"Flavones" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
A group of 4-keto-FLAVONOIDS.
| Descriptor ID |
D047309
|
| MeSH Number(s) |
D03.383.663.283.266.450.260 D03.633.100.150.266.450.260
|
| Concept/Terms |
Flavones- Flavones
- 2-Phenyl-2-Ene-Benzopyran-4-One Compounds
|
Below are MeSH descriptors whose meaning is more general than "Flavones".
Below are MeSH descriptors whose meaning is more specific than "Flavones".
This graph shows the total number of publications written about "Flavones" by people in this website by year, and whether "Flavones" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2010 | 2 | 0 | 2 |
| 2011 | 3 | 0 | 3 |
| 2012 | 0 | 2 | 2 |
| 2013 | 1 | 0 | 1 |
| 2021 | 0 | 1 | 1 |
| 2022 | 2 | 0 | 2 |
| 2025 | 0 | 1 | 1 |
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Below are the most recent publications written about "Flavones" by people in Profiles.
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Targeting the hepatic circadian clock concomitant with tyrosine kinase inhibition reverses late-stage hepatocellular carcinoma. Cell Rep. 2025 Nov 25; 44(11):116313.
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ROR activation by Nobiletin enhances antitumor efficacy via suppression of I?B/NF-?B signaling in triple-negative breast cancer. Cell Death Dis. 2022 04 19; 13(4):374.
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The clock modulator Nobiletin mitigates astrogliosis-associated neuroinflammation and disease hallmarks in an Alzheimer's disease model. FASEB J. 2022 03; 36(3):e22186.
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Guaianolide Sesquiterpene Lactones from Centaurothamnus maximus. Molecules. 2021 Apr 03; 26(7).
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Hispidulin attenuates bone resorption and osteoclastogenesis via the RANKL-induced NF-?B and NFATc1 pathways. Eur J Pharmacol. 2013 Sep 05; 715(1-3):96-104.
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Anti-angiogenic and anti-tumor activity of Bavachinin by targeting hypoxia-inducible factor-1a. Eur J Pharmacol. 2012 Sep 15; 691(1-3):28-37.
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Systematic studies of sulfation and glucuronidation of 12 flavonoids in the mouse liver S9 fraction reveal both unique and shared positional preferences. J Agric Food Chem. 2012 Mar 28; 60(12):3223-33.
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Evaluation of 3,3',4'-trihydroxyflavone and 3,6,4'-trihydroxyflavone (4'-O-glucuronidation) as the in vitro functional markers for hepatic UGT1A1. Mol Pharm. 2011 Dec 05; 8(6):2379-89.
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Acacetin causes a frequency- and use-dependent blockade of hKv1.5 channels by binding to the S6 domain. J Mol Cell Cardiol. 2011 Dec; 51(6):966-73.
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Sulfation of selected mono-hydroxyflavones by sulfotransferases in vitro: a species and gender comparison. J Pharm Pharmacol. 2011 Jul; 63(7):967-70.