4419-94-7
Chemical Structure
p-Nitrophenyl β-D-lactoside
- CAS No.: 4419-94-7
- Formula:C18H25NO13
- Molecular Weight:463.39
IUPAC Name: (2S,3R,4S,5R,6R)-2-(((2R,3S,4R,5R,6S)-4,5-dihydroxy-2-(hydroxymethyl)-6-(4-nitrophenoxy)tetrahydro-2H-pyran-3-yl)oxy)-6-(hydroxymethyl)tetrahydro-2H-pyran-3,4,5-triol
InChIKey: IAYJZWFYUSNIPN-MUKCROHVSA-N
SMILES: OC[C@@H](O[C@H]([C@@H]([C@H]1O)O)OC2=CC=C(C=C2)[N+]([O-])=O)[C@H]1O[C@@H]3O[C@@H]([C@@H]([C@@H]([C@H]3O)O)O)CO
Biological Activity: p-Nitrophenyl β-D-lactoside is a substrate of β-lactosidase and can be used to determine β-lactosinase activity. p-Nitrophenyl β-D-lactoside is a substrate of cellobiohydrolase. p-Nitrophenyl β-D-lactoside is a class of biochemical reagents used in glycobiology research[1][2].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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p-Nitrophenyl β-D-lactoside | 96.14% | p-Nitrophenyl β-D-lactoside is a substrate of β-lactosidase and can be used to determine β-lactosinase activity. p-Nitrophenyl β-D-lactoside is a substrate of cellobiohydrolase. p-Nitrophenyl β-D-lactoside is a class of biochemical reagents used in glycobiology research. | ||||||||||||||||||||
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References
- [1]. Paolo Riccio, et al. Extraction and immobilization in one step of two β-glucosidases released from a yeast strain of Debaryomyces hansenii. Enzyme and Microbial Technology. Volume 24, Issues 3-4, February-March 1999, Pages 123-129.
- [2]. Jalak J, et al. Mechanism of initial rapid rate retardation in cellobiohydrolase catalyzed cellulose hydrolysis. Biotechnol Bioeng. 2010 Aug 15;106(6):871-83. [Content Brief]
