7724-09-6

Usage

Uses

Used in Pharmaceutical Industry:
2-Hydroxybenzyl beta-D-glucopyranoside is used as a therapeutic agent for its antioxidant and anti-inflammatory properties, making it a potential candidate for treating conditions related to oxidative stress and inflammation.
Used in Diabetes Management:
2-Hydroxybenzyl beta-D-glucopyranoside is used as a compound for regulating blood sugar levels and improving insulin sensitivity, showing promise in the management of diabetes and metabolic syndrome.

Upstream product

• 2280-44-6 D-Glucose 
• 90-01-7 salicylic alcohol 
• 2492-87-7 4-nitrophenyl-β-D-glucoside 
• 15921-67-2 (2-hydroxy-benzyl)-(tetra-O-acetyl-β-D-glucopyranoside) 
• 1464-44-4 phenyl-β-D-glucopyranoside 
• 572-09-8 2,3,4,6-tetra-O-acetyl-α-D-glucopyranosyl bromide 
• 89-95-2 2-methyl-benzyl alcohol 
• 57-50-1 Sucrose 

Downstream Products

• 492-62-6 alpha-D-glucopyranose 
• 90-01-7 salicylic alcohol 

Relevant academic research and scientific papers

Enzymatic resolution of (RS)-1-phenylalkyl β-D-glucosides to (R)-1-phenylalkyl β-primeverosides and (S)-1-phenylalkyl β-D-glucosides via plant xylosyltransferase

The stereoselective xylosylation of (RS)-1-phenylalkyl β-D-glucosides was investigated using plant xylosyltransferase isolated from cultured Catharanthus roseus cells. Enzymatic xylosylation of (RS)-1-phenylethyl β-D-glucoside afforded (R)-1-phenylethyl β

Biotransformation of benzaldehyde-type and acetophenone-type derivatives by Pharbitis nil hairy roots

The glucosylation of some coumarin and flavone derivatives on incubation with the hairy roots of morning glory (Pharbitis nil) was previously reported. We further studied the biotransformation of benzaldehyde- and acetophenone-type derivatives. Vanillin a

Simple synthesis of β-D-glycopyranosides using β-glycosidase from almonds

Enzymatic glycosidation of twenty-one kinds of alcohols (n-hepanol, n-octanol, 2-phenylethanol, 3-phenylpropanol, 4-phenylbutanol, 5-phenylpentanol, 6-phenylhexanol, furfury alcohol, 2-pyridinemethanol, isobutanol, isopentanol, p-methoxycinnamylalcohol) including secondary alcohols (isopropanol, cyclohexanol, 1-phenylethanol) and 1, ω-alkanediols (1,5-pentanediol, 1,6-hexanediol, 1,7-heptanediol, 1,8-octanediol, 1,9-nonanediol), salicyl alcohol and 4-nitrophenyl β-D-glucopyranoside (5) using β-glucosidase from almonds stereoselectively gave the corresponding β-D-glucopyranosides in moderate yield.

Enzyme-catalysed synthesis of alkyl β-D-Glucosides in organic media

The synthetic potential of Almond β-D-Glucosidase for the synthesis of alkyl glucosides was studied. The regio and stereoselectivity of the synthesis were analysed for the reverse hydrolysis and the transglucosylation methods in tert-butanol and acetonitrile media.

Synthesis of β-Alkyl Glucosides by Enzymic Transglucosylation

Lactase from Kluyveromyces lactis was found to have high transglucosylation activity, transferring the glucosyl group of aryl glucoside to an alcoholic hydroxyl group in high yield.Both primary and secondary alcohols can accept the glucosyl group.Transglucosylation to glycol yielded a single kind of glucoside.A very hydrophilic alcohol, such as glycerol, could not serve as a substrate in this system.Hydrophobic alcohols slightly soluble in water were glucosylated in a two-phase system consisting of water and an organic solvent immiscible with water.Keywords - transglucosylation; transglycosylation; β-glucoside; lactase; Kluyveromyce s lactis; phenyl β-D-glucopyranoside; hydrophobic alcohol; two-phase system; alkyl glucoside; enzymic transglucosylation