151963-95-0
Chemical Structure
N-Benzyl-2,3,4,6-tetra-O-benzyl-1,5-dideoxy-imino-L-iditol
- CAS No.: 151963-95-0
- Formula:C41H43NO4
- Molecular Weight:613.78
IUPAC Name: (2S,3R,4R,5S)-1-benzyl-3,4,5-tris(benzyloxy)-2-((benzyloxy)methyl)piperidine
InChIKey: UMMMXEDKZOXSCP-LETRWZBTSA-N
SMILES: C1(CO[C@@H]2[C@@H](N(C[C@@H]([C@H]2OCC3=CC=CC=C3)OCC4=CC=CC=C4)CC5=CC=CC=C5)COCC6=CC=CC=C6)=CC=CC=C1
Biological Activity: N-Benzyl-2,3,4,6-tetra-O-benzyl-1,5-dideoxy-imino-L-iditol 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].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
|
N-Benzyl-2,3,4,6-tetra-O-benzyl-1,5-dideoxy-imino-L-iditol | N-Benzyl-2,3,4,6-tetra-O-benzyl-1,5-dideoxy-imino-L-iditol 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. | |||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
