5-Amino-1MQ

5-Amino-1MQ is a small molecule that inhibits the enzyme nicotinamide N-methyltransferase (NNMT); it is not a peptide. Mouse studies report effects on weight, fat tissue, and aged muscle; no published human study exists.

Bottom lineAll findings on 5-Amino-1MQ come from cell and mouse experiments, largely from a single research team. Efficacy and safety in humans are unknown; it is not a licensed drug anywhere, and the “peptide” label is misleading.

How does it act?

  • NNMT enzyme: NNMT converts nicotinamide (a form of vitamin B3) to 1-methylnicotinamide by adding a methyl group; 5-amino-1MQ was developed as a selective inhibitor of this reaction.
  • NAD+ and SAM: In fat cell culture, NNMT inhibitors increased intracellular NAD+ and S-adenosylmethionine (SAM) levels and reduced fat synthesis; this is a cell finding.
Explore the details

At a glance

  • 5-Amino-1MQ is a small molecule developed to inhibit the enzyme NNMT; its chemical structure is a methylquinolinium derivative, not an amino acid chain. [1]
  • All findings on weight, fat tissue, blood sugar, and aged muscle come from mouse and cell experiments. [1] [3]
  • As of October 19, 2026, ClinicalTrials.gov lists no registered human study of 5-amino-1MQ. [7]
  • In 2026, FDA sent a warning letter to an outsourcing facility registered under 503B that was compounding drugs with this substance, stating that the substance is not on the 503B bulk substances list. [8]
  • No licensed 5-amino-1MQ product exists in Türkiye. [11]
  • This guide gives no dose, method-of-use, or product-sourcing information.

What is 5-Amino-1MQ, and why is it not a peptide?

5-Amino-1MQ is the abbreviation of “5-amino-1-methylquinolinium.” In 2018, a team at the University of Texas Medical Branch in Galveston, USA, compared a series of small molecules that inhibit the enzyme nicotinamide N-methyltransferase (NNMT); these compounds with a methylquinolinium scaffold crossed cell membranes easily and did not inhibit similar methyl-transferring enzymes or enzymes in the NAD+ salvage pathway. One of the most potent of them, 5-amino-1MQ, was taken into a mouse experiment. [1]

Peptides are chains formed by linking amino acids together. 5-Amino-1MQ, by contrast, is a small molecule built on a quinoline ring and contains no amino acid chain; in the FDA’s 2026 warning letter, the substance is also referred to as “5-amino-1-methylquinolinium iodide,” that is, as a salt. [8] Being sold online next to “research peptide” products does not make it a peptide; that classification belongs to marketing. What peptides are is covered in a separate guide: What are peptides?

What does the NNMT enzyme do?

NNMT adds a methyl group to nicotinamide, a form of vitamin B3. In this reaction the methyl donor S-adenosylmethionine (SAM) is consumed, and nicotinamide is excreted as 1-methylnicotinamide instead of returning to the production of NAD+, which has a role in cellular energy metabolism. A mouse study published in Nature in 2014 showed that NNMT is elevated in the fat tissue and liver of obese and diabetic mice; silencing the enzyme at the gene level in these tissues (with an antisense oligonucleotide) protected mice from diet-induced obesity and increased energy expenditure. [2]

5-Amino-1MQ is a test of this idea with a drug-like molecule. In cell culture, NNMT inhibitors lowered 1-methylnicotinamide levels, raised intracellular NAD+ and SAM levels, and reduced fat synthesis in fat cells. [1] All of these findings were obtained in a culture dish or in mice; no change in NAD+ or SAM measured with 5-amino-1MQ in human tissue has been published.

What do the mouse studies show?

The table below lists the published animal studies conducted with 5-amino-1MQ, with their model and limitation. All were done in mice.

StudyModelReported findingLimitationGrade
Neelakantan et al., 2018Male mice made obese with a high-fat diet, 9 per group; 11 days of subcutaneous administrationBody weight fell 5.1% in the treated group and rose 1.4% in the control group; abdominal fat tissue shrank by about 35%, and fat cell size by more than 30%; total cholesterol dropped about 30%; food intake did not change and no observable side effects were reported. [1]11 days; a single male group; long-term effect and safety not measuredE — not studied in humans
Babula et al., 2024Obese mice, 8 per group; subcutaneous administration once daily for about 4 weeks, two dosesAt the high dose, weight gain was limited to 0.9 g (5.4 g in controls, 5.2 g at the low dose); glucose tolerance, insulin sensitivity, and fatty liver improved. [5]The low dose did not limit weight gain; no significant change in lean massE — not studied in humans

Read together, the two studies show that 5-amino-1MQ could limit weight gain and shrink fat tissue in obese mice. However, the effect was dose-dependent: in the 2024 study, the low-dose group did not differ from the control group in weight. [5] Weight percentages in mouse models cannot be translated into weight loss in humans; whether a substance works in humans can only be shown by a human study.

Do oral capsules work?

This question has not been answered in humans. In the 2024 study, the absolute bioavailability of orally given 5-amino-1MQ in mice was about 3.5%. Although the substance dissolves very well in water, it was absorbed only to a limited extent from the gut; the authors explained the low rate by limited absorption and high first-pass breakdown in the liver. With subcutaneous administration, distribution to fat, muscle, and liver tissue was shown. [5] This means that only a very small fraction of an oral dose in mice reaches the blood; absorption in humans has not been measured.

Aged muscle and exercise claims

The marketing of 5-amino-1MQ as “muscle-protective” rests on two studies in aged mice.

  • Repair after muscle injury (2019): Chemical injury was induced in the leg muscle of 24-month-old mice, and the animals were treated for 1 or 3 weeks. In treated mice, proliferation of muscle stem cells increased, the cross-sectional area of repaired muscle fibers grew about 2-fold, and the peak contractile force of the injured muscle was about 70% higher than in controls. [3]
  • Combined with exercise (2024): 35 female mice aged 22 months were divided into four groups over 8 weeks. Grip strength was about 40% higher in the sedentary treated group than in sedentary controls, about 20% higher in the exercise-only group, and about 60% higher in the group receiving treatment and exercise together. [4]

These models mimic some features of age-related muscle loss (sarcopenia), but no human muscle mass, strength, or fall outcome has been measured. In the 2024 study, the groups consisted of 7–10 animals. [4]

Where does the evidence come from?

All four 5-amino-1MQ mouse studies summarized on this page carry the signature of the same researchers (Watowich and Neelakantan). In the 2018 and 2019 papers, the authors declared no conflict of interest. [1] [3] In the 2024 papers, the senior author was declared as the founder of a company developing NNMT inhibitors, and some of the other authors as current or former employees of the same company. [4] [5] This does not invalidate the results, but it indicates that the findings have not been replicated by independent laboratories.

What is the NAD+ and aging claim based on?

5-Amino-1MQ is often presented as an “NAD+ booster” and “anti-aging.” The source of this claim is that NNMT diverts nicotinamide away from the NAD+ pathway and that inhibitors raised NAD+ levels in fat cell culture. [1] There is no NAD+ change, aging marker, or lifespan outcome measured in humans with 5-amino-1MQ. The human evidence for NAD+ precursors is covered in separate guides: NAD+, NMN.

The overall state of the field is also cautious. A 2026 review examining the clinical translation of NNMT inhibitors writes that, because of inadequate target engagement, low bioavailability, and unknown safety profiles, these molecules have shown limited success even at the preclinical stage, and that newer-generation compounds are trying to address these problems. Two authors of the review are listed as inventors on a patent application filed for a different NNMT inhibitor. [6]

Is it safe? What is known and unknown

There are no human safety data. No observable side effects were reported in mouse studies; in the 2018 study, the dose-finding phase was carried out with only two mice. [1] In the 2024 study, a laboratory screen across a broad panel of targets observed that 5-amino-1MQ also inhibited human MAO-A (67.4% inhibition at 10 µM); the authors wrote that part of the improvement in glucose tolerance might stem from this effect. [5] The significance of this off-target effect in humans and drug interactions have not been examined.

The unknowns are these: absorption and elimination in humans, liver, kidney, and nervous system safety with long-term use, pregnancy, and drug interactions. Whether the labeled substance is actually present in unregulated products, and its purity, are also unknown. General injection-related risks are covered in a separate guide: Peptide side effects

United States

In the FDA’s May 14, 2026 nomination list for 503A (pharmacy compounding), 5-amino-1MQ is not in any of categories 1, 2, or 3. [9] In a warning letter dated January 20, 2026, FDA found that an outsourcing facility registered under 503B was compounding drugs with 5-amino-1MQ and NAD+. According to the letter, because these substances are not on the 503B bulk substances list and were not used to make a drug on the drug shortage list, products compounded with them cannot benefit from the 503B exemptions; the facility could not document the fate of these products or that production had stopped. [8] The legal and practical meaning of the “for research purposes” label is covered in a separate guide: What does research peptide mean?

Sport (WADA)

5-Amino-1MQ is not named in the WADA list valid from January 1, 2026. Section S0 of the list prohibits at all times, in and out of competition, any pharmacological substance not covered by later sections and not approved by any governmental health authority for human therapeutic use, for example drugs in preclinical or clinical development. [10] Published data on 5-amino-1MQ are at the preclinical level; the classification of a specific substance is within WADA’s authority.

Türkiye

The October 16, 2026 TİTCK Licensed Human Medicinal Products List contains no product with 5-amino-1MQ as active ingredient. [11] There is also no row naming it in the Ministry of Agriculture and Forestry Supplement Restricted Substances List (September 21, 2026). [14]

Article 19 of Law No. 1262 punishes with imprisonment of one to five years those who manufacture unlicensed preparations and those who knowingly sell, offer for sale, or have them sold; the same penalty is provided for those who sell or advertise a product with the claim of diagnosing or treating diseases even if it is not a preparation. Importing unlicensed preparations for commercial purposes counts as smuggling. Additional Article 7 of the Law provides that the Ministry may permit the bringing in of unlicensed preparations for examination, trial, or personal treatment, within an amount to be accepted by the Ministry; this is a permit mechanism. [12] Under Article 24 of Law No. 6197, medicines cannot be sold online or in any other electronic medium. [13]

The general legal framework for peptides and similar products: Are peptides legal?

Evidence table: claim, population, and limits

ClaimPopulation studiedLimitation
Causes weight loss, burns fatMale mice made obese with diet (8–9 per group)11 days–4 weeks; low dose ineffective; no human data. [1] [5]
Corrects blood sugar and fatty liverObese miceSeen at the high dose; MAO-A effect may have contributed. [5]
Prevents muscle loss in old age22–24-month-old miceMuscle injury model and grip strength; no muscle outcome measured in humans. [3] [4]
Raises NAD+, slows agingFat cell cultureNo NAD+, aging, or lifespan measured in humans. [1]
Works as a capsuleMice (pharmacokinetics)Oral bioavailability about 3.5%. [5]
Is a “peptide”—A small molecule, a methylquinolinium derivative. [8]

One final point completes this table: as of October 19, 2026, no registered study appears on ClinicalTrials.gov with either a “5-amino-1MQ” or a “5-amino-1-methylquinolinium” search. [7] Efficacy and safety in humans remain a question not yet asked.

Limits of this guide

This page summarizes published animal studies on 5-amino-1MQ and documents from official institutions. It gives no dose, cycle, preparation, administration technique, or product-sourcing information; procedures in animal studies cannot be transferred to humans. Drugs with evidence for weight management are covered in separate guides: GLP-1 agonists

What does the evidence say?

What it does and does not affect
What do the A–E grades mean?

The letter describes the strength of evidence for a specific claim, not the size of the benefit or a usage recommendation. E does not mean ineffectiveness has been proven.

AStrong
Established physiology (e.g. correcting a deficiency) or strong, consistent, direct human studies
BModerate
Supportive human evidence; small effect or some limitations
CLimited
A single randomised trial, mixed results or low-certainty human findings
DInsufficient
Small, uncontrolled or indirect evidence; not enough to judge
ENo benefit shown / not studied in humans
No benefit shown for the claim, or only animal or cell data exist

These grades are Half-Life Journal’s editorial evidence summary; they are not a formal GRADE rating or independent medical approval.

The letter shows evidence strength; it is not a score for positive effect or a usage recommendation.

Frequently asked questions

What is 5-Amino-1MQ?

5-Amino-1MQ (5-amino-1-methylquinolinium) is a small laboratory-developed molecule that inhibits the enzyme nicotinamide N-methyltransferase (NNMT). It is not a peptide because it has no amino acid chain; being sold alongside “research peptide” products does not change this.

Does 5-Amino-1MQ cause weight loss in humans?

Unknown. Findings on weight and fat loss come from mice made obese with a high-fat diet; as of October 19, 2026, ClinicalTrials.gov lists no registered human study of 5-amino-1MQ.

Are oral 5-Amino-1MQ capsules absorbed?

Not measured in humans. In mice, the bioavailability of orally given 5-amino-1MQ was about 3.5%; the authors attributed this to limited absorption from the gut and high first-pass breakdown in the liver.

Is 5-Amino-1MQ banned in doping control?

It is not named in the WADA 2026 list. Section S0 of the list always prohibits substances not covered by other sections and not approved by any governmental health authority for human therapeutic use, for example preclinical drugs; WADA makes the concrete classification.

Is 5-Amino-1MQ legal in Türkiye?

The October 16, 2026 list of licensed products from TİTCK (Turkish Medicines and Medical Devices Agency) contains no drug with 5-amino-1MQ, and it is not named in the Ministry of Agriculture and Forestry restricted substances list for supplements. Law No. 1262 punishes manufacturing an unlicensed preparation and knowingly selling it with imprisonment.

Sources

  1. Animal Neelakantan H et al. — Selective and membrane-permeable small molecule inhibitors of nicotinamide N-methyltransferase reverse high fat diet-induced obesity in mice (Biochem Pharmacol) (2018)Back to text ↑
  2. Animal Kraus D et al. — Nicotinamide N-methyltransferase knockdown protects against diet-induced obesity (Nature) (2014)Back to text ↑
  3. Animal Neelakantan H et al. — Small molecule nicotinamide N-methyltransferase inhibitor activates senescent muscle stem cells and improves regenerative capacity of aged skeletal muscle (Biochem Pharmacol) (2019)Back to text ↑
  4. Animal Dimet-Wiley AL et al. — Nicotinamide N-methyltransferase inhibition mimics and boosts exercise-mediated improvements in muscle function in aged mice (Sci Rep) (2024)Back to text ↑
  5. Animal Babula JJ et al. — Nicotinamide N-methyltransferase inhibition mitigates obesity-related metabolic dysfunction (Diabetes Obes Metab) (2024)Back to text ↑
  6. Guideline / review Puleo N et al. — Emerging opportunities for nicotinamide N-methyltransferase (NNMT) inhibitor clinical translation (Trends Pharmacol Sci) (2026)Back to text ↑
  7. Source ClinicalTrials.gov — “5-amino-1MQ” ve “5-amino-1-methylquinolinium” aramaları (19.10.2026) (2026)Back to text ↑
  8. Institution FDA — Uyarı mektubu, WL 718739 (20.01.2026): 503B tesisinde 5-Amino-1MQ ile ilaç hazırlanması (2026)Back to text ↑
  9. Institution FDA — Bulk Drug Substances Nominated for Use in Compounding Under Section 503A (kategori 1–3 listesi; güncelleme 14.05.2026) (2026)Back to text ↑
  10. Institution WADA — 2026 Yasaklılar Listesi (Prohibited List; 1 Ocak 2026’dan itibaren geçerli) (2026)Back to text ↑
  11. Institution TİTCK — Ruhsatlı Beşeri Tıbbi Ürünler Listesi (16.10.2026) (2026)Back to text ↑
  12. Institution 1262 sayılı İspençiyari ve Tıbbi Müstahzarlar Kanunu (mevzuat.gov.tr, güncel metin) (2025)Back to text ↑
  13. Institution 6197 sayılı Eczacılar ve Eczaneler Hakkında Kanun (madde 24; 6514 sayılı Kanunla değişik)Back to text ↑
  14. Institution T.C. Tarım ve Orman Bakanlığı — Takviye Edici Gıdalar Kısıtlı Maddeler Listesi (son güncelleme 21/09/2026) (2026)Back to text ↑

Method: Institutional clinical guidance and relevant studies were compared. Each finding is presented with its population, outcome, sources and limitations. Independent medical review has not yet been completed.

Updated

This content is for information only and is not medical advice. It does not recommend doses, products or vendors. Talk to your clinician before making any health decision.