Search results for "TYR"

showing 10 items of 2017 documents

A system for rapid radiochemical separations from aqueous solutions

1969

Abstract For the study of short-lived fission products, an automatic system has been developed that allows to irradiate aqueous solutions sealed in polystyrene capsules, to separate chemically the radioactive products formed, and to start counting, all within a few seconds. Irradiations are performed in a pneumatic tube system installed in a horizontal beam hole of a reactor. The capsule is projected into a separation apparatus where it breaks by impact. Its content is then sucked through a thin reactive layer that takes up the desired product. The whole sequence of irradiation, transportation, chemical separation, and counting is controlled by automatic timers. The adaption of this techniq…

Chemical separationchemistry.chemical_compoundFission productsAqueous solutionMaterials sciencechemistryRadiochemistryGeneral MedicineIrradiationPolystyreneLayer (electronics)Pneumatic tubeBeam (structure)Nuclear Instruments and Methods
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Cytotoxicity and antileishmanial activity of Annona muricata pericarp

2000

Abstract Hexane, ethyl acetate and methanol extracts of Annona muricata pericarp were tested in vitro against Leishmania braziliensis and L. panamensis promastigotes, and against cell line U-937. The ethyl acetate extract was more active than the other extracts and even of Glucantime® used as reference substance. Its fractionation led to the isolation of three acetogenins — annonacin, annonacin A and annomuricin A.

Chemical structureAntiprotozoal AgentsEthyl acetateAnnonacinFractionationCell LineLactoneschemistry.chemical_compound4-ButyrolactoneDrug DiscoveryAnimalsHumansFuransMedicinal plantsCytotoxicityAnnona muricataLeishmaniaPharmacologyPlants MedicinalbiologyTraditional medicinePlant ExtractsGeneral Medicinebiology.organism_classificationLeishmania braziliensischemistryBiochemistryFitoterapia
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From Spherical Mesopores to Worm-Shaped Mesopores : Morphology Transition in Titania–Polystyrene-b-poly(ethylene oxide) Composite Films with Increasi…

2013

A morphology transition from spherical mesopores to worm-shaped mesopores within titania block copolymer composite thin films has been observed by varying the sol–gel reaction time from 40 min to 48 h in the four-component templating system of polystyrene-$\mathit{b}$-poly(ethylene oxide) (PS-$\mathit{b}$-PEO), 1,4-dioxane, concentrated HCl, and titanium tetraisopropoxide (TTIP) with a PS-$\mathit{b}$-PEO mass concentration of 0.25 wt.-%. The impact of the sol–gel reaction time on the local structure, long-range lateral structure, and vertical structure of the as-prepared, calcined, and UV-degraded thin films as well as the structural changes in solution have been systematically investigate…

ChemieNanotechnologyMicellelaw.inventionInorganic ChemistryX-ray reflectivitychemistry.chemical_compoundDynamic light scatteringchemistryChemical engineeringlawddc:540Grazing-incidence small-angle scatteringCalcinationPolystyreneMesoporous materialSol-gel
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Kinetics of styrene biodegradation by Pseudomonas sp. E-93486

2011

The research into kinetics of styrene biodegradation by bacterial strain Pseudomonas sp. E-93486 coming from VTT Culture Collection (Finland) was presented in this work. Microbial growth tests in the presence of styrene as the sole carbon and energy source were performed both in batch and continuous cultures. Batch experiments were conducted for initial concentration of styrene in the liquid phase changed in the range of 5–90 g m−3. The Haldane model was found to be the best to fit the kinetic data, and the estimated constants of the equation were: μm = 0.1188 h−1, KS = 5.984 mg l−1, and Ki = 156.6 mg l−1. The yield coefficient mean value \documentclass[12pt]{minimal} \usepackage{amsmath} \…

ChemistryBatch experimentKineticsAnalytical chemistryGeneral MedicineChemostatBacterial growthApplied Microbiology and BiotechnologyBiotechnological Products and Process EngineeringCarbonDilutionStyreneKineticschemistry.chemical_compoundChemostatPseudomonasYield (chemistry)Organic chemistrySensitivity (control systems)Energy sourceStyreneBiotransformationBiotechnologyApplied Microbiology and Biotechnology
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Size Dependence of Tracer Diffusion in Supercooled Liquids

1996

We have determined by forced Rayleigh scattering the diffusion coefficients D of several photochromic tracers with van der Waals radii between 0.38 and 8 nm (the largest ones being photolabeled polystyrene micronetworks) in 10 glass-forming liquids at temperatures between the glass temperature Tg and ∼1.2Tg. The results were analyzed in terms of power law plots, D(T) ∝ T/η(T)ξ, where η is the solvent shear viscosity, and temperature shifts, D(T) ∝ T/η(T + ΔT). The shift ΔT was related with the width of the rotational correlation time distribution via the time−temperature superposition principle.

ChemistryDiffusionGeneral EngineeringThermodynamicsPower lawPhysics::Fluid DynamicsCondensed Matter::Soft Condensed Mattersymbols.namesakeSuperposition principlechemistry.chemical_compoundsymbolsVan der Waals radiusPolystyrenePhysical and Theoretical ChemistrySupercoolingGlass transitionRotational correlation timeThe Journal of Physical Chemistry
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ChemInform Abstract: Enantioselective Henry Addition of Methyl 4-Nitrobutyrate to Aldehydes. Chiral Building Blocks for 2-Pyrrolidinones and Other De…

2010

The reaction is applied to a wide range or aromatic and aliphatic aldehydes and proceeds with moderate to good diastereoselectivities.

ChemistryEnantioselective synthesisOrganic chemistryGeneral MedicinePyrrolidinonesMethyl 4-nitrobutyratePyrrole derivativesChemInform
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A theoretical study of the electronic spectrum of styrene

1999

Abstract The electronic spectrum of styrene has been studied by using multiconfigurational second-order perturbation theory (CASPT2). The study includes geometry optimization of the ground state, the lowest triplet state, and the lowest singlet excited state. The covalent 2 1 A ′ state placed vertically at 4.34 eV is assigned to the first band. The 1 1 A ′→3 1 A ′ transition located at 4.97 eV is responsible for the second band. The most intense feature involves the 5 1 A ′ state, which is calculated to lie 6.19 eV above the ground state. The lowest singlet–singlet Rydberg transition (3s) is predicted to occur at 5.85 eV.

ChemistryGeneral Physics and AstronomyEnergy minimizationStyrenesymbols.namesakechemistry.chemical_compoundComputer Science::Systems and ControlExcited stateRydberg formulasymbolsSinglet statePhysical and Theoretical ChemistryPerturbation theoryTriplet stateAtomic physicsGround stateChemical Physics Letters
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Control of the mutagenicity of aromatic amines by protein kinases and phosphatases

1997

The role of protein kinase C and protein phosphatases was examined in the control of mutagenic metabolites of aromatic amines. Various metabolic activating systems derived from rat liver were treated with: 12-O-tetradecanoylphorbol-13-acetate (TPA), a protein kinase C modulator; okadaic acid (OA), a potent inhibitor of serine/threonine protein phosphatases (PP1 and PP2A); and ortho-vanadate (OV), an inhibitor of tyrosine phosphatases. TPA used over a wide concentration range (10−9–10−6 M) did not affect the bacterial mutagenicity of the aromatic amines and of the aromatic amide investigated, 2-aminoanthracene, 2-aminofluorene and 2-acetylaminofluorene (2AAF). At the molecular level, TPA did…

ChemistryHealth Toxicology and MutagenesisPhosphataseProtein phosphatase 1General MedicineProtein phosphatase 2Protein tyrosine phosphataseOkadaic acidToxicologychemistry.chemical_compoundBiochemistryPhosphorylationProtein Phosphatase InhibitorProtein kinase CArchives of Toxicology
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Ancillary Ligand Effect on Single-Site Styrene Polymerization:  Isospecificity of Group 4 Metal Bis(phenolate) Catalysts

2003

Styrene is polymerized isospecifically by group 4 metal complexes that contain a C2-symmetrically coordinated 1,4-dithiabutane-linked bis(phenolato) ligand activated by methylaluminoxane.

ChemistryLigandMethylaluminoxaneGeneral ChemistryBiochemistryCatalysisStyreneCatalysisMetalchemistry.chemical_compoundColloid and Surface ChemistryPolymerizationSingle siteGroup (periodic table)visual_artPolymer chemistryvisual_art.visual_art_mediumJournal of the American Chemical Society
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Bioinspired self-assembly of tyrosinase-modified silicatein and fluorescent core-shell silica spheres.

2014

Inspired by the intermolecular cross-linking of mussel foot proteins and their adhesive properties, tyrosinase has been used to modify recombinant silicatein. DOPA/DOPAquinone-mediated cross-linking and interfacial interactions enhanced both self-assembly of silicatein building blocks and templating of core–shell silica spheres, resulting in fluorescent biomimetic silicatein–silica hybrid mesofibers.

ChemistryMonophenol MonooxygenaseTyrosinaseBiophysicsNanotechnologySilicon DioxideBiochemistryFluorescenceCathepsinsPoriferaCore shellNanoporesBiomimetic MaterialsMaterials TestingMolecular MedicineAnimalsSelf-assemblyAdhesiveEngineering (miscellaneous)NanospheresBiotechnologyFluorescent DyesBioinspirationbiomimetics
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