IGF-1 LR3 is an 83-amino-acid IGF-1 analog with reduced IGFBP binding, extending half-life from ~15 minutes to ~20–30 hours — the most studied long-acting IGF-1 analog in preclinical research.

Growth Hormone Peptides

IGF-1LR3

IGF-1 LR3 (Insulin-like Growth Factor 1 Long R3) is a 83-amino-acid analog of human IGF-1, engineered to have dramatically reduced binding to IGF-binding proteins (IGFBPs) and a consequently extended biological half-life. It is one of the most studied anabolic signaling peptides in the preclinical research literature. The research significance of IGF-1 LR3 versus native IGF-1 is its binding profile. Native IGF-1 is rapidly bound by a family of IGFBPs in circulation, severely limiting its available half-life and bioavailability. The LR3 modification — adding 13 amino acids to the N-terminus and substituting arginine for glutamate at position 3 — dramatically reduces IGFBP affinity, extending the effective half-life from approximately 15 minutes (native IGF-1) to 20–30 hours in animal models. Preclinical research on IGF-1 LR3 has examined its role in muscle protein synthesis, satellite cell activation, glucose uptake in skeletal muscle, adipose tissue metabolism, and anabolic signaling through the PI3K/Akt/mTOR pathway. The compound binds the same IGF-1 receptor as native IGF-1 but with prolonged receptor engagement due to reduced IGFBP scavenging. For researchers studying IGF-1 signaling, anabolic pathways, muscle biology, metabolic regulation, or GH-IGF axis downstream effects, IGF-1 LR3 is the most pharmacokinetically favorable analog with the most extensive published research profile. This listing is for laboratory and preclinical research purposes only. Not for human or veterinary use.

Product Information

Shipping & Returns

From $3,000.00
IGF-1LR3-
$3,000.00

Product definition

What is IGF-1LR3?

IGF-1 LR3 is an 83-amino-acid IGF-1 analog with reduced IGFBP binding, extending half-life from ~15 minutes to ~20–30 hours — the most studied long-acting IGF-1 analog in preclinical research.

IGF-1 Long R3 is a modified form of human IGF-1 developed to circumvent the binding protein problem that limits native IGF-1's utility in research and therapeutic contexts. The modification involves substitution of glutamate with arginine at position 3 and addition of a 13-amino-acid extension to the N-terminus, together producing a molecule with <1% of native IGF-1's IGFBP-3 binding affinity. In preclinical research, IGF-1 LR3 is investigated for its role in muscle protein synthesis, satellite cell activation, myotube hypertrophy, glucose transporter expression in skeletal muscle, and anabolic signaling through PI3K/Akt/mTOR. The extended half-life relative to native IGF-1 makes it significantly more practical for animal studies examining sustained IGF-1 receptor engagement.

Research context

How is IGF-1LR3 described in the research literature?

IGF-1 LR3 binds IGF-1 receptors with comparable affinity to native IGF-1 but with dramatically reduced binding to IGF-binding proteins (IGFBPs), prolonging its effective half-life in vivo. Receptor engagement activates the PI3K/Akt/mTOR pathway, stimulating muscle protein synthesis and satellite cell activation in preclinical models. The LR3 modification is the critical pharmacokinetic distinction from native IGF-1.

Compound profile

Key facts about IGF-1LR3

Class
Long-acting IGF-1 analog
Amino acids
83
Molecular weight
~9,117 Da
Half-life
~20–30 hours in vivo (vs ~15 min for native IGF-1)
IGFBP binding
<1% of native IGF-1 binding
Key modification
R3 substitution + 13 AA N-terminal extension
Research category
Anabolic signaling, muscle biology, metabolic research
Storage
Lyophilized: −20°C. Reconstituted: 2–8°C, use within 14 days

Research areas

What research areas is IGF-1LR3 associated with?

  • Half-life of ~20–30 hours vs. ~15 minutes for native IGF-1 — dramatically better for research protocols
  • Studied in preclinical models for muscle protein synthesis and satellite cell activation
  • Investigated for glucose uptake promotion in skeletal muscle via GLUT-4 translocation
  • Examined for PI3K/Akt/mTOR anabolic signaling pathway activation in muscle biology research
  • Reduced IGFBP binding (<1% of native IGF-1) allows sustained IGF-1 receptor engagement
  • Reference compound for IGF-1 axis research requiring prolonged receptor activation

Research audience

Who researches IGF-1LR3?

IGF-1 LR3 is used by researchers in muscle biology, sports science preclinical work, metabolic signaling, GH-IGF axis research, and anabolic pathway pharmacology. It is the standard long-acting IGF-1 analog used when extended receptor engagement is required for a study protocol.

Preclinical research overview

What does the preclinical literature say about IGF-1LR3?

IGF-1 LR3 was developed as a research tool to extend the effective window of IGF-1 receptor engagement beyond what native IGF-1 allows due to rapid IGFBP sequestration. The compound is manufactured by multiple research suppliers and has been used across hundreds of published preclinical studies examining anabolic signaling and metabolism. In muscle biology research, IGF-1 LR3 is studied for its effects on satellite cell proliferation and differentiation — key events in skeletal muscle repair and hypertrophy. In cell culture systems, it produces robust PI3K/Akt/mTOR activation at nanomolar concentrations, making it a standard tool for signaling pathway studies. In in vivo rodent studies, it has been used to examine body composition effects, muscle mass responses, and metabolic parameters. The compound also shows binding to the insulin receptor, though with approximately 11% of native insulin's potency. This cross-reactivity is relevant for metabolic research designs and should be considered when interpreting in vivo results.

Common questions

Frequently asked about IGF-1LR3

Why use IGF-1 LR3 instead of native IGF-1?

Native IGF-1 is rapidly bound by IGFBPs in circulation, reducing its effective half-life to approximately 15 minutes. IGF-1 LR3's modifications reduce IGFBP binding to <1% of native levels, extending effective half-life to 20–30 hours. For research protocols requiring sustained receptor engagement, IGF-1 LR3 is dramatically more practical and the standard choice in the field.

Does IGF-1 LR3 affect insulin signaling?

IGF-1 LR3 shows partial agonism at insulin receptors — approximately 11% of insulin's potency at the insulin receptor. This cross-reactivity is relevant for metabolic research designs and should be accounted for when interpreting results from studies using high concentrations. At typical research concentrations in muscle biology studies, the primary effect is IGF-1 receptor-mediated.

What is the recommended storage protocol for IGF-1 LR3?

Lyophilized IGF-1 LR3 is stable at −20°C. Once reconstituted, it should be stored at 2–8°C and used within approximately 14 days — a shorter window than many other peptides due to reduced stability in reconstituted form. Avoid repeated freeze-thaw cycles of reconstituted solution.

Research Use Only

Sold for laboratory and research purposes only. Not approved for, nor intended for, human or veterinary consumption, diagnostic use, or therapeutic application. These products have not been evaluated by the Food and Drug Administration. Keep out of reach of children. For use by qualified researchers only.

Nothing on this page constitutes medical advice, a treatment recommendation, or a clinical protocol. Consult a qualified healthcare provider before making any health or treatment decisions.

By accessing this product page you confirm that you are a qualified researcher aged 18 or older and that you will use this product solely for lawful laboratory research purposes. View Research Use Policy