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STROMUSC Aicar 10mg*100Tablets For Bodybuilding CAS:3031-94-5

STROMUSC Aicar 10mg*100Tablets For Bodybuilding CAS:3031-94-5

Within the relentless pursuit of physical perfection, bodybuilders and elite athletes are perpetually searching for compounds that can provide a legitimate edge. Beyond the well-trodden path of anabolic steroids and SARMs lies a more niche, yet profoundly intriguing agent: AICAR, typically encountered in 10mg dosages. This compound operates on a fundamentally different principle than tissue-building anabolics, targeting instead the very engine of performance: cellular metabolism. This in-depth analysis will dissect AICAR 10mg, exploring its unique mechanism, theoretical applications, nuanced benefits, and the significant practical considerations for any individual contemplating its use.

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Description

   What is AICAR? A Primer on the Molecule

    AICAR, an acronym for 5-Aminoimidazole-4-carboxamide ribonucleotide, is an analog of adenosine monophosphate (AMP), a fundamental cellular metabolite. To understand AICAR, one must first understand cellular energy status. During intense exertion, ATP (adenosine triphosphate) is consumed, leading to a rise in AMP levels. This increase is a primary signal of low cellular energy.

    AICAR is pharmacologically designed to mimic this low-energy signal. When introduced into the body, it is converted into its active form, ZMP, which impersonates AMP. This "deception" has profound downstream effects, primarily through the activation of a critical cellular enzyme known as AMPK (AMP-activated protein kinase).

    Think of AMPK as the body's master metabolic regulator. Its activation shifts the body's energy dynamics from an anabolic (building-up) state to a catabolic (breaking-down) state, but in a highly targeted and potentially beneficial manner. It is this precise, scientific mechanism that forms the basis of AICAR's appeal in performance contexts.

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Features and Mechanism: The "Metabolic Switch"

    The defining feature of AICAR is its role as a direct AMPK activator. Unlike compounds that stimulate hormone receptors, AICAR works deep within the cell, influencing gene expression and metabolic pathways. Its key features include:

    1.Direct AMPK Activation: It bypasses the natural triggers for AMPK (like ATP depletion from exercise) and directly initiates the cascade of effects associated with this enzyme.

    2.Non-Hormonal Action: Its effects are not mediated through the androgen receptor or growth hormone pathways, making its action profile distinct from traditional anabolics.

    3.Metabolic Reprogramming: It instructs muscle cells to become more efficient at utilizing energy, primarily by enhancing fat oxidation and glucose uptake.

Applications in Bodybuilding: Beyond Mere Fat Loss

    While often simplistically labeled a "fat loss" drug, AICAR's applications in a sophisticated bodybuilding regimen are more nuanced and strategic.

    1.The "Off-Season" Conditioning Agent: During a mass-gaining phase, caloric surplus is essential but often leads to unwanted fat gain. AICAR could theoretically be employed to enhance the body's metabolic efficiency, potentially directing more calories toward muscle tissue growth and away from adipose storage by chronically upregulating fat-burning pathways. This could allow for a "cleaner" bulk with a more favorable muscle-to-fat gain ratio.

    2.The "Cardio-Sparing" Elixir: This is perhaps its most legendary and sought-after application. The theory posits that AICAR can mimic certain adaptations to endurance training. By enhancing mitochondrial biogenesis (the creation of new cellular power plants) and improving muscular endurance, an athlete could maintain a higher level of cardiovascular fitness with less actual time spent on strenuous cardio. This is invaluable during a pre-contest phase where preserving hard-earned muscle mass is paramount, and excessive cardio can become catabolic.

    3.Enhanced Recovery and Endurance Within Workouts: By improving the metabolic efficiency of muscle cells, AICAR could potentially reduce lactate accumulation and delay the onset of fatigue during high-rep training or intense supersets. This allows for more volume and higher quality work in each session, indirectly contributing to greater muscular stimulation over time.

Postulated Benefits: A Theoretical Framework

    The benefits of AICAR are derived from its mechanism and must be framed within the context of its experimental nature.

    ●Increased Fat Oxidation: The most consistent and documented effect. Activation of AMPK promotes the burning of fatty acids for fuel, leading to a reduction in adipose tissue.

    ●Improved Endurance Capacity: By enhancing the muscles' energy efficiency and mitochondrial density, users report being able to train harder for longer before hitting a wall of fatigue.

    ●Metabolic Flexibility: It may help the body become better at switching between fuel sources (fats and carbohydrates), a hallmark of a fit and efficient metabolism.

    ●Potential Insulin Sensitization: AMPK activation stimulates glucose uptake into muscles independently of insulin, which can improve overall insulin sensitivity-a critical factor in nutrient partitioning.

    It is crucial to state that many of these benefits, while grounded in sound physiology, are largely anecdotal in the bodybuilding community due to a lack of controlled human trials for this specific application.

Dosage, Cycle, and Half-Life: A Pragmatic Guide

    Handling AICAR, especially in its common 10mg research peptide form, requires careful consideration.

    ●Dosage: The 10mg vial is a standard unit. In performance-enhancement circles, a common dosage ranges from 50mg to 100mg per day, typically administered via subcutaneous injection. This means reconstituting a 10mg vial as part of a larger batch to achieve the desired single dose. Starting at the lower end of this range is imperative to assess individual tolerance.

    ●Cycle Length: AICAR is not a compound for year-round use. Cycles are typically short, ranging from 2 to 6 weeks. Its effects are metabolic and adaptive; prolonged use could lead to a downregulation of its pathways or other unforeseen homeostatic compensations. It is often cycled in conjunction with other compounds, most notably GW501516 (Cardarine), which acts on the PPAR-delta pathway to further enhance endurance. This combination is believed to have a synergistic effect, targeting endurance from two different angles.

    ●Half-Life: The half-life of AICAR is relatively short, estimated to be in the range of 2 to 4 hours. This necessitates once-daily dosing, often timed pre-workout to leverage the acute endurance benefits during training, or in the morning to influence metabolism throughout the day.

PTC (Post-Cycle Therapy): A Necessary Consideration

    Since AICAR is non-hormonal, it does not suppress the hypothalamic-pituitary-testicular (HPTT) axis in the way that anabolic steroids or even some SARMs do. Therefore, a traditional PCT aimed at restarting natural testosterone production is not required.

    However, this does not mean the body requires no support after an AICAR cycle. The concept of a "Metabolic PCT" is more appropriate. The body's metabolic system has been artificially manipulated, and it is prudent to support its return to baseline homeostasis. This should include:

    ●Robust Nutrient Timing: Ensuring a diet rich in whole foods, with careful attention to micronutrients that support metabolic function, such as B vitamins, magnesium, and chromium.

    ●Continued Physical Activity: Maintaining a consistent training regimen that includes both resistance and cardiovascular exercise to "hold on" to the enhanced metabolic adaptations.

    ●Natural AMPK Supporters: Incorporating natural substances known to support healthy AMPK activity, such as berberine, resveratrol, or alpha-lipoic acid, can help maintain metabolic health without external chemical stimulation.

    ●Comprehensive Blood Work: Monitoring markers like lipid profiles, fasting glucose, and liver enzymes is wise to ensure all systems have returned to normal parameters.

The Inherent Risks and the Final Verdict

    AICAR is not a benign supplement. It is a potent research chemical with a limited safety profile in healthy humans. Potential risks include:

    ●Unknown Long-Term Toxicity: Its long-term effects are simply not known.

    ●Cardiovascular Stress: Artificially altering fundamental energy pathways could have unintended consequences on heart muscle and vascular function.

    ●Dosage Inaccuracy: As a reconstituted peptide, the risk of improper dosing, bacterial contamination, or injecting an incorrectly mixed solution is high.

Clinical Data

Brand

STROMUSC

Trade names

Aminoimidazole carboxamide ribonucleotide,

AICA ribonucleotide, ZMP

CAS

3031-94-5

Molar mass

338.213

MF

C9H15N4O8P

Purity

Above 98%

Apprarance

10mg*100

 

 

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Conclusion

    AICAR 10mg represents a fascinating, high-tech foray into metabolic manipulation for bodybuilding purposes. It is not a muscle-builder but a performance and conditioning optimizer that operates at the cellular level. Its potential to enhance endurance, promote fat loss, and improve metabolic efficiency is powerful in theory. However, it remains a tool shrouded in significant risk and uncertainty, firmly in the domain of experimental use. For the vast majority of athletes, mastering the fundamentals of diet, training, and recovery will yield far greater and safer returns than venturing into the complex and uncharted territory of metabolic modulators like AICAR.

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