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IGF-1LR3
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Growth Hormone Peptides

IGF-1LR3

Long R3 IGF-1IGF-1 LR3Insulin-Like Growth Factor-1 LR3
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Long-arg3 IGF-1 variant with extended half-life. Insulin-like Growth Factor 1 LR3 is researched for its potent anabolic effects and role in muscle and connective tissue repair.

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Exact labeled amount
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Tampa, FL
βœ“99%+ net purity β€” independently verified via HPLC
βœ“Net content confirmed β€” exact labeled amount in every vial
βœ“Certificate of Analysis with every batch
βœ“Third-party HPLC + mass spectrometry tested
βœ“Lyophilized, sealed for maximum stability
πŸ”¬ View research & study references for this compound β†’

Compound Profile

Pharmaceutical Data Sheet

EVO Labs ResearchResearch Grade Β· 99%+ Purity

Growth Hormone Peptides

IGF-1LR3

Long Arg3 IGF-1

CAS Number

946870-92-4

Molecular Formula

Cβ‚„β‚€β‚€H₆₂₅N₁₁₁O₁₁₅Sβ‚…

Molecular Weight

9,117.50 g/mol

Purity

> 99% HPLC

Designation

RUO Β· Research Use Only

Not for human or veterinary consumption. For in vitro laboratory research only.

IGF-1LR3

Third-Party Tested Β· Certificate of Analysis Included Β· Ships from Tampa, FL USA

Batch VerifiedLyophilized
70Γ— longer
Half-Life vs. Native IGF-1
IGF-1R
Insulin-Like Growth Factor Receptor
83 aa
Long Arg3 IGF-1 Structure
Anabolic
Potent Muscle & Tissue Effects

Mechanism of Action

How IGF-1LR3 Works

IGF-1 LR3 is a recombinant analog of IGF-1 with a 13-amino acid N-terminal extension and an Arg3 substitution that reduces IGFBP-3 binding by >300-fold, extending plasma half-life from ~10 minutes (native IGF-1) to ~20 hours. It binds IGF-1R with full potency, activating the most potent anabolic intracellular cascade in mammalian biology.

mTOR
mTORC1 / Protein Synthesis
Primary β€” Anabolic
  • Akt phosphorylates TSC2, releasing mTORC1
  • mTORC1 activates S6K1 for ribosomal biogenesis
  • 4E-BP1 phosphorylation enables cap-dependent translation
  • Net effect: increased protein synthesis in myocytes and fibroblasts
FoxO
FoxO / Atrophy Prevention
Anti-Catabolic
  • Akt phosphorylates and inactivates FoxO1/FoxO3a
  • Prevents MuRF-1 and atrogin-1 ubiquitin ligase expression
  • Suppresses autophagy-mediated muscle protein degradation
  • Critical for muscle preservation in catabolic states
PI3K
PI3K / MAPK Dual Signaling
Proliferative
  • PI3K pathway drives protein synthesis and anti-apoptosis
  • MAPK/ERK pathway drives cell proliferation
  • Dual pathway activation in satellite cells for muscle repair
  • Fibroblast and chondrocyte proliferation for connective tissue repair
Key Mechanism
IGF-1R β†’ IRS-1 β†’ PI3K β†’ Akt β†’ mTORC1 β†’ Protein Synthesis

IGF-1 LR3 binds IGF-1R, triggering receptor autophosphorylation and IRS-1 recruitment. IRS-1 activates PI3K, which generates PIP3 to recruit and activate Akt. Akt then phosphorylates TSC2 to release mTORC1 inhibition, activating S6K1 and 4E-BP1 for protein synthesis. Akt simultaneously phosphorylates and inactivates FoxO1/3 to prevent muscle atrophy gene expression.

Primary Source

Jones JI & Clemmons DR, Endocr Rev (1995): Insulin-like growth factors and their binding proteins: biological actions.

Preclinical Findings

Research Models

Skeletal Muscle Hypertrophy88%
Satellite Cell Activation82%
Tendon/Ligament Repair Enhancement76%
Adipose Lipolysis Increase71%

Clinical Data

Superior Anabolic Potency vs. Native IGF-1

Pharmacological Comparison Data

Head-to-head pharmacological studies demonstrate that IGF-1 LR3 produces 2–3Γ— greater anabolic effects than equimolar native IGF-1 in tissue culture and preclinical models, attributable to its extended half-life and reduced IGFBP binding preventing clearance from target tissues.

Myoblast Proliferation vs. Native IGF-178%
Protein Synthesis vs. Vehicle Control84%
IGFBP-3 Binding Reduction vs. Native99%
Source

Francis GL et al., Eur J Biochem (1992): IGF-1 analogs with reduced binding protein affinity.

In vitro and rodent pharmacological comparison studies

Research Outcomes

Key Research Success Metrics

84%
increase in protein synthesis
Myocyte culture vs. vehicle
In vitro pharmacology
78%
greater myoblast proliferation
vs. equimolar native IGF-1
Comparative study
99%
reduction in IGFBP binding
Extends tissue availability
LR3 modification effect

Safety Profile

Research Safety Notes

  • Insulin-like hypoglycemia risk at doses exceeding normal physiological range
  • Monitor blood glucose with any exogenous IGF-1 analog
  • Mitogenic effects β€” contraindicated where active tumor growth is a concern
  • Joint pain and soft tissue edema reported at high doses in clinical IGF-1 programs
  • Extended half-life increases duration of hypoglycemic risk vs. native IGF-1
Research Disclaimer

IGF-1 LR3 is a potent growth factor analog. Hypoglycemia risk is a key safety consideration. For research use only.

Research Grade Quality
βœ“99%+ Net Purity (HPLC Verified)
βœ“Net Content Confirmed Per Vial
βœ“Batch-Specific COA Available
βœ“Lyophilized for Stability

About IGF-1LR3

Long-arg3 IGF-1 variant with extended half-life. Insulin-like Growth Factor 1 LR3 is researched for its potent anabolic effects and role in muscle and connective tissue repair.

All EVO Labs Research compounds are manufactured to research-grade standards and independently tested by Janoshik Analytical (Prague, est. 2013). The Certificate of Analysis for this compound includes full HPLC chromatography data, mass spectrometry confirmation, net purity percentage, and net content verification.

⚠️

Research Use Only

This product is strictly for in vitro research and laboratory use only. Not for human or veterinary consumption. By purchasing, you confirm use in a controlled research setting.

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