Hypolaetin
Chemical structure of hypolaetin.
Names
IUPAC name
3′,4′,5,7,8-Pentahydroxyflavone
Systematic IUPAC name
2-(3,4-Dihydroxyphenyl)-5,7,8-trihydroxy-4H-1-benzopyran-4-one
Other names
8-Hydroxyluteolin
Identifiers
3D model (JSmol)
ChemSpider
UNII
  • InChI=1S/C15H10O7/c16-7-2-1-6(3-8(7)17)12-5-10(19)13-9(18)4-11(20)14(21)15(13)22-12/h1-5,16-18,20-21H
    Key: ASOIXDIITRKTOX-UHFFFAOYSA-N
  • InChI=1/C15H10O7/c16-7-2-1-6(3-8(7)17)12-5-10(19)13-9(18)4-11(20)14(21)15(13)22-12/h1-5,16-18,20-21H
    Key: ASOIXDIITRKTOX-UHFFFAOYAN
  • C1=CC(=C(C=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)O)O)O
Properties
C15H10O7
Molar mass 302.23 g/mol
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

Hypolaetin is a flavone. It is the aglycone of hypolaetin 8-glucuronide, a compound found in the liverwort Marchantia berteroana.[1] Hypolaetin 8-glucoside can be found in Sideritis leucantha.[2]

References

  1. ^ Isoscutellarein and hypolaetin 8-glucuronides from the liverwort Marchantia berteroana. Kenneth R. Markham and Lawrence J. Porter, Phytochemistry, April 1975, Volume 14, Issue 4, Pages 1093–1097, doi:10.1016/0031-9422(75)85194-6
  2. ^ Hypolaetin 8-glucoside from Sideritis leucantha. Francisco Tomas, Bernard Voirina, Francisco A.T. Barberan and Philippe Lebreton, Phytochemistry, 1985, Volume 24, Issue 7, Pages 1617–1618, doi:10.1016/S0031-9422(00)81082-1
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