Search results for "Oxidation."

showing 10 items of 1877 documents

Effects of free fatty acids, lysophosphatides and phospholipase treatment on lipid peroxidation of myocardial homogenates and membrane fractions

1987

The effects of various free fatty acids, lysophosphatides and phospholipase treatments on the enzymatic and the non-enzymatic lipid peroxidation capacities in the heart homogenates and subcellular fractions were studied. The results showed a dose related inhibition of both the enzymatic and non-enzymatic lipid peroxidation with free fatty acids. A significant inhibition occurred as early as at the concentration of 25–50 μM of several fatty acids both in homogenates and in organelle fractions. In general, the inhibition was greatest with cis-unsaturated, long-chain fatty acids. The inhibition was also induced by the pretreatment of the homogenates with phospholipase A2 but not with phospholi…

chemistry.chemical_classificationbiologyPhospholipaseLipid peroxidationchemistry.chemical_compoundEnzymePhospholipase A2MembranechemistryBiochemistryOrganelleAmphiphilebiology.proteinInhibitory effect
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Experimental evidence for proton motive force-dependent catalysis by the diheme-containing succinate:menaquinone oxidoreductase from the Gram-positiv…

2006

In Gram-positive bacteria and other prokaryotes containing succinate:menaquinone reductases, it has previously been shown that the succinate oxidase and succinate:menaquinone reductase activities are lost when the transmembrane electrochemical proton potential, Deltap, is abolished by the rupture of the bacteria or by the addition of a protonophore. It has been proposed that the endergonic reduction of menaquinone by succinate is driven by the electrochemical proton potential. Opposite sides of the cytoplasmic membrane were envisaged to be separately involved in the binding of protons upon the reduction of menaquinone and their release upon succinate oxidation, with the two reactions linked…

chemistry.chemical_classificationbiologyProtonophoreChemiosmosisSuccinic AcidProton-Motive ForceBacillusVitamin K 2HemeReductasebiology.organism_classificationBiochemistryRedoxCatalysisSuccinate DehydrogenaseEnzymeBiochemistrychemistryBacterial ProteinsFumaratesOxidoreductaseBacillus licheniformisOxidoreductasesOxidation-ReductionBacteriaBiochemistry
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Succinate dehydrogenase functioning by a reverse redox loop mechanism and fumarate reductase in sulphate-reducing bacteria.

2006

Sulphate- or sulphur-reducing bacteria with known or draft genome sequences (Desulfovibrio vulgaris, Desulfovibrio desulfuricans G20, Desulfobacterium autotrophicum [draft], Desulfotalea psychrophila and Geobacter sulfurreducens) all contain sdhCAB or frdCAB gene clusters encoding succinate : quinone oxidoreductases. frdD or sdhD genes are missing. The presence and function of succinate dehydrogenase versus fumarate reductase was studied. Desulfovibrio desulfuricans (strain Essex 6) grew by fumarate respiration or by fumarate disproportionation, and contained fumarate reductase activity. Desulfovibrio vulgaris lacked fumarate respiration and contained succinate dehydrogenase activity. Succi…

chemistry.chemical_classificationbiologySulfatesSuccinate dehydrogenaseMolecular Sequence DataSuccinic AcidBacillus subtilisFumarate reductasebiology.organism_classificationMicrobiologySuccinate DehydrogenaseEnzymechemistryBiochemistryFumaratesMultigene Familybiology.proteinDesulfovibrioSDHDAmino Acid SequenceDesulfovibrio vulgarisGeobacter sulfurreducensOxidation-ReductionBacteriaMicrobiology (Reading, England)
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Synthese von Benzo[b]thioxanthenen

1995

Synthesis of Benzo[b]thioxanthenes Benzo[b]thioxanthenes, heterocyclic compounds related to tetracenes and tetracyclines can be obtained by the reaction of 2H-benzo[b]thiete (1) and 1,4-naphthoquinones (3a–g). The primary cycloadducts 4a–g undergo an autoxidation process leading to the quinones 6a–g. The dihydroxy compound 4e shows an additional isomerization by a tetrafold H transfer (4e 5e′). Another preparative route to benzo[b]thioxanthenes makes use of the cycloadditon reaction of 1 and 1,4-epoxynaphthalenes (7a–d). The primary adducts can be transformed to the title compounds by catalytic dehydration processes (8a–d 9a-d). An alternate regioselective opening of the oxygen bridge can b…

chemistry.chemical_classificationchemistry.chemical_compoundKetonechemistryAutoxidationSulfoniumStereochemistryThioxanthenesRegioselectivityGeneral MedicineIsomerizationCatalysisAdductJournal f�r Praktische Chemie/Chemiker-Zeitung
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Über die synthese von oligophenylenes mit einer o-verknüpfung. 10. Mitteilung

1960

Es werden zwei Wege zur Darstellung von Oligophenylenen mit einer o-Winkelung beschrieben. Als Ausgangssubstanzen dienen der Mono-enolather des Cyclohexandion (1,2) bzw. Cyclohexenoxyd. Die Darstellung des Mono-enolathylathers des Cyclohexandion (1,2) wird beschrieben. Durch Oxydation nach OPPENAUER mit Chinon als Wasserstoffacceptor konnen die als Zwischenprodukte der Oligophenylene erhaltenen Cyclohexanolderivate in 90%iger Ausbeute in die benotigten Ketone ubergefuhrt werden. Folgende o-gewinkelten Oligophenylene wurden synthetisiert : o-Terphenyl; 2o2-Quater-phenyl ; 32, 43-Dimethyl-2o2-quaterphenyl ; 3o2-Quinquiphenyl ; 12, 23-Dimethyl-3o2-quinquiphenyl ; 12, 23, 42, 53-Tetramethyl-3o2…

chemistry.chemical_classificationchemistry.chemical_compoundKetonechemistryYield (chemistry)Polymer chemistryMelting pointCyclohexanolOppenauer oxidationAcceptorQuinoneDie Makromolekulare Chemie
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Mo-Based Oxidizers as Powerful Tools for the Synthesis of Thia- and Selenaheterocycles.

2019

A highly efficient synthetic protocol for the synthesis of thia- and selenaheterocycles has been developed. By employing a MoCl5 -mediated intramolecular dehydrogenative coupling reaction, a broad variety of structural motifs was isolated in yields up to 94 %. The electrophilic key transformation is tolerated by several labile moieties like halides and tertiary alkyl groups. Due to the use of disulfide or diselenide precursors, a high atom efficiency was achieved.

chemistry.chemical_classificationcyclization010405 organic chemistryChemistryoxidationOrganic ChemistryHalideGeneral Chemistry010402 general chemistry01 natural sciencesCombinatorial chemistryCatalysisCoupling reactionC−H activationsulfur heterocycles0104 chemical sciencesDiselenidemolybdenumAtom economyIntramolecular forceElectrophileStructural motifAlkylChemistry (Weinheim an der Bergstrasse, Germany)
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Enzymatic Resolution of 3-oxodicyclopentadiene on a Decagram Scale

2018

The chiral building block 3-oxodicyclopentadiene (1) can be readily resolved on a decagram scale by a short sequence consisting of (1) reduction to the corresponding endo-alcohol, (2) enzymatic oxidative resolution with a ketoreductase enzyme to give (+)-1 and the (+)-form of the endo-alcohol, and (3) reoxidation of the (+)-endo-alcohol with another ketoreductase to give (–)-1. With a selectivity factor of 310, the enantiomeric ratios of the resolved (+)-endo-alcohol and (+)-ketone are both >99:1. Both enzymatic oxidations could be performed with a at least 300:1 substrate/catalyst ratio (w/w).

chemistry.chemical_classificationentsyymithapetustetrahydromethanoindenoneResolution (mass spectrometry)alkoholit (yhdisteet)ChemistryStereochemistryoxidationOrganic ChemistrySubstrate (chemistry)resolutionAlcoholCatalysisalcoholsgram-scale synthesischemistry.chemical_compoundEnzymeEnantiomerSelectivity
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Enhancing Selectivity In Photocatalytic Formation Of P-Anisaldehyde In Aqueous Suspension Under Solar Light Irradiation Via Tio2 N-Doping

2012

The photocatalytic partial oxidation of 4-methoxybenzyl alcohol to the corresponding aldehyde (p-anisaldehyde) was performed under simulated solar irradiation by using home prepared N-doped TiO2 catalysts. The photocatalysts were prepared by a sol–gel method, using TiCl4 as TiO2 precursor and NH4Cl, urea or NH4OH as N-doping sources. A commercial TiO2 (Degussa P25) was also used for comparison aims. The prepared catalysts were characterized by BET specific surface area, XRD, ESEM and UV-vis spectroscopy. The reactivity results show that (i) the doped catalysts are predominantly amorphous, and they show selectivity values far higher than those of the corresponding undoped ones and of well cr…

chemistry.chemical_classificationinorganic chemicalsChemistryInorganic chemistryGeneral ChemistryAldehydeCatalysisCatalysisSpecific surface areaMaterials ChemistryPhotocatalysisReactivity (chemistry)Partial oxidationIrradiationN doping TiO2 photocatalysis partial oxidationSelectivity
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Age-related changes in antioxidant status and oxidative damage to lipids and dna in mitochondria of rat liver

2005

To investigate the correlation between oxidative stress and mitochondrial damage with aging, antioxidant system, levels of oxidative DNA damage and as an index of the loss of plasma membrane integrity lipid peroxidation and membrane potential were studied. Results showed that the activities of antioxidant enzymes superoxide dismutase (SOD) and catalase significantly decreased during aging, however glutathione peroxidase (GSH-PX) increased in the aged mitochondria and glutathione (GSH) did not change during aging. No statistical difference was observed in the lipid peroxidation of mitochondria between young and old animals. The level of oxidative DNA damage (measured as 8oxo-dG) tended to in…

chemistry.chemical_classificationmedicine.medical_specialtyAntioxidantbiologyChemistryDNA damagemedicine.medical_treatmentGlutathione peroxidaseBioengineeringGlutathioneMitochondrionmedicine.disease_causeApplied Microbiology and BiotechnologyBiochemistrySuperoxide dismutaseLipid peroxidationchemistry.chemical_compoundEndocrinologyBiochemistryInternal medicinemedicinebiology.proteinOxidative stressProcess Biochemistry
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Early reductive stress followed by a late onset oxidative stress in acute myocardial infarction

2018

Introduction The idea that the cells might suffer from reductive rather than oxidative stress and that such stress may be relevant in pathophysiology has gained momentum. Aim We aimed at studying markers of oxidative stress and damage as well as the expression of antioxidant enzymes in a swine model of acute myocardial infarction (AMI) followed by reperfusion. Results and Discussion We found an increase in the GSH to GSSG ratio, a decrease in protein glutathionylation and a decrease in p38 MAPK phosphorylation after 90 minutes of ischaemia in heart samples. It was accompanied by an increase in the expression of Thioredoxin (TrX) and Peroxiredoxin (PrX) and a decrease in the expression of Gl…

chemistry.chemical_classificationmedicine.medical_specialtyProtein CarbonylationGlutathione peroxidaseGlutathione reductaseGlutathioneProtein glutathionylationmedicine.disease_causeBiochemistryLipid peroxidationchemistry.chemical_compoundEndocrinologychemistryPhysiology (medical)Internal medicinemedicineThioredoxinOxidative stressFree Radical Biology and Medicine
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