Search results for "ammonium"

showing 10 items of 1070 documents

Cryo-negative staining

1998

Abstract A procedure is presented for the preparation of thin layers of vitrified biological suspensions in the presence of ammonium molybdate, which we termcryo-negative staining. The direct blotting of sample plus stain solution on holey carbon supports produces thin aqueous films across the holes, which are routinely thiner than the aqueous film produced by conventional negative staining on a continuous carbon layer. Because of this, a higher than usual concentration of negative stain (ca. 16% rather than 2%) is required for cryo-negative staining in order to produce an optimal image contrast. The maintenance of the hydrated state, the absence of adsorption to a carbon film and associate…

Proteasome Endopeptidase ComplexAnalytical chemistryGeneral Physics and AstronomyNegative Staininglaw.inventionMultienzyme ComplexesStructural BiologylawImage Processing Computer-AssistedTobacco mosaic virusAnimalsGeneral Materials ScienceColoring AgentsMolybdenumAmmonium molybdateTurnip yellow mosaic virusbiologyChemistryChaperonin 60Cell BiologyCatalasebiology.organism_classificationNegative stainStainingCysteine EndopeptidasesMicroscopy ElectronCrystallographyFreeze DryingElectron diffractionHemocyaninsVirusesCattleElectron microscopeTomato bushy stunt virusMicron
researchProduct

A novel oxalate-based three-dimensional coordination polymer showing magnetic ordering and high proton conductivity

2017

A novel three-dimensional (3D) coordination polymer with the formula (C3N2H5)4[MnCr2(ox)6]·5H2O (2), where ox = oxalate and C3N2H5 = imidazolium cation, is reported. Single crystal X-ray diffraction reveals that this porous coordination polymer adopts a chiral three-dimensional quartz-like architecture, with the guest imidazolium cations and water molecules being hosted in its pores. This novel multifunctional material exhibits both a ferromagnetic ordering at TC = 3.0 K, related to the host MnCr2 network, and high proton conductivity [1.86 × 10−3 S cm−1 at 295 K and 88% relative humidity (RH)] due to the presence of the acidic imidazolium cations and free water molecules. The similarity of…

ProtonChemistryCoordination polymerInorganic chemistry02 engineering and technologyConductivity010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesOxalate0104 chemical sciencesInorganic ChemistryCrystallographychemistry.chemical_compoundFerromagnetismMolecule[CHIM]Chemical SciencesAmmonium0210 nano-technologySingle crystalComputingMilieux_MISCELLANEOUS
researchProduct

A one-pot cascade to protoberberine alkaloids via Stevens rearrangement of nitrile-stabilized ammonium ylides.

2015

A facile one-pot synthesis of protoberberines from readily accessible 1,2,3,4-tetrahydroisoquinoline-1-carbonitriles and 1,2-bis(bromomethyl)arenes is described. The reaction cascade comprises four consecutive transformations, all of which can be effected under a single set of conditions. Ten protoberberines, including the alkaloids pseudopalmatine and pseudoepiberberine, were prepared in yields up to 86% according to this strategy. No chromatographic purification of the products is required, and the route is devoid of any protecting group manipulations.

PseudopalmatineNitrileMolecular StructureOrganic ChemistryBerberine Alkaloidschemistry.chemical_compoundAlkaloidschemistryStevens rearrangementCascadeTetrahydroisoquinolinesAmmonium CompoundsNitrilesOrganic chemistryMoleculeAmmoniumProtecting groupThe Journal of organic chemistry
researchProduct

ChemInform Abstract: A One-Pot Cascade to Protoberberine Alkaloids via Stevens Rearrangement of Nitrile-Stabilized Ammonium Ylides.

2015

This method gives access to quaternary protoberberines including naturally occurring pseudopalmatine (IIIf) and pseudoepiberberine (IIIg).

Pseudopalmatinechemistry.chemical_compoundNitrilechemistryStevens rearrangementCascadePolymer chemistryAmmoniumGeneral MedicineChemInform
researchProduct

Relaxant and antiadrenergic effects of ranolazine in human saphenous vein.

2019

Abstract OBJECTIVES Ranolazine improves vascular function in animal models. We evaluate the effects of ranolazine on vascular function and adrenergic response in human saphenous vein. METHODS Rings from 53 patients undergoing coronary artery bypass grafting were mounted in organ baths. Concentration–response curves to ranolazine were constructed in rings precontracted with phenylephrine, endothelin-1, vasopressin, KCl and the thromboxane A2 analogue U-46619. In rings precontracted with phenylephrine, relaxation to ranolazine was tested in the absence and presence of endothelial factors inhibitors, K+ channel blockers and verapamil. The effects of ranolazine on frequency–response and concent…

Pulmonary and Respiratory MedicineAdrenergic AntagonistsCharybdotoxinAdrenergicRanolazine030204 cardiovascular system & hematologyPharmacologyNitric Oxide03 medical and health scienceschemistry.chemical_compoundPotassium Channels Calcium-Activated0302 clinical medicineRanolazineMedicineAnimalsHumansChannel blockerSaphenous Vein030212 general & internal medicinePhenylephrineTetraethylammoniumbusiness.industryGeneral MedicineNG-Nitroarginine Methyl EsterchemistryVerapamilSurgeryEndothelium Vascularmedicine.symptomCardiology and Cardiovascular MedicinebusinessVasoconstrictionmedicine.drugEuropean journal of cardio-thoracic surgery : official journal of the European Association for Cardio-thoracic Surgery
researchProduct

Nanocomplexes for gene therapy of respiratory diseases: Targeting and overcoming the mucus barrier

2015

Gene therapy, i.e. the delivery and expression of therapeutic genes, holds great promise for congenital and acquired respiratory diseases. Non-viral vectors are less toxic and immunogenic than viral vectors, although they are characterized by lower efficiency. However, they have to overcome many barriers, including inflammatory and immune mediators and cells. The respiratory and airway epithelial cells, the main target of these vectors, are coated with a layer of mucus, which hampers the effective reaching of gene therapy vectors carrying either plasmid DNA or small interfering RNA. This barrier is thicker in many lung diseases, such as cystic fibrosis. This review summarizes the most impor…

Pulmonary and Respiratory MedicineCystic FibrosisGenetic enhancementContext (language use)Gene deliveryVectors in gene therapyPolyethylene GlycolsViral vectorPolyethyleinimine Poly-L-lysine Ethylene glycol Chitosan PAMAM G0 dendrimer N-(1-(23-Dioleyloxy)propyl)-NNNtrimethylammonium chloride 12-Dioleoylphosphatidylethanolamine N-acetylcystein 12-Dioctadecanoyl-sn-glycero-3-phosphoethanolaminemedicineHumansTechnology PharmaceuticalPharmacology (medical)RNA Small InterferingLungExpectorantsInflammationLungbusiness.industryBiochemistry (medical)Gene Transfer TechniquesGenetic TherapyMucusMucusmedicine.anatomical_structureSettore CHIM/09 - Farmaceutico Tecnologico ApplicativoImmunologyNanoparticlesInflammation MediatorsbusinessPlasmidsRespiratory tract
researchProduct

IV. An Improved Separation Method for Twenty two Compounds Related to Purine and 6-Thiopurine Metabolism Using High-Pressure Liquid Cation-Exchange C…

1977

Abstract An improved method is described for the separation of 22 compounds normally related to purine and 6-thiopurine metabolism in biological materials using high-pressure liquid cation-exchange chromatography on strongly acidic exchange resin. The column (0.18 × 100 cm) is eluted with 0.4 ᴍ ammonium formate, pH 4.6, at a linear flow velocity of 5.2 cm · min-1 at 50 °C. The elution volumes of sulphate anions, allopurinol, 6-thioxanthine, adenine, adenosine, and guanosine are demonstrated additionally to further 16 purine and 6-thiopurine compounds.

PurineChromatographyChemistryElutionIon chromatographyGuanosineAllopurinolMetabolismAdenosineGeneral Biochemistry Genetics and Molecular Biologychemistry.chemical_compoundmedicineAmmonium formatemedicine.drugZeitschrift für Naturforschung C
researchProduct

Opioid Inhibition of Oxytocin Release, but not Autoinhibition of Dopamine Release May Involve Activation of Potassium (K+) Channels

1991

ABSTRACT Release of oxytocin (Ox) or dopamine (DA) from the isolated neural lobes or neurointermediate lobes, respectively, was evoked by high K + (30 or 45 mM). Naloxone (1-10 μmol/l) which largely enhances the impulse-induced release of Ox had no effect on Ox release evoked by 30 or 45 mM K + . In the presence of 10 mM tetraethylammonium (TEA), Ox release evoked by 30 or 45 mM K + was increased 2-3fold; nevertheless, naloxone caused a further 2-3fold increase. Barium (500 μM) and quinidine (300 μM) antagonized the effect of naloxone observed in the presence of TEA. (-)-Sulpiride (10 μM) enhanced the release of DA evoked by 30 and 45 mM K + by 94 % and 19 %, respectively. TEA enhanced the …

Quinidinemedicine.medical_specialtyTetraethylammoniumChemistrymedicine.drug_class(+)-NaloxonePotassium channelchemistry.chemical_compoundEndocrinologyOpioidOpioid receptorDopamine receptorInternal medicinemedicineAutoreceptormedicine.drug
researchProduct

ESR response to 60Co-rays of ammonium tartrate pellets using as additive

2007

Abstract This work presents experimental results regarding a new ammonium tartrate blend for ESR dosimetry, with a higher sensitivity and a lower lowest detectable dose (LDD) to Co 60 γ -rays than the recently used pure ammonium tartrate. The blend composed by ammonium tartrate and gadolinium-oxide ( Gd 2 O 3 ) shows a greater sensitivity ( ∼ 2 times) and a smaller LDD than ammonium tartrate. The increased sensitivity was mainly attributed to the great atomic number ( Z = 64 ) of gadolinium, that increases the effective atomic number of the blend; the interaction probability with photons and consequently the radical yield is therefore enhanced. Moreover ammonium tartrate with Gd 2 O 3 has a…

RadiationGadoliniumInorganic chemistrychemistry.chemical_elementTartratechemistry.chemical_compoundchemistryYield (chemistry)AmmoniumAtomic numberCobalt-60Isotopes of cobaltInstrumentationEffective atomic numberNuclear chemistryRadiation Measurements
researchProduct

Unexpected Reaction of the Unsaturated Cluster Host and Catalyst [Pd3(3-CO)(dppm)3]2+ with the Hydroxide Ion: Spectroscopic and Kinetic Evidence of a…

2006

The title cluster, [Pd(3)(mu(3)-CO)(dppm)(3)](2+) (dppm=bis(diphenylphosphino)methane), reacts with one equivalent of hydroxide anions (OH(-)), from tetrabutylammonium hydroxide (Bu(4)NOH), to give the paramagnetic [Pd(3)(mu(3)-CO)(dppm)(3)](+) species. Reaction with another equivalent of OH(-) leads to the zero-valent compound [Pd(3)(mu(3)-CO)(dppm)(3)](0). From electron paramagnetic resonance analysis of the reaction medium using the spin-trap agent 5,5-dimethyl-1-pyrroline-N-oxide (DMPO), the 2-tetrahydrofuryl or methyl radicals, deriving from the tetrahydrofuran (THF) or dimethyl sulfoxide (DMSO) solvent, respectively, were detected. For both [Pd(3)(mu(3)-CO)(dppm)(3)](2+) and [Pd(3)(mu…

RadicalInner sphere electron transfersolvent effects[CHIM.INOR]Chemical Sciences/Inorganic chemistry010402 general chemistryPhotochemistry01 natural sciencesMedicinal chemistryCatalysislaw.inventionAdductchemistry.chemical_compoundlawElectron paramagnetic resonancehydroxide anionsTetrahydrofuranComputingMilieux_MISCELLANEOUS010405 organic chemistryTetrabutylammonium hydroxideOrganic Chemistry[ CHIM.INOR ] Chemical Sciences/Inorganic chemistryGeneral Chemistrypalladium0104 chemical scienceschemistrydensity functional calculationsHydroxidecluster compoundsSolvent effects
researchProduct