UDP-6-azido-6-doexy-GalNAc.2Na
UDP-6-N3-GalNAc.2Na
Formula of UDP-6-azido-6: C17H24N6Na2O16P2
CAS: 1202854-87-2
MW: 676.65
Purity: min 98% by HPLC
UDP-6-deoxy-GalNAc. 2Na is a synthetic nucleotide sugar analogue. It consists of a modified UDP-GalNAc (uridine diphosphate N-acetylgalactosamine) molecule where the 6th position of the sugar has been substituted with an azido group (-N₃) and a sodium counterion for stability.
### Key Features:
– **UDP-GalNAc Analogue**: UDP-GalNAc is a donor substrate involved in glycosylation, particularly in the biosynthesis of O-linked glycoproteins.
– **Azido Modification**: The azido group at the 6th position is chemically reactive, allowing for bioorthogonal chemistry, particularly in click chemistry reactions. This makes it useful for tracking and labeling glycoconjugates in biological studies.
– **Applications**: Commonly used in glycoengineering, metabolic labeling, and studying glycosylation pathways. The azido group enables subsequent functionalization, making it an ideal choice for research in glycomics and drug development.
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| Size | 10 MG, 100 MG, 50 MG, Other |
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Related Products
| Name | UDP-GlcNAc.2Na |
| Catalog No. | GN02009 |
| CAS Number | 91183-98-1 |
| Formula | C17H25N3O17P2Na2 |
| M.W. | 651.32 |
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| Name | UDP-a-L-Rha Sodium Salt |
| Catalog No. | GN02020 |
| CAS Number | 1526988-33-9 |
| Formula | C15H22N2Na2O16P2 |
| M.W. | 594.27 |
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| Name | dTDP-a-L-Rha.2Na |
| Catalog No. | GN02031 |
| CAS Number | 2147-59-3, 16268-29-4 |
| Formula | C16H24N2Na2O16P2 |
| M.W. | 608.27 |
| Purity | min 90% by HPLC |
10 in stock
| Chemical Name | Uridine-5’-diphospho-6-azido-6-deoxy-D-glucose, Disodium Salt |
|---|---|
| Synonyms | UDP-6-N3-Glc·2Na, UDP-α-6N3-Glucose Disodium Salt, UDP-6-Azido-6-deoxy-D-Glucose Disodium Salt |
| Molecular Formula | C15H21N5O16P2 · 2Na |
| Molecular Weight | 635.28 g/mol (disodium salt) |
| CAS No. | 537039-67-1 |
| Appearance | White to off-white lyophilized powder |
| Purity | ≥95% (HPLC) |
| Solubility | Soluble in water |
| Storage | −20°C, protect from moisture and light |
| Application | Azido-modified nucleotide sugar donor substrate for glucosyltransferases; the C6-azido handle enables bioorthogonal detection via copper-catalyzed azide–alkyne cycloaddition (CuAAC) and strain-promoted azide–alkyne cycloaddition (SPAAC); used for selective labeling of 5-hydroxymethylcytosine (5-hmC) in genomic DNA, glycan imaging, and glycoproteomic profiling |
10 in stock
