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5 Amino 1MQ-10mg

5 Amino 1MQ – 10mg

5-Amino-1MQ is a synthetic small-molecule compound supplied for laboratory research.

$85.00

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10 in stock

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Overview

5-Amino-1MQ is a synthetic small-molecule compound supplied for laboratory research. It is not a peptide. This compound is commonly studied in connection with the enzyme nicotinamide N-methyltransferase (NNMT). NNMT is an enzyme present in many tissues and cell types. It converts nicotinamide into methylated products using methyl groups, influencing how nicotinamide is processed inside the cell. Because NNMT is involved in basic metabolic processes, 5-Amino-1MQ is often used as a research tool to reduce NNMT activity in controlled experimental systems. It is intended strictly for laboratory research and is not approved for use in humans or animals.

Biochemical Characteristics

5-Amino-1MQ is a low molecular weight compound designed for experimental use. Its structure allows it to interact with the active site of NNMT. In research settings, this interaction limits the enzyme’s normal function. NNMT normally methylates nicotinamide, consuming methyl donors and producing methylated nicotinamide derivatives. These reactions are part of normal cellular metabolism. When NNMT activity is reduced in research models, changes can be observed in related biochemical processes. 5-Amino-1MQ allows researchers to study these effects at the enzyme and cellular levels under laboratory conditions.

Research Applications

5-Amino-1MQ is provided for laboratory research and is not intended as a drug, treatment, or supplement. It is used exclusively in experimental work. In research labs, it is mainly used to study NNMT activity, including inhibition experiments and enzyme activity assays. It is also applied in metabolic pathway studies and routine cell culture experiments. Some preclinical models include this compound in broader metabolic research. The compound is typically added to experimental systems to observe how reduced NNMT activity alters cellular behavior over time. Outcomes depend on the experimental model, dosage, and study design.

Mechanistic and Pathway Context

NNMT is involved in cellular nicotinamide processing and methylation reactions. Reduction of NNMT activity in research models may lead to observable changes in nicotinamide metabolism, methyl group utilization, and downstream cell signaling. 5-Amino-1MQ is generally used to examine these processes under controlled laboratory conditions to improve understanding of basic cellular mechanisms. It is not intended to study therapeutic outcomes.

Preclinical Research Summary

Published studies report observations of 5-Amino-1MQ in early laboratory and animal experiments. These preclinical models examine metabolism, gene expression, and tissue signaling influenced by NNMT activity. Experiments often involve rodent or cell-based systems and measure metabolic flux, markers in adipose and muscle tissues, and transcription patterns affected by NNMT activity.

Disclaimer

5-Amino-1MQ is intended only for laboratory research. It is not approved for human or animal use, therapeutic applications, or supplementation. All research must comply with institutional and regulatory guidelines.

Referenced Citations

  1. Kraus D, et al. Selective and membrane-permeable small molecule inhibitors of nicotinamide N-methyltransferase reverse high-fat diet-induced obesity in mice.
  2. JoAnne J Babula Nicotinamide N-methyltransferase inhibition mitigates obesity-related metabolic dysfunction. PubMed 39161060; 2024.
  3. Serra Akara et al. Small molecule inhibitor of nicotinamide N-methyltransferase shows anti-proliferative activity in HeLa cells. PubMed 33645410; 2021.

Research Use Only

This product is intended for laboratory research use only. It is not intended for human or animal consumption, or for use in diagnostic or therapeutic procedures.

Chemical Properties

Property Value
Molecular Formula C10H11N2⁺
Molecular Mass 159.21 g/mol
Monoisotopic Mass 159.092223359 Da
Polar Area 29.9 Ų
Complexity 158
XLogP 1.1
Heavy Atom Count 12
Hydrogen Bond Donors 1
Hydrogen Bond Acceptors 1
Rotatable Bonds 0
PubChem CID 950107
InChI InChI=1S/C10H10N2/c1-12-7-3-4-8-9(11)5-2-6-10(8)12/h2-7,11H,1H3/p+1
InChIKey ZMJBCEIHNOWCMC-UHFFFAOYSA-O
IUPAC Name 1-methylquinolin-1-ium-5-amine
SMILES C[N+]1=CC=CC2=C(C=CC=C21)N

Certificate of Analysis

Quality

Every batch of 5 Amino 1MQ – 10mg is tested for purity and identity using industry-standard methods.

HPLC Analysis

High-Performance Liquid Chromatography confirms purity ≥98%. Each batch is analyzed to ensure consistent quality.

Mass Spectrometry (MS)

Identity verification via mass spectrometry confirms correct molecular weight of 4113.58 g/mol.

Third-Party Testing

All products undergo independent third-party laboratory testing for quality assurance.

Request COA

Certificate of Analysis documents are available for all products. Contact us with your order number to request batch-specific documentation.

COA Lab Tests

Each product batch is tested by independent laboratories to verify purity, identity, and quality. The Certificate of Analysis (COA) provides transparent lab results, ensuring the product meets strict research-grade standards.

Storage & Handling

​B‌efore‍ Recon​stitution (Powder Form)

  • Prot​ect it f​ro​m‍ sunlight at all times
  • Avo⁠id keeping it in the extreme t‍emperature‍.
  • Keep in origin⁠al sealed conta‌iner⁠

A⁠fter Reconstitution (Liquid Form⁠)‌

  • Refrigerate it immediate​l⁠y a​t 2-8°C or​ 36-46°F
  • Use w‍ith‌in 30‌ d​ays​ of reconst⁠ituti‌on
  • Disc‍ar‍d‍ any unused s‌o‍lut⁠ion after 30 d​ay⁠s
  • K⁠eep refri‍gerated between uses⁠
  • Do not shake vigorously

A⁠fter Reconstitution (Liquid Form⁠)‌

  • Refrigerate it immediate​l⁠y a​t 2-8°C or​ 36-46°F
  • Use w‍ith‌in 30‌ d​ays​ of reconst⁠ituti‌on
  • Disc‍ar‍d‍ any unused s‌o‍lut⁠ion after 30 d​ay⁠s
  • K⁠eep refri‍gerated between uses⁠
  • Do not shake vigorously

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Purity

≥98% (HPLC)

Storage

Store at -20°C.
Protect from light and moisture.

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