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7,3',4'-Trihydroxy-3-benzyl-2H-chroMene

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7,3',4'-Trihydroxy-3-benzyl-2H-chroMene Basic information

Product Name:
7,3',4'-Trihydroxy-3-benzyl-2H-chroMene
Synonyms:
  • 4-((7-Hydroxy-2H-chroMen-3-yl)Methyl)benzene-1,2-diol
  • 1,2-Benzenediol, 4-[(7-hydroxy-2H-1-benzopyran-3-yl)methyl]-
  • benzyl-2H-chromene7,3',4'-Trihydroxy-3-
  • 4-[(7-Hydroxy-2H-1-benzopyran-3-yl)methyl]-1,2-benzenediol
  • 4'-Trihydroxy-3-benzyl-2H-chromene
  • 7,3',4'-Trihydroxy-3-benzyl-2H-chromene
  • 7,3',4'-Trihydroxy-3-benzyl-2H-chromene
CAS:
1111897-60-9
MF:
C16H14O4
MW:
270.27996
Mol File:
1111897-60-9.mol
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7,3',4'-Trihydroxy-3-benzyl-2H-chroMene Chemical Properties

Boiling point:
540.8±50.0 °C(Predicted)
Density 
1.406±0.06 g/cm3(Predicted)
pka
9.75±0.20(Predicted)
form 
Solid
color 
Brown to black
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7,3',4'-Trihydroxy-3-benzyl-2H-chroMene Usage And Synthesis

Uses

7,3',4'-Trihydroxy-3-benzyl-2H-chromene is an reversible noncompetitive neuraminidase (NA) inhibitor. 7,3',4'-Trihydroxy-3-benzyl-2H-chromene can be isolated from the dried heartwood of Caesalpinia sappan L. 7,3',4'-Trihydroxy-3-benzyl-2H-chromene has potent NAs inhibitory activities with IC50 values of 34.6 μM [H1N1], 39.5 μM [H3N2], and 50.5μM [H9N2], respectively. 7,3',4'-Trihydroxy-3-benzyl-2H-chromene can be used for the research of influenza virus[1][2].

References

[1] Hyung Jae Jeong, et al. Homoisoflavonoids from Caesalpinia sappan displaying viral neuraminidases inhibition. Biol Pharm Bull. 2012;35(5):786-90. DOI:10.1248/bpb.35.786
[2] Huanxin Zhao, et al. A new homoisoflavan from Caesalpinia sappan. J Nat Med. 2008 Jul;62(3):325-7. DOI:10.1007/s11418-008-0231-6

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