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Apiin

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Apiin
Apigenin
Names
IUPAC name
7-[(2S,3R,4S,5S,6R)-3-[(2S,3R,4R)-3,4-Dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5-hydroxy-2-(4-hydroxyphenyl)chromen-4-one
Other names
Apioside
Apigenin-7-apioglucoside
Apigenin-7-O-apioglucoside
Identifiers
3D model (JSmol)
ChEBI
ChEMBL
ChemSpider
ECHA InfoCard 100.043.421 Edit this at Wikidata
  • InChI=1S/C26H28O14/c27-8-18-20(32)21(33)22(40-25-23(34)26(35,9-28)10-36-25)24(39-18)37-13-5-14(30)19-15(31)7-16(38-17(19)6-13)11-1-3-12(29)4-2-11/h1-7,18,20-25,27-30,32-35H,8-10H2/t18-,20-,21+,22-,23+,24-,25+,26-/m1/s1 checkY
    Key: NTDLXWMIWOECHG-YRCFQSNFSA-N checkY
  • O=C\4c5c(O)cc(O[C@@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O[C@@H]1OC[C@](O)(CO)[C@H]1O)cc5O/C(c3ccc(O)cc3)=C/4
Properties
C26H28O14
Molar mass 564.496 g·mol−1
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 ?)

Apiin is a natural flavonoid, a diglycoside of the flavone apigenin found in the winter-hardy plants parsley[1] and celery.[2] The glycoside moity at carbon-7 of apiin, O-β-D-apiofuranosyl(→)2-β-D-glucosyl, is carried by several other flavones in parsley plant and seed.[3] The sugar apiose possibly play a role in winter hardiness of celery, duckweed and parsley.[4]

See also

References

  1. ^ H. Meyer; A. Bolarinwa; G. Wolfram; J. Linseisen (2006). "Bioavailability of Apigenin from Apiin-Rich Parsley in Humans". Ann Nutr Metab. 50 (3): 167–172. doi:10.1159/000090736. PMID 16407641.
  2. ^ S. R. Gupta. "A study of apiin from the parsley seeds and plant". doi:10.1007/BF03172503. Retrieved 12 October 2014. {{cite journal}}: Cite journal requires |journal= (help)
  3. ^ page 245 "Methods in plant biochemistry" volume 2: "Carbohydrates", ISBN 0080984207
  4. ^ page 136 "Advances in Carbohydrate Chemistry and Biochemistry", Volume 31, ISBN 0080562906



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