35978-96-2
![N-[(ε-Benzyloxycarbonylamino)caproyl]-β-L-fucopyranosylamine Chemical Structure](http://file.medchemexpress.cn/product_pic/hy-w698802.gif "N-[(ε-Benzyloxycarbonylamino)caproyl]-β-L-fucopyranosylamine Chemical Structure")
Chemical Structure
N-[(ε-Benzyloxycarbonylamino)caproyl]-β-L-fucopyranosylamine
- CAS No.: 35978-96-2
- Formula:C20H30N2O7
- Molecular Weight:410.46
IUPAC Name: benzyl (6-oxo-6-(((2S,3S,4R,5S,6S)-3,4,5-trihydroxy-6-methyltetrahydro-2H-pyran-2-yl)amino)hexyl)carbamate
InChIKey: MDHPQXZYOTUIEH-LRMKFPBYSA-N
SMILES: O=C(OCC1=CC=CC=C1)NCCCCCC(N[C@@H]2[C@H]([C@@H]([C@@H]([C@@H](O2)C)O)O)O)=O
Biological Activity: N-[(ε-Benzyloxycarbonylamino)caproyl]-β-L-fucopyranosylamine 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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N-[(ε-Benzyloxycarbonylamino)caproyl]-β-L-fucopyranosylamine | N-[(ε-Benzyloxycarbonylamino)caproyl]-β-L-fucopyranosylamine 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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