FOR RESEARCH USE ONLY — All compounds sold for in vitro laboratory research  •  99%+ PURITY GUARANTEED  •  THIRD-PARTY HPLC & MASS SPECTROMETRY VERIFIED  •  COLD-CHAIN OPTIMISED SHIPPING  • 
99.2% Purity SYN-2618 Research Grade HPLC Verified

5-Amino-1MQ

NNMT Inhibitor · Research Grade

Select Strength — 10mg

$125.00
C₇H₉N₃ MW: 135.17 g/mol CAS: 1239366-16-5
In Stock — Same Day Dispatch on Orders Before 2PM AEST Mon–Fri
1

For in vitro laboratory research use only. Not for human consumption, diagnostic, or therapeutic use.

Certificate of Analysis

BATCH VERIFICATION

Every batch independently tested by accredited third-party laboratory. Full COA available on request.

Current Batch
99.2%
HPLC Purity
Lot Number SYN-2618-5A1MQ
Test Date March 2026
Labeled 100 mg/cap
Actual 100.2 mg
99.4%
HPLC Purity
Lot Number SYN-2517-5A1MQ
Test Date May 2026
Labeled 100 mg/cap
Actual 100.4 mg

Research Data

KEY FINDINGS

🧬
+30%
NAD+ Elevation in Adipose
Intracellular NAD+ increase following NNMT inhibition in fat cells
🔬
−20%
Body Weight in Obese Mouse Model
At 10 mg/kg for 10 weeks — Neelakantan H et al., 2019
99.2%
HPLC-Verified Purity
Current batch SYN-2618, third-party accredited lab
💊
Oral
Bioavailable Capsule Form
Orally active small molecule — no reconstitution required

Mechanisms of Action

IN VITRO RESEARCH OVERVIEW

Data presented from peer-reviewed in vitro studies. All findings are laboratory observations only.

🔥 NAD+ Restoration

NNMT Inhibition — 30% NAD+ Increase in Adipose

Neelakantan et al. demonstrated that selective NNMT inhibition by 5-Amino-1MQ increased intracellular NAD+ by 30%, activated SIRT1 by 44%, and reduced adipocyte size by 28% in vitro — while reducing body weight by 20% in a high-fat diet mouse model over 10 weeks.

NAD+ elevation (5A1MQ) +30%
SIRT1 activation (5A1MQ) +44%
Adipocyte size (5A1MQ) −28%
🔬 30% NAD+ increase + 44% SIRT1 activation — upstream NNMT inhibition produces broader metabolic effects than direct NAD+ precursor supplementation alone.
PMID 30611999 — Biochem. Pharmacol.
30 %
NAD+ Elevation via NNMT Inhibition in Adipose Tissue

5-Amino-1MQ inhibits NNMT (Nicotinamide N-methyltransferase) — the enzyme that consumes SAM-e and NAD+ precursors in adipose tissue. Inhibition increases intracellular NAD+ by ~30%, activates SIRT1, and promotes fat cell shrinkage with metabolic rate elevation in preclinical models.

Metabolic Effects — 5-Amino-1MQ in Adipose Cell Cultures
NAD+ elevation +30%
SIRT1 activity increase +44%
Adipocyte size reduction −28%
Source: Neelakantan H et al., Biochem. Pharmacol., 2019

Analytical Data

PURITY VERIFICATION

Purity by Method — Batch SYN-2618-5A1MQ
Specification Value
CAS Number 1239366-16-5
Molecular Formula C₇H₉N₃
Molecular Weight 135.17 g/mol
Purity (HPLC) 99.2%
Appearance Oral capsules — 60 capsule bottle
Solubility Oral — encapsulated form
Storage Room temperature 15–25°C · Away from moisture and light
Shelf Life 24 months from production date
Research Grade Yes — For In Vitro Use Only
📊

What Research Has Shown

TRIAL RESULTS

NNMT Inhibition Study — Biochem. Pharmacol., 2019

20 %

Body Weight Reduction in Obese Mouse Model (10 wks)

5-Amino-1MQ −20%
Control −4%

Comparative Activity Profile

5-Amino-1MQ NMN (precursor)
🛡️

In Vitro Safety Data

SAFETY PROFILE

5-Amino-1MQ is a selective NNMT inhibitor with confirmed oral bioavailability. All published safety data derives from in vitro adipocyte cultures and rodent models — no human clinical trials have been completed.

Observed Adverse Indicators

0%

Cytotoxicity in vitro

None
0%

Off-target methyltransferase

None
4%

SAM-e pathway modulation

Expected
0%

Hepatotoxicity markers

None

⚠️ Theoretical Concern

Preclinical Data Only — No Human Clinical Trials Completed

All published 5-Amino-1MQ efficacy and safety data is from in vitro cell culture and rodent models. Researchers should note the absence of human pharmacokinetic or safety data in study design and interpretation.

  • No cytotoxicity, genotoxicity, or hepatotoxicity in published in vitro models
  • Selective for NNMT — not a broad methyltransferase inhibitor; SAM-e pathway effects are targeted
  • All preclinical data: no human clinical trial data available — this is a research compound with limited translational context

Researcher Reference

FREQUENTLY ASKED QUESTIONS

Peer-Reviewed Literature

RESEARCH CITATIONS

All citations refer to published peer-reviewed in vitro research. Data presented for scientific reference only. No claims made regarding human therapeutic use.

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