Search results for "Biochanin A"

showing 5 items of 5 documents

Characterization of particle morphology of biochanin A molecularly imprinted polymers and their properties as a potential sorbent for solid-phase ext…

2014

Abstract Molecularly imprinted polymers (MIPs) with biochanin A as a template were obtained using a bulk polymerization with non-covalent imprinting approach. The polymers were prepared in acetonitrile as porogen, using ethylene glycol dimethacrylate (EDMA) as cross-linking agent. The synthesis, with an application of 1′,1′-azobis(cyclohexanecarbonitrile) (ACHN) as an initiator, has been performed thermally. During the synthesis process the effect of different functional monomers such as methacrylic acid (MAA), acrylamide (AA) and 4-vinylpyridine (4-VP) was investigated. The application of nitrogen sorption porosimetry, scanning electron microscopy (SEM), and Fourier transform infrared spec…

AcetonitrilesMaterials scienceNitrogenPolymersPyridinesEthylene glycol dimethacrylateBioengineeringPolymerizationBiochanin ABiomaterialschemistry.chemical_compoundSpectroscopy Fourier Transform Infraredsolid-phase extractionSolid phase extractionFourier transform infrared spectroscopyChromatography High Pressure Liquidchemistry.chemical_classificationphytoestrogensAcrylamideChromatographySolid Phase ExtractionMolecularly imprinted polymerPolymerGenisteinIsoflavonesCross-Linking ReagentschemistryMethacrylic acidMechanics of MaterialsadsorptionMicroscopy Electron ScanningMethacrylatesmolecular imprintingMolecular imprintingNuclear chemistryMaterials Science & Engineering C-Materials for Biological Applications
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Prenylated isoflavones from the stem bark of Erythrina sacleuxii

2018

Abstract Two new prenylated isoflavones, named erysacleuxin A (1) and B (2), along with eight known compounds, biochanin A (3), 5′-(3-methylbut-2-enyl)pratensein (4), 7-demethylrobustigenin (5), 3′-(3-methylbut-2-enyl)biochanin A (6) abyssinone V-4′-methyl ether (7), sigmoidin E (8), erythrinasinate (9), and burtinone (10) were isolated from the stem bark of Erythrina sacleuxii Hua (Leguminosae). The structures were determined based on spectroscopic and spectrometric data. All isolated compounds were evaluated for antifungal activity against Botrytis cinerea, Candida albicans, Eremothecium coryli, Penicillium notatum, Pyricularia oryzae, and Rhizomucor miehei with compounds 3, 4 and 6 showi…

Eremothecium corylibiologyTraditional medicine010405 organic chemistryRhizomucor mieheiPratenseinPlant ScienceIsoflavonesbiology.organism_classification01 natural sciencesBiochemistry0104 chemical sciencesBiochanin A010404 medicinal & biomolecular chemistrychemistry.chemical_compoundchemistryPenicilliumErythrina sacleuxiiAgronomy and Crop ScienceBiotechnologyBotrytis cinereaPhytochemistry Letters
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Acute effects of three isoflavone class phytoestrogens and a mycoestrogen on cerebral microcirculation.

2007

Phytoestrogens and mycoestrogens are naturally occurring plant and fungus secondary metabolites with estrogen-like structure and/or actions. We aimed to check the hypothesis that phytoestrogens and mycoestrogens, due to their ability to elicit cerebral vasodilation, can induce acute increases in brain blood perfusion. For this purpose, we continuously recorded cerebrocortical perfusion by laser-Doppler flowmetry in anesthetized rats receiving intracarotid infusions (1 mg/kg) of one of the following estrogenic compounds: biochanin A, daidzein, genistein or zearalanone. We have shown the ability of two isoflavone class phytoestrogens (daidzein and biochanin A) and the mycoestrogen zearalanone…

Maleendocrine systemmedicine.medical_specialtyPharmaceutical SciencePhytoestrogensPharmacologyBiochanin Achemistry.chemical_compoundCerebral circulationInternal medicineDrug DiscoverymedicineAnimalsZearalanoneRats WistarPharmacologyChemistryMicrocirculationDaidzeinfood and beveragesMycoestrogenBrainIsoflavonesIsoflavonesRatsEndocrinologyComplementary and alternative medicineCerebral blood flowCerebrovascular CirculationMolecular MedicineZearalenonePhytoestrogensPhytomedicine : international journal of phytotherapy and phytopharmacology
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Surface molecularly imprinted silica for selective solid-phase extraction of biochanin A, daidzein and genistein from urine samples

2015

Selective molecularly imprinted silica polymer (SiO2MIP) for extraction of biochanin A, daidzein and genistein was synthesized using the surface molecular imprinting technique with the silica gel as a support. Biochanin A (BCA) was used as a template, 3-aminopropyltriethoxysilane (APTES) as a functional monomer, and tetraethoxysilicane (TEOS) as a cross-linker. Non-imprinted polymer with the sol–gel process (SiO2NIP) was also prepared for comparison. The synthesized polymers were characterized by Fourier transform infrared spectrometry (FTIR), scanning electron microscopy (SEM) and a standard Brunauer-Emett-Teller (BET) and Barret–Joyner–Halenda (BJH) analysis. The obtained results indicate…

PolymersSilica Gelmolecularly imprinted polymerBiochemistryAnalytical ChemistryBiochanin AMolecular Imprintingchemistry.chemical_compoundHumanssolid-phase extractionSolid phase extractionFourier transform infrared spectroscopyChromatographyPropylaminesChemistrySilica gelSolid Phase ExtractionOrganic ChemistryExtraction (chemistry)DaidzeinMolecularly imprinted polymerWaterGeneral MedicineSilanesSilicon DioxideGenisteinIsoflavonesurineCross-Linking ReagentsNanoparticlesFemaleMolecular imprintingPorosityJournal of Chromatography A
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Efficient extraction and preparative separation of four main isoflavonoids from Dalbergia odorifera T. Chen leaves by deep eutectic solvents-based ne…

2016

In this study, green and efficient deep eutectic solvent-based negative pressure cavitation-assisted extraction (DES-NPCE) followed by macroporous resin column chromatography was developed to extract and separate four main isoflavonoids, i.e. prunetin, tectorigenin, genistein and biochanin A from Dalbergia odorifera T. Chen leaves. The extraction procedure was optimized systematically by single-factor experiments and a Box-Behnken experimental design combined with response surface methodology. The maximum extraction yields of prunetin, tectorigenin, genistein and biochanin A reached 1.204, 1.057, 0.911 and 2.448mg/g dry weight, respectively. Moreover, the direct enrichment and separation of…

TectorigeninChromatographyPlant ExtractsDalbergia010401 analytical chemistryClinical BiochemistryExtraction (chemistry)Cell BiologyGeneral Medicine010402 general chemistryIsoflavones01 natural sciencesBiochemistry0104 chemical sciencesAnalytical ChemistryDeep eutectic solventBiochanin APlant Leaveschemistry.chemical_compoundPrunetinColumn chromatographychemistryResponse surface methodologyChromatography LiquidEutectic systemJournal of Chromatography B
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