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Usage

Uses

Used in Pharmaceutical Industry:
(2'-METHOXYCARBONYL)PHENYL-2-,3,4,6-TETRA-O-ACETYL-BETA-D-GLUCOPYRANOSE is used as an intermediate in the synthesis of glycosylated metabolites for the development of new pharmaceutical compounds. Its unique structure allows for the creation of glycosylated derivatives that can exhibit improved pharmacological properties, such as enhanced solubility, stability, and bioavailability. This makes it a valuable component in the design and synthesis of novel drug candidates with potential therapeutic applications.
Used in Organic Synthesis:
In the field of organic synthesis, (2'-METHOXYCARBONYL)PHENYL-2-,3,4,6-TETRA-O-ACETYL-BETA-D-GLUCOPYRANOSE serves as a versatile building block for the preparation of various complex organic molecules. Its functional groups, such as the ester linkage and acetyl groups, can be selectively modified or removed to generate a wide range of glycosylated products. This versatility makes it an essential component in the synthesis of natural products, pharmaceuticals, and other bioactive compounds.
Used in Research and Development:
(2'-METHOXYCARBONYL)PHENYL-2-,3,4,6-TETRA-O-ACETYL-BETA-D-GLUCOPYRANOSE is also used in research and development settings to study the properties and behavior of glycosylated compounds. Its unique structure allows researchers to investigate the effects of glycosylation on the biological activity, pharmacokinetics, and pharmacodynamics of various compounds. This knowledge can be applied to the design of new drugs and the optimization of existing ones, ultimately contributing to the advancement of pharmaceutical science.

Upstream product

• 108-24-7 acetic anhydride 
• 10019-60-0 o-methoxycarbonylphenyl β-D-glucopyranoside 
• 572-09-8 2,3,4,6-tetra-O-acetyl-D-glucopyranosyl bromide 
• 119-36-8 methyl salicylate 
• 572-09-8 2,3,4,6-tetra-O-acetyl-α-D-glucopyranosyl bromide 

Downstream Products

• 1338564-86-5 C₁₈H₂₂O₁₀ 
• 490-67-5 gaultherin 
• 10366-91-3 2-hydroxy-3-O-β-D-glucopyranosylbenzoic acid 
• 10019-60-0 o-methoxycarbonylphenyl β-D-glucopyranoside 

Relevant academic research and scientific papers

Synthesis and anti-nociceptive and anti-inflammatory effects of gaultherin and its analogs

The synthesis of gaultherin (1) and its analogs was carried out to provide 11 glycosides under phase-transfer catalytic conditions. The activities of all synthesized compounds were evaluated by nitric oxide production inhibitory assay in vitro. Methyl 2-O-(4-O-β- d-galactopyranosyl)- β- d-glucopyranosylbenzoate (5f) showed significantly anti-nociceptive and anti-inflammatory effects by the evaluation in vivo. Structure-activity relationships within these compounds were discussed.

Glycosidically Bound Eugenol and Methyl Salicylate in the Fruit of Edible Passiflora Species

The β-D-glucopyranoside and 6-O-α-L-rhamnopyranosyl-β-D-glucopyranoside of methyl salicylate and the β-D-glucopyranoside of eugenol have been characterized in purple passion fruit (Passiflora edulis SIMS) by GC and GC/MS of their trifluoroacetylated deriv

Synthesis and Characterization of the Salicylic Acid β-D-glucopyranoside

Simple unambiguous synthesis of salicylic acid β-D-glucopyranoside is described.Analytical and spectral characteristics of the compound, which is important for studies in plant physiology, is presented. Key words: glycosylation, carboxyphenyl, glucoside,

PHOTOCYCLISATION DE PHENYL-GLYCOSIDES ORTHOCARBONYLES: VOIES D'ACCES STEREOSELECTIVES AUX DIOXASPIRANNONES AROMATIQUES

The photolysis of 2-carbonylphenyl β-D-glucopyranosides gave, by a stereoselective, Norrish-type II carbocyclisation, hydroxy-aromatic, spiro C-1 sugars, having the β-D configuration.The α-D anomers were easily obtained by acid isomerisation of the β-D an