CAS 36948-77-3

4H-1-Benzopyran-4-one, 7-(β-D-glucopyranosyloxy)-5-hydroxy-6-methoxy-2-phenyl-

Description:

The chemical substance known as "4H-1-Benzopyran-4-one, 7-(β-D-glucopyranosyloxy)-5-hydroxy-6-methoxy-2-phenyl-" with CAS number 36948-77-3 is a flavonoid glycoside, characterized by its complex structure that includes a benzopyran core, a glucopyranosyl moiety, and multiple hydroxyl and methoxy functional groups. This compound exhibits properties typical of flavonoids, such as antioxidant activity, which is attributed to the presence of hydroxyl groups that can scavenge free radicals. The glucopyranosyl group enhances its solubility in water and may influence its bioavailability and pharmacological effects. Additionally, the presence of the phenyl group contributes to its potential interactions with biological targets. Such compounds are often studied for their therapeutic potential, including anti-inflammatory, antimicrobial, and anticancer activities. The specific arrangement of substituents on the benzopyran ring can significantly affect the compound's reactivity and biological activity, making it a subject of interest in medicinal chemistry and natural product research.

Formula: C₂₂H₂₂O₁₀

Synonyms:

• oroxylin A-7-O-glucoside
• 4H-1-Benzopyran-4-one, 7-(β-D-glucopyranosyloxy)-5-hydroxy-6-methoxy-2-phenyl-
• Oroxylin 7-O-glucoside

oroxylin A 7-O-β-d-glucuronide

CAS: 36948-77-3

oroxylin A 7-O-β-d-glucuronide

Purity: ≥98%

Molecular weight: 446.4g/mol

Ref: 54-BUP00817

Oroxylin A-7-O-glucoside

CAS: 36948-77-3

Formula: C₂₂H₂₂O₁₀

Purity: 95%~99%

Molecular weight: 446.408

Ref: BP-BP4662

Oroxylin A 7-O-glucoside

CAS: 36948-77-3

Oroxylin A 7-O-glucoside was a new alkaloid which found in the bulbs of Lycoris radiata.

Formula: C₂₂H₂₂O₁₀

Purity: 98.70% - 99.02%

Color and Shape: Solid

Molecular weight: 446.4

Ref: TM-TN6782

Oroxylin A-7-o-glucoside

CAS: 36948-77-3

Oroxylin A-7-o-glucoside is a flavonoid compound, specifically a glucoside derivative of Oroxylin A. It is sourced from various plant species, particularly those within the Scutellaria genus. The compound exhibits its mode of action through its antioxidant properties, which involve scavenging free radicals and modulating redox-sensitive signaling pathways. This flavonoid derivative has been studied for its potential biological effects, such as anti-inflammatory, anticancer, and neuroprotective activities. Its applications span across pharmacological research focused on developing therapeutic agents that may alleviate oxidative stress-related conditions and modulate inflammatory responses. Scientists are particularly interested in Oroxylin A-7-o-glucoside for its potential to contribute to the development of novel drugs targeting chronic diseases driven by oxidative damage and inflammation. The exploration of this compound continues to provide valuable insights into its molecular mechanisms and therapeutic potential in various biomedical fields.

Formula: C₂₂H₂₂O₁₀

Purity: Min. 95%

Molecular weight: 446.4 g/mol

Ref: 3D-LBA94877