Structure via PubChem · Public domain (PubChem)
apiforol
Sign in to saveAlso known as flavan-4,4',5,7-tetrol, (2S)-apiforol, leucoapigeninidin
Apiforol is a chemical compound belonging to the flavan-4ol class of flavonoids.
In the Vinony graph
Vinony's link graph records 49 inbound references to apiforol, and connects out to (2S)-flavan-4-ol, maize and apple.
It is catalogued under topics including Chembox image size set, Chemical articles with multiple compound IDs and Flavan-4-ols.
Vinony links it to 6 Wikipedia language editions.
Chemical data
- Formula
- C15H14O5
- Molecular weight
- 274.27 g/mol
- IUPAC name
- (2S)-2-(4-hydroxyphenyl)-3,4-dihydro-2H-chromene-4,5,7-triol
- SMILES
- C1[C@H](OC2=CC(=CC(=C2C1O)O)O)C3=CC=C(C=C3)O
- InChIKey
- RPKUCYSGAXIESU-ABLWVSNPSA-N
- XLogP
- 1.6
- Polar surface area
- 90.2 Ų
- H-bond donors
- 4
- H-bond acceptors
- 5
- Formal charge
- 0
via PubChem
Wikidata facts
- Mass
- 274.084124
Show 3 more facts
- canonical SMILES
- C1C(C2=C(C=C(C=C2OC1C3=CC=C(C=C3)O)O)O)O
- chemical formula
- C₁₅H₁₄O₅
- isomeric SMILES
- C1[C@H](OC2=CC(=CC(=C2C1O)O)O)C3=CC=C(C=C3)O
Sources (2)
via Wikidata · CC0
~1 min read
Encyclopedic overview
2 sectionsContents
- Metabolism
- References
Apiforol is a chemical compound belonging to the flavan-4ol class of flavonoids.
==Metabolism== Flavanone 4-reductase is an enzyme transforming naringenin into apiforol. This enzyme can be found in Columnea hybrida, in Malus domestica, in Pyrus communis, in Sinningia cardinalis, and in Zea mays.
Excerpted from Wikipedia’s “apiforol” article, available under the CC BY-SA 4.0 licence.