Apiforol

Apiforol
Names

IUPAC name (2S)-2-(4-hydroxyphenyl)-3,4-dihydro-2H-chromene-4,5,7-triol
Identifiers
CAS Number	55167-29-8^Y
ChEBI	CHEBI:74812^N
ChemSpider	391780^Y
Jmol interactive 3D	Image Image
PubChem	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	274.26 g/mol
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
N verify (what is ^YN ?)
Infobox references

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

Types of flavan-4-ols

Flavan-4-ols:	Apiforol Luteoforol

Glycosides	abacopterins A B C D Triphyllin A 6,8-dimethyl-7-hydroxy-4‘-methoxyanthocyanidin-5-O-β-d-glucopyranoside

This article is issued from Wikipedia - version of the Saturday, November 28, 2015. The text is available under the Creative Commons Attribution/Share Alike but additional terms may apply for the media files.