Rosinidin
Names
IUPAC name
3,4′,5-Trihydroxy-3′,7-dimethoxyflavylium
Systematic IUPAC name
3,5-Dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-7-methoxy-1λ4-benzopyran-1-ylium
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
  • Oc1cc2c(O)cc(OC)cc2[o+]c1c3cc(OC)c(O)cc3
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 derived from Cyanidin. 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.
  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

External links

Anthocyanidins and their anthocyanin glucosides
Category