Search results for "Catalysis"

showing 10 items of 5944 documents

Determination of molecular mass, Stokes' radius, frictional coefficient and isomer-type of non-denatured proteins by time-dependent pore gradient gel…

1988

Molecular mass, Stoke's radius, frictional coefficient and isomer-type of non-denatured proteins can be obtained by time-dependent gradient gel electrophoresis by evaluating the resulting data using a two-step mathematical procedure. Provided a histochemical staining procedure is available to locate the position of an enzyme in the gel, crude cell extracts can be used for estimating their molecular size properties. The computation of molecular properties of non-denatured proteins is demonstrated for isozymes of aspartate aminotransferase (EC 2.6.1.1), peroxidase (EC 1.11.1.42) and glucose-6-phosphate dehydrogenase (EC 1.1.1.49) from current-year needles of spruce. The resulting data as well…

Gel electrophoresisShikimate dehydrogenaseChromatographyMolecular massChemistryGlutamate dehydrogenaseClinical BiochemistryReproducibility of ResultsDehydrogenaseEnvironmental pollutionStereoisomerismBiochemistryCatalysisAnalytical ChemistryEnzymesMolecular WeightCalibrationElectrophoresis Polyacrylamide GelPolyacrylamide gel electrophoresisStokes radiusPlant ProteinsElectrophoresis
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1989

Synthese a partir du dibromo-1,5 di t-butyl-3,7 naphtalene via un monomere bifonctionnel (action du butyllithium et du triisopropoxyborane)

Gel permeation chromatographyTert butylchemistry.chemical_compoundChemistryStereochemistryMoleculechemistry.chemical_elementSolubilityMedicinal chemistryOligomerCatalysisPalladiumDie Makromolekulare Chemie, Rapid Communications
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Geminal ionic liquids: a combined approach to investigate their three-dimensional organisation.

2009

Different investigations, such as 1D and 2D NMR spectroscopy, resonance light scattering spectroscopy and molecular dynamics simulations, have been jointly used to achieve a deeper understanding of the degree of structural order in two geminal ionic liquids. In particular, 3,3'-di-n-butyl-1,1'-(1,3-phenylenedimethylene)diimidazolium and 3,3'-di-n-butyl-1,1'-(1,4-phenylenedimethylene)diimidazolium bis[bis(trifluoromethanesulfonyl)imide] have been studied. These geminal ionic liquids were chosen because of the presence of both a rigid phenylenedimethylene link between two imidazolium rings, which should give a high degree of order to the solvent system, and the different shapes of the two cat…

GeminalOrganic ChemistryInorganic chemistryGeneral ChemistryNuclear magnetic resonance spectroscopyResonance (chemistry)Catalysischemistry.chemical_compoundMolecular dynamicschemistryIonic liquidPhysical chemistryImideSpectroscopyTwo-dimensional nuclear magnetic resonance spectroscopyChemistry (Weinheim an der Bergstrasse, Germany)
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The “Janus” Role of C/EBPs Family Members in Cancer Progression

2020

CCAAT/enhancer-binding proteins (C/EBPs) constitute a family of transcription factors composed of six members that are critical for normal cellular differentiation in a variety of tissues. They promote the expression of genes through interaction with their promoters. Moreover, they have a key role in regulating cellular proliferation through interaction with cell cycle proteins. C/EBPs are considered to be tumor suppressor factors due to their ability to arrest cell growth (contributing to the terminal differentiation of several cell types) and for their role in cellular response to DNA damage, nutrient deprivation, hypoxia, and genotoxic agents. However, C/EBPs can elicit completely opposi…

Gene isoformCell typeDNA damagetumor suppressorCellular differentiationReviewBiologyCatalysisInorganic Chemistrylcsh:ChemistryStructure-Activity RelationshipSettore BIO/13 - Biologia ApplicataNeoplasmsAnimalsHumansProtein IsoformscancerPhysical and Theoretical ChemistryCell Cycle ProteinMolecular BiologyTranscription factorlcsh:QH301-705.5SpectroscopyCell growthOrganic Chemistrytumor promoterPromoterGeneral MedicineC/EBPComputer Science ApplicationsCell biologyGene Expression Regulation Neoplasticlcsh:Biology (General)lcsh:QD1-999Multigene FamilyCCAAT-Enhancer-Binding ProteinsDisease ProgressionDisease SusceptibilityProtein BindingSignal TransductionInternational Journal of Molecular Sciences
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Model of a six immunoglobulin-like domain fragment of filamin A (16-21) built using residual dipolar couplings.

2012

Filamins are actin-binding proteins that participate in a wide range of cell functions, including cell morphology, locomotion, membrane protein localization, and intracellular signaling. The three filamin isoforms found in humans, filamins A, B, and C, are highly homologous, and their roles are partly complementary. In addition to actin, filamins interact with dozens of other proteins that have roles as membrane receptors and channels, enzymes, signaling intermediates, and transcription factors. Filamins are composed of an N-terminal actin-binding domain and 24 filamin-type immunoglobulin-like domains (FLN) that form tail-to-tail dimers with their C-terminal FLN domain. Many of the filamin …

Gene isoformModels Molecularanimal structuresMagnetic Resonance SpectroscopyProtein ConformationFilaminsIntegrinBiomolecular structuremacromolecular substances010402 general chemistryFilaminCell morphologyCrystallography X-Ray01 natural sciencesBiochemistryCatalysis03 medical and health sciencesColloid and Surface ChemistryContractile ProteinsHumansTranscription factorImmunoglobulin FragmentsActin030304 developmental biologychemistry.chemical_classification0303 health sciencesbiologyChemistryMicrofilament ProteinsGeneral Chemistry0104 chemical sciencesCell biologybody regionsbiology.proteinGlycoproteinJournal of the American Chemical Society
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Disparity between Inter-Patient Molecular Heterogeneity and Repertoires of Target Drugs Used for Different Types of Cancer in Clinical Oncology

2020

Inter-patient molecular heterogeneity is the major declared driver of an expanding variety of anticancer drugs and personalizing their prescriptions. Here, we compared interpatient molecular heterogeneities of tumors and repertoires of drugs or their molecular targets currently in use in clinical oncology. We estimated molecular heterogeneity using genomic (whole exome sequencing) and transcriptomic (RNA sequencing) data for 4890 tumors taken from The Cancer Genome Atlas database. For thirteen major cancer types, we compared heterogeneities at the levels of mutations and gene expression with the repertoires of targeted therapeutics and their molecular targets accepted by the current guideli…

Gene mutationMedical OncologychemotherapyGenomeTranscriptomelcsh:ChemistryDrug Delivery SystemsProstateNeoplasmstumor heterogeneityMedicineCluster AnalysisMolecular Targeted TherapyPathology MolecularPrecision Medicinelcsh:QH301-705.5targeted therapeuticscancer drugsSpectroscopyExome sequencingGeneral MedicineGenomicspersonalized medicineComputer Science ApplicationsDrug repositioningmedicine.anatomical_structureAntineoplastic AgentsComputational biologyCatalysisArticleInorganic Chemistrymolecular diagnosticsGenetic HeterogeneityDrug TherapyExome SequencingHumansPhysical and Theoretical ChemistryMolecular Biologygenomeclinical oncologybusiness.industryOrganic ChemistryMolecular diagnosticsmutationslcsh:Biology (General)lcsh:QD1-999MutationPersonalized medicinebusinesstranscriptomeInternational Journal of Molecular Sciences
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Modelling wet-air oxidation of phenol in a trickle-bed reactor using active carbon as a catalyst

2014

BACKGROUND Catalytic wet air oxidation (CWAO) of phenol in a trickle-bed reactor has been investigated (operating parameters: P=1.85 MPa, T=393, 413, 433 K, L=0.17–1.77 kg m−2 s−1 and G=0.2–0.62 kg m−2 s−1). Activated carbon was used as a catalyst. The experimental results have been simulated by Eulerian multifluid model (CFD) and for comparison by the plug flow model. RESULTS The experiments proved that active carbon can be applied as a catalyst in the phenol oxidation processes revealing a catalytic activity comparable with that of commonly used metal oxides. The highest conversion of phenol obtained in long-lasting experimental runs carried out at stable catalytic activity (PO2 = 0.31 MP…

General Chemical Engineering02 engineering and technologyCatalysisInorganic ChemistryMetalchemistry.chemical_compound020401 chemical engineeringmedicinePhenolWet oxidation0204 chemical engineeringPorosityWaste Management and DisposalChromatographyPlug flowRenewable Energy Sustainability and the EnvironmentChemistryOrganic ChemistryTrickle-bed reactor021001 nanoscience & nanotechnologyPollutionFuel TechnologyChemical engineeringvisual_artvisual_art.visual_art_medium0210 nano-technologyBiotechnologyActivated carbonmedicine.drugJournal of Chemical Technology & Biotechnology
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Electrochemically reduced titanocene dichloride as a catalyst of reductive dehalogenation of organic halides

2006

Abstract We have studied a reaction between the reduced form of titanocene dichloride (Cp 2 TiCl 2 ) and a group of organic halides: benzyl derivatives (4-X C 6 H 4 CH 2 Cl, X = H, NO 2 , CH 3 ; 4-X C 6 H 4 CH 2 Br, X = H, NO 2 , PhC(O); 4-X C 6 H 4 CH 2 SCN, X = H, NO 2 ) as well as three aryl halides (4-NO 2 C 6 H 4 Hal, Hal = Cl, Br; 4-CH 3 O-C 6 H 4 Cl). It has been shown that the electrochemical reduction of Cp 2 TiCl 2 in the presence of these benzyl halides leads to a catalytic cycle resulting in the reductive dehalogenation of these organic substrates to yield mostly corresponding toluene derivatives as the main product. No dehalogenation has been observed for aryl derivatives. Base…

General Chemical EngineeringArylTitanocene dichlorideHalogenationHalidePhotochemistryMedicinal chemistryHeterolysisCatalysischemistry.chemical_compoundchemistryCatalytic cycleElectrochemistryMetalloceneElectrochimica Acta
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Green and Direct Synthesis of Benzaldehyde and Benzyl Benzoate in One Pot

2018

High yields of valued benzaldehyde and benzyl benzoate are obtained in one pot starting from benzyl alcohol using oxygen as only oxidant under mild conditions (2 bar O2, 100 °C) along with an ultralow amount (0.02 mol %) of Au nanoparticles heterogenized over a spherical ORMOSIL mesoporous support. The process is remarkably selective and the catalyst is stable.

General Chemical EngineeringBenzyl benzoateORMOSILchemistry.chemical_elementGold catalysis010402 general chemistry01 natural sciencesOrmosilOxygenMedicinal chemistryBenzaldehydechemistry.chemical_compoundBenzyl benzoateEnvironmental ChemistryOne pot010405 organic chemistryRenewable Energy Sustainability and the EnvironmentSolagel catalysisGeneral ChemistrySettore CHIM/06 - Chimica OrganicaBenzaldehyde0104 chemical scienceschemistryBenzyl alcoholAerobic oxidationSolâgel catalysis
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3D Ruthenium Nanoparticle Covalent Assemblies from Polymantane Ligands for Confined Catalysis

2020

International audience; The synthesis of metal nanoparticle (NP) assemblies stabilized by functional molecules is an important research topic in nanoscience, and the ability to control interparticle distances and positions in NP assemblies is one of the major challenges in designing and understanding functional nanostructures. Here, two series of functionalized adamantanes, bis-adamantanes, and diamantanes, bearing carboxylic acid or amine functional groups, were used as building blocks to produce, via a straightforward method, networks of ruthenium NPs. Both the nature of the ligand and the Ru/ligand ratio affect the interparticle distance in the assemblies. The use of 1,3-adamantanedicarb…

General Chemical EngineeringCarboxylic acidchemistry.chemical_elementNanoparticle02 engineering and technology010402 general chemistryLigands01 natural sciencesCatalysischemistry.chemical_compound[CHIM.GENI]Chemical Sciences/Chemical engineeringOrganic acidsMaterials ChemistryGénie chimique[SPI.GPROC]Engineering Sciences [physics]/Chemical and Process EngineeringAminesGénie des procédéschemistry.chemical_classificationCatalystsLigandDecarbonylationGeneral Chemistry021001 nanoscience & nanotechnologyCombinatorial chemistry0104 chemical sciencesRutheniumchemistryPhenylacetyleneMetalsDensity functional theory0210 nano-technology
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