Search results for "chemistry [Oligopeptides]"

showing 10 items of 211 documents

Synthesis of iodobiaryls and dibenzofurans by direct coupling at BDD anodes.

2014

The first direct oxidative phenol-arene cross-coupling reactions of an iodine-containing guaiacol derivative and the possible over-oxidation products of electron-rich phenols are described. Hereby, a "green" and targeted synthesis for dibenzofurans was developed.

HalogenationChemistryGuaiacolHalogenationOxidation reductionGreen Chemistry TechnologyCatalysisAnodeCatalysischemistry.chemical_compoundPhenolsOrganic chemistryDirect couplingPhenolsGuaiacolPhysical and Theoretical ChemistryDiamondElectrodesOxidation-ReductionDerivative (chemistry)BenzofuransBoronFaraday discussions
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Speciation of methylmercury in market seafood by thermal degradation, amalgamation and atomic absorption spectroscopy

2014

Sample thermal decomposition followed by mercury amalgamation and atomic absorption has been employed for the determination of methylmercury (MeHg) in fish. The method involves HBr leaching of MeHg, extraction into toluene, and back-extraction into an aqueous l-cysteine solution. Preliminary studies were focused on the extraction efficiency, losses, contaminations, and species interconversion prevention. The limit of detection was 0.018µgg(-1) (dry weight). The intraday precision for three replicate analysis at a concentration of 4.2µgg(-1) (dry weight) was 3.5 percent, similar to the interday precision according to analysis of variance (ANOVA). The accuracy was guaranteed by the use of for…

Health Toxicology and Mutagenesischemistry.chemical_elementlaw.inventionchemistry.chemical_compoundDry weightlawAnimalsCysteineMethylmercuryDetection limitChemistrySpectrophotometry AtomicFishesPublic Health Environmental and Occupational HealthGreen Chemistry TechnologyMercuryGeneral MedicineReplicateMethylmercury CompoundsPollutionMercury (element)Certified reference materialsSeafoodEnvironmental chemistryLeaching (metallurgy)Atomic absorption spectroscopyEnvironmental MonitoringEcotoxicology and Environmental Safety
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Pressurized hot water extraction (PHWE) for the green recovery of bioactive compounds and steviol glycosides from Stevia rebaudiana Bertoni leaves

2018

Stevia rebaudiana Bertoni leaves are a natural source of diterpenic glycosides, and various bioactive compounds. The objectives were to characterize antioxidants and steviol glycosides in the extracts obtained from Stevia after "green" pressurized hot water extraction (PHWE). PHWE extracts were obtained at different temperatures (100, 130, 160 °C); static extraction times (5 and 10 min), and cycle numbers (1, 2, 3) using a constant pressure of 10.34 MPa. Temperature was the most important parameter for extraction, where the highest recoveries of all bioactive compounds (except for carotenoids) were at 160 °C. Extracts obtained at longer static times had more steviol glycosides, condensed ta…

Hot TemperatureSteviolChemical FractionationAntioxidantsAnalytical Chemistrychemistry.chemical_compound0404 agricultural biotechnologyGlucosidesPressureSteviaPhenolsCarotenoidchemistry.chemical_classificationChromatographyExtraction (chemistry)WaterGlycosideGreen Chemistry Technology04 agricultural and veterinary sciencesGeneral Medicine040401 food scienceGreen extraction ; Total phenolics ; Condensed tannins ; Chlorophylls/carotenoids ; Stevioside/rebaudioside APlant LeavesHot water extractionStevia rebaudianachemistryProanthocyanidinDiterpenes KauraneFood ScienceFood Chemistry
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New Cathepsin Inhibitors to Explore the Fluorophilic Properties of the S 2 Pocket of Cathepsin B: Design, Synthesis, and Biological Evaluation

2011

5 páginas, 1 figura, 2 tablas -- PAGS nros. 5256-5260

Hydrocarbons FluorinatedStereochemistryStereoisomerismhydrolasesstereoselectivityCatalysisCathepsin BCathepsin BNitrilesinhibitorsCombinatorial Chemistry TechniquesHumansMoleculefluorinated ligandsBiological evaluationCathepsinMolecular StructureCombinatorial Chemistry TechniquesligandsChemistryOrganic ChemistryStereoisomerismDipeptidesGeneral Chemistryfluorinated fluorinatedDesign synthesisDrug DesignpeptidesStereoselectivityChemistry – A European Journal
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Tetrathiafulvalene-Capped Hybrid Materials for the Optical Detection of Explosives

2013

[EN] Mesoporous silica microparticles capped with TTF moieties and containing a ruthenium dye in the pores were used for the turn-on optical detection of the nitroaromatic explosives Tetryl and TNT via a selective pore uncapping and release of the entrapped dye.

INGENIERIA DE LA CONSTRUCCIONMaterials scienceExplosive materialInorganic chemistrychemistry.chemical_elementChemistry Techniques AnalyticalNitroaromatic explosivesMolecular Gateschemistry.chemical_compoundQUIMICA ORGANICANitroaromatic explosivesExplosive AgentsHeterocyclic CompoundsQUIMICA ANALITICAControlled releaseGeneral Materials ScienceChemosensorsQUIMICA INORGANICAMesoporous solidsMesoporous silicaSilicon DioxideTetrylControlled releaseRutheniumchemistryTetrathiafulvaleneHybrid materialPorosityTetrathiafulvaleneTrinitrotolueneACS Applied Materials & Interfaces
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Optical chemosensors and reagents to detect explosives

2012

[EN] This critical review is focused on examples reported from 1947 to 2010 related to the design of chromo-fluorogenic chemosensors and reagents for explosives (141 references). © 2012 The Royal Society of Chemistry.

INGENIERIA DE LA CONSTRUCCIONMaterials scienceOptical PhenomenaExplosive materialNanotechnologyLight related phenomenaColorimetry (chemical method)Chemistry Techniques AnalyticalNitroaromatic explosivesQUIMICA ORGANICAExplosive AgentsQUIMICA ANALITICAIndicatorsChemical analysisDyesReagentsQUIMICA INORGANICAOptical ProcessesGeneral ChemistryMarkers and buffersExplosive AgentsSpectrometry FluorescenceSpectrofluorometryIndicators and ReagentsColorimetryOptical Processes
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Analytical tools used for the identification and quantification of pectin extracted from plant food matrices, wastes and by-products: A review

2018

Pectin is the methylated ester of polygalacturonic acid and has a wide range of applications. It can be used in food and animal feed as well as in pharmaceutical and cosmetic products. Pectin is traditionally used as a gelling agent in fruit-based products, as a stabilizer in some fruit juices and milk drinks and fruit filling for bakery and confectionary products, but their potential applications differ according to their chemical composition. Therefore, at this stage of development, it is of a great importance to find fast, reliable methods to not only identify and quantify pectin, but also to determine its chemical structure and composition when it is extracted from plant matrices, waste…

Identificationfood.ingredientPectinAnimal feedChemical structure02 engineering and technologyPlant foodsChemistry Techniques AnalyticalAnalytical Chemistry0404 agricultural biotechnologyfoodSettore AGR/13 - CHIMICA AGRARIAQuantificationAnalytical toolsAnimalsFood scienceChemical compositionWaste ProductsEvaporative light scatteringMass spectrometryPectin ; Analytical tools ; Identification ; Quantification ; HPLC ; Evaporative light scattering ; Mass spectrometryChemistryfood and beverages04 agricultural and veterinary sciencesGeneral MedicinePlants021001 nanoscience & nanotechnologyPectin040401 food scienceAnalytical tools; Evaporative light scattering; HPLC; Identification; Mass spectrometry; Pectin; Quantification;Fruit and Vegetable JuicesStructural compositionPectinsHPLC0210 nano-technologyFood AnalysisFood ScienceStabilizer (chemistry)
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Synthesis of tumor-associated MUC1-glycopeptides and their multivalent presentation by functionalized gold colloids

2014

The mucin MUC1 is a glycoprotein involved in fundamental biological processes, which can be found over-expressed and with a distinctly altered glycan pattern on epithelial tumor cells; thus it is a promising target structure in the quest for effective carbohydrate-based cancer vaccines and immunotherapeutics. Natural glycopeptide antigens indicate only a low immunogenicity and a T-cell independent immune response; however, this major drawback can be overcome by coupling of glycopeptide antigens multivalently to immunostimulating carrier platforms. In particular, gold nanoparticles are well suited as templates for the multivalent presentation of glycopeptide antigens, due to their remarkably…

Immunoassaychemistry.chemical_classificationGlycanbiologyImmunogenicityMucin-1Organic ChemistryGlycopeptidesChemistry Techniques SyntheticGold ColloidBiochemistryCombinatorial chemistryGlycopeptideImmobilized ProteinsImmune systemchemistryAntigenBiochemistryColloidal goldQuartz Crystal Microbalance Techniquesbiology.proteinPhysical and Theoretical ChemistryGlycoproteinMUC1Organic & Biomolecular Chemistry
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Two-Step Route to Indoles and Analogues from Haloarenes: A Variation on the Fischer Indole Synthesis

2012

In a new variation on the Fischer indole synthesis, readily available haloarenes are converted into a wide range of indoles in just two steps by halogen-magnesium exchange and quenching with di-tert-butyl azodicarboxylate, followed by reaction with aldehydes or ketones under acidic conditions. The protocol, which is readily extended to the preparation of indole isosteres, 4- and 6-azaindoles and thienopyrroles, obviates the need to prepare potentially toxic aryl hydrazines, simultaneously avoiding undesirable anilines such as naphthylamines.

Indole testQuenching (fluorescence)IndolesHalogenationChemistryArylOrganic ChemistryTwo stepFischer synthesiHalogenationGreen Chemistry TechnologyChemistry Techniques SyntheticHydrocarbons AromaticSettore CHIM/08 - Chimica Farmaceuticachemistry.chemical_compoundIndoleFischer indole synthesisOrganic chemistrythienopyrrolesMagnesiumFischer synthesis; Indoles; azaindoles; thienopyrrolesFischer synthesisazaindolesazaindole
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Synthesis of Functionalized Indoles with a Trifluoromethy-Substituted Stereogenic Tertiary Carbon Atom Through an Enantioselective Friedel-Crafts Alk…

2010

[EN] Chiral complexes of BINOL-based ligands with zirconium tert-butoxide catalyze the Friedel-Crafts alkylation reaction of indoles with beta-trifluoromethyl-alpha,beta-unsaturated ketones to give functionalized indoles with an asymmetric tertiary carbon center attached to a trifluoromethyl group. The reaction can be applied to a large number of substituted alpha-trifluoromethyl enones and substituted indoles. The expected products were obtained with good yields and ees of up to 99%.

IndolesHydrocarbons FluorinatedAlkylationEnonesStereoisomerismAlkylationElectrophilic aromatic substitutionLigandsMedicinal chemistryCatalysisCatalysisStereocenterchemistry.chemical_compoundAsymmetric catalysisOrganic chemistryCombinatorial Chemistry TechniquesAromatic substitutionFriedel–Crafts reactionTrifluoromethylMolecular StructureChemistryOrganic ChemistryEnantioselective synthesisStereoisomerismGeneral ChemistryKetonesCarbonFISICA APLICADAZirconiumFluorinated compounds
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