CAS 15486-34-7

5-Hydroxy-3,7,4′-trimethoxyflavone

Description:

5-Hydroxy-3,7,4′-trimethoxyflavone, with the CAS number 15486-34-7, is a flavonoid compound characterized by its polyphenolic structure, which includes multiple methoxy groups and a hydroxyl group. This compound typically exhibits a yellow to orange color and is soluble in organic solvents, reflecting its lipophilic nature. It is known for its potential antioxidant properties, which may contribute to various biological activities, including anti-inflammatory and anticancer effects. The presence of hydroxyl and methoxy groups enhances its reactivity and interaction with biological systems. Flavonoids like this one are often studied for their role in plant defense mechanisms and their potential health benefits in human nutrition. Additionally, 5-Hydroxy-3,7,4′-trimethoxyflavone may be found in certain plants and is of interest in pharmacological research for its therapeutic potential. Its stability and reactivity can be influenced by environmental factors such as pH and temperature, making it a subject of interest in both natural product chemistry and medicinal chemistry.

Formula: C₁₈H₁₆O₆

InChI: InChI=1S/C18H16O6/c1-21-11-6-4-10(5-7-11)17-18(23-3)16(20)15-13(19)8-12(22-2)9-14(15)24-17/h4-9,19H,1-3H3

InChI key: InChIKey=WSQWAMGRHJQANC-UHFFFAOYSA-N

SMILES: O(C)C1=C(OC=2C(C1=O)=C(O)C=C(OC)C2)C3=CC=C(OC)C=C3

Synonyms:

• 3,4′,7-Tri-O-methylkaempferol
• 3,4′,7-Trimethylkaempferol
• 3,7,4′-Tri-O-methylkaempferol
• 3,7,4′-Trimethylkaempferol
• 4H-1-Benzopyran-4-one, 5-hydroxy-3,7-dimethoxy-2-(4-methoxyphenyl)-
• 5-Hydroxy-3,4′,7-trimethoxyflavone
• 5-Hydroxy-3,7,4′-trimethoxyflavone
• 5-Hydroxy-3,7-dimethoxy-2-(4-methoxyphenyl)-4H-1-benzopyran-4-one
• 5-hydroxy-3,7-dimethoxy-2-(4-methoxyphenyl)-4H-chromen-4-one
• Flavone, 5-hydroxy-3,4′,7-trimethoxy-
• Kaempferol 3,4′,7-trimethyl ether
• Kaempferol 3,7,4′-trimethyl ether
• Kaempferol trimethylether
• Kaempferol-3,7,4'-trimethylether

Kaempferol-3,4',7-trimethylether

CAS: 15486-34-7

Kaempferol-3,4',7-trimethylether analytical standard provided with chromatographic purity, to be used as reference material for qualitative determination.

Formula: C₁₈H₁₆O₆

Purity: (HPLC) ≥95%

Color and Shape: Powder

Molecular weight: 328.33

Ref: 11-1070

Kaempferol-3,7,4'-trimethyl ether

CAS: 15486-34-7

Formula: C₁₈H₁₆O₆

Purity: 95%

Molecular weight: 328.3160

Ref: IN-DA00APGT

Kaempferol 3,7,4''-trimethyl ether

CAS: 15486-34-7

Formula: C₁₈H₁₆O₆

Molecular weight: 328.32

Ref: 7W-GY2577

Kaempferol 3,7,4'-trimethyl ether

CAS: 15486-34-7

Kaempferol 3,7,4'-trimethyl ether

Purity: ≥98%

Molecular weight: 328.32g/mol

Ref: 54-BUP02532

Kaempferol 3,7,4'-trimethyl ether

CAS: 15486-34-7

Formula: C₁₈H₁₆O₆

Purity: 95%~99%

Molecular weight: 328.32

Ref: BP-SBP03000

Kaempferol 3,7,4'-trimethyl ether

CAS: 15486-34-7

Kaempferol 3,7,4'-trimethyl ether (Kaempferol 3,7,4'-trimethylether) shows selective cyctoxic activities against the nine tested cancer cell lines.

Formula: C₁₈H₁₆O₆

Purity: 99.72% - 99.98%

Color and Shape: Solid

Molecular weight: 328.32

Ref: TM-TN1817

Kaempferol-3,7,4'-trimethyl ether

CAS: 15486-34-7

Kaempferol-3,7,4'-trimethyl ether is a methylated flavonoid compound, which is naturally derived from various plant sources known for their rich polyphenol content. This compound is characterized by its three methoxy groups attached to the kaempferol structure, enhancing its hydrophobic nature and overall stability. The primary mode of action of Kaempferol-3,7,4'-trimethyl ether involves modulation of various cellular signaling pathways, including those related to antioxidant and anti-inflammatory processes. It exerts its effects by interacting with key enzymes and receptors, leading to the modulation of gene expression linked to cellular stress responses.

Formula: C₁₈H₁₆O₆

Purity: Min. 98 Area-%

Color and Shape: Powder

Molecular weight: 328.32 g/mol

Ref: 3D-FK65525