Search results for "Tetra"

showing 10 items of 6481 documents

Identification of Potential Distinguishing Markers for the Use of Cannabis-Based Medicines or Street Cannabis in Serum Samples

2021

Increasing prescription numbers of cannabis-based medicines raise the question of whether uptake of these medicines can be distinguished from recreational cannabis use. In this pilot study, serum cannabinoid profiles after use of cannabis-based medicines were investigated, in order to identify potential distinguishing markers. Serum samples after use of Sativex®, Dronabinol or medical cannabis were collected and analyzed for 18 different cannabinoids, using a validated liquid chromatography-tandem mass spectrometry (LC-MS/MS) method. Analytes included delta-9-tetrahydrocannabinol, 11-hydroxy-tetrahydrocannabinol, 11-nor-9-carboxy-tetrahydrocannabinol, cannabidiol, cannabinol, cannabigerol, …

Cannabigerolprincipal component analysisEndocrinology Diabetes and MetabolismTetrahydrocannabivarin01 natural sciencesBiochemistryMicrobiologyArticleCannabicyclol03 medical and health sciencesCannabichromenechemistry.chemical_compoundcannabinoids0302 clinical medicinemedicineserum concentrations030216 legal & forensic medicineDronabinolLC-MS/MSMolecular BiologybiologyTraditional medicinebusiness.industry010401 analytical chemistrymedical cannabisbiology.organism_classificationSativexQR1-5020104 chemical scienceschemistryCannabinolCannabisDronabinolbusinessCannabidiolmedicine.drugMetabolites
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Gas—liquid chromatographic analyses

1984

Abstract The gas chromatography (GC) of n -alkyl acetates (CH 3 COOR), chloroacetates (CH 2 ClCOOR), dichloroacetates (CHCl 2 COOR) and trichloroacetates (CCl 3 COOR), where the alcohol chain length (R) varied between 1 and 8, and certain of their monochlorinated derivatives, 176 compounds altogether, has been studied on SE-30 and OV-351 glass capillary columns under the same operating conditions. The isomeric monochlorinated esters are eluted in direct order from the 1- chloro to the ω-chloro isomer, the separation of the isomers being complete on OV- 351. On SE-30, however, the peaks of the 6- and 7-chlorooctyl esters are partly overlapped. The separation of the mixtures of odd- and e…

Capillary actionAnalytical chemistryAlcoholFormyl groupAldehydeBiochemistryAnalytical Chemistrychemistry.chemical_compoundCapillary columnStraight chainpolycyclic compoundsStructural isomerOrganic chemistryMethyleneBenzoic acidchemistry.chemical_classificationPrimary (chemistry)General MedicineCapillary gas chromatographyBoiling pointChromatographic separationSalicylaldehydeNitrobenzoatesPolarlipids (amino acids peptides and proteins)Aliphatic compoundResolution (mass spectrometry)Polarity (physics)Carboxylic acidchemistry.chemical_elementBranching (polymer chemistry)Isothermal processTurn (biochemistry)ChlorinePhenolsQuartzAlkylTetradecaneChlorophenolDegree of unsaturationChromatographyGeminalElutionOrganic ChemistryChloroacetatesComplete resolutionReverse orderChain lengthchemistryChlorobenzeneFunctional groupNitroKovats retention indexNon polarGas chromatographyVicinalGas liquid chromatographicJournal of Chromatography A
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DFT calculation of 1J(119Sn,13C) and 2J(119Sn,1H) coupling constants in di- and trimethyltin(IV) compounds

2008

We have tested several computational protocols, at the nonrelativistic DFT level of theory, for the calculation of 1J(119Sn, 13C) and 2J(119Sn, 1H) spin-spin coupling constants in di- and trimethyltin(IV) derivatives with various ligands. Quite a good agreement with experimental data has been found with several hybrid functionals and a double-zeta basis set for a set of molecules comprising tetra-, penta-, and hexa-coordinated tin(IV). Then, some of the protocols have been applied to the calculation of the 2J(119Sn, 1H) of the aquodimethyltin(IV) ion and dimethyltin(IV) complex with D-ribonic acid and to the calculation of 1J(119Sn, 13C) and 2J(119Sn, 1H) of the dimethyltin(IV)-glycylglycin…

Carbon Isotopes; Dipeptides; Glycylglycine; Hydrogen; Organotin Compounds; Solvents; Tin; Trimethyltin Compounds; Water; Quantum Theorychemistry.chemical_elementInorganic ChemistryOrganotin(IV) DFT NMR relativistic effects tin couplingsComputational chemistryOrganotin CompoundsMoleculePhysical and Theoretical ChemistryBasis setCoupling constantCarbon IsotopesNMR tin derivatives coupling constantsTrimethyltin CompoundsbiologyGlycylglycineWaterDipeptidesbiology.organism_classificationHybrid functionalSolventchemistryTinSolventsQuantum TheoryTetraSolvent effectsTinHydrogen
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Stereoselective construction of the tetracyclic scalarane skeleton from carvone

1999

The tetracyclic scalarane skeleton 22 has been constructed from (S)-(+)-carvone using two intramolecular Diels–Alder reactions as key synthetic steps. Abad Somovilla, Antonio, Antonio.Abad@uv.es ; Agullo Blanes, M Consuelo, Consuelo.Agullo@uv.es ; Cuñat Romero, Ana Carmen, Ana.Cunat@uv.es ; Llosa Blasco, Maria Carmen, Carmen.Llosa@uv.es

CarvoneSynthetic stepsStereochemistryChemistryUNESCO::QUÍMICA:QUÍMICA::Química orgánica [UNESCO]Metals and AlloysGeneral ChemistrySkeleton (category theory)Carvone:QUÍMICA [UNESCO]CatalysisStereoselective TetracyclicStereoselective Tetracyclic ; Carvone ; Diels-Alder reactiones ; Synthetic stepsSurfaces Coatings and FilmsElectronic Optical and Magnetic Materialschemistry.chemical_compoundIntramolecular forceDiels-Alder reactionesMaterials ChemistryCeramics and CompositesOrganic chemistryStereoselectivityUNESCO::QUÍMICA::Química orgánica
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Exceptional affinity of nanostructured organic-inorganic hybrid materials towards dioxygen: confinement effect of copper complexes

2007

We report the exceptional reactivity towards dioxygen of a nanostructured organic-inorganic hybrid material due to the confinement of copper cyclam within a silica matrix. The key step is the metalation reaction of the ligand, which can occur before or after xerogel formation through the sol-gel process. The incorporation of a Cu(II) center into the material after xerogel formation leads to a bridged Cu(I)/Cu(II) mixed-valence dinuclear species. This complex exhibits a very high affinity towards dioxygen, attributable to auto-organization of the active species in the solid. The remarkable properties of these copper complexes in the silica matrix demonstrate a high cooperative effect for O(2…

Cations DivalentMetalationInorganic chemistrychemistry.chemical_elementLigands010402 general chemistry01 natural sciencesCatalysischemistry.chemical_compoundAdsorptionHeterocyclic CompoundsCyclamPolymer chemistryOrganometallic CompoundsLamellar structureReactivity (chemistry)ComputingMilieux_MISCELLANEOUSdioxygen bindingBinding Sites010405 organic chemistryLigandsol-gel processesSpectrum AnalysisOrganic ChemistryTemperatureGeneral Chemistry[CHIM.MATE]Chemical Sciences/Material chemistrySilicon DioxideCopperEnzymesNanostructuresPeroxides0104 chemical sciencesOxygenchemistrytetraazamacrocyclesMultiprotein Complexescopper[ CHIM.MATE ] Chemical Sciences/Material chemistryAnisotropyAdsorptionHybrid materialGelsorganic-inorganic hybrid composites
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Superoxide generation by human neutrophils induced by low doses of Escherichia coli hemolysin.

1991

Escherichia coli hemolysin (Hly) was isolated from bacterial culture supernatants by polyethylene glycol precipitation and centrifugation in glycerol density gradients. The toxin preparations contained less than 1 mol of lipopolysaccharide per 10 mol of protein, and they had no fatty acids. The capacity of purified hemolysin to stimulate superoxide anion production in polymorphonuclear leukocytes was monitored kinetically in a lumimeter by using the lucigenin assay and was correlated with the kinetics of transmembrane pore formation. When applied to leukocytes suspended in protein-free buffer, very low concentrations (0.02 to 0.1 HU/ml) of the toxin strongly stimulated the production of sup…

Cell Membrane PermeabilityNeutrophilsImmunologyBacterial ToxinsBiologymedicine.disease_causeHemolysin ProteinsMicrobiologychemistry.chemical_compoundHemolysin ProteinsBacterial ProteinsSuperoxidesmedicineEscherichia coliHumansCentrifugationLucigeninEscherichia coliSuperoxideToxinEscherichia coli ProteinsHemolysinFlow CytometryRespiratory burstKineticsInfectious DiseaseschemistryBiochemistryTetradecanoylphorbol AcetateParasitologyPropidiumResearch ArticleInfection and immunity
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An approach to As(III) and As(V) bioavailability studies with Caco-2 cells

2005

Foods and drinking water are the main sources of human exposure to inorganic arsenic [As(III) and As(V)]. After oral ingestion, the intestinal epithelium is the first barrier to absorption of these species. A human intestinal cell line (Caco-2) was used to evaluate cell retention and transport of As(III) (15.6-156.0 microM) and/or As(V) (15.4-170.6 microM). Cell monolayer integrity, cell viability, membrane damage and effects on cell metabolism were evaluated. Only the highest concentrations assayed [As(III): 156.0 microM; As(V): 170.6 microM] produced a cytotoxic effect with different cellular targets: As(III) altered the permeability of tight junctions, and As(V) caused uncoupling of the …

Cell SurvivalChemistryArsenateRespiratory chainBiological AvailabilityTetrazolium SaltsGeneral MedicineAbsorption (skin)ToxicologyIntestinal epitheliumMolecular biologyArsenicBioavailabilityThiazoleschemistry.chemical_compoundIntestinal AbsorptionBiochemistryCaco-2Electric ImpedanceHumansViability assayCaco-2 CellsIntestinal MucosaArseniteToxicology in Vitro
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Toxicity evaluation of individual and mixed enniatins using an in vitro method with CHO-K1 cells

2013

Enniatins (ENs) A, A1, B and B1 are produced by Fusarium species. They are known as emerging fusario- toxins, and can cause outbreaks in both humans and animals. ENs elicits a wide range of different biolog- ical properties and toxicological effects, and their co-occurrence may enhance the extent of these hazards. As the potential toxins reach in vitro cells in the same way as they would in vivo, cytotoxicity was studied with CHO-K1, which is considered one of the most sensitive cell lines for preliminary screen- ing of cytotoxicity studies. In this study, individual cytotoxic effects of ENs were evaluated by MTT assay after exposing ENs to CHO-K1 cells for 24, 48, and 72 h. The IC50 values…

Cell SurvivalStereochemistryTetrazolium SaltsCHO CellsGeneral MedicineMycotoxinsBiologyToxicologyMolecular biologyIn vitroThiazolesSensitive cellCricetulusIn vivoCricetinaeDepsipeptidesToxicity TestsToxicityAnimalsCytotoxic T cellMTT assayCytotoxicityAntagonismToxicology in Vitro
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Anti-inflammatory effects of chemically modified tetracyclines by the inhibition of nitric oxide and interleukin-12 synthesis in J774 cell line

2001

We investigated the effects of chemically modified tetracyclines (CMTs) on the production of nitric oxide (NO) and on the synthesis of some cytokines: tumour necrosis factor alpha (TNF-alpha), interleukin(IL)-10 and IL-12 in lipopolysaccharide (LPS)-treated J774 cell line. Furthermore, we studied the ability of these drugs to modify the viability in LPS-stimulated J774 macrophages. CMTs decreased, in a dose-dependent manner, inducible NO synthase (iNOS) activity and, consequently, nitrite formation in J774 cultures. The CMT-induced decrease in NO production is due to the inhibition of enzyme activity rather than to a direct effect on enzyme expression. The absence of the inhibition in mRNA …

Cell Survivalmedicine.medical_treatmentImmunologyNitric Oxide Synthase Type IIApoptosisEnzyme-Linked Immunosorbent AssayNitric OxideCell LineNitric oxideMicechemistry.chemical_compoundEthidiumIn Situ Nick-End LabelingmedicineAnimalsImmunology and AllergyRNA MessengerViability assayEnzyme InhibitorsFluorescent DyesPharmacologybiologyReverse Transcriptase Polymerase Chain ReactionAnti-Inflammatory Agents Non-SteroidalInterleukinBiological activityInterleukin-12Acridine OrangeCell biologyNitric oxide synthaseInterleukin 10CytokinechemistryBiochemistryTetracyclinesApoptosisbiology.proteinCytokinesElectrophoresis Polyacrylamide GelIndicators and ReagentsNitric Oxide SynthaseInternational Immunopharmacology
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Characterization of the Receptor Protein-Tyrosine Kinase Gene from the Marine Sponge Geodia cydonium

1996

Cells are provided with well-defined receptor structures (signal receivers) which interact with their corresponding ligands (signal molecules) and initiate a signal transduction pathway resulting in a change of cellular behavior or metabolism (Stoddard et al. 1992). It is well established that cells from both eukaryotic protists (single-cell organisms) and from Metazoa (multicellular organisms) respond to signals emanating from the extracellular environment. The extracellular signals to which protists respond are mainly nutrients which diffuse to their surfaces, and in most cases cross the cell membrane. In addition, they are able to bind peptide hormones, e.g., insulin or adrenocorticotrop…

Cell membraneMulticellular organismmedicine.anatomical_structurebiologymedicineTetrahymenaExtracellularSignal transductionReceptorbiology.organism_classificationTyrosine kinaseGeneCell biology
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