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4-Nitrophenyl α-D-Glucopyranoside

$395.00

Catalog Number: B2012259 (100 mg)
4-Nitrophenyl α-D-Glucopyranoside is a high quality Substrate for α-D-Glucosidase. This product has been used as molecular tool for various biochemical applications. It has also been used in a wide array of other chemical and immunological applications. Custom bulk amounts of this product are available upon request.

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SKU: B2012259 Categories: , Tag:

Description

4-Nitrophenyl α-D-Glucopyranoside
Catalog number: B2012259
Lot number: Batch Dependent
Expiration Date: Batch dependent
Amount: 100 mg
Molecular Weight or Concentration: 301.3 g/mol
Supplied as: Powder
Applications: molecular tool for various biochemical applications
Storage: -20C
Keywords: p-Nitrophenyl α-D-glucopyranoside
Grade: Biotechnology grade. All products are highly pure. All solutions are made with Type I ultrapure water (resistivity >18 MΩ-cm) and are filtered through 0.22 um.

References:
1: Kanellopoulos PN, Pavlou K, Perrakis A, Agianian B, Vorgias CE, Mavrommatis C, Soufi M, Tucker PA, Hamodrakas SJ. The crystal structure of the complexes of concanavalin A with 4′-nitrophenyl-alpha-D-mannopyranoside and 4′-nitrophenyl-alpha-D-glucopyranoside J Struct Biol. 1996 May-Jun;116(3):345-55.
2: Binder TP, Robyt JF. p-Nitrophenyl alpha-D-glucopyranoside, a new substrate for glucansucrases Carbohydr Res. 1983 Dec 23;124(2):287-99.
3: Vlahopoulos V, Jakinovich W Jr. Antagonism of the gerbil’s sucrose taste response by p-nitrophenyl alpha-D-glucopyranoside and chloramphenicol J Neurosci. 1986 Sep;6(9):2611-5.
4: Nishio T, Hakamata W, Kimura A, Chiba S, Takatsuki A, Kawachi R, Oku T. Glycon specificity profiling of alpha-glucosidases using monodeoxy and mono-O-methyl derivatives of p-nitrophenyl alpha-D-glucopyranoside Carbohydr Res. 2002 Apr 2;337(7):629-34.
5: Strompen S, Miranda-Molina A, López-Munguía A, Castillo E, Saab-Rincón G. Acceptor-induced modification of regioselectivity in CGTase-catalyzed glycosylations of p-nitrophenyl-glucopyranosides Carbohydr Res. 2015 Mar 2;404:46-54.
6: Côté GL, Ahlgren JA. The hydrolytic and transferase action of alternanase on oligosaccharides Carbohydr Res. 2001 Jun 15;332(4):373-9.
7: Tagomori BY, Dos Santos FC, Barbosa-Tessmann IP. Recombinant expression, purification, and characterization of an α-amylase from Massilia timonae 3 Biotech. 2021 Jan;11(1):13.
8: Omichi K, Ikenaka T. Differential rate assay of human pancreatic and salivary alpha-amylases in serum using two coupled enzymes J Biochem. 1986 Nov;100(5):1353-8.
9: Heydari Z, Mohammadi-Khanaposhtani M, Imanparast S, Faramarzi MA, Mahdavi M, Ranjbar PR, Larijani B. Pyrano[3,2-c]quinoline Derivatives as New Class of α-glucosidase Inhibitors to Treat Type 2 Diabetes: Synthesis, in vitro Biological Evaluation and Kinetic Study Med Chem. 2019;15(1):8-16.
10: Guo FN , Wang YT , Wu N , Feng LX , Zhang HC , Yang T , Wang JH . Carbon nitride nanoparticles as ultrasensitive fluorescent probes for the detection of α-glucosidase activity and inhibitor screening Analyst. 2021 Feb 7;146(3):1016-1022.

Products Related to 4-Nitrophenyl α-D-Glucopyranoside can be found at Substrates

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