5-Amino-1MQ Vial

Lyophilized 5-Amino-1MQ research material for laboratory reconstitution. The vial format supports precise dose-response studies in cell-culture and animal models of NNMT inhibition and adipose-tissue metabolic regulation. HPLC-tested, third-party COA per batch.

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Description

5-Amino-1MQ (5-amino-1-methylquinolinium iodide) is a small-molecule, membrane-permeable inhibitor of nicotinamide N-methyltransferase (NNMT), the enzyme that converts nicotinamide and S-adenosyl-l-methionine (SAM) into 1-methylnicotinamide and S-adenosyl-l-homocysteine. NNMT is upregulated in the white adipose tissue of obese animals and humans, and its activity is mechanistically linked to depleted cellular NAD+ and SAM pools. 5-Amino-1MQ was developed as a research tool to selectively block NNMT in vitro and in vivo, primarily by the Watowich group at the University of Texas at Austin.

The strongest published finding is from the foundational Biochemical Pharmacology study by Neelakantan et al.: in diet-induced obese mice, daily 5-Amino-1MQ administration produced reductions in body weight, white adipose tissue mass, and adipocyte size without any significant change in food intake.1

Important Note on the Evidence Base

The published evidence base for 5-Amino-1MQ is preclinical. All controlled studies referenced below were conducted in cell culture (3T3-L1 adipocytes, primary muscle stem cells) or rodent models (diet-induced obese mice, aged C57BL/6J mice). No human clinical trials of 5-Amino-1MQ in obesity, sarcopenia, or any other indication have been published in peer-reviewed journals. The peer-reviewed literature is also concentrated within a single research group (Watowich lab, University of Texas at Austin) and its industry partner Ridgeline Therapeutics, with limited independent replication to date. Animal-to-human amount translation is not straightforward and requires allometric scaling, and human pharmacokinetics, safety, and efficacy remain uncharacterized in published literature. This product is for laboratory research only.

Published Research on 5-Amino-1MQ

Foundational DIO Mouse Study — Neelakantan et al., Biochemical Pharmacology (2018)

This paper introduced 5-Amino-1MQ as a selective and membrane-permeable small molecule inhibitor of NNMT and tested it in 3T3-L1 adipocytes and in male C57BL/6J mice maintained on a high-fat diet. Daily intraperitoneal administration for 11 days reduced body weight gain, decreased white adipose tissue mass by approximately 35%, and reduced adipocyte size, while food intake between treated and control groups did not differ significantly. The compound showed an in vitro NNMT IC50 of approximately 1.2 μM and did not inhibit related methyltransferases at concentrations tested.1

Aged Muscle Stem Cell Rejuvenation — Neelakantan et al., Biochemical Pharmacology (2019)

In a follow-up study, the authors tested whether NNMT inhibition could reverse the age-related decline in muscle stem cell (satellite cell) function. NNMT was confirmed to be upregulated in aged versus young mouse skeletal muscle. In 24-month-old mice subjected to muscle injury, 5-Amino-1MQ treatment increased satellite cell proliferation and myofiber cross-sectional area approximately 2-fold compared with vehicle controls. The authors framed the data as first clear evidence that NNMT inhibitors constitute a viable pharmacological approach to enhance regenerative capacity in aged skeletal muscle.2

Grip Strength and Exercise Endurance in Aged Mice — Dimet-Wiley et al., Scientific Reports (2024)

This study compared 5-Amino-1MQ treatment, voluntary wheel-running exercise (PoWeR), and combined treatment in aged C57BL/6J mice. 5-Amino-1MQ alone improved grip strength to a greater degree than rigorous exercise training alone, and combined treatment produced sustained increases in daily running distance that did not taper off in the way exercise-alone groups did, suggesting reduced post-exercise muscle recovery requirement. The authors interpreted the data as supporting NNMT inhibition as a candidate exercise-mimetic.3

Extended Administration Pharmacokinetics in DIO Mice — Neelakantan et al., Biochemical Pharmacology (2024)

This study reported a 28-day once-daily administration protocol of 5-Amino-1MQ in diet-induced obese mice, characterizing plasma pharmacokinetics, tissue distribution, and effects on body composition, fatty liver pathology, and circulating biomarkers. Extended treatment continued to limit body weight gain and white adipose tissue mass, lowered total plasma cholesterol, and showed measurable accumulation in adipose tissue consistent with the compound’s lipophilic profile. The work supports the chronic-administration tolerability of 5-Amino-1MQ in mouse models of obesity-linked type 2 diabetes.4

About the Compound

5-Amino-1MQ is a quinolinium salt — a small, water-soluble, membrane-permeable molecule (not a peptide). Its mechanism is competitive inhibition within the NNMT catalytic pocket, blocking the methyl transfer from SAM to nicotinamide. Two downstream consequences are mechanistically central: nicotinamide is preserved for re-entry into the NAD+ salvage pathway (raising intracellular NAD+ availability), and SAM is preserved for other methylation reactions. The combination has been associated with elevated sirtuin activity, altered adipocyte differentiation markers, and changes in muscle stem cell quiescence and proliferation in the cited preclinical literature.

  • Compound class: small-molecule NNMT inhibitor; quinolinium salt (non-peptide)
  • Synonyms: 5A1MQ, 5-amino-1-methylquinolinium iodide
  • CAS Number: 13441-78-4
  • Molecular Formula: C10H11IN2
  • Molecular Weight: 286.11 g/mol
  • Solubility: water-soluble; dissolves readily in PBS and culture media
  • Primary research origin: Watowich group, University of Texas at Austin
  • Mechanism: competitive NNMT inhibition; preserves NAD+ salvage and SAM availability
  • Regulatory status: not approved by the FDA or any other regulatory authority; research compound only

Product Specifications

  • Format: lyophilized powder in vial (reconstitute with bacteriostatic water)
  • Strengths available: 10 mg per vial; 50 mg per vial
  • Purity: ≥99% (HPLC verified)
  • Container: sealed glass vial (lyophilized powder)
  • Certificate of Analysis: lot-specific COA available

See the FDA Disclosure, Storage Instructions, and RUO tabs for handling, storage, and regulatory information.

References

  1. Neelakantan H, Vance V, Wetzel MD, et al. Selective and membrane-permeable small molecule inhibitors of nicotinamide N-methyltransferase reverse high fat diet-induced obesity in mice. Biochem Pharmacol. 2018;154:161-171. doi:10.1016/j.bcp.2018.05.003
  2. Neelakantan H, Brightwell CR, Graber TG, et al. Small molecule nicotinamide N-methyltransferase inhibitor activates senescent muscle stem cells and improves regenerative capacity of aged skeletal muscle. Biochem Pharmacol. 2019;163:481-492. doi:10.1016/j.bcp.2019.02.008
  3. Dimet-Wiley A, Latham CM, Brightwell CR, et al. NNMT inhibition combined with exercise enhances skeletal muscle endurance and grip strength in aged mice. Sci Rep. 2024;14:14305. doi:10.1038/s41598-024-65310-y
  4. Neelakantan H, Hommel JD, Watowich SJ, et al. Nicotinamide N-methyltransferase inhibition mitigates obesity-related metabolic dysfunctions in diet-induced obese mice. Biochem Pharmacol. 2024;229:116476. doi:10.1016/j.bcp.2024.116476
For research use only. Not for human consumption.