![{[Name]}](/probes/images/structure-default.jpg?v=2025011501)
![{[Name]}](https://resource.bocsci.com/structure/361154-30-5.gif?v=2025011501)
![{[Name]}](https://resource.bocsci.com/structure/1398044-52-4.gif?v=2025011501)
![{[Name]}](https://resource.bocsci.com/structure/1817735-35-5.gif?v=2025011501)
![{[Name]}](https://resource.bocsci.com/structure/1835759-68-6.gif?v=2025011501)
Inquiry Basket
1,3,4,6-Tetra-O-acetyl-N-azidoacetylglucosamine | CAS 98924-81-3
| Catalog Number | R14-0015 |
| Category | Azides |
| Molecular Formula | C16H22N4O10 |
| Molecular Weight | 430.37 |
* Please be kindly noted products are not for therapeutic use. We do not sell to patients.
Product Introduction
1,3,4,6-Tetra-O-acetyl-N-azidoacetylglucosamine, a vital compound employed in biomedical research, serves as an indispensable intermediate. It finds extensive utility in synthesizing glycosylated biomolecules, including glycopeptides and glycoproteins. Possessing an azido functional group, this compound facilitates efficient bioconjugation and labeling investigations. Its versatility stretches to the exploration of cell surface glycans, glycosylation pathways, and glycoengineering. Additionally, it aids in examining cell-surface interactions and potential therapeutic interventions associated with anomalous glycosylation, thereby contributing significantly to the realm of disease management.
Chemical Information
Product Specification
Application
| Synonyms | N-azidoacetylglucosamine-tetraacylated (Ac4GlcNAz);GlcNAz tetraacetate; 1,3,4,6-Tetra-O-acetyl-2-(2-azidoacetamido)-2-deoxy-b-D-glucopyranose; N-Azidoacetylglucosamine tetraacylated; Ac4GlcNAz |
| Purity | 90% |
| IUPAC Name | [(2R,3S,4R,5R)-3,4,6-triacetyloxy-5-[(2-azidoacetyl)amino]oxan-2-yl]methyl acetate |
| Canonical SMILES | CC(=O)OCC1C(C(C(C(O1)OC(=O)C)NC(=O)CN=[N+]=[N-])OC(=O)C)OC(=O)C |
| InChI | InChI=1S/C16H22N4O10/c1-7(21)26-6-11-14(27-8(2)22)15(28-9(3)23)13(16(30-11)29-10(4)24)19-12(25)5-18-20-17/h11,13-16H,5-6H2,1-4H3,(H,19,25)/t11-,13-,14-,15-,16?/m1/s1 |
| InChIKey | HGMISDAXLUIXKM-ALTVCHKUSA-N |
| Storage | -20 °C |
1,3,4,6-Tetra-O-acetyl-N-azidoacetylglucosamine is a chemically modified sugar molecule derived from N-acetylglucosamine, which is an essential building block of various glycoconjugates in biological systems. This compound is characterized by having its hydroxyl groups acetylated and an azide group introduced to the N-acetyl position. Acetylation increases the lipid solubility of the molecule, making it more permeable to cellular membranes, while the azide group serves as a reactive handle for subsequent chemical modifications. This unique structure facilitates its incorporation into glycan structures in cells, thereby enabling various innovative biological and chemical applications.
One of the key applications of 1,3,4,6-Tetra-O-acetyl-N-azidoacetylglucosamine is in the field of metabolic glycoengineering. By introducing this modified sugar into cellular systems, researchers can metabolically incorporate it into glycoproteins on the cell surface. This incorporation allows for subsequent bio-orthogonal labeling because the azide group can participate in the Staudinger ligation or click chemistry reactions. Such labeling techniques enable the visualization and study of glycans in vivo, thus providing insights into glycosylation processes that are crucial for understanding various biological functions and disease mechanisms.
Another significant application is in the development of glycan-based vaccines. The azide-modified sugar can be incorporated into pathogen glycan structures, allowing researchers to create vaccines that present these glycans in a more recognizable form to the human immune system. This approach aids in generating a robust immune response, thereby providing a strategy for vaccine development against pathogens that depend heavily on glycan structures for infectivity and immune evasion, such as certain bacteria and viruses.
1,3,4,6-Tetra-O-acetyl-N-azidoacetylglucosamine also plays a crucial role in the synthesis of glycan microarrays. These microarrays are used to probe the specific interactions between glycans and proteins, which are vital for biological recognition and signaling processes. By using this compound, glycans can be chemically modified to allow their immobilization on solid surfaces, thereby creating a diverse array of glycans that can be used to screen for glycan-binding proteins, antibodies, or other biomolecules. This technology is essential for deciphering glycan functions in health and disease.
Lastly, in the realm of materials science, this modified sugar finds application in the development of biofunctional materials. The presence of the reactive azide group allows for its attachment to various polymers and nanoparticles, which can be further functionalized for targeted delivery and release systems in drug delivery applications. These materials can mimic natural glycan structures, enhancing their compatibility and functionality in biological environments, thus paving the way for new innovations in biomedical engineering and therapeutics.
Recommended Services
Recommended Articles
- Hoechst Dyes: Definition, Structure, Mechanism and Applications
- Mastering the Spectrum: A Comprehensive Guide to Cy3 and Cy5 Dyes
- Fluorescent Probes: Definition, Structure, Types and Application
- Fluorescent Dyes: Definition, Mechanism, Types and Application
- Coumarin Dyes: Definition, Structure, Benefits, Synthesis and Uses
- BODIPY Dyes: Definition, Structure, Synthesis and Uses
- Cyanine Dyes: Definition, Structure, Types and Uses
- Fluorescein Dyes: Definition, Structure, Synthesis and Uses
- Rhodamine Dyes: Definition, Structure, Uses, Excitation and Emission
- Unlocking the Power of Fluorescence Imaging: A Comprehensive Guide
- Cell Imaging: Definitions, Systems, Protocols, Dyes, and Applications
- Lipid Staining: Definition, Principles, Methods, Dyes, and Uses
- Flow Cytometry: Definition, Principles, Protocols, Dyes, and Uses
- Nucleic Acid Staining: Definition, Principles, Dyes, Procedures, and Uses
- DNA Staining: Definition, Procedures, Benefits, Dyes and Uses
- Cell Staining: Definition, Principles, Protocols, Dyes, and Uses
- Ion Imaging: Definition, Principles, Benefits, Dyes, and Uses
- Fluorescent Labeling: Definition, Principles, Types and Applications
Recommended Products
Online Inquiry
