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
Hemolysis D006461 131 associated lipids
Stomach Ulcer D013276 75 associated lipids
Diabetes Mellitus D003920 90 associated lipids
Neoplasms, Experimental D009374 10 associated lipids
Adenocarcinoma D000230 166 associated lipids
Dermatitis, Contact D003877 59 associated lipids
Pain D010146 64 associated lipids
Lupus Erythematosus, Systemic D008180 43 associated lipids
Lung Neoplasms D008175 171 associated lipids
Pancreatic Neoplasms D010190 77 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

Download all related citations
Per page 10 20 50 100 | Total 1492
Authors Title Published Journal PubMed Link
Brieskorn CH and Biechele W [Flavones from Salvia officinalis L. 22. Components of Salvia off. L]. 1971 Arch Pharm Ber Dtsch Pharm Ges pmid:5284536
Matern U et al. Further characterization and regulation of malonyl-coenzyme A: flavonoid glucoside malonyltransferases from parsley cell suspension cultures. 1983 Arch. Biochem. Biophys. pmid:6639051
Mukai R et al. Suppression mechanisms of flavonoids on aryl hydrocarbon receptor-mediated signal transduction. 2010 Arch. Biochem. Biophys. pmid:20450880
JURD L et al. The flavonoid constituents of Spirodela oligorrhiza. II. The flavone constituents. 1957 Arch. Biochem. Biophys. pmid:13425623
Tammela P et al. Permeability characteristics and membrane affinity of flavonoids and alkyl gallates in Caco-2 cells and in phospholipid vesicles. 2004 Arch. Biochem. Biophys. pmid:15111127
Henry EC and Gasiewicz TA Molecular determinants of species-specific agonist and antagonist activity of a substituted flavone towards the aryl hydrocarbon receptor. 2008 Arch. Biochem. Biophys. pmid:18294953
Schrag ML and Wienkers LC Covalent alteration of the CYP3A4 active site: evidence for multiple substrate binding domains. 2001 Arch. Biochem. Biophys. pmid:11414684
Velázquez I and Pardo JP Kinetic characterization of the rotenone-insensitive internal NADH: ubiquinone oxidoreductase of mitochondria from Saccharomyces cerevisiae. 2001 Arch. Biochem. Biophys. pmid:11370674
Cook SA and Shiemke AK Evidence that a type-2 NADH:quinone oxidoreductase mediates electron transfer to particulate methane monooxygenase in methylococcus capsulatus. 2002 Arch. Biochem. Biophys. pmid:11811946
Sutter A et al. Oxidation of flavanone to flavone with cell-free extracts from young parsley leaves. 1975 Arch. Biochem. Biophys. pmid:242261
Hausen BM et al. 5,8-dihydroxyflavone (primetin) the contact sensitizer of Primula mistassinica Michaux. 1983 Arch. Dermatol. Res. pmid:6660907
Rostom SA et al. Synthesis and biological evaluation of some polymethoxylated fused pyridine ring systems as antitumor agents. 2009 Arch. Pharm. (Weinheim) pmid:19714673
Ertan R et al. Synthesis of new annellated flavonoid derivatives possessing spasmolytic activity--VII. 1989 Arch. Pharm. (Weinheim) pmid:2751412
Aitken RA et al. Synthesis and antitumour activity of new derivatives of flavone-8-acetic acid (FAA). Part 4: Variation of the basic structure. 2000 Arch. Pharm. (Weinheim) pmid:10909190
Da Re P et al. Beta-adrenergic blocking agents of the flavone group. [(author's transl)]. 1975 Arch. Pharm. (Weinheim) pmid:236740
Yenjai C et al. Structural modification of 5,7-dimethoxyflavone from Kaempferia parviflora and biological activities. 2009 Arch. Pharm. Res. pmid:19784571
Liao Z et al. Antidiabetic effect of flavones from Cirsium japonicum DC in diabetic rats. 2010 Arch. Pharm. Res. pmid:20361298
Lee HJ et al. Protection of prenylated flavonoids from Mori Cortex Radicis (Moraceae) against nitric oxide-induced cell death in neuroblastoma SH-SY5Y cells. 2012 Arch. Pharm. Res. pmid:22297755
Kim SJ et al. Inhibition of nitric oxide production from lipopolysaccharide-treated RAW 264.7 cells by synthetic flavones: structure-activity relationship and action mechanism. 2004 Arch. Pharm. Res. pmid:15473664
Rudolf JL et al. The influence of diet composition on phase I and II biotransformation enzyme induction. 2008 Arch. Toxicol. pmid:18488195