Search results for "Conjugate"

showing 10 items of 644 documents

Immunochemical rapid determination of quinoxyfen, a priority hazardous pollutant

2018

In 2013, quinoxyfen was included in the list of priority hazard pollutants of the European Water Framework Directive due to its toxicity to aquatic organisms. However, few analytical methods for the analysis of this fungicide have been reported and no rapid immunochemical methods have been published so far. In the present study, immunoreagents for quinoxyfen analysis were generated for the first time and an enzyme-linked immunosorbent assay was developed. Two carboxylated derivatives of quinoxyfen were designed on the basis of the minimum energy conformation of the target compound. Active esters of those novel compounds were prepared using N,N′-disuccinimidyl carbonate, and purified for cov…

Environmental EngineeringHealth Toxicology and MutagenesisEnzyme-Linked Immunosorbent Assay010501 environmental sciencesMass spectrometry01 natural sciencesMass SpectrometryAntibodiesAquatic organismsmedicineEnvironmental ChemistryWater pollutant0105 earth and related environmental sciencesDetection limitPollutantImmunoassayChromatographyBioconjugationmedicine.diagnostic_testChemistry010401 analytical chemistryPublic Health Environmental and Occupational HealthGeneral MedicineGeneral ChemistryPollution0104 chemical sciencesFungicides IndustrialBioconjugatesHaptenImmunoassayQuinolinesImmunochemical methodsHaptenHaptensWater Pollutants ChemicalConjugate
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Synthesis and Structure-Activity Relationships of Amino Acid Conjugates of Cholanic Acid as Antagonists of the EphA2 Receptor

2013

The Eph–ephrin system plays a critical role in tumor growth and vascular functions during carcinogenesis. We had previously identified cholanic acid as a competitive and reversible EphA2 antagonist able to disrupt EphA2-ephrinA1 interaction and to inhibit EphA2 activation in prostate cancer cells. Herein, we report the synthesis and biological evaluation of a set of cholanic acid derivatives obtained by conjugation of its carboxyl group with a panel of naturally occurring amino acids with the aim to improve EphA2 receptor inhibition. Structure-activity relationships indicate that conjugation of cholanic acid with linear amino acids of small size leads to effective EphA2 antagonists whereas …

EphA2 antagonistsStereochemistryStructure-activity relationship studiesPharmaceutical Sciencemedicine.disease_causeArticleProtein Structure SecondaryAnalytical Chemistrylcsh:QD241-441Inhibitory Concentration 50Structure-Activity Relationshipchemistry.chemical_compoundamino acid conjugateslcsh:Organic chemistryEphA2 anatgonistscholanic acid; amino acid conjugates; EphA2 antagonists; structure-activity relationshipsCell Line TumorDrug DiscoveryAromatic amino acidsmedicineHumansPhosphorylationPhysical and Theoretical ChemistryReceptorbile acids; EphA2 anatgonists; Structure-activity relationship studies; amino acid conjugatesbile acidschemistry.chemical_classificationBinding SitesReceptor EphA1Receptor EphA2structure-activity relationshipsOrganic ChemistryAntagonistCholic AcidsHydrogen BondingEPH receptor A2Amino acidMolecular Docking SimulationCholanic acidcholanic acidchemistryBiochemistryChemistry (miscellaneous)Molecular MedicineCarcinogenesisProtein Processing Post-TranslationalProtein BindingConjugateMolecules
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Glycoconjugate expression in the extracellular matrix of the mouse lung (87.7)

2014

Extracellular matrixchemistry.chemical_classificationchemistryGlycoconjugateGeneticsMouse LungMolecular BiologyBiochemistryBiotechnologyCell biologyThe FASEB Journal
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Firing characteristics of vestibular nuclei neurons in the alert monkey after bilateral vestibular neurectomy

1992

After destruction of the peripheral vestibular system which is not activated by moving large-field visual stimulation, not only labyrinthine-ocular reflexes but also optokinetic-ocular responses related to the "velocity storage" mechanism are abolished. In the normal monkey optokinetic-ocular responses are reflected in sustained activity changes of central vestibular neurons within the vestibular nuclei. To account for the loss of optokinetic responses after labyrinthectomy, inactivation of central vestibular neurons consequent on the loss of primary vestibular activity is assumed to be of major importance. To test this hypothesis we recorded the neural activity within the vestibular nuclea…

Eye Movementsgenetic structuresWheat Germ AgglutininsWheat Germ Agglutinin-Horseradish Peroxidase ConjugateVestibular NerveSmooth pursuitVestibular nucleiotorhinolaryngologic diseasesAnimalsHorseradish PeroxidaseNeuronsVestibular systemHistocytochemistryMuscimolGeneral NeuroscienceVestibular pathwayAnatomyOptokinetic reflexVestibular NucleiMacaca mulattaElectrophysiologyEar InnerReflexsense organsVestibulo–ocular reflexPsychologyNeurosciencePhotic StimulationExperimental Brain Research
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A second-order sparse factorization method for Poisson's equation with mixed boundary conditions

1992

Abstract We propose an algorithm for solving Poisson's equation on general two-dimensional regions with an arbitrary distribution of Dirichlet and Neumann boundary conditions. The algebraic system, generated by the five-point star discretization of the Laplacian, is solved iteratively by repeated direct sparse inversion of an approximating system whose coefficient matrix — the preconditioner — is second-order both in the interior and on the boundary. The present algorithm for mixed boundary value problems generalizes a solver for pure Dirichlet problems (proposed earlier by one of the authors in this journal (1989)) which was found to converge very fast for problems with smooth solutions. T…

Fast solverPreconditionerfactorization methodApplied MathematicsMathematical analysisBoundary (topology)Dirichlet and Neumann conditionsMixed boundary conditionPreconditioned Conjugate Gradient methodComputational Mathematicssymbols.namesakeDirichlet boundary conditionConjugate gradient methodgeneral regionsNeumann boundary conditionsymbolsBoundary value problemPoisson's equationMathematicsJournal of Computational and Applied Mathematics
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On irreducible products of characters

2021

Abstract We study the problem when the product of two non-linear Galois conjugate characters of a finite group is irreducible. We also prove new results on irreducible tensor products of cross-characteristic Brauer characters of quasisimple groups of Lie type.

Finite groupPure mathematicsAlgebra and Number Theory010102 general mathematicsType (model theory)01 natural sciencesTensor productProduct (mathematics)0103 physical sciences010307 mathematical physics0101 mathematicsMathematics::Representation TheoryMathematicsConjugateJournal of Algebra
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Local Effects of Longitudinal Heat Conduction in Plate Heat Exchangers

2007

Abstract In a plate heat exchanger, heat transfer from the hot to the cold fluid is a multi-dimensional conjugate problem, in which longitudinal heat conduction (LHC) along the dividing walls often plays some role and can not be neglected. Large-scale , or end-to-end, LHC is always detrimental to the exchanger’s effectiveness. On the contrary, if significant non-uniformities exist in the distribution of either convective heat transfer coefficient, small-scale , or local, LHC may actually enhance the exchanger’s performance by improving the thermal coupling between high heat transfer spots located on the opposite sides of the dividing wall.

Fluid Flow and Transfer ProcessesMaterials scienceConvective heat transferMechanical Engineeringlongitudinal heat conductionPlate heat exchangerThermodynamicsconjugate heat transferHeat transfer coefficientMechanicsHeat sinkCondensed Matter Physicsplate heat exchangerHeat transferHeat spreaderMicro heat exchangerPlate fin heat exchangerSettore ING-IND/19 - Impianti Nucleari
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Self-pumped phase conjugation in a BaTiO3:Rh waveguide

2002

We present a self-pumped phase conjugator originated by self-bending of the incident beam at λ = 515 nm in a BaTiO3:Rh waveguide elaborated by three successive He+ ion implantations. Phase conjugate reflectivity reached is 28 %.

Four-wave mixingWaveguide (electromagnetism)Materials sciencebusiness.industryPhase (matter)Incident beamOptoelectronicsPhase conjugationbusinessReflectivityIonConjugateNonlinear Guided Waves and Their Applications
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3,6-Bis(2-arylethenyl)-1,2,4,5-tetrazine - Synthese, Fl�ssigkristallinit�t und Photochemie

1995

3,6-Bis(2-arylethenyl)-1,2,4,5-tetrazines - Synthesis, LC Properties and Photochemistry The (E,E)-3,6-Bis(2-arylethenyl)-1,2,4,5-tetrazines 8 were prepared in a synthetic sequence starting with aromatic aldehydes 1 and cinnamic acids 2, respectively (Scheme 1). The rod-like conjugated molecules represent calamitic mesogens as well as extended chromophores. Hence, we investigated the formation of liquid crystals, achieved by the introduction of long flexible side chains, and the photochemical behaviour that is characterized by the fragmentation of the central ring (Scheme 3).

Fragmentation (mass spectrometry)Liquid crystalChemistryPolymer chemistrySide chainMoleculeSequence (biology)Conjugated systemChromophoreRing (chemistry)Journal f�r Praktische Chemie/Chemiker-Zeitung
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Of Thiols and Disulfides: Methods for Chemoselective Formation of Asymmetric Disulfides in Synthetic Peptides and Polymers.

2018

In protein or peptide chemistry, thiols are frequently chosen as a chemical entity for chemoselective modification reactions. Although it is a well-established methodology to address cysteines and homocysteines in aqueous media to form S-C bonds, possibilities for the chemoselective formation of asymmetric disulfides have been less approached. Focusing on bioreversibility in conjugation chemistry, the formation of disulfide bonds is highly desirable for the attachment of thiol-containing bioactive agents to proteins or in cross-linking reactions, because disulfide bonds can combine stability in blood with degradability inside cells. In this Concept article, recent approaches in the field of…

Free RadicalsPolymersPeptide02 engineering and technologyConjugated system010402 general chemistryMicroscopy Atomic Force01 natural sciencesCatalysisPolymerizationReactivity (chemistry)DisulfidesSulfhydryl CompoundsProtecting groupSolid-Phase Synthesis Techniqueschemistry.chemical_classificationAqueous mediumOrganic ChemistryGeneral ChemistryPolymer021001 nanoscience & nanotechnologyCombinatorial chemistry0104 chemical scienceschemistryThiolQuantum TheorySelf-assembly0210 nano-technologyPeptidesChemistry (Weinheim an der Bergstrasse, Germany)
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