2-Azido-2-deoxy-1,3,4,6-tetra-O-acetyl-α-D-glucopyranose

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2-Azido-2-deoxy-1,3,4,6-tetra-O-acetyl-α-D-glucopyranose
(4-hydroxybutyl)azanediyl)bis(hexane-6,1-diyl)bis(2-hexyldecanoate)

2-Azido-2-deoxy-1,3,4,6-tetra-O-acetyl-α-D-glucopyranose

Original price was: $1,795.00.Current price is: $895.00.

Catalog Number: B2027286 (1 g)
2-Azido-2-deoxy-1,3,4,6-tetra-O-acetyl-α-D-glucopyranose is a peracetylated azidosugar derivative widely utilized as a key building block in carbohydrate chemistry and chemical biology. The presence of the azido functional group enables efficient modification via copper-catalyzed or strain-promoted azide-alkyne cycloaddition (click chemistry) reactions. Provided as a high-purity biochemical reagent, it is suitable for metabolic labeling of glycans, chemical synthesis, and molecular probe development. Custom bulk amounts of this product are available upon request.

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Product Description

5/5 - (2 votes)

2-Azido-2-deoxy-1,3,4,6-tetra-O-acetyl-α-D-glucopyranose
Catalog number: B2027286
Lot number: Batch Dependent
Expiration Date: Batch dependent
Amount: 1 g
Molecular Weight or Concentration: 373.32
Supplied as: Powder
Storage: NA
Keywords: 1,3,4,6-Tetra-O-acetyl-2-azido-2-deoxy-α-D-glucopyranose, 2-Azido-2-deoxy-α-D-glucopyranose tetraacetate

References:
1. Vocadlo DJ, Hang HC, Kim EJ, Hanover JA, Bertozzi CR. A chemical approach to detect O-GlcNAc glycosylation in nuclear and cytoplasmic proteins. Proceedings of the National Academy of Sciences. 2003;100(16):9116-9121.
2. Saxon E, Bertozzi CR. Cell surface engineering by a modified Staudinger reaction. Science. 2000;287(5460):2007-2010.
3. Hang HC, Yu C, Kato DL, Bertozzi CR. A metabolic labeling approach toward proteomic analysis of mucin-type O-linked glycosylation. Proceedings of the National Academy of Sciences. 2003;100(25):14846-14851.
4. Laughlin ST, Bertozzi CR. Imaging the glycome in living organisms. ACS Chemical Biology. 2007;2(10):661-665.
5. Chang PV, Prescher JA, Sletten EM, et al. Copper-free click chemistry in living animals. Proceedings of the National Academy of Sciences. 2010;107(5):1821-1826.
6. Lemieux GA, Yarema KJ, Jacobs CL, Bertozzi CR. Biocompatible antigen delivery: coupling bioorthogonal chemistry to MHC class I antigen presentation. Journal of the American Chemical Society. 2003;125(16):4708-4709.
7. Agard NJ, Prescher JA, Bertozzi CR. A strain-promoted [3 + 2] azide-alkyne cycloaddition for covalent modification of biomolecules in living systems. Journal of the American Chemical Society. 2004;126(46):15046-15047.
8. Boyce M, Carrico IS, Ganguli AS, et al. Metabolic cross-talk allows labeling of O-GlcNAc-modified proteins via the N-acetylglucosamine salvage pathway. Proceedings of the National Academy of Sciences. 2011;108(8):3141-3146.
9. Zaro BW, Yang YY, Hang HC, Pratt MR. Chemical reporters for fluorescent detection and identification of O-GlcNAc-modified proteins distinct from glycosyltransferase labeling. ChemBioChem. 2011;12(11):1701-1707.
10. Luchansky SJ, Hang HC, Saxon E, et al. Constructing cell surfaces with unnatural sialic acids. Methods in Enzymology. 2003;362:249-272.
2-Azido-2-deoxy-1,3,4,6-tetra-O-acetyl-α-D-glucopyranose

Products Related to 2-Azido-2-deoxy-1,3,4,6-tetra-O-acetyl-α-D-glucopyranose can be found at Carbohydrates

Additional Information

Weight 0.15 oz
Dimensions 2 × 0.5 × 0.5 in
5/5 - (2 votes)

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