14982-11-7

Basic information

• Product Name: 4H-1-Benzopyran-4-one,7-(b-D-glucopyranosyloxy)-2,3-dihydro-5-hydroxy-2-(4-hydroxy-3-methoxyphenyl)-,(2S)-
• Synonyms: 4H-1-Benzopyran-4-one,7-(b-D-glucopyranosyloxy)-2,3-dihydro-5-hydroxy-2-(4-hydroxy-3-methoxyphenyl)-,(S)-; Flavanone, 4',5,7-trihydroxy-3'-methoxy-, 7-b-D-glucopyranoside (8CI); (2S)-Homoeriodictyol 7-O-b-D-glucoside; Homoeriodictyol7-glucoside; Homoeriodictyol-7-O-glucoside; Viscumside A
• CAS NO: 14982-11-7
• Molecular Formula: C22H24 O11
• Molecular Weight: 464.426
• Mol File: 14982-11-7.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 4H-1-Benzopyran-4-one,7-(b-D-glucopyranosyloxy)-2,3-dihydro-5-hydroxy-2-(4-hydroxy-3-methoxyphenyl)-,(2S)-(CAS DataBase Reference)
• NIST Chemistry Reference: 4H-1-Benzopyran-4-one,7-(b-D-glucopyranosyloxy)-2,3-dihydro-5-hydroxy-2-(4-hydroxy-3-methoxyphenyl)-,(2S)-(14982-11-7)
• EPA Substance Registry System: 4H-1-Benzopyran-4-one,7-(b-D-glucopyranosyloxy)-2,3-dihydro-5-hydroxy-2-(4-hydroxy-3-methoxyphenyl)-,(2S)-(14982-11-7)

Safety Data

• Hazardous Substances Data: 14982-11-7(Hazardous Substances Data)

Usage

General Description

The chemical "4H-1-Benzopyran-4-one,7-(b-D-glucopyranosyloxy)-2,3-dihydro-5-hydroxy-2-(4-hydroxy-3-methoxyphenyl)-,(2S)-" is a compound with a benzopyranone core structure, containing a glucopyranosyl group attached to the 7-position. It also has a 2,3-dihydro-5-hydroxy-2-(4-hydroxy-3-methoxyphenyl) moiety, with a stereochemistry of (2S). This chemical is a flavonoid glycoside, with potential biological activities such as antioxidant, anti-inflammatory, and anti-cancer properties. It is commonly found in plants and natural products, and may have potential pharmaceutical and medicinal applications.

Upstream product

• 133-89-1 UDP-glucose 
• 446-71-9 homoeriodictyol 

Relevant articles and documents

Identification of a flavonoid 7-O-glucosyltransferase from Andrographis paniculata

Andrographis paniculata is an important traditional medicinal herb in which flavonoids are part of the primary specialized metabolites. A flavonoid glucosyltransferase with broad substrate spectrum (named ApUGT3) was successfully identified by screening homologous glycosyltransferase genes from A. paniculata. The enzyme displayed glycosylation activity toward multiple flavonoids in?vitro, and the major products were identified as 7-O-glucosides. Phylogenetic analysis revealed that ApUGT3 is the first reported glycosyltransferase from the Acanthaceae family that belongs to cluster I, suggesting that ApUGT3 is a new flavonoid glycosyltransferase of this subcluster. This enzyme is potentially useful as powerful glycosylation catalysts to modify flavonoid-like compounds and improve their biological activities. (Figure presented.).