Genkwanin

Genkwanin is a lipid of Polyketides (PK) class. The involved functions are known as Synthesis, Gene Expression, nodulation, Signal Transduction and conjugation. The associated genes with Genkwanin are Genes, Bacterial.

Cross Reference

Introduction

To understand associated biological information of Genkwanin, 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 Genkwanin?

There are no associated biomedical information in the current reference collection.

Possible diseases from mapped MeSH terms on references

We collected disease MeSH terms mapped to the references associated with Genkwanin

MeSH term MeSH ID Detail
Osteosarcoma D012516 50 associated lipids
Acne Vulgaris D000152 35 associated lipids
Total 2

PubChem Associated disorders and diseases

What pathways are associated with Genkwanin

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 Genkwanin?

There are no associated biomedical information in the current reference collection.

What functions are associated with Genkwanin?


Related references are published most in these journals:

Function Cross reference Weighted score Related literatures

What lipids are associated with Genkwanin?

There are no associated biomedical information in the current reference collection.

What genes are associated with Genkwanin?

Related references are published most in these journals:


Gene Cross reference Weighted score Related literatures

What common seen animal models are associated with Genkwanin?

There are no associated biomedical information in the current reference collection.

NCBI Entrez Crosslinks

All references with Genkwanin

Download all related citations
Per page 10 20 50 100 | Total 75
Authors Title Published Journal PubMed Link
pmid:
Zhang J et al. [Quality of processed samples of Daphne genkwa Sieb. et Zucc]. 1997 Zhongguo Zhong Yao Za Zhi pmid:10743197
Ahmed MS et al. A weakly antimalarial biflavanone from Rhus retinorrhoea. 2001 Phytochemistry pmid:11576606
Zahid M et al. Flavonoid glycosides from Salvia moorcroftiana wall. 2002 Carbohydr. Res. pmid:11861014
Yuan S et al. [Comprehensive evaluation and practical confirmation on processing technology of Daphne genkwa Sieb. et Zucc]. 1999 Zhongguo Zhong Yao Za Zhi pmid:12205864
Ibañez E et al. Subcritical water extraction of antioxidant compounds from rosemary plants. 2003 J. Agric. Food Chem. pmid:12517098
Kraft C et al. In vitro antiplasmodial evaluation of medicinal plants from Zimbabwe. 2003 Phytother Res pmid:12601673
del Baño MJ et al. Phenolic diterpenes, flavones, and rosmarinic acid distribution during the development of leaves, flowers, stems, and roots of Rosmarinus officinalis. Antioxidant activity. 2003 J. Agric. Food Chem. pmid:12848492
Santos-Gomes PC et al. Determination of phenolic antioxidant compounds produced by calli and cell suspensions of sage (Salvia officinalis L.). 2003 J. Plant Physiol. pmid:14593803
Kim AR et al. Active components from Artemisia iwayomogi displaying ONOO(-) scavenging activity. 2004 Phytother Res pmid:14750192
Cao S et al. Cytotoxic triterpenoids from Acridocarpus vivy from the Madagascar rain forest. 2004 J. Nat. Prod. pmid:15217279
Martini ND et al. Biological activity of five antibacterial flavonoids from Combretum erythrophyllum (Combretaceae). 2004 J Ethnopharmacol pmid:15234754
del Baño MJ et al. Flavonoid distribution during the development of leaves, flowers, stems, and roots of Rosmarinus officinalis. postulation of a biosynthetic pathway. 2004 J. Agric. Food Chem. pmid:15291464
Zhang W et al. [Studies on the chemical constituents in roots of Daphne odora var. atrocaulis]. 2005 Zhongguo Zhong Yao Za Zhi pmid:16011095
Leonard E et al. Expression of a soluble flavone synthase allows the biosynthesis of phytoestrogen derivatives in Escherichia coli. 2006 Appl. Microbiol. Biotechnol. pmid:16025328
Park BY et al. Isolation of flavonoids, a biscoumarin and an amide from the flower buds of Daphne genkwa and the evaluation of their anti-complement activity. 2006 Phytother Res pmid:16685682
Sadhu SK et al. Prostaglandin inhibitory and antioxidant components of Cistus laurifolius, a Turkish medicinal plant. 2006 J Ethnopharmacol pmid:16814498
Pérez-Fons L et al. Rosemary (Rosmarinus officinalis) diterpenes affect lipid polymorphism and fluidity in phospholipid membranes. 2006 Arch. Biochem. Biophys. pmid:16949545
Zhang YH et al. [Studies on chemical constituents in spikes of Schizonepeta tenuifolia]. 2006 Zhongguo Zhong Yao Za Zhi pmid:17048568
Jones WP et al. Cytotoxic constituents from the fruiting branches of Callicarpa americana collected in southern Florida. 2007 J. Nat. Prod. pmid:17279798
Hara H et al. Laxative effect of agarwood leaves and its mechanism. 2008 Biosci. Biotechnol. Biochem. pmid:18256503
Saito T et al. Sakuranetin induces adipogenesis of 3T3-L1 cells through enhanced expression of PPARgamma2. 2008 Biochem. Biophys. Res. Commun. pmid:18522800
Brozic P et al. Flavonoids and cinnamic acid derivatives as inhibitors of 17beta-hydroxysteroid dehydrogenase type 1. 2009 Mol. Cell. Endocrinol. pmid:18835421
Su J et al. Flavonoids from Daphne giraldii Nitsche. 2008 Nat. Prod. Res. pmid:19023794
Jeon YM et al. Biological synthesis of 7-O-methyl Apigenin from naringenin using escherichia coli expressing two genes. 2009 J. Microbiol. Biotechnol. pmid:19494697
Androutsopoulos VP et al. CYP1-mediated antiproliferative activity of dietary flavonoids in MDA-MB-468 breast cancer cells. 2009 Toxicology pmid:19666078
Henchiri H et al. Sesquiterpenoids from Teucrium ramosissimum. Phytochemistry pmid:19766274
Pérez-Fons L et al. Relationship between the antioxidant capacity and effect of rosemary (Rosmarinus officinalis L.) polyphenols on membrane phospholipid order. 2010 J. Agric. Food Chem. pmid:19924866
Tamaki Y et al. Activated glutathione metabolism participates in protective effects of carnosic acid against oxidative stress in neuronal HT22 cells. 2010 Planta Med. pmid:19941258
Bai N et al. Flavonoids and phenolic compounds from Rosmarinus officinalis. 2010 J. Agric. Food Chem. pmid:20397728
Mohammadi M et al. Two new coumarins from the chloroform extract of Angelica urumiensis from Iran. 2010 Chem. Pharm. Bull. pmid:20410639
Lai HY et al. Blechnum orientale Linn - a fern with potential as antioxidant, anticancer and antibacterial agent. 2010 BMC Complement Altern Med pmid:20429956
Liu RH et al. [Studies on the chemical constituents from Daphne tangutica]. 2009 Zhong Yao Cai pmid:20432900
Devkota HP et al. Flavonoids from the aerial parts of Diplomorpha canescens. 2010 Chem. Pharm. Bull. pmid:20523001
Brechenmacher L et al. Soybean metabolites regulated in root hairs in response to the symbiotic bacterium Bradyrhizobium japonicum. 2010 Plant Physiol. pmid:20534735
Li YN et al. A simple and efficient protocol for large-scale preparation of three flavonoids from the flower of Daphne genkwa by combination of macroporous resin and counter-current chromatography. 2010 J Sep Sci pmid:20535750
Tohno H et al. Evaluation of estrogen receptor Beta binding of pruni cortex and its constituents. 2010 Yakugaku Zasshi pmid:20606380
Jordán MJ et al. Introduction of distillate rosemary leaves into the diet of the Murciano-Granadina goat: transfer of polyphenolic compounds to goats' milk and the plasma of suckling goat kids. 2010 J. Agric. Food Chem. pmid:20608728
Mizuochi K et al. New iridoid diesters of glucopyranose from Linaria canadensis (L.) Dum. 2011 J Nat Med pmid:20635154
Kunwar RM et al. Traditional herbal medicine in far-west Nepal: a pharmacological appraisal. 2010 J Ethnobiol Ethnomed pmid:21144003
Androutsopoulos VP et al. Comparative CYP1A1 and CYP1B1 substrate and inhibitor profile of dietary flavonoids. 2011 Bioorg. Med. Chem. pmid:21482471
Maia GL et al. Flavonoids from Praxelis clematidea R.M. King and Robinson modulate bacterial drug resistance. 2011 Molecules pmid:21666549
Borrás Linares I et al. Comparison of different extraction procedures for the comprehensive characterization of bioactive phenolic compounds in Rosmarinus officinalis by reversed-phase high-performance liquid chromatography with diode array detection coupled to electrospray time-of-flight mass spectrometry. 2011 J Chromatogr A pmid:21835416
Ben Sghaier M et al. Flavonoids and sesquiterpenes from Tecurium ramosissimum promote antiproliferation of human cancer cells and enhance antioxidant activity: a structure-activity relationship study. 2011 Environ. Toxicol. Pharmacol. pmid:22004952
Piao GC et al. Cytotoxic fraction from Artemisia sacrorum Ledeb. against three human cancer cell lines and separation and identification of its compounds. 2012 Nat. Prod. Res. pmid:22008023
Sati SC et al. Bioactive constituents and medicinal importance of genus Alnus. 2011 Pharmacogn Rev pmid:22279375
Hyldgaard M et al. Essential oils in food preservation: mode of action, synergies, and interactions with food matrix components. 2012 Front Microbiol pmid:22291693
Favela-Hernández JM et al. Antibacterial and antimycobacterial lignans and flavonoids from Larrea tridentata. 2012 Phytother Res pmid:22422605
Escandón-Rivera S et al. α-glucosidase inhibitors from Brickellia cavanillesii. 2012 J. Nat. Prod. pmid:22587572
Chang CW et al. Daphne Genkwa sieb. Et zucc. Water-soluble extracts act on enterovirus 71 by inhibiting viral entry. 2012 Viruses pmid:22590685