5-Amino-1MQ vs AOD-9604

Side-by-side comparison of mechanisms, dosing, interactions, and stacking potential.

✅ Stacking Partners — These compounds are commonly used together and may have synergistic effects.
5-Amino-1MQAOD-9604
CategoryPeptidesGrowth Factors
Standard DoseResearch indicates 50-150 mg daily via oral administration, typically divided into 1-2 doses.Research indicates 250-300 mcg daily via subcutaneous injection, administered in the morning on an empty stomach.
TimingMorning dosing preferred. Can be taken with or without food.Morning administration on empty stomach, at least 30 minutes before eating. Fasted state enhances lipolytic effect.
Cycle Duration8-12 week cycles.12-20 week cycles.
Evidence Levelanimal_plus_anecdotalmoderate_human
A

5-Amino-1MQ

Peptides

Mechanism

5-Amino-1MQ is a small molecule inhibitor of nicotinamide N-methyltransferase (NNMT), an enzyme that catalyzes the transfer of a methyl group from S-adenosylmethionine (SAM) to nicotinamide, generating 1-methylnicotinamide (1-MNA). By inhibiting NNMT, 5-Amino-1MQ increases intracellular NAD+ levels, reduces 1-MNA production, suppresses lipogenesis in adipocytes, and modulates the methionine-homocysteine cycle. In vivo, it significantly reduces body weight, white adipose mass, and adipocyte size through enhanced energy expenditure and altered lipid metabolism.

Standard Dosing

Research indicates 50-150 mg daily via oral administration, typically divided into 1-2 doses.

Timing

Morning dosing preferred. Can be taken with or without food.

Cycle Duration

8-12 week cycles.

Side Effects

  • Mild GI discomfort
  • Headache
  • Diarrhea (uncommon)
  • Nausea at higher doses

Contraindications

  • Pregnancy and breastfeeding
  • Severe hepatic impairment
  • Active cancer (NAD+ modulation concern)

Best Stacking Partners

MOTS-cAOD-9604TesofensineSemaglutide
B

AOD-9604

Growth Factors

Mechanism

AOD-9604 is a synthetic 16-amino acid fragment (residues 176-191) of the C-terminal domain of human growth hormone with a tyrosine substitution at the N-terminus. It selectively stimulates lipolysis by upregulating beta-3 adrenergic receptors in adipose tissue while inhibiting lipogenesis. It modulates lipid and glucose metabolism through beta-adrenergic and AMPK-related pathways without influencing IGF-1 activity, growth, or insulin sensitivity — retaining GH's fat-burning properties without its growth-promoting effects.

Standard Dosing

Research indicates 250-300 mcg daily via subcutaneous injection, administered in the morning on an empty stomach.

Timing

Morning administration on empty stomach, at least 30 minutes before eating. Fasted state enhances lipolytic effect.

Cycle Duration

12-20 week cycles.

Side Effects

  • Injection site reactions
  • Headache
  • Mild nausea
  • Transient hypoglycemia (rare)

Contraindications

  • Active cancer
  • Pregnancy and breastfeeding
  • Type 1 diabetes (use with caution)
  • Limited human evidence and sourcing variability

Best Stacking Partners

5-Amino-1MQMOTS-cCJC-1295/IpamorelinTesofensine

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