73208-80-7
Chemical Structure
N-Acetyl-2-O-methyl-α-neuraminic acid methyl ester 4,7,8,9-tetraacetate
- CAS No.: 73208-80-7
- Formula:C21H31NO13
- Molecular Weight:505.47
IUPAC Name: (1S,2R)-1-((2R,3R,4S,6R)-3-acetamido-4-acetoxy-6-methoxy-6-(methoxycarbonyl)tetrahydro-2H-pyran-2-yl)propane-1,2,3-triyl triacetate
InChIKey: BDVAGIAWBFWKLD-YKFXCJJJSA-N
SMILES: CC(OC[C@@H](OC(C)=O)[C@H]([C@@]1([H])[C@@H]([C@H](C[C@@](OC)(O1)C(OC)=O)OC(C)=O)NC(C)=O)OC(C)=O)=O
Biological Activity: N-Acetyl-2-O-methyl-α-neuraminic acid methyl ester 4,7,8,9-tetraacetateis 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-Acetyl-2-O-methyl-α-neuraminic acid methyl ester 4,7,8,9-tetraacetate | N-Acetyl-2-O-methyl-α-neuraminic acid methyl ester 4,7,8,9-tetraacetateis 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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