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
Neoplasm Invasiveness D009361 23 associated lipids
Cystitis D003556 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
Weight Loss D015431 56 associated lipids
Dermatitis, Contact D003877 59 associated lipids
Pain D010146 64 associated lipids
Mammary Neoplasms, Experimental D008325 67 associated lipids
Melanoma D008545 69 associated lipids
Carcinoma, Non-Small-Cell Lung D002289 72 associated lipids
Hyperlipidemias D006949 73 associated lipids
Stomach Ulcer D013276 75 associated lipids
Pancreatic Neoplasms D010190 77 associated lipids
Diabetes Mellitus, Experimental D003921 85 associated lipids
Diabetes Mellitus D003920 90 associated lipids
Glioma D005910 112 associated lipids
Hypertension D006973 115 associated lipids
Cell Transformation, Neoplastic D002471 126 associated lipids
Prostatic Neoplasms D011471 126 associated lipids
Hemolysis D006461 131 associated lipids
Carcinoma, Hepatocellular D006528 140 associated lipids
Edema D004487 152 associated lipids
Colonic Neoplasms D003110 161 associated lipids
Adenocarcinoma D000230 166 associated lipids
Lung Neoplasms D008175 171 associated lipids
Body Weight D001835 333 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
Takada Y and Aggarwal BB Flavopiridol inhibits NF-kappaB activation induced by various carcinogens and inflammatory agents through inhibition of IkappaBalpha kinase and p65 phosphorylation: abrogation of cyclin D1, cyclooxygenase-2, and matrix metalloprotease-9. 2004 J. Biol. Chem. pmid:14630924
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
Galietta LJ et al. Novel CFTR chloride channel activators identified by screening of combinatorial libraries based on flavone and benzoquinolizinium lead compounds. 2001 J. Biol. Chem. pmid:11262417
Lotito SB and Frei B Dietary flavonoids attenuate tumor necrosis factor alpha-induced adhesion molecule expression in human aortic endothelial cells. Structure-function relationships and activity after first pass metabolism. 2006 J. Biol. Chem. pmid:16987811
Huang MT et al. Specificity in the activation and inhibition by flavonoids of benzo[a]pyrene hydroxylation by cytochrome P-450 isozymes from rabbit liver microsomes. 1981 J. Biol. Chem. pmid:6270135
Harlow GR and Halpert JR Alanine-scanning mutagenesis of a putative substrate recognition site in human cytochrome P450 3A4. Role of residues 210 and 211 in flavonoid activation and substrate specificity. 1997 J. Biol. Chem. pmid:9038138
Skizim NJ et al. Metabolic pathways for photobiological hydrogen production by nitrogenase- and hydrogenase-containing unicellular cyanobacteria Cyanothece. 2012 J. Biol. Chem. pmid:22128188
Guo AJ et al. Baicalin, a flavone, induces the differentiation of cultured osteoblasts: an action via the Wnt/beta-catenin signaling pathway. 2011 J. Biol. Chem. pmid:21652696
Martins VP et al. Mitochondrial function in the yeast form of the pathogenic fungus Paracoccidioides brasiliensis. 2008 J. Bioenerg. Biomembr. pmid:18797987
Wei Z et al. Cardamonin protects septic mice from acute lung injury by preventing endothelial barrier dysfunction. 2012 J. Biochem. Mol. Toxicol. pmid:22696397
Aslan E and Adem S In vitro effects of some flavones on human pyruvate kinase isoenzyme M2. 2015 J. Biochem. Mol. Toxicol. pmid:25388478
Li BH et al. Structure-activity relationship of polyphenols that inhibit fatty acid synthase. 2005 J. Biochem. pmid:16428296
Kasai N et al. Atypical kinetics of cytochromes P450 catalysing 3'-hydroxylation of flavone from the white-rot fungus Phanerochaete chrysosporium. 2010 J. Biochem. pmid:19819902
Perry JD et al. Evaluation of novel chromogenic substrates for the detection of bacterial beta-glucosidase. 2007 J. Appl. Microbiol. pmid:17241346
Novy P et al. In vitro synergistic effects of baicalin with oxytetracycline and tetracycline against Staphylococcus aureus. 2011 J. Antimicrob. Chemother. pmid:21421582
Zhang J et al. Threshold dissociation and molecular modeling of transition metal complexes of flavonoids. 2005 J. Am. Soc. Mass Spectrom. pmid:15694764
Fabre N et al. Determination of flavone, flavonol, and flavanone aglycones by negative ion liquid chromatography electrospray ion trap mass spectrometry. 2001 J. Am. Soc. Mass Spectrom. pmid:11401161
Ma YL et al. Internal glucose residue loss in protonated O-diglycosyl flavonoids upon low-energy collision-induced dissociation. 2000 J. Am. Soc. Mass Spectrom. pmid:10689666
Pikulski M et al. Tunable transition metal-ligand complexation for enhanced elucidation of flavonoid diglycosides by electrospray ionization mass spectrometry. 2007 J. Am. Soc. Mass Spectrom. pmid:17112735
Caddick S et al. Synthetic ligands for apo-neocarzinostatin. 2006 J. Am. Chem. Soc. pmid:16568976
Klier L et al. Lewis acid-triggered selective zincation of chromones, quinolones, and thiochromones: application to the preparation of natural flavones and isoflavones. 2012 J. Am. Chem. Soc. pmid:22860983
Gauci AJ et al. Identification of polyphenolic compounds and black tea extract as potent inhibitors of lipid membrane destabilization by Aβ₄₂ aggregates. 2011 J. Alzheimers Dis. pmid:21891862
Weng Z et al. The novel flavone tetramethoxyluteolin is a potent inhibitor of human mast cells. 2015 J. Allergy Clin. Immunol. pmid:25498791
Rayyan S et al. Flavone C-glycosides from seeds of fenugreek, Trigonella foenum-graecum L. 2010 J. Agric. Food Chem. pmid:20486688
Fiorentino A et al. Identification and assessment of antioxidant capacity of phytochemicals from kiwi fruits. 2009 J. Agric. Food Chem. pmid:19358604
Jeong SH et al. Tyrosinase inhibitory polyphenols from roots of Morus lhou. 2009 J. Agric. Food Chem. pmid:19166303
Gobbo-Neto L and Lopes NP Online identification of chlorogenic acids, sesquiterpene lactones, and flavonoids in the Brazilian arnica Lychnophora ericoides Mart. (Asteraceae) leaves by HPLC-DAD-MS and HPLC-DAD-MS/MS and a validated HPLC-DAD method for their simultaneous analysis. 2008 J. Agric. Food Chem. pmid:18237124
Morimoto M et al. Insect antifeedant activity of flavones and chromones against Spodoptera litura. 2003 J. Agric. Food Chem. pmid:12517100
Yang L et al. Purification and characterization of an isoflavone-conjugates-hydrolyzing beta-glucosidase from endophytic bacterium. 2004 J. Agric. Food Chem. pmid:15053533
Kim H et al. Effects of naturally occurring compounds on fibril formation and oxidative stress of beta-amyloid. 2005 J. Agric. Food Chem. pmid:16248550
Xiao J et al. Noncovalent interaction of dietary polyphenols with common human plasma proteins. 2011 J. Agric. Food Chem. pmid:21863815
Appeldoorn MM et al. Some phenolic compounds increase the nitric oxide level in endothelial cells in vitro. 2009 J. Agric. Food Chem. pmid:19722703
Caristi C et al. Flavonoids detection by HPLC-DAD-MS-MS in lemon juices from Sicilian cultivars. 2003 J. Agric. Food Chem. pmid:12769519
Hamada M et al. TCDD-induced CYP1A1 expression, an index of dioxin toxicity, is suppressed by flavonoids permeating the human intestinal Caco-2 cell monolayers. 2006 J. Agric. Food Chem. pmid:17090139
Nørbaek R et al. Flavone C-glycoside, phenolic acid, and nitrogen contents in leaves of barley subject to organic fertilization treatments. 2003 J. Agric. Food Chem. pmid:12537462
Manthey JA and Guthrie N Antiproliferative activities of citrus flavonoids against six human cancer cell lines. 2002 J. Agric. Food Chem. pmid:12358447
Xu B and Chang SK Phenolic substance characterization and chemical and cell-based antioxidant activities of 11 lentils grown in the northern United States. 2010 J. Agric. Food Chem. pmid:20058926
Marín FR and Del Río JA Selection of hybrids and edible citrus species with a high content in the diosmin functional compound. Modulating effect of plant growth regulators on contents. 2001 J. Agric. Food Chem. pmid:11453775
Bandaruk Y et al. Evaluation of the inhibitory effects of quercetin-related flavonoids and tea catechins on the monoamine oxidase-A reaction in mouse brain mitochondria. 2012 J. Agric. Food Chem. pmid:23009399
Chang TL Inhibitory effect of flavonoids on 26S proteasome activity. 2009 J. Agric. Food Chem. pmid:19795881
Rossi A et al. Inhibition of inducible nitric oxide synthase expression by an acetonic extract from Feijoa sellowiana Berg. fruits. 2007 J. Agric. Food Chem. pmid:17550270
Kim S et al. Promotion of Glucose Uptake in C2C12 Myotubes by Cereal Flavone Tricin and Its Underlying Molecular Mechanism. 2017 J. Agric. Food Chem. pmid:28474889
Kwon HM et al. Anti-inflammatory inhibition of endothelial cell adhesion molecule expression by flavone derivatives. 2005 J. Agric. Food Chem. pmid:15969490
Yang JM et al. Hispidulin sensitizes human ovarian cancer cells to TRAIL-induced apoptosis by AMPK activation leading to Mcl-1 block in translation. 2010 J. Agric. Food Chem. pmid:20734985
Lin YC et al. Hispidulin potently inhibits human glioblastoma multiforme cells through activation of AMP-activated protein kinase (AMPK). 2010 J. Agric. Food Chem. pmid:20698539
Ho YC et al. Re-examination of chromogenic quantitative assays for determining flavonoid content. 2012 J. Agric. Food Chem. pmid:22352692
Choi CW et al. Yeast α-glucosidase inhibition by isoflavones from plants of Leguminosae as an in vitro alternative to acarbose. 2010 J. Agric. Food Chem. pmid:20734984
Zbidah M et al. Apigenin-induced suicidal erythrocyte death. 2012 J. Agric. Food Chem. pmid:22132906
Lee SE et al. Inhibitory effects of naturally occurring compounds on aflatoxin B(1) biotransformation. 2001 J. Agric. Food Chem. pmid:11714299
Echeverry C et al. Pretreatment with natural flavones and neuronal cell survival after oxidative stress: a structure-activity relationship study. 2010 J. Agric. Food Chem. pmid:20095615