Search results for "carbamate"

showing 10 items of 219 documents

Genetic transfer of the mcd gene in soil.

2003

Aims: To investigate the role of horizontal gene transfer of mcd (methylcarbamate-degrading) gene in high genetic diversity of carbofuran-degrading bacteria. Methods and Results: The actuality of genetic transfer from degraders to an Agrobacterium tumefaciens strain was determined in liquid medium. The mcd gene was chosen for transfer experiments. Transconjugants were obtained irrespective of the type of the donor strain (Gram-positive or Gram-negative), size of the inoculum, or nature and concentration of the pesticide in the medium. Soil microcosms, inoculated with or without the donor and/or recipient strains were used. The size of the initial degrading population (treated or untreated s…

Gene Transfer HorizontalAgrobacteriumPopulationApplied Microbiology and BiotechnologyCARBOFURANEMicrobiologyCarbofuranPseudomonaseducation[SDV.MP] Life Sciences [q-bio]/Microbiology and ParasitologySoil MicrobiologyElectrophoresis Agar Geleducation.field_of_studybiologyStrain (chemistry)Genetic transferPseudomonasGeneral MedicineAgrobacterium tumefaciensbiology.organism_classification[SDV.MP]Life Sciences [q-bio]/Microbiology and ParasitologyBiodegradation EnvironmentalAgrobacterium tumefaciensGenes BacterialConjugation GeneticHorizontal gene transferCarbamatesBacteriaBiotechnologyJournal of applied microbiology
researchProduct

Eel ATPase activity as biomarker of thiobencarb exposure

2003

Abstract European eels ( Anguilla anguilla ) were exposed to a sublethal thiobencarb concentration of 0.22 mg/L in a flow-through system for 96 h. Mg 2+ and Na + –K + adenosine triphosphatase (ATPase) activities were evaluated in gill and muscle tissues at 2, 12, 24, 48, 72, and 96 h of thiobencarb exposure. Gill ATPase activities were rapidly inhibited from 2 h of contact onward. Highest inhibition was registered for Na + , K + -ATPase (85%) from 2 to 12 h. Both Mg 2+ and total ATPase were inhibited (>73%) during the first hours of toxicant exposure. At the end of the exposure period (96 h) ATPase activities were still different from those of the controls (>50%). Significant inhibition was…

GillsMuscle tissueGillmedicine.medical_specialtyHealth Toxicology and MutagenesisATPasechemistry.chemical_compoundThiocarbamatesAnguillidaeInternal medicinemedicineAnimalsTissue DistributionMuscle SkeletalAdenosine Triphosphataseschemistry.chemical_classificationbiologyHerbicidesPublic Health Environmental and Occupational HealthEnvironmental ExposureGeneral MedicineAnguillabiology.organism_classificationPollutionmedicine.anatomical_structureEnzymeEndocrinologychemistryBiochemistryEnzyme inhibitorToxicitybiology.proteinBiomarkersWater Pollutants ChemicalToxicantEcotoxicology and Environmental Safety
researchProduct

Gold-Catalyzed Intramolecular Hydroamination of o-Alkynylbenzyl Carbamates: A Route to Chiral Fluorinated Isoindoline and Isoquinoline Derivatives

2013

Enantiomerically pure fluorinated isoindoline and dihydroisoquinoline scaffolds have been prepared through a diastereoselective addition of fluorinated nucleophiles to Ellman’s N-(tert-butanesulfinyl)imines followed by a sequence of Sonogashira cross-coupling/gold(I)-catalyzed cycloisomerization of the corresponding carbamate. A more favored 5-exo-dig mechanism was observed mainly due to an electronic effect of the fluorinated group.

Hydrocarbons FluorinatedMolecular StructureChemistryOrganic ChemistrySonogashira couplingStereoisomerismIsoindolineIsoindolesIsoquinolinesBiochemistryMedicinal chemistryCatalysischemistry.chemical_compoundCycloisomerizationNucleophileIntramolecular forceElectronic effectOrganic chemistryHydroaminationCarbamatesGoldPhysical and Theoretical ChemistryIsoquinolineAmines
researchProduct

Validation of Dissolution Testing with Biorelevant Media: An OrBiTo Study.

2017

Dissolution testing with biorelevant media has become widespread in the pharmaceutical industry as a means of better understanding how drugs and formulations behave in the gastrointestinal tract. Until now, however, there have been few attempts to gauge the reproducibility of results obtained with these methods. The aim of this study was to determine the interlaboratory reproducibility of biorelevant dissolution testing, using the paddle apparatus (USP 2). Thirteen industrial and three academic laboratories participated in this study. All laboratories were provided with standard protocols for running the tests: dissolution in FaSSGF to simulate release in the stomach, dissolution in a singl…

IndolesInterlaboratory reproducibilityChemistry PharmaceuticalPhenylcarbamatesPharmaceutical ScienceIbuprofen02 engineering and technologyPharmacology030226 pharmacology & pharmacyBiopharmaceuticsTosyl Compounds03 medical and health sciences0302 clinical medicineDrug DiscoveryIntestine SmallDissolution testingTransfer modelDissolutionSulfonamidesChromatographyChemistryReproducibility of ResultsHydrogen-Ion Concentration021001 nanoscience & nanotechnologyDrug LiberationSolubilityGastric MucosaMolecular Medicine0210 nano-technologyTabletsMolecular pharmaceutics
researchProduct

Organometallic Nickel(II) Complexes Containing Thiolate and Dithiocarbamate Ligands

2000

Inorganic Chemistrychemistry.chemical_classificationNickelChemistryOrganic chemistrychemistry.chemical_elementBioinorganic chemistryDithiocarbamateEuropean Journal of Inorganic Chemistry
researchProduct

Effects of four carbamate compounds on antioxidant parameters

2009

Abstract The effect of four carbamates, aldicarb and its metabolites (aldicarb sulfone and aldicarb sulfoxide) and propoxur on glutathione content and the activity of the enzymes involved in the sulfur-redox cycle in the mammalian cellular model CHO-K1 cells after 24-h exposure were determined. Carbamate exposure resulted in a depletion of intracellular reduced glutathione (GSH) content, no change was observed in oxidized glutathione (GSSG) and a decrease in GSH/GSSG ratio was detected. After carbamates exposition a GSH/GSSG decreases in ranged from 12.44% to 21.35% of control was observed. Depletion of GSH levels was accompanied by the induction of glutathione reductase (GR) after 24 h exp…

InsecticidesCarbamateAntioxidantAldicarbHealth Toxicology and Mutagenesismedicine.medical_treatmentGlutathione reductaseCHO CellsPropoxurmedicine.disease_causeAntioxidantschemistry.chemical_compoundCricetulusCricetinaemedicineAnimalschemistry.chemical_classificationGlutathione PeroxidaseGlutathione DisulfideGlutathione peroxidasePublic Health Environmental and Occupational HealthGeneral MedicineGlutathionePropoxurGlutathionePollutionOxidative StressGlutathione ReductasechemistryBiochemistryEnzyme InductionAldicarbOxidative stressEcotoxicology and Environmental Safety
researchProduct

Flow-Injection Spectrophotometric Determination of Phenolic Drugs and Carbamate Pesticides by Coupling with Diazotized 2,4,6-Trimethylaniline

1999

Abstract A flow-injection (FI) spectrophotometric system is proposed for the determination of phenols and carbamates. In the FI manifolds, the solutions of phenols or carbamates (the latter after hydrolysis with NaOH) were injected into a diazonium ion carrier stream at pH 9.5 (buffered with tetrahydroborate), which was formed by mixing 2,4,6-trimethylaniline (TMA) with nitrate in a sodium dodecyl sulfate aqueous micellar medium. Absorbance was measured at 550 nm. The system combines the advantages derived from the use of TMA for the coupling of phenols in basic micellar media, because of the inhibition of the self-coupling reaction of the reagent, with the precision and speed of the FI pro…

InsecticidesCarbamateEpinephrineMethiocarbmedicine.medical_treatmentAnalytical Chemistrychemistry.chemical_compoundPhenolsmedicineEnvironmental ChemistryPhenolsSodium dodecyl sulfateAcetaminophenPharmacologyFlow injection analysisAniline CompoundsChromatographyAqueous solutionHerbicidesGuaiacolWaterDiazonium CompoundsHydrogen-Ion ConcentrationPharmaceutical PreparationschemistrySpectrophotometryReagentFlow Injection AnalysisPromecarbIndicators and ReagentsCarbamatesAgronomy and Crop ScienceFood ScienceJournal of AOAC INTERNATIONAL
researchProduct

Assessment of Pesticide Residues in Honey Samples from Portugal and Spain

2003

Fifty samples of honey collected from local markets of Portugal and Spain during year 2002 were analyzed for 42 organochlorine, carbamate, and organophosphorus pesticide residues. An analytical procedure based on solid-phase extraction with octadecyl sorbent followed by gas chromatography-mass spectrometry (GC-MS), for organochlorines, and by liquid chromatography-atmospheric pressure chemical ionization-mass spectrometry (LC-APCI-MS), for organophosphorus and carbamates, has been developed. Recoveries of spiked samples ranged from 73 to 98%, except for dimethoate (40%), with relative standard deviations from 3 to16% in terms of repeatability, and from 6 to 19% in terms of reproducibility. …

InsecticidesChromatographyPesticide residueMethiocarbPortugalPesticide ResiduesGeneral ChemistryMethidathionHoneyPesticidePirimicarbSensitivity and Specificitychemistry.chemical_compoundOrganophosphorus CompoundschemistrySpainCarbarylParathion methylHydrocarbons ChlorinatedCarbamatesGeneral Agricultural and Biological SciencesCarbofuran
researchProduct

Solid-phase microextraction-liquid chromatography-mass spectrometry applied to the analysis of insecticides in honey

2007

An approach based on solid-phase microextraction-liquid chromatography-mass spectrometry (SPME-LC-MS) has been developed for determining 12 insecticides (bromophos ethyl, chlorpyrifos methyl, chlorpyrifos ethyl, diazinon, fenoxycarb, fonofos, phenthoate, phosalone, pirimiphos methyl, profenofos, pyrazophos, and temephos) in honey. The influence of several parameters on the efficiency of the SPME was systematically investigated. Under optimal conditions, the procedure provided excellent linearity (>0.990), detection and quantification limits (between 0.001 and 0.1 microg g(-1) and between 0.005 and 0.5 microg g(-1), respectively), and precision (<19% at the quantification limits and from 6 t…

InsecticidesDiazinonHealth Toxicology and MutagenesisFonofosToxicologySolid-phase microextractionMass Spectrometrychemistry.chemical_compoundOrganophosphorus CompoundsLiquid chromatography–mass spectrometryPhosaloneSolid Phase MicroextractionChromatographyPyrazophosPesticide ResiduesPublic Health Environmental and Occupational HealthPirimiphos-methylHoneyGeneral ChemistryGeneral MedicinechemistryLinear ModelsCarbamatesMaximum Allowable ConcentrationPhenthoateChromatography LiquidFood ScienceFood Additives &amp; Contaminants: Part A
researchProduct

PERSISTENCE OF SOME PESTICIDES IN THE AQUATIC ENVIRONMENT

1992

InsecticidesEcologyHealth Toxicology and MutagenesisWaterGeneral MedicinePesticideToxicologyPollutionPersistence (computer science)Aquatic toxicologychemistry.chemical_compoundchemistryDrug StabilityAquatic environmentSpainThiocarbamatesDiazinonEnvironmental scienceWater qualityPesticidesWater pollutionEndosulfanEndosulfanHexachlorocyclohexaneWater Pollutants Chemical
researchProduct