Search results for "ethylenediamine"

showing 10 items of 142 documents

EGTA treatment causes the synthesis of heat shock proteins in sea urchin embryos.

2000

Paracentrotus lividus embryos, at post-blastular stage, when subjected to a rise in temperature from physiologic (20 degrees C) to 31 degrees C, synthesize a large group of heat shock proteins (hsps), and show a severe inhibition of bulk protein synthesis. We show, by mono- and two-dimensional electrophoresis, that also EGTA (ethylene glycol-bis[beta-aminoethyl ether] tetraacetic acid) treatment induces in sea urchin embryos both marked inhibition of bulk protein synthesis and the synthesis of the entire set of hsps. Furthermore, EGTA-treated sea urchin embryos are able to survive at a temperature otherwise lethal (35 degrees C) becoming thermotolerant. Because incubation with a different c…

Embryo NonmammalianbiologyEthylenediaminetetraacetic acidbiology.organism_classificationParacentrotus lividuschemistry.chemical_compoundEGTAchemistryBiochemistrybiology.animalHeat shock proteinSea UrchinsProtein biosynthesisBiophysicsAnimalsChelationElectrophoresis Gel Two-DimensionalMolecular BiologySea urchinIncubationEgtazic AcidEdetic AcidHeat-Shock ProteinsChelating AgentsMolecular cell biology research communications : MCBRC
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Behaviour of EDTA in marine microcosms

2000

Laboratory-scale microcosm tests were carried out in sea water with and without sediment to investigate the importance of ultraviolet (UV) light and microbes in the temperature-dependent degradation of metal complexes of ethylenediaminetetraacetic acid (EDTA). After 17 weeks, 44% and 48% of the original EDTA (initial concentration 385 microg/L) were converted at 10 degrees C and 22 degrees C, respectively. The degradation was more influenced by UV light than by sediment microbes, although the latter were very important. At both temperatures, absorption of EDTA to the sediment phase reached a maximum in the initial stage of the experiments (4 weeks): at 10 degrees C about 4% and at 22 degree…

Environmental EngineeringHealth Toxicology and MutagenesisPublic Health Environmental and Occupational HealthEnvironmental engineeringSedimentEthylenediaminetetraacetic acidGeneral MedicineGeneral ChemistryBiodegradationPollutionchemistry.chemical_compoundchemistryEnvironmental chemistryEnvironmental ChemistryDegradation (geology)SeawaterChelationWater pollutionMicrocosmChemosphere
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Palladium on pumice: new catalysts for the stereoselective semihydrogenation of alkynes to (Z)-alkenes

2001

Abstract High selectivities (93–99%) and excellent stereoselectivities (>99%) in the semihydrogenation of CC triple bonds were achieved using palladium on pumice with a metal loading of 0.5, 1.5 or 3.0% wt as catalyst. The reactions were carried out in ethanol or tetrahydrofuran with only 2.5% of ethylenediamine allowing a self-terminating semihydrogenation independently on the CC triple bond.

EthanolOrganic Chemistrychemistry.chemical_elementEthylenediamineTriple bondBiochemistryCatalysischemistry.chemical_compoundchemistryPumiceDrug DiscoveryPolymer chemistryStereoselectivityTetrahydrofuranPalladiumTetrahedron Letters
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ChemInform Abstract: Palladium on Pumice: New Catalysts for the Stereoselective Semihydrogenation of Alkynes to (Z)-Alkenes.

2010

Abstract High selectivities (93–99%) and excellent stereoselectivities (>99%) in the semihydrogenation of CC triple bonds were achieved using palladium on pumice with a metal loading of 0.5, 1.5 or 3.0% wt as catalyst. The reactions were carried out in ethanol or tetrahydrofuran with only 2.5% of ethylenediamine allowing a self-terminating semihydrogenation independently on the CC triple bond.

Ethanolchemistry.chemical_elementEthylenediamineGeneral MedicineTriple bondCatalysischemistry.chemical_compoundchemistryPumicePolymer chemistryOrganic chemistryStereoselectivityTetrahydrofuranPalladiumChemInform
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Determination of Kinetic and Thermochemical Parameters of a Substitution Reaction at a Square-Planar Palladium(II) Complex in Water/AOT/n-Heptane Mic…

1995

Abstract The substitution reaction [Pd(bipy)(en)] 2+ + en → [Pd(en) 2 ] 2+ + bipy (where bipy = 2,2′-bipyridine and en = ethylenediamine) has been studied in water and water/AOT/ n -heptane microemulsions at various values of the molar ratio R ( R = [water]/[AOT]) by flow microcalorimetry. From calorimetric data, molar enthalpies of reaction and rate constants were obtained. These quantities indicate that, by increasing R , the reaction becomes less exothermic and its rate constant decreases, trending to the value observed in water. These features can be reasonably rationalized in terms of the peculiar solvation state of reactants inside the AOT reversed micelles and/or the peculiar physico…

Exothermic reactionIsothermal microcalorimetryHeptaneChemistryEnthalpySolvationEthylenediamineSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsBiomaterialschemistry.chemical_compoundColloid and Surface ChemistryReaction rate constantOrganic chemistryPhysical chemistryMicroemulsionJournal of Colloid and Interface Science
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Application of graphene quantum dots in heavy metals and pesticides detection

2020

Graphene Quantum Dots (GQDs) were produced using electrochemical oxidation of graphite rods. Obtained GQDs were gamma-irradiated in the presence of the N atoms source, ethylenediamine. Both structural and morphological changes were investigated using UV-Vis, X-ray photoelectron and photoluminescence (PL) spectroscopy as well as atomic force microscopy. The ability of both types of dots to change PL intensity in the presence of pesticides such as malathion and glyphosate, as well as copper (II) ions was detected. These preliminary results indicated a high potential of produced GQDs to be applied as non-enzymatic PL sensors for the detection of selected pesticides and metal ions. 26th Interna…

Graphene Quantum DotsX-ray photoelectron spectroscopymalathionatomic force microscopyphotoluminescence sensorsUV-Vis spectroscopycopper (II) ionglyphosatephotoluminescence spectroscopyGraphene Quantum Dotelectrochemical oxidationethylenediaminecopper (II) ionsgraphite rodgraphite rods
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Study of supramolecular structures released from the cell wall of Candida albicans by ethylenediamine treatment

1996

Candida albicans cell wall components were analyzed by ethylenediamine (EDA) treatment. Based on their different solubility properties, the cell wall components produced three fractions (A, B, and C). Fractions B (EDA-soluble, water-insoluble) and C (EDA-insoluble) contained glucan, chitin, and protein in different proportions. After zymolyase (mainly a beta-glucanase complex) or chitinase treatment of fractions B and C, more polysaccharides and proteins were solubilized by a second EDA treatment, suggesting that the solubility of the polymers in EDA depends on the degree of polymer interactions. Western blot analysis using two monoclonal antibodies (1B12 and 4C12) revealed electrophoretic …

HydrolasesBlotting WesternChitinCalcofluor-whitePolysaccharideBiochemistryMicrobiologyFungal ProteinsCell wallchemistry.chemical_compoundAgglutininChitinCell WallPolysaccharidesCandida albicansGeneticsCandida albicansGlucansMolecular BiologyGlucanchemistry.chemical_classificationbiologyChitinasesGeneral MedicineEthylenediaminesbiology.organism_classificationMicroscopy ElectronMicroscopy FluorescenceBiochemistrychemistryChitinasebiology.proteinArchives of Microbiology
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Chemoselective heterogeneous iridium catalyzed hydrogenation of cinnamalaniline

2020

International audience; Selective hydrogenation of unsaturated imines over heterogeneous catalysts is an ecologically feasible and effective way to produce commercially valuable saturated imines and unsaturated amines under mild conditions, avoiding the utilization of toxic halides. The liquid-phase hydrogenation of a model imine, cinnamalaniline, over Ir, Ru, Pd and Au catalysts was studied in polar protic (methanol, 2-propanol), polar aprotic (methyl tert-butyl ether) and non-polar aprotic (toluene) solvents at 40-80°C under atmospheric hydrogen pressure. Different metal oxides (Al 2 O 3 , ZrO 2 , SiO 2) and carbon composites based on carbon nitrides synthesized by pyrolysis of ethylenedi…

Iminechemistry.chemical_elementEthylenediamineplatinametallit010402 general chemistry01 natural sciences7. Clean energyCatalysisCatalysischemistry.chemical_compoundkatalyytitOrganic chemistryIridiumtyppiyhdisteetChemoselectivityhydrausorgaaniset yhdisteetkemiallinen synteesi010405 organic chemistry0104 chemical sciencesSolvent[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistrychemistry13. Climate actionkatalyysiAmine gas treatingMethanol
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In vitro evaluation of poloxamer in situ forming gels for bedaquiline fumarate salt and pharmacokinetics following intramuscular injection in rats

2019

Graphical abstract

In situPO Propylene oxideIV IntravenousP338 Poloxamer 338lcsh:RS1-441Pharmaceutical Sciencechemistry.chemical_compoundn Sample sizeSD Standard deviationIM Intramuscularchemistry.chemical_classificationC0 Analyte plasma concentration at time zeroDoE Design of experimentsUV UltravioletPharmacology. TherapyK2.EDTA Potassium ethylenediaminetetraacetic acidLC–MS/MS Liquid chromatography-tandem mass spectrometryH&E Hematoxylin and eosintmax Sampling time to reach the maximum observed analyte plasma concentrationIn situ forming gelsCMC Critical micellar concentrationCmax Maximum observed analyte plasma concentrationIntramuscular injectionDN Dose normalizedGPT Gel point temperaturePLGA Poly-(DL-lactic-co-glycolic acid)TFA Trifluoroacetic acidCAN AcetonitrileATP Adenosine 5′ triphosphateSalt (chemistry)Polyethylene glycolPoloxamerArticlelcsh:Pharmacy and materia medicaPharmacokineticsIn vivoUHPLC Ultra-high performance liquid chromatographyPharmacokineticsAUClast Area under the analyte concentration versus time curve from time zero to the time of the last measurable (non-below quantification level) concentrationEO Ethylene oxideNMP N-methyl-2-pyrrolidoneComputingMethodologies_COMPUTERGRAPHICSAUC∞ Area under the analyte concentration vs time curve from time zero to infinite timeP407 Poloxamer 407In vitro releasePoloxamerCMT Critical micellar temperatureGel erosionIn vitrot1/2 Apparent terminal elimination half-lifechemistryMDR-TB Multi-drug resistant tuberculosisAUC80h Area under the analyte concentration versus time curve from time zero to 80 htlast Sampling time until the last measurable (non-below quantification level) analyte plasma concentrationMRM Multiple reaction monitoringNuclear chemistrySustained releaseInternational Journal of Pharmaceutics: X
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Sequestering ability of some chelating agents towards methylmercury(II).

2013

A study on the interactions between CH3Hg+ and some S, N and O donor ligands (2-mercaptopropanoic acid (thiolactic acid (H2 TLA)), 3-mercaptopropanoic acid (H2 MPA), 2-mercaptosuccinic acid (thiomalic acid (H3 TMA)), d,l-penicillamine (H2 PSH), l-cysteine (H2 CYS), glutathione (H3 GSH), N,N′-bis(3-aminopropyl)-1-4-diaminobutane (spermine (SPER)), 1,2,3,4,5,6-benzenehexacarboxylic acid (mellitic acid (H6 MLT)) and ethylenediaminetetraacetic acid (H4 EDTA)) is reported. The speciation models in aqueous solution and the possible structures of the complexes formed are discussed on the basis of potentiometric, calorimetric, UV spectrophotometric and electrospray mass spectrometric results. For t…

Inorganic chemistryElectrospray ionisation mass spectrometry (ESI-MS)Ethylenediaminetetraacetic acidCalorimetryBiochemistrySequestering ability of S N and O donor ligandAnalytical Chemistrychemistry.chemical_compoundHydrolysisSettore CHIM/01 - Chimica AnaliticaChelationMellitic acidThiomalic acidEnvironmental Restoration and RemediationChelating AgentsThiolactic acidAqueous solutionMolecular StructureLigandMethylmercury(II) cationMethylmercury CompoundsKineticschemistryMethylmercury(II) cation; Sequestering ability of S; N and O donor ligands; UV–spectrophotometry; Electrospray ionisation mass spectrometry (ESI-MS); PotentiometryPotentiometryEnvironmental PollutantsUV–spectrophotometryNuclear chemistryAnalytical and bioanalytical chemistry
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