Search results for "dimethyl sulfoxide"

showing 10 items of 200 documents

The gap junctional intercellular communication is no prerequisite for the stabilization of xenobiotic metabolizing enzyme activities in primary rat l…

1995

In primary monocultures of adult rat liver parenchymal cells (PC), the activities of the xenobiotic metabolizing enzymes microsomal epoxide hydrolase (mEHb), soluble epoxide hydrolase (sEH), glutathione S-transferases (GST), and phenolsulfotransferase (ST) were reduced after 7 d to values below 33% of the initial activities. Furthermore, the gap junctional intercellular communication (GJIC), measured after microinjection by dye transfer, decreased from 90% on Day 1 to undetectable values after 5 d in monoculture. Co-culture of PC with nonparenchymal rat liver epithelial cells (NEC) increased (98% on Day 1) and stabilized (82% on Day 7) the homotypic GJIC of PC. Additionally, most of the mea…

Epoxide hydrolase 2MaleCell CommunicationBiologyCell LineDDTXenobioticsRats Sprague-Dawleychemistry.chemical_compoundAnimalsDimethyl SulfoxideMicroinjectionGlutathione TransferaseEpoxide HydrolasesDimethyl sulfoxideGap JunctionsCell DifferentiationEpithelial CellsCell BiologyGeneral MedicineGlutathioneArylsulfotransferaseIn vitroRatsEnzyme ActivationchemistryBiochemistryLiverCell cultureMicrosomal epoxide hydrolaseIntracellularDevelopmental BiologyIn vitro cellulardevelopmental biology. Animal
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In vivo survival rate of rabbit morulae after vitrification in a medium without serum protein.

2000

The in vivo survival rate of rabbit morulae after vitrification in a mixture of dimethyl sulphoxide and ethylene glycol solution without protein supplement (WPS) was compared with two types of protein supplements: rabbit serum (RS) and bovine serum albumin (BSA). Significant dif- ferences were observed in the percentage of transferable embryos (undamaged embryos after devit- rification, 80.4 % versus 93.2 and 92.1 %, WPS, BSA and RS, respectively, P < 0.05) and live born rate (40.9 % versus 56.1 %, WPS and BSA, respectively, P < 0.05). Non-significant differences were, however, observed in the percentages of implanted embryos at 12 days post-ovulation induc- tion (56.7, 69.7 and 68.6 %), po…

Ethylene GlycolMorulaAndrologychemistry.chemical_compoundCryoprotective AgentsPregnancyIn vivo[SDV.BDD] Life Sciences [q-bio]/Development BiologyAnimalsDimethyl SulfoxideVitrificationEmbryo ImplantationBovine serum albuminFetal DeathSurvival rate[SDV.BDLR] Life Sciences [q-bio]/Reproductive BiologyCryopreservationLagomorphabiologySerum Albumin BovineEmbryo cultureBlood ProteinsEmbryo Transferbiology.organism_classificationEmbryo transfer[SDV.AEN] Life Sciences [q-bio]/Food and NutritionBloodchemistryBiochemistrybiology.proteinFemaleRabbitsEthylene glycol
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Estimation of formamide harmonic and anharmonic modes in the Kohn-Sham limit using the polarization consistent basis sets.

2010

Formamide harmonic and anharmonic frequencies of fundamental vibrations in the gas phase and in several solvents were successfully estimated in the B3LYP Kohn-Sham complete basis set limit (KS CBS). CBS results were obtained by extrapolating a power function (two-parameter formula) to the results calculated with polarization-consistent basis sets. Anharmonic corrections using the second order perturbation treatment (PT2) and hybrid B3LYP functional combined with polarization consistent pc-n (n = 0, 1, 2, 3, 4) and several Pople’s basis sets were analyzed for all fundamental formamide vibrational modes in the gas phase and solution. Solvent effects were modeled within a PCM method. The anhar…

FormamideAcetonitrilesMolecular ConformationAnharmonic vibrationSolvent effectMolecular physicsCatalysisInorganic ChemistryAcetonechemistry.chemical_compoundComputational chemistryScissoringHexanesComputer SimulationDimethyl SulfoxideHarmonic vibrationPhysical and Theoretical ChemistryPhysics::Chemical PhysicsCarbon TetrachlorideBasis setQuantitative Biology::BiomoleculesOriginal PaperFormamidesOrganic ChemistryAnharmonicityWaterComplete basis set limitFormamideComputer Science ApplicationsComputational Theory and MathematicschemistryModels ChemicalMolecular vibrationHarmonicSolventsThermodynamicsFermi resonanceChloroformGasesSolvent effectsJournal of molecular modeling
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RAB3GAP1 and RAB3GAP2 modulate basal and rapamycin-induced autophagy

2014

Macroautophagy is a degradative pathway that sequesters and transports cytosolic cargo in autophagosomes to lysosomes, and its deterioration affects intracellular proteostasis. Membrane dynamics accompanying autophagy are mostly elusive and depend on trafficking processes. RAB GTPase activating proteins (RABGAPs) are important factors for the coordination of cellular vesicle transport systems, and several TBC (TRE2-BUB2-CDC16) domain-containing RABGAPs are associated with autophagy. Employing C. elegans and human primary fibroblasts, we show that RAB3GAP1 and RAB3GAP2, which are components of the TBC domain-free RAB3GAP complex, influence protein aggregation and affect autophagy at basal an…

GTPase-activating proteinlipid dropletsrab3 GTP-Binding ProteinsATG16L1DMSO dimethyl sulfoxideFEZ20302 clinical medicineATG autophagy-relatedPhagosomesDAPI 4’ 6-diamidino-2-phenylindoleSQSTM1 sequestosome 1ATG16L1MAP1LC3 microtubule-associated protein 1 light chain 3GFP green fluorescent protein0303 health sciencesGABARAP GABA(A) receptor-associated proteinGTPase-Activating ProteinsCell biologyRAB3GAP1RAB3GAP2RABGAP RAB GTPase activating proteinATG3autophagyCALCOCO2 calcium binding and coiled-coil domain 2Basic Research PaperseV empty vectorATG8ATG5PBS phosphate-buffered salineBiologyPE phosphatidylethanolamineTBC domain TRE2-BUB2-CDC16 domainBAG3GEF guanine nucleotide exchange factor03 medical and health sciencesC. elegans Caenorhabditis elegansAnimalsHumansCaenorhabditis elegansMolecular Biology030304 developmental biologySirolimusDPH 1 6-diphenyl-1 3 5-hexatrieneproteostasisAutophagyBiological TransportCell BiologyFEZ1Bafi bafilomycin A1FEZ fasciculation and elongation protein zetaNBR1 neighbor of BRCA1 gene 1ProteostasissiRNA small interfering RNABSA bovine serum albuminRabLysosomes030217 neurology & neurosurgeryAutophagy
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Synthesis of fluorinated oxadiazoles with gelation and oxygen storage ability

2012

A new family of fluorinated low molecular weight (LMW) gelators has been synthesized through SNAr substitution of 5-polyfluoroaryl-3-perfluoroheptyl-1,2,4-oxadiazoles with glycine ester. The obtained compounds give thermal and pH-sensitive hydrogels or thermo-reversible organogels in DMSO. Oxygen solubility studies showed the ability to maintain high oxygen levels in solution and in gel blend with plate counter agar (PCA).

HalogenationOxygen storageGlycinechemistry.chemical_elementBiochemistryPhase TransitionNucleophilic aromatic substitutionOrganic chemistryDimethyl SulfoxidePhysical and Theoretical ChemistrySolubilityOxadiazolesHydrogen bondChemistryOrganic ChemistryHalogenationEstersHydrogen BondingFluorineSettore CHIM/06 - Chimica OrganicaHydrogen-Ion ConcentrationMolecular WeightOxygenSolubilityGlycineSelf-healing hydrogelsFluorineMicroscopy Electron Scanninglow molecular weight gelators(LMWG) oxadiazoles fluorinated compounds oxgyen carriersThermodynamicsGels
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Contact Sensitizers Specifically Increase MHC Class II Expression on Murine Immature Dendritic Cells

2000

Contact sensitivity is a T-cell-mediated immune disease that can occur when low-molecular-weight chemicals penetrate the skin. In vivo topical application of chemical sensitizers results in morphological modification of Langerhans cells (LC). Moreover, within 18 h, LC increase their major histocompatibility complex (MHC) class II antigens expression and migrate to lymph nodes where they present the sensitizer to T lymphocytes. We wanted to determine if such an effect could also be observed in vitro. However, because of the high genetic diversity encountered in humans, assays were performed with dendritic cells (DC) obtained from a Balb/c mouse strain. The capacity of a strong sensitizer, DN…

Health Toxicology and MutagenesisGenes MHC Class IIBone Marrow CellsSodium ChlorideBiologyAnimal Testing AlternativesToxicologyMajor histocompatibility complexCell LineImmunophenotypingOxazoloneMicechemistry.chemical_compoundImmune systemAntigens CDIn vivoCell AdhesionmedicineAnimalsDimethyl SulfoxideBenzothiazolesCells CulturedSensitizationMice Inbred BALB CMHC class IIHistocompatibility Antigens Class IIOxazoloneSodium Dodecyl SulfateDendritic CellsDendritic cellMolecular biologyIn vitroThiazolesmedicine.anatomical_structureGene Expression RegulationchemistryAntigens SurfaceDermatitis Allergic ContactImmunologyIrritantsbiology.proteinDinitrofluorobenzeneFemaleHaptensIn Vitro &amp; Molecular Toxicology
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Ethyl 5-amino-3-(pyridin-4-yl)-1-(2,4,6-trichlorophenyl)-1H-pyrazole-4-carboxylate dimethyl sulfoxide hemisolvate

2012

The asymmetric unit of the title compound, C17H13Cl3N4O2&amp;#183;0.5C2H6OS, contains two almost identical molecules and one dimethyl sulfoxide (DMSO-d6) solvent molecule. The pyrazole ring forms dihedral angles of 54.6&amp;#8197;(4) and 80.0&amp;#8197;(4)&amp;#176; in one molecule, and dihedral angles of 54.2&amp;#8197;(4) and 81.2&amp;#8197;(4)&amp;#176; in the other molecule, with the directly attached pyridine and trichlorophenyl rings, respectively. The dihedral angles of the pyridine and trichlorophenyl rings are 51.2&amp;#8197;(4) and 52.0&amp;#8197;(4)&amp;#176;, respectively. The crystal packing is characterized by intra- and intermolecular hydrogen bonds. The crystal is a nonmeroh…

Hydrogen bondDimethyl sulfoxideGeneral ChemistryDihedral anglePyrazoleCondensed Matter PhysicsRing (chemistry)BioinformaticsOrganic PapersMedicinal chemistrySolventlcsh:Chemistrychemistry.chemical_compoundchemistrylcsh:QD1-999PyridineGeneral Materials ScienceEthyl groupActa Crystallographica Section E
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Liver X Receptor Regulates Arachidonic Acid Distribution and Eicosanoid Release in Human Macrophages

2013

Objective— Liver X receptors (LXRs) are oxysterol-activated nuclear receptors that are highly expressed in macrophages and regulate lipid homeostasis and inflammation. Among putative LXR target genes, lysophosphatidylcholine acyltransferase 3 (LPCAT3) involved in the Lands cycle controls the fatty acid composition at the sn-2 position of glycerophospholipids and, therefore, the availability of fatty acids, such as arachidonic acid (AA), used for eicosanoid synthesis. The aim of our study was to determine whether LXRs could regulate the Lands cycle in human macrophages, to assess the consequences in terms of lipid composition and inflammatory response, and to work out the relative contribut…

InflammationBiologySensitivity and SpecificityDinoprostoneMonocyteschemistry.chemical_compoundDownregulation and upregulationmedicineHumansDimethyl SulfoxideRNA MessengerLiver X receptorReceptorCells CulturedLiver X ReceptorsInflammationArachidonic AcidMacrophagesLysophospholipid acyltransferase activity1-Acylglycerophosphocholine O-AcyltransferaseMicroarray AnalysisOrphan Nuclear ReceptorsUp-RegulationchemistryEicosanoidNuclear receptorBiochemistryEicosanoidslipids (amino acids peptides and proteins)Arachidonic acidmedicine.symptomCardiology and Cardiovascular MedicineArteriosclerosis, Thrombosis, and Vascular Biology
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The Difficult Marriage of Triarylcorroles with Zinc and Nickel Ions.

2022

The coordination chemistry of corrole has witnessed a great improvement in the past few years and its Periodic Table has been widened to be so large that it is compared with that of porphyrins. However, Ni and Zn ions, commonly used with porphyrins for both synthetic and theoretical purposes, are sparsely reported in the case of corroles. Here, we report synthetic protocols for preparing Ni and Zn triarylcorrole complexes. In the case of Zn, the preliminary oxidation of the free base corrole in DMSO to the neutral corrole radical is a necessary step to obtain the coordination of the metal ion, because the direct reaction led to the formation of an open-chain tetrapyrrole. The Ni complex cou…

Inorganic ChemistryIonskemiallinen synteesiaromaattiset yhdisteetZincsinkki (metallit)PorphyrinsNickelSettore CHIM/07Dimethyl SulfoxidekompleksiyhdisteetPhysical and Theoretical ChemistrynikkeliInorganic chemistry
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Stereospezifische Überführung chiraler acyclischer tertiärer Phosphinsulfide in die entsprechenden tertiären Phosphinoxide mit Dimethylsulfoxid (DMSO)

1975

Die Uberfuhrung chiraler acyclischer tertiarer Phosphinsulfide in die entsprechenden tertiaren Phosphinoxide mit DMSO in saurer Losung erfolgt unter vollstandiger Inversion der Konfiguration am zentralen Phosphoratom. Aufgrund dieses stereochemischen Verlaufs wird ein Mechanismus fur die Reaktion zur Diskussion gestellt. Stereospecific Conversion of Chiral Acyclic Tertiary Phosphine Sulfides into the Corresponding Tertiary Phosphine Oxides by Means of Dimethyl Sulfoxide (DMSO) The conversion of chiral acyclic tertiary phosphine sulfides into the corresponding tertiary phosphine oxides by means of DMSO in acidic solution proceeds with complete inversion of configuration at the central phosph…

Inorganic ChemistryReaction mechanismchemistry.chemical_compoundStereospecificityChemistryStereochemistryComplete inversionDimethyl sulfoxidePhosphorus atomMedicinal chemistryPhosphineChemische Berichte
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