35785-42-3
Chemical Structure
4-Nitrobenzyl 2,3,4,6-tetra-O-acetyl-1-thio-β-D-galactopryranoside
- CAS No.: 35785-42-3
- Formula:C21H25NO11S
- Molecular Weight:499.49
IUPAC Name: (2R,3S,4S,5R,6S)-2-(acetoxymethyl)-6-((4-nitrobenzyl)thio)tetrahydro-2H-pyran-3,4,5-triyl triacetate
InChIKey: ZHFJYPUDGFUYCK-IFLJBQAJSA-N
SMILES: CC(O[C@@H]1[C@H]([C@@H](O[C@@H]([C@@H]1OC(C)=O)COC(C)=O)SCC2=CC=C(C=C2)[N+]([O-])=O)OC(C)=O)=O
Biological Activity: 4-Nitrobenzyl 2,3,4,6-tetra-O-acetyl-1-thio-β-D-galactopryranoside 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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4-Nitrobenzyl 2,3,4,6-tetra-O-acetyl-1-thio-β-D-galactopryranoside | 4-Nitrobenzyl 2,3,4,6-tetra-O-acetyl-1-thio-β-D-galactopryranoside 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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