5-Amino-1MQ
Small-molecule NNMT inhibitor
Identifier graph
Cross-references to canonical chemistry knowledge graphs. Each binding is the same identity used in PubMed-indexed literature.
- ChEMBL
- CHEMBL1191168
- Molecular formula
C10H12N2- Molecular weight
- 174.21 g/mol
What is 5-Amino-1MQ?
5-Amino-1-methylquinolinium (5-Amino-1MQ, sometimes written 5A1MQ) is a small-molecule selective inhibitor of nicotinamide N-methyltransferase (NNMT) — an enzyme that consumes S-adenosyl-methionine (SAM) and nicotinamide (a NAD⁺ precursor) to produce 1-methyl-nicotinamide. NNMT activity is elevated in adipose tissue, hepatocytes and tumour cells, and its inhibition has been investigated as a strategy for improving cellular NAD⁺ status and methyl-donor availability.
Molecular formula C₁₀H₁₂N₂, molecular weight 174.21 g/mol. ChEMBL ID CHEMBL1191168. The compound is unusual in this catalogue as a small molecule rather than a peptide.
Mechanism of action
NNMT (nicotinamide N-methyltransferase) catalyses the methylation of nicotinamide using SAM as the methyl donor, producing 1-methyl-nicotinamide. Elevated NNMT activity depletes both the NAD⁺-precursor pool (nicotinamide) and the cellular methyl-donor pool (SAM). 5-Amino-1MQ is a selective competitive inhibitor of NNMT, and inhibition is reported to restore nicotinamide and SAM availability in cells where NNMT is upregulated.
Research context
Investigated in preclinical models of adipose-tissue metabolism, obesity, hepatic steatosis, cancer biology, and NAD⁺ depletion in ageing tissue. The compound represents a distinct mechanistic approach to NAD⁺ support compared to direct precursor supplementation (e.g. nicotinamide riboside, NMN, or direct NAD⁺ administration).
Analytical specifications
Every batch of 5-Amino-1MQ supplied by NMChem is characterised by reversed-phase HPLC for purity determination and by mass spectrometry for identity confirmation. Certificate of Analysis (COA) documents are issued per batch and made available on request.
Identity is confirmed by ESI-MS and proton NMR (¹H NMR) where structurally informative. Purity is determined by HPLC with UV detection; NMChem specification is ≥99% by area-under-curve. Material ships as crystalline solid or hygroscopic powder depending on the compound; consult the per-batch Certificate of Analysis for the appropriate storage and reconstitution protocol.
UK regulatory status
Supplied as a research-grade reference standard for laboratory use only. Not a licensed medicinal product in the United Kingdom and not approved by the MHRA for human or veterinary administration. Sale is restricted to researchers, institutions and laboratory professionals; the compound must be retained within research premises. End-user compliance with the Human Medicines Regulations 2012, the Misuse of Drugs Act 1971 (where applicable) and local institutional biosafety policy is the responsibility of the buyer.
Research literature
Selected peer-reviewed publications from PubMed referencing this compound.
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NAD
Yang M et al. · Journal for immunotherapy of cancer · 2024
PubMed PMID 39067875 -
Small molecule inhibitor of nicotinamide N-methyltransferase shows anti-proliferative activity in HeLa cells.
Akar S et al. · Journal of obstetrics and gynaecology : the journal of the Institute of Obstetrics and Gynaecology · 2021
PubMed PMID 33645410 -
Reduced calorie diet combined with NNMT inhibition establishes a distinct microbiome in DIO mice.
Dimet-Wiley A et al. · Scientific reports · 2022
PubMed PMID 35013352
Related compounds
Other research compounds in adjacent mechanism classes or commonly used alongside 5-Amino-1MQ.
Frequently asked questions about 5-Amino-1MQ
What is NNMT and why is it a research target?
How is 5-Amino-1MQ different from NAD⁺ precursors like NMN?
Get research-grade 5-Amino-1MQ from NMChem
UK supplier · HPLC and MS verified · Per-batch Certificate of Analysis · Tracked Royal Mail dispatch.