Search results for "Benzene"

showing 10 items of 1701 documents

Discerning the Origins of the Amplitude Fluctuations in Dynamic Raman Nanospectroscopy

2012

International audience; We introduce a novel experimental and analytical method for discerning rare surface-enhanced Raman scattering (SERS) events observable at the nanoscale. We show that the kinetics of the Raman activity recorded on an isolated nanostructure is punctuated by intense and rare events of large amplitude and spectral variations. The fluctuations of thousands of SERS spectra were analyzed statistically in terms of power density functions, and the occurrence of the rare events was quantified by a wavenumber statistics. Our analysis enables one to extract valuable and unique spectroscopic signature of Raman variations usually hidden in time-average or space-average measurement…

NanostructureSURFACEELECTRODESBENZENETHIOL02 engineering and technology010402 general chemistry01 natural sciencesMolecular physicsSpectral lineRESONANCE FLUORESCENCEsymbols.namesakeOpticsRare eventsBLINKINGWavenumberSCATTERINGPhysical and Theoretical ChemistrySPECTROSCOPYChemistrybusiness.industrySERSObservable021001 nanoscience & nanotechnologySTATISTICS0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsGeneral EnergyAmplitudesymbolsADATOMS0210 nano-technologyRaman spectroscopybusinessRaman scattering
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Sorafenib, but not sunitinib, affects function of dendritic cells and induction of primary immune responses

2008

AbstractThe tyrosine kinase inhibitors sorafenib and sunitinib are approved for the treatment of patients with malignant diseases. To analyze the possible use of these compounds in combination with immunotherapeutic approaches, we analyzed the effects of both inhibitors on the immunostimulatory capacity of human dendritic cells (DCs) and the induction of primary immune responses in vivo. Sorafenib, but not sunitinib, inhibits function of DCs, characterized by reduced secretion of cytokines and expression of CD1a, major histocompatibility complex, and costimulatory molecules in response to TLR ligands as well as by their impaired ability to migrate and stimulate T-cell responses. These inhib…

NiacinamideSorafenibIndolesPyridinesImmunologyAntineoplastic AgentsApoptosisCD8-Positive T-LymphocytesPharmacologyBiologyurologic and male genital diseasesMajor histocompatibility complexT-Lymphocytes RegulatoryBiochemistryPeripheral blood mononuclear cellMiceImmune systemCell MovementIn vivoSunitinibmedicineAnimalsHumansCytotoxic T cellPyrrolesCells CulturedSunitinibPhenylurea CompoundsBenzenesulfonatesGranulocyte-Macrophage Colony-Stimulating FactorDextransDendritic CellsCell BiologyHematologySorafenibEndocytosisfemale genital diseases and pregnancy complicationsMice Inbred C57BLToll-Like Receptor 4biology.proteinCytokinesFemaleInterleukin-4Lymphocyte Culture Test MixedTyrosine kinaseCell DivisionSignal Transductionmedicine.drugBlood
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Novel inhibitors in development for hepatocellular carcinoma

2010

The multikinase inhibitor sorafenib was the first agent to demonstrate a survival benefit for patients with locally advanced or metastatic hepatocellular carcinoma (HCC). Although sorafenib represents a landmark in the treatment of HCC and proved molecularly targeted therapy to be effective in this disease, it represents just the first step towards an improvement in systemic therapy. Since then, novel inhibitors have been evaluated in early clinical trials, showing potential activity.This article aims to review novel inhibitors emerging in the field of advanced HCC. An Internet-based search was performed to identify abstracts, clinical trials ( www.clinicaltrials.gov , last accessed 30 Nove…

NiacinamideSorafenibOncologymedicine.medical_specialtyCarcinoma HepatocellularPyridinesmedicine.medical_treatmentMEDLINEAntineoplastic AgentsDiseasePharmacologySystemic therapyTargeted therapyDrug Delivery SystemsInternal medicinemedicineCarcinomaAnimalsHumansPharmacology (medical)PharmacologyClinical Trials as Topicbusiness.industryPhenylurea CompoundsBenzenesulfonatesLiver NeoplasmsDrugs InvestigationalGeneral MedicineSorafenibmedicine.diseasedigestive system diseasesClinical trialDrug DesignHepatocellular carcinomabusinessSignal Transductionmedicine.drugExpert Opinion on Investigational Drugs
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Pyrene-functionalized nanoparticles: two independent sensors, the excimer and the monomer.

2012

The high surface-to-volume ratio of nanoparticles has been used to obtain a high local concentration of pyrene units on their periphery, making the formation of both pyrene emissive species possible using amazingly small pyrene concentrations. The sensing properties of model pyrene-functionalized nanoparticles was investigated by using different nitroaromatic compounds [m-nitroaniline and p-nitroaniline] and nitrobenzenes [nitrobenzene, p-nitrotoluene, 2,4-dinitrotoluene, and 2,6-dinitrotoluene]. The hybrid system acts as a dual-fluorescence sensor, in which the decrease of the pyrene emission, induced by the quencher, is hardly reflected in the pyrene excimer emission. The encapsulation ca…

NitrobenzeneAnalytechemistry.chemical_compoundMonomerFunctionalized nanoparticleschemistryNanoparticlePyreneExcimerPhotochemistryAnalytical ChemistryAnalytical chemistry
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Understanding the Mechanism of Nitrobenzene Nitration with Nitronium Ion: A Molecular Electron Density Theory Study

2019

Nitrobenzenechemistry.chemical_compoundElectron densitychemistryNitrationNitronium ionMolecular mechanismGeneral ChemistryElectrophilic aromatic substitutionPhotochemistryMechanism (sociology)ChemistrySelect
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Synthesis of pyrido[2,3-d]pyrimidinones by the reaction of aminopyrimidin-4-ones with benzylidene meldrum's acid derivatives

1997

A series of pyrido[2,3-d]pyrimidine-4,7-diones 5a-h were prepared from 6-amino-4-pyrimidones 1 and benzylidene Meldrum's acid derivatives 2 by cyclization reactions in boiling nitrobenzene. The structure of 5, determined by nmr measurements, reveals a selective orientation of 1 and 2 in the addition step.

Nitrobenzenechemistry.chemical_compoundPyrimidinoneschemistryBoilingOrganic ChemistryOrientation (graph theory)Meldrum's acidMedicinal chemistryJournal of Heterocyclic Chemistry
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ChemInform Abstract: Synthesis of Pyrido(2,3-d)pyrimidinones by the Reaction of Aminopyrimidin-4-ones with Benzylidene Meldrum′s Acid Derivatives.

2010

A series of pyrido[2,3-d]pyrimidine-4,7-diones 5a-h were prepared from 6-amino-4-pyrimidones 1 and benzylidene Meldrum's acid derivatives 2 by cyclization reactions in boiling nitrobenzene. The structure of 5, determined by nmr measurements, reveals a selective orientation of 1 and 2 in the addition step.

Nitrobenzenechemistry.chemical_compoundPyrimidinoneschemistryOrganic chemistryGeneral MedicineMeldrum's acidChemInform
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Growth of polyoxymethylene crystals during cationic polymerization of trioxane in nitrobenzene

1973

Nitrobenzenechemistry.chemical_compoundTrioxanePolyoxymethyleneChemistryPolymer chemistryGeneral EngineeringCationic polymerizationGeneral Materials SciencePhotochemistryJournal of Polymer Science: Polymer Letters Edition
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First transformations of pyrano[3,4-b]indol-3-ones to salvadoricine and 2,3-diacylindoles

1992

The readily available methylated pyrano[3,4-b]indol-3-ones 1a and 1b were hydrolyzed to furnish the 2-acetylindol-3-alkanoic acids 2 and 4. Compound 2 was easily transformed selectively to 2-acetyl-3-methylindole (3, salvadoricine). Substrate 1b reacts with molecular oxygen from the air only in the presence of a catalyst to give 2,3-diacetylindole (5) while 1a reacts with nitrosobenzene via a proposed Diels-Alder step to yield 2-acetylindole-3-carbaldehyde (6). The latter product can also be obtained in low yield from the reaction of 1a with molecular oxygen from the air.

Nitrosobenzenechemistry.chemical_classificationchemistry.chemical_compoundHydrolysischemistryBicyclic moleculeYield (chemistry)Organic ChemistrySubstrate (chemistry)Organic chemistryMolecular oxygenLactoneCatalysisJournal of Heterocyclic Chemistry
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By-products in the rearrangement of N-methyl-N-phenylnitramine

1998

Abstract N-Methyl-N-phenylnitramine was rearranged in the aqueous dioxane — sulphuric acid mixture to 2-nitro- and 4-nitro-N-methylanilines. The isomer ratio was independent of the acidity within the range of −0.3 > Ho > −2.8. Some by-products were isolated and identified e.g. N-methyl-N-nitrosoaniline, its 2-nitro and 4-nitro derivatives, nitrosobenzene and 4′,4″-bis-(N-methylamino)-3′,3″-dinitrodiphenylmethane. The mechanism of the nitramine rearrangement is discussed.

Nitrosobenzenechemistry.chemical_compoundAqueous solutionchemistryOrganic ChemistryDrug DiscoveryOrganic chemistryBiochemistryMedicinal chemistryTetrahedron
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