Vitexin

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Vitexin
Vitexin.svg
Names
Other names
Identifiers
3681-93-4 YesY
ChEBI CHEBI:16954 YesY
ChEMBL ChEMBL487417 YesY
ChemSpider 4444098 YesY
Jmol 3D model Interactive image
PubChem 5280441
  • InChI=1S/C21H20O10/c22-7-14-17(27)18(28)19(29)21(31-14)16-11(25)5-10(24)15-12(26)6-13(30-20(15)16)8-1-3-9(23)4-2-8/h1-6,14,17-19,21-25,27-29H,7H2/t14-,17-,18+,19-,21+/m1/s1 YesY
    Key: SGEWCQFRYRRZDC-VPRICQMDSA-N YesY
  • InChI=1/C21H20O10/c22-7-14-17(27)18(28)19(29)21(31-14)16-11(25)5-10(24)15-12(26)6-13(30-20(15)16)8-1-3-9(23)4-2-8/h1-6,14,17-19,21-25,27-29H,7H2/t14-,17-,18+,19-,21+/m1/s1
    Key: SGEWCQFRYRRZDC-VPRICQMDBU
  • O=C2\C=C(/Oc1c(c(O)cc(O)c12)[C@@H]3O[C@@H]([C@@H](O)[C@H](O)[C@H]3O)CO)c4ccc(O)cc4
Properties
C21H20O10
Molar mass 432.38 g/mol
Appearance Light yellow powder
Melting point 203 to 204 °C (397 to 399 °F; 476 to 477 K)
Vapor pressure {{{value}}}
Supplementary data page
Refractive index (n),
Dielectric constantr), etc.
Thermodynamic
data
Phase behaviour
solid–liquid–gas
UV, IR, NMR, MS
YesY verify (what is YesYN ?)
Infobox references

Vitexin is an apigenin flavone glucoside, a chemical compound found in the passion flower, Vitex agnus-castus (chaste tree or chasteberry), in the Phyllostachys nigra bamboo leaves,[1] in the pearl millet (Pennisetum millet),[2] and in Hawthorn.[citation needed]

Metabolism

Goitrogenicity of millet flavones : Vitexin inhibits thyroid peroxidase thus contributing to goiter.[3][4]

See also

Isovitexin (or homovitexin, saponaretin) is the apigenin-6-C-glucoside.

References

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External links