Search results for "oxidation-reduction"

showing 10 items of 689 documents

Role of Redox Signaling, Protein Phosphatases and Histone Acetylation in the Inflammatory Cascade in Acute Pancreatitis: Therapeutic Implications

2010

Acute pancreatitis starts as a local inflammation of the pancreatic tissue but often leads to the systemic inflammatory response syndrome and death by multiple organ failure. Pro-inflammatory cytokines, particularly TNF-alpha and Il-1beta, play a pivotal role together with oxidative stress and glutathione depletion in the inflammatory response in this disease. Most inflammatory mediators act through mitogen activated protein kinases and nuclear factor kB. Nevertheless, elucidation of the precise mechanisms involved in activation and attenuation phases of the inflammatory cascade is still underway. Redox signaling mediated by inactivation of protein phosphatases and histone acetylation trigg…

Phosphodiesterase InhibitorsImmunologyPhosphataseBiologyHistonesDual-specificity phosphatasePhosphoprotein PhosphatasesHumansImmunology and AllergyPancreasHistone AcetyltransferasesInflammationPharmacologyHistone AcetyltransferasesKinaseAcetylationGeneral MedicineProtein phosphatase 2ChromatinCell biologyHistone Deacetylase InhibitorsHistonePancreatitisBiochemistryAcetylationAcute Diseasebiology.proteinSignal transductionOxidation-ReductionSignal TransductionInflammation & Allergy - Drug Targets
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Enhanced electron-transfer properties of cofacial porphyrin dimers through pi-pi interactions

2009

pi-pi assisted: Photoinduced electron transfer from cofacial porphyrin dimers to electron acceptors is prominently accelerated, whereas the back electron transfer is decelerated, relative to the corresponding porphyrin monomer (see figure).The radical cation of zinc tetrapentylporphyrin is dimerized with an excess of the neutral counterpart to form the dimer radical cation in which the unpaired electron is delocalized over both porphyrin rings. The dimeric radical cation exhibits an NIR absorption spectrum characteristic of weak pi-bond formation between the porphyrin rings. When cofacial porphyrin dimers, linked by different spacers, are oxidized such pi-bond formation between the porphyri…

Photosynthetic reaction centrePorphyrinsPhotosynthetic Reaction Center Complex ProteinsElectron donorpi interactionsPhotochemistry010402 general chemistry01 natural sciencesPhotoinduced electron transferCatalysisElectron Transportchemistry.chemical_compoundElectron transferredox chemistrypolycyclic compoundsComputingMilieux_MISCELLANEOUSchemistry.chemical_classificationphotosynthesisphotochemistryMolecular StructureChemistry010405 organic chemistryOrganic ChemistryGeneral ChemistryElectron acceptorelectron transferPorphyrinMarcus theory0104 chemical sciences[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistryZincUnpaired electronModels Chemical[ CHIM.THEO ] Chemical Sciences/Theoretical and/or physical chemistryThermodynamicsOxidation-ReductionAlgorithms
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Molecular Mechanisms of the Crosstalk Between Mitochondria and NADPH Oxidase Through Reactive Oxygen Species—Studies in White Blood Cells and in Anim…

2014

Aims: Oxidative stress is involved in the development of cardiovascular disease. There is a growing body of evidence for a crosstalk between different enzymatic sources of oxidative stress. With the present study, we sought to determine the underlying crosstalk mechanisms, the role of the mitochondrial permeability transition pore (mPTP), and its link to endothelial dysfunction. Results: NADPH oxidase (Nox) activation (oxidative burst and translocation of cytosolic Nox subunits) was observed in response to mitochondrial reactive oxygen species (mtROS) formation in human leukocytes. In vitro, mtROS-induced Nox activation was prevented by inhibitors of the mPTP, protein kinase C, tyrosine kin…

PhysiologyNeutrophilsClinical BiochemistryBiologyMitochondrionmedicine.disease_causeBiochemistryModels BiologicalSuperoxide dismutaseCyclophilinsMiceForum Original Research CommunicationsMitochondria (A. Daiber Ed.)medicineLeukocytesAnimalsHumansMolecular BiologyGeneral Environmental ScienceRespiratory Burstchemistry.chemical_classificationMice KnockoutReactive oxygen speciesNADPH oxidaseSuperoxide DismutaseAngiotensin IINADPH OxidasesBiological TransportCell BiologyRespiratory burstMitochondriaPeroxidesEnzyme ActivationCrosstalk (biology)Oxidative StressMitochondrial permeability transition poreBiochemistrychemistrybiology.proteincardiovascular systemGeneral Earth and Planetary SciencesReactive Oxygen SpeciesOxidation-ReductionOxidative stressCyclophilin D
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DC polarographic reduction of chloroguanide hydrochloride.

1984

Chloroguanide hydrochloride, an antimalarial drug, shows one well-defined DC polarographic wave in Britton-Robinson buffered media. In the pH range 3–9 the observed reduction wave is related to the reduction of the two azomethine centers on the monoprotonated biguanide group (BH+). The effects of pH and other experimental variables on the limiting current and half-wave potentials as well as the reduction mechanism are discussed.

PolarographyBiguanidemedicine.drug_classChemistryProguanil HydrochlorideInorganic chemistryLimiting currentPharmaceutical ScienceDimethylformamideHydrogen-Ion ConcentrationReduction (complexity)DiffusionProguanilPh rangemedicineOxidation-ReductionPolarographyJournal of pharmaceutical sciences
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Evaluation of Charge‐Regulated Supramolecular Copolymerization to Tune the Time Scale for Oxidative Disassembly of β‐Sheet Comonomers

2019

A multistimuli-responsive supramolecular copolymerization is reported. The copolymerization is driven by hydrogen bond encoded β-sheet-based charge co-assembly into 1D nanorods in water, using glutamic acid or lysine residues in either of the peptide comonomers. The incorporation of methionine as hydrophobic amino acid supports β-sheet formation, but oxidation of the thioether side-chain to a sulfoxide functional group destabilizes the β-sheet ordered domains and induces disassembly of the supramolecular polymers. Using H2 O2 as reactive oxygen species, the time scale and kinetics of the oxidative disassembly are probed. Compared to the charge neutral homopolymers, it is found that the oxid…

Polymers and PlasticsMacromolecular SubstancesPolymersSupramolecular chemistryBeta sheet02 engineering and technology010402 general chemistry01 natural scienceschemistry.chemical_compoundThioetherAmphiphilePolymer chemistryMaterials ChemistryCopolymerAmino Acidschemistry.chemical_classificationNanotubesHydrogen bondOrganic ChemistryHydrogen BondingSulfoxideHydrogen-Ion Concentration021001 nanoscience & nanotechnology0104 chemical sciencesSupramolecular polymerschemistryProtein Conformation beta-StrandPeptidesReactive Oxygen Species0210 nano-technologyOxidation-ReductionMacromolecular Rapid Communications
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Oxidative Addition of Halogens on Open Metal Sites in a Microporous Spin-Crossover Coordination Polymer

2009

PolymersCoordination polymeroxidative additionMolecular ConformationchemisorptionPhotochemistryCatalysisMetalchemistry.chemical_compoundHalogensX-Ray Diffractionspin crossoverSpin crossoverPlatinumporous compoundsBinding SitesGeneral ChemistryMicroporous materialGeneral MedicineOxidative additioncoordination polymerschemistryMetalsChemisorptionvisual_artX-ray crystallographyHalogenvisual_art.visual_art_mediumOxidation-ReductionAngewandte Chemie
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Porphyrin amino acids-amide coupling, redox and photophysical properties of bis(porphyrin) amides.

2013

New trans-AB2C meso-substituted porphyrin amino acid esters with meso-substituents of tunable electron withdrawing power (B = mesityl, 4-C6H4F, 4-C6H4CF3, C6F5) were prepared as free amines 3a-3d, as N-acetylated derivatives Ac-3a-Ac-3d and corresponding zinc(II) complexes Zn-Ac-3a-Zn-Ac-3d. Several amide-linked bis(porphyrins) with a tunable electron density at each porphyrin site were obtained from the amino porphyrin precursors by condensation reactions (4a-4d) and mono- and bis(zinc(II)) complexes Zn(2)-4d and Zn(1)Zn(2)-4d were prepared. The electronic interaction between individual porphyrin units in bis(porphyrins) 4 is probed by electrochemical experiments (CV, EPR), electronic abso…

PorphyrinsAbsorption spectroscopyMetalationchemistry.chemical_elementZincPhotochemistryRedoxlaw.inventionInorganic Chemistrychemistry.chemical_compoundlawAmidePolymer chemistryOrganometallic CompoundsAmino AcidsElectron paramagnetic resonanceMolecular StructureElectron Spin Resonance SpectroscopyCondensation reactionPhotochemical ProcessesPorphyrinAmidesZincchemistryQuantum TheoryOxidation-ReductionDalton transactions (Cambridge, England : 2003)
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Application of 3-Quinolinoyl Picket Porphyrins to the Electroreduction of Dioxygen to Water: Mimicking the Active Site of Cytochromec Oxidase

2001

International audience

PorphyrinsHemeproteinReducing agentIronchemistry.chemical_elementPhotochemistryElectrochemistry[ CHIM ] Chemical SciencesBiochemistryOxygenElectron Transport Complex IVO-O activationcytochrome c oxidase[CHIM]Chemical SciencesCytochrome c oxidaseBinding siteMolecular BiologyComputingMilieux_MISCELLANEOUSBinding SitesbiologyChemistryMolecular MimicryOrganic ChemistryActive siteElectron Transport Complex IVheme proteinsoxidoreductasesOxygenelectrochemistryReducing Agentsbiology.proteinMolecular MedicineIndicators and ReagentsSpectrophotometry UltravioletOxidation-ReductionCopperChemBioChem
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Clarification of the oxidation state of cobalt corroles inheterogeneous and homogeneous catalytic reduction of dioxygen

2008

Co(III) corroles were investigated as efficient catalysts for the reduction of dioxygen in the presence of perchloric acid in both heterogeneous and homogeneous systems. The investigated compounds are (5,10,15-tris(pentafluorophenyl)corrole)cobalt (TPFCor)Co, (10-pentafluorophenyl-5,15-dimesitylcorrole)cobalt (F 5PhMes 2Cor)Co, and (5,10,15-trismesitylcorrole)cobalt (Mes 3Cor)Co, all of which contain bulky substituents at the three meso positions of the corrole macrocycle. Cyclic voltammetry and rotating ring-disk electrode voltammetry were used to examine the catalytic activity of the compounds when adsorbed on the surface of a graphite electrode in the presence of 1.0 M perchloric acid, a…

PorphyrinsInorganic chemistrychemistry.chemical_element010402 general chemistry01 natural sciencesRedoxMedicinal chemistryCatalysisInorganic Chemistry[ CHIM.CATA ] Chemical Sciences/Catalysischemistry.chemical_compoundcorroleOxidation stateElectrochemistryOrganometallic CompoundsPerchloric acidPhysical and Theoretical ChemistryCorroleElectrodesComputingMilieux_MISCELLANEOUSPerchlorates010405 organic chemistryElectron Spin Resonance Spectroscopy[CHIM.CATA]Chemical Sciences/Catalysiscobaltcatalytic reduction of dioxygen0104 chemical sciencesOxygenBenzonitrilechemistryRadical ionSpectrophotometry UltravioletCyclic voltammetryOxidation-ReductionCobalt
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Greatly enhanced intermolecular π-dimer formation of a porphyrin trimer radical trications through multiple π bonds.

2010

A trefoil-like porphyrin trimer linked by triphenylamine (TPA-TPZn(3)) was synthesized. A three-electron oxidation of TPA-TPZn(3) forms a radical trication (TPA-TPZn(3)(3+)), in which each porphyrin ring undergoes a one-electron oxidation. The radical trication TPA-TPZn(3)(3+) spontaneously dimerizes to afford (TPA-TPZn(3))(2)(6+) in CH(2)Cl(2) . The characteristic charge-resonance band due to the charge delocalization over the π system of (TPA-TPZn(3))(2)(6+) was observed in the NIR region. The initial oxidation potential of TPA-TPZn(3) is negatively shifted relative to that of the corresponding monomer porphyrin, which results from the stabilization of the oxidized state of TPA-TPZn(3) as…

PorphyrinsMolecular StructureDimerOrganic ChemistryElectron Spin Resonance SpectroscopyTemperatureTrimerElectronsGeneral ChemistryPhotochemistryTriphenylaminePorphyrinCatalysislaw.inventionchemistry.chemical_compoundchemistryRadical ionlawStability constants of complexesCationsPi interactionElectron paramagnetic resonanceDimerizationOxidation-ReductionChemistry (Weinheim an der Bergstrasse, Germany)
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