Luteolin-4'-O-glucoside

CAS: 6920-38-3

Ref. 3D-FL137961

Produktinformation

• Name: Luteolin-4'-O-glucoside
• Synonyme: 3',4',5,7-Tetrahydroxyflavone-4'-glucoside, 2-[4-(β-<span class="text-smallcaps">D</span>-Glucopyranosyloxy)-3-hydroxyphenyl]-5,7-dihydroxy-4H-1-benzopyran-4-one, 3′,4′,5,7-Tetrahydroxyflavone 4′-β-<span class="text-smallcaps">D</span>-glucoside, 4-(5,7-Dihydroxy-4-oxo-4H-chromen-2-yl)-2-hydroxyphenyl b-D-glucopyranoside, 4H-1-Benzopyran-4-one, 2-[4-(β-<span class="text-smallcaps">D</span>-glucopyranosyloxy)-3-hydroxyphenyl]-5,7-dihydroxy-, 4H-1-benzopyran-4-one, 2-[4-(beta-D-glucopyranosyloxy)-3-hydroxyphenyl]-5,7-dihydroxy-, 4′-β-<span class="text-smallcaps">D</span>-Glucosylluteolin, 5,7-Dihydroxy-2-(3-hydroxy-4-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl]oxy}phenyl)-4H-chromen-4-on, 5,7-Dihydroxy-2-(3-hydroxy-4-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl]oxy}phenyl)-4H-chromen-4-one, Flavone, 3′,4′,5,7-tetrahydroxy-, 4′-β-<span class="text-smallcaps">D</span>-glucopyranoside, Glucopyranoside, luteolin-4′, β-<span class="text-smallcaps">D</span>-, Juncein, Luteolin 4′-O-glucoside, Luteolin 4′-O-β-<span class="text-smallcaps">D</span>-glucopyranoside, Luteolin 4′-O-β-<span class="text-smallcaps">D</span>-glucoside, Luteolin-4'-glucoside, bêta-D-Glucopyranoside de 4-(5,7-dihydroxy-4-oxo-4H-chromén-2-yl)-2-hydroxyphényle, 4-(5,7-Dihydroxy-4-oxo-4H-chromen-2-yl)-2-hydroxyphenyl-beta-D-glucopyranoside, Flavone, 3′,4′,5,7-tetrahydroxy-, 4′-β-D-glucopyranoside, 4-(5,7-Dihydroxy-4-oxo-4H-chromen-2-yl)-2-hydroxyphenyl beta-D-glucopyranoside, 4H-1-Benzopyran-4-one, 2-[4-(β-D-glucopyranosyloxy)-3-hydroxyphenyl]-5,7-dihydroxy-, 2-[4-(β-D-Glucopyranosyloxy)-3-hydroxyphenyl]-5,7-dihydroxy-4H-1-benzopyran-4-one, Glucopyranoside, luteolin-4′, β-D-

Beschreibung

Luteolin-4'-O-glucoside is a flavonol glycoside that is found in plants such as licorice, celery, and parsley. Luteolin-4'-O-glucoside has been shown to inhibit the growth of Coccidioides neoformans by binding to the cell membrane surface and blocking the synthesis of phospholipids. It also inhibits cancer cells in culture by reducing their viability. The structural analysis of luteolin-4'-O-glucoside revealed an hydroxyl group on its aromatic ring, which may be responsible for its anti-inflammatory effects. Luteolin-4'-O-glucoside has been shown to be effective against inflammatory diseases, such as rheumatoid arthritis and asthma, and may also have a protective effect against certain types of cancer, such as cervical cancer. Luteolin-4'-O-glucoside has also been shown to

• Marke: Biosynth

Chemische Eigenschaften

• Molekulargewicht: 448.38 g/mol
• Formel: C₂₁H₂₀O₁₁
• Reinheit: Min. 95%
• Farbe/Form: Powder