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
Adenocarcinoma D000230 166 associated lipids
Adenoma D000236 40 associated lipids
Asthma D001249 52 associated lipids
Body Weight D001835 333 associated lipids
Carcinoma, Non-Small-Cell Lung D002289 72 associated lipids
Cell Transformation, Neoplastic D002471 126 associated lipids
Colonic Neoplasms D003110 161 associated lipids
Cystitis D003556 23 associated lipids
Dermatitis, Contact D003877 59 associated lipids
Diabetes Mellitus D003920 90 associated lipids
Diabetes Mellitus, Experimental D003921 85 associated lipids
Edema D004487 152 associated lipids
Encephalitis D004660 15 associated lipids
Glioma D005910 112 associated lipids
Hemolysis D006461 131 associated lipids
Carcinoma, Hepatocellular D006528 140 associated lipids
Hyperlipidemias D006949 73 associated lipids
Hypertension D006973 115 associated lipids
Leukemia P388 D007941 43 associated lipids
Lung Neoplasms D008175 171 associated lipids
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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
Kim SY et al. Cis-2', 3'-dihydrodiol production on flavone B-ring by biphenyl dioxygenase from Pseudomonas pseudoalcaligenes KF707 expressed in Escherichia coli. 2003 Antonie Van Leeuwenhoek pmid:14574103
Fang H et al. Study of 202 natural, synthetic, and environmental chemicals for binding to the androgen receptor. 2003 Chem. Res. Toxicol. pmid:14565775
Lin HY et al. Inhibition of lipopolysaccharide-induced nitric oxide production by flavonoids in RAW264.7 macrophages involves heme oxygenase-1. 2003 Biochem. Pharmacol. pmid:14563492
Uyemura SA et al. Oxidative phosphorylation and rotenone-insensitive malate- and NADH-quinone oxidoreductases in Plasmodium yoelii yoelii mitochondria in situ. 2004 J. Biol. Chem. pmid:14561763
Mackenzie CA et al. Gonadal differentiation in frogs exposed to estrogenic and antiestrogenic compounds. 2003 Environ. Toxicol. Chem. pmid:14552012
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KOEPPEN BH et al. The flavone C-glycosides and flavonol O-glycosides of Aspalathus acuminatus (rooibos tea). 1962 Biochem. J. pmid:14457727
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van der Logt EM et al. Induction of rat hepatic and intestinal UDP-glucuronosyltransferases by naturally occurring dietary anticarcinogens. 2003 Carcinogenesis pmid:12869420
Wenzel U et al. Nitric oxide suppresses apoptosis in human colon cancer cells by scavenging mitochondrial superoxide anions. 2003 Int. J. Cancer pmid:12866025
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Gabrieli C and Kokkalou E A new acetylated glucoside of luteolin and two flavone glucosides from Lavandula stoechas ssp. stoechas. 2003 Pharmazie pmid:12857010
Maçanita AL et al. Photochemistry of flavothione and hydroxyflavothiones: mechanisms and kinetics. 2003 Photochem. Photobiol. pmid:12856878
Kesava Reddy M et al. A new chalcone and a flavone from Andrographis neesiana. 2003 Chem. Pharm. Bull. pmid:12843595
Díaz F et al. Cytotoxic flavone analogues of vitexicarpin, a constituent of the leaves of Vitex negundo. 2003 J. Nat. Prod. pmid:12828478
Zhang P et al. A maize QTL for silk maysin levels contains duplicated Myb-homologous genes which jointly regulate flavone biosynthesis. 2003 Plant Mol. Biol. pmid:12825685
Vieira RF et al. Chemical profiling of Ocimum americanum using external flavonoids. 2003 Phytochemistry pmid:12809716
Topcu G et al. Studies on di- and triterpenoids from Salvia staminea with cytotoxic activity. 2003 Planta Med. pmid:12802732
Jameson MB et al. Clinical aspects of a phase I trial of 5,6-dimethylxanthenone-4-acetic acid (DMXAA), a novel antivascular agent. 2003 Br. J. Cancer pmid:12799625
Caristi C et al. Flavonoids detection by HPLC-DAD-MS-MS in lemon juices from Sicilian cultivars. 2003 J. Agric. Food Chem. pmid:12769519
Martínez-Richa A and Joseph-Nathan P Carbon-13 CP-MAS nuclear magnetic resonance studies of teas. 2003 Solid State Nucl Magn Reson pmid:12763559
Gleye C et al. Acaricidal activity of tonka bean extracts. Synthesis and structure-activity relationships of bioactive derivatives. 2003 J. Nat. Prod. pmid:12762809
Tombola F et al. Plant polyphenols inhibit VacA, a toxin secreted by the gastric pathogen Helicobacter pylori. 2003 FEBS Lett. pmid:12753930
Suzuki R et al. Two flavone C-glycosides from the style of Zea mays with glycation inhibitory activity. 2003 J. Nat. Prod. pmid:12713418
Gafner S et al. Inhibition of [3H]-LSD binding to 5-HT7 receptors by flavonoids from Scutellaria lateriflora. 2003 J. Nat. Prod. pmid:12713409
Selloum L et al. Anti-inflammatory effect of rutin on rat paw oedema, and on neutrophils chemotaxis and degranulation. 2003 Exp. Toxicol. Pathol. pmid:12710715
Boué SM et al. Identification of flavone aglycones and glycosides in soybean pods by liquid chromatography-tandem mass spectrometry. 2003 J Chromatogr A pmid:12703901
Rustin GJ et al. 5,6-dimethylxanthenone-4-acetic acid (DMXAA), a novel antivascular agent: phase I clinical and pharmacokinetic study. 2003 Br. J. Cancer pmid:12698178