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
Loading... please refresh the page if content is not showing up.

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
Colonic Neoplasms D003110 161 associated lipids
Diabetes Mellitus, Experimental D003921 85 associated lipids
Mammary Neoplasms, Experimental D008325 67 associated lipids
Body Weight D001835 333 associated lipids
Edema D004487 152 associated lipids
Prostatic Neoplasms D011471 126 associated lipids
Osteosarcoma D012516 50 associated lipids
Melanoma D008545 69 associated lipids
Asthma D001249 52 associated lipids
Glioma D005910 112 associated lipids
Cell Transformation, Neoplastic D002471 126 associated lipids
Leukemia P388 D007941 43 associated lipids
Carcinoma, Hepatocellular D006528 140 associated lipids
Hypertension D006973 115 associated lipids
Hyperlipidemias D006949 73 associated lipids
Adenoma D000236 40 associated lipids
Cystitis D003556 23 associated lipids
Carcinoma, Non-Small-Cell Lung D002289 72 associated lipids
Encephalitis D004660 15 associated lipids
Weight Loss D015431 56 associated lipids
Neoplasm Invasiveness D009361 23 associated lipids
Lymphedema D008209 4 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
Loading... please refresh the page if content is not showing up.

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
Loading... please refresh the page if content is not showing up.

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
Loading... please refresh the page if content is not showing up.

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
Fernández SP et al. Synergistic interaction between hesperidin, a natural flavonoid, and diazepam. 2005 Eur. J. Pharmacol. pmid:15840404
Furtmueller R et al. 6,3'-Dinitroflavone is a low efficacy modulator of GABA(A) receptors. 2008 Eur. J. Pharmacol. pmid:18639544
Geraets L et al. Flavone as PARP-1 inhibitor: its effect on lipopolysaccharide induced gene-expression. 2007 Eur. J. Pharmacol. pmid:17643414
Patanasethanont D et al. Modulation of function of multidrug resistance associated-proteins by Kaempferia parviflora extracts and their components. 2007 Eur. J. Pharmacol. pmid:17481606
Toton E et al. The tetramethoxyflavone zapotin selectively activates protein kinase C epsilon, leading to its down-modulation accompanied by Bcl-2, c-Jun and c-Fos decrease. 2012 Eur. J. Pharmacol. pmid:22381066
Cai M et al. The neuroprotective effect of eupatilin against ischemia/reperfusion-induced delayed neuronal damage in mice. 2012 Eur. J. Pharmacol. pmid:22683875
Guo W et al. Antagonistic effect of flavonoids on NSC-741909-mediated antitumor activity via scavenging of reactive oxygen species. 2010 Eur. J. Pharmacol. pmid:20854805
Ren L et al. Effects of flavone 6-substitutions on GABAA receptors efficacy. 2011 Eur. J. Pharmacol. pmid:21914441
Jansakul C et al. Relaxant mechanisms of 3, 5, 7, 3', 4'-pentamethoxyflavone on isolated human cavernosum. 2012 Eur. J. Pharmacol. pmid:22800934
Yin Y et al. Jaceosidin inhibits contact hypersensitivity in mice via down-regulating IFN-γ/STAT1/T-bet signaling in T cells. 2011 Eur. J. Pharmacol. pmid:21093428
Hall BJ et al. Flumazenil-independent positive modulation of gamma-aminobutyric acid action by 6-methylflavone at human recombinant alpha1beta2gamma2L and alpha1beta2 GABAA receptors. 2004 Eur. J. Pharmacol. pmid:15102527
Benabdallah H and Gharzouli K Effects of flavone on the contractile activity of the circular smooth muscle of the rabbit middle colon in vitro. 2015 Eur. J. Pharmacol. pmid:25895637
Alexandrakis M et al. Flavones inhibit proliferation and increase mediator content in human leukemic mast cells (HMC-1). 2003 Eur. J. Haematol. pmid:14703695
Hirvonen T et al. Flavonol and flavone intake and the risk of intermittent claudication in male smokers. 2004 Eur. J. Epidemiol. pmid:15180100
Park HJ et al. Baicalin induces NAD(P)H:quinone reductase through the transactivation of AP-1 and NF-kappaB in Hepa 1c1c7 cells. 2004 Eur. J. Cancer Prev. pmid:15548947
Philpott M et al. The antitumour agent 5,6-dimethylxanthenone-4-acetic acid acts in vitro on human mononuclear cells as a co-stimulator with other inducers of tumour necrosis factor. 2001 Eur. J. Cancer pmid:11576850
Ebel J and Hahlbrock K Enzymes of flavone and flavonol-glycoside biosynthesis. Coordinated and selective induction in cell-suspension cultures of Petroselinum hortense. 1977 Eur. J. Biochem. pmid:862617
Jasso-Chávez R and Moreno-Sánchez R Cytosol-mitochondria transfer of reducing equivalents by a lactate shuttle in heterotrophic Euglena. 2003 Eur. J. Biochem. pmid:14653820
Hayeshi R et al. The potential inhibitory effect of antiparasitic drugs and natural products on P-glycoprotein mediated efflux. 2006 Eur J Pharm Sci pmid:16846720
Raghav N and Garg S SAR studies of o-hydroxychalcones and their cyclized analogs and study them as novel inhibitors of cathepsin B and cathepsin H. 2014 Eur J Pharm Sci pmid:24780403
Rajesh G et al. Effect of hydroxyl substitution of flavone on angiogenesis and free radical scavenging activities: a structure-activity relationship studies using computational tools. 2010 Eur J Pharm Sci pmid:19874890
Duchnowicz P et al. Hypolipidemic and antioxidant effects of hydroxycinnamic acids, quercetin, and cyanidin 3-glucoside in hypercholesterolemic erythrocytes (in vitro study). 2012 Eur J Nutr pmid:21755326
Torres-Piedra M et al. A comparative study of flavonoid analogues on streptozotocin-nicotinamide induced diabetic rats: quercetin as a potential antidiabetic agent acting via 11beta-hydroxysteroid dehydrogenase type 1 inhibition. 2010 Eur J Med Chem pmid:20346546
Liao SY et al. QSAR, action mechanism and molecular design of flavone and isoflavone derivatives with cytotoxicity against HeLa. 2008 Eur J Med Chem pmid:18082913
Park H et al. Synthesis and inhibition of PGE2 production of 6,8-disubstituted chrysin derivatives. 2005 Eur J Med Chem pmid:15963606
Kothandan G et al. Docking and 3D-QSAR (quantitative structure activity relationship) studies of flavones, the potent inhibitors of p-glycoprotein targeting the nucleotide binding domain. 2011 Eur J Med Chem pmid:21723648
Rane RA et al. Synthesis and evaluation of novel marine bromopyrrole alkaloid-based hybrids as anticancer agents. 2013 Eur J Med Chem pmid:23584542
Dong JJ et al. Synthesis, biological evaluation and molecular docking studies of flavone and isoflavone derivatives as a novel class of KSP (kinesin spindle protein) inhibitors. 2013 Eur J Med Chem pmid:24184776
Neves MP et al. Prenylated derivatives of baicalein and 3,7-dihydroxyflavone: synthesis and study of their effects on tumor cell lines growth, cell cycle and apoptosis. 2011 Eur J Med Chem pmid:21496973
Kant R et al. Synthesis of newer 1,2,3-triazole linked chalcone and flavone hybrid compounds and evaluation of their antimicrobial and cytotoxic activities. 2016 Eur J Med Chem pmid:26922227
Imran S et al. Synthesis of novel flavone hydrazones: in-vitro evaluation of α-glucosidase inhibition, QSAR analysis and docking studies. 2015 Eur J Med Chem pmid:26491979
Ahmed N et al. Design, synthesis and antiproliferative activity of functionalized flavone-triazole-tetrahydropyran conjugates against human cancer cell lines. 2014 Eur J Med Chem pmid:24941129
Mitra I et al. Chemometric modeling of free radical scavenging activity of flavone derivatives. 2010 Eur J Med Chem pmid:20800321
Alvarez G et al. Massive screening yields novel and selective Trypanosoma cruzi triosephosphate isomerase dimer-interface-irreversible inhibitors with anti-trypanosomal activity. 2010 Eur J Med Chem pmid:20889239
Ilboudo O et al. Targeting structural motifs of flavonoid diglycosides using collision-induced dissociation experiments on flavonoid/Pb2+ complexes. 2012 Eur J Mass Spectrom (Chichester, Eng) pmid:23221119
Kammalla AK et al. Comparative pharmacokinetic interactions of Quercetin and Rutin in rats after oral administration of European patented formulation containing Hipphophae rhamnoides and Co-administration of Quercetin and Rutin. 2015 Eur J Drug Metab Pharmacokinet pmid:24888486
Kerr DJ and Kaye SB Flavone acetic acid--preclinical and clinical activity. 1989 Eur J Cancer Clin Oncol pmid:2680512
Hill S et al. Vascular collapse after flavone acetic acid: a possible mechanism of its anti-tumour action. 1989 Eur J Cancer Clin Oncol pmid:2591434
Ching LM and Baguley BC Hyporesponsiveness of macrophages from C3H/HeJ (endotoxin-resistant) mice to the antitumour agent flavone acetic acid (NSC 347512). 1989 Eur J Cancer Clin Oncol pmid:2591444
Ching LM and Baguley BC Reduction of cytotoxic effector cell activity in colon 38 tumours following treatment with flavone acetic acid. 1989 Eur J Cancer Clin Oncol pmid:2597283
Baguley BC et al. Comparison of the effects of flavone acetic acid, fostriecin, homoharringtonine and tumour necrosis factor alpha on colon 38 tumours in mice. 1989 Eur J Cancer Clin Oncol pmid:2702981
Lewis CR et al. Autonomic neuropathy following treatment with flavone acetic acid. 1989 Eur J Cancer Clin Oncol pmid:2703010
Ching LM and Baguley BC Effect of flavone acetic acid (NSC 347,512) on splenic cytotoxic effector cells and their role in tumour necrosis. 1989 Eur J Cancer Clin Oncol pmid:2737219
Ching LM and Baguley BC Enhancement of in vitro cytotoxicity of mouse peritoneal exudate cells by flavone acetic acid (NSC 347512). 1988 Eur J Cancer Clin Oncol pmid:3181272
Dodion P et al. Sensitivity of normal human bone marrow myeloid progenitor cells to anthracycline, cisplatin, anthracene and flavone acetic acid derivatives, and its relevance for the prediction of human plasma concentrations of anticancer drugs. 1987 Eur J Cancer Clin Oncol pmid:3436354
Ching LM and Baguley BC Induction of natural killer cell activity by the antitumour compound flavone acetic acid (NSC 347 512). 1987 Eur J Cancer Clin Oncol pmid:3665989
Capolongo LS et al. Antiproliferative properties of flavone acetic acid (NSC 347512) (LM 975), a new anticancer agent. 1987 Eur J Cancer Clin Oncol pmid:3678316
Dodion PF et al. Clinical and pharmacokinetic phase I trial with the diethylaminoester of flavone acetic acid (LM985, NSC 293015). 1987 Eur J Cancer Clin Oncol pmid:3653200
Schroyens WA et al. In vitro chemosensitivity testing of flavone acetic acid (LM975; NSC 347512) and its diethylaminoethyl ester derivative (LM985; NSC 293015). 1987 Eur J Cancer Clin Oncol pmid:3653209
Smith GP et al. Flavone acetic acid (NSC 347512) induces haemorrhagic necrosis of mouse colon 26 and 38 tumours. 1987 Eur J Cancer Clin Oncol pmid:3653213