Date published: 2026-4-23

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3-Acetamido-3-deoxy-D-glucose (CAS 14086-88-5)

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CAS Number:
14086-88-5
Molecular Weight:
221.21
Molecular Formula:
C8H15NO6
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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3-Acetamido-3-deoxy-D-glucose, also known as N-acetylglucosamine (GlcNAc), is a fundamental building block of complex carbohydrates and glycoconjugates found abundantly in nature. Its mechanism of action is complexly linked to its role in various biological processes, particularly in post-translational modification of proteins and cell surface glycosylation. GlcNAc serves as a substrate for glycosyltransferase enzymes responsible for adding N-acetylglucosamine residues to proteins during glycosylation, a crucial process that modulates protein stability, folding, and function. In research, GlcNAc is widely utilized in studying the dynamics of protein glycosylation and its impact on cellular processes. Researchers employ GlcNAc analogs labeled with isotopic tracers for metabolic labeling experiments, allowing the tracking of glycosylation events in live cells and elucidating the glycosylation pathways involved in various cellular processes, such as cell signaling, immune response, and cell-cell interactions. Additionally, GlcNAc serves as a precursor for the synthesis of diverse glycan structures, including chitin, a polysaccharide found in fungal cell walls and the exoskeletons of arthropods, enabling investigations into chitin biosynthesis and fungal cell wall remodeling. Furthermore, GlcNAc derivatives are utilized in the development of glycan-based vaccines and carbohydrate-based materials, highlighting its importance in glycobiology research and its potential applications in biotechnology and biomaterials science.


3-Acetamido-3-deoxy-D-glucose (CAS 14086-88-5) References

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  2. A Novel Bovine beta-1,4-Galactosyltransferase Reaction To Yield beta-D-Galactopyranosyl-(1-3)-Linked Disaccharides from L-Sugars The authors are grateful for the funding of the Regional Leading Research Project of Shizuoka Prefecture from the Ministry of Science and Technology of the Japanese Government, and for funding from the Deutsche Forschungsgemeinschaft.  |  Nishida, Y., et al. 2000. Angew Chem Int Ed Engl. 39: 2000-2003. PMID: 10941010
  3. Synthesis and antibacterial activity of aminodeoxyglucose derivatives against Listeria innocua and Salmonella typhimurium.  |  Muhizi, T., et al. 2009. J Agric Food Chem. 57: 8770-5. PMID: 19725544
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  7. Galactosyl transfer onto p-nitrophenyl beta-D-glucoside using beta-D-galactosidase from Bacillus circulans.  |  Murata, T., et al. 1997. Biosci Biotechnol Biochem. 61: 1118-20. PMID: 9255974
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Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

3-Acetamido-3-deoxy-D-glucose, 25 mg

sc-220852
25 mg
$380.00