Search results for "SITES"

showing 10 items of 2851 documents

Modular functionalized polyphosphines for supported materials: previously unobserved (31)P-NMR «through-space» ABCD spin systems and heterogeneous pa…

2014

The modular design of polyphosphines, diversely functionalized for facile immobilization on virtually any kind of support, is reported. Previously unobserved ABCD (31)P NMR spin-spin systems evidence the control exercised on the polyphosphines conformation. We illustrate the catalytic performance at low Pd loading of the recyclable immobilized polyphosphines in C-C bond formation reactions.

StereochemistryMetals and Alloyschemistry.chemical_elementGeneral ChemistryBond formationCombinatorial chemistryCatalysisSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsCatalysischemistryMaterials ChemistryCeramics and CompositesSpin (physics)PalladiumChemical communications (Cambridge, England)
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Polyamines containing naphthyl groups as pH-regulated molecular machines driven by light

2001

A series of compounds made up by linking methylnaphthalene fragments at both ends of different polyamine chains have shown to behave as pH-regulated molecular machines driven by light and fluorescence emission studies have proved the formation of an excimer between the two naphthalene units whose appearance, fluorescence intensity and decay times depend on the pH value of the media. Albelda Gimeno, Maria Teresa, Teresa.Albelda@uv.es ; Garcia-España Monsonis, Enrique, Enrique.Garcia-Es@uv.es ; Soriano Soto, Concepción, Concepcion.Soriano@uv.es

StereochemistryPHUNESCO::QUÍMICAPhotochemistryExcimerNaphthyl:QUÍMICA [UNESCO]CatalysisFluorescencechemistry.chemical_compoundMaterials ChemistryPolyaminesUNESCO::QUÍMICA::Química orgánicaMethylnaphthaleneNaphthalene:QUÍMICA::Química orgánica [UNESCO]Metals and AlloysGeneral ChemistryFluorescenceMolecular machineSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsFluorescence intensitychemistryPolyamines ; Naphthyl ; Methylnaphthalene ; PH ; FluorescenceCeramics and CompositesPolyamine
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α-Adrenoceptor Interaction of Tetrandrine and Isotetrandrine in the Rat: Functional and Binding Assays

1998

Abstract The action of 1S,1′S-tetrandrine, a bisbenzyltetrahydroisoquinoline alkaloid, on α1-adrenoceptors has been compared with that of its isomer 1R,1′S-isotetrandrine. The work includes binding assays to analyse the affinity of these products for the [3H]prazosin binding site of rat cerebral cortical membranes and functional studies on rat isolated aorta to examine the effects of both alkaloids on intracellular calcium processes related or not to α-adrenoceptor activation. A radioligand receptor-binding study showed that both compounds interacted with the α1-adrenoceptors displacing [3H]prazosin from the specific binding site. The Ki values (inhibition constants) were 0.69±0.12 and 1.6±…

StereochemistryPharmaceutical Sciencechemistry.chemical_elementAorta ThoracicIn Vitro TechniquesBiologyPharmacologyCalciumTritiumBenzylisoquinolinesBinding CompetitiveMuscle Smooth VascularCalcium in biologyNorepinephrinechemistry.chemical_compoundAlkaloidsPrazosinmedicineExtracellularAnimalsDrug InteractionsRats WistarCerebral CortexPharmacologyBinding SitesMolecular StructureAlkaloidBiological activityPrazosinReceptors Adrenergic alphaCalcium Channel BlockersRatsTetrandrinechemistryCalciumFemaleIntracellularMuscle ContractionProtein Bindingmedicine.drugJournal of Pharmacy and Pharmacology
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A second pathway of activation of the Torpedo acetylcholine receptor channel

1991

We have studied the interaction of the reversible acetylcholine esterase inhibitor (-)physostigmine (D-eserine) with the nicotinic acetylcholine receptor (nAChR) from Torpedo marmorata electric tissue by means of ligand-induced ion flux into nAChR-rich membrane vesicles and of equilibrium binding. We find that (-) physostigmine induces cation flux (and also binds to the receptor) even in the presence of saturating concentrations of antagonists of acetylcholine, such as D-tubocurarine, alpha-bungarotoxin or antibody WF6. The direct action on the acetylcholine receptor is not affected by removal of the methylcarbamate function from the drug and thus is not due to carbamylation of the receptor…

StereochemistryPhysostigmineCesiumTubocurarineReceptors NicotinicTorpedoBiochemistryIon ChannelsAcetylcholine bindingCationsMuscarinic acetylcholine receptor M5medicineAnimalsBinding siteAcetylcholine receptorElectric OrganBinding SitesChemistryCell MembraneAntibodies MonoclonalMuscarinic acetylcholine receptor M3BungarotoxinsQuaternary Ammonium CompoundsNicotinic acetylcholine receptorNicotinic agonistBiophysicsCarbamatesAcetylcholinemedicine.drugEuropean Journal of Biochemistry
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Highlights from the 42nd EUCHEM Conference on Stereochemistry, Bürgenstock, Switzerland, April 2007.

2007

StereochemistryPolitical scienceMaterials ChemistryMetals and AlloysCeramics and CompositesGeneral ChemistryCatalysisSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsChemical communications (Cambridge, England)
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Attracted or repelled?--a matter of two neurons, one pheromone binding protein, and a chiral center.

1998

Abstract Two species of scarab beetles, the Osaka beetle (Anomala osakana) and the Japanese beetle (Popillia japonica), utilize the opposite enantiomers of japonilure, (Z)-5-(1-decenyl)oxacyclopentan-2-one, as their sex pheromones. Each species produces only one of the enantiomers that functions as its own sex pheromone and as a very strong behavioral antagonist for the other species. Using an integrated approach we tested whether the discrimination of these two opposite signals is due to selective filtering by pheromone binding proteins or whether it originates in the specificity of ligand–receptor interactions. We found that the antennae of each of these two scarab species contain only a …

StereochemistryProtein ConformationMolecular Sequence DataBiophysicsBiochemistryPheromonesPopilliaBotanymedicineAnimalsPheromone bindingAmino Acid SequenceCloning MolecularMolecular BiologySensillumNeuronsOlfactory receptorBinding SitesbiologyStereoisomerismCell Biologybiology.organism_classificationChemoreceptor CellsColeopteramedicine.anatomical_structureSex pheromonePheromoneEnantiomerPheromone binding proteinSequence AlignmentSignal TransductionBiochemical and biophysical research communications
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Efficient synthesis of hexahydroindenopyridines and their potential as melatoninergic ligands.

2014

Hexahydroindenopyridine (HHIP) is an interesting tricyclic piperidine nucleus that is structurally related to melatonin, a serotonin-derived neurohormone. Melatonin receptor ligands have applications in several cellular, neuroendocrine and neurophysiological disorders, including depression and/or insomnia. We report herein an efficient two-step method to prepare new HHIP via enamine C-alkylation-cyclization. The influence of substituents on the benzene ring and the nitrogen atom on melatoninergic receptors has been studied. Among the 25 synthesized HHIPs, some of them containing methylenedioxy (series 2) and 8-chloro-7-methoxy substituents (series 4) on the benzene ring revealed affinity fo…

StereochemistryPyridinesRing (chemistry)LigandsMelatonin receptorMethylenedioxyEnaminechemistry.chemical_compoundStructure-Activity RelationshipDrug DiscoveryHumansReceptorCells CulturedPharmacologychemistry.chemical_classificationBinding SitesDose-Response Relationship DrugMolecular StructureReceptor Melatonin MT2Receptor Melatonin MT1Organic ChemistryGeneral MedicineHEK293 CellschemistryPiperidineAcetamideTricyclicEuropean journal of medicinal chemistry
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Effects of side chains of oxatub[4]arene on its conformational interconversion, molecular recognition and macroscopic self-assembly.

2017

A series of oxatub[4]arenes with different alkyl side chains have been synthesized. The conformational interconversion, molecular recognition and macroscopic self-assembly behaviour of oxatub[4]arene derivatives were investigated. The difference in side chains slightly changes the binding affinities, but results in different self-assembly morphologies at the solid state.

StereochemistrySolid-state010402 general chemistry01 natural sciencesCatalysisside chainsoxatubarenesMolecular recognitionMaterials ChemistrySide chainta116makromolekyylitAlkylBinding affinitieschemistry.chemical_classification010405 organic chemistryChemistryMetals and Alloysself-assemblyGeneral Chemistry0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsCeramics and CompositesSelf-assemblyaromaattiset hiilivedytChemical communications (Cambridge, England)
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The mechanism of hydrolysis of beta-glycerophosphate by kidney alkaline phosphatase.

1975

1. To identify the functional groups that are involved in the conversion of β-glycerophosphate by alkaline phosphatase (EC 3.1.3.1) from pig kidney, the kinetics of alkaline phosphatase were investigated in the pH range 6.6-10.3 at substrate concentrations of 3 μM-30 mM. From the plots of log ṼH+ against pH and log ṼH+/KH+m against pH one functional group with pK = 7.0 and two functional groups with pK = 9.1 were identified. These groups are involved in substrate binding. Another group with pK = 8.8 was found, which in its unprotonated form catalyses substrate conversion. 2. GSH inhibits the alkaline phosphatase reversibly and non-competitively by attacking the bound Zn(II). 3. The influenc…

StereochemistrySwineKidneyBiochemistrychemistry.chemical_compoundHydrolysisAnimalsMagnesiumBinding siteMolecular Biologychemistry.chemical_classificationBinding SitesHydrolysisSubstrate (chemistry)Cell BiologyGlutathioneHydrogen-Ion ConcentrationPhosphateAlkaline PhosphataseGlutathioneKineticsZincEnzymechemistryModels ChemicalGlycerophosphatesFunctional groupAlkaline phosphataseResearch ArticleThe Biochemical journal
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Cu2+-Induced formation of cage-like compounds containing pyrazole macrocycles

2002

The crystal structure of the complex [Cu4(H22L)2(H2O)2- (ClO4)2](ClO4)2·2H2O where L is a new pyrazole ligand containing 1,5-diaminopentane spacers represents a new form of obtaining metal ion-induced inorganic–organic cages. Escarti Alemany, Francisco, franesa@alumni.uv.es ; Latorre Saborit, Julio, Julio.Latorre@uv.es ; Garcia-España Monsonis, Enrique, Enrique.Garcia-Es@uv.es

StereochemistryUNESCO::QUÍMICACrystal structurePyrazole:QUÍMICA [UNESCO]CatalysisMetalchemistry.chemical_compoundCu2Crystal estructurePolymer chemistryMaterials ChemistryInorganic organicInorganic-organicUNESCO::QUÍMICA::Química inorgánicaMetals and AlloysGeneral ChemistryPyrazole ligands:QUÍMICA::Química inorgánica [UNESCO]Surfaces Coatings and FilmsElectronic Optical and Magnetic Materialschemistryvisual_artPyrazoleCeramics and Compositesvisual_art.visual_art_mediumPyrazole ; Crystal estructure ; Cu2 ; Inorganic-organicCageChemical Communications
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