How Does 5-Amino-1MQ Work? Benefits + Side Effects

Medically reviewed by
Dr. Michael Fortunato, MD

Written by
All About Peptides Team

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This article is for informational purposes only and does not constitute medical advice. Always consult with a qualified healthcare provider before considering any peptide therapy.


5-Amino-1MQ, also known as 5-amino-1-methylquinolinium, is a promising wellness compound that may support fat burning, energy production, and healthy aging. As a small molecule, 5-Amino-1MQ acts on specific enzymes in the body to exert its effects. Rather than being a traditional weight loss compound, 5-Amino-1MQ is a nicotinamide N-methyltransferase (NNMT) inhibitor.

NNMT is an enzyme that depletes cellular stores of nicotinamide adenine dinucleotide (NAD+), a critical molecule involved in mitochondrial energy production and longevity pathways. NNMT activity is often upregulated in obesity, leading to reduced NAD+ levels and contributing to metabolic dysfunction.

By inhibiting NNMT, 5-Amino-1MQ may help maintain NAD+ levels, support mitochondrial function, and activate pathways associated with longevity.

But 5-Amino-1MQ isn’t yet FDA-approved. Most evidence comes from animal studies, not human clinical trials. Let’s examine what the science actually shows.

Quick Takeaways

  • 5-Amino-1MQ blocks an enzyme called NNMT that depletes cellular energy stores, helping preserve NAD+ levels needed for metabolism and longevity.
  • Animal studies show reductions in body weight (5.1%) and fat mass (35%) without changes in appetite or food intake.
  • The compound appears to increase grip strength by approximately 40% in aged mice and may work synergistically with exercise.
  • Human clinical trial data is absent, so current use remains experimental despite favorable animal safety profiles.

What is 5-Amino-1MQ Peptide Therapy?

Most weight loss compounds work through appetite suppression or stimulant effects. 5-Amino-1MQ takes a different approach by addressing cellular metabolism directly.

The compound is a selective NNMT inhibitor, not a peptide. Research shows it specifically targets fat cells and liver tissue, where NNMT expression increases up to two-fold in obesity[1]. This selectivity may explain its apparent safety profile in animal studies.

In obese individuals, NNMT activity correlates strongly with insulin resistance and type 2 diabetes[2]. By inhibiting this enzyme, 5-Amino-1MQ appears to reverse some metabolic dysfunction at the cellular level. The effect happens without requiring changes to diet or exercise, though combining it with lifestyle modifications likely produces better results.

How Does 5-Amino-1MQ Work?

Bodybuilder flexing his back muscles in the gym.

Understanding how 5-Amino-1MQ affects your body requires looking at three interconnected processes: enzyme inhibition, energy preservation, and metabolic activation.

Blocking NNMT Enzyme Activity

NNMT catalyzes the methylation of nicotinamide (vitamin B3) into 1-methylnicotinamide (1-MNA). This process consumes both nicotinamide and S-adenosylmethionine (SAM), depleting two compounds your cells need for energy production and methylation[1].

When 5-Amino-1MQ blocks NNMT, it prevents this wasteful reaction. The result is higher NAD+ availability.

In differentiated adipocytes, 5-Amino-1MQ treatment increased intracellular NAD+ levels by 1.2 to 1.6-fold at concentrations of 1-60 µM. The compound reduced 1-MNA levels by up to 60% at effective concentrations[3].

NAD+ Preservation Fuels Energy Production

NAD+ serves as a coenzyme in the electron transport chain, driving ATP synthesis in mitochondria. When NNMT is overactive, it drains NAD+ pools. When blocked, those pools stay full and increase NAD availability for cellular functions.

Higher NAD+ availability triggers several metabolic benefits:

  • Increased mitochondrial energy production and improved mitochondrial health
  • Activation of sirtuins (longevity proteins)
  • Support for DNA repair mechanisms
  • Enhanced cellular stress resistance

The preservation of NAD+ may explain why 5-Amino-1MQ affects multiple aspects of aging beyond just reducing fat storage. NAD+ levels naturally decline with age, and restoring them has become a target for longevity research.

SIRT1 Activation and Metabolic Effects

Elevated NAD+ activates SIRT1, a NAD+-dependent enzyme often called the “longevity gene.” SIRT1 regulates multiple metabolic pathways related to aging and metabolism[4].

When SIRT1 activates, it triggers:

  • Enhanced fat oxidation through PGC-1α activation
  • Improved glucose regulation and insulin sensitivity
  • Reduced systemic inflammation via NF-κB modulation
  • Muscle mass preservation during caloric restriction

Research published in Nature Medicine demonstrated that NNMT inhibition in white adipose tissue increased energy expenditure, reduced fat mass, and improved insulin sensitivity in animal models. These effects appear to stem largely from SIRT1 activation downstream of NAD+ preservation[2].


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What Does Research Show?

The scientific evidence for 5-Amino-1MQ comes primarily from animal models, with studies examining weight loss, physical performance, and metabolic changes.

Weight Loss and Body Composition Changes

The most comprehensive preclinical data comes from a 2017 study published in Biochemical Pharmacology. Diet-induced obese mice received 20 mg/kg of 5-Amino-1MQ subcutaneously three times daily for 11 days[1].

Results included:

MeasurementChange
Body weight-5.1% (while controls gained 1.4%)
Epididymal fat mass-35% reduction
Fat cell size-30% decrease
Fat cell volume-40% reduction
Total cholesterol-30% decrease
Food intakeNo change

Food intake remained unchanged between treatment and control groups. This means weight loss occurred through increased metabolic rate, not appetite suppression. No toxic or behavioral effects appeared at these doses.

Physical Performance Improvements

A 2024 study in Scientific Reports examined 5-Amino-1MQ’s effects on muscle function in aged mice[5]. The findings revealed improvements in physical performance:

  • Sedentary mice: 40% increase in grip strength versus untreated controls
  • Exercise alone: 20% improvement in grip strength
  • Combined treatment and exercise: 60% increase in grip strength

The additive effect suggests 5-Amino-1MQ influences molecular pathways differently from exercise training. This makes it potentially complementary to physical training for those interested in peptides for endurance athletes.

Combined Diet and Treatment Studies

When diet-induced obese mice switched from a Western diet to a lean diet while receiving 5-Amino-1MQ[6], the combination:

  • Accelerated body weight and fat loss beyond diet change alone
  • Increased whole-body lean mass to body weight ratio
  • Reduced liver adiposity and improved hepatic steatosis
  • Normalized body composition to levels seen in lean controls
  • Produced unique metabolomic signatures in adipose tissue

The pharmacokinetic study in rats showed 38.4% oral bioavailability, considered favorable for oral administration. Terminal elimination half-life was 6.90 hours orally[7].

Potential Benefits of 5-Amino-1MQ

Based on preclinical research, 5-Amino-1MQ shows promise across several areas of health and wellness, from body composition to energy levels.

Metabolic Health and Weight Management

5-Amino-1MQ appears to promote fat loss without appetite suppression. The compound:

  • Reduces body weight and fat mass while preserving lean muscle
  • Decreases fat cell size, particularly visceral (abdominal) fat
  • Improves insulin sensitivity and glucose metabolism
  • Reduces plasma cholesterol levels
  • Supports metabolic syndrome management

The focus on visceral fat reduction matters. This type of fat closely links to metabolic disease risk more than subcutaneous fat.

Those interested in peptides for fat loss often ask how 5-Amino-1MQ compares to other options like AOD-9604. The mechanisms differ, with 5-Amino-1MQ working through NAD+ preservation while AOD-9604 directly stimulates lipolysis.

Energy and Cellular Function

By preserving NAD+ levels, 5-Amino-1MQ may:

  • Increase cellular ATP production through enhanced mitochondrial function
  • Boost basal metabolic rate without stimulant effects
  • Promote mitochondrial biogenesis through SIRT1-PGC-1α activation
  • Reduce oxidative stress and support cellular energy balance

The compound increases energy expenditure at the cellular level. This means the body burns more calories even at rest.

Muscle Function and Recovery

Research shows 5-Amino-1MQ can:

  • Improve grip strength and muscle function in aged subjects
  • Boost exercise endurance and reduce recovery time
  • Provide additive benefits when combined with exercise training
  • Support muscle mass preservation during weight loss

For those exploring peptides for men focused on body composition, this preservation of lean mass during fat loss represents a key advantage.

Longevity and Anti-Aging Support

The activation of SIRT1 and preservation of NAD+ suggest potential longevity benefits:

  • Support for DNA repair through maintained NAD+ levels
  • Reduction in inflammation markers
  • Activation of cellular stress resistance pathways
  • Support for healthy aging markers

Dr. Dwayne Jackson, a peptide researcher with over 30 years of experience, describes 5-Amino-1MQ as “a small molecule that blocks the enzyme NNMT, which helps preserve NAD+ levels and may enhance fat metabolism, muscle regeneration, and anti-aging effects.”


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What Are the Side Effects?

Understanding the potential side effects of 5-Amino-1MQ requires examining both animal safety data and limited human reports.

Preclinical Safety Profile

Animal studies show a favorable safety profile. In the comprehensive 2017 study, mice treated with 5-Amino-1MQ at effective doses showed[1]:

  • No observable adverse effects
  • No behavioral changes
  • No signs of toxicity
  • No impact on food intake

Cell viability studies showed no cytotoxicity at concentrations up to 10 µM, well above therapeutic ranges. Modest cytotoxicity appeared only at 100-300 µM, far exceeding effective dosing.

The compound demonstrated high selectivity for NNMT with no inhibition of related enzymes including DNMT1, PRMT3, COMT, NAMPT, or SIRT1. This selectivity minimizes risk of off-target effects.

Limited Human Data

Here’s what you need to know: human clinical trials for 5-Amino-1MQ are limited or non-existent in peer-reviewed literature.

Most safety and efficacy data comes from animal studies. Anecdotal reports from clinical use suggest mild, transient side effects:

  • Temporary digestive changes in the first few days
  • Mild headaches (often related to hydration)
  • Transient muscle soreness as fat oxidation increases
  • Sleep disturbances in rare cases

No documented serious side effects exist in clinical or research settings to date. Medical oversight is recommended, particularly for those with metabolic conditions or taking medications.

Important Cautions

You should avoid 5-Amino-1MQ if you’re:

  • Pregnant or breastfeeding (no safety data available)
  • Undergoing active cancer treatment (more research needed)
  • Taking medications without medical supervision

Research on cardiovascular effects reveals complexity. While NNMT inhibition may improve metabolic health, NNMT’s product (1-MNA) can exert protective effects through NRF2 activation[8]. Long-term cardiovascular implications of chronic NNMT inhibition remain unclear.

How to Use 5-Amino-1MQ Safely

Before considering 5-Amino-1MQ, you need to understand its regulatory status, appropriate dosing approaches, and how it compares to other metabolic compounds.

Regulatory Status

5-Amino-1MQ is not FDA-approved for medical use. In the United States, it’s available through:

  • Licensed compounding pharmacies under physician oversight
  • Specialized telehealth clinics offering peptide therapy
  • Research suppliers (for laboratory use only)

The FDA has not reviewed 5-Amino-1MQ for safety or efficacy in humans. It should be considered investigational.

Dosing Considerations

While human clinical dosing protocols aren’t established through formal trials, typical patterns in clinical practice include:

  • Starting dose: 50 mg per day orally, divided into two doses
  • Standard dose: 50-100 mg per day (25-50 mg twice daily)
  • Alternative: 150 mcg subcutaneously once daily
  • Treatment cycles: 3-4 months followed by breaks

Some protocols recommend taking 5-Amino-1MQ 30 minutes after NAD+ supplementation for synergistic effects. Avoid taking close to bedtime as NAD+ elevation may impact circadian signaling.

For detailed dosing protocols and calculator, see our guide on 5-Amino-1MQ dosage.

Comparing Options

Those researching metabolic compounds often compare 5-Amino-1MQ to SLU-PP-332, another emerging metabolic modulator. Both work through different mechanisms, with 5-Amino-1MQ focusing on NNMT inhibition while SLU-PP-332 acts as a selective PPARδ modulator.

Bottom Line

5-Amino-1MQ represents an approach to metabolic health through NNMT inhibition and NAD+ preservation. Preclinical evidence shows benefits for weight management, metabolic health, and physical performance without apparent toxicity in animal models.

The lack of human clinical trials means its use remains experimental. Dr. Jackson emphasizes that “while early data looks promising, the compound’s safety, efficacy, and long-term effects in humans remain unproven,” and warns that “online anecdotal use is experimental and risky.” Those considering 5-Amino-1MQ should work with qualified healthcare providers who can monitor safety and efficacy given the limited human data available.

References

  1. Neelakantan H, Vance V, Wetzel MD, Wang HYL, McHardy SF, Finnerty CC, et al. Selective and membrane-permeable small molecule inhibitors of nicotinamide N-methyltransferase reverse high fat diet-induced obesity in mice. Elsevier BV; 2018. https://doi.org/10.1016/j.bcp.2017.11.007
  2. Kraus D, Yang Q, Kong D, Banks AS, Zhang L, Rodgers JT, et al. Nicotinamide N-methyltransferase knockdown protects against diet-induced obesity. Springer Science and Business Media LLC; 2014. https://doi.org/10.1038/nature13198
  3. Liu JR, Deng ZH, Zhu XJ, Zeng YR, Guan XX, Li JH. Roles of Nicotinamide N‐Methyltransferase in Obesity and Type 2 Diabetes. Wiley; 2021. https://doi.org/10.1155/2021/9924314
  4. Hubbard BP, Sinclair DA. Small molecule SIRT1 activators for the treatment of aging and age-related diseases. Elsevier BV; 2014. https://doi.org/10.1016/j.tips.2013.12.004
  5. Dimet-Wiley AL, Latham CM, Brightwell CR, Neelakantan H, Keeble AR, Thomas NT, et al. Nicotinamide N-methyltransferase inhibition mimics and boosts exercise-mediated improvements in muscle function in aged mice. Springer Science and Business Media LLC; 2024. https://doi.org/10.1038/s41598-024-66034-9
  6. Sampson CM, Dimet AL, Neelakantan H, Ogunseye KO, Stevenson HL, Hommel JD, et al. Combined nicotinamide N-methyltransferase inhibition and reduced-calorie diet normalizes body composition and enhances metabolic benefits in obese mice. Springer Science and Business Media LLC; 2021. https://doi.org/10.1038/s41598-021-85051-6
  7. Awosemo O, Neelakantan H, Watowich S, Ma J, Wu L, Chow DSL, et al. Development & validation of LC–MS/MS assay for 5-amino-1-methyl quinolinium in rat plasma: Application to pharmacokinetic and oral bioavailability studies. Elsevier BV; 2021. https://doi.org/10.1016/j.jpba.2021.114255
  8. Jawaria, Zarlashat Y, Philippovich M, Dósa E. Nicotinamide N-Methyltransferase in Cardiovascular Diseases: Metabolic Regulator and Emerging Therapeutic Target. MDPI AG; 2025. https://doi.org/10.3390/biom15091281

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