| Chemical Formula | C18H27N3O15P2 |
|
|---|---|---|
| Molecular Weight | 587.37 Daltons | |
| Monoisotopic Mass | 589.1073902979999 Daltons |
| Chemical Formula | C16H26N3O14P2 |
|
|---|---|---|
| Molecular Weight | 546.34 Daltons | |
| Monoisotopic Mass | 547.0968256117 Daltons |
Name: GDP-6-AIkyne-L-Fuc
CAS: N/A
MW: 643.30
Chemical Formula: C16H22N8Na2O15P2
Synonym: Guanosine 5′-diphospho-b-6-alkyne-L-fucose disodium salt
| Chemical Name | Guanosine-5’-diphospho-6-azido-6-deoxy-L-fucose, Disodium Salt |
|---|---|
| Synonyms | GDP-6-N3-L-Fuc, GDP-6-Azido-Fucose, GDP-6-Azido-6-deoxy-L-Fucose |
| Molecular Formula | C16H22N8O15P2 · 2Na |
| Molecular Weight | 674.32 g/mol (disodium salt) |
| CAS No. | N/A — research-grade compound |
| 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 fucosyltransferases; enables bioorthogonal click chemistry labeling of fucosylated glycans via azide–alkyne cycloaddition (CuAAC/SPAAC); used for glycan imaging and glycoproteomic profiling |
| Name | GDP-6-deoxy-D-talose; GDP-6-deoxy-alpha-D-talose |
|---|---|
| Formula | C16H25N5O15P2 |
| Exact mass | 589.0822 |
| Mol weight | 589.34 |
| Chemical Name | Guanosine-5’-diphospho-α-D-mannose, Disodium Salt |
|---|---|
| Synonyms | GDP-D-Man·2Na, GDP-Mannose Disodium Salt, GDP-α-D-Mannose Disodium Salt |
| Molecular Formula | C16H23N5O16P2 · 2Na |
| Molecular Weight | 649.30 g/mol (disodium salt) |
| CAS No. | 103301-73-1 (disodium salt); 3123-67-9 (free acid) |
| Appearance | White powder |
| Purity | ≥95% (HPLC) |
| Source | Enzymatic synthesis |
| Solubility | Soluble in water |
| Storage | −20°C, protect from moisture |
| Application | Activated sugar nucleotide donor substrate for mannosyltransferases; essential for N-linked glycoprotein biosynthesis, GPI-anchor assembly, and ascorbic acid (vitamin C) biosynthesis in plants |
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| Chemical Name | Guanosine-5’-diphospho-β-L-fucose, Disodium Salt |
|---|---|
| Synonyms | GDP-L-Fuc·2Na, GDP-Fucose Disodium Salt, GDP-β-L-Fucose Disodium Salt |
| Molecular Formula | C16H23N5O15P2 · 2Na |
| Molecular Weight | 633.31 g/mol (disodium salt) |
| CAS No. | 148296-47-3 (disodium salt); 15839-70-0 (free acid) |
| Appearance | White to off-white solid/powder |
| Purity | ≥95% (HPLC) |
| Solubility | Soluble in water |
| Storage | −20°C, protect from moisture and light |
| Application | Activated nucleotide sugar donor substrate for fucosyltransferases (FUTs); essential for biosynthesis of fucosylated glycans including Lewis antigens, ABO blood group determinants, and core fucosylation of N-glycans |
| Chemical Name | Uridine-5’-diphospho-2-alkyne-N-acetylgalactosamine |
|---|---|
| Synonyms | UDP-GalNAlk, UDP-2-Alkyne-GalNAc, UDP-2-Alkyne-N-Acetylgalactosamine |
| Molecular Formula | C18H29N3O17P2 (approximate) |
| Molecular Weight | ~645 g/mol |
| CAS No. | N/A — research-grade compound |
| Appearance | White to off-white lyophilized powder |
| Purity | ≥95% (HPLC) |
| Solubility | Soluble in water |
| Storage | −20°C, protect from moisture and light |
| Application | Alkyne-modified nucleotide sugar donor substrate for GalNAc-transferases (ppGalNAcTs) and O-GlcNAc transferase (OGT); enables bioorthogonal click chemistry labeling of O-GalNAc glycans and O-GlcNAcylated proteins via copper-catalyzed azide–alkyne cycloaddition (CuAAC); used for glycoproteomic profiling, glycan imaging, and metabolic labeling |
| Chemical Name | Uridine-5’-diphospho-2-alkyne-N-acetylglucosamine |
|---|---|
| Synonyms | UDP-GlcNAlk, UDP-2-Alkyne-GlcNAc, UDP-2-Alkyne-N-Acetylglucosamine |
| Molecular Formula | C19H27N3O17P2 |
| Molecular Weight | 645.40 g/mol |
| CAS No. | N/A — research-grade compound |
| Appearance | White to off-white lyophilized powder |
| Purity | ≥95% (HPLC) |
| Solubility | Soluble in water |
| Storage | −20°C, protect from moisture and light |
| Application | Alkyne-modified nucleotide sugar donor substrate; used for remodeling of cell-surface glycans and O-GlcNAc profiling; the terminal alkyne handle enables bioorthogonal detection via copper-catalyzed azide–alkyne cycloaddition (CuAAC); less susceptible to epimerization than the corresponding GalNAc analog; applied in glycoproteomic profiling, glycan imaging, and metabolic labeling |
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