Scutellarein

Scutellarein
Ball-and-stick model of scutellarein
Names
IUPAC name
4′,5,6,7-Tetrahydroxyflavone
Systematic IUPAC name
5,6,7-Trihydroxy-2-(4-hydroxyphenyl)-4H-1-benzopyran-4-one
Other names
6-Hydroxyapigenin
Identifiers
CAS Number
  • 529-53-3 checkY
3D model (JSmol)
  • Interactive image
ChEBI
  • CHEBI:9062 ☒N
ChEMBL
  • ChEMBL55415 ☒N
ChemSpider
  • 4445014 ☒N
PubChem CID
  • 5281697
UNII
  • P460GTI853 checkY
CompTox Dashboard (EPA)
  • DTXSID40200946 Edit this at Wikidata
InChI
  • InChI=1S/C15H10O6/c16-8-3-1-7(2-4-8)11-5-9(17)13-12(21-11)6-10(18)14(19)15(13)20/h1-6,16,18-20H ☒N
    Key: JVXZRQGOGOXCEC-UHFFFAOYSA-N ☒N
  • InChI=1/C15H10O6/c16-8-3-1-7(2-4-8)11-5-9(17)13-12(21-11)6-10(18)14(19)15(13)20/h1-6,16,18-20H
    Key: JVXZRQGOGOXCEC-UHFFFAOYAD
  • C13=C(OC(=CC1=O)C2=CC=C(O)C=C2)C=C(O)C(=C3O)O
Properties
Chemical formula
C15H10O6
Molar mass 286.241 g/mol
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Infobox references
Chemical compound

Scutellarein is a flavone that can be found in Scutellaria lateriflora and other members of the genus Scutellaria, as well as the fern Asplenium belangeri.[1]

Glycosides

The scutellarin (Scutellarein-7-glucuronide) is transformed by hydrolysis into scutellarein.

References

  1. ^ UmiKalsom, Yusuf; Harborne, Jeffrey B. (1991). "Flavonoid distribution in asplenioid ferns". Pertanika. 14 (3): 297–300.
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Flavones and their conjugates
Aglycones
Monohydroxyflavone
Dihydroxyflavones
Trihydroxyflavones
Tetrahydroxyflavones
Pentahydroxyflavones
O-methylated flavones
Glycosides
of apigenin
of baicalein
of hypolaetin
  • Hypolaetin 8-glucoside
  • Hypolaetin 8-glucuronide
of luteolin
Acetylated
  • Artocarpetin A
  • Artoindonesianin P
  • Sulfated glycosidesPolymersDrugs
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