51471-40-0
![2-Deoxy-2-[[(4-methoxyphenyl)methylene]amino]-β-D-glucopyranose Chemical Structure](http://file.medchemexpress.cn/product_pic/hy-w354410.gif "2-Deoxy-2-[[(4-methoxyphenyl)methylene]amino]-β-D-glucopyranose Chemical Structure")
Chemical Structure
2-Deoxy-2-[[(4-methoxyphenyl)methylene]amino]-β-D-glucopyranose
- CAS No.: 51471-40-0
- Formula:C14H19NO6
- Molecular Weight:297.30
IUPAC Name: (2R,3R,4R,5S,6R)-6-(hydroxymethyl)-3-(((E)-4-methoxybenzylidene)amino)tetrahydro-2H-pyran-2,4,5-triol
InChIKey: NMMULIPYJSFGRK-HKDDVOALSA-N
SMILES: COC(C=C1)=CC=C1/C=N/[C@@H]2[C@H]([C@@H]([C@H](O[C@H]2O)CO)O)O
Biological Activity: 2-Deoxy-2-[[(4-methoxyphenyl)methylene]amino]-β-D-glucopyranose 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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2-Deoxy-2-[[(4-methoxyphenyl)methylene]amino]-β-D-glucopyranose | 2-Deoxy-2-[[(4-methoxyphenyl)methylene]amino]-β-D-glucopyranose 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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