Search results for "Azine"

showing 10 items of 1589 documents

Humic substances as catalysts in condensation reactions

2001

Humic substances (HS) demonstrate appreciable impact on the rate of the condensation reactions as shown in the example of the reaction between hydrazine and 4-(dimethylamino)-benzaldhyde in an aquatic environment. The catalytic activity of HS has also been demonstrated in Knoevenagel and Claisen-Schmidt reactions for condensation of carbonyl compounds with CH acids. The aquatic fulvic acids are the most active in these reactions. The velocity of the studied reactions also depends on pH, temperature, the concentration and origin of HS used. A possible micellar and acid-base catalysis mechanism in aquatic media has been suggested.

Environmental EngineeringChemical PhenomenaHealth Toxicology and MutagenesisHydrazineInorganic chemistryAldehydeCatalysisCatalysischemistry.chemical_compoundEnvironmental ChemistryOrganic chemistryHumic acidBenzopyransHumic Substanceschemistry.chemical_classificationClaisen condensationChemistry PhysicalCondensationTemperaturePublic Health Environmental and Occupational HealthGeneral MedicineGeneral ChemistryHydrogen-Ion ConcentrationCondensation reactionPollutionchemistryKnoevenagel condensationWater Pollutants ChemicalChemosphere
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Kinetics and metabolism of 14C-lindane and 14C-atrazine in early life stages of zebrafish (Brachydanio Rerio)

1990

Abstract Fertilized eggs, yolk sac larvae, and juveniles of zebrafish were exposed to 14C-lindane and 14C-atrazine under static conditions and the uptake was studied for a period of 48 hours. After 24 hours, a number of animals were transferred into pesticide-free running water and the elimination was examined for another 24 hours. The bioconcentration factors (BCFs) as well as the rate constants for uptake and elimination were calculated. Except for the lindane uptake by eggs and the atrazine uptake by juveniles, the steady state was reached within five hours. For all tested developmental stages the bioconcentration factor of lindane distinctly exceeded 100, whereas it was less than 10 in …

Environmental EngineeringHealth Toxicology and MutagenesisPublic Health Environmental and Occupational HealthBioconcentrationGeneral MedicineGeneral ChemistryMetabolismPesticideBiologyPollutionchemistry.chemical_compoundAnimal sciencemedicine.anatomical_structurechemistryEnvironmental chemistryToxicitymedicineEnvironmental ChemistryAtrazineSteady state (chemistry)Yolk sacLindaneChemosphere
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Transfer of hexazinone and glyphosate through undisturbed soil columns in soils under Christmas tree cultivation.

2004

Abstract Field studies monitoring pesticide pollution in the Morvan region (France) have revealed surface water contamination by some herbicides. The purpose of this study was to investigate in greater detail the transport of two herbicides, used in Christmas tree production in the Morvan, under controlled laboratory conditions. Thus, the leaching of hexazinone (3-cyclohexyl-6-dimethyl-amino-1-methyl-1,3,5-triazine-2,4 (1H,3H) dione) and glyphosate ( N -(phosphono-methyl-glycine)) through structured soil columns was studied using one loamy sand and two sandy loams from sites currently under Christmas tree cultivation in the Morvan. The three soils were cultivated sandy brunisol [Sound refer…

Environmental EngineeringHealth Toxicology and MutagenesisRainGlycineSoil scienceTreeschemistry.chemical_compoundSoilWorld Reference Base for Soil ResourcesEnvironmental ChemistryLeaching (agriculture)Organic ChemicalsCambisolHerbicidesTriazinesPublic Health Environmental and Occupational HealthGeneral MedicineGeneral ChemistrySoil carbonPollutionHexazinoneSoil contaminationCarbonchemistryAgronomyLoamSoil waterEnvironmental sciencePorosityWater Pollutants ChemicalEnvironmental MonitoringChemosphere
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Trimeprazine is enantioselectively degraded by an activated sludge in ready biodegradability test conditions

2018

[EN] A great number of available pharmaceuticals are chiral compounds. Although they are usually manufactured as racemic mixtures, they can be enantioselectively biodegraded as a result of microbial processes. In this paper, a biodegradability assay in similar conditions to those recommended in OECD tests of enantiomers of trimeprazine (a phenothiazine employed as a racemate) is carried out. Experiments were performed in batch mode using a minimal salts medium inoculated with an activated sludge (collected from a Valencian Waste Water Treatment Plant, WWTP) and supplemented with the racemate. The concentration of the enantiomers of trimeprazine were monitored by means of a chiral HPLC metho…

Environmental EngineeringTrimeprazineEnantioselectivity010501 environmental sciences01 natural scienceschemistry.chemical_compoundMonod equationCurve fittingCelluloseWaste Management and DisposalChromatography High Pressure Liquid0105 earth and related environmental sciencesWater Science and TechnologyCivil and Structural EngineeringChromatographySewageEcological ModelingBatch experiment010401 analytical chemistryBiodegradability testEnantioselective synthesisStereoisomerismAntipruriticsTrimeprazinePrecisionBiodegradationPollution0104 chemical sciencesChiral column chromatographyBiodegradation EnvironmentalActivated sludgechemistryEnantiomerWater Pollutants ChemicalWater Research
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On the activity of trifluoperazine and palmitoylcarnitine in mice: Delayed hypersensitivity models

2001

Abstract The effect of pre- and post-challenge treatments with trifluoperazine and palmitoylcarnitine, two protein kinase C (PKC) inhibitors characterised by their interaction with the phospholipid enzyme cofactor, on the inflammation caused by delayed hypersensitivity (DTH) to dinitrofluorobenzene (DNFB) and sheep red blood cells (SRBC) in mice is reported. The activity of dexamethasone and two immunosupressors, azathioprine and methotrexate, is also evaluated. The effectiveness of pre-treatment with each of the test drugs diminished when the DNFB challenge dose increased, whereas trifluoperazine and azathioprine were more active when administered after the challenge at the high DNFB dose.…

ErythrocytesAnti-Inflammatory Agentschemical and pharmacologic phenomenaInflammationTrifluoperazinePharmacologyDexamethasoneGeneral Biochemistry Genetics and Molecular BiologyMicechemistry.chemical_compoundAzathioprinemedicineAnimalsHypersensitivity DelayedEnzyme InhibitorsGeneral Pharmacology Toxicology and PharmaceuticsProtein Kinase CPalmitoylcarnitineProtein kinase CDexamethasoneSheepbusiness.industryPalmitoylcarnitineGeneral MedicineTrifluoperazineMethotrexatechemistryDelayed hypersensitivityDinitrofluorobenzeneFemaleMethotrexatemedicine.symptombusinessHaptenImmunosuppressive Agentsmedicine.drugLife Sciences
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Distribution of chlorpromazine in a simplified blood influenced by various drugs

1973

The binding of chlorpromazine to erythrocytes and to albumin as influenced by other drugs was studied in a simplified blood (31.5±0.3% bovine erythrocytes, 4 g-% bovine serum albumin in 0.02 M phosphate buffer solution containing 0.15 M NaCl). the total concentration of chlorpromazine in the simplified blood was 10−4 M, the concentration of the displacing drugs was 10−3 M. After an incubation period of 3 h at 22° C the chlorpromazine concentration was determined in the albumin solution after centrifugation of the blood at 3000×g and in the aqueous phase after ultracentrifugation at 150000×g. Under control conditions 68.1±0.9% of chlorpromazine was bound to the erythrocytes, 28.5±0.9% was bo…

ErythrocytesChlorpromazineIndomethacinSuraminBenzoatesBinding CompetitiveIncubation periodCoumarinsmedicineAnimalsDistribution (pharmacology)CentrifugationThiopentalBovine serum albuminChlorpromazinePharmacologySulfonamidesBinding SitesChromatographyQuininebiologyProbenecidChemistryFatty AcidsAqueous two-phase systemAlbuminSerum Albumin BovineGeneral MedicineChlorothiazideTetracyclineAntidepressive AgentsSalicylatesAcetazolamidePhenylbutazoneSolubilityPhenytoinbiology.proteinCattleUltracentrifugeDeoxycholic AcidProtein Bindingmedicine.drugNaunyn-Schmiedeberg's Archives of Pharmacology
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Swellable microparticles containing Suprofen: evaluation of in vitro release and photochemical behaviour

1998

Suprofen, an anti-inflammatory drug was incorporated in polymer networks based on biocompatible macromolecules, such as alpha,beta-polyasparthydrazide (PAHy) and alpha,beta-poly(N-hydroxyethyl)-DL-aspartamide (PHEA) crosslinked by glutaraldehyde or gamma-rays, respectively. Swelling tests carried out in aqueous media showed that pH value affects the swelling degree of the prepared hydrogels. In vitro release tests were performed in simulated gastrointestinal fluids (pH 1/6.8) using the pH variation method and in phosphate-buffered saline, pH 7.4. Experimental data indicated that Suprofen was released in a sustained way both from PAHy and PHEA microparticles. Further, incorporation of Suprof…

ErythrocytesPlasma SubstitutesSuprofenPharmaceutical ScienceSuprofenHemolysisDosage formchemistry.chemical_compoundmedicineHumansOrganic chemistryParticle SizeActive ingredientGastric JuicePhotosensitizing AgentsChromatographyAnti-Inflammatory Agents Non-SteroidalHydrogen-Ion ConcentrationNylonsCross-Linking ReagentsHydrazineschemistryGlutaralDelayed-Action PreparationsSelf-healing hydrogelsLiberationGlutaraldehydeSwellingmedicine.symptomPeptidesDrug carrierGelsmedicine.drugJournal of Controlled Release
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Convenient Access to α‐Amino‐ω‐Hydroxyl Heterobifunctional PEG and PPO via a Sacrificial Hexahydro‐Triazine Star Strategy

2019

The anionic ring opening polymerizations of ethylene oxide (EO) and propylene oxide (PO) are performed by using 1,3,5-triethanol hexahydro-1,3,5-triazine (TrAz) as a "sacrificial" trifunctional initiator. Well-defined three-arm star polymers are obtained with a narrow molecular weight distribution (M w /M n < 1.1). Molecular weights range from 3-15 kg mol-1 . Since these star polymers possess an acid-labile hexahydro-triazine core, acidic hydrolysis leads to cleavage of the arms. This gives access to well-defined α-amino-ω-hydroxyl heterobifunctional poly(ethylene glycol) (PEG) and poly(propylene oxide) (PPO) in the molecular weight range of 1-5 kg mol-1 and low dispersity M w /M n < 1.1. T…

Ethylene OxidePolymers and PlasticsPolymersDispersity02 engineering and technologyPolyethylene glycol010402 general chemistry01 natural sciencesPolymerizationchemistry.chemical_compoundPolyolPolymer chemistryMaterials ChemistryPropylene oxideTriazinechemistry.chemical_classificationEthylene oxideTriazinesOrganic Chemistry021001 nanoscience & nanotechnology0104 chemical sciencesMolecular WeightchemistryPropylene GlycolsMolar mass distributionEpoxy Compounds0210 nano-technologyEthylene glycolMacromolecular Rapid Communications
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Metal-organic magnets with large coercivity and ordering temperatures up to 242°C.

2020

International audience; Magnets derived from inorganic materials (e.g., oxides, rare-earth–based, and intermetallic compounds) are key components of modern technological applications. Despite considerable success in a broad range of applications, these inorganic magnets suffer several drawbacks, including energetically expensive fabrication, limited availability of certain constituent elements, high density, and poor scope for chemical tunability. A promising design strategy for next-generation magnets relies on the versatile coordination chemistry of abundant metal ions and inexpensive organic ligands. Following this approach, we report the general, simple, and efficient synthesis of light…

FabricationMaterials sciencemagneettiset ominaisuudetPyrazineMetal ions in aqueous solutionmagneetitIntermetallicNanotechnology02 engineering and technologyorganometalliyhdisteet010402 general chemistrylarge coercivity7. Clean energy01 natural sciencesordering temperaturesCoordination complexchemistry.chemical_compoundMoleculechemistry.chemical_classificationMultidisciplinarymetal-organic magnets[CHIM.MATE]Chemical Sciences/Material chemistrykompleksiyhdisteetCoercivity021001 nanoscience & nanotechnologykiteet0104 chemical scienceschemistryMagnetlämpötila0210 nano-technologyScience (New York, N.Y.)
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A History of the Pharmacological Treatment of Bipolar Disorder.

2018

In this paper, the authors review the history of the pharmacological treatment of bipolar disorder, from the first nonspecific sedative agents introduced in the 19th and early 20th century, such as solanaceae alkaloids, bromides and barbiturates, to John Cade&rsquo;s experiments with lithium and the beginning of the so-called &ldquo;Psychopharmacological Revolution&rdquo; in the 1950s. We also describe the clinical studies and development processes, enabling the therapeutic introduction of pharmacological agents currently available for the treatment of bipolar disorder in its different phases and manifestations. Those drugs include lithium salts, valproic acid, carbamazepine, new antiepilep…

Farmacología veterinariamedicine.drug_classPsychopharmacologyFarmacologíaantipsychotic drugsAtypical antipsychoticCariprazineReviewPharmacologyLamotrigineLithiumHistory 21st CenturyCatalysisTreatment of bipolar disorderInorganic Chemistrylcsh:Chemistry03 medical and health scienceschemistry.chemical_compound0302 clinical medicinepharmacological treatmentmedicineAsenapineAnimalsHumansZiprasidoneantiepileptic drugsPhysical and Theoretical ChemistryMolecular Biologylcsh:QH301-705.5SpectroscopyPsiquiatríaLurasidonebipolar disorderbusiness.industrymood stabilizer drugsOrganic ChemistryHistory 19th CenturyGeneral MedicineHistory 20th Century030227 psychiatryComputer Science ApplicationsTranquilizing Agentschemistrylcsh:Biology (General)lcsh:QD1-999Quetiapinebusiness030217 neurology & neurosurgerymedicine.drug
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