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Evidence review

5-Amino-1MQ: What the Evidence Actually Shows

5-Amino-1MQ has real mouse data behind it and zero human trials. Here's what the actual NNMT-inhibitor research shows, and what it doesn't.

Written by David ChenClinical Evidence & Regulatory Editor

5-Amino-1MQ is sold across the longevity-supplement market as an oral capsule, marketed for fat loss and "cellular energy" through a mechanism most other compounds on this site don't share at all: it isn't a peptide, and it isn't administered like one.

What it actually is, and why it isn't on this site's calculator hub

5-Amino-1MQ (5-amino-1-methylquinolinium) is a small molecule, not a peptide — it has no amino-acid sequence. It's an inhibitor of nicotinamide N-methyltransferase (NNMT), an enzyme that methylates and clears nicotinamide, the same building block cells use to make NAD+. The mechanistic pitch is that blocking NNMT redirects more nicotinamide toward NAD+ synthesis and reduces methylation-driven epigenetic changes linked to fat storage. That's a real, published cell-biology mechanism — described below — but the underlying pharmacology is also why this article doesn't come with a reconstitution calculator the way most of this site's compound pages do: as a small, stable molecule rather than a peptide, 5-Amino-1MQ is orally bioavailable, and a live check of the market confirms oral capsules are the dominant real-world form. Several sellers — including longevity-supplement brands that don't carry any other research peptide at all — sell it exclusively as an oral capsule; only a minority of research-chemical-specific vendors also list an injectable vial. Building a vial-to-syringe tool for a compound whose real-world dominant form is a capsule would misrepresent how it's actually taken, so this site doesn't.

The mechanism — real, and entirely mouse-tested

NNMT enzyme

Normally methylates and clears nicotinamide, a building block for NAD+

5-Amino-1MQ inhibits NNMT

Small molecule, not a peptide — orally bioavailable

Result in obese mice: reduced weight and adipose mass

A real preclinical finding — not yet tested in any human study

A genuine, published mouse finding: NNMT inhibition reduced body weight and adipose mass in diet-induced obese mice without affecting food intake.

The actual research: real, but entirely in mice

A research group at the University of Texas Medical Branch (Watowich lab) has published an active line of work on small-molecule NNMT inhibitors as an anti-obesity strategy. Their 2018 paper describes methylquinolinium-scaffold NNMT inhibitors that reduced body weight and white adipose mass in diet-induced obese mice, without affecting food intake or producing observable adverse effects1. A 2022 follow-up study from the same group explicitly names the compound used as "5-amino-1-methylquinolinium" — confirming this is the same substance sold today — and reports that combining it with a reduced-calorie diet produced dramatic weight and adiposity loss in obese mice, rapidly normalizing their measurements to those of lean, age-matched control animals; a calorie-reduced diet alone did not achieve the same result in the same timeframe2. That is a real, positive, mechanistically-grounded finding — and it is entirely a mouse result. A live, dedicated PubMed search for the exact compound name "5-amino-1MQ" returns zero results; searching by its full chemical name returns exactly three papers, all from this same research line, all in mice.

What's actually been tested, by claim

  • Mouse obesity/adiposity data (compound-specific)MODERATE evidence

    Two published studies from the same research group, one explicitly naming 5-amino-1-methylquinolinium, both in diet-induced obese mice.

  • Broader NNMT-as-a-drug-target research (other chemistries)MODERATE evidence

    A genuinely active field (cancer, fibrosis, kidney disease) — but this is research on the TARGET, not evidence for this specific molecule.

  • 5-Amino-1MQ — any human study, any dose, any routeNONE evidence

    A dedicated PubMed search for the exact compound name returns zero results.

A real, active mouse research program — with a gap at the exact point where a human dosing or safety claim would need to start.

What this doesn't tell you: nothing about a human dose, or a human effect

NNMT itself is a genuinely active area of broader drug-target research — a live search turns up dozens of 2024-2026 papers on NNMT inhibition in cancer, kidney fibrosis, and metabolic disease. That broader research momentum is real, but it is not the same claim as "5-Amino-1MQ has been tested in those contexts" — most of that literature studies NNMT as a target using different inhibitor chemistries, or studies the enzyme's biology without testing any inhibitor drug at all. This article does not conflate general NNMT-target interest with evidence for the specific molecule sold as 5-Amino-1MQ. No human trial of 5-Amino-1MQ, for any use, at any dose, was located for this article — no published safety data, no published pharmacokinetics, no published effective dose in a person. Any specific milligram amount attached to a "5-Amino-1MQ protocol" online is not sourced to a human study; it can't be, because none exists.

The regulatory picture: entirely off FDA's radar

5-Amino-1MQ has never been nominated to FDA for compounding-bulk-substance review of any kind — checked live against both FDA's current 503A Bulks List (updated May 14, 2026) and its companion page tracking substances with documented safety concerns, including historically-withdrawn nominations; neither document contains any match for "1MQ," "methylquinolinium," or "5-amino." DailyMed's structured-product-label search returns zero results, confirming no FDA-approved product exists3. openFDA's FAERS adverse-event database returns zero reports4 — the second of this five-compound batch, alongside IGF-1 LR3, with a fully null safety-report history, which again reflects the absence of any formal use record rather than a demonstrated safety profile.

The regulatory picture, checked live

5-Amino-1MQ
Ever nominated to FDA for 503A/503B compounding review?No — absent from the current list and its historical/withdrawn section alike
FDA-approved product?No — zero results in DailyMed
FAERS adverse-event reports (all time)0
Predominant real-world market formOral capsule (multiple longevity-supplement brands); a minority of vendors also sell an injectable vial
Sold by a board-reviewed provider on this site?No
Re-verified directly against FDA's current 503A Bulks List, its companion significant-safety-risk page, DailyMed, and openFDA's FAERS database for this article.

What this means if you're considering it

None of the 31 providers this site's own reviews cover sell 5-Amino-1MQ as a primary, boarded product — this site's own identity-layer research confirms it is not tagged to any reviewed seller. The mouse research behind 5-Amino-1MQ is real, mechanistically coherent, and comes from a legitimate, ongoing academic research program — a genuinely different starting point than a compound with no research behind it at all. But "real mouse data" and "tested in humans" are different claims, and this compound has only the first. If you're weighing it against other metabolically-marketed compounds this site now covers, our AOD-9604 evidence review has the opposite profile — a compound that reached and then failed a human efficacy trial, after passing six human safety trials — which makes it a more informative comparison than a reassuring one.

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Frequently asked questions

Is 5-Amino-1MQ a peptide?

No. It's a small molecule (5-amino-1-methylquinolinium), not a peptide — it has no amino-acid sequence. That's also why this site doesn't carry a reconstitution calculator for it: as an orally bioavailable small molecule, it's predominantly sold and taken as a capsule, not reconstituted and injected the way most compounds on this site's calculator hub are.

What does the research on 5-Amino-1MQ actually show?

A research group at the University of Texas Medical Branch has published mouse studies showing that 5-Amino-1MQ, an inhibitor of the NNMT enzyme, reduces body weight and adipose mass in diet-induced obese mice, especially when combined with a reduced-calorie diet. That research is real and mechanistically coherent — but it is entirely in mice. A dedicated search of the published literature found zero human trials of the compound, for any use, at any dose.

Is 5-Amino-1MQ FDA-approved or regulated?

It has never been nominated to FDA for compounding-bulk-substance review of any kind — confirmed against both FDA's current 503A Bulks List and its companion page tracking historical safety concerns and withdrawn nominations. No FDA-approved product exists; DailyMed returns zero results, and openFDA's adverse-event database returns zero reports.

References

  1. Neelakantan H, Vance V, Wetzel MD, Wang HL, McHardy SF, Finnerty CC, Hommel JD, Watowich SJ (2018). Selective and membrane-permeable small molecule inhibitors of nicotinamide N-methyltransferase reverse high fat diet-induced obesity in mice. Biochemical Pharmacology. https://pubmed.ncbi.nlm.nih.gov/29155147/
  2. Dimet-Wiley A, Wu Q, Wiley JT, Eswar A, Neelakantan H, Savidge T, Watowich S (2022). Reduced calorie diet combined with NNMT inhibition establishes a distinct microbiome in DIO mice. Scientific Reports. https://pubmed.ncbi.nlm.nih.gov/35013352/
  3. National Library of Medicine (2026). DailyMed structured-product-label search for "5-amino-1MQ" — zero results (no FDA-approved drug label on file). DailyMed — U.S. National Library of Medicine (official archive of FDA-approved drug labeling). https://dailymed.nlm.nih.gov/dailymed/services/v2/spls.json?drug_name=5-amino-1MQ
  4. U.S. Food and Drug Administration (2026). FDA Adverse Event Reporting System (FAERS) — zero reports for "5-AMINO-1MQ" as a medicinal-product name search, data last updated July 30, 2026. openFDA — drug/event public API. https://api.fda.gov/drug/event.json?search=patient.drug.medicinalproduct:%225-AMINO-1MQ%22

Medical disclaimer: This content is for general educational purposes only and is not medical advice, diagnosis, or treatment. Always consult a licensed healthcare professional before starting, stopping, or changing any treatment.