Format
Sealed research vial
Trust signal
COA-backed inventory
99%+ Purity
Lab-grade supply. Limited AU stock.
A$269
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Fast AU dispatch, tracked delivery, and documentation-ready inventory.
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High purity, consistent supply, and fast AU-wide dispatch.
Certificate of Analysis
COA library
Browse the current COA library and available product documentation.
5-Amino is 5-amino-1-methylquinolinium (5-amino-1MQ), a small-molecule nicotinamide N-methyltransferase (NNMT) inhibitor used in one-carbon metabolism and epigenetic methylation research.
Unlike the peptides in this catalogue, 5-amino-1MQ is a quinolinium small molecule — its research applications centre on enzyme inhibition biochemistry, one-carbon cycle flux analysis, and epigenomic profiling rather than receptor pharmacology. Isotope tracing experiments (¹³C-methionine or ²H-SAM) are frequently used alongside NNMT inhibitors to map methyl group flux quantitatively.
Browse Inventory
In research literature, 5-Amino is generally treated as 5-amino-1-methylquinolinium (5-amino-1MQ), a small-molecule nicotinamide N-methyltransferase (NNMT) inhibitor used in one-carbon metabolism and epigenetic methylation research. 5-amino-1MQ competitively inhibits NNMT — an enzyme that converts nicotinamide (vitamin B3) to 1-methylnicotinamide using S-adenosylmethionine (SAM) as the methyl donor. By blocking this reaction, 5-amino-1MQ increases the cellular SAM:SAH (S-adenosylhomocysteine) ratio, which enhances the methyl-donor capacity of the one-carbon pool available to histone and DNA methyltransferases. This shifts the epigenetic landscape toward increased H3K4me3 and H3K27me3 marks in cell models, linking NNMT inhibition to chromatin remodelling research. NNMT is overexpressed in multiple adipose tissue depots and certain cancer types, making it a target of interest in both metabolic and oncology research contexts.
Unlike the peptides in this catalogue, 5-amino-1MQ is a quinolinium small molecule — its research applications centre on enzyme inhibition biochemistry, one-carbon cycle flux analysis, and epigenomic profiling rather than receptor pharmacology. Isotope tracing experiments (¹³C-methionine or ²H-SAM) are frequently used alongside NNMT inhibitors to map methyl group flux quantitatively. For laboratory teams, the practical emphasis is usually on sequence identity, receptor or pathway relevance where documented, and whether 5-Amino behaves consistently across stability, purity, and analytical verification workflows. Variant labels on this page support clearer internal referencing when multiple labelled variants are under review.
Potential research applications for 5-Amino should be framed strictly in analytical and laboratory terms. Typical reasons a team might review this product page include:
Handling decisions should always follow the vial label, internal SOPs, and any product-specific documentation. A conservative laboratory baseline for 5-Amino is:
If a product-specific file is not attached to this listing, the wider COA library remains the correct reference point for current published documentation. The COA section is useful for confirming how the product is labelled in the catalogue, whether purity information has been published, and whether the laboratory record for the material is complete before bench use.
When teams compare 5-Amino with Glow, BPC-157 + TB-500, and Klow, COA access also helps keep comparator decisions grounded in documented material identity rather than assumption. That is especially important for research pages that combine pricing, variant selection, and analytical records on a single URL.
Certificate of Analysis
COA library
Browse the current COA library and available product documentation.
It brings together 1 labelled variant: 50mg, current pricing context, stock visibility, COA access, and internal links to related catalogue pages so a laboratory buyer can review the material from a single reference URL.
5-Amino is generally discussed as 5-amino-1-methylquinolinium (5-amino-1MQ), a small-molecule nicotinamide N-methyltransferase (NNMT) inhibitor used in one-carbon metabolism and epigenetic methylation research. The most relevant background is sequence behaviour, pathway or receptor context where documented, and analytical consistency under controlled laboratory conditions.
Use the label, COA, and internal SOPs as the primary guide. In general, store the material under controlled laboratory conditions, minimise avoidable environmental exposure, and keep variant tracking records current.
This page links the broader COA library when a product-specific document is not attached. Laboratories should use the published documentation set that is currently available for the listing.
No. The page should be interpreted strictly in a research and laboratory context. It does not provide dosage guidance, treatment claims, or human or animal use instructions.
