Search results for "Pyrene"

showing 10 items of 260 documents

Pyrene-Derived Novel One- and Two-Component Organogelators

2003

A new class of alkyl-chain-appended pyrene derivatives 4-14 were synthesized and evaluated for their gelation abilities. Depending on the nature of the linking group, these compounds gelated a number of organic solvents, either in the presence or in the absence of the acceptor molecule 2,4,7-trinitrofluorenone (TNF). Compounds with ester, ether, or alkyl linkages gelated a number of hydroxylic and hydrocarbon solvents by means of a charge-transfer interaction with TNF, while compounds with amide, urethane and urea linkers formed gels on their own in a variety of solvents by means of pi-pi stacking and hydrogen-bonding interactions. The Xray crystal structure of urethane (S)-12 showed hydrog…

chemistry.chemical_classificationHydrogen bondOrganic ChemistryStackingEtherGeneral ChemistryAcceptorCatalysischemistry.chemical_compoundchemistryAmideOrganic chemistryMoleculePyreneAlkylChemistry - A European Journal
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Self-organization of hydrophobized polyzwitterions

1992

Abstract Several series of copolymers of different geometry were synthesized from zwitterionic surfactant monomers and polar non-ionic comonomers. Bulk properties were investigated by d.s.c. and X-ray scattering. The copolymers were amorphous, but exhibited superstructures up to high commonomer contents. Solubility of the copolymers was determined as a function of geometry and composition. From the results, a main chain spacer model has been derived. All water-soluble copolymers exhibited characteristic features of classical polysoaps, as shown by surface tension measurements and by solubilization of pyrene. But gradual differences depending on the polymer geometry were observed for the sol…

chemistry.chemical_classificationMaterials sciencePolymers and PlasticsOrganic ChemistryPolymerMicelleSurface tensionchemistry.chemical_compoundMonomerChemical engineeringchemistryPulmonary surfactantPolymer chemistryMaterials ChemistryCopolymerPyreneSolubilityPolymer
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The Distribution of Carcinogen Metabolizing Enzymes in the Mouse Liver: Comparison of Parenchymal and Non-Parenchymal Cell Populations

1987

The distribution of aminopyrine N-demethylase (APND), ethoxy- resorufin O-deethylase (ERRD), epoxide hydrolase (EH) and glutathione transferase (GST) activities in parenchymal (PC) and non-parenchymal (NPC) cell populations of control and Aroclor 1254-treated C57BL/6N and DBA/2N mice was determined. Furthermore, the metabolism of benzo(a)- pyrene (BP) in PC and NPC of both Aroclor 1254-treated mice strains was examined. Measurable activities of all enzymes investigated were detected in control PC as well as NPC of both mice strains; in all instances the PC possessed greater enzyme activities than did the NPC. The PC and NPC of DBA/ 2N mice had significantly lower ERRD and EH activities than…

chemistry.chemical_classificationMetabolismOxidative phosphorylationMolecular biologystomatognathic diseaseschemistry.chemical_compoundEnzymeBenzo(a)pyrenechemistryotorhinolaryngologic diseasesInducerEpoxide hydrolaseReceptorCarcinogen
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Reduction of benzo(a)pyrene mutagenicity by dihydrodiol dehydrogenase

1979

THE enigma of how inert chemicals can exert potent mutagenic, carcinogenic, allergenic and cytotoxic effects has been much debated. It has been learned that such compounds are metabolically converted to chemically reactive species1. In the case of aromatic or olefinic compounds, monooxygenases located in the membranes of the cell can transform these compounds into epoxides2–5 which by virtue of electrophilic reactivity can bind chemically to cellular macromolecules such as DNA, RNA and proteins, thereby disturbing biochemical control mechanisms and leading to the above mentioned toxic effects. The same membranes in which such epoxides are produced possess an enzyme, epoxide hydratase, which…

chemistry.chemical_classificationMultidisciplinarybiologyChemistryEpoxideMonooxygenaseCofactorAlcohol OxidoreductasesMiceStructure-Activity Relationshipchemistry.chemical_compoundEnzymeBiochemistryBenzo(a)pyreneMutationMicrosomes Liverpolycyclic compoundsbiology.proteinAnimalsPyreneBenzopyrenesBiotransformationCarcinogenDNANature
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α ,ω n -Heterotelechelic Hyperbranched Polyethers Solubilize Carbon Nanotubes

2010

The synthesis of novel linear-hyperbranched (linhb) polyether block copolymers based on poly(ethylene oxide) and branched poly(glycerol), bearing a single pyrene or myristyl moiety at the α-position of the linear chain is described. The polymers exhibit low polydispersity (M w /M n < 1.3) and controlled molecular weights (M n = 5 000 g·mol -1 ). The mainly hydrophilic block copolymers with multiple hydroxyl end groups readily dissolve multiwalled carbon nanotubes (MWCNTs) in water by mixing and subsequent sonification, resulting in noncovalent attachment of the linhb hybrid structure to the carbon nanotubes (CNTs). Transmission electron microscopy (TEM) was employed to visualize the solubil…

chemistry.chemical_classificationPolymers and PlasticsEthylene oxideOrganic ChemistryDispersityCarbon nanotubePolymerCondensed Matter Physicslaw.inventionchemistry.chemical_compoundEnd-groupchemistrylawPolymer chemistryMaterials ChemistryCopolymerMoietyPyrenePhysical and Theoretical ChemistryMacromolecular Chemistry and Physics
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UV-B-Induced acute toxicity of pyrene to the waterflea Daphnia magna in natural freshwaters.

1999

Abstract The effects of various water characteristics in natural freshwaters on the acute toxicity of one polycyclic aromatic hydrocarbon (PAH), pyrene, to a pelagic invertebrate Daphnia magna was studied under ultraviolet B (UV-B) radiation and in the dark. Pyrene was photoactivated and was more toxic to D. magna in the presence of UV-B radiation. Dissolved organic material (DOM), measured as dissolved organic carbon (DOC), significantly reduced the photoenhanced toxicity of pyrene. Under UV-B radiation the EC50 values were lower and in relation to the amount of DOM, ranging from 3.0 to 30.0 μg/L pyrene, whereas in the dark they were between 29.2 and 54.8 μg/L and not related to the amount…

chemistry.chemical_classificationPyrenesbiologyDose-Response Relationship DrugUltraviolet RaysHealth Toxicology and MutagenesisDaphnia magnaPublic Health Environmental and Occupational HealthPolycyclic aromatic hydrocarbonFresh WaterGeneral Medicinebiology.organism_classificationPollutionAcute toxicitychemistry.chemical_compoundchemistryCladoceraDaphniaEnvironmental chemistryDissolved organic carbonToxicityPyreneAnimalsOrganic matterOrganic ChemicalsEcotoxicology and environmental safety
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Photoinduced electron transfer in molecular organizates at the gas-water interface

1994

Abstract The influence of the molecular geometry is of fundamental importance for a better understanding of the photoinduced electron transfer mechanism. Because of their typical molecular structures, cyclophane rings have proved to be suitable for this purpose as electron acceptor molecules adsorbed under an amphiphile monolayer. We used a pyrene-labelled phospholipid derivative both as molecular anchor for the cyclophane ring and electron donor molecule. The co-spreading technique was used to prepare the complex monolayers. Surface pressure and surface potential measurements have indicated similar monolayer behaviour as with dimyristoylphosphatidic acid as anchor molecule, leading to the …

chemistry.chemical_classificationQuenching (fluorescence)ChemistryMetals and AlloysElectron donorSurfaces and InterfacesElectron acceptorPhotochemistryPhotoinduced electron transferSurfaces Coatings and FilmsElectronic Optical and Magnetic Materialschemistry.chemical_compoundElectron transferMonolayerMaterials ChemistryPyreneCyclophaneThin Solid Films
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ISOLATION OF RAT LIVER EPOXIDE HYDRATASE: PROPERTIES AND SUBSTRATE SPECIFICITY OF THE PURE ENZYME

1977

ABSTRACT The microsomal enzyme epoxide hydratase has been purified to homogeneity as judged by electrophoretical, ultracentrifugal and immunological criteria and by C- and N-terminal analysis. The preparation procedure consisted of solubilisation using the non-ionic detergent cutscum, (NH4)2SO4 precipitation, ion-exchange chromatography on DEAE-cellulose and cellulose phosphate and hydrophobic chromatography on butyl-sepharose. The product was detergent-free, had a relatively high content of hydrophobic amino acids and tended to aggregate in aqueous solutions. The protein had a minimum molecular weight of 49,000 ± 500 with a sedimentation coefficient of S20w≃ 3. Antibodies raised against th…

chemistry.chemical_classificationSedimentation coefficientchemistry.chemical_compoundAqueous solutionEnzymeChromatographychemistryAlkeneStyrene oxideMicrosomePyreneOrganic chemistryAmino acid
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Sensitive and selective determination of metabolically formed trans -dihydrodiols and phenols of benzo[ a ]pyrene in water and urine samples by HPLC …

1998

A method has been developed to separate hydroxylated metabolites of the carcinogenic polycyclic aromatic hydrocarbon benzo[a]pyrene, i. e. trans-4,5-, 7,8-, 9,10-dihydrodiol and 1-, 3-, 7-, and 9-phenol, by HPLC with amperometric detection employing an isocratic methanol/water eluent (70:30, v/v) containing 0.5 g/L sulfuric acid and 1 g/L lithium perchlorate. Compared with the usually applied fluorescence (λex = 265 nm, λem = 460 nm) and ultraviolet (λ = 265 nm) detection, the amperometric technique is about 2–12 times more sensitive for the determination of all metabolites investigated. The method was applied to the determination of the seven metabolites of benzo[a]pyrene in different wate…

chemistry.chemical_classificationchemistry.chemical_compoundChromatographyColumn chromatographychemistryBenzo(a)pyreneMetabolitePolycyclic aromatic hydrocarbonPyrenePhenolPhenolsBiochemistryHigh-performance liquid chromatographyFresenius' Journal of Analytical Chemistry
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Metabolic Inactivation of Reactive Metabolites

1978

ABSTRACT Many compounds which are not electrophilically reactive as such are transformed by mammalian enzymes to reactive metabolites which are, in many cases, responsible for cytotoxic, mutagenic and/or carcinogenic effects of the compounds in question. The essential role of activating systems in this situation has become common knowledge during the last decade. However, many reactive metabolites are also subject to inactivation by mammalian enzymes. This important parameter is frequently not taken into account. Compounds possessing aromatic or olefinic moieties are very widely occurring and activation of these often proceeds via an electrophilically reactive epoxide. This may be transform…

chemistry.chemical_classificationchemistry.chemical_compoundCytosolEnzymechemistryMetabolic InactivationBiochemistryStereochemistryEpoxidePyreneGlutathioneMonooxygenaseCarcinogen
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