Annulatin

Last updated
Annulatin
Chemical structure of annulatin Annulatin.svg
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
3D model (JSmol)
ChemSpider
PubChem CID
UNII
  • 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,1H3 Yes check.svgY
    Key: XWTLYULBWZQAAZ-UHFFFAOYSA-N Yes check.svgY
  • 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,1H3
    Key: XWTLYULBWZQAAZ-UHFFFAOYAS
  • COc1c(=O)c2c(cc(cc2oc1c3cc(c(c(c3)O)O)O)O)O
Properties
C16H12O8
Molar mass 332.264 g·mol−1
Density 1.807 g/mL
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Yes check.svgY  verify  (what is  Yes check.svgYX mark.svgN ?)

Annulatin is an O-methylated flavonol found in the roots of Pteroxygonum giraldii . [1]

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.
This page is based on this Wikipedia article
Text is available under the CC BY-SA 4.0 license; additional terms may apply.
Images, videos and audio are available under their respective licenses.