Search results for "PORP"

showing 10 items of 567 documents

Antenna effects in truxene-bridged BODIPY triarylzinc(ii)porphyrin dyads: evidence for a dual Dexter–Förster mechanism

2014

The antenna process from an energy donor (BODIPY; 4′,4′-difluoro-1′,3′,5′,7′-tetramethyl-4′-bora-3a′,4a′-diaza-s-indacene) in its singlet state to two acceptors (two zinc(II) 5,15-p-tolyl-10-phenylporphyrin) bridged by a central truxene residue (5′,5′′,10′,10′′,15′,15′′-hexabutyltruxene), 5, has been analysed by means of comparison of the energy transfer rates with those of a structurally similar β-substituted BODIPY-(zinc(II) 5,10,15-p-tolyl-porphyrin), 6, where no conjugation is present between the donor and the two acceptors using the Forster resonance energy transfer (FRET) approximation. It is estimated that the energy transfer in 5 operates mostly via a Dexter mechanism (>99%), and th…

Inorganic Chemistrychemistry.chemical_compoundFörster resonance energy transferChemistryEnergy transferchemistry.chemical_elementSinglet stateZincBODIPYPhotochemistryPorphyrinDalton Trans.
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Thermodynamic and kinetic control over the oxidation mechanism of the natural vanadyl porphyrin series (DPEP)VO in methylene chloride: electrogenerat…

2006

The electrochemical behavior of the natural (DPEP)VO series (where DPEP is the dianion deoxophylloerythroetioporphyrinate) is studied in methylene chloride. The investigated compounds, which were extracted from oil shales of Tarfaya (Morocco), exhibit a typical electrochemical behavior as compared to that of related synthetic vanadyl porphyrins. The electro-oxidation of (DPEP)VO is characterized by a splitting of the peaks when carried out at a glassy carbon electrode. This can be explained by two possible paths (CE and EC mechanisms) which are characterized by a “square diagram” where the chemical step, C, corresponds to a dimerization (radical–radical or substrate–substrate reaction). The…

Inorganic chemistryKinetics010402 general chemistryElectrochemistry01 natural sciencesChlorideKinetic controlCatalysislaw.inventionchemistry.chemical_compoundlawMaterials Chemistrymedicine[CHIM.COOR]Chemical Sciences/Coordination chemistryMethyleneSpectroscopyElectron paramagnetic resonanceComputingMilieux_MISCELLANEOUS010405 organic chemistryChemistry[ CHIM.COOR ] Chemical Sciences/Coordination chemistryGeneral ChemistryPorphyrin0104 chemical sciences[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistry[ CHIM.THEO ] Chemical Sciences/Theoretical and/or physical chemistrymedicine.drug
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Interfacial Self-Assembly of Water-Soluble Cationic Porphyrins for the Reduction of Oxygen to Water

2012

Meet at the border: Assembly of the water-soluble cobalt tetrakis(N-methylpyridinium-4-yl)porphyrin [CoTMPyP]4+ at soft interfaces is enhanced and stabilized by its interfacial interaction with the lipophilic anion (C6F5)4B−. The supramolecular structure thus formed (see picture) provides excellent catalytic activity in the four-electron reduction of oxygen.

Inorganic chemistrySupramolecular chemistry2Nd-Harmonic Generationchemistry.chemical_element010402 general chemistryporphyrinsOxygen01 natural sciencesCatalysisMolecular ElectrocatalysisCatalysisinterfacesPolarized Interfacechemistry.chemical_compound[SPI]Engineering Sciences [physics]AggregationPolymer chemistry[CHIM]Chemical Sciencesliquid-liquid interfacesComputingMilieux_MISCELLANEOUS[PHYS]Physics [physics]oxygen reduction reactionDioxygen010405 organic chemistryCationic polymerizationGeneral ChemistryGeneral Medicineself-assemblyPorphyrin3. Good health0104 chemical scienceschemistryTetrathiafulvaleneSelf-assemblyImmiscible Electrolyte-SolutionsCobaltTetrathiafulvalene
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Hemin-coupled iron(III)-hydroxide nanoparticles show increased uptake in Caco-2 cells

2011

Abstract Objectives The absorption of commonly used ferrous iron salts from intestinal segments at neutral to slightly alkaline pH is low, mainly because soluble ferrous iron is easily oxidized to poorly soluble ferric iron and ferrous iron but not ferric iron is carried by the divalent metal transporter DMT-1. Moreover, ferrous iron frequently causes gastrointestinal side effects. In iron(III)-hydroxide nanoparticles hundreds of ferric iron atoms are safely packed in nanoscaled cores surrounded by a solubilising carbohydrate shell, yet bioavailability from such particles is insufficient when compared with ferrous salts. To increase their intestinal uptake iron(III)-hydroxide nanoparticles …

Inorganic chemistryTetrazolium SaltsPharmaceutical ScienceNanoparticleFerrozineIron Chelating AgentsFerric CompoundsFerrouschemistry.chemical_compoundMicroscopy Electron TransmissionSpectroscopy Fourier Transform InfraredmedicineHumansScattering RadiationParticle SizeColoring AgentsHemePharmacologyChemistryIron Chelating AgentsIron deficiencymedicine.diseaseCulture MediaThiazolesHeminNanoparticlesHydroxideColorimetrySpectrophotometry UltravioletProtoporphyrinCaco-2 CellsHeminJournal of Pharmacy and Pharmacology
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Electrochemistry and germanium porphyrins in nonaqueous media. Reactions of water and hydroxide ligands associated with (P)Ge(ClO4)2 and (P)Ge(OH)2, …

1988

Inorganic chemistrychemistry.chemical_elementGermaniumElectrochemistryMedicinal chemistryInorganic ChemistryBenzonitrilechemistry.chemical_compoundTransition metalchemistryTetraphenylporphyrinHydroxidePhysical and Theoretical ChemistryCyclic voltammetryPlatinumInorganic Chemistry
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Dynamics of closure of zinc bis-porphyrin molecular tweezers with copper(II) ions and electron transfer.

2011

Zinc bis-porphyrin molecular tweezers composed of a N(4) spacer bound through pyridyl units to the meso position of porphyrins were synthesized, and the tweezers are closed by the coordination of a copper(II) ion inside the spacer ligand. The effect of the π-π interaction between the porphyrin rings in the closed conformation on the absorption spectra of multi-electron oxidized species and the reduction potentials were clarified by chemical and electrochemical oxidation of the closed form of the zinc bis-porphyrin molecular tweezers in comparison with the open form without copper(II) ion and the corresponding porphyrin monomer. The shifts in redox potentials and absorption spectrum of the p…

IonsLigandMetalloporphyrinsOrganic Chemistrychemistry.chemical_elementGeneral ChemistryZincElectrochemical TechniquesPhotochemistryPorphyrinCopperCatalysisDicationElectron TransportElectron transferchemistry.chemical_compoundchemistryTweezerspolycyclic compoundsheterocyclic compoundsSpectrophotometry UltravioletMolecular tweezersOxidation-ReductionCopperChemistry (Weinheim an der Bergstrasse, Germany)
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Effect of boldine, secoboldine, and boldine methine on angiotensin II-induced neutrophil recruitment in vivo.

2005

AbstractAngiotensin-II (Ang-II) has inflammatory activity and is involved in different diseases associated with the cardiovascular system. This study has evaluated the effect of boldine (B), and two phenanthrene alkaloids semisynthesized by us, secoboldine (SB) and boldine methine (BM), on Ang-II-induced neutrophil recruitment. Intraperitoneal administration of 1 nM Ang-II induced significant neutrophil accumulation, which was maximal at 4–8 h. BM inhibited neutrophil infiltration into the peritoneal cavity at 4 h and 8 h by 73% and 77%, respectively, SB at 8 h by 55%, and B had no effect on this response. Although BM inhibited the release of cytokine-inducible neutrophil chemoattractant/ke…

KeratinocytesMaleChemokineAporphinesEndotheliumNeutrophilsImmunologyChemokine CXCL2InflammationPharmacologyRats Sprague-Dawleychemistry.chemical_compoundIn vivomedicineImmunology and AllergyBoldineAnimalsHumansInfusions ParenteralPlatelet Activating FactorReceptorchemistry.chemical_classificationReactive oxygen speciesbiologyMolecular StructureAngiotensin IIMonokinesInterleukin-8Endothelial CellsCell BiologyPhenanthrenesAngiotensin IIRatsP-Selectinmedicine.anatomical_structureBiochemistrychemistrybiology.proteinIntercellular Signaling Peptides and Proteinsmedicine.symptomChemokinesReactive Oxygen SpeciesChemokines CXCJournal of leukocyte biology
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Oxidative DNA damage induced by visible light in mammalian cells: extent, inhibition by antioxidants and genotoxic effects

1998

The extent of the indirect DNA damage generated in mammalian cells by visible light because of the presence of endogenous photosensitizers was studied by means of repair endonucleases. In immortalized human keratinocytes (HaCaT cells) exposed to low doses of natural sunlight, the yield of oxidative DNA base modifications sensitive to the repair endonuclease formamidopyrimidine-DNA glycosylase (Fpg protein) generated by this indirect mechanism was 10% of that of pyrimidine dimers (generated by direct DNA excitation). A similar yield of Fpg-sensitive modifications, which include 8-hydroxyguanine, was observed in primary keratinocytes. The relative yield of oxidative base modifications decreas…

KeratinocytesMalePorphyrinsLightDNA damageRiboflavinPyrimidine dimerAscorbic AcidBiologyToxicologyIndirect DNA damageAntioxidantsMiceCricetinaeGeneticsAnimalsHumansN-Glycosyl HydrolasesMolecular BiologyCells CulturedMutagenesisInfant NewbornInfantEndonucleasesAscorbic acidHaCaTDNA-Formamidopyrimidine GlycosylaseBiochemistryMutagenesisDNA glycosylaseChild PreschoolBiophysicsL1210 cellsOxidation-ReductionDNA DamageMutation Research/DNA Repair
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Electron-Transfer Kinetics for Generation of Organoiron(IV) Porphyrins and the Iron(IV) Porphyrin π Radical Cations

1999

Homogeneous electron-transfer kinetics for the oxidation of seven different iron(III) porphyrins using three different oxidants were examined in deaerated acetonitrile, and the resulting data were evaluated in light of the Marcus theory of electron transfer to determine reorganization energies of the rate-determining oxidation of iron(III) to iron(IV). The investigated compounds are represented as (P)Fe(R), where P = the dianion of 2,3,7,8,12,13,17,18-octaethyl-5,10,15,20-tetraphenylporphyrin (OETPP) and R = C6H5, 3,5-C6F2H3, 2,4,6-C6F3H2, or C6F5 or P = the dianion of 2,3,7,8,12,13,17,18-octaethylporphyrin (OEP) and R = C6H5, 2,4,6-C6F3H2, or 2,3,5,6-C6F4H. The first one-electron transfer …

KineticsInorganic chemistryGeneral ChemistryBiochemistryPorphyrinMedicinal chemistryCatalysisMarcus theorychemistry.chemical_compoundElectron transferColloid and Surface ChemistrychemistryHomogeneousAcetonitrileJournal of the American Chemical Society
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Porphyromonas gingivalis, Periodontal and Systemic Implications: A Systematic Review

2019

In recent scientific literature, oral infections and systemic manifestations, or correlations between oral health and systemic diseases are a topic of discussion. Porphyromonas gingivalis is one of the bacteria implicated in the biofilm formation of bacterial plaque, and plays an important role in the progression of periodontal disease. In this systematic review authors have evaluated the literature of the last 10 years on P. gingivalis and all the systemic implications proven. This study therefore evaluates all the districts of the organism in which this bacterium may have implications. From the results it emerges that P. gingivalis has implications in the onset of different systemic patho…

LPSOral healthbrain diseasesArthritisBacteremiaReviewOral healthPorphyromonas gingivaliNeurodegenerative disease03 medical and health sciences0302 clinical medicinePeriodontal diseasemedicineneurodegenerative diseasesperiodontitisGeneral DentistryPorphyromonas gingivalisOrganismBrain disease030304 developmental biologyPeriodontitis0303 health sciencesbiologybusiness.industryPeriodontiti030206 dentistryCardiovascular diseasemedicine.diseasebiology.organism_classificationcardiovascular diseasesarthritisRheumatoid arthritisImmunologybusinessPorphyromonas gingivalisArthritiDentistry Journal
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