IGF-1 LR3
Also known as: Long R3 IGF-1 · Insulin-like Growth Factor 1 Long R3 · LR3-IGF-1
A modified, long-acting form of IGF-1 with 3x the potency of natural IGF-1, capable of promoting muscle hyperplasia and enhanced nutrient partitioning.
Overview
IGF-1 LR3 (Long R3 Insulin-like Growth Factor-1) is a modified, more potent version of the naturally occurring IGF-1 peptide. The modification involves replacing the glutamic acid at position 3 with arginine (R3) and adding a 13-amino-acid extension at the N-terminus (Long), which dramatically reduces its binding to IGF binding proteins (IGFBPs). In the body, natural IGF-1 is largely bound to IGFBPs which limit its bioavailability and activity — approximately 98% of circulating IGF-1 is protein-bound. IGF-1 LR3's reduced IGFBP binding means it remains active in the bloodstream for much longer (half-life of 20-30 hours vs.
12-15 hours for standard IGF-1) and has approximately three times the potency of regular IGF-1. IGF-1 is the primary mediator of growth hormone's anabolic effects — when GH is released, the liver produces IGF-1, which then drives muscle growth, fat metabolism, and tissue repair. IGF-1 LR3 directly activates the IGF-1 receptor (IGF-1R), triggering the PI3K/Akt and MAPK/ERK signaling cascades that promote protein synthesis, cell proliferation, and inhibit apoptosis. It is one of the most potent anabolic peptides available, capable of promoting muscle hyperplasia (creation of new muscle cells) rather than just hypertrophy (enlargement of existing cells).
It also enhances nutrient partitioning, directing calories toward muscle tissue and away from fat storage. Due to its potency, IGF-1 LR3 requires careful dosing and is typically used in shorter cycles.
Mechanism of Action
IGF-1 LR3 binds to the IGF-1 receptor (IGF-1R), a transmembrane tyrosine kinase receptor present on virtually all cell types. Upon binding, it activates two major intracellular signaling cascades: the PI3K/Akt/mTOR pathway (which drives protein synthesis, cell growth, and survival) and the Ras/MAPK/ERK pathway (which promotes cell proliferation and differentiation). The key difference from standard IGF-1 is that IGF-1 LR3 has dramatically reduced affinity for the six IGF binding proteins (IGFBP-1 through IGFBP-6), which normally sequester and inactivate circulating IGF-1. This means IGF-1 LR3 remains in its free, bioactive form for much longer, providing sustained receptor activation. At the muscle level, IGF-1 LR3 activates satellite cells — the muscle stem cells responsible for creating new myonuclei and, potentially, entirely new muscle fibers (hyperplasia). It also directly stimulates mTORC1, the master regulator of protein synthesis, and inhibits the ubiquitin-proteasome pathway that breaks down muscle protein.
Key Benefits
Potential Side Effects
Common Stacks
This peptide is commonly combined with the following compounds for synergistic effects:
Known Interactions
The following interactions have been documented for IGF-1 LR3. Always consult a healthcare professional before combining compounds.
Use Caution (3)
Both raise IGF-1 levels significantly. Combined use may push IGF-1 to supraphysiological levels, increasing risk of unwanted cell proliferation.
IGF-1 LR3 provides exogenous IGF-1 while CJC-1295 stimulates endogenous GH/IGF-1. Combined use may result in excessive IGF-1 levels.
Both are growth factors that promote cell proliferation. Combined use may cause excessive growth signaling. Use at different times — PEG-MGF post-workout, IGF-1 LR3 on off days.
Scientific References
Quick Reference
Typical Dose
Research doses: 20-100 mcg/day. Common protocol: 40-80 mcg/day, divided into 1-2 injections (bilateral site injections post-workout are common). Start at lower doses to assess tolerance. Due to potency, conservative dosing is recommended.
Frequency
Once or twice daily (often post-workout)
Route
Subcutaneous or intramuscular injection (site-specific IM injections are common)
Half-Life
~20-30 hours
Cycle Length
4-6 weeks on, 4-6 weeks off (to prevent receptor desensitization and manage insulin sensitivity)
FDA Status
Research chemical — not FDA approved for human use. Recombinant IGF-1 (mecasermin/Increlex) is FDA-approved only for severe IGF-1 deficiency.
Need to calculate dosing?
Use our reconstitution calculator to determine exact syringe measurements.
Open CalculatorThis information is for educational purposes only. Consult a qualified healthcare professional before using any peptide. Dosing information reflects commonly reported protocols and may not be appropriate for everyone.
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