Not a peptide
5-Amino-1MQ is 5-amino-1-methylquinolinium, a quinolinium derivative. It is a small molecule with no amino acid sequence, and it is not a peptide.
It is not the only one in this position. AICAR is a nucleoside, and SLU-PP-332 is a synthetic receptor agonist; both are sold through peptide catalogues for the same commercial reasons, and the two make an instructive pair — one has been given to more than three thousand people and failed, the other has never been given to anybody.
It shares a catalogue page with peptides, and very little else.
There is a visible clue, if anyone is looking for one: it is usually sold as a capsule to be swallowed. Peptides are generally destroyed in the digestive tract, which is why almost everything else in this library is injected — the reason is set out in the primer on what a peptide actually is. A compound that survives being swallowed is telling you something about what it is.
What it does
It inhibits an enzyme called nicotinamide N-methyltransferase, usually shortened to NNMT.
NNMT is involved in how cells process nicotinamide, which sits close to the NAD+ pathway — and NAD+ is the reason this compound gets filed alongside the compounds sold for longevity and metabolic products. MOTS-c, the other NAD+-adjacent entry here reaches the same shelf by a different route, and is at least a peptide. The reasoning is: NNMT consumes something the cell could otherwise use for NAD+; block the enzyme, and more is available.
That is a coherent piece of biochemistry. Whether pulling that lever produces a useful effect in a person is a different question, and the published record does not answer it.
What has actually been shown
In mice: selective, membrane-permeable NNMT inhibitors reversed obesity induced by a high-fat diet. This is the finding almost every claim about the compound traces back to.
Among the other compounds sold for fat loss, the construct that targets the blood vessels feeding fat tissue is the one whose mechanism differs most from everything here — it is designed to kill cells rather than to alter a signalling pathway.
In cells: 5-amino-1MQ at 30 micromolar for 24 hours changed intracellular NAD+ and nicotinic acid levels and the ratio between them in differentiated fat cells. Related work found that NNMT inhibitors did not affect the viability of 3T3-L1 pre-adipocytes at concentrations up to 100 micromolar. Separate work found the compound inhibited the proliferation of HeLa cells in a concentration- and time-dependent way.
In people: nothing was found in the published record.
Where that leaves it
The mouse result is genuinely interesting, and NNMT is a real target that serious groups are working on. What does not follow is that swallowing this compound produces fat loss or muscle regeneration in a person. That step has not been taken in the literature, and every confident statement about human results is filling a gap rather than reporting one.
It is not approved anywhere, for anything.
Last checked
2026-09-07.
