Search results for "molecular conformation"

showing 10 items of 376 documents

Synthesis, configuration, and calcium modulatory properties of enantiomerically pure 5-oxo-1,4,5,6,7,8-hexahydroquinoline-3-carboxylates.

1992

Enantiomerically pure hexahydroquinolinones of the structural type 9 were prepared by a variation of the Hantzsch synthesis in which an optically active acetoacetate served as a chiral auxiliary reagent. Determinations of the de and ee values are described. The absolute configurations of the optically pure products were characterized by single-crystal X-ray analysis. The antipodes 9a and 9b exhibited calcium antagonistic activities on smooth musculature; the (S)-(-)-enantiomer 9b was the more potent compound with regard to the EC50 values which differed by a factor of 100; the intrinsic activity of 9b was 1.2, compared with a value of 0.54 for 9a. On the other hand, R-(+)-9a exerted positiv…

MaleIntrinsic activityGuinea PigsMolecular Conformationchemistry.chemical_elementCalciumQuinolonesMedicinal chemistrychemistry.chemical_compoundX-Ray DiffractionIleumDrug DiscoveryAnimalsHeart AtriaAortaChiral auxiliaryBicyclic moleculeMolecular StructureEnantioselective synthesisAbsolute configurationBiological activityStereoisomerismPapillary MusclesAtrial FunctionCalcium Channel BlockersElectric StimulationchemistryReagentMolecular MedicineFemaleMuscle ContractionJournal of medicinal chemistry
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Selective action of two aporphines at alpha 1-adrenoceptors and potential-operated Ca2+ channels.

1993

Abstract Contractions evoked by noradrenaline (1 μM) or a depolarizing solution of 60 mM KCI were concentration dependently depressed by the aporphine alkaloids (S)-boldine and (R)-apomorphine in rataorta. Both drugs had a greater inhibitory potency on the contraction elicited by noradrenaline. Dose-response curves for noradrenaline were shifted to the right in presence of (S)-boldine. (R)-Apomorphine acted by a complex mechanism at α 1 -adrenoceptors and its inhibitory effects was irreversible. The conformational features of these alkaloids may explain their different behaviour at α 1 -adrenoceptors. In Ca 2+ -free solution, the alkaloids inhibited the contraction evoked by noradrenaline b…

MaleReceptor complexAporphinesApomorphineStereochemistryPhosphodiesterase InhibitorsMolecular ConformationIn Vitro TechniquesMuscle Smooth VascularPotassium Chloridechemistry.chemical_compoundNorepinephrineRadioligand AssaymedicinePrazosinBoldineAnimalsAporphineRats WistarEvoked PotentialsPharmacologyMembranesAlkaloidDihydropyridinePhosphodiesteraseReceptors Adrenergic alphaRatsAntitussive AgentsMechanism of actionchemistryCattleCalcium Channelsmedicine.symptommedicine.drugMuscle ContractionEuropean journal of pharmacology
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Organometallic complexes with biological molecules. XVIII. Alkyltin(IV) cephalexinate complexes: synthesis, solid state and solution phase investigat…

2004

Abstract Dialkyltin(IV) and trialkyltin(IV) complexes of the deacetoxycephalo-sporin-antibiotic cephalexin [7-( d -2-amino-2-phenylacetamido)-3-methyl-3-cephem-4-carboxylic acid] (Hceph) have been synthesized and investigated both in solid and solution phase. Analytical and thermogravimetric data supported the general formula Alk 2 SnOHceph · H 2 O and Alk 3 Snceph · H 2 O (Alk=Me, n -Bu), while structural information has been gained by FT-IR, 119 Sn Mossbauer and 1 H, 13 C, 119 Sn NMR data. In particular, IR results suggested polymeric structures both for Alk 2 SnOHceph · H 2 O and Alk 3 Snceph · H 2 O. Moreover, cephalexin appears to behave as monoanionic tridentate ligand coordinating th…

MaleThermogravimetric analysisDenticitySpectrophotometry InfraredStereochemistryMolecular Conformationchemistry.chemical_elementorganotin(IV)proton nuclear magnetic resonanceBiochemistryMedicinal chemistryChromosomesMossbauerInorganic ChemistrySpectroscopy Mossbauerchemistry.chemical_compoundantibiotic; cephalexin; organotin(IV); Mossbauer; cytotoxicitySpermatocytescomplex formationantibioticMössbauer spectroscopyOrganotin CompoundsAnimaliaAnimalsMoietyBrachidontes pharaoniCarboxylateNuclear Magnetic Resonance BiomolecularCephalexinMolecular StructureChemistryarticlesolid stateNuclear magnetic resonance spectroscopycarbon nuclear magnetic resonanceBivalviaAnti-Bacterial AgentsspermatocyteSettore CHIM/03 - Chimica Generale E InorganicaMolluscaThermogravimetryMössbauercytotoxicitycefalexinorganometallic compoundChromosome breakagedrug synthesiTinMutagensJournal of Inorganic Biochemistry
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Isomorphous replacement of MII ions in MII–GdIII dimers (MII = CuII, MnII, NiII, CoII, ZnII): magnetic studies of the products

2011

Complexes [M(II)Gd(III){pyCO(OEt)pyC(OH)(OEt)py}₃](ClO₄)₂·EtOH [M(II) = Cu(II) (1), Mn(II) (2), Ni(II) (3), Co(II) (4) and Zn(II) (5)] crystallize in the monoclinic Cc space group and contain one hexacoordinate M(II) ion and one enneacoordinate Gd(III) ion, bridged by three {pyCO(OEt)pyC(OH)(OEt)py}⁻ ligands. Magnetic susceptibility measurements indicate a ferromagnetic interaction for 1 and antiferromagnetic interactions for 2-4. Using the Ĥ = -JŜ(Gd(III))Ŝ(M(II)) spin Hamiltonian formalism, fits to the magnetic susceptibility data yielded J values of +0.32 cm⁻¹ for 1, -1.7 cm⁻¹ for 2, and -0.22 cm⁻¹ for 3. In complex 4, the orbital contributions of Co(II) precluded the determination of th…

ManganeseChemistryStereochemistryMolecular ConformationHexacoordinateSpin hamiltonianGadoliniumCobaltCrystallography X-RayMagnetic susceptibilityInductive couplingIonInorganic ChemistryMagneticsZincCrystallographyFerromagnetismCoordination ComplexesMetalsNickelAntiferromagnetismDimerizationCopperMonoclinic crystal systemDalton Transactions
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Drug release from alpha,beta-poly(N-2-hydroxyethyl)-DL-aspartamide-based microparticles.

2004

Abstract Spherical pH-sensitive microparticles have been prepared by reverse phase suspension polymerization technique. Starting polymer has been α , β -poly( N -2-hydroxyethyl)- dl -aspartamide (PHEA) partially derivatized with glycidylmethacrylate (GMA). PHEA-GMA copolymer (PHG) has been crosslinked in the presence of acrylic acid (AA) or methacrylic acid (MA) at various concentration. The obtained microparticles have been characterized by FT-IR spectrophotometry, particle size distribution analysis and scanning electron microscopy. In order to have information about water affinity of the prepared samples, swelling measurements have been carried out in aqueous media which simulate some bi…

Materials scienceChemical structureBiophysicsDrug Evaluation PreclinicalMolecular ConformationBioengineeringAbsorptionBiomaterialsDiffusionchemistry.chemical_compoundDrug Delivery SystemsSpectrophotometryPolymer chemistrymedicineCopolymerParticle SizeAcrylic acidchemistry.chemical_classificationDrug Carriersmedicine.diagnostic_testWaterHydrogelsPolymerMicrospheresBody FluidschemistryMethacrylic acidPharmaceutical PreparationsMechanics of MaterialsDelayed-Action PreparationsCeramics and CompositesSuspension polymerizationSwellingmedicine.symptomPeptidesNuclear chemistryBiomaterials
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Influence of the Number of Nanoparticles on the Enhancement Properties of Surface-Enhanced Raman Scattering Active Area: Sensitivity versus Repeatabi…

2011

In the present work, the combination of chemical immobilization with electron beam lithography enables the production of sensitive and reproducible SERS-active areas composed of stochastic arrangements of gold nanoparticles. The number of nanoparticles was varied from 2 to 500. Thereby a systematic analysis of these SERS-active areas allows us to study SERS efficiency as a function of the number of nanoparticles. We found that the experimental parameters are critical, in particular the size of the SERS-active area must be comparable to the effective area of excitation to obtained reproducible SERS measurements. The sensitivity has also been studied by deducing the number of NPs that generat…

Materials scienceLightMacromolecular SubstancesSurface PropertiesMolecular ConformationGeneral Physics and AstronomyNanoparticleNanotechnology02 engineering and technologySpectrum Analysis Raman010402 general chemistry01 natural sciencessymbols.namesakeMaterials TestingScattering RadiationGeneral Materials ScienceSensitivity (control systems)Particle SizeSurface plasmon resonanceComputingMilieux_MISCELLANEOUS[PHYS.PHYS.PHYS-OPTICS]Physics [physics]/Physics [physics]/Optics [physics.optics]General Engineering021001 nanoscience & nanotechnologyNanostructures0104 chemical sciencesColloidal goldsymbolsSurface modificationCrystallization0210 nano-technologyElectron-beam lithographyExcitationRaman scatteringACS Nano
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Quantum dot-block copolymer hybrids with improved properties and their application to quantum dot light-emitting devices.

2009

To combine the optical properties of CdSe@ZnS quantum dots (QDs) with the electrical properties of semiconducting polymers, we prepared QD/polymer hybrids by grafting a block copolymer (BCP) containing thiol-anchoring moieties (poly(para-methyl triphenylamine-b-cysteamine acrylamide)) onto the surfaces of QDs through the ligand exchange procedure. The prepared QD/polymer hybrids possess improved processability such as enhanced solubility in various organic solvents as well as the film formation properties along with the improved colloidal stability derived from the grafted polymer shells. We also demonstrated light-emitting diodes based on QD/polymer hybrids, exhibiting the improved device …

Materials scienceMacromolecular SubstancesPolymersSurface PropertiesMolecular ConformationGeneral Physics and AstronomyNanotechnologyColloidMaterials TestingQuantum DotsCopolymerNanotechnologyGeneral Materials ScienceSolubilityLightingchemistry.chemical_classificationtechnology industry and agricultureGeneral EngineeringPolymerEquipment Designequipment and suppliesGraftingEquipment Failure AnalysischemistryQuantum dotQuantum efficiencyHybrid materialCrystallizationACS nano
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Double-stranded RNA polyinosinic-polycytidylic acid immobilized onto gamma-Fe2O3 nanoparticles by using a multifunctional polymeric linker.

2007

Materials scienceMacromolecular SubstancesPolymersSurface PropertiesMolecular ConformationNanoparticleMaterials testingFerric CompoundsBiomaterialschemistry.chemical_compoundCoated Materials BiocompatibleMaterials TestingNanotechnologyGeneral Materials ScienceParticle SizeRNA Double-Strandedchemistry.chemical_classificationFerric CompoundsImmunomagnetic SeparationRNAGeneral ChemistryDouble stranded rnaPolymerCombinatorial chemistryNanostructuresPoly I-CchemistryBiochemistryPolyinosinic:polycytidylic acidCrystallizationLinkerBiotechnologySmall (Weinheim an der Bergstrasse, Germany)
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Comparative evaluation of the swelling and degrees of cross-linking in three organic gel packings for SEC through some geometric parameters.

2003

Abstract The size exclusion chromatographic (SEC) behavior of five solvent/polymer systems in three organic column packings based on polystyrene/divinylbenzene (PS/DVB) copolymer, TSK-Gel H HR , μ-styragel and TSK-Gel H XL , has been compared. All the packings offer similar characteristics (pore size, particle size and efficiency) but some differences have been found when eluting the same systems. The different elution behavior observed in both polymeric gels has been analyzed in terms of their swelling and cross-linking degrees and of the fractal parameters. From the Universal Calibration plots, values of the chromatographic partition coefficient, K p , have been obtained and using some eq…

Materials scienceMacromolecular SubstancesSize-exclusion chromatographyBiophysicsAnalytical chemistryMolecular ConformationBiochemistryFractal dimensionchemistry.chemical_compoundMaterials TestingmedicineOrganic ChemicalsParticle SizeViscositySolvationDivinylbenzenePartition coefficientEquipment Failure AnalysisCross-Linking ReagentschemistryVolume fractionCalibrationChromatography GelParticle sizeSwellingmedicine.symptomGelsPorosityJournal of biochemical and biophysical methods
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Nanostructuring with a crosslinkable discotic material.

2007

A high-yielding synthesis afforded a hexa-peri-hexabenzocoronene carrying acrylate units at the end of six attached alkyl spacers. The polymerization of these acrylate moieties could be initiated with thermal energy and through direct photoactivation without the addition of a photoinitiator. This allowed the organization of the liquid-crystalline material to be fixed in either the crystalline state or the mesophase, which preserved the organization in the respective phase. The use of a focused synchrotron beam permitted selected regions of a thin film to be rendered insoluble. After "developing" the film in this lithographic process by dissolving the soluble, unpolymerized material, defined…

Materials scienceMacromolecular SubstancesSurface PropertiesMolecular ConformationBiomaterialschemistry.chemical_compoundPhase (matter)Polymer chemistryMaterials TestingNanotechnologyGeneral Materials ScienceParticle SizeAlkylchemistry.chemical_classificationTitaniumAcrylateMesophaseGeneral ChemistryLiquid CrystalsNanostructuresMembraneCross-Linking ReagentsPolymerizationchemistryAcrylatesMesoporous materialCrystallizationPhotoinitiatorBiotechnologySmall (Weinheim an der Bergstrasse, Germany)
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