Metabolic & GLP-1Small moleculeEvidence C4 cited

5-Amino-1MQ

NNMT Inhibitor

aka 5-amino-1-methylquinolinium · NNMT inhibitor

A small molecule researched for blocking NNMT enzyme to boost NAD+ levels and fat metabolism.

Molecular wt
159.21g/mol
Formula
C10H11N2+
CAS
685079-15-6
Half-life
4 h
estimated
Tmax
1 h
Route
Oral

Sequence

Read this before quoting the sequence
Not a peptide. 5-Amino-1MQ is a small-molecule quaternary quinolinium cation (5-amino-1-methylquinolin-1-ium), a nicotinamide N-methyltransferase (NNMT) inhibitor. No amino acid sequence exists.
Source ↗

Mechanism of action

5-Amino-1MQ works by inhibiting the nicotinamide N-methyltransferase (NNMT) enzyme, which plays a role in the regulation of energy metabolism. By blocking NNMT, this compound increases the availability of nicotinamide adenine dinucleotide (NAD+), a crucial coenzyme in cellular energy production. This enhancement of NAD+ levels supports improved mitochondrial function and energy expenditure. Additionally, it may influence fat metabolism by altering the expression of genes involved in adipogenesis.

What the evidence actually shows

Grade C

There are currently no published human clinical trials specifically investigating 5-Amino-1MQ. Most evidence comes from animal studies and in vitro experiments, which suggest potential benefits in metabolic regulation and fat loss. Human studies are needed to confirm these effects and establish safety profiles.

Regulatory status

Status
Not an approved drug in any jurisdiction identified. No registered human clinical trial for 5-Amino-1MQ was found on ClinicalTrials.gov.
Clinical stage
Preclinical (rodent and in vitro only)
UK
research_compound

5-Amino-1MQ is not approved for medical use in the UK and is considered a research compound. It is not regulated by the MHRA for therapeutic use.

Source ↗

Pharmacokinetics

Half-life
4 h
Tmax
1 h
Absorption
oral
Elimination
hepatic
Washout
3 days
Low-confidence pharmacokinetics
These figures are recorded as estimated rather than measured in a published PK study. Treat them as an order of magnitude. Anything downstream of them — accumulation, steady state, washout — inherits that uncertainty.

Dosing — what backs each figure

Nothing is known about dosing 5-amino-1MQ in humans: there are no published human trials and no registered clinical studies. All published in-vivo work is in diet-induced obese mice at 32 mg/kg/day by subcutaneous injection; the source paper notes 5-amino-1MQ has poor oral bioavailability in mice, which directly contradicts the claim that animal studies used oral administration.

PreclinicalAnimal studies — not a human dose
  • 32 mg/kg/day of active pharmaceutical ingredient (4 mg/mL 5-amino-1MQ monochloride salt in saline, dosed at 10 mL/kg body weight), once daily, alongside a low-fat diet switch

    mouse (diet-induced obese C57BL/6) · subcutaneous injection · PMID 35013352

  • Once-daily dosing for 28 days; dose-dependent reduction in body weight and fat mass. Plasma/tissue PK characterised after intravenous, oral and subcutaneous dosing. Exact mg/kg levels are in the full text, not the abstract.

    mouse (diet-induced obese) · subcutaneous (efficacy arm); IV/oral/SC compared for PK · PMID 39161060

  • Systemic administration of a potent methylquinolinium NNMT inhibitor reduced body weight, white adipose mass and adipocyte size; dose in full text only

    mouse (diet-induced obese, high-fat diet) · systemic (intraperitoneal) · PMID 29155147

Animal doses do not convert to human doses by body weight alone. Route matters too — a compound dosed intraperitoneally in mice tells you little about subcutaneous use.

Commonly circulatedNot established by any study
Dose
50-150 mg/day
Frequency
Daily

Why this isn't evidence
There is no registered or published human trial of 5-amino-1MQ at all, and the only published in-vivo regimen is 32 mg/kg/day given SUBCUTANEOUSLY in mice — a route the authors chose explicitly because 5-amino-1MQ has poor oral bioavailability in mice — so a flat oral 50-150 mg/day human figure is not derived from any source.

This figure is shown because it is what circulates and what people search for — not because it is supported. Cycle lengths in particular tend to be convention copied between compounds rather than anything derived from a compound's own pharmacokinetics.

No established human dose
No approved label or completed human trial establishes a dosing regimen for this compound. Anything presented as a standard protocol for it — anywhere — is someone's convention rather than a finding.

Handling and storage

No compound-specific stability data exists
No stability/storage study for 5-Amino-1MQ was located. Note that PubChem CID 950107 is the free cation; material is normally handled as a salt (e.g. iodide), whose formula and mass differ from the cation values above. No compound-specific stability study (lyophilised or reconstituted) was located in a primary/regulatory source during this verification pass. Only generic synthetic-peptide handling guidance exists for this compound; no specific temperatures or durations are recorded here rather than fabricating them. General peptide handling still applies — reconstitute gently, keep it cold, keep it dark — but any specific figure you see quoted for this compound elsewhere is someone's assumption, not a measurement.

Safety

Commonly reported
  • ·Gastrointestinal discomfort
Rarely reported
  • ·Potential liver enzyme alterations
Contraindications
  • ·Pregnancy
  • ·Breastfeeding
Drug interactions
  • ·Nicotinamide supplements, which may alter NAD+ metabolism

Reported combinations

Reported as synergistic
  • ·Resveratrol, which also enhances NAD+ levels
Reported as antagonistic
  • ·High-dose niacin, which may interfere with NAD+ pathways

Combination claims in this dataset are largely unsourced and should be treated as folk knowledge until a citation appears beside them.

References (4)

Data provenance

Chemistry and citations on this page were checked against primary sources on 2026-08-14. Values that could not be verified were left blank rather than filled with a plausible guess.

Could not verify
sequence, storage.lyophilized, storage.reconstituted, storage.lightSensitive, reconstitution.solvent, regulatory.wada

Research use only
This profile is educational reference material. It is not medical advice, not a prescription, and not an endorsement of self-administration. Compounds discussed here are research chemicals and most are not approved for human therapeutic use.