Kraus et al. — obese mice
NNMT knockdown in obese mice produced lean-mass-preserving weight loss without caloric restriction.
A small-molecule NNMT inhibitor (not technically a peptide, but sold alongside). Blocks the enzyme that disposes of methyl groups, which keeps SAM high and biases metabolism toward lean-mass preservation. Research-grade only.
A small-molecule NNMT inhibitor (not technically a peptide, but sold alongside). Blocks the enzyme that disposes of methyl groups, which keeps SAM high and biases metabolism toward lean-mass preservation. Research-grade only.
Blocks an enzyme (NNMT) that slows down fat cell metabolism. When you block it, fat cells burn more, and muscle cells keep their anabolic signaling.
Cycles of 8–12 weeks. Very new; monitor closely.
Blocks an enzyme (NNMT) that slows down fat cell metabolism. When you block it, fat cells burn more, and muscle cells keep their anabolic signaling.
Selective inhibitor of nicotinamide N-methyltransferase (NNMT). NNMT overexpression in adipose tissue correlates with obesity. Inhibition raises intracellular nicotinamide adenine dinucleotide levels and SAM, stimulating fat-cell energy expenditure and skeletal muscle protein synthesis.
NNMT knockdown in obese mice produced lean-mass-preserving weight loss without caloric restriction.
Established 5-amino-1MQ as a potent, selective NNMT inhibitor with oral bioavailability.
These are reported protocols from research literature and practitioner accounts, not prescriptions. No FDA-approved human dose exists for research compounds. Anyone using 5-Amino-1MQ should work with a qualified physician and source from a supplier providing third-party COAs.
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