Search results for " Modification"

showing 10 items of 781 documents

Low-cost materials for boron adsorption from water

2012

[EN] Knowing the affinity of boron aqueous species for cis-diol organic groups, five different hybrid materials have been prepared by anchoring glucose groups onto the surface of silica matrices with a different surface topology: UVM-7 bimodal mesoporous silica, UVM-11 unimodal non-templated mesoporous silica, commercial silica fume and two silica xerogels with pores within the mesoporous range (13-50 nm). After optimizing the experimental conditions, a comparison was made of the boron adsorption capacities in water. The relationship of the structural and functionalization parameters is discussed and the importance of the surface topology in the final adsorption behaviour is revealed. Hence…

INGENIERIA DE LA CONSTRUCCIONMaterials scienceSilica fumeInorganic chemistrychemistry.chemical_elementAdsorptionQUIMICA ORGANICAMaterials ChemistryReverse-OsmosisNanoparticulated SilicasBoronChemical ControlAzomethine-H MethodAqueous-SolutionQUIMICA INORGANICAGeneral ChemistryMesoporous silicaMesoporous organosilicachemistryMesoporous OxidesSurface-PropertiesSurface modificationMesoporous materialHybrid materialRemovalPorosityIon-Exchange
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Stability of different mesoporous silica particles during an in vitro digestion

2016

Mesoporous silica materials have the ability to entrap drugs, nutrients and functional biomolecules and can be able to act as smart delivery systems capable to control and target the release of their cargo in a particular part of the gastrointestinal tract when administrated orally. However, the aptness of these encapsulation supports in in vivo oral controlled release relies on their chemical stability through the digestive tube. In this context, we have evaluated the stability of four different mesoporous silica particles, frequently used as encapsulating supports, during an in vitro digestion process comprising buccal, stomach and intestinal phases. Results showed that after 4 h of diges…

INGENIERIA DE LA CONSTRUCCIONTECNOLOGIA DE ALIMENTOSNanoparticle02 engineering and technology010402 general chemistryElectron Microscopy Service of the UPV01 natural sciencesMesoporous silica particlesQUIMICA ORGANICAQUIMICA ANALITICAOrganic chemistryMoietyGeneral Materials ScienceAmine-functionalizationchemistry.chemical_classificationChemistryBiomoleculeQUIMICA INORGANICAIn vitro digestionGeneral ChemistryBuccal administrationMesoporous silica021001 nanoscience & nanotechnologyCondensed Matter PhysicsControlled release0104 chemical sciencesChemical engineeringMechanics of MaterialsSurface modificationChemical stability0210 nano-technologyStabilityMicroporous and Mesoporous Materials
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"Table 4" of "Measurement of prompt photon production in $\sqrt{s_\mathrm{NN}} = 8.16$ TeV $p$+Pb collisions with ATLAS"

2019

The nuclear modification factor R_pPb for prompt, isolated photons with rapidity in (1.09,1.90).

InclusiveNuclear Modification8000.0Proton-Lead Scattering
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"Table 5" of "Measurement of prompt photon production in $\sqrt{s_\mathrm{NN}} = 8.16$ TeV $p$+Pb collisions with ATLAS"

2019

The nuclear modification factor R_pPb for prompt, isolated photons with rapidity in (−1.84,0.91).

InclusiveNuclear Modification8000.0Proton-Lead Scattering
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"Table 6" of "Measurement of prompt photon production in $\sqrt{s_\mathrm{NN}} = 8.16$ TeV $p$+Pb collisions with ATLAS"

2019

The nuclear modification factor R_pPb for prompt, isolated photons with rapidity in (−2.83,−2.02).

InclusiveNuclear Modification8000.0population characteristicscardiovascular diseasesProton-Lead Scattering
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Palladium-catalyzed dehydrogenative β'-functionalization of β-keto esters with indoles at room temperature.

2012

The dehydrogenative β′-functionalization of α-substituted β-keto esters with indoles proceeds with high regioselectivities (C3-selective for the indole partner and β′-selective for the β-keto ester) and good yields under mild palladium catalysis at room temperature with a variety of oxidants. Two possible mechanisms involving either late or early involvement of indole are presented.

Indole testColloid and Surface Chemistrychemistrychemistry.chemical_elementSurface modificationOrganic chemistryGeneral Chemistryta116BiochemistryCatalysisPalladiumCatalysisJournal of the American Chemical Society
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Palladium-catalyzed domino C-H/N-H functionalization: an efficient approach to nitrogen-bridged heteroacenes.

2015

Palladium-catalyzed domino C-H/N-H functionalization for the synthesis of novel nitrogen-bridged thienoacenes and 10H-benzo[4,5]thieno[3,2-b]indole derivatives from dihaloarene is reported. This domino sequence consists of initial C-H functionalization of the benzo[b]thiophene moiety, followed by Buchwald-Hartwig coupling. This transformation is also useful for the synthesis of highly π-extended compounds.

Indole testStereochemistryOrganic Chemistrychemistry.chemical_elementGeneral ChemistryMedicinal chemistryCatalysisDominoCatalysischemistry.chemical_compoundchemistryThiopheneMoietySurface modificationAminationPalladiumChemistry (Weinheim an der Bergstrasse, Germany)
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ChemInform Abstract: Palladium-Catalyzed Dehydrogenative β′-Functionalization of β-Keto Esters with Indoles at Room Temperature.

2012

The dehydrogenative β′-functionalization of α-substituted β-keto esters with indoles proceeds with high regioselectivities (C3-selective for the indole partner and β′-selective for the β-keto ester) and good yields under mild palladium catalysis at room temperature with a variety of oxidants. Two possible mechanisms involving either late or early involvement of indole are presented.

Indole testchemistrychemistry.chemical_elementSurface modificationGeneral MedicineCombinatorial chemistryPalladiumCatalysisChemInform
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ChemInform Abstract: Palladium-Catalyzed Domino C-H/N-H Functionalization: An Efficient Approach to Nitrogen-Bridged Heteroacenes.

2015

Palladium-catalyzed domino CH/NH functionalization for the synthesis of novel nitrogen-bridged thienoacenes and 10H-benzo[4,5]thieno[3,2-b]indole derivatives from dihaloarene is reported. This domino sequence consists of initial CH functionalization of the benzo[b]thiophene moiety, followed by Buchwald–Hartwig coupling. This transformation is also useful for the synthesis of highly π-extended compounds.

Indole testchemistry.chemical_compoundChemistryThiophenechemistry.chemical_elementMoietySurface modificationGeneral MedicineMedicinal chemistryNitrogenDominoCatalysisPalladiumChemInform
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Synthesis and in Vitro Evaluation of Biotinylated RG108:  A High Affinity Compound for Studying Binding Interactions with Human DNA Methyltransferases

2006

Small-molecule inhibitors of DNA methyltransferases such as RG108 represent promising candidates for cancer drug development. We report the synthesis and in vitro analysis of a biotinylated RG108 conjugate, 2-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-3-(5-[3-[5-(2-oxo-hexahydro-thieno[3,4-d]imidazol-4-yl)pentanoylamino]propoxy]-1H-indol-3-yl)propionic acid (bio-RG108), for the evaluation of interactions with DNA methyltransferase enzymes. The structural design of the chemically modified inhibitor was aided by molecular modeling, which suggested the possibility for extensive chemical modifications at the 5-position of the tryptophan moiety in RG108. The inhibitory activity of the corresponding d…

IndolesMethyltransferaseMolecular modelStereochemistryBiomedical EngineeringBiotinPharmaceutical SciencePhthalimidesBioengineeringDNA methyltransferaseCell-free systemchemistry.chemical_compoundAffinity chromatographyHumansDNA Modification MethylasesNuclear Magnetic Resonance BiomolecularPharmacologychemistry.chemical_classificationCell-Free SystemMolecular StructureChemistryOrganic ChemistryTryptophanEnzymeBiochemistryBiotinylationPropionatesDNAProtein BindingBiotechnologyBioconjugate Chemistry
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