Search results for "Hydrogen"

showing 10 items of 4254 documents

Energy Metabolism Characterization of a Novel Cancer Stem Cell-Like Line 3AB-OS

2013

Cancer stem cells (CSC) have a central role in driving tumor growth. Since metabolism is becoming an important diagnostic and therapeutic target, characterization of CSC line energetic properties is an emerging need. Embryonic and adult stem cells, compared to differentiated cells, exhibit a reduced mitochondrial activity and a stronger dependence on aerobic glycolysis. Here, we aimed to comparatively analyze bioenergetics features of the human osteosarcoma 3AB-OS CSC-like line, and the parental osteosarcoma MG63 cells, from which 3AB-OS cells have been previously selected. Our results suggest that 3AB-OS cells depend on glycolytic metabolism more strongly than MG63 cells. Indeed, growth in…

education.field_of_studyLactate dehydrogenase ACellular differentiationCell BiologyMitochondrionBiologyBiochemistryCell biologyBiochemistryAnaerobic glycolysisCancer stem cellCancer cellStem celleducationMolecular BiologyAdult stem cellJournal of Cellular Biochemistry
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Influence of Bond Fixation in Benzo-Annulated N-Salicylideneanilines and Their ortho-C(O)X Derivatives (X = CH3, NH2, OCH3) on Tautomeric Equilibria …

2007

1H, 13C, and 15N NMR spectra show that an ortho-C(=O)X group present in the molecules of N-salicylideneanthranilamide (X = NH2), methyl N-salicylideneanthranilate (X = OCH3), N-salicylidene-o-aminoacetophenone (X = CH3), and their benzo analogues have only a minor effect on the tautomeric OH/NH-equilibrium in solution. Only two of three possible tautomers were detected. Lability of the absent form was proved by theoretical calculations. Calculated energies show that the enolimino form (OH) is less stable than the enaminone (NH) form only for dibenzo-annulated N-salicylideneanilines. The population of each species in the tautomeric mixture was found to be inversely proportional to its energy…

education.field_of_studyStereochemistryHydrogen bondOrganic ChemistryCarbon-13PopulationAromaticityTautomerEnolNMR spectra databaseCrystallographychemistry.chemical_compoundchemistryMoleculeeducationThe Journal of Organic Chemistry
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Syntheses of Trifluoroethylated N-Heterocycles from Vinyl Azides and Togni’s Reagent Involving 1,n-Hydrogen-Atom Transfer Reactions

2020

2,2,2-Trifluoroethyl-substituted 3-oxazolines, 3-thiazolines, and 5,6-dihydro-2H-1,3-oxazines have been obtained by reacting substituted vinyl azides with a combination of Togni’s reagent and substoichiometric amounts of iron(II) chloride. The results of density functional theory calculations support the proposed mechanism involving 1,n-hydrogen-atom transfer reactions. peerReviewed

eetteritenergia010405 organic chemistryChemistryOrganic ChemistryreagentsHydrogen atom010402 general chemistry01 natural sciencesBiochemistryChloride0104 chemical sciencesetherssubstituentsReagentredox reactionsPolymer chemistryreagenssitmedicineDensity functional theoryPhysical and Theoretical Chemistryenergymedicine.drugOrganic Letters
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Experimental tests on hydrogen production from seawaves energy

2017

In this paper we propose the use of Wave Energy Converter and saline water to produce hydrogen. Two different scheme and technology are proposed. The objective of this research is to design an electrolyzing system capable of utilizing sea. In particular, we present the results obtained by two different prototype of electrolyzer: one with steel electrodes and the second with titanium electrodes. Further experiments were carried out by changing the electrolytic solution of water and sodium chloride in real seawater. Finally, the electrical load has been changed as imposing electric current with a distorted waveform. © 2017 Marine Technology Society.

electrolysis hydrogen new fuel sea waterSettore ING-IND/32 - Convertitori Macchine E Azionamenti Elettrici
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Precision measurement of the mass difference between light nuclei and anti-nuclei

2015

The measurement of the mass differences for systems bound by the strong force has reached a very high precision with protons and anti-protons. The extension of such measurement from (anti-)baryons to (anti-)nuclei allows one to probe any difference in the interactions between nucleons and anti-nucleons encoded in the (anti-)nuclei masses. This force is a remnant of the underlying strong interaction among quarks and gluons and can be described by effective theories, but cannot yet be directly derived from quantum chromodynamics. Here we report a measurement of the difference between the ratios of the mass and charge of deuterons and anti-deuterons, and $^{3}{\rm He}$ and $^3\overline{\rm He}…

electronQuarkspectroscopyAntiparticleParticle physicsPhysics of Elementary Particles and FieldsCPT symmetryStrong interactionNuclear TheoryantunucleiFOS: Physical sciencesAntiprotonGeneral Physics and Astronomy[PHYS.NEXP]Physics [physics]/Nuclear Experiment [nucl-ex]ElectronHigh Energy Physics - ExperimentNuclear physicsHigh Energy Physics - Experiment (hep-ex)Physics and Astronomy (all)[PHYS.HEXP]Physics [physics]/High Energy Physics - Experiment [hep-ex]Nuclear Physics - ExperimentNuclear Experiment (nucl-ex)Nuclear ExperimentNuclear ExperimentAntihydrogenSpectroscopyNuclear Physicsantihydrogenmass measurementQuantum chromodynamicsPhysicsanti-nucleita114SPECTROSCOPY; ANTIHYDROGEN; ANTIPROTON; ELECTRONmass difference nuclei antunucleiHigh Energy Physics::Phenomenologymass differenceNATURAL SCIENCES. Physics.3. Good healthGluonPRIRODNE ZNANOSTI. Fizika.antiprotonnucleiQuark–gluon plasmamassmass difference ; nuclei ; anti-nuclei ; ALICE ; CERNHigh Energy Physics::ExperimentNucleon
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Synthesis of phosphine derivatives of [Fe2(CO)6(μ-sdt)] (sdt = SCH2SCH2S) and investigation of their proton reduction capabilities

2023

The reactions of [Fe2(CO)6(μ-sdt)] (1) (sdt = SCH2SCH2S) with phosphine ligands have been investigated. Treatment of 1 with dppm (bis(diphenylphosphino)methane) or dcpm (bis(dicyclohexylphosphino)methane) affords the diphosphine-bridged products [Fe2(CO)4(μ-sdt)(μ-dppm)] (2) and [Fe2(CO)4(μ-sdt)(μ-dcpm)] (3), respectively. The complex [Fe2(CO)4(μ-sdt)(κ2-dppv)] (4) with a chelating diphosphine was obtained by reacting 1 with dppv (cis-1,2-bis(diphenylphosphino)ethene). Reaction of 1 with dppe (1,2-bis(diphenylphosphino)ethane) produces [{Fe2(CO)4(μ-sdt)}2(μ-κ1-dppe)] (5) in which the diphosphine forms an intermolecular bridge between two diiron cluster fragments. Three products were obtaine…

elektrokatalyysielectrocatalysisphosphinehydrogenaseiron carbonyl complexkompleksiyhdisteetproton reductioncyclic voltammetry
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The endopolygalacturonase 1 from botrytis cinerea activates grapevine defense reactions unrelated to its enzyumatic activity

2003

A purified glycoprotein from Botrytis cinerea(strain T4), identified as endopolygalacturonase 1 (T4BcPG1) by mass spectrometry analysis, has been shown to activate defense reactions in grapevine (Vitis vinifera cv. Gamay). These reactions include calcium influx, production of active oxygen species, activation of two mitogen-activated protein kinases, defense gene transcript accumulation, and phytoalexin production. Most of these defense reactions were also activated in grapevine in response to purified oligogalacturonides (OGA) with a degree of polymerization of 9 to 20. In vivo, these active OGA might be a part of the released products resulting from endopolygalacturonase activity on plan…

elicitor; endopolygalacturonase 1; Botrytis cinerea; plant defenceplant defencePhysiologyMolecular Sequence DataOligosaccharidesBiologyCell wallBotrytis cinereaGene Expression Regulation PlantSequence Homology Nucleic Acid[SDV.BBM] Life Sciences [q-bio]/Biochemistry Molecular Biology[SDV.BBM]Life Sciences [q-bio]/Biochemistry Molecular BiologyVitisAmino Acid SequencePectinaseendopolygalacturonase 1ComputingMilieux_MISCELLANEOUSBotrytis cinereachemistry.chemical_classificationelicitorBase SequenceSequence Homology Amino AcidKinasePhytoalexinfood and beveragesGeneral MedicineHydrogen Peroxidebiology.organism_classificationImmunity InnateElicitorEnzyme ActivationEnzymePolygalacturonasechemistryBiochemistryCalciumBotrytisMitogen-Activated Protein KinasesGlycoproteinAgronomy and Crop Science
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Crystal structures of allyltriphenyl-phosphonium halogenocuprates(I)

2013

Alternating-current electrochemical synthesis is used to obtain for the first time halogenocuprates of an allyl derivative of phosphonium of the composition (CH2=CHCH2(C6H5)3P)CuX2 (X = Br (I), Cl (II)). Compound I crystallizes in the space group P21, a = 9.6341(3) A, b = 12.4167(4) A, c = 9.9618(4) A, β = 117.484(5)°, Z = 2. Compound II crystallizes in the space group P21/n, a = 9.9725(5) A, b = 15.4586(8) A, c = 13.7557(5) A, β = 90.429(4)°, Z = 4. In the structures of I and II quasilinear CuX 2 − anions are held by C-H…X hydrogen bonds inside a framework formed by the stacking of phenyl groups from CH2=CHCH2(C6P5)3P+ cations. Allyl groups are not involved in coordination with copper(I) a…

embracecrystal structurehyperconjugationphenylStereochemistryHydrogen bondStackingchemistry.chemical_elementCrystal structureHyperconjugationElectrochemistryhomoconjugationCoppercopper(I)weak hydrogen bondsInorganic Chemistrychemistry.chemical_compoundCrystallographychemistrystackingallyl phosphoniumMaterials ChemistryPhosphoniumPhysical and Theoretical ChemistryDerivative (chemistry)Journal of Structural Chemistry
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Investigations of methyl lactate in the presence of reverse micelles by vibrational spectroscopy and circular dichroism

2012

Abstract The FT-IR and vibrational circular dichroism (VCD) spectra of ( S )- and -( R )-methyl lactate have been recorded for neat samples and at various concentrations in CCl 4 and DMSO solutions. These spectra are used to analyse the FT-IR and VCD spectra of methyl lactates in presence of sodium bis(2-ethylhexyl)sulfosuccinate (AOT) in CCl 4 , where the surfactant molecules are known to form reverse micelles. Some tendency of methyl lactate to interact with AOT micellar aggregates is observed, but not as well defined as previously observed for dimethyl tartrate in analogous circumstances. Besides, near infrared (NIR) absorption and VCD data have been obtained for most of the above system…

endocrine systemCircular dichroismChemistryHydrogen bondAnalytical chemistryInfrared spectroscopyMethyl lactateMicellechemistry.chemical_compoundVibrational circular dichroismMoleculePhysical chemistryAbsorption (chemistry)Methyl lactate Sodium bis(2-ethylhexyl)sulfosuccinate (AOT) Reverse micelles VCD NIR AnharmonicitySpectroscopyVibrational Spectroscopy
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Context dependent variation in corticosterone and phenotypic divergence of Rana arvalis populations along an acidification gradient

2022

Background Physiological processes, as immediate responses to the environment, are important mechanisms of phenotypic plasticity and can influence evolution at ecological time scales. In stressful environments, physiological stress responses of individuals are initiated and integrated via the release of hormones, such as corticosterone (CORT). In vertebrates, CORT influences energy metabolism and resource allocation to multiple fitness traits (e.g. growth and morphology) and can be an important mediator of rapid adaptation to environmental stress, such as acidification. The moor frog, Rana arvalis, shows adaptive divergence in larval life-histories and predator defense traits along an acidi…

endocrine systemviitasammakkoRanidaeEvolutionAcidification; Adaptive divergence; Amphibians; Corticosterone; Environmental stress; Evolutionary physiology; Phenotypic plasticityEnvironmental stressPhenotypic plasticitykortikosteroniEvolutionsbiologiAcidificationAmphibiansAdaptive divergencehappamoituminenQH359-425polycyclic compoundsAnimalsHumanshormonaaliset vaikutuksetQH540-549.5sopeutuminenEkologiEvolutionary BiologyEcologysammakkoeläimetHydrogen-Ion ConcentrationAdaptation PhysiologicalLarvaEvolutionary physiologyfenotyyppiAnuraCorticosteroneAcidsympäristönmuutoksethormones hormone substitutes and hormone antagonistsfysiologiset vaikutuksetResearch ArticleBMC Ecology and Evolution
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