flavone
Sign in to savethumb|Molecular structure of the flavone backbone with numbers
Research
19,098 papers- Flavones and flavone synthases.Phytochemistry · 2005
- Plant flavone Chrysin as an emerging histone deacetylase inhibitor for prosperous epigenetic-based anticancer therapy.Phytotherapy research : PTR · 2021
- Neuroprotective effects of flavone luteolin in neuroinflammation and neurotrauma.BioFactors (Oxford, England) · 2021
- Report on the mutagenicity of flavone derivatives and their contribution to advancing scientific knowledge.Proceedings of the Japan Academy. Series B, Physical and biological sciences · 2024
- Eggerthella lenta down regulated flavone and flavonol biosynthesis promoted Kawasaki disease.Virulence · 2025
via PubMed
Wikidata facts
Show 5 more facts
- Commons category
- Flavones
- topic's main category
- Category:Flavones
- different from
- flavone
- canonical SMILES
- O1C2=C(C(C(=C1C3=C(C(=C(C(=C3*)*)*)*)*)*)=O)C(=C(C(=C2*)*)*)*
- SMARTS notation
- *-[#6]-1=[#6](-[#8]-c2c(-*)c(-*)c(-*)c(-*)c2-[#6]-1=O)-c1c(-*)c(-*)c(-*)c(-*)c1-*
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Encyclopedic overview
9 sectionsContents
- Intake and elimination
- Drug interactions
- Biosynthesis
- Organic chemistry
- {{anchor|Wessely-Moser rearrangement}} Wessely–Moser rearrangement
- Common flavones
- Research
- References
- External links
thumb|Molecular structure of the flavone backbone with numbers
Flavones (from Latin flavus "yellow") are a class of flavonoids based on the backbone of 2-phenylchromen-4-one (2-phenyl-1-benzopyran-4-one) (as shown in the first image of this article).
Excerpted from Wikipedia’s “flavone” article, available under the CC BY-SA 4.0 licence.