FLAVONE

FLAVONE is a lipid of Polyketides (PK) class. Flavone is associated with abnormalities such as Cardiovascular Diseases, Cerebrovascular accident, DERMATITIS HERPETIFORMIS, FAMILIAL, Hyperinsulinism and Inflammatory disorder. The involved functions are known as Oxidation-Reduction, Metabolic Inhibition, Inflammation, Phosphorylation and antioxidant activity. Flavone often locates in Endothelium, Hepatic, Protoplasm, Body tissue and Extracellular. The associated genes with FLAVONE are ICAM1 gene, BCL2L1 gene, MYC gene, TP53 gene and cytochrome c''. The related lipids are Promega, Steroids and Total cholesterol. The related experimental models are Knock-out, Disease model and Animal Disease Models.

Cross Reference

Introduction

To understand associated biological information of FLAVONE, we collected biological information of abnormalities, associated pathways, cellular/molecular locations, biological functions, related genes/proteins, lipids and common seen animal/experimental models with organized paragraphs from literatures.

What diseases are associated with FLAVONE?

FLAVONE is suspected in Diabetes Mellitus, Non-Insulin-Dependent, Obesity, Chronic Disease, Disintegration, Cardiovascular Diseases, Cerebrovascular accident and other diseases in descending order of the highest number of associated sentences.

Related references are mostly published in these journals:

Disease Cross reference Weighted score Related literature
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Possible diseases from mapped MeSH terms on references

We collected disease MeSH terms mapped to the references associated with FLAVONE

MeSH term MeSH ID Detail
Lymphedema D008209 4 associated lipids
Neoplasms, Experimental D009374 10 associated lipids
Encephalitis D004660 15 associated lipids
Cystitis D003556 23 associated lipids
Neoplasm Invasiveness D009361 23 associated lipids
Adenoma D000236 40 associated lipids
Leukemia P388 D007941 43 associated lipids
Lupus Erythematosus, Systemic D008180 43 associated lipids
Osteosarcoma D012516 50 associated lipids
Asthma D001249 52 associated lipids
Per page 10 20 50 | Total 32

PubChem Associated disorders and diseases

What pathways are associated with FLAVONE

There are no associated biomedical information in the current reference collection.

PubChem Biomolecular Interactions and Pathways

Link to PubChem Biomolecular Interactions and Pathways

What cellular locations are associated with FLAVONE?

Related references are published most in these journals:

Location Cross reference Weighted score Related literatures
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What functions are associated with FLAVONE?


Related references are published most in these journals:

Function Cross reference Weighted score Related literatures

What lipids are associated with FLAVONE?

Related references are published most in these journals:

Lipid concept Cross reference Weighted score Related literatures
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What genes are associated with FLAVONE?

Related references are published most in these journals:


Gene Cross reference Weighted score Related literatures

What common seen animal models are associated with FLAVONE?

Knock-out

Knock-out are used in the study 'MATE2 mediates vacuolar sequestration of flavonoid glycosides and glycoside malonates in Medicago truncatula.' (Zhao J et al., 2011) and Knock-out are used in the study 'How can research on plants contribute to promoting human health?' (Martin C et al., 2011).

Disease model

Disease model are used in the study 'How can research on plants contribute to promoting human health?' (Martin C et al., 2011).

Animal Disease Models

Animal Disease Models are used in the study 'How can research on plants contribute to promoting human health?' (Martin C et al., 2011).

Related references are published most in these journals:

Model Cross reference Weighted score Related literatures
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NCBI Entrez Crosslinks

All references with FLAVONE

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Per page 10 20 50 100 | Total 1492
Authors Title Published Journal PubMed Link
Golub AG et al. Discovery and characterization of synthetic 4'-hydroxyflavones-New CK2 inhibitors from flavone family. 2013 Bioorg. Med. Chem. pmid:24011954
Kuemmerle J et al. Synthesis of caged 2,3,3a,7a-tetrahydro-3,6-methanobenzofuran-7(6H)-ones: Evaluating the minimum structure for apoptosis induction by gambogic acid. 2008 Bioorg. Med. Chem. pmid:18337106
Springsteel MF et al. Benzoflavone activators of the cystic fibrosis transmembrane conductance regulator: towards a pharmacophore model for the nucleotide-binding domain. 2003 Bioorg. Med. Chem. pmid:12927873
Betti L et al. Design, synthesis, and alpha(1)-adrenoceptor binding properties of new arylpiperazine derivatives bearing a flavone nucleus as the terminal heterocyclic molecular portion. 2004 Bioorg. Med. Chem. pmid:15018926
Wang TC et al. Synthesis, antiproliferative, and antiplatelet activities of oxime- and methyloxime-containing flavone and isoflavone derivatives. 2005 Bioorg. Med. Chem. pmid:15990314
Boumendjel A et al. Acridone derivatives: design, synthesis, and inhibition of breast cancer resistance protein ABCG2. 2007 Bioorg. Med. Chem. pmid:17317193
Dei S et al. Design and synthesis of aminoester heterodimers containing flavone or chromone moieties as modulators of P-glycoprotein-based multidrug resistance (MDR). 2018 Bioorg. Med. Chem. pmid:29162309
Ullah Mughal E et al. Synthesis and antibacterial activity of substituted flavones, 4-thioflavones and 4-iminoflavones. 2006 Bioorg. Med. Chem. pmid:16603364
Dong X et al. Identification of SVM-based classification model, synthesis and evaluation of prenylated flavonoids as vasorelaxant agents. 2008 Bioorg. Med. Chem. pmid:18678502
Greeff J et al. Antioxidant properties of 4-quinolones and structurally related flavones. 2012 Bioorg. Med. Chem. pmid:22197671
Göker H et al. Synthesis and potent antimicrobial activity of some novel 2-phenyl or methyl-4H-1-benzopyran-4-ones carrying amidinobenzimidazoles. 2005 Bioorg. Med. Chem. pmid:15698788
Valenti P et al. Synthesis and biological activity of some rigid analogues of flavone-8-acetic acid. 2000 Bioorg. Med. Chem. pmid:10968283
Marder M et al. Molecular modeling and QSAR analysis of the interaction of flavone derivatives with the benzodiazepine binding site of the GABA(A) receptor complex. 2001 Bioorg. Med. Chem. pmid:11249125
Lewin G et al. Synthesis of antiproliferative flavones from calycopterin, major flavonoid of Calycopteris floribunda Lamk. 2011 Bioorg. Med. Chem. pmid:21146994
Li HQ et al. Synthesis of C(7) modified chrysin derivatives designing to inhibit beta-ketoacyl-acyl carrier protein synthase III (FabH) as antibiotics. 2009 Bioorg. Med. Chem. pmid:19664929
Lewin G et al. Influence of the skeleton on the cytotoxicity of flavonoids. 2012 Bioorg. Med. Chem. pmid:22257529
Mays JR et al. The synthesis and evaluation of flavone and isoflavone chimeras of novobiocin and derrubone. 2010 Bioorg. Med. Chem. pmid:19932969
Liu H et al. New synthetic flavone derivatives induce apoptosis of hepatocarcinoma cells. 2010 Bioorg. Med. Chem. pmid:20674374
Wang SQ et al. Flavonoids from Dracocephalum tanguticum and their cardioprotective effects against doxorubicin-induced toxicity in H9c2 cells. 2010 Bioorg. Med. Chem. Lett. pmid:20932762
Nilsson J et al. Azaflavones compared to flavones as ligands to the benzodiazepine binding site of brain GABA(A) receptors. 2008 Bioorg. Med. Chem. Lett. pmid:18851913
Chen WQ et al. A new antifungal and cytotoxic C-methylated flavone glycoside from Picea neoveitchii. 2012 Bioorg. Med. Chem. Lett. pmid:22901896
An JY et al. Identification and structure activity relationship of novel flavone derivatives that inhibit the production of nitric oxide and PGE2 in LPS-induced RAW 264.7 cells. 2017 Bioorg. Med. Chem. Lett. pmid:28408221
Nakagawa-Goto K et al. Total synthesis and bioactivity of unique flavone desmosdumotin B and its analogs. 2005 Bioorg. Med. Chem. Lett. pmid:15913998
Auffret G et al. Synthesis and antimalarial evaluation of a series of piperazinyl flavones. 2007 Bioorg. Med. Chem. Lett. pmid:17166718
Ryu YB et al. Structural characteristics of flavanones and flavones from Cudrania tricuspidata for neuraminidase inhibition. 2009 Bioorg. Med. Chem. Lett. pmid:19660948
Lebeau J et al. Beneficial effects of different flavonoids, on functional recovery after ischemia and reperfusion in isolated rat heart. 2001 Bioorg. Med. Chem. Lett. pmid:11140725
Balboni G et al. Flavones and structurally related 4-chromenones inhibit carbonic anhydrases by a different mechanism of action compared to coumarins. 2012 Bioorg. Med. Chem. Lett. pmid:22487176
Choe H et al. Structure-based design of flavone-based inhibitors of wild-type and T315I mutant of ABL. 2013 Bioorg. Med. Chem. Lett. pmid:23790540
Hyup YH et al. 2,3-Diarylbenzopyran derivatives as a novel class of selective cyclooxygenase-2 inhibitors. 2003 Bioorg. Med. Chem. Lett. pmid:12565941
Tamura S et al. New inhibitors for expression of IgE receptor on human mast cell. 2010 Bioorg. Med. Chem. Lett. pmid:20202836
Kang Y et al. Inhibitory potential of flavonoids on PtdIns(3,4,5)P3 binding with the phosphoinositide-dependent kinase 1 pleckstrin homology domain. 2017 Bioorg. Med. Chem. Lett. pmid:28049590
Hatnapure GD et al. Synthesis and biological evaluation of novel piperazine derivatives of flavone as potent anti-inflammatory and antimicrobial agent. 2012 Bioorg. Med. Chem. Lett. pmid:22981334
Ahmed N et al. Synthesis, characterization, and estrogen receptor binding affinity of flavone-, indole-, and furan-estradiol conjugates. 2007 Bioorg. Med. Chem. Lett. pmid:17379515
Shin SY et al. Relationship between the structures of flavonoids and their NF-κB-dependent transcriptional activities. 2011 Bioorg. Med. Chem. Lett. pmid:21907578
Ono M et al. 99mTc/Re complexes based on flavone and aurone as SPECT probes for imaging cerebral β-amyloid plaques. 2010 Bioorg. Med. Chem. Lett. pmid:20797860
Gao L et al. 3D QSAR and docking study of flavone derivatives as potent inhibitors of influenza H1N1 virus neuraminidase. 2011 Bioorg. Med. Chem. Lett. pmid:21843936
Jin J et al. Design, synthesis and biological evaluation of new arylpiperazine derivatives bearing a flavone moiety as α1-adrenoceptor antagonists. 2011 Bioorg. Med. Chem. Lett. pmid:21236664
Baxter A et al. Non-covalent inhibitors of rhinovirus 3C protease. 2011 Bioorg. Med. Chem. Lett. pmid:21183345
Liu XH et al. Synthesis and molecular docking studies of novel 2-chloro-pyridine derivatives containing flavone moieties as potential antitumor agents. 2010 Bioorg. Med. Chem. Lett. pmid:20538457
Aboul-Enein HY et al. Scavenging effects of phenolic compounds on reactive oxygen species. 2007 Biopolymers pmid:17373654
Xu H et al. Molecular cloning and characterization of phenylalanine ammonia-lyase, cinnamate 4-hydroxylase and genes involved in flavone biosynthesis in Scutellaria baicalensis. 2010 Bioresour. Technol. pmid:20708926
Kim JH et al. Characterization of flavonoid 7-O-glucosyltransferase from Arabidopsis thaliana. 2006 Biosci. Biotechnol. Biochem. pmid:16794327
Kanho H et al. Glucosylation of phenolic compounds by Pharbitis nil hairy roots: I. Glucosylation of coumarin and flavone derivatives. 2004 Biosci. Biotechnol. Biochem. pmid:15502347
Ueda H et al. A hydroxyl group of flavonoids affects oral anti-inflammatory activity and inhibition of systemic tumor necrosis factor-alpha production. 2004 Biosci. Biotechnol. Biochem. pmid:14745173
Han DH et al. Relationship between estrogen receptor-binding and estrogenic activities of environmental estrogens and suppression by flavonoids. 2002 Biosci. Biotechnol. Biochem. pmid:12224631
Matsui T et al. Luteolin, a flavone, does not suppress postprandial glucose absorption through an inhibition of alpha-glucosidase action. 2002 Biosci. Biotechnol. Biochem. pmid:12005074
Gao H et al. Structure-activity relationships for alpha-glucosidase inhibition of baicalein, 5,6,7-trihydroxyflavone: the effect of A-ring substitution. 2004 Biosci. Biotechnol. Biochem. pmid:14981300
Yun CS et al. Expression of parsley flavone synthase I establishes the flavone biosynthetic pathway in Arabidopsis thaliana. 2008 Biosci. Biotechnol. Biochem. pmid:18391443
Feng XT et al. Pollen Typhae total flavone improves insulin resistance in high-fat diet and low-dose streptozotocin-induced type 2 diabetic rats. 2014 Biosci. Biotechnol. Biochem. pmid:25273139
Watanabe J et al. Coumarin and flavone derivatives from estragon and thyme as inhibitors of chemical mediator release from RBL-2H3 Cells. 2005 Biosci. Biotechnol. Biochem. pmid:15665459