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Agnuside

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Agnuside
Names
IUPAC name pyran-7-yl]methyl 4-hydroxybenzoate
Systematic IUPAC name oxy}-1,4a,5,7a-tetrahydrocyclopentapyran-7-yl]methyl 4-hydroxybenzoate
Identifiers
CAS Number
3D model (JSmol)
ChEBI
ChemSpider
ECHA InfoCard 100.208.702 Edit this at Wikidata
KEGG
PubChem CID
UNII
CompTox Dashboard (EPA)
InChI
  • InChI=1S/C22H26O11/c23-8-15-17(26)18(27)19(28)22(32-15)33-21-16-11(7-14(25)13(16)5-6-30-21)9-31-20(29)10-1-3-12(24)4-2-10/h1-7,13-19,21-28H,8-9H2/t13-,14+,15+,16+,17+,18-,19+,21-,22-/m0/s1Key: GLACGTLACKLUJX-QNAXTHAFSA-N
  • InChI=1/C22H26O11/c23-8-15-17(26)18(27)19(28)22(32-15)33-21-16-11(7-14(25)13(16)5-6-30-21)9-31-20(29)10-1-3-12(24)4-2-10/h1-7,13-19,21-28H,8-9H2/t13-,14+,15+,16+,17+,18-,19+,21-,22-/m0/s1Key: GLACGTLACKLUJX-QNAXTHAFBH
SMILES
  • C1=CO(21(C=C2COC(=O)C3=CC=C(C=C3)O)O)O4((((O4)CO)O)O)O
Properties
Chemical formula C22H26O11
Molar mass 466.439 g·mol
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). Infobox references
Chemical compound

Agnuside is a chemical compound found in Vitex agnus-castus. Agnuside is the ester of aucubin and p-hydroxybenzoic acid.

References

  1. Eva Hoberg, Beat Meier and Otto Sticher (September–October 2000). "An analytical high performance liquid chromatographic method for the determination of agnuside and p-hydroxybenzoic acid contents in Agni-casti fructose". Phytochemical Analysis. 11 (5): 327–329. doi:10.1002/1099-1565(200009/10)11:5<327::AID-PCA523>3.0.CO;2-0.
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