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GlycoDepot

dTDP-D-GlcNAc

dTDP-D-GlcNAc (dTDP-N-acetyl-D-glucosamine) is a nucleotide sugar that consists of thymidine diphosphate (dTDP) linked to N-acetylglucosamine (GlcNAc). It serve…

dTDP-D-GlcNAc
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  • ISO 9001:2015 facilities · CoA + batch tracking with every shipment
  • Worldwide shipping · dry-ice option for thermolabile reagents
  • Research Use Only — not for human or veterinary clinical use

About this product

dTDP-D-GlcNAc (dTDP-N-acetyl-D-glucosamine) is a nucleotide sugar that consists of thymidine diphosphate (dTDP) linked to N-acetylglucosamine (GlcNAc). It serves as a sugar donor in glycosylation reactions and plays a vital role in the biosynthesis of complex glycans, including glycoproteins, glycolipids, and bacterial cell wall components. Structure & Properties: Molecular Weight (MW): 605.1 Chemical Formula: C18H29N3O16P2 Synonyms: dTDP-N-acetylglucosamine, thymidine diphospho-N-acetyl-D-glucosamine Functional Groups: Contains an N-acetylglucosamine sugar linked to thymidine diphosphate (dTDP), characterized by an acetyl group (-COCH3) attached to the amino group on the glucosamine ring. Biological Role: Biosynthesis Pathway: dTDP-D-GlcNAc is synthesized via enzymatic pathways that convert GlcNAc into the nucleotide sugar form. This process involves attaching N-acetylglucosamine to the thymidine diphosphate molecule. Function: dTDP-D-GlcNAc acts as a donor of GlcNAc in glycosylation reactions. It is crucial in constructing various glycoconjugates, such as bacterial surface glycans and glycosylated proteins. Applications: Bacterial Glycobiology: dTDP-D-GlcNAc is essential in constructing bacterial cell wall glycans, including lipopolysaccharides (LPS) and peptidoglycan, which are critical for bacterial survival, immune evasion, and virulence. Glycan Engineering: In synthetic biology and glycosylation research, dTDP-D-GlcNAc is used to create custom glycans in vitro or in engineered cells to study the roles of glycosylation in biological systems. Significance in Research: Pathogen Glycan Diversity: dTDP-D-GlcNAc is involved in generating diverse bacterial glycan structures, contributing to the virulence and immune evasion of pathogens. Therapeutic Targeting: Disrupting dTDP-D-GlcNAc biosynthesis or the pathways it participates in can impair the production of essential glycans, offering potential avenues for developing antibacterial agents. Key Roles: Peptidoglycan Biosynthesis: dTDP-D-GlcNAc is involved in the biosynthesis of peptidoglycan, a critical component of bacterial cell walls. This makes it an essential factor in bacterial growth and division. Lipopolysaccharides (LPS): dTDP-D-GlcNAc is also a building block for LPS, which play roles in bacterial virulence and interaction with host immune systems. Storage and Stability: Storage: dTDP-D-GlcNAc should be stored at -20°C in a moisture-free and light-protected environment. Stability: Under these conditions, it remains stable, but exposure to moisture, light, or heat may lead to degradation. Research Applications: Glycan Synthesis: dTDP-D-GlcNAc is used to synthesize N-acetylglucosamine-containing glycans, which are critical for studying glycosylation processes in various organisms. Drug Development: Investigating the role of dTDP-D-GlcNAc in bacterial glycan biosynthesis can guide the development of new antibacterial therapies that target glycosylation pathways. Potential Impact: Antibacterial Strategies: By targeting enzymes that produce or utilize dTDP-D-GlcNAc, researchers can disrupt bacterial glycan biosynthesis, potentially leading to the weakening of bacterial defenses and virulence. Synthetic Glycans: dTDP-D-GlcNAc can be used in the design of synthetic glycans for therapeutic or diagnostic applications, particularly in bacterial glycosylation studies. Key Research Areas: Bacterial Virulence and Immune Evasion: dTDP-D-GlcNAc-containing glycans contribute to bacterial mechanisms for evading the host immune system, making them key targets for research on immune modulation and antibacterial therapies. Enzyme Inhibition: Research into the enzymes that synthesize dTDP-D-GlcNAc offers opportunities to develop inhibitors that block bacterial glycan formation. Conclusion: dTDP-D-GlcNAc (dTDP-N-acetyl-D-glucosamine) is a crucial nucleotide sugar involved in the biosynthesis of bacterial glycans, including peptidoglycan and LPS. Its role in bacterial virulence, glycosylation, and immune evasion makes it a valuable target for antibacterial research and therapeutic development. Additionally, dTDP-D-GlcNAc is an important tool in glycan engineering for studying glycosylation pathways and designing novel glycoconjugates for research and potential clinical applications.

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