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
Lupus Erythematosus, Systemic D008180 43 associated lipids
Lymphedema D008209 4 associated lipids
Mammary Neoplasms, Experimental D008325 67 associated lipids
Melanoma D008545 69 associated lipids
Neoplasm Invasiveness D009361 23 associated lipids
Neoplasms, Experimental D009374 10 associated lipids
Pain D010146 64 associated lipids
Pancreatic Neoplasms D010190 77 associated lipids
Prostatic Neoplasms D011471 126 associated lipids
Osteosarcoma D012516 50 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
Yun CS et al. Expression of parsley flavone synthase I establishes the flavone biosynthetic pathway in Arabidopsis thaliana. 2008 Biosci. Biotechnol. Biochem. pmid:18391443
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
Aboul-Enein HY et al. Scavenging effects of phenolic compounds on reactive oxygen species. 2007 Biopolymers pmid:17373654
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
Cabrera M et al. Identification of chalcones as in vivo liver monofunctional phase II enzymes inducers. 2010 Bioorg. Med. Chem. pmid:20639112
Chen IL et al. Synthesis and antiproliferative evaluation of amide-containing flavone and isoflavone derivatives. 2008 Bioorg. Med. Chem. pmid:18662883
Lin YM et al. Chalcones and flavonoids as anti-tuberculosis agents. 2002 Bioorg. Med. Chem. pmid:12057669
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
Ono M et al. Synthesis and characterization of styrylchromone derivatives as beta-amyloid imaging agents. 2007 Bioorg. Med. Chem. pmid:17035032
Lameira J et al. Structure-activity relationship study of flavone compounds with anti-HIV-1 integrase activity: a density functional theory study. 2006 Bioorg. Med. Chem. pmid:16890444
Kubo I et al. Flavonols from Heterotheca inuloides: tyrosinase inhibitory activity and structural criteria. 2000 Bioorg. Med. Chem. pmid:10976523
Ullah Mughal E et al. Synthesis and antibacterial activity of substituted flavones, 4-thioflavones and 4-iminoflavones. 2006 Bioorg. Med. Chem. pmid:16603364
Xiang H et al. Synthesis and biological evaluation of isoflavone fatty acid esters with potential weight loss and hypolipidemic activities. 2010 Bioorg. Med. Chem. pmid:20392645
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
Iori F et al. Theoretical quantitative structure-activity relationships of flavone ligands interacting with cytochrome P450 1A1 and 1A2 isozymes. 2005 Bioorg. Med. Chem. pmid:15914008
Malolanarasimhan K et al. Synthesis and biological study of a flavone acetic acid analogue containing an azido reporting group designed as a multifunctional binding site probe. 2005 Bioorg. Med. Chem. pmid:15781383
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
Amato E et al. Investigation of fluorinated and bifunctionalized 3-phenylchroman-4-one (isoflavanone) aromatase inhibitors. 2014 Bioorg. Med. Chem. pmid:24345481
Valenti P et al. Synthesis and biological activity of some rigid analogues of flavone-8-acetic acid. 2000 Bioorg. Med. Chem. pmid:10968283
Mavel S et al. Synthesis and biological evaluation of a series of flavone derivatives as potential radioligands for imaging the multidrug resistance-associated protein 1 (ABCC1/MRP1). 2006 Bioorg. Med. Chem. pmid:16263302
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
Pick A et al. Structure-activity relationships of flavonoids as inhibitors of breast cancer resistance protein (BCRP). 2011 Bioorg. Med. Chem. pmid:21354800
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