Encyclopedia · Metabolic & Weight Loss

5-Amino-1MQ

Evidence review

Evidence grade D

Evidence is primarily from animal and laboratory studies; human efficacy and an established dose are absent.

Reviewed Aug 10, 2026 10 linked authoritative sources

5-Amino-1MQ is frequently marketed and searched for as a "peptide," but that label is chemically inaccurate. The compound, formally 5-amino-1-methylquinolinium, is a small synthetic molecule rather than a chain of amino acids, and it is listed as such in chemical databases like PubChem and the FDA's Global…

What It Is

5-Amino-1MQ is frequently marketed and searched for as a "peptide," but that label is chemically inaccurate. The compound, formally 5-amino-1-methylquinolinium, is a small synthetic molecule rather than a chain of amino acids, and it is listed as such in chemical databases like PubChem and the FDA's Global Substance Registration System.[1] It is studied as a selective, membrane-permeable inhibitor of an enzyme called nicotinamide N-methyltransferase, or NNMT.

Because online body-composition and longevity content often lumps metabolic research compounds together with true peptides, 5-Amino-1MQ shows up in peptide-therapy searches despite its distinct chemical class. Common naming variants include 5-Amino-1MQ, 5-amino-1-methylquinolinium, 5-AMQ, and 5A-1MQ, all referring to the same research molecule.

How It Works

NNMT is an enzyme that transfers a methyl group from S-adenosylmethionine (SAM) to nicotinamide (a form of vitamin B3). This reaction sits at a crossroads of NAD-related energy metabolism and methylation biology, and NNMT activity varies by tissue, playing different roles in liver, fat, muscle, and cancer cells.[2]

By blocking NNMT, 5-Amino-1MQ is hypothesized to shift this balance in ways that affect fat cell metabolism. In cultured fat cells, NNMT inhibitors lowered 1-methylnicotinamide while raising NAD+ and SAM, and suppressed the pathway that builds new fat. A separate discovery using genetic knockdown of NNMT, rather than the drug itself, found that removing NNMT protected mice from diet-induced obesity, lending plausibility to the target. None of this proves that inhibiting NNMT produces clinical benefit in people.

What the Research Shows

The evidence for 5-Amino-1MQ is preclinical. In diet-induced-obese mice, the compound reduced body weight, white-fat mass, adipocyte size, and cholesterol without reducing food intake.[2] A follow-up mouse study combining an NNMT inhibitor with a reduced-calorie diet reported improvements in body composition and liver fat compared with diet change alone.[5] Separate mouse work examined aged muscle and exercise responses, while a pharmacokinetic study characterized the compound in rats rather than people.[6][13]

No registered or completed human efficacy study of 5-Amino-1MQ was identified in the sources reviewed through August 10, 2026.[20] Claims about human fat loss, longevity, mitochondrial health, or disease treatment therefore remain extrapolations from animal and cell experiments.

Safety & Side Effects

Human safety data for 5-Amino-1MQ were not identified. A 2018 mouse experiment reported no observable adverse effects during its short treatment period, but that result cannot establish human safety.[2] Long-term toxicity, reproductive safety, organ impairment, medicine interactions, and the consequences of inhibiting an enzyme with tissue-dependent roles in cancer biology remain unknown.[10]

An absence of adverse-event reports is not reassuring when there is no systematic human exposure program. Products sold as compounded or research-grade 5-Amino-1MQ add identity, concentration, impurity, and manufacturing risks; FDA does not review compounded drugs for safety, effectiveness, or quality before marketing.[15]

Regulatory Status

5-Amino-1MQ is not an FDA-approved drug and has no approved label, indication, or human dose. PubChem and FDA's Global Substance Registration System contain chemical identity records for 5-amino-1-methylquinolinium, but FDA explicitly states that assignment of a UNII or inclusion in GSRS does not imply regulatory review or approval.[1][9]

Section 503A places conditions on the use of bulk substances in compounding; an online product labeled "compounded" or "research use" is not thereby an approved medicine or a clinically validated formulation.[17] No standard human regimen should be inferred from the mouse and rat studies.

Evidence review

Sources and evidence

Citation numbers in the article link to the exact regulator records, trial registrations, and publications reviewed.

  1. NIH PubChem5-Amino-1-methylquinolinium compound record (2026)
  2. Biochemical Pharmacology5-Amino-1MQ and diet-induced obesity in mice (2018)
  3. Scientific ReportsNNMT inhibition plus reduced-calorie diet in obese mice (2021)
  4. Journal of Pharmaceutical and Biomedical Analysis5-Amino-1MQ pharmacokinetics and oral bioavailability in rats (2021)
  5. U.S. FDA GSRS5-Amino-1-methylquinolinium substance record (2026)
  6. Cell Death & DiseaseComplex roles of NNMT in cancer progression (2022)
  7. Scientific ReportsNNMT inhibition and muscle function in aged mice (2024)
  8. U.S. FDAUnderstanding the risks of compounded drugs (2026)
  9. U.S. FDABulk drug substances used in compounding under section 503A (2026)
  10. ClinicalTrials.govExact-name study search for 5-Amino-1MQ (2026)