Search results for " radical"

showing 10 items of 757 documents

Does catalase play a role in Adriamycin induced cardiotoxicity?

1980

Summary Adriamycin causes an increase of lipid peroxidation in mouse cardiac homogenates that is dependent on the concentration of the antiblastic. The same phenomenon is not observed in the hearts of mice treated with an elevated dose of Adriamycin in which, conversely, an increase of the antioxidizing enzyme catalase was noticed. The significance of these findings is discussed with relationship to the hypothesis of an enhanced free radicals formation at the basis of Adriamycin induced cardiotoxicity.

chemistry.chemical_classificationPharmacologyCardiotoxicityLipid PeroxidesbiologyFree RadicalsHeart DiseasesMyocardiumPharmacologyNADCatalaseMalonatescarbohydrates (lipids)Lipid peroxidationchemistry.chemical_compoundMiceEnzymechemistryCatalaseDoxorubicinMalondialdehydepolycyclic compoundsbiology.proteinAnimalsFemalePharmacological Research Communications
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Synthesis, crystallographic and spectroscopic characterization and magnetic properties of dimer and monomer ternary copper(II) complexes with sulfona…

2010

Abstract Three dinuclear and one mononuclear copper(II)-1,10-phenanthroline ternary complexes, [Cu(L1)(phen)(OH)]2 (1), [Cu(L2)(phen)(OH)]2·3H2O (2), [Cu(L3)(phen)(OH)]2 (3) and [Cu(L4)2(phen)(H2O)] (4), with thiadiazole sulfonamide derivative ligands: HL1 (N-(5-ethyl-1,3,4-thiadiazol-2-yl)naphthalene-1-sulfonamide), HL2 (N-(5-ethylthio)-1,3,4-thiadiazol-2-yl)-4-methylbenzenesulfonamide), HL3 (N-(5-ethyl-1,3,4-thiadiazol-2-yl)benzenesulfonamide) and HL4 (N-(5-ethyl-1,3,4-thiadiazol-2-yl)-4-methylbenzenesulfonamide) have been synthesized and characterized. In the four complexes each copper atom is five-coordinated. The structure of complexes 1, 2 and 3 consists of a dimeric unit with a C2 sy…

chemistry.chemical_classificationPhenanthrolineDimerchemistry.chemical_elementCleavage (embryo)Ascorbic acidCopperSulfonamideInorganic Chemistrychemistry.chemical_compoundCrystallographyMonomerchemistryMaterials ChemistryHydroxyl radicalPhysical and Theoretical ChemistryPolyhedron
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Evidence for chain transfer in the atom transfer radical polymerization of butyl acrylate

2000

Poly(butyl acrylate) (PBuA) of high molecular weight was synthesized by atom transfer radical polymerization (ATRP) in ethyl acetate. Whereas for low molecular weight polymers, a linear increase of the number-average molecular weight. M n , versus conversion and narrow molecular weight distributions indicate the suppression of side reactions, a downward curvature in the plot of M n versus conversion was observed for high molecular weights (M n > 50 000). This effect is explained by chain transfer reactions, leading to branched polymers. GPC measurements with a viscosity detector give evidence for the branched structure of high molecular weight polymers obtained in ATRP. In addition, transfe…

chemistry.chemical_classificationPolymers and PlasticsAtom-transfer radical-polymerizationButyl acrylateOrganic ChemistryRadical polymerizationChain transferSolution polymerizationPolymerchemistry.chemical_compoundMonomerchemistryCatalytic chain transferPolymer chemistryMaterials ChemistryMacromolecular Rapid Communications
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Patterning of a Surface Immobilized ATRP Initiator with an Inkjet Printer

2010

A new technique for patterning polymer brushes on the micrometer scale has been developed in which an inkjet printer was used to deposit droplets of acid on a surface-immobilized initiator for atom transfer radical polymerization (ATRP). The acid cleaved an ester bond in the ATRP initiator in a saponification reaction. As a result, the ATRP initiator was rendered inactive. To control the degree of defunctionalization, a new initiator containing a weak ester bond was derived from a tertiary alcohol. Comparison to an established ATRP initiator, derived from a primary alcohol, showed that the novel initiator was defunctionalized with a higher efficiency. Control of the reaction time allowed to…

chemistry.chemical_classificationPolymers and PlasticsBulk polymerizationChemistryAtom-transfer radical-polymerizationOrganic ChemistryAlcoholPolymerPrimary alcoholGraftingInorganic Chemistrychemistry.chemical_compoundPolymer chemistryMaterials ChemistryMoleculeSaponificationMacromolecules
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γ-radiation-initiated polymerization of vinylidene fluoride in dense carbon dioxide

2002

The γ-ray-initiated batch polymerization of vinylidene fluoride (VF2) has been investigated in dense carbon dioxide under relatively mild operative conditions (T ≤ 40 °C and P < 25 MPa). When the initial VF2 molar concentration was increased from 3.4 to 6.4 mol/L, monomer conversion increased from 20 to 73%; a similar trend was observed for the number-average molecular weight and the molecular complexity of synthesized poly(vinylidene fluoride) (PVDF) as determined from rheological measurements. Under all adopted experimental conditions, a synthesized PVDF polymer was collected in the form of a white powder. Despite the inherent heterogeneous character of the polymerization process, a homog…

chemistry.chemical_classificationReaction mechanismMolar concentrationGeneral Chemical EngineeringKineticsSolution polymerizationGeneral ChemistryPolymerSettore ING-IND/27 - Chimica Industriale E TecnologicaIndustrial and Manufacturing Engineeringchemistry.chemical_compoundMonomerchemistryPolymerizationsupercritical carbon dioxide free radical polymerization fluoropolymersPolymer chemistryFluorideNuclear chemistry
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The chemistry of melatonin's interaction with reactive species

2002

Melatonin has been shown to be an effective antioxidant in a number of experimental models both in vitro and in vivo. Considering the data available, it is now clear that the indoleamine is involved in antioxidative mechanisms more complex than originally envisaged. These range from the direct radical scavenging of a variety of radicals and reactive species to the control and/or modulation of a number of processes which may trigger a redox imbalance between antioxidant and prooxidant species. This review focuses on the direct radical scavenging activity of melatonin and provides a summary of the mechanisms of the reactions between the indoleamine and reactive species in pure chemical soluti…

chemistry.chemical_classificationReactive oxygen speciesAntioxidantChemistryRadicalmedicine.medical_treatmentmedicine.disease_causeRedoxMelatoninchemistry.chemical_compoundEndocrinologyBiochemistrymedicineHydroxyl radicalReactive nitrogen speciesOxidative stressmedicine.drugJournal of Pineal Research
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Contact probe voltammetry for in situ monitoring of the reactivity of phenolic tomato (Solanum lycopersicum L.) compounds with ROS

2015

The application of an in situ electrochemical contact probe methodology for monitoring reactivity of antioxidant polyphenolic compounds in tomato fruits is described. Upon electrochemical generation of reactive oxygen species (ROS), characteristic voltammetric responses were recorded for compounds resulting from the reaction of such species with tomato compounds. This suggests that new electrochemically oxidizable compounds are generated from the oxidation of highly reactive polyphenolic compounds with ROS. Therefore, an evaluation of the antioxidant capacity of such species could be made from voltammetric data for different tomato varieties.

chemistry.chemical_classificationReactive oxygen speciesAntioxidantbiologyPlant ExtractsChemistrymedicine.medical_treatmentfood and beveragesFree Radical Scavengersbiology.organism_classificationElectrochemistryAnalytical Chemistrychemistry.chemical_compoundSolanum lycopersicumPhenolsPolyphenolFruitElectrochemistrymedicineOrganic chemistryReactivity (chemistry)PhenolsSolanumReactive Oxygen SpeciesVoltammetryTalanta
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ChemInform Abstract: Investigations Concerning the COX/5-LOX Inhibiting and Hydroxyl Radical Scavenging Potencies of Novel 4,5-Diaryl Isoselenazoles.

2008

The aim of this study was to investigate 4,5-diaryl isoselenazoles as multiple target non-steroidal anti-inflammatory drugs (MTNSAIDs) which can intervene into the inflammatory processes via different mechanisms of action creating a new class of compounds. Here we describe the synthesis of COX/LOX inhibitors which additionally reduce the level of reactive oxygen species, such as hydroxyl radicals which are well known for supporting inflammation processes in Parkinson's disease, Alzheimer's disease and rheumatoid arthritis.

chemistry.chemical_classificationReactive oxygen speciesRadicalInflammationGeneral MedicinePharmacologyMultiple targetmedicine.diseasechemistry.chemical_compoundchemistryRheumatoid arthritismedicineHydroxyl radicalmedicine.symptomChemInform
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Magnesium, Oxidative Stress, and Aging Muscle

2014

Abstract Magnesium (Mg) deficiency, aside from having a negative impact on the energy production pathways required by the mitochondria to generate ATP, also reduces the threshold antioxidant capacity of the aging organism and its resistance to free-radical damage. Mg acts as an antioxidant against free radical damage of the mitochondria. Chronic Mg deficiency results in excessive production of oxygen-derived free radicals and low-grade inflammation. Chronic inflammation and oxidative stress have been identified as pathogenic factors in several age-related conditions. Aging is often associated with Mg inadequacy, muscle loss, and sarcopenia. Although the importance of magnesium as a determin…

chemistry.chemical_classificationReactive oxygen speciesmedicine.medical_specialtySettore MED/09 - Medicina InternaAntioxidantbusiness.industryMagnesiummedicine.medical_treatmentchemistry.chemical_elementInflammationMitochondrionmedicine.diseasemedicine.disease_causeEndocrinologychemistrySarcopeniaInternal medicinemedicinemedicine.symptombusinessMagnesium Aging Mg Deficiency Muscle Oxidative stress Chronic inflammation Sarcopenia Free radical Reactive oxygen species Muscle performance IonsOxidative stressFree-radical theory of aging
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Synthesis of .beta.-ionone in an aldehyde/xanthine oxidase/.beta.-carotene system involving free radical formation

1994

The enzymic cooxidation of β-carotene (BC) by xanthine oxidase (XO) in aqueous solutions leads to β-ionone (BI) and derivatives: epoxy-β-ionone (EPBI), dihydroactinidiolide, β-cyclocitral, pseudoionone, etc. We demonstrate, in this article, that this is due to free radical (R . ) formation during the first hour of stirring and the use of aldehydes as substrate. The bleaching of BC does not occur when the common substrate of XO, xanthine, is used; this proves that the superoxide anion O 2 .- alone is not active on BC. BI formation in this case is not observed

chemistry.chemical_classificationSuperoxideStereochemistryDihydroactinidiolideSubstrate (chemistry)XanthineIononeMedicinal chemistryAldehydechemistry.chemical_compoundchemistryXanthine oxidaseFree Radical FormationBiotechnologyBiotechnology Progress
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