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5-Amino-1MQ

Fat Loss
·173 Da·C₁₀H₁₁N₂⁺
Peptide Database
3Mechanisms
4Benefits
20Studies

5-Amino-1MQ (5-amino-1-methylquinolinium) is a synthetic small molecule, not a peptide. It was developed as a selective, cell-permeable inhibitor of the enzyme nicotinamide N-methyltransferase (NNMT).

Research Dosage Notes

Not FDA-approved. Commonly discussed research dosages range from 50-150 mg/day orally, often taken as 50 mg one to three times daily with meals. Typical cycles are 4-12 weeks. Human clinical data is very limited; most evidence is from animal studies.

Mechanisms of Action

3

NNMT inhibition

Strong

Selectively inhibits nicotinamide N-methyltransferase, preventing the methylation of nicotinamide (NAM) and depletion of S-adenosylmethionine (SAM). This preserves intracellular NAD+ levels by preventing the NNMT-mediated 'methyl sink' that drains energy precursors.

NAD+ salvage / one-carbon metabolism

NAD+ upregulation

Strong

By blocking NNMT, intracellular NAD+ concentrations increase, enhancing mitochondrial function and shifting cellular energy metabolism toward fat oxidation over fat storage.

NAD+ / mitochondrial bioenergetics

Lipogenesis suppression

Moderate

Reduces intracellular 1-methylnicotinamide (1-MNA) and suppresses de novo lipogenesis in adipocytes, leading to reduced fat cell size without changes in caloric intake.

Adipocyte lipid metabolism

Benefits

4
60

Fat loss

Body Composition

Animal studies show reductions in fat cell size by 30-40% and notable reduction in visceral fat without changes in calorie intake.

Moderate
60

Increased cellular energy and metabolic rate

Metabolic

By preserving NAD+ levels, mitochondrial function is enhanced, potentially increasing basal metabolic rate and energy expenditure.

Moderate
40

Cholesterol reduction

Metabolic

NNMT inhibition has been associated with improved lipid profiles in preclinical models, including reduced total cholesterol.

Emerging
40

Muscle preservation during fat loss

Body Composition

Unlike caloric restriction alone, NNMT inhibition may preferentially target adipose tissue while preserving lean mass, though human data is limited.

Emerging

Research Studies

20
2025

Emerging evidences suggest that autophagy, a key cellular process responsible for degrading and recy...

Brain research · Rishika Dhapola, Sneha Kumari, Prajjwal Sharma, Balachandar ...

2024

Inhibitors of NAD

International journal of molecular sciences · Moustafa S Ghanem, Irene Caffa, Fiammetta Monacelli, Alessio...

2021

Human neurodegenerative proteinopathies are disorders associated with abnormal protein depositions i...

Human molecular genetics · Meredith Pinkerton, Andrea Ruetenik, Viktoriia Bazylianska, ...

2021

SARM1 is an inducible TIR-domain NAD

Cell reports · Tong Wu, Jian Zhu, Amy Strickland, Kwang Woo Ko, Yo Sasaki

2020

Interleukin-8 drives CD38 to form NAADP from NADP

FASEB journal : official publication of the Federation of American Societies for Experimental Biology · Tae-Sik Nam, Dae-Ryoung Park, So-Young Rah, Tae-Gyu Woo, Hun...

This database is for educational and research purposes only. It is not medical advice. Consult a healthcare professional before using any peptide or supplement.

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