Search results for "Reactivity"

showing 10 items of 880 documents

Kalanchoe pinnata inhibits mast cell activation and prevents allergic airway disease

2011

Aqueous extract of Kalanchoe pinnata (Kp) have been found effective in models to reduce acute anaphylactic reactions. In the present study, we investigate the effect of Kp and the flavonoid quercetin (QE) and quercitrin (QI) on mast cell activation in vitro and in a model of allergic airway disease in vivo. Treatment with Kp and QE in vitro inhibited degranulation and cytokine production of bone marrow-derived mast cells following IgE/FcɛRI crosslinking, whereas treatment with QI had no effect. Similarly, in vivo treatment with Kp and QE decreased development of airway hyperresponsiveness, airway inflammation, goblet cell metaplasia and production of IL-5, IL-13 and TNF. In contrast, treatm…

KalanchoeOvalbuminmedicine.medical_treatmentBasophil Degranulation TestPharmaceutical ScienceInflammationImmunoglobulin EMiceIn vivoDrug DiscoverymedicineAnimalsMast CellsPharmacologyMetaplasiaMice Inbred BALB CGoblet cellInterleukin-13biologyPlant ExtractsTumor Necrosis Factor-alphabusiness.industryDegranulationIn vitroCytokinemedicine.anatomical_structureComplementary and alternative medicineImmunologybiology.proteinMolecular MedicineQuercetinTumor necrosis factor alphaGoblet CellsBronchial HyperreactivityInterleukin-5medicine.symptombusinessPhytotherapyPhytomedicine
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A Combined Experimental and Theoretical Approach to the Photogeneration of 5,6-Dihydropyrimidin-5-yl Radicals in Nonaqueous Media

2016

The chemical fate of radical intermediates is relevant to understand the biological effects of radiation and to explain formation of DNA lesions. A direct approach to selectively generate the putative reactive intermediates is based on the irradiation of photolabile precursors. But, to date, radical formation and reactivity have only been studied in aqueous media, which do not completely mimic the micro environment provided by the DNA structure and its complexes with proteins. Thus, it is also important to evaluate the photogeneration of nucleoside-based radicals in nonaqueous media. The attention here is focused on the independent generation of 5,6-dihydropyrimidin-5-yl radicals in organic…

KetoneTHYMIDINEDNA damageRadicalReactive intermediate010402 general chemistryPhotochemistryHydrogen atom abstraction01 natural sciencesQUIMICA ORGANICAAQUEOUS-SOLUTIONSQUIMICA ANALITICASTRAND SCISSIONReactivity (chemistry)REPAIRchemistry.chemical_classificationAqueous solution010405 organic chemistryOrganic ChemistryINDEPENDENT GENERATION0104 chemical sciences56-DIHYDROTHYMID-5-YLDNA-DAMAGEchemistry2ND-ORDER PERTURBATION-THEORYRADIATIONFlash photolysisHYDROGEN-ATOM ABSTRACTIONThe Journal of Organic Chemistry
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Reaktionskinetik der Polymerisationshemmung durch molekularen Sauerstoff

1957

Die Polymerisationshemmung geschieht bei Styrol nach demselben Mechanismus wie er kurzlich fur Methylmethacrylat berichtet wurde1. Wahrend der Inhibierungsperiode findet streng alternierende Copolymerisation zwischen molekularem Sauerstoff und dem monomeren Styrol statt. Die fur die Anlagerung von O2 an das Radikal RM · masgebende Konstante kMO2 ist etwa von der Grosenordnung 106–107, d. h. die Reaktionsfahigkeit des Sauerstoffs in dieser Reaktion entspricht der eines Radikals. Bruttogeschwindigkeit und kinetische Kettenlange wahrend der Inhibierungsperiode werden auf Grund des Reaktionsmechanismus berechnet und experimentell bestatigt. The inhibition mechanism in the polymerization of styr…

Kinetic chain lengthReaction ratechemistry.chemical_compoundReaction rate constantchemistryPolymerizationPolymer chemistryCopolymerReactivity (chemistry)Molecular oxygenStyreneDie Makromolekulare Chemie
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On the Nucleophilic Reactivity of 4,6-Dichloro-5-nitrobenzofuroxan with Some Aliphatic and Aromatic Amines: Selective nucleophilic substitution

2020

The reaction rates for the nucleophilic aromatic substitution of 4,6-dichloro-5-nitrobenzofuroxan 1 with eight aliphatic amines (characterized by very different basicities/ nucleophilicities) and three anilines have been measured in both methanol and toluene. The obtained rates have been related to the basicity (pKaH in water and Kb in benzene) or nucleophilicity (N Mayr constants) of the tested amines. The whole of the obtained kinetic data has furnished useful information on the high nucleophilic reactivity of benzofuroxan derivatives, which has been related essentially to two factors: the high electron-drawing ability/power of the condensed furoxan ring and the low aromatic character of …

KineticOrganic ChemistryFuroxanBenzofuroxanTolueneMedicinal chemistrySNArchemistry.chemical_compoundchemistryNucleophileNucleophilic aromatic substitutionAromaticity IndexNucleophilic substitutionMayr constantReactivity (chemistry)MethanolBenzene
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CO Oxidation on Cationic Gold Clusters: A Theoretical Study

2008

Aiming at understanding the elementary steps governing the oxidation of CO catalyzed by dispersed or supported gold nanoclusters, the reactivity of molecular species, such as O2 and CO, on neutral and positively charged Au13 clusters have been studied using a DFT approach. Two CO oxidation mechanisms have been simulated, involving respectively the adsorption of CO and O2 on adjacent catalytic sites (two-sites mechanism) and the competitive interaction of the reactants on the same site (single-site mechanism). It is demonstrated that in the former scheme a definite interaction of CO and O2 with both the charged and neutral cluster is effective, but that a chemical reaction between the adsorb…

Latter mechanismInorganic chemistryReaction pathPhotochemistryChemical reactionNeutral clusterNanoclustersCatalysisMolecular specieAdsorptionCompetitive interactionCluster (physics)Reactivity (chemistry)Physical and Theoretical ChemistrySupported golds Engineering main heading: Carbon monoxideEngineering controlled terms: AdsorptionPositively chargedOxidation Engineering uncontrolled terms: Catalytic siteDioxygenChemistryElementary stepCationic polymerizationOxidation of COCatalytic oxidationCO oxidationSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsFlow interactionGeneral EnergyCarbon dioxideCatalytic oxidationChemical oxygen demandCarbon clusterCationic gold clusterChemical reactionGold compoundThe Journal of Physical Chemistry C
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Factors affecting copper(II) binding to multiarmed cyclam-grafted mesoporous silica in aqueous solution

2009

Single- as well as multi-anchored cyclam-functionalized silica samples have been prepared by grafting amorphous silica gel (K60) and mesostructured silica (SBA-15) with silylated cyclam precursors bearing one, two, or four triethoxysilyl groups, respectively ascribed to cyclam-mono, cyclam-di, and cyclam-tetra. Their reactivity toward copper(II) has been thoroughly investigated in aqueous solution and discussed with respect to the number of arms tethering the ligand to the silica surface and the structural ordering of the adsorbent in terms of capacity, long-term stability, and speed of access to the binding sites. Less-than-complete metal ion uptake was always observed, even in excess of c…

Ligand field theoryStereochemistrychemistry.chemical_element02 engineering and technology010402 general chemistry01 natural scienceschemistry.chemical_compoundCyclamPolymer chemistryElectrochemistryGeneral Materials ScienceReactivity (chemistry)SpectroscopyAlkylComputingMilieux_MISCELLANEOUSchemistry.chemical_classificationAqueous solutionSilica gelSurfaces and Interfaces[CHIM.MATE]Chemical Sciences/Material chemistryMesoporous silica021001 nanoscience & nanotechnologyCondensed Matter PhysicsCopper0104 chemical scienceschemistry[ CHIM.MATE ] Chemical Sciences/Material chemistry0210 nano-technology
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Monitoring Thiol–Ligand Exchange on Au Nanoparticle Surfaces

2018

Surface functionalization of nanoparticles (NPs) plays a crucial role in particle solubility and reactivity. It is vital for particle nucleation and growth as well as for catalysis. This raises the quest for functionalization efficiency and new approaches to probe the degree of surface coverage. We present an (in situ) proton nuclear magnetic resonance (1H NMR) study on the ligand exchange of oleylamine by 1-octadecanethiol as a function of the particle size and repeated functionalization on Au NPs. Ligand exchange is an equilibrium reaction associated with Nernst distribution, which often leads to incomplete surface functionalization following “standard” literature protocols. Here, we show…

LigandNanoparticle02 engineering and technologySurfaces and Interfaces010402 general chemistry021001 nanoscience & nanotechnologyCondensed Matter PhysicsPhotochemistry01 natural sciences0104 chemical scienceschemistry.chemical_compoundsymbols.namesakechemistryOleylamineElectrochemistryProton NMRsymbolsSurface modificationGeneral Materials ScienceReactivity (chemistry)Nernst equationParticle size0210 nano-technologySpectroscopyLangmuir
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Novel unsymmetrical ortho-metalated dirhodium (II) catalysts: trans influence of the axial ligand

1999

Inductive effects of an X axial group which are transmitted through the RhRh bond influence the reactivity of ortho-metalated dirhodium complexes 3 in the cyclization of 1-diazo-5-penten-2-one (4).

LigandTrans effectGroup (periodic table)ChemistryOrganic ChemistryDrug DiscoveryReactivity (chemistry)BiochemistryMedicinal chemistryCatalysisTetrahedron Letters
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Selective Processing of Food– and Body–Related Information and Autonomic Arousal in Patients with Eating Disorders

1998

Both attentional bias (using the modified Stroop Task) and autonomic reactivity (skin conductance level) to food- and body-related information were assessed in 25 patients with eating disorders (15 patients with anorexia, 10 patients with bulimia) and 18 women controls. Patients with anorexia showed the greatest interference in color-naming food-related words. However, on this occasion there were no differences in body condition, probably because of heterogeneity of clinical samples and because the control group were staff members, so the target information was very familiar to them. The groups differed in their autonomic reactivity while performing the Stroop, the patients with anorexia re…

Linguistics and Languagemedicine.medical_specialtyAutonomic arousaldigestive oral and skin physiologyAnorexiaAttentional biasAudiologymedicine.diseaseLanguage and LinguisticsCognitive biasDevelopmental psychologyEating disordersmental disordersmedicineIn patientmedicine.symptomPsychologyReactivity (psychology)General PsychologyStroop effectThe Spanish Journal of Psychology
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Multinuclear 1H, 13C and 15N NMR study of some substituted 2-amino-4-nitropyridines and their N-oxides.

2002

1H, 13C and 15N NMR chemical shift assignments based on pulsed field gradient selected PFG 1H,X (X = 15C and 15N) HMQC and HMBC experiments are reported for three 4-nitropyridine N-oxides and four 4-nitropyridines. It was found that an ortho effect of a methyl group inhibits the deshielding effect of the 4-nitro group and that this effect and the so-called back donation is influenced by electronegativity and position of substituents in the multisubstituted pyridine N-oxides. The shielding effect of N-oxide group is most pronounced in the 15N NMR chemical shifts of the studied compounds. This effect is further modified by methylamino, methylnitramino, 5- or 3-methyl and 4-nitro groups. Among…

Magnetic Resonance SpectroscopyChemistryNitrogenPyridinesUltraviolet RaysChemical shiftNuclear magnetic resonance spectroscopyAtomic and Molecular Physics and OpticsCarbonAnalytical ChemistryElectronegativityOxygenchemistry.chemical_compoundCrystallographyModels ChemicalComputational chemistryPyridineNucleophilic substitutionShielding effectReactivity (chemistry)InstrumentationSpectroscopyMethyl groupSpectrochimica acta. Part A, Molecular and biomolecular spectroscopy
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