73208-61-4
Chemical Structure
N-Acetyllactosamine Heptaacetate
- CAS No.: 73208-61-4
- Formula:C28H39NO18
- Molecular Weight:677.61
IUPAC Name: (2S,3R,4S,5S,6R)-2-(((2R,3S,4R,5R)-5-acetamido-4,6-diacetoxy-2-(acetoxymethyl)tetrahydro-2H-pyran-3-yl)oxy)-6-(acetoxymethyl)tetrahydro-2H-pyran-3,4,5-triyl triacetate
InChIKey: XKTWMUHXXMTTHP-FYFQELNQSA-N
SMILES: CC(O[C@H]([C@H](C(O[C@@H]1COC(C)=O)OC(C)=O)NC(C)=O)[C@@H]1O[C@H]2[C@@H]([C@H]([C@H]([C@H](O2)COC(C)=O)OC(C)=O)OC(C)=O)OC(C)=O)=O
Biological Activity: N-Acetyllactosamine Heptaacetate is a class of biochemical reagents used in glycobiology research. Glycobiology studies the structure, synthesis, biology, and evolution of sugars. It involves carbohydrate chemistry, enzymology of glycan formation and degradation, protein-glycan recognition, and the role of glycans in biological systems. This field is closely related to basic research, biomedicine, and biotechnology[1].
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N-Acetyllactosamine Heptaacetate | N-Acetyllactosamine Heptaacetate is a class of biochemical reagents used in glycobiology research. Glycobiology studies the structure, synthesis, biology, and evolution of sugars. It involves carbohydrate chemistry, enzymology of glycan formation and degradation, protein-glycan recognition, and the role of glycans in biological systems. This field is closely related to basic research, biomedicine, and biotechnology. | |||||||||||||||||||||
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Keywords
