Acacetin 7-O-methyl ether

CAS : 5128-44-9

Ref. 3D-FA65396

Informations sur le produit

• Nom: Acacetin 7-O-methyl ether
• Synonymes: 4',7-Dimethoxy-5-hydroxyflavone4',7-O-Dimethylapigenin, 4',7-DimethoxyapigeninApigenin-4',7-di-O-methyl ether, 4',7-Dimethylapigenin, 4H-1-Benzopyran-4-one, 5-hydroxy-7-methoxy-2-(4-methoxyphenyl)-, 4H-1-Benzopyran-4-one, 5-hydroxy-7-methoxy-2-(4-methoxyphenyl)- (9CI), 4′,7-Di-O-methylapigenin, 4′,7-Dimethylapigenin, 4′-Methoxytectochrysin, 5-Hydroxy-4',7-dimethoxyflavone, 5-Hydroxy-4′,7-dimethoxyflavone, 5-Hydroxy-7,4′-dimethoxyflavone, 5-Hydroxy-7-methoxy-2-(4-methoxyphenyl)-4H-1-benzopyran-4-one, 5-hydroxy-7-methoxy-2-(4-methoxyphenyl)-4H-chromen-4-one, 7,4′-Di-O-methylapigenin, 7,4′-Dimethylapigenin, 7-Methylacacetin, 7-O-Methylacacetin, Acacetin 7-methyl ether, Apigenin 4',7-dimethyl ether, Apigenin 4′,7-dimethyl ether, Apigenin 7,4'-dimethyl ether, Apigenin dimethyl ether, Apigenin dimethylether, Flavone, 5-hydroxy-4',7-dimethoxy- (8CI), Flavone, 5-hydroxy-4,7-dimethoxy-, Genkwanin 4'-methyl ether, Nsc 94547, 5-Hydroxy-7-methoxy-2-(4-methoxyphenyl)-4-benzopyrone

Description

Acacetin 7-O-methyl ether is a natural compound belonging to the class of phenylpropanoids. It has been found to be active against cancer cells and has been shown to inhibit the proliferation of endothelial cells. Acacetin 7-O-methyl ether inhibits the growth of cervical cancer cells by preventing their proliferation. This compound also reacts with light, releasing energy that can be used in chemical reactions. Acacetin 7-O-methyl ether is structurally similar to protocatechuic acid, a phenolic compound found in plants such as etoac extract and acetate extract.

• Marque: Biosynth

Propriétés chimiques

• Masse moléculaire: 298.29 g/mol
• Formule: C₁₇H₁₄O₅
• Degré de pureté: Min. 95%
• Couleur/Forme: White Powder
• InChI: InChI=1S/C17H14O5/c1-20-11-5-3-10(4-6-11)15-9-14(19)17-13(18)7-12(21-2)8-16(17)22-15/h3-9,18H,1-2H3
• Code InChI: InChIKey=LZERJKGWTQYMBB-UHFFFAOYSA-N
• SMILES: COc1ccc(-c2cc(=O)c3c(O)cc(OC)cc3o2)cc1