Search results for "N-oxide"

showing 10 items of 155 documents

Suppression of intestinal microbiota-dependent production of pro-atherogenic trimethylamine N-oxide by shifting L-carnitine microbial degradation.

2014

Abstract Aims Trimethylamine-N-oxide (TMAO) is produced in host liver from trimethylamine (TMA). TMAO and TMA share common dietary quaternary amine precursors, carnitine and choline, which are metabolized by the intestinal microbiota. TMAO recently has been linked to the pathogenesis of atherosclerosis and severity of cardiovascular diseases. We examined the effects of anti-atherosclerotic compound meldonium, an aza-analogue of carnitine bioprecursor gamma-butyrobetaine (GBB), on the availability of TMA and TMAO. Main methods Wistar rats received L-carnitine, GBB or choline alone or in combination with meldonium. Plasma, urine and rat small intestine perfusate samples were assayed for L-car…

TrimethylamineTrimethylamine N-oxideBacterial growthBiologyGeneral Biochemistry Genetics and Molecular BiologyStatistics NonparametricCholinechemistry.chemical_compoundMethylaminesBetaineTandem Mass SpectrometryCarnitineBlood plasmamedicineCholineAnimalsCarnitineGeneral Pharmacology Toxicology and PharmaceuticsRats WistarChromatography High Pressure LiquidMeldoniumCarbon IsotopesMicrobiotaGeneral MedicineBiosynthetic PathwaysRatsBetaineGastrointestinal TractBiochemistrychemistrymedicine.drugMethylhydrazinesLife sciences
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2,2′-[2,3,5,6-Tetramethyl-p-phenylenebis(methylenethio)]bis(pyridineN-oxide)

2008

Mol-ecules of the title compound, C(22)H(24)N(2)O(2)S(2), lie across centres of inversion. The two thio-pyridine N-oxide groups adopt a stepped trans configuration with respect to the benzene ring, by virtue of the symmetry. The oxopyridinium ring forms a dihedral angle of 79.9 (2)° with the benzene ring. The crystal structure is stabilized by a strong π-π inter-action between the pyridinium rings of adjacent mol-ecules [ring centroid-centroid distance = 3.464 (3) Å].

biologyPyridine-N-oxideGeneral ChemistryCrystal structureDihedral angleCondensed Matter Physicsbiology.organism_classificationRing (chemistry)BioinformaticsOrganic PapersMedicinal chemistrychemistry.chemical_compoundchemistryTetraGeneral Materials SciencePyridiniumBenzeneEne reactionActa Crystallographica Section E Structure Reports Online
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Tin compounds interaction with membranes of egg lecithin liposomes.

2007

This work is a continuation of earlier research concerning the influence of tin compounds on the dynamic properties of liposome membranes produced with lecithin hen egg yolks (EYL). The experiments were carried out at room temperature (about 25 ∞C). Four tin compounds were chosen, including three organic ones, (CH3)4Sn, (C2H5)4Sn and (C3H7)3SnCl, and one inorganic, SnCl2. The investigated compounds were admixed to water dispersions of liposomes. The content of the admixture changed within the range 0 mol-% to 11mol-% in proportion to EYL. Two spin probes were used in the experiment: 2,2,6,6-tetramethylpiperidine- 1-oxyl (TEMPO) and 2-ethyl-2-(15-methoxy-15-oxopentadecyl)-4,4-dimethyl-3-oxaz…

chemistry.chemical_classificationEgg lecithinLiposomefood.ingredientChromatographyIonic bondingchemistry.chemical_elementLecithinEgg YolkGeneral Biochemistry Genetics and Molecular BiologyCyclic N-Oxideschemistry.chemical_compoundfoodMembraneHydrocarbonchemistryLiposomesChlorinePhosphatidylcholinesAnimalsFemaleSpin LabelsTinChickensNuclear chemistryZeitschrift fur Naturforschung. C, Journal of biosciences
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2-(Mesitylmethylsulfanyl)pyridineN-oxide–18-crown-6 (2/1)

2008

In the title compound, 2C(15)H(17)NOS·C(12)H(24)O(6), the asymmetric unit consists of one N-oxide derivative and one-half of the 18-crown-6 ether, which lies on an inversion centre. In the crown ether, the O-C-C-O torsion angles indicate a gauche conformation of the ethyl-eneoxy units, while the C-O-C-C torsion angles indicate planarity of these segments. In the N-oxide unit, the dihedral angle between the pyridine and benzene rings is 85.88 (12)°. The crystal packing is stabilized by weak C-H⋯O hydrogen bonds and C-H⋯π inter-actions.

chemistry.chemical_classificationHydrogen bond18-Crown-6Pyridine-N-oxideEtherGeneral ChemistryDihedral angleCondensed Matter PhysicsBioinformaticsOrganic PapersPlanarity testingchemistry.chemical_compoundCrystallographychemistryPyridineGeneral Materials ScienceCrown etherActa Crystallographica Section E Structure Reports Online
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Bimodal Effect of Amphiphilic Biocide Concentrations on Fluidity of Lipid Membranes

1996

Abstract Using the spin label method (ESR) it has been shown that biologically active, amphiphilic compounds (quaternary ammonium salts -AS) containing polar heads with single and double positive charge caused, at low concentrations, decrease fluidity of liposome membranes formed with egg yolk lecithin (EYL). At higher concentrations an increase in fluidity was observed. With compounds having a single positive charge minimum fluidity of membrane structure occurs in the range of 1 to 3%, with compounds containing double positive charge -in the range of 4 -6 % . That effect does not depend on polar head size and length of alkyl chains of the AS used. Analysis of the electrostatic interaction …

chemistry.chemical_classificationLiposomefood.ingredientMembrane FluidityBinding energyInorganic chemistryElectron Spin Resonance SpectroscopyEgg YolkModels BiologicalLecithinGeneral Biochemistry Genetics and Molecular BiologyDivalentCyclic N-OxidesQuaternary Ammonium CompoundsMembranefoodchemistryBiochemistryLiposomesPhosphatidylcholinesMembrane fluiditySpin LabelsUltrasonicsSpin labelAlkylZeitschrift für Naturforschung C
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Stimuli-Responsive Y-Shaped Polymer Brushes Based on Junction-Point-Reactive Block Copolymers

2012

Reversibly responsive, thin or ultrathin polymer fi lms, often referred to as “smart surfaces”, can alter their properties upon application of external stimuli. [ 1 , 2 ] One particular application fi eld represents the engineering of nanostructured fi lms mimicking cell membranes. [ 3 , 4 ] Such materials offer application potential for sensors, textiles, construction materials, and smart coatings due to a rapid change in surface energy and morphology. [ 5–7 ] The surface response can be triggered by various external stimuli such as light, temperature, electrical potential, mechanical force, magnetic fi eld, pH change, or selective solvent treatment. [ 1 , 8–12 ] A variety of different thi…

chemistry.chemical_classificationMaterials scienceStimuli responsivePolymersSurface PropertiesMechanical EngineeringTemperatureWaterNanotechnologyPolymerSmart surfacesSurface energyAnionic addition polymerizationMembranechemistryMechanics of MaterialsJunction pointPolymer chemistryWettabilityCopolymerPolystyrenesGeneral Materials SciencePolyvinylpyridine N-OxidePolytetrafluoroethyleneAdvanced Materials
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Host-guest complexes of C-propyl-2-bromoresorcinarene with aromatic N-oxides*

2018

The host-guest complexes of C-propyl-2-bromoresorcinarene with pyridine N-oxide, 3-methylpyridine N-oxide, quinoline N-oxide and isoquinoline N-oxide are studied using single crystal X-ray crystallography and 1H NMR spectroscopy. The C-propyl-2-bromoresorcinarene forms endo-complexes with the aromatic N-oxides in the solid-state when crystallised from either methanol or acetone. In solution, the endo-complexes were observed only in methanol-d4. In DMSO the solvent itself is a good guest, and crystallisation provides only solvate endo-complexes. The C-propyl-2-bromoresorcinarene shows remarkable flexibility when crystallised from either methanol or acetone, and packs into one-dimensional sel…

crystal structurekemiaSupramolecular chemistryCrystal structurechemistry010402 general chemistry01 natural scienceschemistry.chemical_compoundPolymer chemistryPyridinecrystalssupramolekulaarinen kemiaAcetoneresorcinarenesmoleculesIsoquinolineta116Biochemistry Biophysics and Structural Biologyvetysidoksetta114010405 organic chemistryHydrogen bondQuinolinemolekyylitGeneral Chemistrykiteet0104 chemical sciencesaromatic N-oxidesSolventChemistrychemistryvetyhydrogenhydrogen bondsSupramolecular chemistrySUPRAMOLECULAR CHEMISTRY
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One-pot synthesis of fluorinated 2-amino-pyrimidine-N-oxides. Competing pathways in the four-atom side-chain rearrangements of 1,2,4-oxadiazoles

2006

Abstract Trifluoromethylated 2-amino-pyrimidine N-oxides have been synthesized by reaction of the 3-amino-5-methyl-1,2,4-oxadiazole with trifluoromethyl-β-diketones in the presence of perchloric acid, followed by hydrolysis. In this ring-to-ring transformation an initial formation of (unisolated) 1,2,4-oxadiazole-pyrimidinium salts, and subsequent ring-opening at the oxadiazole moiety occurs. Isolation of 2-(hydroxyamino)-pyrimidine from the reaction mixture evidenced the presence of a competing pathway where the N(4) nitrogen of the oxadiazole is involved in the formation of a regioisomeric pyrimidinium salt. The effect of the trifluoromethyl group on the product distribution is discussed.…

fluoropyrimidine derivativecrystal structurepyrimidine N-oxidePyrimidinesynthesisStereochemistryOne-pot synthesisOxadiazoleX ray analysis3 diketoneBiochemistryMedicinal chemistryperchloric acidnitrogenchemistry.chemical_compoundside-chain rearrangementDrug DiscoveryStructural isomerSide chainMoietyPerchloric acidring openingfluorinated heterocycle3 diketone fluoropyrimidine derivative ketone derivative nitrogen oxide perchloric acid; article crystal structure hydrolysis priority journal reaction analysis ring opening synthesis X ray analysisTrifluoromethylChemistryOrganic Chemistryarticle124-oxadiazoleketone derivativereaction analysishydrolysispriority journaloxide
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Liposomes modified by mono- and bis-phthalocyanines: A comprehensive EPR study.

2016

The impact of selected metallophthalocyanines, featuring diverse molecular structure, upon the fluidity of liposome membranes was studied using the spin label EPR technique. The “mono”-type MPc’s (M = Zn, Sn; Pc = C32H16N8 is the phthalocyanine ligand) and sandwich LnPc2 complexes (Ln = Nd, Sm, Gd) were explored. Liposomes were obtained in a sonication process, from egg yolk lecithin (EYL) in water. TEMPO and 16-DOXYL spin labels were used to monitor the peripheral and central part of the lipid double layer, respectively, which allowed to localize the phthalocyanine additive within the bilayer, as well as to perform independent measurements of changes in fluidity upon addition thereof. All …

food.ingredientBiophysics02 engineering and technologyLecithinlaw.inventionCyclic N-Oxides03 medical and health scienceschemistry.chemical_compoundSonication0302 clinical medicineNuclear magnetic resonancefoodlawLecithinsOrganometallic CompoundsGeneral Materials ScienceLipid bilayerElectron paramagnetic resonanceSpin labelLiposomeChemistryLiquid crystalsBilayerElectron Spin Resonance SpectroscopySurfaces and InterfacesGeneral Chemistry021001 nanoscience & nanotechnologyCrystallographyMembraneSoft Matter030220 oncology & carcinogenesisLiposomesPhthalocyanine0210 nano-technologyBiotechnologyThe European physical journal. E, Soft matter
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Non-covalent interactions of N-phenyl-1,5-dimethyl-1H-imidazole-4-carboxamide 3-oxide derivatives—a case of intramolecular N-oxide hydrogen bonds

2017

The crystal structures of new N-phenyl-1,5-dimethyl-1H-imidazole-4-carboxamide 3-oxide derivatives are reported. The results of X-ray diffraction showed the existence of intramolecular hydrogen bonding between carboxamide nitrogen donors and N-oxide oxygen acceptors. The use of Quantum Theory of Atoms in Molecules allowed its classification as a strong interaction, with energy about 10 kcal/mol, and of intermediate character between closed shell and shared bonds. Comparison of experimental data and quantum theoretical calculations indicated that a substituent attached to the phenyl ring in the para position influences the strength and geometry of the title hydrogen bonding. Stronger π-elect…

medicine.drug_classLow-barrier hydrogen bondintramolecular hydrogen bondSubstituentCarboxamideN-oxide group010402 general chemistry01 natural scienceschemistry.chemical_compoundComputational chemistrymedicineNon-covalent interactionsHirshfeld surface analysisPhysical and Theoretical Chemistrychemistry.chemical_classification010405 organic chemistryHydrogen bondIntermolecular forceAtoms in moleculesCondensed Matter Physicshydrogen bonding0104 chemical sciencesCrystallographychemistryQTAIMIntramolecular forcesubstituent effectStructural Chemistry
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