97276-96-5
Chemical Structure
Methyl 3-O-benzyl-4,6-O-benzylidene-2-deoxy-2-N-phthalimido- β-D-glucopyranoside
- CAS No.: 97276-96-5
- Formula:C29H27NO7
- Molecular Weight:501.53
IUPAC Name: 2-((4aR,6R,7R,8R,8aS)-8-(benzyloxy)-6-methoxy-2-phenylhexahydropyrano[3,2-d][1,3]dioxin-7-yl)isoindoline-1,3-dione
InChIKey: HYDHLSHOGOVBCQ-DIFZJPFWSA-N
SMILES: CO[C@H](O[C@@]1([H])[C@@]2([H])OC(C3=CC=CC=C3)OC1)[C@H](N4C(C5=CC=CC=C5C4=O)=O)[C@H]2OCC6=CC=CC=C6
Biological Activity: Methyl 3-O-benzyl-4, 6-O-Benzylidene-2-deoxy-2-N-Phthalimido-β-d-Glucopyranoside is a class of biochemical reagents used in the study of glycobiology. Glycobiology studies the structure, synthesis, biology, and evolution of sugars. It deals with carbohydrate chemistry, glycan formation and degradation enzymology, protein-glycan recognition, and the role of glycans in biological systems. The field is closely related to basic research, biomedicine and biotechnology[1].
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Methyl 3-O-benzyl-4,6-O-benzylidene-2-deoxy-2-N-phthalimido- β-D-glucopyranoside | Methyl 3-O-benzyl-4, 6-O-Benzylidene-2-deoxy-2-N-Phthalimido-β-d-Glucopyranoside is a class of biochemical reagents used in the study of glycobiology. Glycobiology studies the structure, synthesis, biology, and evolution of sugars. It deals with carbohydrate chemistry, glycan formation and degradation enzymology, protein-glycan recognition, and the role of glycans in biological systems. The field is closely related to basic research, biomedicine and biotechnology. | |||||||||||||||||||||
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