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