| Identification | Back Directory | [Name]
LUTEOLIN-3',7-DI-O-GLUCOSIDE | [CAS]
52187-80-1 | [Synonyms]
LUTEOLIN-7,3'-DIGLUCOSIDE
LUTEOLIN-3',7-DIGLUCOSIDE
LUTEOLIN-3',7-DI-O-GLUCOSIDE
LUTEOLIN-7,3'-DI-O-GLUCOSIDE
Luteolin 3′,7-O- diglucoside
Luteolin-7,3'-di-O-gflucoside
LUTEOLIN-3'',7-DIGLUCOSIDE hplc
LUTEOLIN-7,3''-DIGLUCOSIDE WITH HPLC
LUTEOLIN-7,3''-DI-O-GLUCOSIDE WITH HPLC
2-(3-β-D-Glucopyranosyloxy-4-hydroxyphenyl)-7-(β-D-glucopyranosyloxy)-5-hydroxy-4H-1-benzopyran-4-one
7-(β-D-Glucopyranosyloxy)-2-[3-(β-D-glucopyranosyloxy)-4-hydroxyphenyl]-5-hydroxy-4H-1-benzopyran-4-one
4H-1-Benzopyran-4-one,7-(b-D-glucopyranosyloxy)-2-[3-(b-D-glucopyranosyloxy)-4-hydroxyphenyl]-5-hydroxy-
4H-1-Benzopyran-4-one, 7-(β-D-glucopyranosyloxy)-2-[3-(β-D-glucopyranosyloxy)-4-hydroxyphenyl]-5-hydroxy-
7-(beta-D-glucopyranosyloxy)-2-[3-(beta-D-glucopyranosyloxy)-4-hydroxyphenyl]-5-hydroxy-4H-1-benzopyran-4-one
5-hydroxy-2-[4-hydroxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one
5-hydroxy-2-[4-hydroxy-3-[[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)-2-oxanyl]oxy]phenyl]-7-[[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)-2-oxanyl]oxy]-1-benzopyran-4-one | [EINECS(EC#)]
257-724-7 | [Molecular Formula]
C27H30O16 | [MDL Number]
MFCD00017467 | [MOL File]
52187-80-1.mol | [Molecular Weight]
610.52 |
| Chemical Properties | Back Directory | [Melting point ]
220-250°C | [Boiling point ]
998.0±65.0 °C(Predicted) | [density ]
1.742±0.06 g/cm3(Predicted) | [pka]
6.09±0.40(Predicted) | [LogP]
-3.490 (est) |
| Hazard Information | Back Directory | [Uses]
Luteolin-3′,7-diglucoside is a glycoside that can be isolated from R. luteolin. Luteolin-3′,7-diglucoside significantly inhibits cataracts induced in ovine lenses. Luteolin-3′,7-diglucoside inhibits the activity of Ureaplasma urealyticumATCC and clinical strains[1][2][3]. | [Definition]
ChEBI:Luteolin-3',7-di-O-glucoside is a member of flavonoids and a glycoside. | [References]
[1] Cristea D, et al. Identification and quantitative HPLC analysis of the main flavonoids present in weld (Reseda luteola L.)[J]. Dyes and Pigments, 2003, 57(3): 267-272.
[2] Vit P, et al. Putative anticataract properties of honey studied by the action of flavonoids on a lens culture model[J]. Journal of Health Science, 2008, 54(2): 196-202.
[3] Bisignano C, et al. In Vitro Efficacy of Crataegus oxycantha L.(Hawthorn) and Its Major Components against ATCC and Clinical Strains of Ureaplasma urealyticum[J]. Advances in Microbiology, 2016, 6(12): 909-916. |
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