks:

  • Hypoglycemia (insulin-like effects)
  • Theoretical cancer concerns
  • No approved medical uses
  • Limited human safety data

Comparison with Other IGF-1 Forms

FormHalf-lifePotencyIGFBP Binding
IGF-1MinutesBaselineHigh
IGF-1 LR3HoursEnhancedVery low
IGF-1 DESMinutesHigherLower

Summary

IGF-1 LR3 offers enhanced potency and duration through modifications that prevent binding protein sequestration, making it a subject of research interest despite safety unknowns.

Key Points:

  • Classification: Modified IGF-1
  • Modifications: R3 substitution + N-terminal extension
  • Effect: ~2-3x potency of native IGF-1
  • Status: Research compound, not approved

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