Search results for "Sulfhydryl compounds"

showing 10 items of 85 documents

The aminothiol redox status in haemodialysis patients does not improve with folate therapy.

2008

Patients on haemodialysis suffer from high cardiovascular morbidity and mortality, and oxidative stress may play a role in the pathophysiology of cardiovascular disease in these patients. Hyperhomocysteinemia is common in dialysis patients and may have pro-oxidant effects. Moreover, the redox status of the major plasma aminothiols (homocysteine [Hcy], cysteine and cysteinylglycine) may be regarded as a biomarker of oxidative stress. In the present study, we investigated the aminothiol redox status during a period of homocysteine-lowering therapy with folinic acid.In the first part of the study, 32 stable patients receiving maintenance haemodialysis were compared with 32 reference subjects. …

Malemedicine.medical_specialtyHyperhomocysteinemiaHomocysteineClinical Biochemistrymedicine.disease_causeGastroenterologychemistry.chemical_compoundFolinic acidFolic AcidRenal DialysisInternal medicinemedicineHumansSulfhydryl CompoundsAgedbusiness.industryGeneral MedicineMiddle Agedmedicine.diseaseRedox statusPathophysiologySurgerychemistryBiomarker (medicine)FemalebusinessOxidation-ReductionOxidative stressCysteinemedicine.drugScandinavian journal of clinical and laboratory investigation
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Thioether-Bearing Hyperbranched Polyether Polyols with Methionine-Like Side-Chains: A Versatile Platform for Orthogonal Functionalization

2016

The synthesis of thioether-bearing hyperbranched polyether polyols based on an AB/AB2 type copolymerization (cyclic latent monomers) is introduced. The polymers are prepared by anionic ring-opening multibranching copolymerization of glycidol and 2-(methylthio)ethyl glycidyl ether (MTEGE), which is conveniently accessible in a single etherification step. Slow monomer addition provides control over molecular weights. Moderate dispersities (Đ = 1.48–1.85) are obtained, given the hyperbranched structure. In situ 1H NMR copolymerization kinetics reveal reactivity ratios of rG = 3.7 and rMTEGE = 0.27. Using slow monomer addition, copolymer composition can be systematically varied, allowing for th…

Materials sciencePolymers and PlasticsPolymersAllyl glycidyl ether02 engineering and technology010402 general chemistryBranching (polymer chemistry)01 natural sciencesPolymerizationchemistry.chemical_compoundMethionineThioetherPolymer chemistryMaterials ChemistryCopolymerOrganic chemistrySulfhydryl CompoundsPropylene oxideMolecular StructureOrganic ChemistryTemperatureGlycidol021001 nanoscience & nanotechnologyIsocyanate0104 chemical sciencesMonomerchemistry0210 nano-technologyEthersMacromolecular Rapid Communications
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Transition to Reinforced State by Percolating Domains of Intercalated Brush-Modified Cellulose Nanocrystals and Poly(butadiene) in Cross-Linked Compo…

2013

The classic nanocomposite approach aims at percolation of low fraction of exfoliated individual reinforcing nanoscale elements within a polymeric matrix. By contrast, many of the mechanically excellent biological nanocomposites involve self-assembled and space-filled structures of hard reinforcing and soft toughening domains, with high weight fraction of reinforcements. Here we inspect a new concept toward mimicking such structures by studying whether percolation of intercalated domains consisting of alternating rigid and reinforcing, and soft rubbery domains could allow a transition to a reinforced state. Toward that, we present the functionalization of rigid native cellulose nanocrystals …

Materials sciencePolymers and PlasticsSurface PropertiesUltraviolet RaysComposite numberta221NanoparticleBioengineering02 engineering and technology010402 general chemistryElastomer01 natural sciencesNanocompositesBiomaterialsTensile StrengthButadienesMaterials ChemistrySulfhydryl CompoundsComposite materialCelluloseta116ta218Nanocompositeta214ta114021001 nanoscience & nanotechnology0104 chemical sciencesElastomersNanocrystalPercolationMicroscopy Electron ScanningClick chemistryNanoparticlesSurface modificationClick Chemistry0210 nano-technologyBiomacromolecules
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The thiol switch C684 in Mitofusin-2 mediates redox-induced alterations of mitochondrial shape and respiration

2017

Mitofusin-2 (MFN2) is a GTPase in the outer mitochondrial membrane involved in the regulation of mitochondrial fusion and bioenergetics. MFN2 also plays a role in mitochondrial fusion induced by changes in the intracellular redox state. Adding oxidized glutathione (GSSG), the core cellular stress indicator, to mitochondrial preparations stimulates mitochondrial fusion by inducing disulphide bond-mediated oligomer formation of MFN2 and its homolog MFN1 which involve cysteine 684 (C684) of MFN2. Mitochondrial hyperfusion represents an adaptive stress response that confers transient protection by increasing mitochondrial ATP production but how this depends on the thiol switch C684 in MFN2 has …

Mice Knockout0301 basic medicineCell RespirationMFN2Cell BiologyOxidative phosphorylationMitochondrionBiologyMitochondrial apoptosis-induced channelGTP PhosphohydrolasesMitochondriaCell biologyMice03 medical and health sciencesCellular and Molecular NeuroscienceMitofusin-2030104 developmental biologymitochondrial fusionAnimalsMFN1Sulfhydryl CompoundsATP–ADP translocaseCell ShapeOxidation-ReductionCells CulturedNeurochemistry International
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The gold-sulfur interface at the nanoscale.

2012

Thiolate-protected gold surfaces and interfaces, relevant for self-assembled monolayers of organic molecules on gold, for passivated gold nanoclusters and for molecule-gold junctions, are archetypal systems in various fields of current nanoscience research, materials science, inorganic chemistry and surface science. Understanding this interface at the nanometre scale is essential for a wide range of potential applications for site-specific bioconjugate labelling and sensing, drug delivery and medical therapy, functionalization of gold surfaces for sensing, molecular recognition and molecular electronics, and gold nanoparticle catalysis. During the past five years, considerable experimental …

Models MolecularChemistrySurface PropertiesGeneral Chemical EngineeringNanoparticleMolecular electronicsNanotechnologyStereoisomerismGeneral ChemistryCrystallography X-RayNanoclustersMolecular recognitionDrug Delivery SystemsMonolayerSurface modificationNanotechnologyNanometreGoldSulfhydryl CompoundsNanoscopic scaleSulfurNature chemistry
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Coordination polymers based on diiron tetrakis(dithiolato) bridged by alkali metals, electrical bistability around room temperature, and strong antif…

2015

Coordination polymer chains have been formed by the direct reaction between HSC6H2Cl2SH and FeCl3·6H2O in the presence of an aqueous solution of the corresponding alkali-metal hydroxide (M = Li, Na, and K) or carbonate (M = Rb and Cs). The structures consist of dimeric [Fe2(SC6H2Cl2S)4](2-) entities bridged by [M2(THF)4] [M = K (1), Rb (2), and Cs (3); THF = tetrahydrofuran] or {[Na2(μ-H2O)2(THF)2] (5 and 5') units. The smaller size of the lithium atom yields an anion/cation ion-pair molecule, [Li(THF)4]2[Fe2(SC6H2Cl2S)4] (4), in which the dianionic moieties are held together by Cl···Cl interactions. Electrical characterization of these compounds shows a general semiconductor behavior in wh…

Models MolecularCoordination polymerMetals AlkaliPolymersInorganic chemistryElectric ConductivityTemperatureAlkali metalIonInorganic Chemistrychemistry.chemical_compoundCrystallographychemistrySemiconductorsAntiferromagnetismHydroxideMoleculeFerrous CompoundsSulfhydryl CompoundsPhysical and Theoretical ChemistryTetrahydrofuranLithium atomInorganic chemistry
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Thioetherification of Chloroheteroarenes: A Binuclear Catalyst Promotes Wide Scope and High Functional-Group Tolerance

2014

A constrained binuclear palladium catalyst system affords selective thioetherification of a wide range of functionalized arenethiols with chloroheteroaromatic partners with the highest turnover numbers (TONs) reported to date and tolerates a large variety of reactive functions. The scope of this system includes the coupling of thiophenols with six- and five-membered 2-chloroheteroarenes (i.e., functionalized pyridine, pyrazine, quinoline, pyrimidine, furane, and thiazole) and 3-bromoheteroarenes (i.e., pyridine and furane). Electron-rich congested thiophenols and fluorinated thiophenols are also suitable partners. The coupling of unprotected amino-2-chloropyridines with thiophenol and the s…

Models MolecularHalogenationPyrazinePhosphinesPyridineschemistry.chemical_elementSulfidesLigandsCatalysisCatalysischemistry.chemical_compoundPhenolsPyridineOrganic chemistrySulfhydryl CompoundsFuransThiazoleThiophenolOrganic ChemistryQuinolineGeneral ChemistryCombinatorial chemistryThiazoleschemistryPyrazinesFunctional groupQuinolinesPalladiumPalladiumChemistry - A European Journal
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Nondestructive Size Determination of Thiol-Stabilized Gold Nanoclusters in Solution by Diffusion Ordered NMR Spectroscopy

2013

Diffusion ordered NMR spectroscopy (DOSY) was used as an analytical tool to estimate the size of thiol-stabilized gold nanoclusters in solution, namely, phenylethanethiol (PET) stabilized Au25(PET)18, Au38(PET)24, and Au144(PET)60. This was achieved by determining the diffusion coefficient and hydrodynamic radius from solution samples that were confirmed to be monodispersed by electrospray ionization mass spectrometry. The average cluster diameters obtained by this technique were estimated to be 1.7, 2.2, and 3.1 nm for the Au25(PET)18, Au38(PET)24, and Au144(PET)60 nanoclusters, respectively, which were shown to agree well with the average diameters of the corresponding single crystal or t…

Models MolecularMagnetic Resonance SpectroscopyHydrodynamic radiusChemistryDiffusionElectrospray ionizationta221Analytical chemistryNanoparticleNuclear magnetic resonance spectroscopyNanostructuresAnalytical ChemistryCharacterization (materials science)NanoclustersDiffusionGoldSulfhydryl CompoundsParticle SizeSingle crystalta116Analytical Chemistry
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A chirality-induced alpha phase and a novel molecular magnetic metal in the BEDT-TTF/tris(croconate)ferrate(iii) hybrid molecular system

2006

The novel paramagnetic and chiral anion [Fe(C5O5)3]32 has been combined with the organic donor BEDT-TTF (= ET = bis(ethylenedithio)tetrathiafulvalene) to yield the first chirality- induced α phase and a paramagnetic metal. Gomez Garcia, Carlos, Carlos.Gomez@uv.es ; Coronado Miralles, Eugenio, Eugenio.Coronado@uv.es ; Gimenez Saiz, Carlos, Carlos.Gimenez@uv.es

Models MolecularMagnetic metalUNESCO::QUÍMICAIronInorganic chemistryMolecular ConformationCyclopentanesCrystallography X-RayFerric Compounds:QUÍMICA [UNESCO]CatalysisIonMetalMagneticsParamagnetismchemistry.chemical_compoundPhase (matter)Materials ChemistryMoleculeSulfhydryl CompoundsNovelOrganicMolecular StructureChemistryUNESCO::QUÍMICA::Química analíticaTemperatureMetals and AlloysGeneral ChemistrySurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsParamagneticCrystallographyvisual_artYield (chemistry)Paramagnetic ; Organic ; Magnetic metal ; Novel:QUÍMICA::Química analítica [UNESCO]Ceramics and Compositesvisual_art.visual_art_mediumChirality (chemistry)TetrathiafulvaleneChem. Commun.
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On the Structure of Thiolate-Protected Au25

2008

Density functional theory is used to explore the structure of Au25(RS)18. The preferred structure consists of an icosahedral Au13 core protected by 6 RS-Au-RS-Au-RS units. The enhanced stability of the structure as an anion is found to originate from closure of an eight-electron shell for delocalized Au(6s) electrons. The evaluated XRD pattern and optical spectra are in good agreement with experimental data.

Models MolecularMolecular StructureChemistryIcosahedral symmetrySuperatomShell (structure)General ChemistryElectronCrystallography X-RayLigandsBiochemistryCatalysisIonCrystallographyDelocalized electronColloid and Surface ChemistryModels ChemicalNanoparticlesMoleculeDensity functional theorySulfhydryl CompoundsOrganogold CompoundsJournal of the American Chemical Society
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