210110-89-7
Chemical Structure
5-Bromo-4-chloro-3-indolyl 2-acetamido-2-deoxy-α-D-galactopyranoside
- CAS No.: 210110-89-7
- Formula:C16H18BrClN2O6
- Molecular Weight:449.68
IUPAC Name: N-((2R,3R,4R,5R,6R)-2-((5-bromo-4-chloro-1H-indol-3-yl)oxy)-4,5-dihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-3-yl)acetamide
InChIKey: SUWPNTKTZYIFQT-IRHMCKRBSA-N
SMILES: BrC1=CC=C2C(C(O[C@@H]3[C@@H]([C@H]([C@H]([C@H](O3)CO)O)O)NC(C)=O)=CN2)=C1Cl
Biological Activity: 5-Bromo-4-chloro-3-indolyl 2-acetamido-2-deoxy-α-D-galactopyranoside 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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5-Bromo-4-chloro-3-indolyl 2-acetamido-2-deoxy-α-D-galactopyranoside | 5-Bromo-4-chloro-3-indolyl 2-acetamido-2-deoxy-α-D-galactopyranoside 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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