
From Peptidepedia, the trusted peptide wiki.


DES IGF-1 (Des(1-3)IGF-1) is a truncated, highly potent analog of insulin-like growth factor-1 that lacks the first three amino acids of the native IGF-1 molecule. This structural modification dramatically increases its bioactivity by preventing binding to IGF binding proteins (IGFBPs), allowing it to act directly on target tissues with approximately 10 times greater potency than standard IGF-1. DES IGF-1 is popular among bodybuilders, athletes, and biohackers seeking localized muscle growth, enhanced recovery, and tissue repair. Typical dosages range from 20–100 mcg per injection, administered subcutaneously or intramuscularly into target muscle groups, with cycles typically lasting 4–6 weeks.
DES IGF-1, formally known as Des(1-3)IGF-1, is a synthetic peptide consisting of 67 amino acids—three fewer than the 70-amino-acid native human IGF-1 molecule. The removal of the N-terminal tripeptide (Gly-Pro-Glu) creates a compound that does not bind to the six known IGF binding proteins that normally sequester and regulate circulating IGF-1 in the bloodstream.
The primary distinction of DES IGF-1 lies in its enhanced bioavailability. Native IGF-1 circulates bound to IGFBPs, which extend its half-life but also limit its immediate biological activity. DES IGF-1 bypasses this regulatory mechanism entirely, resulting in rapid, direct receptor activation. Research published in the Journal of Neurophysiology demonstrated that des-IGF-1 was specifically used in experiments "to avoid interactions with IGF binding proteins that normally sequester circulating IGF-1."
This characteristic makes DES IGF-1 particularly attractive for localized applications, as it acts quickly at the injection site before being metabolized. Its half-life is estimated at only 20–30 minutes, compared to several hours for IGF-1 LR3.
Users report several potential benefits from DES IGF-1 administration:
DES IGF-1 exerts its effects primarily through binding to the IGF-1 receptor (IGF-1R), a transmembrane tyrosine kinase receptor. Upon binding, the receptor undergoes autophosphorylation, initiating a cascade of intracellular signaling events. Research has demonstrated that des-IGF-1 application results in a concentration-dependent increase in cellular activity, with effects initiated within 5 minutes of application.
The phosphoinositide 3-kinase (PI3K)/Akt pathway represents a critical downstream signaling mechanism. Studies using PI3K inhibitors (wortmannin and LY 294002) demonstrated that des-IGF-1's enhancement effects were "significantly reduced" when this pathway was blocked, confirming its central role in mediating the peptide's biological actions.
This pathway regulates:
Interestingly, research has revealed that des-IGF-1 specifically enhances AMPA receptor-mediated synaptic transmission via a postsynaptic mechanism. Studies showed a 34% increase in AMPA-mediated excitatory postsynaptic currents, while NMDA receptor-mediated currents remained unaffected. This selective action may contribute to cognitive and neuromuscular benefits.
IGF-1 and its analogs regulate skeletal muscle protein synthesis and protein degradation via the ubiquitin-proteasome system (UPS) and autophagy pathways. DES IGF-1's enhanced potency means these anabolic effects occur more rapidly and intensely at the injection site.
Dosing DES IGF-1 requires careful consideration of experience level, goals, and the specific muscle groups being targeted.
Beginner Protocol: 20–30 mcg per injection, once daily, administered bilaterally into target muscles. This conservative approach allows assessment of individual response and tolerance.
Intermediate Protocol: 40–50 mcg per injection, 1–2 times daily. Users at this level typically inject pre-workout or immediately post-workout for maximum effect.
Advanced Protocol: 60–100 mcg per injection, up to twice daily. Higher doses are generally reserved for experienced users who have established tolerance and understand their individual response patterns.
Standard cycling protocols recommend:
Extended use beyond 6 weeks is generally discouraged due to potential receptor desensitization and diminishing returns.
DES IGF-1 can be administered via two primary routes:
Subcutaneous Injection: Injected into the fatty tissue beneath the skin, typically in the abdominal area. This method provides systemic distribution but less localized effect.
Intramuscular Injection: The preferred method for targeted muscle growth. Users inject directly into the muscle belly of the target area, often bilaterally (both sides) to ensure symmetrical development. Common injection sites include:
For intramuscular administration, insulin syringes (29–31 gauge) are typically used. The injection should be performed slowly, and the site should be rotated to prevent tissue damage or scar tissue formation.
Timing Considerations: Due to its short half-life, DES IGF-1 is most effective when administered in close proximity to training. Many users prefer bilateral injections into the target muscle group immediately before or after working that specific body part.
Week 1–2: Initial effects may include enhanced muscle pumps during training, improved recovery between sessions, and subtle increases in muscle fullness at injection sites.
Week 3–4: More noticeable localized muscle development becomes apparent. Users often report improved mind-muscle connection and visible changes in targeted areas.
Week 5–6: Peak effects are typically observed during this period, with measurable improvements in muscle size and definition at injection sites. Recovery capacity often reaches its maximum enhancement.
Post-Cycle: Effects gradually diminish over 2–4 weeks following cessation. Some users report retention of gains, particularly when combined with proper nutrition and continued training.
Scientific investigation of des-IGF-1 has primarily occurred in laboratory and animal model settings. A landmark study published in the Journal of Neurophysiology characterized the acute effects of des-IGF-1 on hippocampal excitatory synaptic transmission, demonstrating a 40% increase in field excitatory postsynaptic potential (fEPSP) slope at concentrations of 40 ng/ml.
Research on IGF-1 and its analogs has shown significant effects on skeletal muscle regulation. A comprehensive review in PMC detailed how IGF-1 regulates skeletal muscle protein synthesis and protein degradation through multiple pathways and mechanisms.
Studies examining growth hormone and IGF-1 use for anabolic purposes have reported dosage ranges of 3–8 mg/day for bodybuilding applications, administered three to four times weekly in cycles of four to six weeks.
It should be noted that human clinical trials specifically examining DES IGF-1 for muscle-building purposes remain limited, and much of the evidence supporting its use comes from preclinical research and anecdotal user reports.
DES IGF-1 is frequently combined with other compounds to enhance results:
With IGF-1 LR3: Some users alternate between DES IGF-1 (for localized, immediate effects) and IGF-1 LR3 (for systemic, longer-lasting effects). This combination theoretically provides both targeted and whole-body anabolic stimulation.
With Growth Hormone: GH administration increases endogenous IGF-1 production, potentially synergizing with exogenous DES IGF-1. This stack is popular among advanced users seeking maximum anabolic effect.
With Anabolic Steroids: DES IGF-1 is sometimes incorporated into steroid cycles to enhance muscle-building effects, particularly during mass-gaining phases.
With Insulin: An advanced and potentially dangerous combination that requires extreme caution due to hypoglycemia risk. This stack is not recommended for inexperienced users.
Reconstitution Protocol:
Storage Requirements:
Some sources recommend using 0.6% acetic acid solution instead of bacteriostatic water for improved stability and extended shelf life of reconstituted IGF-1 peptides.
DES IGF-1 shares many potential side effects with other IGF-1 analogs and growth factors:
Common Side Effects:
Potential Serious Concerns:
Users should monitor blood glucose levels, particularly during initial use, and consume adequate carbohydrates around administration times.
DES IGF-1 is not approved by the U.S. Food and Drug Administration (FDA) for any human therapeutic use. It is classified as a research chemical and is legally sold for "research purposes only" or "not for human consumption."
The FDA has approved only one IGF-1-based medication—mecasermin (Increlex)—for the treatment of severe primary IGF-1 deficiency in children. DES IGF-1 and other IGF-1 analogs sold through peptide suppliers do not have FDA approval and are not subject to pharmaceutical-grade manufacturing standards.
Possession for personal use exists in a legal gray area in many jurisdictions. Users should research their local laws regarding peptide possession and use.
IGF-1 and all its analogs, including DES IGF-1, are explicitly prohibited by the World Anti-Doping Agency (WADA). The substance appears on the Prohibited List under the category of "Peptide Hormones, Growth Factors, Related Substances, and Mimetics."
According to USADA: "Insulin-like Growth factor-1 (IGF-1) is a prohibited substance on the World Anti-Doping Agency (WADA) Prohibited List. It is included in the class of peptide hormones, growth factors and related substances."
This prohibition applies:
Athletes subject to drug testing should be aware that IGF-1 analogs are detectable through modern testing methods, and violations carry significant penalties including competition bans.
DES IGF-1 represents one of the most potent IGF-1 analogs available, offering unique advantages for localized muscle development due to its inability to bind to IGF binding proteins. Its short half-life and rapid action make it particularly suited for targeted applications, distinguishing it from longer-acting variants like IGF-1 LR3.
While preclinical research demonstrates clear biological activity through well-characterized mechanisms including PI3K/Akt pathway activation and AMPA receptor modulation, human clinical data specifically supporting muscle-building applications remains limited. Users should approach DES IGF-1 with appropriate caution, understanding both its potential benefits and risks.
The peptide's prohibited status in competitive sports and lack of FDA approval underscore the importance of informed decision-making. Those choosing to use DES IGF-1 should prioritize proper reconstitution, storage, and administration protocols while monitoring for adverse effects.
What is the difference between DES IGF-1 and IGF-1 LR3?
DES IGF-1 has a very short half-life (20–30 minutes) and acts locally at the injection site, making it ideal for targeted muscle growth. IGF-1 LR3 has an extended half-life (20–30 hours) due to its modified structure and provides more systemic, whole-body effects. DES IGF-1 is typically used for site-specific enhancement, while LR3 is preferred for overall anabolic support.
How quickly does DES IGF-1 work?
DES IGF-1 begins acting within minutes of injection due to its direct receptor binding without IGFBP interference. Research shows cellular effects initiating within 5 minutes of application. However, visible muscle changes typically require 3–4 weeks of consistent use.
Can DES IGF-1 cause cancer?
Elevated IGF-1 levels have been epidemiologically associated with increased risk of certain cancers. However, the relationship is complex, and short-term, cycled use at moderate doses has not been definitively linked to cancer development. Users with personal or family history of cancer should exercise particular caution.
Is DES IGF-1 detectable in drug tests?
Yes. IGF-1 and its analogs are detectable through specialized testing methods used by WADA-accredited laboratories. Athletes subject to anti-doping testing should not use DES IGF-1 or any IGF-1 analog.
What happens if I miss a dose?
Due to DES IGF-1's short half-life, missing a single dose has minimal impact on overall results. Simply resume your normal dosing schedule; do not double the next dose to compensate.
Can women use DES IGF-1?
Yes, women can use DES IGF-1. Recommended dosages for women are typically lower (20–40 mcg per injection) compared to men. Women should monitor for any virilizing effects, though these are less common with IGF-1 peptides than with androgenic compounds.
How should I time DES IGF-1 injections around meals?
To minimize hypoglycemia risk, DES IGF-1 should be administered with or shortly before a meal containing carbohydrates and protein. Avoid injecting on an empty stomach, particularly at higher doses.
Can DES IGF-1 be used for injury recovery?
Some users report accelerated recovery from muscle strains and soft tissue injuries when using DES IGF-1. While preclinical evidence supports IGF-1's role in tissue repair, clinical data specifically for DES IGF-1 in injury recovery is limited. Consult a healthcare provider for serious injuries.
