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Rosinidin

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Rosinidin
Names
IUPAC name
2-(4-Hydroxy-3-methoxyphenyl)-7-methoxychromenylium-3,5-diol
Other names
2-(4-Hydroxy-3-methoxy-phenyl)-7-methoxy-chromene-3,5-diol
Identifiers
3D model (JSmol)
ChEBI
ChemSpider
  • InChI=1S/C17H14O6/c1-21-10-6-13(19)11-8-14(20)17(23-15(11)7-10)9-3-4-12(18)16(5-9)22-2/h3-8H,1-2H3,(H2-,18,19,20)/p+1 ☒N
    Key: GNONHFYAESLOCB-UHFFFAOYSA-O ☒N
  • InChI=1/C17H14O6/c1-21-10-6-13(19)11-8-14(20)17(23-15(11)7-10)9-3-4-12(18)16(5-9)22-2/h3-8H,1-2H3,(H2-,18,19,20)/p+1
    Key: GNONHFYAESLOCB-IKLDFBCSAN
  • COC1=CC2=[O+]C(=C(C=C2C(=C1)O)O)C3=CC(=C(C=C3)O)OC
Properties
C17H15O6+
Molar mass 315.30 g/mol
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
☒N verify (what is checkY☒N ?)

Rosinidin is an O-methylated anthocyanidin. It is a pigment found in the flowers of Catharanthus roseus[1] and, in lower concentration, in Primula rosea.[2]

References

  1. ^ Toki K, Saito N, Irie Y, Tatsuzawa F, Shigihara A, Honda T (March 2008). "7-O-Methylated anthocyanidin glycosides from Catharanthus roseus". Phytochemistry. 69 (5): 1215–9. doi:10.1016/j.phytochem.2007.11.005. PMID 18164044.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  2. ^ The Structure and Distribution of the Flavonoids in Plants. Tsukasa Iwashina, Journal of Plant Research, 2000, Volume 113, Number 3, pages 287-299, doi:10.1007/PL00013940