Search results for "AGENT"

showing 10 items of 8904 documents

Preparation of 2,3-seco-5α-cholestane-2,3-diol and 4α-methyl-2,3-seco-5α-cholestane-2,3-diol and its reactions with o-nitrophenyl selenocyanate

1984

The reaction of 2,3-seco-5 alpha-cholestane-2,3-diol and 4 alpha-methyl-2,3-seco-5 alpha-cholestane-2,3-diol with o-nitrophenyl selenocyanate was studied. The diols were synthesized from cholesterol.

inorganic chemicalsMagnetic Resonance SpectroscopyChemical PhenomenaOptical RotationSpectrophotometry InfraredClinical BiochemistryDiolBiochemistrychemistry.chemical_compoundEndocrinologySpectrophotometryNitrilespolycyclic compoundsmedicineSecosteroidsOrganic chemistryMolecular BiologyPharmacologyintegumentary systemmedicine.diagnostic_testorganic chemicalsOrganic ChemistryNuclear magnetic resonance spectroscopyChemistrychemistryIndicators and ReagentsCholestaneCholestanolshormones hormone substitutes and hormone antagonistsSteroids
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Synthesis, Characterization, and Cu(2+) Coordination Studies of a 3-Hydroxy-4-pyridinone Aza Scorpiand Derivative.

2016

The synthesis, acid-base behavior, and Cu(2+) coordination chemistry of a new ligand (L1) consisting of an azamacrocyclic core appended with a lateral chain containing a 3-hydroxy-2-methyl-4(1H)-pyridinone group have been studied by potentiometry, cyclic voltammetry, and NMR and UV-vis spectroscopy. UV-vis and NMR studies showed that phenolate group was protonated at the highest pH values [log K = 9.72(1)]. Potentiometric studies point out the formation of Cu(2+) complexes of 1:2, 2:2, 4:3, 1:1, and 2:1 Cu(2+)/L1 stoichiometries. UV-vis analysis and electrochemical studies evidence the implication of the pyridinone moieties in the metal coordination of the 1:2 Cu(2+)/L1 complexes. L1 shows …

inorganic chemicalsMagnetic Resonance SpectroscopyStereochemistryPyridinesPyridonesPotentiometric titrationProtonationChemistry Techniques Synthetic010402 general chemistry010403 inorganic & nuclear chemistryElectrochemistryCrystallography X-Ray01 natural sciencesMedicinal chemistryAntioxidantsCoordination complexInorganic Chemistrychemistry.chemical_compoundStructure-Activity RelationshipCoordination ComplexesHumansChelationPhysical and Theoretical ChemistryCell ProliferationChelating Agentschemistry.chemical_classificationLigandHydrogen-Ion Concentration0104 chemical scienceschemistryPotentiometrySpectrophotometry UltravioletCyclic voltammetryDerivative (chemistry)CopperHeLa CellsInorganic chemistry
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Amino-Acid-Based Polymerizable Surfactants for the Synthesis of Chiral Nanoparticles

2016

Amino-acid-based chiral surfactants with polymerizable moieties are synthesized, and a versatile approach to prepare particles thereof with a chiral surface functionality is presented. As an example of an application, the synthesized particles are tested for their ability as nucleating agents in the enantioselective crystallization of amino acid conglomerate systems, taking rac-asparagine as a model system. Particles resulting from chiral surfactants with different tail groups are compared and the results demonstrate that only the chiral nanoparticles made of the polymerizable surfactant are able to act efficiently as nucleation agent in enantioselective crystallization.

inorganic chemicalsMaterials sciencePolymers and PlasticsPolymersNucleationNanoparticleModel system02 engineering and technology010402 general chemistry01 natural sciencesPolymerizationlaw.inventionSurface-Active AgentsPulmonary surfactantlawMaterials ChemistryOrganic chemistryAmino AcidsCrystallizationchemistry.chemical_classificationMolecular Structureorganic chemicalsOrganic Chemistrytechnology industry and agricultureEnantioselective synthesisStereoisomerism021001 nanoscience & nanotechnologyCombinatorial chemistry0104 chemical sciencesAmino acidchemistryNanoparticles0210 nano-technologyChirality (chemistry)Macromolecular Rapid Communications
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One pot light assisted green synthesis, storage and antimicrobial activity of dextran stabilized silver nanoparticles.

2014

Background Green synthesis of nanomaterials finds the edge over chemical methods due to its environmental compatibility. Herein, we report green synthesis of silver nanoparticles (Ag NPs) mediated with dextran. Dextran was used as a stabilizer and capping agent to synthesize Ag NPs using silver nitrate (AgNO3) under diffused sunlight conditions. Results UV–vis spectra of as synthesized Ag nanoparticles showed characteristic surface plasmon band in the range from ~405-452 nm. Scanning electron microscopy (SEM) and atomic force microscopy (AFM) studies showed spherical Ag NPs in the size regime of ~50-70 nm. Face centered cubic lattice of Ag NPs was confirmed by powder X-ray diffraction (PXRD…

inorganic chemicalsMaterials scienceSilverReducing agentScanning electron microscopeeducationBiomedical EngineeringDrug Evaluation PreclinicalMedicine (miscellaneous)Pharmaceutical ScienceMetal NanoparticlesNanotechnologyBioengineeringMicrobial Sensitivity TestsAntimicrobial activityMicroscopy Atomic ForceApplied Microbiology and BiotechnologySilver nanoparticleNanomaterialsStorage of nanoparticleschemistry.chemical_compoundAnti-Infective AgentsX-Ray DiffractionDiffused sun lightSpectroscopy Fourier Transform InfraredThin filmhealth care economics and organizationsAg nanoparticlesResearchtechnology industry and agricultureDextransGreen Chemistry TechnologySilver nitrateDextranchemistryMicroscopy Electron ScanningMolecular MedicineSilver NitrateSpectrophotometry UltravioletPowder diffractionNuclear chemistryJournal of nanobiotechnology
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Synergistic Anticancer Therapy by Ovalbumin Encapsulation-Enabled Tandem Reactive Oxygen Species Generation

2020

Abstract The anticancer efficacy of photodynamic therapy (PDT) is limited due to the hypoxic features of solid tumors. We report synergistic PDT/chemotherapy with integrated tandem Fenton reactions mediated by ovalbumin encapsulation for improved in vivo anticancer therapy via an enhanced reactive oxygen species (ROS) generation mechanism. O2 .− produced by the PDT is converted to H2O2 by superoxide dismutase, followed by the transformation of H2O2 to the highly toxic .OH via Fenton reactions by Fe2+ originating from the dissolution of co‐loaded Fe3O4 nanoparticles. The PDT process further facilitates the endosomal/lysosomal escape of the active agents and enhances their intracellular deliv…

inorganic chemicalsNanomedicines | Hot PaperOvalbuminmedicine.medical_treatmentRadicalsynergisticcisplatinPhotodynamic therapyAntineoplastic Agents010402 general chemistry01 natural sciencesCatalysisSuperoxide dismutasechemistry.chemical_compoundMicemedicineAnimalsHumansResearch Articleschemistry.chemical_classificationCisplatinReactive oxygen speciesOxidase testPhotosensitizing Agentsbiology010405 organic chemistryFenton reactionsDrug SynergismGeneral MedicineGeneral ChemistryhypoxicEndocytosis0104 chemical sciencesOvalbuminchemistryphotodynamic therapybiology.proteinBiophysicsMCF-7 CellsReactive Oxygen SpeciesNicotinamide adenine dinucleotide phosphatemedicine.drugResearch Article
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Sol-gel entrapped chromium(VI): a new selective, efficient and recyclable oxidizing system

2001

Abstract The sol-gel entrapment of chromium(VI) within a silica matrix, obtained by oxidation with ozone of the corresponding entrapped chromium(III), was found to be an efficient and recyclable oxidizing system (at least up to 16 times) for benzylic alcohols. No leaching of chromium in solution was observed, which prevented any environmental pollution.

inorganic chemicalsOzoneChemistryOrganic ChemistryInorganic chemistrytechnology industry and agriculturechemistry.chemical_elementEnvironmental pollutionBiochemistryChromiumchemistry.chemical_compoundSilica matrixDrug DiscoveryOxidizing agentotorhinolaryngologic diseasesLeaching (metallurgy)Sol-gelTetrahedron Letters
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ChemInform Abstract: Sol-Gel Entrapped Chromium(VI): A New Selective, Efficient and Recyclable Oxidizing System.

2010

Abstract The sol-gel entrapment of chromium(VI) within a silica matrix, obtained by oxidation with ozone of the corresponding entrapped chromium(III), was found to be an efficient and recyclable oxidizing system (at least up to 16 times) for benzylic alcohols. No leaching of chromium in solution was observed, which prevented any environmental pollution.

inorganic chemicalsOzonetechnology industry and agriculturechemistry.chemical_elementEnvironmental pollutionGeneral Medicinechemistry.chemical_compoundChromiumchemistrySilica matrixOxidizing agentotorhinolaryngologic diseasesLeaching (metallurgy)Nuclear chemistrySol-gelChemInform
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Role of glutathione in the formation of the active form of the oxygen sensor FNR ([4Fe-4S]·FNR) and in the control of FNR function

2000

The oxygen sensor regulator FNR (fumarate nitrate reductase regulator) of Escherichia coli is known to be inactivated by O2 as the result of conversion of a [4Fe-4S] cluster of the protein into a [2Fe-2S] cluster. Further incubation with O2 causes loss of the [2Fe-2S] cluster and production of apoFNR. The reactions involved in cluster assembly and reductive activation of apoFNR isolated under anaerobic or aerobic conditions were studied in vivo and in vitro. In a gshA mutant of E. coli that was completely devoid of glutathione, the O2 tension for the regulatory switch for FNR-dependent gene regulation was decreased by a factor of 4–5 compared with the wild-type, suggesting a role for glutat…

inorganic chemicalsReducing agentCysteine desulfuraseMutantRegulatormacromolecular substancesGlutathioneBiologymedicine.disease_causeNitrate reductaseenvironment and public healthBiochemistryenzymes and coenzymes (carbohydrates)chemistry.chemical_compoundchemistryBiochemistrymedicinebacteriaEscherichia coliCysteineEuropean Journal of Biochemistry
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Formation and growth of palladium nanoparticles inside porous poly(4-vinyl-pyridine) monitored by operando techniques: The role of different reducing…

2017

In this work we followed the formation of palladium nanoparticles, starting from palladium (II) acetate precursor, inside a poly(4-vinylpyridine-co-divinylbenzene) polymer in presence of different reducing agents. The formation and growth of palladium nanoparticles in presence of H-2 was followed as a function of temperature by simultaneous XANES-SAXS techniques, coupled with DRIFT spectroscopy in operando conditions. It was found that the pyridyl functional groups in the polymer plays a fundamental role in the stabilization of the palladium (II) acetate precursor, as well as in the stabilization of the palladium nanoparticles. The effect of a thermal treatment in alcohol (ethanol and 2-pro…

inorganic chemicalsReducing agentInfrared spectroscopychemistry.chemical_element02 engineering and technologyThermal treatment010402 general chemistryPhotochemistry01 natural sciencesAEROBIC ALCOHOL OXIDATIONCatalysisCatalysiCatalysisP4VPRUTHENIUM NANOPARTICLESMoleculeOrganic chemistryOperandoCATALYTIC-ACTIVITYchemistry.chemical_classificationPD NANOPARTICLESDRIFT; Operando; P4VP; Palladium nanoparticles; SAXS; XANESChemistryIN-SITUChemistry (all)SAXSGeneral ChemistryPolymerPalladium nanoparticleSELECTIVE OXIDATION021001 nanoscience & nanotechnologyPalladium nanoparticlesXANESX-RAY-SCATTERINGPARTICLE-SIZE0104 chemical sciencesDRIFTColloidal goldGOLD NANOPARTICLESVIBRATIONAL PROPERTIESDRIFT; Operando; P4VP; Palladium nanoparticles; SAXS; XANES; Catalysis; Chemistry (all)0210 nano-technologyPalladiumCatalysis Today
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Thieme Chemistry Journals Awardees – Where Are They Now? Molybdenum(V)-Mediated Synthesis of Nonsymmetric Diaryl and Aryl Alkyl Chalcogenides

2017

Oxidative chalcogenation reaction using molybdenum(V) reagents provides fast access to a wide range of nonsymmetric aryl sulfides and selenides. The established protocol is tolerated by a variety of labile functions, protecting groups, and aromatic heterocycles. In particular, when labile moieties are present, the use of molybdenum(V) reagents provides superior yields compared to other oxidants.

inorganic chemicalschemistry.chemical_classificationmolybdenum pentachloridedisulfides010405 organic chemistryArylOrganic Chemistrychemistry.chemical_elementMolybdenum pentachloride010402 general chemistryoxidative coupling01 natural sciences0104 chemical scienceschemistry.chemical_compoundchemistryMolybdenumReagentcross-couplingOrganic chemistryOxidative coupling of methaneC–S bond formationAlkylSynlett
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