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4-Nitrophenyl α-D-Glucopyranoside

<strong>4-Nitrophenyl α-D-Glucopyranoside</strong>_x000D_ <strong>Catalog number:</strong> B2012259_x000D_ <strong>Lot number:</strong> Batch Dependent_x000D_ <strong>Expiration Date:</strong> Batch dependent_x000D_ <strong>Amount:</strong> 100 mg_x000D_ <strong>Molecular Weight or Concentration:</strong> 301.3 g/mol_x000D_ <strong>Supplied as:</strong> Powder_x000D_ <strong>Applications:</strong> molecular tool for various biochemical applications_x000D_ <strong>Storage:</strong> -20C_x000D_ <strong>Keywords:</strong> p-Nitrophenyl α-D-glucopyranoside_x000D_ <strong>Grade:</strong> Biotechnology grade. All products are highly pure. All solutions are made with Type I ultrapure water (resistivity &gt;18 MŒ©-cm) and are filtered through 0.22 um._x000D_ _x000D_ <strong>References:</strong>_x000D_ 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._x000D_ 2: Binder TP, Robyt JF. p-Nitrophenyl alpha-D-glucopyranoside, a new substrate for glucansucrases Carbohydr Res. 1983 Dec 23;124(2):287-99._x000D_ 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._x000D_ 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._x000D_ 5: Strompen S, Miranda-Molina A, L√≥pez-Mungu√≠a A, Castillo E, Saab-Rinc√≥n G. Acceptor-induced modification of regioselectivity in CGTase-catalyzed glycosylations of p-nitrophenyl-glucopyranosides Carbohydr Res. 2015 Mar 2;404:46-54._x000D_ 6: C√¥t√© GL, Ahlgren JA. The hydrolytic and transferase action of alternanase on oligosaccharides Carbohydr Res. 2001 Jun 15;332(4):373-9._x000D_ 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._x000D_ 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._x000D_ 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._x000D_ <a href="https://pubmed.ncbi.nlm.nih.gov/33295353">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. </a>_x000D_ _x000D_ <strong>Products Related to 4-Nitrophenyl α-D-Glucopyranoside can be found at</strong> <a href="https://moleculardepot.com/product-category/Substrates/"> Substrates</a>

Product Specifications

Short Description

Catalog Number: B2012259 (100 mg)

Weight

0.15

Length

2

Width

0.5

Height

0.5

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