4-Nitrophenyl β-D-cellotetraoside | Gentaur

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4-Nitrophenyl β-D-cellotetraoside

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804-HY-138111

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4-Nitrophenyl β-D-cellotetraoside

CAS Number: 129411-62-7
UNSPSC Description: 4-Nitrophenyl β-D-cellotetraoside (p-Nitopheyl β-D-cellotetaoside) is a small molecule cellulose mimetic consisting of a tetramer of D-glucose units linked by β-1-4 glycosidic bonds. The fragmentation pattern of 4-Nitrophenyl β-D-cellotetraoside after enzymatic hydrolysis can be analyzed by TLC or by the release of 4-nitrophenol, which has a strong absorbance at 395 nm in alkaline solutions. 4-Nitrophenyl β-D-cellotetraoside can be used in cellulose degradation studies to determine the specificity of cellulases[1].
Target Antigen: Fluorescent Dye
Type: Dye Reagents
Related Pathways: Others
Field of Research: Others
Assay Protocol: https://www.medchemexpress.com/4-nitrophenyl-β-d-cellotetraoside.html
Smiles: OC[C@@H](O[C@H]1O[C@@H]([C@@H]([C@H]2O)O)[C@H](O[C@H]2OC(C=C3)=CC=C3[N](=O)=O)CO)[C@H]([C@@H]([C@H]1O)O)O[C@@H]([C@@H]([C@H]4O)O)O[C@@H]([C@H]4O[C@@H]([C@@H]([C@H]5O)O)O[C@@H]([C@H]5O)CO)CO
Molecular Weight: 787.67
References & Citations: [1]Hakamada Y, et al. Enzymatic properties, crystallization, and deduced amino acid sequence of an alkaline endoglucanase from Bacillus circulans[J]. Biochimica et Biophysica Acta (BBA)-General Subjects, 2002, 1570(3): 174-180.
Shipping Conditions: Room temperature
Clinical Information: No Development Reported

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