Search results for "Catechols"

showing 5 items of 25 documents

Cooperative Catechol-Functionalized Polypept(o)ide Brushes and Ag Nanoparticles for Combination of Protein Resistance and Antimicrobial Activity on M…

2018

Prevention of biofouling and microbial contamination of implanted biomedical devices is essential to maintain their functionality and biocompatibility. For this purpose, polypept(o)ide block copolymers have been developed, in which a protein-resistant polysarcosine (pSar) block is combined with a dopamine-modified poly(glutamic acid) block for surface coating and silver nanoparticles (Ag NPs) formation. In the development of a novel, versatile, and biocompatible antibacterial surface coating, block lengths pSar were varied to derive structure-property relationships. Notably, the catechol moiety performs two important tasks in parallel; primarily it acts as an efficient anchoring group to me…

SilverPolymers and PlasticsBiocompatibilityDopamineCatecholsOxideBioengineering02 engineering and technology010402 general chemistry01 natural sciencesSilver nanoparticleBiomaterialsBiofoulingchemistry.chemical_compoundAnti-Infective AgentsMaterials ChemistryCopolymerMoietyCatecholOxides021001 nanoscience & nanotechnologyCombinatorial chemistry0104 chemical sciencesSurface coatingPolyglutamic AcidchemistryNanoparticles0210 nano-technologyBiomacromolecules
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Hydroxylation and conjugation of phenol by the frog Rana temporaria.

1985

1. Frogs injected with phenol excrete 67–95% of dose in 15h; 32–87% of dose are metabolites.2. Metabolites identified were phenyl sulphate (15–44% of dose), phenyl glucuronide (10–25% of dose), catechol sulphate (up to 7% of dose), quinol sulphate (1–25% of dose), resorcinol and catechol (traces).

StereochemistryHealth Toxicology and MutagenesisRana temporariaCatecholsGlucuronatesResorcinolSulfuric Acid EstersToxicologyHydroxylationBiochemistryHydroxylationchemistry.chemical_compoundPhenolsSalientiaPhenolAnimalsCarbon RadioisotopesChromatography High Pressure LiquidPharmacologyCatecholChromatographybiologyPhenolGeneral MedicineMetabolismResorcinolsbiology.organism_classificationHydroquinoneschemistryGRENOUILLEGlucuronideXenobiotica; the fate of foreign compounds in biological systems
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Purification and spectroscopic studies on catechol oxidases from Lycopus europaeus and Populus nigra: evidence for a dinuclear copper center of type …

1999

We purified two catechol oxidases from Lycopus europaeus and Populus nigra which only catalyze the oxidation of catechols to quinones without hydroxylating tyrosine. The molecular mass of the Lycopus enzyme was determined to 39,800 Da and the mass of the Populus enzyme was determined to 56,050 Da. Both catechol oxidases are inhibited by thiourea, N-phenylthiourea, dithiocarbamate, and cyanide, but show different pH behavior using catechol as substrate. Atomic absorption spectrosopic analysis found 1.5 copper atoms per protein molecule. Using EPR spectroscopy we determined 1.8 Cu per molecule catechol oxidase. Furthermore, EPR spectroscopy demonstrated that catechol oxidase is a copper enzym…

TyrosinaseCatecholschemistry.chemical_elementPhotochemistrySpectrum Analysis RamanBiochemistrylaw.inventionTreesInorganic Chemistrychemistry.chemical_compoundlawPolymer chemistryEnzyme InhibitorsElectron paramagnetic resonanceCatechol oxidaseCatecholBinding SitesCyanidesbiologyMonophenol MonooxygenaseSpectrophotometry AtomicElectron Spin Resonance SpectroscopySubstrate (chemistry)Bridging ligandHydrogen-Ion ConcentrationPlantsPhenylthioureaCopperMolecular WeightchemistryHemocyaninsbiology.proteinSpectrophotometry UltravioletOxygen bindingCatechol OxidaseCopperJournal of biological inorganic chemistry : JBIC : a publication of the Society of Biological Inorganic Chemistry
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Acute toxicity of some chlorinated phenols, catechols and cresols to trout.

1981

biologyChemistryTroutHealth Toxicology and MutagenesisCatecholsGeneral MedicineToxicologybiology.organism_classificationPollutionAcute toxicityLethal Dose 50TroutCresolsChlorinated phenolsPhenolsEnvironmental chemistryEcotoxicologyAnimalsBiotransformationSalmonidaeChlorophenolsBulletin of environmental contamination and toxicology
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Direct Visualization of Molecule Deprotonation on an Insulating Surface

2012

Elucidating molecular-scale details of basic reaction steps on surfaces is decisive for a fundamental understanding of molecular reactivity within many fields, including catalysis and on-surface synthesis. Here, the deprotonation of 2,5-dihydroxybenzoic acid (DHBA) deposited onto calcite (101;4) held at room temperature is followed in situ by noncontact atomic force microscopy. After deposition, the molecules form two coexisting phases, a transient striped phase and a stable dense phase. A detailed analysis of high-resolution noncontact atomic force microscopy images indicates the transient striped phase being a bulk-like phase, which requires hydrogen bonds between the carboxylic acid moie…

noncontact atomic force microscopyCarboxylic acidCatecholsGeneral Physics and AstronomyMicroscopy Atomic ForceKelvin probe force microscopy530Calcium Carbonatechemistry.chemical_compoundDeprotonationPhase (matter)Materials TestingHydroxybenzoatesMoleculeGeneral Materials ScienceReactivity (chemistry)CarboxylateParticle Sizechemistry.chemical_classificationKelvin probe force microscopeHydrogen bondinsulating surfaceGeneral EngineeringElectric ConductivityMolecular ImagingNanostructuresCrystallographychemistrydeprotonationProtons
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