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Annulatin

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Annulatin
Chemical structure of annulatin
Chemical structure of annulatin
Names
IUPAC name 3′,4′,5,5′,7-Pentahydroxy-3-methoxyflavone
Systematic IUPAC name 5,7-Dihydroxy-3-methoxy-2-(3,4,5-trihydroxyphenyl)-4H-1-benzopyran-4-one
Other names Myricetin 3-Methylether
Identifiers
CAS Number
3D model (JSmol)
ChemSpider
PubChem CID
UNII
CompTox Dashboard (EPA)
InChI
  • InChI=1S/C16H12O8/c1-23-16-14(22)12-8(18)4-7(17)5-11(12)24-15(16)6-2-9(19)13(21)10(20)3-6/h2-5,17-21H,1H3Key: XWTLYULBWZQAAZ-UHFFFAOYSA-N
  • InChI=1/C16H12O8/c1-23-16-14(22)12-8(18)4-7(17)5-11(12)24-15(16)6-2-9(19)13(21)10(20)3-6/h2-5,17-21H,1H3Key: XWTLYULBWZQAAZ-UHFFFAOYAS
SMILES
  • COc1c(=O)c2c(cc(cc2oc1c3cc(c(c(c3)O)O)O)O)O
Properties
Chemical formula C16H12O8
Molar mass 332.264 g·mol
Density 1.807 g/mL
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). checkverify (what is  ?) Infobox references
Chemical compound

Annulatin is an O-methylated flavonol found in the roots of Pteroxygonum giraldii.

References

  1. Li, Bao-Lin; Yang, Zhan-Jun; Jiang, Lin-Ling; Zhang, Xi-Quan; Gu, Hong-Mei; Wang, Hui-Chun; Tian, Xian-Hua (2009). "ChemInform Abstract: Antioxidant Flavone Glycosides from the Root of Pteroxygonum giraldii". ChemInform. 40 (49). doi:10.1002/chin.200949203.
Flavonols and their conjugates
Backbone
Aglycones
Flavonols
Aglycones
Conjugates
Glycosides of herbacetin
Glycosides of kaempferol
Glycosides of myricetin
Conjugates of quercetin
Sulfates
Glycosides
O-Methylated flavonols
Aglycones
Glycosides
of isorhamnetin
other
Derivative flavonols
Aglycones
Glycosides
Pyranoflavonols
Aglycones
Furanoflavonols
Aglycones
Glycosides
Semisynthetic
Glycosides
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