Search results for "Epoxy Compounds"

showing 10 items of 77 documents

Induction of rat liver microsomal epoxide hydrolase by its endogenous substrate 16α, 17α-epoxyestra-1,3,5-trien-3-ol

1995

1. The influence of the endogenous steroid epoxides 16 alpha, 17 alpha-epoxyestra-1,3,5(10)-trien-3-ol (estroxide) and 16 alpha, 17 alpha-expoxiandrost-4-en-3-one (androstene oxide) and their metabolic precursors estra-1,3,5(10), 16-tetraen-3-ol (estratetraenol) and androsta-4, 16-dien-3-one (androstadienone) on the specific activities of hepatic microsomal and soluble epoxide hydrolase, glutathione S-transferase, dihydrodiol dehydrogenase, and 7-ethoxycoumarin deethylase was investigated in the male Sprague-Dawley rat. 2. Both estroxide and estratetraenol induced microsomal epoxide hydrolase activity towards styrene oxide and estroxide itself 2-2.5-fold and glutathione conjugation of 1-chl…

MaleEpoxide hydrolase 2Health Toxicology and Mutagenesis7-Alkoxycoumarin O-DealkylaseToxicologyBiochemistryRats Sprague-Dawleychemistry.chemical_compoundEstratetraenolStyrene oxideAnimalsEpoxide hydrolaseGlutathione TransferaseEpoxide HydrolasesPharmacologyEstriolChemistryAndrostadienoneGeneral MedicineGlutathioneRatsBiochemistryEnzyme InductionMicrosomal epoxide hydrolaseMicrosomes LiverMicrosomeEpoxy CompoundsOxidoreductasesXenobiotica
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Ethoxyquin feeding to rats increases liver microsome-catalyzed formation of benzo(a)pyrene diol epoxide--DNA adduct.

1978

Abstract The ability of rat liver microsomes to catalyze the formation of benzo(a)pyrene 7,8-diol-9,10-epoxide — DNA nucleoside adduct was increased threefold by feeding 0.5% ethoxyquin to the animals. Microsomal epoxide hydratase activity was enhanced i parallel by a factor of 3 while aryl hydrocarbon hydroxylase activity was not induced. Liver microsomes from rat pretreated with 3-methylcholanthrene produced an increased proportion of diol epoxide — DNA adduct when ethoxyquin had been fed to the animals. The main chromatographic peak formed by microsomes from 3-methylcholanthrene treated rats which contains DNA adducts of secondary benzo(a)pyrene phenol metabolites is reduced when the ani…

MaleEthoxyquinChemistryBiophysicsEpoxideCell BiologyDNABiochemistryAdductRatschemistry.chemical_compoundEthoxyquinBiochemistryBenzo(a)pyreneDNA adductMethylcholanthreneMicrosomeMicrosomes LiverQuinolinesPyreneAnimalsEpoxy CompoundsBenzopyrenesMolecular BiologyMethylcholanthreneBiochemical and biophysical research communications
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Use of monoclonal and polyclonal antibodies as structural and topographical probes for hepatic epoxide hydrolase

1983

AbstractMonoclonal antibodies have been prepared against rat liver epoxide hydrolase (EH), some of which gave precipitation lines on immunodiffusion against pure EH suggesting the presence of repetitive structural domains on the enzyme. Using ELISA, with polyclonal antibodies to rat and rabbit liver EH, reactivity and therefore structural similarities between EH of all species tested, including human, were observed. This was in contrast to immunodiffusion results demonstrating the limitations of the latter technique. Using monoclonal antibodies in ELISA, greatest structural similarity was between rat, mouse, and Syrian hamster EH and relatively little between rat and human. Two of the antib…

MalePrimatesMonoclonal antibodyImmunodiffusionmedicine.drug_classGuinea PigsBiophysicsHamsterEpoxide hydrolaseMonoclonal antibodyBiochemistryAntibodiesMiceEnzyme-linked immunosorbent assayStructural BiologyCricetinaeGeneticsmedicineAnimalsHumansEpoxide hydrolaseMolecular BiologyEpoxide HydrolasesbiologyChemistryEndoplasmic reticulumAntibodies MonoclonalRats Inbred StrainsCell BiologyMolecular biologyRatsImmunodiffusionLiverBiochemistryPolyclonal antibodiesMembrane topologyMonoclonalProtein structurebiology.proteinEpoxy CompoundsRabbitsAntibodyFEBS Letters
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Metabolic epoxidation of trans-4-acetylaminostilbene: A protective mechanism against its activation to a mutagen

1976

Abstract Trans -4-acetylaminostilbene is activated by liver preparations to mutagens for Salmonella typhimurium . Since this compound is metabolized to the trans -α,β-epoxide and since many epoxides are ultimate mutagens, this epoxide was tested for direct mutagenicity. It was, however, found to be non-mutagenic, and, in contrast to the parent compound, the epoxide was no longer activated by liver preparations to mutagens. The same was found for the β-ketone and for the threo -α,β-dihydrodiol, which are formed metabolically from trans -4-acetylaminostilbene and from its α,β-epoxide. 4-Acetylaminobibenzyl showed a very weak mutagenic activity in the presence of the liver preparation. Thus, i…

MaleSalmonella typhimuriumendocrine systemStereochemistryBiophysicsEpoxideMutagenmedicine.disease_causeBiochemistryMicechemistry.chemical_compoundStilbenesmedicineAnimalsMolecular BiologyMolecular Structurefungifood and beveragesCell BiologyTrans-4-acetylaminostilbeneLiverchemistryBiochemistryEpoxy CompoundsLiver preparationMutagensBiochemical and Biophysical Research Communications
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Vitamin K epoxide reductase activity in the metabolism of epoxides

1985

Abstract The importance of vitamine K epoxide reductase for the metabolism of a range of structurally diverse epoxides has been investigated. Vitamin K 1 epoxide is reduced by rat liver microsomes at a rate of 0.47 nmoles/g liver/min. The rate of menadione oxide reduction is not significantly higher than the non-enzymatic reduction rate. No measurable reduction of benzo[ a ]pyrene 4,5-oxide, benzo[ a ]pyrene 7,8-oxide, phenanthrene 9,10-oxide, styrene 7,8-oxide, and dieldrin has been detected, nor could trichothecene T-2 toxin inhibit reduction of vitamin K 1 epoxide. Thus, vitamin K epoxide reductase is very specific for vitamin K 1 epoxide. Taking into account the range of structurally di…

MaleStereochemistryEpoxideIn Vitro TechniquesReductaseBiochemistryMixed Function Oxygenaseschemistry.chemical_compoundMenadioneEthers CyclicVitamin K Epoxide ReductasesAnimalsEpoxide hydrolaseTrichloroepoxypropaneEpoxide HydrolasesPharmacologyRats Inbred StrainsVitamin K 1MetabolismRatschemistryBiochemistryMicrosomal epoxide hydrolaseMicrosomes LiverMicrosomeEpoxy CompoundsVitamin K epoxide reductaseBiochemical Pharmacology
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Aliphatic polycarbonates based on carbon dioxide, furfuryl glycidyl ether, and glycidyl methyl ether: reversible functionalization and cross-linking.

2014

Well-defined poly((furfuryl glycidyl ether)-co-(glycidyl methyl ether) carbonate) (P((FGE-co-GME)C)) copolymers with varying furfuryl glycidyl ether (FGE) content in the range of 26% to 100% are prepared directly from CO2 and the respective epoxides in a solvent-free synthesis. All materials are characterized by size-exclusion chromatography (SEC), (1)H NMR spectroscopy, and differential scanning calorimetry (DSC). The furfuryl-functional samples exhibit monomodal molecular weight distributions with Mw/Mn in the range of 1.16 to 1.43 and molecular weights (Mn) between 2300 and 4300 g mol(-1). Thermal properties reflect the amorphous structure of the polymers. Both post-functionalization and…

Methyl EthersMaterials scienceMagnetic Resonance SpectroscopyPolymers and PlasticsPolymersEtherMaleimideschemistry.chemical_compoundDifferential scanning calorimetryPolymer chemistryMaterials ChemistryCopolymerOrganic chemistryFuransMaleimidechemistry.chemical_classificationPolycarboxylate CementCalorimetry Differential ScanningCycloaddition ReactionMolecular StructureOrganic ChemistryTemperaturePolymerCarbon DioxideAmorphous solidchemistryModels ChemicalProton NMRChromatography GelSurface modificationEpoxy CompoundsMacromolecular rapid communications
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Glutathione Conjugation of Bay- and Fjord-Region Diol Epoxides of Polycyclic Aromatic Hydrocarbons by Glutathione Transferases M1-1 and P1-1

1997

Metabolism of polycyclic aromatic hydrocarbons in mammalian cells results in the formation of vicinal diol epoxides considered as ultimate carcinogens if the oxirane ring is located in a bay- or fjord-region of the parent compound. In the present study, individual stereoisomers of the bay-region diol epoxides of chrysene, dibenz[a,h]anthracene, and benzo[a]pyrene as well as of the fjord-region diol epoxides of benzo[c]phenanthrene, benzo[c]chrysene, and benzo[g]-chrysene have been incubated with GSH in the presence of human glutathione transferases GSTM1-1 (a mu-class enzyme) and GSTP1-1 (a pi-class enzyme). As previously shown with GSTA1-1 (an alpha-class enzyme) both M1-1 and P1-1 demonst…

Models MolecularChryseneStereochemistryConjugated systemToxicologySubstrate Specificitychemistry.chemical_compoundpolycyclic compoundsHumansPolycyclic Aromatic HydrocarbonsCarcinogenGlutathione TransferaseBay-Region Polycyclic Aromatic Hydrocarbonchemistry.chemical_classificationAnthraceneintegumentary systemStereoisomerismGeneral MedicineGlutathionePhenanthreneGlutathioneIsoenzymesKineticsEnzymechemistryCarcinogensEpoxy CompoundsPyreneCrystallizationChemical Research in Toxicology
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Sporogen, S14-95, and S-curvularin, three inhibitors of human inducible nitric-oxide synthase expression isolated from fungi.

2003

The induction of human inducible nitric-oxide synthase (iNOS) expression depends (among other factors) on activation of the signal transducer and activator of transcription 1 (STAT1) pathway. Therefore, the STAT1 pathway may be an appropriate target for the development of inhibitors of iNOS expression. HeLa S3 cells transiently transfected with a gamma-activated site (GAS)/interferon-stimulated response element-driven reporter gene construct were used as the primary screening system. Using this system, three novel inhibitors of interferon-gamma-dependent gene expression, namely, sporogen, S14-95, and S-curvularin, were isolated from different Penicillium species. These three compounds also …

Nitric Oxide Synthase Type IIINitric Oxide Synthase Type IIGene expressionHumansRNA MessengerEnzyme InhibitorsPromoter Regions GeneticCells CulturedNitritesPharmacologyRegulation of gene expressionReporter genebiologyPenicilliumNitric Oxide Synthase Type IIITransfectionCurvularinMolecular biologyNitric oxide synthaseDNA-Binding ProteinsSTAT1 Transcription FactorGene Expression Regulationbiology.proteinSTAT proteinTrans-ActivatorsMolecular MedicineEpoxy CompoundsZearalenoneNitric Oxide SynthaseCell DivisionMolecular pharmacology
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Inverse solvent effects in the heterogeneous and homogeneous epoxidation of cis-2-heptene with [2-percarboxyethyl]-functionalized silica and meta-chl…

2014

The rate constants for the epoxidation of cis-2-heptene with [2-percarboxyethyl]-functionalized silica (1a) and meta-chloroperbenzoic acid (mCPBA) (1b) in different solvents have been determined at temperatures in the −10 to 40 °C range. The heterogeneous epoxidation exhibits a dependence of the reaction rate on solvent polarity opposite to its homogeneous counterpart and anomalous activation parameters in n-hexane, which are interpreted in terms of the surface-promoted solvent structure at the solid–liquid interface. The results show that highly polar solvents can strongly inhibit heterogeneous reactions performed with silica-supported reagents or catalysts.

Organic ChemistryPhotochemistrySilicon DioxideBiochemistryHepteneCatalysisHeptanesSolventReaction rateChlorobenzoateschemistry.chemical_compoundKineticsReaction rate constantchemistryReagentSolventsPolarEpoxy CompoundsHexanesThermodynamicsPhysical and Theoretical ChemistrySolvent effectsOxidation-ReductionOrganicbiomolecular chemistry
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Differential effect of the enantiomers of phenprocoumon and warfarin on the vitamin K1-epoxide/vitamin K1 ratio in rat plasma.

1979

PharmacologyVitaminMaleTime FactorsDose-Response Relationship DrugWarfarinPharmaceutical ScienceEpoxideStereoisomerism4-HydroxycoumarinsVitamin K 1PharmacologyRatsPhenprocoumonchemistry.chemical_compoundchemistrymedicinePhenprocoumonAnimalsEpoxy CompoundsWarfarinEnantiomermedicine.drugThe Journal of pharmacy and pharmacology
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