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5-Hydroxy-3',4',7-trimethoxyflavone

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5-Hydroxy-3',4',7-trimethoxyflavone Basic information

Product Name:
5-Hydroxy-3',4',7-trimethoxyflavone
Synonyms:
  • 4H-1-Benzopyran-4-one, 2-(3,4-diMethoxyphenyl)-5-hydroxy-7-Methoxy-
  • Gonzalitosin I
  • Luteolin 7,3',4'-trimethyl ether
  • 2-(3,4-DiMethoxyphenyl)-5-hydroxy-7-Methoxy-4H-chroMen-4-one
  • 7,3',4'-Tri-O-methylluteolin (5-Hydroxy-3',4',7-trimethoxyflavone)
  • 2-(3,4-dimethoxyphenyl)-5-hydroxy-7-methoxychromen-4-one
  • Rutoside Trihydrate Impurity 12
  • COX,TNFR,7,3',4'TriOmethylluteolin,lipopolysaccharide,Tumor Necrosis Factor Receptor,Inflammation-related diseases,pro-inflammatory cytokines,RAW 264.7 macrophage,Interleukin Related,inhibit,TNF Receptor,Cyclooxygenase,7,3',4' Tri O methylluteolin,Inhibitor
CAS:
29080-58-8
MF:
C18H16O6
MW:
328.32
Mol File:
29080-58-8.mol
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5-Hydroxy-3',4',7-trimethoxyflavone Chemical Properties

Melting point:
163 °C
Boiling point:
536.3±50.0 °C(Predicted)
Density 
1.314±0.06 g/cm3(Predicted)
storage temp. 
2-8°C
solubility 
Soluble in DMSO
pka
6.32±0.40(Predicted)
form 
Solid
color 
White to yellow
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5-Hydroxy-3',4',7-trimethoxyflavone Usage And Synthesis

Uses

7,3',4'-Tri-O-methylluteolin (5-Hydroxy-3',4',7-trimethoxyflavone), a flavonoid compound, possesses potent anti-inflammatory effects in LPS-induced macrophage cell line mediated by inhibition of release of inflammatory mediators, NO, PGE2, and pro-inflammatory cytokines. 7,3',4'-Tri-O-methylluteolin significantly induces reduction in the mRNA expressions of inducible nitric oxide synthase and cyclooxygenase-2[1].

IC 50

IL-6; IL-1β; COX-2

References

[1] Sudha, A, et al. Protective effect of 5-hydroxy-3′,4′,7-trimethoxyflavone against inflammation induced by lipopolysaccharide in RAW 264.7 macrophage: in vitro study and in silico validation. Medicinal Chemistry Research, 2016,25(9), 1754–1767.

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