Search results for " Ultraviolet"

showing 10 items of 337 documents

Trefoil factor TFF1-induced protection of conjunctival cells from apoptosis at premitochondrial and postmitochondrial levels.

2008

PURPOSE. Goblet cells of the conjunctival epithelium synthesize and secrete TFF1 (Trefoil factor 1), a small protease-resistant peptide that, together with mucins, is responsible for the rheologic properties of the tear film. This study aimed to determine whether TFF1, whose synthesis increases in inflammatory conditions such as pterygium, could protect conjunctival cells from apoptosis. METHODS. Chang conjunctival cells, either wild-type or expressing TFF1 through stable transfection, were exposed to benzalkonium chloride (BAK) and ultraviolet (UV) irradiation to trigger apoptosis. The authors used cell fractionation to detect lipid raft‐associated proteins, coimmunoprecipitation to explor…

MESH : Cell LineMESH : Chromosomes Human Pair 21Chromosomes Human Pair 21CellApoptosisMESH: Flow CytometryMESH: Caspase 8Membrane Potentials0302 clinical medicineMESH: Mitochondrial MembranesMESH: Chromosomes Human Pair 21MESH : Membrane Potentials0303 health sciencesCaspase 8MESH : Caspase 8MESH : Benzalkonium CompoundsMESH : Tumor Suppressor ProteinsChromosome MappingFas receptorFlow CytometryXIAPMitochondriaMESH : Epithelial Cellsmedicine.anatomical_structureMESH: Epithelial Cells030220 oncology & carcinogenesisMitochondrial MembranesTrefoil Factor-1MESH : MitochondriaMESH : TransfectionBenzalkonium CompoundsConjunctivaMESH: Benzalkonium CompoundsProgrammed cell deathMESH: Enzyme ActivationMESH : ConjunctivaUltraviolet RaysMESH : Flow CytometryMESH: MitochondriaMESH: ConjunctivaCaspase 3BiologyInhibitor of apoptosisCaspase 8TransfectionCell Line03 medical and health sciencesMESH : Mitochondrial Membranesmedicine[SDV.BBM] Life Sciences [q-bio]/Biochemistry Molecular BiologyHumansMESH: Membrane PotentialsMESH: Tumor Suppressor Proteins[SDV.BBM]Life Sciences [q-bio]/Biochemistry Molecular Biology[ SDV.BBM ] Life Sciences [q-bio]/Biochemistry Molecular Biology030304 developmental biologyMESH: HumansTumor Suppressor ProteinsMESH: ApoptosisMESH: TransfectionMESH : HumansEpithelial CellsMolecular biologyMESH: Cell LineEnzyme ActivationApoptosisMESH : Ultraviolet RaysMESH: Ultraviolet RaysMESH : Enzyme ActivationMESH: Chromosome MappingMESH : ApoptosisMESH : Chromosome Mapping
researchProduct

A Functionalized Noncovalent Macrocyclic Multiporphyrin Assembly from a Dizinc(II) Bis-Porphyrin Receptor and a Free-Base Dipyridylporphyrin

2003

The bis-porphyrin system ZnP 2 , in which two zinc porphyrins are connected by a phenanthroline linker in an oblique fashion, acts as a bifunctional receptor towards the complexation of free-base meso-5,10-bis(4'-pyridyl)-15,20-diphenylporphyrin (4'-cisDPyP). In solution, NMR spectroscopy evidenced quantitative formation of the tris-porphyrin macrocyclic assembly ZnP 2 (4'-cisDPyP), in which the two fragments are held together by two axial 4'-N(pyridyl)-Zn interactions. The remarkable stability of the edifice (an association constant of about 6 x 10 8 M - 1 was determined by UV/Vis absorption and emission titration experiments in toluene) is due to the almost perfect geometrical match betwe…

Macromolecular SubstancesMetalloporphyrinsPhenanthrolineOrganic ChemistryFree baseGeneral ChemistryNuclear magnetic resonance spectroscopyChromophoreCrystallography X-RayPhotochemistryPorphyrinMass SpectrometryCatalysisZincchemistry.chemical_compoundCrystallographyModels ChemicalchemistrySpectrophotometry UltravioletSelf-assemblySinglet stateBifunctionalChemistry - A European Journal
researchProduct

5-Methoxyuridine, a new modified constituent in tRNAs of Bacillaceae.

1976

Magnetic Resonance SpectroscopyBiophysicsBacillusBacillus subtilisMass spectrometryBiochemistryMass Spectrometrychemistry.chemical_compoundRNA TransferSpecies SpecificityStructural BiologyGeneticsMolecular BiologyUridineBacillus (shape)BacillaceaebiologyCell BiologyNuclear magnetic resonance spectroscopyRibonucleotidesbiology.organism_classificationChromatography Ion ExchangeUridinechemistryBiochemistrySpectrophotometry UltravioletBacillus subtilisFEBS letters
researchProduct

Circumdatin H, a new inhibitor of mitochondrial NADH oxidase, from Aspergillus ochraceus

2005

Circumdatin H (1), a new alkaloid from the culture broth of Aspergillus ochraceus, has been isolated, together with a known circumdatin, circumdatin E (2) and other known compounds: flavacol (3) and stephacidin A (4). The structure of 1 was established on the basis of chemical and spectral evidence. All of these alkaloids showed biological activity as inhibitors of the mammalian mitochondrial respiratory chain.

Magnetic Resonance SpectroscopyChemical PhenomenaSpectrophotometry InfraredStereochemistryCircumdatin HMass SpectrometryElectron Transportchemistry.chemical_compoundMultienzyme ComplexesDrug Discoveryheterocyclic compoundsNADH NADPH OxidoreductasesEnzyme InhibitorsPharmacologyAspergillus ochraceusBenzodiazepinonesbiologyChemistry PhysicalAlkaloidStephacidinBiological activityGeneral Medicinebiology.organism_classificationMitochondriaCircumdatin EMitochondrial respiratory chainchemistryBiochemistryFermentationNADH oxidaseSpectrophotometry UltravioletAspergillus ochraceus
researchProduct

The dynamic properties of the M121H azurin metal site as studied by NMR of the paramagnetic Cu(II) and Co(II) metalloderivatives

1998

The M121H azurin mutant in solution presents various species in equilibrium that can be detected and studied by 1H NMR of the Cu(II) and Co(II) paramagnetic metalloderivatives. In both cases up to three species are observed in slow exchange, the proportions of which are different for the two metalloderivatives. Above pH 5 the major species displays a tetrahedral coordination in which the His121 can be observed as a coordinated residue. Its metal site corresponds to a new type of site that is defined as a type 1.5 site. The second and third species resemble the wild type (type 1) azurin and, above pH 4.5, they are present only at a low concentration. At low pH a protonation process increases…

Magnetic Resonance SpectroscopyChemistryInorganic chemistryWild typeElectron Spin Resonance SpectroscopyTemperatureProtonationCell BiologyNuclear magnetic resonance spectroscopyCobaltHydrogen-Ion ConcentrationBiochemistryMetalParamagnetismCrystallographyResidue (chemistry)Azurinvisual_artvisual_art.visual_art_mediumSpectrophotometry UltravioletAzurinMolecular BiologyCopperCoordination geometry
researchProduct

Synthesis of a polymer-bound galactosylamine and its application as an immobilized chiral auxiliary in stereoselective syntheses of piperidine and am…

2004

A 2,3,4-tri-O-pivaloylated beta-D-galactopyranosyl azide bearing a hydroxy-functionalized spacer unit at the C-6 position of the galactose was synthesized and immobilized on the solid phase by using a polymer-bound chlorosilane. The azide was reduced to the corresponding galactopyranosylamine, which served as a versatile chiral auxiliary in highly diastereoselective Ugi four-component condensation reactions at ambient temperature. Fluoride-induced cleavage from the polymeric support furnished N-glycosylated N-acylated alpha-amino acid amides. The reaction of the immobilized galactosylamine with aldehydes gave rise to the corresponding aldimines, which underwent a domino Mannich-Michael cond…

Magnetic Resonance SpectroscopyDienePolymersMolecular ConformationGalactosamineCatalysisMass Spectrometrychemistry.chemical_compoundSolid-phase synthesisPiperidinesPolymer chemistryOrganic chemistryLewis acids and basesAmino AcidsChiral auxiliaryOrganic ChemistryDiastereomerStereoisomerismGeneral ChemistryCondensation reactionchemistryIndicators and ReagentsSpectrophotometry UltravioletAzidePiperidineChromatography Thin LayerChromatography LiquidChemistry (Weinheim an der Bergstrasse, Germany)
researchProduct

Synthesis of Soluble Donor-Acceptor Double-Cable polymers based on polythiophene and tetracyanoanthraquinodimethane (TCAQ).

2003

[structure: see text] Novel suitably functionalized tetracyanoanthraquinodimethane (TCAQ) derivatives covalently linked to thiophene moieties have been synthesized. The thiophene-based monomers have been chemically polymerized and copolymerized to yield new and soluble donor-acceptor double-cable polymers. The absorption and emission data reveal that the optical properties can be finely tuned by modifying the ratio of monomers in the copolymerization process.

Magnetic Resonance SpectroscopyFotoricettoriPolymersAnthraquinonesThiophenesmacromolecular substancesBiochemistryIndicators and Reagentchemistry.chemical_compoundSpettroscopiaThiophenePolymer chemistryCopolymerThiophenePhysical and Theoretical ChemistryPolymerPolimerichemistry.chemical_classificationOrganic Chemistrytechnology industry and agriculturePolymerSettore CHIM/06 - Chimica OrganicaMonomerchemistryPolymerizationCovalent bondLuminescent MeasurementLuminescent MeasurementsPolythiopheneMolecular MedicineAnthraquinoneIndicators and ReagentsSpectrophotometry UltravioletAbsorption (chemistry)Celle solariSintesi
researchProduct

DIFFERENTIAL SCANNING CALORIMETRY STUDY ON DRUG RELEASE FROM AN INULIN-BASED HYDROGEL AND ITS INTERACTION WITH A BIOMEMBRANE MODEL:pH AND LOADING EFF…

2008

Inulin has been derivatized with methacrylic anhydride (MA) and succinic anhydride (SA) to obtain a methacrylated/succinilated derivative (INU-MA-SA) able to produce a pH sensitive hydrogel after UV irradiation. The hydrogel was characterized and loaded with diflunisal (10.4, 17 and 24%, w/w) chosen as a model drug. The drug release from INU-MA-SA-based hydrogel to a biomembrane model made by unilamellar vesicles of dimyristoylphosphatidyl-choline (DMPC) was investigated at pH 4.0 and 7.4 by differential scanning calorimetry (DSC) that appears to be a suitable technique to follow the transfer kinetics of a drug from a controlled release system to a biomembrane model. The drug release from t…

Magnetic Resonance SpectroscopyINULIN HYDROGELS DRUG RELEASE DIFFERENTIAL SCANNING CALORIMETRYPharmaceutical ScienceDiflunisalMethacrylic anhydrideCentrifugationInsulysinDosage formchemistry.chemical_compoundDifferential scanning calorimetryX-Ray DiffractionSpectroscopy Fourier Transform InfraredmedicineHypoglycemic AgentsChromatography High Pressure LiquidChromatographyCalorimetry Differential ScanningVesicleAnti-Inflammatory Agents Non-Steroidaltechnology industry and agricultureSuccinic anhydrideInulinHydrogelsMembranes ArtificialSuccinatesHydrogen-Ion ConcentrationDiflunisalControlled releaseMolecular WeightchemistryChemical engineeringSolubilitySelf-healing hydrogelsSpectrophotometry UltravioletChromatography Thin LayerDimyristoylphosphatidylcholinemedicine.drug
researchProduct

Inulin-iron complexes: a potential treatment of iron deficiency anaemia.

2007

The aim of this work was that to synthesize macromolecular derivatives based on inulin able to complex iron and useful in the treatment of iron deficiency anaemia. Carboxylated or thiolated/carboxylated inulin derivatives were obtained by single or double step reactions, respectively. The first one was obtained by reaction of inulin (INU) with succinic anhydride (SA) alone obtaining INU-SA derivative; the second one was obtained by the reaction of INU with succinic anhydride and subsequent reaction of INU-SA with cysteine; both derivatives were treated with ferric chloride in order to obtain the INU-SA-Fe(III) and INU-SA-Cys-Fe(III) complexes. Both complexes showed an excellent biodegradabi…

Magnetic Resonance SpectroscopyIronInulinPharmaceutical Sciencechemistry.chemical_compoundSpectroscopy Fourier Transform InfraredmedicineMucoadhesionOrganic chemistryHumansInulinaseChromatography High Pressure LiquidAnemia Iron-DeficiencyPolyacrylic acidSuccinic anhydrideInulinInulin iron anaemiaGeneral MedicineIron deficiencymedicine.diseasechemistryIron-deficiency anemiaSettore CHIM/09 - Farmaceutico Tecnologico ApplicativoFerricSpectrophotometry UltravioletBiotechnologyNuclear chemistrymedicine.drugEuropean journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V
researchProduct

3-Oxo-rhazinilam:  A New Indole Alkaloid from Rauvolfia serpentina × Rhazya stricta Hybrid Plant Cell Cultures

2000

A new monoterpenoid indole alkaloid, 3-oxo-rhazinilam (1), was isolated from intergeneric somatic hybrid cell cultures of Rauvolfia serpentina and Rhazya stricta, and the structure was determined by detailed 1D and 2D NMR analysis. It was also proved that 3-oxo-rhazinilam (1) is a natural constituent of the hybrid cells.

Magnetic Resonance SpectroscopyLactamsPharmaceutical SciencePharmacognosyRhazya strictaRhazinilamMass SpectrometryRauwolfiaAnalytical Chemistrychemistry.chemical_compoundAlkaloidsRauvolfia serpentinaDrug DiscoveryBotanyCells CulturedPharmacologyPlants MedicinalIndole alkaloidbiologyApocynaceaeOrganic ChemistryIndolizinesbiology.organism_classificationCoculture TechniquesTerpenoidSomatic fusionComplementary and alternative medicinechemistryMolecular MedicineSpectrophotometry UltravioletJournal of Natural Products
researchProduct