Names | |
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IUPAC name
(2S)-2-(4-Hydroxyphenyl)-3,4-dihydro-2H-chromene-4,5,7-triol
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Identifiers | |
3D model (
JSmol)
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ChEBI | |
ChemSpider | |
KEGG | |
PubChem
CID
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CompTox Dashboard (
EPA)
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Properties | |
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).
|
Apiforol is a chemical compound belonging to the flavan-4ol class of flavonoids.
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]
Names | |
---|---|
IUPAC name
(2S)-2-(4-Hydroxyphenyl)-3,4-dihydro-2H-chromene-4,5,7-triol
| |
Identifiers | |
3D model (
JSmol)
|
|
ChEBI | |
ChemSpider | |
KEGG | |
PubChem
CID
|
|
CompTox Dashboard (
EPA)
|
|
| |
| |
Properties | |
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).
|
Apiforol is a chemical compound belonging to the flavan-4ol class of flavonoids.
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]