General Information of Natural Product (ID: NP2053)
  Natural Product Name
Luteolin-7-o-glucuronide
  Synonyms
luteolin-7-o-glucuronide|Luteolin-7-beta-D-glucuronide|29741-10-4|Luteolin-7-glucuronide|BCP29714|2-(3,4-Dihydroxyphenyl)-5-hydroxy-4-oxo-4H-1-benzopyran-7-yl-|A-D-glucopyranosiduronic acid|3 inverted exclamation marka,4 inverted exclamation marka,5,7-Tetrahydroxy-7-|A-D-glucopyranuronoside flavone|6-[2-(3,4-dihydroxyphenyl)-5-hydroxy-4-oxochromen-7-yl]oxy-3,4,5-trihydroxyoxane-2-carboxylic acid|Luteolin-7-glucuronide;Luteolin 7-O-beta-D-glucuronopyranoside; Luteolin 7-O-beta-glucuronide;Luteolin 7-O-beta-glucuronopyranoside
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  Formula C21H18O12
  Weight 462.4
  Structure Could Not Find 2D Structure
3D Structure Download 2D Structure Download
  InChI InChI=1S/C21H18O12/c22-9-2-1-7(3-10(9)23)13-6-12(25)15-11(24)4-8(5-14(15)32-13)31-21-18(28)16(26)17(27)19(33-21)20(29)30/h1-6,16-19,21-24,26-28H,(H,29,30)
  InChI Key VSUOKLTVXQRUSG-UHFFFAOYSA-N
  Isomeric SMILES C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)C(=O)O)O)O)O)O)O)O
  Canonical SMILES C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)C(=O)O)O)O)O)O)O)O
  External Links PubChem ID 13607752
CAS ID 29741-10-4

 The Content Variation of Natural Product Induced by Different Factor(s)
      Species Name: Chrysanthemum morifolium Ram. cv. 'Gaya yellow'
  Factor Name: Photosynthetic Active Radiation Treatment [1]
              Species Info Factor Info
               Experiment Detail
After acclimation, the plants were grown independently in different light treatment chambers at 20 ± 0.2 &#8451 and 65 ± 2% humidity until the harvest date (35 days after light treatment). The white fluorescent light (70 ± 5 µmol/m2/s) was maintained for 12 h, and then each of the blue, green, red, and white lights was irradiated at 70 ± 5 µmol/m2/s for 4 h using LED arrays (DR LED Networks Co., Seoul, Republic of Korea). The spectral energy distribution of four different LED arrays was measured from 300 to 800 nm with a spectroradiometer (International Light, RPS-900, U.S.). Their maximum spectral wavelengths were 463 (blue), 518 (green), and 632 nm (red); the white LEDs had a broad spectrum. Irradiance was measured using a quantum sensor (LI-COR, LI-191, Lincoln, NE, U.S.). Water was supplied daily with top irrigation and a nutrient solution (Hoagland, pH = 5.9 ± 0.2, electrical conductivity = 1.2 dS/m) every 4 days until harvest.
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               Factor Function
A quantitation and principal component analysis biplot demonstrated that luteolin-7-O-glucoside (2), luteolin-7-O-glucuronide (3), and quercetagetin-trimethyl ether (8) were the highest polyphenols yielded under green light, and dicaffeoylquinic acid isomer (4), dicaffeoylquinic acid isomer (5), naringenin (7), and apigenin-7-O-glucuronide (6) were greatest under red light. Chlorogenic acid (1) and 1,2,6-trihydroxy-7,8-dimethoxy-3-methylanthraquinone (9) were produced in similar concentrations under both light types. The white and blue light appeared inefficient for polyphenol production.
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               Factor Part Location NP Content
 
Under blue light (spectral wavelengths: 463 nm)
leaf Korea
NP Content: 71.6 ± 1.0 mg/kg
 
Under green light (spectral wavelengths: 518 nm)
leaf Korea
NP Content: 145.1 ± 1.0 mg/kg
 
Under red light (spectral wavelengths: 632 nm)
leaf Korea
NP Content: 143.9 ± 2.2 mg/kg
 
Under white light (spectral wavelengths: broad spectrum)
leaf Korea
NP Content: 55.5 ± 0.7 mg/kg
References
1 Influences of four different light-emitting diode lights on flowering and polyphenol variations in the leaves of chrysanthemum (Chrysanthemum morifolium)