Search results for "nap"

showing 10 items of 2226 documents

Total oxidation of naphthalene with high selectivity using a ceria catalyst prepared by a combustion method employing ethylene glycol.

2009

Abstract During the catalytic combustion of naphthalene, compounds other than CO 2 are often obtained. These products, as polymerized polycyclic aromatic hydrocarbons, oxygenated aromatic compounds and benzene derivate compounds, are usually more toxic than naphthalene. At the present work it is shown a nanocrystalline cerium oxide prepared by a combustion method employing a proper ethylene glycol concentration that exhibits very high activity in the decomposition of naphthalene in the presence of air and, most importantly, a selectivity value towards CO 2 of 100% for any range of conversions and/or temperatures used. In addition, it has been demonstrated that the amount of ethylene glycol …

Cerium oxideEthylene GlycolEnvironmental EngineeringHealth Toxicology and MutagenesisInorganic chemistryCatalytic combustionNaphthalenesCatalysisCatalysischemistry.chemical_compoundX-Ray DiffractionEnvironmental ChemistryBenzeneWaste Management and DisposalNaphthalenechemistry.chemical_classificationAir PollutantsAirTemperatureCarbon DioxidePollutionOxygenHydrocarbonchemistryMicroscopy Electron ScanningNanoparticlesGasesSelectivityCrystallizationEthylene glycolJournal of hazardous materials
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Synthesis and inhibitory activity of dimethylamino-chalcone derivatives on the induction of nitric oxide synthase.

2002

A series of nine dimethylamino-chalcone derivatives (1,3-diaryl-propenones) was synthesized and screened as potential inhibitors of NO and PGE(2) production in the RAW 264.7 macrophage cell line. 4-Dimethylamino-2',5'-dimethoxychalcone (6) was found to be the most potent and dual inhibitor (IC(50s) in the submicromolar range) of NO and PGE(2) production. 2',6'-Dimethoxylation appeared to be an effective requirement for selective and potent inhibition of nitric oxide synthase induction as it was confirmed by Western blot analysis. Chalcone (6) at 25 mg kg(-1) by oral route, inhibited significantly the formation of oedema in the carrageenan-induced model of inflammation in mice.

ChalconeAnti-Inflammatory AgentsDrug Evaluation PreclinicalAdministration OralNitric Oxide Synthase Type IIInflammationInhibitory postsynaptic potentialChemical synthesisDinoprostoneNitric oxideCell Linechemistry.chemical_compoundMiceStructure-Activity RelationshipChalconeWestern blotDrug DiscoverymedicineOral routeAnimalsEdemaPharmacologychemistry.chemical_classificationmedicine.diagnostic_testbiologyMacrophagesOrganic ChemistryDual inhibitorMacrophage cellGeneral MedicineMolecular biologyNitric oxide synthaseEnzymeBiochemistrychemistryEnzyme inhibitorCell cultureEnzyme Inductionbiology.proteinmedicine.symptomNitric Oxide SynthaseDimethylaminesEuropean journal of medicinal chemistry
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Neural inflammation alters synaptic plasticity probed by 10 Hz repetitive magnetic stimulation

2020

ABSTRACTSystemic inflammation is associated with alterations in complex brain functions such as learning and memory. However, diagnostic approaches to functionally assess and quantify inflammation-associated alterations in synaptic plasticity are not well-established. In previous work, we demonstrated that bacterial lipopolysaccharide (LPS)-induced systemic inflammation alters the ability of hippocampal neurons to express synaptic plasticity, i.e., the long-term potentiation (LTP) of excitatory neurotransmission. Here, we tested whether synaptic plasticity induced by repetitive magnetic stimulation (rMS), a non-invasive brain stimulation technique used in clinical practice, is affected by L…

ChemistryBrain stimulationSynaptic plasticityExcitatory postsynaptic potentialStimulationTumor necrosis factor alphaLong-term potentiationNeurotransmissionHippocampal formationNeuroscience
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Theoretical study on hydration of symmetrically different diazanaphthalenes

2005

Abstract Quinazoline (symmetrical) and quinoxaline (unsymmetrical), diazanaphthalenes involved in certain biological reactions, have been studied computational with the purpose of comparing their protonation and covalent hydration mechanisms. Geometry optimizations of neutral, mono and diprotonated cations and hydrated products have been carried out at three levels of theory. Geometry optimizations were performed at HF, DFT/B3LYP levels of theory using 6-311G* basis set and single point energies were calculated at the MP2 level of theory using the same basis set. In agreement with experimental results, calculations predict a two steps mechanism resulting in a hydrated cation in which the OH…

ChemistryDiazanaphthaleneProtonationCondensed Matter PhysicsEnergy minimizationBiochemistrychemistry.chemical_compoundQuinoxalineCovalent bondComputational chemistryQuinazolineMoleculePhysical and Theoretical ChemistryBasis setJournal of Molecular Structure: THEOCHEM
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A Tale of Two Isomers: Enhanced Antiaromaticity/Diradical Character versus Deleterious Ring‐Opening of Benzofuran‐fused s ‐Indacenes and Dicyclopenta…

2021

We examine the effects of fusing two benzofurans to s-indacene (indacenodibenzofurans, IDBFs) and dicyclopenta[b,g]naphthalene (indenoindenodibenzofurans, IIDBFs) to control the strong antiaromaticity and diradical character of these core units. Synthesis via 3-functionalized benzofuran yields syn-IDBF and syn-IIDBF. syn-IDBF possesses a high degree of paratropicity, exceeding that of the parent hydrocarbon, which in turn results in strong diradical character for syn-IIDBF. In the case of the anti-isomers, synthesized via 2-substituted benzofurans, these effects are decreased; however, both derivatives undergo an unexpected ring-opening reaction during the final dearomatization step. All th…

ChemistryDiradicalStereochemistryGeneral ChemistryGeneral MedicineRing (chemistry)CatalysisElectronegativityTurn (biochemistry)chemistry.chemical_compoundCharacter (mathematics)BenzofuranAntiaromaticityNaphthaleneAngewandte Chemie
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A current source density analysis of field potentials evoked in slices of visual cortex

1987

The method of one-dimensional current source density (CSD) analysis was applied to field potentials recorded from 350 microns thick slices of the primary visual cortex of rats and cats. Field potentials were elicited by stimulation of the white matter and recorded along trajectories perpendicular to the cortical layers at spatial intervals of 25 to 50 microns. The resulting CSD distributions resembled closely those recorded from the cat visual cortex "in vivo". The responses with the shortest latency were distinct sinks in layers IV and VI probably reflecting monosynaptic EPSP's from specific thalamic afferents. From layer IV activity was relayed along three major routes: 1. to the supragra…

ChemistryGeneral NeuroscienceAge FactorsRats Inbred StrainsStimulationIn Vitro TechniquesStimulus (physiology)Current sourceElectric StimulationRatsWhite matterVisual cortexmedicine.anatomical_structureIn vivoDensity analysisCatsReaction TimeExcitatory postsynaptic potentialmedicineBiophysicsAnimalsEvoked Potentials VisualNeuroscienceVisual CortexExperimental Brain Research
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Brain choline has a typical precursor profile.

1998

Choline is product and precursor to both acetylcholine and membrane phospholipids, and, in the brain, is ultimately provided by the circulation. The brain is protected from excess choline and choline deprivation by a refined system of homeostatic mechanisms that maintain a level of extracellular choline that, for its role as precursor, meets saturation criteria under normal conditions. The kinetic and activity profiles of choline are typical for a biosynthetic precursor.

ChemistryGeneral NeuroscienceBrainCholine acetyltransferaseAcetylcholineCholinechemistry.chemical_compoundKineticsMembraneBiochemistryPhysiology (medical)SynapsesmedicineExtracellularCholinergicCholineAnimalsHomeostasisHumansCholinergic mechanismsAcetylcholineHomeostasisPhospholipidsmedicine.drugJournal of physiology, Paris
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Volatile constituents of aerial parts of Lasiopogon muscoides

2009

ChemistryLasiopogon muscoides Gnaphaliinae volatile constituentsOrganic chemistrySettore CHIM/06 - Chimica OrganicaSettore BIO/15 - Biologia FarmaceuticaPlant ScienceGeneral ChemistryLasiopogon muscoidesGeneral Biochemistry Genetics and Molecular BiologyChemistry of Natural Compounds
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Organocatalytic asymmetric addition of naphthols and electron-rich phenols to isatin-derived ketimines: highly enantioselective construction of tetra…

2015

A quinine-derived thiourea organocatalyst promoted the highly enantioselective addition of naphthols and activated phenols to ketimines derived from isatins. The reaction afforded chiral 3-amino-2-oxindoles with a quaternary stereocenter in high yields (up to 99%) with excellent enantioselectivity (up to 99% ee). To the best of our knowledge, this transformation is the first highly enantioselective addition of naphthols to ketimines

ChemistryOrganocatalysisIsatinIsatin-derived ketiminesEnantioselective synthesisAsymmetric synthesisGeneral ChemistryNaphtholsGeneral MedicineCatalysisStereocenterReaccions químiqueschemistry.chemical_compoundThioureaCatàlisiOrganocatalysisFISICA APLICADAOrganic chemistryPhenolsFriedel-Crafts reactionsQuímica orgànicaAngewandte Chemie (International ed. in English)
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Pre- and Postsynaptic Effects of Muscarinic Antagonists in the Isolated Guinea Pig Ileum

1986

Several compounds have been claimed to differentiate between subtypes of muscarinic receptors (2). In the experiments described in this chapter we have studied in the guinea-pig ileum whether the presynaptic muscarinic receptors of the cholinergic nerves differ from the postsynaptic muscarinic receptors of the longitudinal muscle in their affinities for several muscarinic antagonists (methylatropine; trihexyphenidyl; clozapine; DAMP). Inhibition by oxotremorine of the evoked release of acetylcholine (ACh) was used as a parameter of presynaptic activity, and the increase by oxotremorine of smooth muscle tension as a postsynaptic parameter. The affinity constants (pA2 values) of the antagonis…

ChemistryPostsynaptic potentialMuscarinic acetylcholine receptormedicineAntagonistOxotremorineMuscarinic antagonistPharmacologyReceptorMuscarinic agonistAcetylcholinemedicine.drug
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