Search results for "Acene"

showing 10 items of 204 documents

Epoxides derived from various polycyclic hydrocarbons as substrates of homogeneous and microsome-bound epoxide hydratase. A general assay and kinetic…

1976

A general assay for epoxide hydratase using epoxides derived from polycyclic aromatic hydrocarbons as substrates is described. Addition of dimethylsulphoxide to the incubation mixture after incubation allowed unreacted epoxide and its phenolic by-product to be extracted into light petroleum whilst the product dihydrodiol remained in the aqueous phase. The product was then extracted into ethyl acetate and estimated radiochemically. This assay gave low extraction blanks (0.8-3.8%) when six K-region epoxides of polycyclic hydrocarbons were used, with high recoveries of the corresponding dihydrodiol in the ethyl acetate phase (65-89%). Radiochromatograms demonstrated that all the radioactivity …

Epoxide HydrolasesAnthraceneEthyl acetateEpoxideSubstrate (chemistry)PhenanthreneBiochemistryRatschemistry.chemical_compoundKineticsStructure-Activity RelationshipchemistryStyrene oxideMicrosomes LiverPyreneOrganic chemistryAnimalsEpoxy CompoundsPolycyclic HydrocarbonsPolycyclic CompoundsHydro-LyasesEuropean journal of biochemistry
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Specificity of mouse liver cytosolic epoxide hydrolase for K-region epoxides derived from polycyclic aromatic hydrocarbons

1980

Mouse liver cytosol epoxide hydrolase, known to be very active for certain alkene oxides, had a specific activity which was 2.1-, 11- and 160-fold lower than that of the microsomal epoxide hydrolase for the arene oxides 7-methylbenz[a]anthracene 5,6-oxide, benz[a]anthracene 5,6-oxide and phenanthrene 9,10-oxide, respectively. For benzo[a]pyrene 4,5-oxide no activity (less than 10 pmol product/mg protein/min) of cytoplasmic epoxide hydrolase was detectable. The specific activity of cytoplasmic epoxide hydrolase was much lower for all K-region epoxides investigated, compared to trans-stilbene oxide used as a positive control and for which a new assay is described. It is concluded from these r…

Epoxide HydrolasesMaleEpoxide hydrolase 2Cancer ResearchAnthracenePhenanthrenesSubstrate SpecificityMicechemistry.chemical_compoundCytosolLiverOncologychemistryBiochemistryEthers CyclicMicrosomal epoxide hydrolaseHydrolaseBenz(a)AnthracenesMicrosomes LiverMicrosomeAnimalsEpoxy CompoundsPyreneSpecific activityEpoxide hydrolaseCancer Letters
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Catalytic oxidation and reduction of polycyclic aromatic hydrocarbons (PAHs) present as mixtures in hydrothermal media

2012

Author's version of an article in the journal: Polycyclic Aromatic Compounds. Also available from the publisher at: http://dx.doi.org/10.1080/10406638.2012.663451 The reactivity of fluorene, anthracene, and fluoranthene under oxidation and reduction conditions were investigated in this study. This project looks at catalytic and green approaches of converting PAHs to less toxic and/or less stable derivatives that are amenable to further degradation. Hydrothermal reactions have been performed at 300°C with pure H2O and Nafion-SiO2 catalyst for oxidation, and pure H2O, HCOOH, Pd-C, and Nafion-SiO2 catalysts for reductive hydrogenation. Time series has been performed for both the oxidation and …

FluorantheneAnthracenehydrothermalPolymers and PlasticsVDP::Mathematics and natural science: 400::Chemistry: 440oxidationOrganic ChemistryanthracenereductionFluorenePhotochemistryRedoxHydrothermal circulationCatalysisfluoranthenechemistry.chemical_compoundfluoreneCatalytic oxidationchemistryMaterials ChemistryOrganic chemistryReactivity (chemistry)
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Hard Cap Espresso Machines in Analytical Chemistry: What Else?

2016

A hard cap espresso machine has been used in combination with liquid chromatography with molecular fluorescence detection for the determination of polycyclic aromatic hydrocarbons (PAHs) from contaminated soils and sediments providing appropriate extraction efficiencies and quantitative results. Naphthalene, acenaphthene, fluorene, phenanthrene, anthracene, fluoranthene, pyrene, benz[a]anthracene, chrysene, benz[b]fluoranthene, benz[k]fluoranthene, benz[a]pyrene, dibenz[a,h]anthracene, benz[ghi]perylene, and indeno[1,2,3-cd]pyrene were used as target compounds. It should be mentioned that the pairs benz[a]anthracene-chrysene and dibenz[a,h]anthracene-benz[ghi]perylene peaks coelute under th…

FluorantheneChryseneDetection limitAnthracene010401 analytical chemistryExtraction (chemistry)Analytical chemistryAcenaphthene010501 environmental sciencesPhenanthrene01 natural sciences0104 chemical sciencesAnalytical Chemistrychemistry.chemical_compoundchemistryPyrene0105 earth and related environmental sciencesAnalytical chemistry
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From small to medium and beyond: a pragmatic approach in predicting properties of Ne containing structures

2013

In this study, we outlined a pragmatic approach for structural studies leading to better understanding of polycarbon structures using 21Ne as a nuclear magnetic resonance (NMR) probe. 21Ne NMR parameters of a single neon atom and its dimer were predicted at the CCSD(T) level in combination with large basis sets. At a lower level of theory, an interaction of neon atom with 1,3-cyclopentadiene ring and with five- and six-membered rings in carbazole was studied using the restricted Hartree–Fock (RHF) and density functional theory (DFT) combined with smaller basis sets. The RHF and DFT modelling of neon interaction with nanosized objects were performed on cyclacenes and selected fullerenes.

Fullerene21Ne NMRDimerBiophysicschemistry.chemical_elementRing (chemistry)Molecular physicsDFTNeonchemistry.chemical_compoundComputational chemistrycarbazoleAtomPhysics::Atomic and Molecular ClustersPhysics::Atomic PhysicsPhysics::Chemical PhysicsPhysical and Theoretical ChemistryMolecular Biologydispersion interactionsBasis (linear algebra)CarbazolefullerenesCondensed Matter PhysicschemistryDensity functional theorycyclacenesMolecular Physics
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Confined growth of carbon nanoforms in one-dimension by fusion of anthracene rings inside the pores of MCM-41

2014

We report a simple two-step procedure that uses anthracene, a cheap polyaromatic hydrocarbon with low melting point, as a molecular precursor to produce carbon nanoforms (CNFs). First, we describe the chemical synthesis of graphite from the fusion of anthracene rings at relatively low temperature (520 °C) followed by cyclodehydrogenation. Next, we extend this protocol to the synthesis of CNFs by confining the molecular precursor in a mesoporous host like MCM-41. The confined environment favors one-dimensional growth of CNFs with sizes controlled by the pores of the mesoporous host.

FusionAnthraceneMaterials scienceLow melting pointchemistry.chemical_elementNanotechnologyChemical synthesischemistry.chemical_compoundChemical engineeringchemistryMCM-41General Materials ScienceGraphiteMesoporous materialCarbonNanoscale
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1988

Synthese par alkylation reductrice de l'anthracene par des electrophiles bifonctionnels comme le dibromo-1,3 propane. Le polymere du titre est un precurseur du polymere redox polyanthrylenetrimethylene

Gel permeation chromatographyAnthracenechemistry.chemical_compoundChain structureReaction mechanismchemistryMolar mass distributionOrganic chemistryAlkylationCharacterization (materials science)Die Makromolekulare Chemie, Rapid Communications
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Crystal and molecular structure of 2,3,6,7-tetramethoxy-9-trichloromethyl-10-carboxymethyl-9,10-dihydroanthracene

1990

Cl3O6C21H21,Mr=475.75, orthorhombic,P212121,a=21.895(3),b=12.101(2), andc=8.237(2) A,V=2182.4(7) A3,Dx=1.45 g cm−3 forZ=4, λ(MoKα)=0.71069 Aμ=3.99 cm−1,F(000) 984, room temperature,R=0.035 for 1877 observed reflections. The molecule exhibits a folded conformation: the dihedral angle between the benzene rings is 28.3(1)°. The central ring is characterized by acis diaxal configuration of hydrogen atoms in the 9, 10 positions, confirming the 13-C NMR results.

General ChemistryCrystal structureNuclear magnetic resonance spectroscopy910-DihydroanthraceneDihedral angleCondensed Matter PhysicsRing (chemistry)chemistry.chemical_compoundCrystallographychemistryStructural BiologyX-ray crystallographyMoleculeOrthorhombic crystal systemSpectroscopyJournal of Crystallographic and Spectroscopic Research
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Overexpression of bone morphogenetic protein-6 (BMP-6) in murine epidermis suppresses skin tumor formation by induction of apoptosis and downregulati…

2001

Bone morphogenetic protein-6 (BMP-6) is a member of the transforming growth factor-beta superfamily. In murine skin, BMP-6 is highly expressed in postmitotic keratinocytes from day 15.5 p.c. till day 6 p.p. Expression in adult skin remains at very low levels, but pathological conditions such as wounding induce the expression of BMP-6. We demonstrate that tumor promotion by TPA (12-O-tetradecanoylphorbol-13-acetate) also induces expression of BMP-6 in suprabasal keratinocytes. This induction is due to post-transcriptional regulation since the level of BMP-6 mRNA remained unchanged. We performed two-stage skin carcinogenesis experiments with transgenic mice epidermally overexpressing BMP-6. T…

Genetically modified mouseKeratinocytesCancer ResearchSkin NeoplasmsBone Morphogenetic Protein 6Transgene910-Dimethyl-12-benzanthraceneDown-RegulationApoptosisMice TransgenicBiologymedicine.disease_causeMiceDownregulation and upregulationGenes junGeneticsmedicineIn Situ Nick-End LabelingTumor Cells CulturedAnimalsRNA MessengerMolecular BiologyIn Situ Hybridizationintegumentary systemActivator (genetics)Reverse Transcriptase Polymerase Chain ReactionGenes fosImmunohistochemistryCell biologyBone morphogenetic protein 6ApoptosisImmunologyBone Morphogenetic ProteinsMutationTetradecanoylphorbol AcetateTumor promotionEpidermisCarcinogenesisCell DivisionOncogene
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The aryl hydrocarbon receptor-dependent deregulation of cell cycle control induced by polycyclic aromatic hydrocarbons in rat liver epithelial cells

2006

Disruption of cell proliferation control by polycyclic aromatic hydrocarbons (PAHs) may contribute to their carcinogenicity. We investigated role of the aryl hydrocarbon receptor (AhR) in disruption of contact inhibition in rat liver epithelial WB-F344 'stem-like' cells, induced by the weakly mutagenic benz[a]anthracene (BaA), benzo[b]fluoranthene (BbF) and by the strongly mutagenic benzo[a]pyrene (BaP). There were significant differences between the effects of BaA and BbF, and those of the strongly genotoxic BaP. Both BaA and BbF increased percentage of cells entering S-phase and cell numbers, associated with an increased expression of Cyclin A and Cyclin A/cdk2 complex activity. Their eff…

Health Toxicology and MutagenesisCyclin AGene ExpressionApoptosisCell Cycle ProteinsCyclin ACell LineBenz(a)AnthracenesBenzo(a)pyreneCytochrome P-450 CYP1A1polycyclic compoundsGeneticsAnimalsRat liver ‘stem-like’ cellsRNA MessengerPolycyclic Aromatic HydrocarbonsRNA Small InterferingMolecular BiologyAryl hydrocarbon receptorCell proliferationCarcinogenCell ProliferationFluorenesBase SequencebiologyChemistryCell growthCell CycleCyclin-Dependent Kinase 2Contact inhibitionEpithelial CellsTransfectionAryl hydrocarbon receptorMolecular biologyPolycyclic aromatic hydrocarbonsPolycyclic Hydrocarbons AromaticRatsReceptors Aryl HydrocarbonBiochemistryApoptosisMultiprotein ComplexesContact inhibitionMutationHepatocytesbiology.proteinCDK inhibitorMutagensMutation Research/Fundamental and Molecular Mechanisms of Mutagenesis
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