Apiforol

Apiforol  Error creating thumbnail: Unable to save thumbnail to destination

Names
IUPAC name

(2S)-2-(4-Hydroxyphenyl)-3,4-dihydro-2H-chromene-4,5,7-triol

Identifiers

CAS Number

* 55167-29-8 Y

3D model (JSmol)

* Interactive image
* Interactive image

ChEBI |

* CHEBI:74812 N

ChemSpider |

* 391780 Y

KEGG |

* C12124

PubChem CID

* 443638

InChI

* 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 Y

Key: RPKUCYSGAXIESU-ABLWVSNPSA-N Y

SMILES

* 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

Chemical formula

| C15H14O5
Molar mass | 274.272 g·mol−1

Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

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Infobox references

Tracking categories (test):

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

## Metabolism

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

1. ↑ 1.0 1.1 EC 1.1.1.234 - flavanone 4-reductase on brenda-enzymes.org
2. ↑ Mizuno, Hiroshi; Yazawa, Takayuki; Kasuga, Shigemitsu; Sawada, Yuji; Kanamori, Hiroyuki; Ogo, Yuko; Hirai, Masami Yokota; Matsumoto, Takashi et al. (2016). "Expression of Flavone Synthase II and Flavonoid 3′-Hydroxylase Is Associated with Color Variation in Tan-Colored Injured Leaves of Sorghum". Frontiers in Plant Science 7: 1718. doi:10.3389/fpls.2016.01718. ISSN 1664-462X. PMID 27917182.

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*[CID]: Compound ID