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2',7-DIHYDROXY-4'-METHOXYISOFLAVAN

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2',7-DIHYDROXY-4'-METHOXYISOFLAVAN Basic information

Product Name:
2',7-DIHYDROXY-4'-METHOXYISOFLAVAN
Synonyms:
  • VESTITOL
  • 2',7-DIHYDROXY-4'-METHOXYISOFLAVAN
  • 3-(2-Hydroxy-4-methoxyphenyl)-7-chromanol
  • 3-(2-Hydroxy-4-methoxyphenyl)-3,4-dihydro-2H-1-benzopyran-7-ol
  • 3-(2-Hydroxy-4-methoxyphenyl)chroman-7-ol
  • 3,4-Dihydro-3-(2-hydroxy-4-methoxyphenyl)-2H-1-benzopyran-7-ol
  • 2H-1-Benzopyran-7-ol, 3,4-dihydro-3-(2-hydroxy-4-methoxyphenyl)-
  • VESTITOL(RG)(PLEASE CALL)
CAS:
56701-24-7
MF:
C16H16O4
MW:
272.3
Product Categories:
  • Iso-Flavones
Mol File:
56701-24-7.mol
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2',7-DIHYDROXY-4'-METHOXYISOFLAVAN Chemical Properties

Melting point:
172-179℃
Boiling point:
418.5±45.0 °C(Predicted)
Density 
1.282±0.06 g/cm3(Predicted)
storage temp. 
Inert atmosphere,Store in freezer, under -20°C
solubility 
DMSO: 2mg/mL, clear
form 
powder
pka
9.53±0.40(Predicted)
color 
white to beige
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2',7-DIHYDROXY-4'-METHOXYISOFLAVAN Usage And Synthesis

Uses

Vestitol is the compound isolated from leaves of Trifolium arvense[1].

Definition

ChEBI: Vestitol is a member of the class of hydroxyisoflavans that is isoflavan substituted by hydroxy groups at positions 7 and 2' and a methoxy group at position 4'. Isolated from Glycyrrhiza uralensis, it exhibits anti-inflammatory activity. It has a role as an anti-inflammatory agent, a plant metabolite and a phytoalexin. It is an aromatic ether, a member of hydroxyisoflavans and a methoxyisoflavan.

Biological Activity

Hydroxyisoflavan isolated from Cuban and Brazilian red propolis th at exhibits potent anti-inflammatory, anti-viral, and antiparasitic activities.

(±)-Vestitol is a hydroxyisoflavan isolated from Cuban and Brazilian red propolis, licorice root and other sources th at exhibits potent anti-inflammatory, anti-viral, and antiparasitic activities. Apparently Vestitol inhibits release of the chemokines CXCL1/KC and CXCL2/MIP-2 from macrophages. Vestitol strongly inhibits Chikungunya virus infection. Vestitol exhibits anti-trypanosomal activity against T. brucei and T. congolense (EC50 3.86 and 4.36 μg/ml).

References

[1] John L. Ingham, et al. Notizen: Isoflavonoid Phytoalexins from Leaves of Trifolium arvense.

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