Trichome

Apiforol
Chemical structure of Apiforol.
Names
IUPAC name
(2S)-2-(4-hydroxyphenyl)-3,4-dihydro-2H-chromene-4,5,7-triol
Identifiers
3D model (JSmol)
ChemSpider
  • InChI=1S/C15H14O5/c16-9-3-1-8(2-4-9)13-7-12(19)15-11(18)5-10(17)6-14(15)20-13/h1-6,12-13,16-19H,7H2/t12?,13-/m0/s1
    Key: RPKUCYSGAXIESU-ABLWVSNPSA-N
  • C1C(C2=C(C=C(C=C2OC1C3=CC=C(C=C3)O)O)O)O
  • Oc1ccc(cc1)[C@H]3Oc2cc(O)cc(O)c2C(O)C3
Properties
C15H14O5
Molar mass 274.26 g/mol
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

Apiforol is a chemical compound belonging to the flavan-4ol class of flavonoids.

Metabolism

(2S)-flavan-4-ol:NADP+ 4-oxidoreductase (flavanone 4-reductase[1]) is an enzyme transforming Naringenin into apiforol[2]. This enzyme can be found in Columnea hybrida, in Malus domestica, in Pyrus communis, in Sinningia cardinalis, and in Zea mays[1].



References

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