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Peptide Profile

IGF-2

Insulin-like Growth Factor 2 · IGF-II

Insulin-like growth factor 2 (IGF-2) is a naturally occurring peptide growth factor structurally homologous to IGF-1 that plays a central role in embryonic development and remains expressed in adult skeletal muscle, where it…

GH / IGF AxisNot EvaluatedResearch Only
Used forperformance
Half-life
~10-20 minutes
Routes
subcutaneous, intramuscular

Educational research information — not medical advice. Review primary sources and consult a qualified professional before any decision.

Educational research tools — not medical advice.

Overview

What IGF-2 is

About IGF-2

Binds IGF-1R and insulin receptor variant A; promotes anabolic signaling in muscle and fat; activates PI3K/Akt/mTOR pathway; different receptor binding profile than IGF-1

Insulin-like growth factor 2 (IGF-2) is a naturally occurring peptide growth factor structurally homologous to IGF-1 that plays a central role in embryonic development and remains expressed in adult skeletal muscle, where it functions as an autocrine regulator of myoblast differentiation and myocyte maturation downstream of MyoD activation. IGF-2 binds both the IGF-1 receptor (IGF-1R), which mediates PI3K/Akt anabolic signaling, and the mannose-6-phosphate/IGF-2 receptor (M6P/IGF-2R), which targets bound ligand for lysosomal degradation rather than intracellular signal transduction; the balance between these receptor populations influences net downstream anabolic signaling. Preclinical and cell biology research demonstrates that autocrine IGF-2 signaling through IGF-1R is required for normal myocyte maturation, and that TGF-β-mediated suppression of IGF-2 autocrine pathways impairs skeletal muscle differentiation, establishing IGF-2 as a functionally important endogenous anabolic signal in muscle regeneration. IGF-2 has no FDA-approved applications in performance enhancement or muscle anabolism; exogenous administration as a research compound is investigational and no human clinical trials have established safety or efficacy for these uses.

IGF-2 Benefits & Research Areas

muscle growthfat metabolismtissue developmentRecovery

Research Signals

Commonly researched in the context of

High Training Load

Population research notes

30s40s50+

These signals reflect research interest areas, not treatment indications.

Pharmacokinetics

IGF-2 half-life calculator

Compound & timing

Half-lifefrom PeptideBase data
Source: "~10-20 minutes" · IGF-2 (PeptideBase)
to show amount remaining
20 min
0%25%50%75%100%021426283104time since dose (min)
Plasma decay curve for IGF-2: 25% to 50% remaining at 20 min after the dose.
range (~10-20 minutes)slower half-life
25%–50%remaining in plasmaat 20 min after the dose
Half-life
10 – 20 min
~97% cleared after
1.7 h

Model: single-dose, first-order (single-compartment) estimate. Real clearance is multi-compartment and varies by individual and route.

The Research

What the evidence says about IGF-2

Research Evidence

based on 6 studies · most recent 2026

Regulatory Status

Availability Status
Research Only
FDA Status
Not Evaluated

Endogenous growth factor. No FDA-approved exogenous IGF-2 drug product. No NDA or IND for IGF-2 as primary active ingredient. Research use only.

Regulatory status reflects publicly available information and may change. This is not legal or medical advice.

Research Sources

6 sources cited · 1 moderate · 5 weak

1 Case series · 2 Reviews · 1 Animal · 2 In vitros

  • IGF-2-mediated hypoglycemia in a patient with a phyllodes tumor of the breast: a rare presentation of non-islet cell tumor hypoglycemia.

    Endocrinol Diabetes Metab Case Rep · 2026

    # Summary Research found that a phyllodes tumor of the breast caused non-islet cell tumor hypoglycemia (NICTH) through IGF-2 secretion, with the diagnosis aided by an elevated IGF-2:IGF-1 ratio rather than absolute IGF-2 levels alone. This study demonstrated that surgical tumor resection completely resolved the patient's recurrent hypoglycemia, confirming IGF-2-mediated NICTH as the underlying cause.

    Case seriesModeratePMID 42214434
  • Proteomics and ex vivo plaque culture identify the insulin-like growth factor axis as a potential regulator of matrix remodelling in carotid plaques.

    Atherosclerosis · 2026

    # Summary Research found that the insulin-like growth factor (IGF) signaling axis, particularly involving IGF-1, IGF-2, and their associated binding proteins, may play a regulatory role in atherosclerotic plaque stability by modulating matrix remodeling proteins. This study demonstrated through proteomics analysis and ex vivo culture that IGF-1 signaling was associated with a more stable plaque phenotype, characterized by decreased matrix-degrading enzymes and increased structural collagen.

    In vitroWeakPMID 42001536
  • TGF-β inhibits muscle differentiation by blocking autocrine signaling pathways initiated by IGF-II

    Molecular Endocrinology · 2011

    Research in mouse and human primary myoblast cultures found that TGF-beta inhibited skeletal muscle differentiation primarily by suppressing IGF-II autocrine signaling, and that exogenous IGF-I or IGF-II restored muscle protein expression and myotube formation despite TGF-beta, identifying IGF-II pathway activation as a strategy to counteract muscle-wasting conditions.

    In vitroWeakPMID 21106882
Show 3 more sources
  • Autocrine growth factor signaling by insulin-like growth factor-II mediates MyoD-stimulated myocyte maturation

    Journal of Biological Chemistry · 2003

    Research in cell culture models identified IGF-II as an early autocrine signal induced by the myogenic transcription factor MyoD, with IGF-II production essential for myocyte fusion and terminal differentiation into myotubes, establishing IGF-II as a key endogenous regulator of skeletal muscle development at the cellular level.

    AnimalWeakPMID 12941952
  • The IGF signaling axis in thyroid cancer: biological complexity and therapeutic challenges.

    Endocr Connect · 2026

    # Summary Research found that dysregulation of the IGF signaling axis, particularly involving IGF-2 and its receptor (IGF-1R), plays an important role in thyroid cancer progression, dedifferentiation, and resistance to radioiodine treatment. This study demonstrated that an IGF-2/IR-A-dominant autocrine circuit is associated with aggressive and treatment-refractory thyroid cancer, though clinical translation of IGF-axis targeting has been limited due to signaling redundancy and adaptive resistance, necessitating combination therapeutic approaches.

    ReviewTheoreticalPMID 42023590
  • Paraneoplastic hypoglycemia as the initial presentation of a pancreatic neuroendocrine tumor.

    Ir J Med Sci · 2026

    ReviewTheoreticalPMID 42348065

IGF-2 Side Effects & Safety Considerations

Research-use compound with limited human data. Evidence strength varies — see the Evidence section.

Absolute contraindications

Under clinical review

Being verified by our medical team before we display contraindications for this peptide.

Consult a qualified healthcare professional before making any health decisions. This information is educational only and does not constitute medical advice.

Frequently Asked Questions — IGF-2

Insulin-like growth factor 2 (IGF-2) is a naturally occurring peptide growth factor structurally homologous to IGF-1 that plays a central role in embryonic development and remains expressed in adult skeletal muscle, where it functions as an autocrine regulator of myoblast differentiation and myocyte maturation downstream of MyoD activation. IGF-2 binds both the IGF-1 receptor (IGF-1R), which mediates PI3K/Akt anabolic signaling, and the mannose-6-phosphate/IGF-2 receptor (M6P/IGF-2R), which targets bound ligand for lysosomal degradation rather than intracellular signal transduction; the balance between these receptor populations influences net downstream anabolic signaling.

muscle growth, fat metabolism, tissue development, Recovery.

Research on IGF-2 primarily documents effects related to muscle growth and fat metabolism and tissue development and Recovery. These are areas covered in preclinical and clinical literature — individual response varies and effects depend on context of use.

For IGF-2, its FDA status is not evaluated by the FDA, and it is designated for research use only. Regulatory status reflects publicly available information and may change. This is not legal or medical advice.

# Summary Research found that a phyllodes tumor of the breast caused non-islet cell tumor hypoglycemia (NICTH) through IGF-2 secretion, with the diagnosis aided by an elevated IGF-2:IGF-1 ratio rather than absolute IGF-2 levels alone. This study demonstrated that surgical tumor resection completely resolved the patient's recurrent hypoglycemia, confirming IGF-2-mediated NICTH as the underlying cause.

Access

How to get IGF-2

Where to buy IGF-2

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