- Saccharides
- Monosaccharides
- Pyranose
Pyranose
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Pyranose (188)
- Formula: C51H99N4O16P
- Molecular Weight: 1055.32
16:0 PA-PEG3-Mannose ammonium is a functionalized lipid.
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- Formula: C6H19Na2O13P
- Molecular Weight: 376.16
α-D-Glucose-1-phosphate disodium tetrahydrate is a derivative of D-glucose (HY-B0389). α-D-Glucose-1-phosphate disodium tetrahydrate serves as a starting material for glucuronic acid synthesis. Glucuronic acid acts as a Ca2+ chelator and also functions as a biosynthetic substrate for the production of linear maltooligosaccharides or α,α-trehalose. α-D-Glucose-1-phosphate disodium tetrahydrate can be used as a cytostatic compound, Antibiotic, and immunosuppressant essential for heart disease management. α-D-Glucose-1-phosphate disodium tetrahydrate is applicable to the research of heart disease.
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- Formula: C6H11N3O5
- Molecular Weight: 205.17
L-Galactose-azide (compound 1b) is an L-fucose analogue synthesized from L-galactose.
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- Formula: C6H14O12P2
- Molecular Weight: 340.12
α-D-Glucose 1,6-bisphosphate is an activator of PMM2 and phosphoglucomutase. α-D-Glucose 1,6-bisphosphate regulates glycogen metabolism, glycolysis, amino sugar synthesis, as well as the formation of bacterial cell walls and capsules. α-D-Glucose 1,6-bisphosphate can be used in studies related to pmm2-cdg (cdg-1a or Jaeken syndrome).
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- Formula: C16H23NO10
- Molecular Weight: 389.35
2-Acetamido-1,3,4,6-tetra-O-acetyl-2-deoxy-alpha-D-glucopyranose can be used in glycobiology research.
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- Formula: C21H26O10
- Molecular Weight: 438.43
1,2,4,6-Tetra-O-acetyl-3-O-benzyl-β-D-glucopyranose can be used in glycobiology research.
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- Formula: C34H28O10
- Molecular Weight: 596.58
2,3,4,6-Tetra-O-benzoyl-β-D-glucopyranose is a D-glucopyranose derivative that has been used in glucosylation reactions.
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- Formula: C12H23N3O8
- Molecular Weight: 337.33
alpha-Man-TEG-N3 is a click chemistry reagent containing an azide group. alpha-Man-TEG-N3 is a click chemistry reagent, it contains an Azide group and can undergo copper-catalyzed azide-alkyne cycloaddition reaction (CuAAc) with molecules containing Alkyne groups. It can also undergo strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with molecules containing DBCO or BCN groups.
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