flavanone

Also known as flavanones

thumb|right|Flavanone skeleton with locants The flavanones, a type of flavonoids, are various aromatic, colorless ketones derived from flavone that often occur in plants as glycosides.

Research

12,994 papers

Trypanocidal Activity of Flavanone Derivatives.Molecules (Basel, Switzerland) · 2020
Molecular Characterisation of Flavanone O-methylation in Eucalyptus.International journal of molecular sciences · 2022
The Extraction, Biosynthesis, Health-Promoting and Therapeutic Properties of Natural Flavanone Eriodictyol.Nutrients · 2024
A new flavanone derivative from the rhizomes of Boesenbergia pandurata.Natural product research · 2022
Citrus flavanone metabolites significantly modulate global proteomic profile in pancreatic β-cells under high-glucose-induced metabolic stress.Biochimica et biophysica acta. Proteins and proteomics · 2023

via PubMed

Wikidata facts

Show 3 more facts

Commons category: Flavanones
canonical SMILES: O1C2=C(C(C(C1C3=C(C(=C(C(=C3*)*)*)*)*)*)=O)C(=C(C(=C2*)*)*)*
SMARTS notation: [$(c);$([cX3H0](c)(c)O),$([cX3H1](c)c)]1[$(c);$([cX3H0](c)(c)O),$([cX3H1](c)c)][$(c);$([cX3H0](c)(c)O),$([cX3H1](c)c)][$(c);$([cX3H0](c)(c)O),$([cX3H1](c)c)][$(c);$([cX3H0](c)(c)O),$([cX3H1](c)c)]c1-[$(C);$([CX4H0](c)(C)(O)O),$([CX4H1](c)(O)C)]2-O-c3[$(c);$([cX3H0](c)(c)O),$([cX3H1](c)c)][$(c);$([cX3H0](c)(c)O),$([cX3H1](c)c)][$(c);$([cX3H0](c)(c)O),$([cX3H1](c)c)][$(c);$([cX3H0](c)(c)O),$([cX3H1](c)c)]c3-C(=O)-[$(C);$([CX4H1](C)(C)O),$([CX4H2](C)C)]2

Sources (3)

via Wikidata · CC0

~1 min read

Article

5 sections

Contents

List of flavanones
Metabolism
Synthesis
References
External links

thumb|right|Flavanone skeleton with locants The flavanones, a type of flavonoids, are various aromatic, colorless ketones derived from flavone that often occur in plants as glycosides.

==List of flavanones== Blumeatin Butin Dichamanetin Eriodictyol Hesperetin Hesperidin Homoeriodictyol Isosakuranetin Kolaflavanone Naringenin Naringin Pinocembrin Poncirin Sakuranetin Sakuranin Sterubin Pinostrobin