Search results for "pyridinium"

showing 10 items of 292 documents

Distinct effects of atypical 1,4-dihydropyridines on 1-methyl-4-phenylpyridinium-induced toxicity.

2006

Our previous data obtained from in vivo experiments demonstrated high neuroprotective effects of three novel atypical neuronal non-calcium antagonistic 1,4-dihydropyridine (DHP) derivatives cerebrocrast, glutapyrone and tauropyrone. The present studies were carried out in vitro to clarify, at least in part, their mechanism of action in primary culture of cerebellar granule cells by use of 1-methyl-4-phenylpyridinium (MPP+) as a neurotoxic agent which causes dramatic oxidative stress. Cerebrocrast (highly lipophilic, with a classical two-ring structure) dose-dependently (0.01-10.0 microM, EC50 = 13 nM) reduced MPP+-induced cell death. At the same time, the calcium antagonist nimodipine (refe…

Membrane potentialNeurons1-Methyl-4-phenylpyridiniumDihydropyridinesCell DeathMolecular Structure1-Methyl-4-phenylpyridiniumClinical BiochemistryCell BiologyGeneral MedicineMitochondrionPharmacologyBiologymedicine.disease_causeBiochemistryNeuroprotectionMechanism of actionmedicinemedicine.symptomMode of actionReactive Oxygen SpeciesOxidative stressIntracellularCells CulturedCell biochemistry and function
researchProduct

Bis(4-aminopyridinium) tetrachloridocobaltate(II)

2009

In the title compound, (C(5)H(7)N(2))(2)[CoCl(4)], the cobalt(II) ion is coordinated by four chloride ions in a slightly distorted tetra-hedral geometry. The crystal packing is stabilized by inter-molecular N-H⋯Cl hydrogen bonding, forming a three-dimensional network. The crystal was a non-merohedral twin emulating tetra-gonal symmetry, but being in fact ortho-rhom-bic.

Metal-Organic PapersCrystallographybiologyChemistryHydrogen bondchemistry.chemical_elementGeneral ChemistryCondensed Matter Physicsbiology.organism_classificationBioinformaticsChlorideIonCrystalCrystallographychemistry.chemical_compoundQD901-999medicineTetraGeneral Materials SciencePyridiniumCobaltmedicine.drugActa Crystallographica Section E Structure Reports Online
researchProduct

Pyridinium bis(pyridine-κN)tetrakis(thiocyanato-κN)ferrate(III) -pyrazine-2-carbonitrile-pyridine (1/4/1)

2013

In the title compound, (C5H6N)[Fe(NCS)4(C5H5N)2]·4C5H3N3·C5H5N, the Fe(III) ion is located on an inversion centre and is six-coordinated by four N atoms of the thio-cyanate ligands and two pyridine N atoms in a trans arrangement, forming a slightly distorted octa-hedral geometry. A half-occupied H atom attached to a pyridinium cation forms an N-H⋯N hydrogen bond with a centrosymmetrically-related pyridine unit. Four pyrazine-2-carbo-nitrile mol-ecules crystallize per complex anion. In the crystal, π-π stacking inter-actions are present [centroid-centroid distances = 3.6220 (9), 3.6930 (9), 3.5532 (9), 3.5803 (9) and 3.5458 (8) Å].

Metal-Organic PapersPyrazinebiologyNitrileHydrogen bondStackingThio-General ChemistryCondensed Matter PhysicsBioinformaticsbiology.organism_classificationMedicinal chemistrychemistry.chemical_compoundchemistryPyridineTetraGeneral Materials SciencePyridiniumta116Acta Crystallographica Section E : Structure Reports Online
researchProduct

Pyridinium bis(pyridine-κN)tetrakis(thiocyanato-κN)ferrate(III)

2013

In the title compound, (C5H6N)[Fe(NCS)4(C5H5N)2], the Fe(III) ion is coordinated by four thio-cyanate N atoms and two pyridine N atoms in a trans arrangement, forming an FeN6 polyhedron with a slightly distorted octa-hedral geometry. Charge balance is achieved by one pyridinium cation bound to the complex anion via N-H⋯S hydrogen bonding. The asymmetric unit consists of one Fe(III) cation, four thio-cyanate anions, two coordinated pyridine mol-ecules and one pyridinium cation. The structure exhibits π-π inter-actions between pyridine rings [centroid-centroid distances = 3.7267 (2), 3.7811 (2) and 3.8924 (2) Å]. The N atom and a neighboring C atom of the pyridinium cation are statistically d…

Metal-Organic PapersbiologyHydrogen bondThio-General ChemistryCondensed Matter Physicsbiology.organism_classificationIonchemistry.chemical_compoundCrystallographychemistryPyridineAtomTetraGeneral Materials SciencePyridiniumActa Crystallographica Section E Structure Reports Online
researchProduct

Oral antiseptics against coronavirus: in-vitro and clinical evidence

2021

Background Angiotensin converting enzyme II (ACE2) is the cellular receptor for SARS-CoV-2, so ACE2-expressing cells can act as target cells and are susceptible to infection. ACE2 receptors are highly expressed in the oral cavity so this may be a potential high-risk route for SARS-CoV-2 infection. Furthermore, the virus can be detected in saliva, even before COVID-19 symptoms appear, with the consequent high risk of virus transmission in asymptomatic/pre-symptomatic patients. Reducing oral viral load could lead to a lower risk of transmission via salivary droplets or aerosols and therefore contribute to the control of the pandemic. Aim To evaluate the available evidence testing the in vitro…

Microbiology (medical)2019-20 coronavirus outbreakmedicine.medical_specialtySalivaCoronavirus disease 2019 (COVID-19)coronavirusesSevere acute respiratory syndrome coronavirus 2 (SARS-CoV-2)virusesMouthwashesCetylpyridiniumReviewmedicine.disease_causeLower riskViruslaw.inventionoral antisepticsRandomized controlled triallawInternal medicinemedicineHumansSalivaLetter to the EditorPandemicsPovidone-IodineCoronavirusMouthSARS-CoV-2Transmission (medicine)business.industryCOVID-19Hydrogen PeroxideGeneral MedicineViral LoadVirologyIn vitroCOVID-19 Drug TreatmentCoronavirusoral rinseInfectious DiseasesSystematic reviewClinical evidenceAnti-Infective Agents LocalCoronavirus InfectionsbusinessViral loadJournal of Hospital Infection
researchProduct

Cetylpyridinium chloride promotes disaggregation of SARS-CoV-2 virus-like particles

2022

ABSTRACT Background SARS-CoV-2 is continuously disseminating worldwide. The development of strategies to break transmission is mandatory. Aim of the study To investigate the potential of cetylpyridinium chloride (CPC) as a viral inhibitor. Methods SARS-CoV-2 Virus Like-Particles (VLPs) were incubated with CPC, a potent surfactant routinely included in mouthwash preparations. Results Concentrations of 0.05% CPC (w/v) commonly used in mouthwash preparations are sufficient to promote the rupture of SARS-CoV-2 VLP membranes. Conclusion Including CPC in mouthwashes could be a prophylactic strategy to keep SARS-CoV-2 from spreading.

Microbiology (medical)Virologiavirusestechnology industry and agriculturevirus diseasesMicrobiologiaInfectious and parasitic diseasesRC109-216macromolecular substancesvirus-like particlesMicrobiologyQR1-502virologybody regionssars-cov-2Infectious Diseasesmembrane disaggregationcetylpyridinium chlorideOriginal ArticleDentistry (miscellaneous)Research ArticleJournal of Oral Microbiology
researchProduct

Morphology of hybrid polystyrene-block-poly(ethylene oxide) micelles: Analytical ultracentrifugation and SANS studies

2006

Abstract Morphology and structure of aqueous block copolymer solutions based on polystyrene- block -poly(ethylene oxide) (PS- b -PEO) of two different compositions, a cationic surfactant, cetyl pyridinium chloride (CPC), and either platinic acid (H 2 PtCl 6 ⋅6H 2 O) or Pt nanoparticles were studied using a combination of analytical ultracentrifugation (AUC), transmission electron microscopy (TEM), and small angle neutron scattering (SANS). These studies combining methods contributing supplemental and analogous structural information allowed us to comprehensively characterize the complex hybrid systems and to discover an isotope effect when H 2 O was replaced with D 2 O. In particular, TEM s…

Models MolecularBlock copolymerHybrid micellesMicellePolyethylene GlycolsBiomaterialsSurface-Active Agentschemistry.chemical_compoundColloid and Surface ChemistrySurfactantPolymer chemistryCopolymerMicellesAqueous solutionCalorimetry Differential ScanningEthylene oxideIsotope effectCationic polymerizationSmall-angle neutron scatteringSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsMicroscopy ElectronchemistryPolystyrenesPhysical chemistryPolystyrenePyridiniumUltracentrifugationJournal of Colloid and Interface Science
researchProduct

4-Aminopyridinium 4-aminobenzoate dihydrate and 4-aminopyridinium nicotinate.

2009

In the title compounds, 4-aminopyridinium 4-aminobenzoate dihydrate, C(7)H(6)NO(2)(-).C(5)H(7)N(2)(+).2H(2)O, (I), and 4-aminopyridinium nicotinate, C(5)H(7)N(2)(+).C(6)H(4)NO(2)(-), (II), the aromatic N atoms of the 4-aminopyridinium cations are protonated. In (I), the asymmetric unit is composed of two 4-aminopyridinium cations, two 4-aminobenzoate anions and four water molecules, and the compound crystallizes in a noncentrosymmetric space group. The two sets of independent molecules of (I) are related by a centre of symmetry which is not part of the space group. In (I), the protonated pyridinium ring H atoms are involved in bifurcated hydrogen bonding with carboxylate O atoms to form an …

Models MolecularMolecular StructureHydrogen bondWaterHydrogen BondingPyridinium CompoundsGeneral MedicineCrystal structureRing (chemistry)Crystallography X-RayNiacinGeneral Biochemistry Genetics and Molecular BiologyAdductchemistry.chemical_compoundCrystallographychemistryIntramolecular forceMoleculeCarboxylatePyridiniumActa crystallographica. Section C, Crystal structure communications
researchProduct

Characterization of isomeric 1,2,4-oxadiazolyl-N-methylpyridinium salts by electrospray ionization tandem mass spectrometry.

2007

The mass spectrometric behavior of 1,2,4-oxadiazolyl- N-methylpyridinium salts has been investigated. These substances are of current interest as perspective ionic liquids, compounds used as green solvents for synthesis, and for their catalytic properties. The studies have been developed through electrospray ionization tandem mass spectrometry (ESI-MS/MS) experiments. The obtained results demonstrate a ready distinction between the two isomeric classes, 3- N-methylpyridinium- and 5- N-methylpyridinium-1,2,4-oxadiazoles, is possible through ESI-MS/MS experiments. A deeper investigation on the principal fragmentation pathways of characteristic ions has been also developed.

Models MolecularSpectrometry Mass Electrospray IonizationProtein mass spectrometry020209 energyElectrospray ionizationIonic Liquids02 engineering and technologyTandem mass spectrometrySample preparation in mass spectrometrychemistry.chemical_compoundIsomerismESI-MS ionic kiquids oxadiazolylpyridiniumComputational chemistry0202 electrical engineering electronic engineering information engineeringDirect electron ionization liquid chromatography–mass spectrometry interfaceSpectroscopyChromatographySelected reaction monitoringExtractive electrospray ionizationGeneral MedicineAtomic and Molecular Physics and OpticschemistryModels ChemicalSpectrometry Mass Matrix-Assisted Laser Desorption-IonizationIonic liquidSaltsEuropean journal of mass spectrometry (Chichester, England)
researchProduct

CCDC 1966174: Experimental Crystal Structure Determination

2020

Related Article: Kwaku Twum, J. Mikko Rautiainen, Shilin Yu, Khai-Nghi Truong, Jordan Feder, Kari Rissanen, Rakesh Puttreddy, Ngong Kodiah Beyeh|2020|Cryst.Growth Des.|20|2367|doi:10.1021/acs.cgd.9b01540

N-methylpyridinium tri-sodium 281420-tetraethyl-46101216182224-octahydroxycalix[4]arene-5111723-tetrayltetrakis(methylenesulfonate) methanol unknown solvateSpace GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
researchProduct