CAS 112448-39-2

3′-Hydroxy-4′,5,6,7,8-pentamethoxyflavone

Description:

3′-Hydroxy-4′,5,6,7,8-pentamethoxyflavone, identified by its CAS number 112448-39-2, is a flavonoid compound characterized by its complex methoxy substitution pattern. This compound features a flavone backbone, which is a type of flavonoid known for its aromatic properties and potential biological activities. The presence of five methoxy groups at the 4′, 5, 6, 7, and 8 positions significantly influences its solubility, stability, and reactivity. The hydroxyl group at the 3′ position contributes to its potential antioxidant properties, making it of interest in pharmacological research. Flavonoids, including this compound, are known for their diverse biological activities, including anti-inflammatory, anticancer, and neuroprotective effects. The unique substitution pattern of 3′-Hydroxy-4′,5,6,7,8-pentamethoxyflavone may enhance its interaction with biological targets, potentially leading to various therapeutic applications. However, further studies are necessary to fully elucidate its mechanisms of action and potential health benefits.

Formula: C₂₀H₂₀O₈

InChI: InChI=1/C20H20O8/c1-23-13-7-6-10(8-11(13)21)14-9-12(22)15-16(24-2)18(25-3)20(27-5)19(26-4)17(15)28-14/h6-9,21H,1-5H3

InChI key: InChIKey=XFYYZBJXMSDKCV-UHFFFAOYSA-N

SMILES: O(C)C1=C2C(=C(OC)C(OC)=C1OC)OC(=CC2=O)C3=CC(O)=C(OC)C=C3

Synonyms:

• 2-(3-Hydroxy-4-methoxyphenyl)-5,6,7,8-tetramethoxy-4H-1-benzopyran-4-one
• 2-(3-Hydroxy-4-methoxyphenyl)-5,6,7,8-tetramethoxychromen-4-one
• 3′-Demethylnobiletin
• 3′-Hydroxy-4′,5,6,7,8-pentamethoxyflavone
• 4H-1-benzopyran-4-one, 2-(3-hydroxy-4-methoxyphenyl)-5,6,7,8-tetramethoxy-
• 3'-Hydroxy-5

3'-Demethylnobiletin

CAS: 112448-39-2

3'-Demethylnobiletin

Purity: ≥98%

Molecular weight: 388.37g/mol

Ref: 54-BUP20758

3'-Demethylnobiletin

CAS: 112448-39-2

3'-Demethylnobiletin is a polymethoxylated flavonoid, which is a naturally occurring compound found in citrus peels. This bioactive flavonoid is primarily sourced from the peel of citrus fruits, particularly those belonging to the genus Citrus. Its structural properties allow it to engage in multiple molecular interactions, providing a wide array of biological effects.

Formula: C₂₀H₂₀O₈

Purity: Min. 95%

Molecular weight: 388.4 g/mol

Ref: 3D-MEA44839

3'-Demethylnobiletin

CAS: 112448-39-2

'3'-Demethylnobiletin inhibits colon cancer growth, causes cell-cycle arrest, and induces apoptosis, affecting key cellular signals.

Formula: C₂₀H₂₀O₈

Purity: 99.87%

Color and Shape: Solid

Molecular weight: 388.37

Ref: TM-TN1244

3'-Demethylnobiletin

CAS: 112448-39-2

Formula: C₂₀H₂₀O₈

Purity: 95%~99%

Molecular weight: 388.372

Ref: BP-BP1805

3''-Demethylnobiletin

CAS: 112448-39-2

Formula: C₂₀H₂₀O₈

Molecular weight: 388.37

Ref: 7W-GY5129