Search results for "Pyrenes"

showing 10 items of 65 documents

Supramolecular Design of Low-dimensional Carbon Nano-hybrids encoding a Polyoxometalate-bis-Pyrene Tweezer

2014

A novel bis-pyrene tweezer anchored on a rigid polyoxometalate scaffold fosters a unique interplay of hydrophobic and electrostatic supramolecular interactions, to shape carbon nanostructures (CNSs)-based extended architectures.

Materials Chemistry2506 Metals and AlloysSurfaces Coatings and FilmCarbon nanotubelaw.inventionCatalysiCoatings and Filmschemistry.chemical_compoundlawhybrid materialsMaterials ChemistryCarbon nanostructures; recognition; hybrid materials; polyoxometalatesMaterials Chemistry2506 Metals and AlloyPyrenesPyreneElectronic Optical and Magnetic MaterialChemistry (all)Metals and AlloysTungsten CompoundsSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsSurfacesSpectrophotometryPolyoxometalatePyrenerecognitionLangmuir-Schaefer filmsHybrid materialHydrophobic and Hydrophilic InteractionsCarbon nanostructuresMaterials scienceStatic ElectricitySupramolecular chemistrychemistry.chemical_elementNanotechnologyCeramics and CompositeCarbon nanotubeCatalysisNano-ElectronicpolyoxometalatesChemistry (all); Catalysis; Ceramics and Composites; Electronic Optical and Magnetic Materials; Surfaces Coatings and Films; Materials Chemistry2506 Metals and Alloys; 2506Optical and Magnetic Materialscarbon nanotubeHybrid materialPolyoxometalateGeneral ChemistryCarbon nanostructuresCarbonNanostructureschemistryCeramics and Composites2506Supramolecular chemistryCarbon
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Uridine uptake inhibition as a cytotoxicity test for a human hepatoma cell line (HepG2 cells): comparison with the neutral red assay

2001

International audience; This study describes a sensitive microassay for measuring cytotoxicity based on the degree of inhibition of RNA synthesis in HepG2 cells. RNA synthesis is measured by the kinetic uptake of radiolabeled uridine. A large number of compounds were tested in a wide range of concentrations. The concentration required to induce 50% inhibition of HepG2 uridine uptake rates (IC50) was determined for each compound and used to rank its potency. These IC50s were compared with IC50s measured with the neutral red assay. 2-acetylaminofluorene, benzo[a]pyrene and methylnitrosourea were not cytotoxic in the neutral red assay. Uridine uptake was always inhibited at lower concentrations…

Neutral redCarcinoma Hepatocellular[SDV.TOX.TCA]Life Sciences [q-bio]/Toxicology/Toxicology and food chainToxicologyXenobiotics03 medical and health scienceschemistry.chemical_compoundInhibitory Concentration 500302 clinical medicineNeutral redToxicity TestsTumor Cells CulturedPotencyCytotoxic T cellHumansBenzopyrenesCytotoxicityColoring AgentsUridine030304 developmental biology0303 health sciencesReproducibility of ResultsMethylnitrosourea2-AcetylaminofluoreneUridine uptakeIn vitroUridineKineticschemistryBiochemistryCytotoxicity-helpG2 cell line[SDV.TOX.TCA] Life Sciences [q-bio]/Toxicology/Toxicology and food chain030220 oncology & carcinogenesisToxicityCarcinogensHepatocytesPyreneRNARegression AnalysisWater Pollutants Chemical
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The capacity of liver microsomes to form benzo[a]pyrene-diolepoxide-DNA adducts and induction of cytochrome P450 1A in feral fish exposed to pulp mil…

1996

An investigation was made of cytochrome P4501A (CYP1A) induction, determined by the activity of EROD (7-ethoxyresorufin O-deethylase), and formation of benzo[a]pyrene-diolepoxide-DNA (BPDE-DNA) adducts, measured by synchronous fluorescence spectrophotometry, in liver microsomes of perch (Perca fluviatilis), bream (Abramis brama), and roach (Rutilus rutilus). Fish were collected from the southern part of Lake Saimaa (Finland), an area polluted by effluents from the pulp and paper industry. In addition, two conjugation enzymes (UDP-glucuronosyltransferase and glutathione S-transferase) were determined. Overall, when compared to an upstream reference, EROD activity was higher in fish at waters…

PaperHealth Toxicology and MutagenesisIndustrial WasteBiologyToxicologychemistry.chemical_compoundDNA AdductsCytochrome P-450 Enzyme SystemBenzo(a)pyreneCytochrome P-450 CYP1A1EcotoxicologyAnimalsBenzopyrenesCarcinogenBiotransformationFinlandPublic Health Environmental and Occupational HealthFishesCytochrome P450General MedicineGlutathionebiology.organism_classificationPollutionchemistryBenzo(a)pyreneEnvironmental chemistryBenzopyreneMicrosomebiology.proteinMicrosomes LiverRutilusWater Pollutants ChemicalEcotoxicology and environmental safety
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Epoxidation of benzo[a]pyrene-7,8-dihydrodiol by human CYP1A1 in reconstituted membranes. Effects of charge and nonbilayer phase propensity of the me…

2002

Human cytochrome P4501A1 (CYP1A1) is one of the key enzymes in the bioactivation of environmental pollutants such as benzo[a]pyrene (B[a]P) and other polycyclic aromatic hydrocarbons. To evaluate the effect of membrane properties and distinct phospholipids on the activity of human CYP1A1 purified insect cell-expressed human CYP1A1 and of human NADPH-P450 reductase were reconstituted into phospholipid vesicle membranes. Conversion rates of up to 36 pmol x min(-1) x pmol(-1) CYP1A1 of the enantiomeric promutagens (-)- and (+)-trans-7,8-dihydroxy-7,8-dihydro-B[a]P (7,8-diol) to the genotoxic diolepoxides were achieved. The highest rates were obtained when negatively charged lipids such as phos…

PhosphatidylethanolamineStereochemistryVesiclePhospholipidMembranes ArtificialPhosphatidylserineBiochemistryRecombinant ProteinsDihydroxydihydrobenzopyreneschemistry.chemical_compoundMembraneBiochemistrychemistryBenzo(a)pyrenepolycyclic compoundsCytochrome P-450 CYP1A1PyreneAnimalsEpoxy CompoundsHumansheterocyclic compoundsPhosphatidylinositolPhospholipidsEuropean journal of biochemistry
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Response of rainbow trout transcriptome to model chemical contaminants.

2004

We used high-density cDNA microarray in studies of responses of rainbow trout fry at sublethal ranges of beta-naphthoflavone, cadmium, carbon tetrachloride, and pyrene. The differentially expressed genes were grouped by the functional categories of Gene Ontology. Significantly different response to the studied compounds was shown by a number of classes, such as cell cycle, apoptosis, signal transduction, oxidative stress, subcellular and extracellular structures, protein biosynthesis, and modification. Cluster analysis separated responses to the contaminants at low and medium doses, whereas at high levels the adaptive reactions were masked with general unspecific response to toxicity. We fo…

ProteomicsProteomeSurvivalTranscription GeneticBiophysicsInformation Storage and RetrievalApoptosisBiologyBiochemistryTranscriptomebeta-NaphthoflavoneComplementary DNAProtein biosynthesisExtracellularAnimalsDatabases ProteinMolecular BiologyGeneCarbon TetrachloridePhylogenyOligonucleotide Array Sequence AnalysisPyrenesDose-Response Relationship DrugCell BiologyMetabolismMolecular biologyBiochemistryGene Expression RegulationOncorhynchus mykissModels AnimalRainbow troutSignal transductionBiomarkersWater Pollutants ChemicalCadmiumEnvironmental MonitoringBiochemical and biophysical research communications
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Retene, pyrene and phenanthrene cause distinct molecular-level changes in the cardiac tissue of rainbow trout (Oncorhynchus mykiss) larvae, Part 2 – …

2020

Polycyclic aromatic hydrocarbons (PAHs) are global contaminants of concern. Despite several decades of research, their mechanisms of toxicity are not very well understood. Early life stages of fish are particularly sensitive with the developing cardiac tissue being a main target of PAHs toxicity. The mechanisms of cardiotoxicity of the three widespread model polycyclic aromatic hydrocarbons (PAHs) retene, pyrene and phenanthrene were explored in rainbow trout (Oncorhynchus mykiss) early life stages. Newly hatched larvae were exposed to sublethal doses of each individual PAH causing no detectable morphometric alterations. Changes in the cardiac proteome and metabolome were assessed after 7 o…

Proteomicsbiologiset vaikutuksetEnvironmental Engineering010504 meteorology & atmospheric sciencestoksiinitDevelopmental toxicitycardiotoxicity010501 environmental sciencesmyrkyllisyys01 natural sciencesproteomiikkaTranscriptomechemistry.chemical_compoundMetabolomicsproteomicsMetabolomeEnvironmental ChemistryAnimalsMetabolomicsdevelopmental toxicityaquatic toxicology14. Life underwaterPolycyclic Aromatic HydrocarbonsWaste Management and Disposal0105 earth and related environmental scienceskalatRetenevesistötPyrenesbiologyChemistryPhenanthrenePhenanthrenesAryl hydrocarbon receptorPollutionmetabolomicsekotoksikologiaBiochemistryLarvaOncorhynchus mykisspolycyclic aromatic hydrocarbons (PAHs)biology.proteinPyrenearomaattiset hiilivedytepäpuhtaudet
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On the Use of Metal Purine Derivatives (M=Ir, Rh) for the Selective Labeling of Nucleosides and Nucleotides

2014

The reactions of neutral or cationic IrIII and RhIII derivatives of phenyl purine nucleobases with unsymmetrical alkynes produce new metallacycles in a predictable manner, which allows for the incorporation of either photoactive (anthracene or pyrene) or electroactive (ferrocene) labels in the nucleotide or nucleoside moiety. The reported methodology (metalation of the purine derivative and subsequent marker insertion) could be used for the postfunctionalization and unambiguous labeling of oligonucleotides.

PurineMetalationIridiumCatalysisNucleobasechemistry.chemical_compoundOrganometallic CompoundsOrganic chemistryMoietyRhodiumNucleotideNuclear Magnetic Resonance BiomolecularPurine NucleotidesAnthraceneschemistry.chemical_classificationPyrenesMolecular StructureOrganic ChemistryCationic polymerizationPurine NucleosidesGeneral ChemistryCombinatorial chemistryFerrocenechemistryAlkynesNucleosideChemistry - A European Journal
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Transcriptome responses to carbon tetrachloride and pyrene in the kidney and liver of juvenile rainbow trout (Oncorhynchus mykiss)

2005

Abstract We report the effects of the hepatotoxic compound carbon tetrachloride (CCl 4 ) and pyrene, a model polycyclic aromatic hydrocarbon, on the transcriptomes of juvenile rainbow trout kidneys and livers. Fish were exposed to sublethal doses for 4 days and expression of 1273 genes was measured using a cDNA microarray. Efforts were focused on differentiating between unspecific responses and those that can be regarded as molecular signatures of CCl 4 and pyrene toxicities. Expression profiles were analyzed in terms of Gene Ontology categories. Universal reactions to chemical toxicity were observed in metallothionein, HSP90 and mitochondrial proteins of oxidative phosphorylation, which we…

PyrenesbiologyFatty acid metabolismGene Expression ProfilingHealth Toxicology and MutagenesisAquatic SciencePeroxisomeKidneydigestive systemHsp90Transcriptomechemistry.chemical_compoundFatty acid desaturaseGene Expression RegulationLiverchemistryBiochemistryOncorhynchus mykissHeat shock proteinbiology.proteinAnimalsMetallothioneinPyreneCarbon TetrachlorideOligonucleotide Array Sequence AnalysisAquatic Toxicology
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An ex vivo model of the rat trachea to study the effect of inhalable toxic compounds

1996

Different cell culture and organ systems are used to evaluate the physiological responses of the airways to the effects of carcinogenic [e.g., benzo(a)pyrene] and anticarcinogenic (e.g., retinoids) compounds on cellular growth and differentiation. However, in contrast to in vivo conditions dissociated epithelial cells or tracheal ring cultures are covered with medium. Therefore, we developed an ex vivo perfusion model enabling evaluation of morphology and metabolism of different compounds under near-physiological conditions. The trachea was surrounded with culture medium and perfused with air by means of a small animal respirator. To test the viability of the system under various experiment…

Retinyl EstersOligosaccharidesBiologyCell morphologyOrgan cultureXenobioticschemistry.chemical_compoundOrgan Culture TechniquesIn vivoLectinsAnimalsBenzopyrenesRats WistarVitamin ACarcinogenVitamin A DeficiencyGeneral MedicineRatsTracheaMicroscopy ElectronBenzo(a)pyrenechemistryBiochemistryCell culturePyreneDiterpenesEx vivoProtein BindingResearch in Experimental Medicine
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Epoxides metabolically produced from some known carcinogens and from some clinically used drugs. I. Differences in mutagenicity.

1975

The epoxide metabolites of two clinically used drugs and an experimental psychotropic agent, carbamazepine 10,11-oxide, cyproheptadine 10,11-oxide and cyclobenzaprine 10,11-oxide, were fully devoid of any mutagenic activity under conditions where K-region-epoxide metabolites of some known carcinogens, such as benzo (a)pyrene, proved to be potent frameshift mutational agents for Salmonella typhimurium TA 1537 and TA 1538. All epoxides tested were non-mutagenic for TA 1535, designed to detect substitution mutations. The 10,11-epoxides of the three drugs, carbamazepine, cyproheptadine and cyclobenzaprine, were not cytotoxic to any of the bacterial tester strains used, precluding that mutagenic…

Salmonella typhimuriumCancer ResearchChemical PhenomenaMutagenesisCyproheptadineEpoxideMutagenOxidesDibenzocycloheptenesCyproheptadinemedicine.disease_causechemistry.chemical_compoundChemistryCarbamazepineOncologyBiochemistrychemistrymedicineMicrosomePyreneBenzopyrenesCytotoxicityCarcinogenmedicine.drugMutagensInternational journal of cancer
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