Brickellin

Brickellin
Names
IUPAC name
2′,5-Dihydroxy-3,4′,5′,6,7-pentamethoxyflavone
Systematic IUPAC name
5-Hydroxy-2-(2-hydroxy-4,5-dimethoxyphenyl)-3,6,7-trimethoxy-4H-1-benzopyran-4-one
Identifiers
3D model (JSmol)
ChEMBL
ChemSpider
UNII
  • InChI=1S/C20H20O9/c1-24-11-6-9(10(21)7-12(11)25-2)18-20(28-5)17(23)15-13(29-18)8-14(26-3)19(27-4)16(15)22/h6-8,21-22H,1-5H3 Y
    Key: USWPTYUGAMOLAB-UHFFFAOYSA-N Y
  • InChI=1/C20H20O9/c1-24-11-6-9(10(21)7-12(11)25-2)18-20(28-5)17(23)15-13(29-18)8-14(26-3)19(27-4)16(15)22/h6-8,21-22H,1-5H3
    Key: USWPTYUGAMOLAB-UHFFFAOYAR
  • COc3cc(C=1Oc2cc(OC)c(OC)c(O)c2C(=O)C=1OC)c(O)cc3OC
Properties
C20H20O9
Molar mass 404.371 g·mol−1
Density 1.443 g/mL
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
N verify (what is YN ?)
Infobox references

Brickellin is an O-methylated flavonol.[1] It can be found in Brickellia veronicifolia.[2]

References

  1. ^ Iinuma, M (1985). "Synthesis and revised structure of the flavone brickellin". Phytochemistry. 24 (6): 1367–1368. Bibcode:1985PChem..24.1367I. doi:10.1016/S0031-9422(00)81135-8.
  2. ^ Brickellin, a novel flavone from Brickellia veronicaefolia and B. chlorolepis. Roberts M. F., Timmermann B. N., Mabry T. J., Brown R. and Matlin S. A., Phytochemistry, 1984, volume 23, no 1, pages 163-165, INIST 9471694
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