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MedChemExpressModel 4-Nitrophenyl ß-D-glucopyranoside -2492-87-7

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4-Nitrophenyl β-D-glucopyranoside is a chromogenic substrate for β-glucosidase. 4-Nitrophenyl β-D-glucopyranoside is converted to a colored product, p-nitrophenol that is easily detected spectrophotometrically at 405 nm when used in a β-glycosidase assay. 4-Nitrophenyl β-D-glucopyranoside is hydrolysed through intramolecular nucleophilic catalysis by the phosphate group in the 2-position. 4-Nitrophenyl β-D-glucopyranoside is promising for research of postmenopausal osteoporosis[1][2][3].
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4-Nitrophenyl β-D-glucopyranoside

MCE China:4-Nitrophenyl β-D-glucopyranoside

Brand:MedChemExpress (MCE)

Cat. No.HY-15927

CAS:2492-87-7

Purity:99.69%

Storage:-20°C, protect from light *In solvent : -80°C, 6 months; -20°C, 1 month (protect from light)

Shipping:Room temperature in continental US; may vary elsewhere.

Description:4-Nitrophenyl β-D-glucopyranoside is a chromogenic substrate for β-glucosidase. 4-Nitrophenyl β-D-glucopyranoside is converted to a colored product, p-nitrophenol that is easily detected spectrophotometrically at 405 nm when used in a β-glycosidase assay. 4-Nitrophenyl β-D-glucopyranoside is hydrolysed through intramolecular nucleophilic catalysis by the phosphate group in the 2-position. 4-Nitrophenyl β-D-glucopyranoside is promising for research of postmenopausal osteoporosis.

In Vitro:4-Nitrophenyl β-D-glucopyranoside (1-20 μM) shows 17%-19% inhibitory effects on adipogenesis at 20 µM treatment in mouse mesenchymal stem cell lines[3].

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References:

[1]. Alhifthi A, et al. Unimolecular, Bimolecular, and Intramolecular Hydrolysis Mechanisms of 4-Nitrophenyl β-d-Glucopyranoside. J Org Chem. 2021 Jul 16;86(14):9530-9539.  [Content Brief]

[2]. Lee KH, et al. Ginkgonitroside, a new nitrophenyl glycoside and bioactive compounds from Ginkgo biloba leaves controlling adipocyte and osteoblast differentiation. Bioorg Med Chem Lett. 2021 Oct 15;50:128322.  [Content Brief]

[3]. Rosie F D. Nucleophilic catalysis of glycoside hydrolysis. The hydrolysis of 4-nitrophenyl α-and β-D-glucopyranoside tetraphosphates[J]. Journal of the Chemical Society, Perkin Transactions 2, 1994 (10): 2085-2090.

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