7-O-Methyl quercetin

CAS: 90-19-7

Ref. 3D-FM25558

Product Information

• Name: 7-O-Methyl quercetin
• Synonyms: 2-(3,4-Dihydroxyphenyl)-5,7-dihydroxy-y-methoxy-4H-1-benzopyran-4-oneRhamnetin3,3',4',5-Tetrahydroxy-7-methoxyflavone, 2-(3,4-Dihydroxyphenyl)-3,5-dihydroxy-7-methoxy-4H-1-benzopyran-4-one, 2-(3,4-Dihydroxyphenyl)-3,5-dihydroxy-7-methoxychromen-4-one, 2-(3,4-dihydroxyphenyl)-3,5-dihydroxy-7-methoxy-4H-chromen-4-one, 3,3′,4′,5-Tetrahydroxy-7-methoxyflavone, 3,5,3′,4′-Tetrahydroxy-7-methoxyflavone, 4H-1-Benzopyran-4-one, 2-(3,4-dihydroxyphenyl)-3,5-dihydroxy-7-methoxy-, 7-Methoxyquercetin, 7-Methylquercetin, 7-O-Methylquercetin, Flavone, 3,3′,4′,5-tetrahydroxy-7-methoxy-, Ly 805921, NSC 19802, Quercetin 7-methyl ether, Rhamnetin, β-Rhamnocitrin
• CAS: 90-19-7

Description

Quercetin is a flavonoid that belongs to the chemical class of polyphenols. It can be found in many plants, fruits, and vegetables. Quercetin has been shown to have anti-cancer properties in vitro assays and in vivo studies by inhibiting the proliferation of cancer cells. It also inhibits pro-inflammatory cytokines such as TNF-α. Quercetin has been shown to inhibit various enzyme activities, including those involved with hydrogen bonding interactions, cardiac effects, or natural compounds. The quercetin molecule contains a basic structure with six hydroxyl groups and three methoxy groups. One of these hydroxyl groups is esterified with an acetate group at position 3′ on the glucose ring (7-O-methyl quercetin). This esterification makes quercetin more lipophilic and increases its membrane permeability. 7-O-Methyl quercetin has been found to have anticancer

• Brand: Biosynth

Chemical properties

• Molecular weight: 316.26 g/mol
• Formula: C₁₆H₁₂O₇
• Purity: 90%
• Color/Form: Powder
• InChI: InChI=1S/C16H12O7/c1-22-8-5-11(19)13-12(6-8)23-16(15(21)14(13)20)7-2-3-9(17)10(18)4-7/h2-6,17-19,21H,1H3
• InChI key: InChIKey=JGUZGNYPMHHYRK-UHFFFAOYSA-N
• SMILES: COc1cc(O)c2c(=O)c(O)c(-c3ccc(O)c(O)c3)oc2c1