Search results for "HeLa"

showing 10 items of 738 documents

(Ni2), (Ni3), and (Ni2 + Ni3): A Unique Example of Isolated and Cocrystallized Ni2 and Ni3 Complexes

2009

Structural and magnetic characterization of compound {[Ni(2)(L)(2)(OAc)(2)][Ni(3)(L)(2)(OAc)(4)]}.2CH(3)CN (3) (HL = the tridentate Schiff base ligand, 2-[(3-methylamino-propylimino)-methyl]-phenol) shows that it is a rare example of a crystal incorporating a dinuclear Ni(II) compound, [Ni(2)(L)(2)(OAc)(2)], and a trinuclear one, [Ni(3)(L)(2)(OAc)(4)]. Even more unusual is the fact that both Ni(II) complexes, [Ni(2)(L)(2)(OAc)(2)] (1) and [Ni(3)(L)(2)(OAc)(4)(H(2)O)(2)].CH(2)Cl(2).2CH(3)OH (2), have also been isolated and structurally and magnetically characterized. The structural analysis reveals that the dimeric complexes [Ni(2)(L)(2)(OAc)(2)] in cocrystal 3 and in compound 1 are almost i…

Inorganic Chemistrychemistry.chemical_compoundCrystallographySchiff baseMolecular geometryTridentate ligandchemistryOctahedral molecular geometryChelationPhysical and Theoretical ChemistryAcetate ionCocrystalInorganic Chemistry
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Highly diastereoselective additions of organometallic reagents to 1-O-silylated 3,4-Di-O-benzyl-L-erythrulose derivatives

1993

Abstract The diastereoselectivity of the addition of several organometallic reagents to the carbonyl group of the title compounds has been investigated. Some organomagnesium reagents display high diastereoselectivities (90–99%) and the major products are those predicted by the α-chelation model.

Inorganic Chemistrychemistry.chemical_compoundNucleophilic additionchemistryReagentOrganic ChemistryOrganic chemistryChelationPhysical and Theoretical ChemistryL-ERYTHRULOSECarbonyl groupCatalysisTetrahedron: Asymmetry
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Imidotungsten(VI) complexes with chelating amino and imino phenolates

2011

The reaction of WOCl(4) with 2,4-di-tert-butyl-6-((isopropylamino)methyl)phenol followed by the reaction with phenyl isocyanate leads to the formation of imidotungsten(VI) complex [W(NPh)Cl(3)(OC(6)H(3)(CH(2)NH-i-Pr)-2-t-Bu(2)-4,6)] 4 with a chelating aminophenolate ligand. When the same procedure was applied using aminophenols with bulkier substituents in the amino group, the final product was an unexpected Schiff-base complex [W(NPh)Cl(3)(OC(6)H(3)(CH=NPh)-2-t-Bu(2)-4,6)] 5, where the ligand is derived from 2,4-di-tert-butyl-6-((phenylimino)methyl)phenol. Complex 5 is also formed in the thermal degradation of 4. On the whole, 5 appears to be formed by a disproportionation of intermediate …

Inorganic Chemistrychemistry.chemical_compoundchemistryStereochemistryLigandPhenolDisproportionationChelationCarbon-13 NMRSolution structureMedicinal chemistryPhenyl isocyanateta116Dalton Transactions
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Synthesis and Complexation of the Metalloligand {(η5-C5H5)[η5-C5Me3-1,2-(PPh2)2]TiCl2} (TiPHOS): The First Example of a 1,2-Bis(diphenylphosphanyl)ti…

2001

The reaction of lithium 1,2-bis(diphenylphosphanyl)trimethylcyclopentadienide (1) with CpTiCl3 leads to the formation of the titanocene diphosphane {(η5-C5H5)[η5-C5Me3-1,2-(PPh2)2]TiCl2} (TiPHOS, 2). This metalloligand reacts readily with (NBD)Cr(CO)4 and W(CO)5(THF) to give, in both cases, the bimetallic chelate complexes (TiPHOS)Cr(CO)4 (3) and (TiPHOS)W(CO)4 (4). The structure of 4 has been determined by X-ray diffraction. The synthesis of a new early-late heterobimetallic complex (TiPHOS)Rh(CO)Cl (5) is reported.

Inorganic Chemistrychemistry.chemical_compoundchemistryStereochemistrychemistry.chemical_elementDiphosphaneLithiumChelationBimetallic stripMedicinal chemistryDerivative (chemistry)RhodiumEuropean Journal of Inorganic Chemistry
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Sequestering ability of some chelating agents towards methylmercury(II).

2013

A study on the interactions between CH3Hg+ and some S, N and O donor ligands (2-mercaptopropanoic acid (thiolactic acid (H2 TLA)), 3-mercaptopropanoic acid (H2 MPA), 2-mercaptosuccinic acid (thiomalic acid (H3 TMA)), d,l-penicillamine (H2 PSH), l-cysteine (H2 CYS), glutathione (H3 GSH), N,N′-bis(3-aminopropyl)-1-4-diaminobutane (spermine (SPER)), 1,2,3,4,5,6-benzenehexacarboxylic acid (mellitic acid (H6 MLT)) and ethylenediaminetetraacetic acid (H4 EDTA)) is reported. The speciation models in aqueous solution and the possible structures of the complexes formed are discussed on the basis of potentiometric, calorimetric, UV spectrophotometric and electrospray mass spectrometric results. For t…

Inorganic chemistryElectrospray ionisation mass spectrometry (ESI-MS)Ethylenediaminetetraacetic acidCalorimetryBiochemistrySequestering ability of S N and O donor ligandAnalytical Chemistrychemistry.chemical_compoundHydrolysisSettore CHIM/01 - Chimica AnaliticaChelationMellitic acidThiomalic acidEnvironmental Restoration and RemediationChelating AgentsThiolactic acidAqueous solutionMolecular StructureLigandMethylmercury(II) cationMethylmercury CompoundsKineticschemistryMethylmercury(II) cation; Sequestering ability of S; N and O donor ligands; UV–spectrophotometry; Electrospray ionisation mass spectrometry (ESI-MS); PotentiometryPotentiometryEnvironmental PollutantsUV–spectrophotometryNuclear chemistryAnalytical and bioanalytical chemistry
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Hemin-coupled iron(III)-hydroxide nanoparticles show increased uptake in Caco-2 cells

2011

Abstract Objectives The absorption of commonly used ferrous iron salts from intestinal segments at neutral to slightly alkaline pH is low, mainly because soluble ferrous iron is easily oxidized to poorly soluble ferric iron and ferrous iron but not ferric iron is carried by the divalent metal transporter DMT-1. Moreover, ferrous iron frequently causes gastrointestinal side effects. In iron(III)-hydroxide nanoparticles hundreds of ferric iron atoms are safely packed in nanoscaled cores surrounded by a solubilising carbohydrate shell, yet bioavailability from such particles is insufficient when compared with ferrous salts. To increase their intestinal uptake iron(III)-hydroxide nanoparticles …

Inorganic chemistryTetrazolium SaltsPharmaceutical ScienceNanoparticleFerrozineIron Chelating AgentsFerric CompoundsFerrouschemistry.chemical_compoundMicroscopy Electron TransmissionSpectroscopy Fourier Transform InfraredmedicineHumansScattering RadiationParticle SizeColoring AgentsHemePharmacologyChemistryIron Chelating AgentsIron deficiencymedicine.diseaseCulture MediaThiazolesHeminNanoparticlesHydroxideColorimetrySpectrophotometry UltravioletProtoporphyrinCaco-2 CellsHeminJournal of Pharmacy and Pharmacology
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Synthesis and characterization of some arsenic, antimony and bismuth complexes of 2-mercaptoaniline

1983

Abstract The complexes of arsenic, antimony and bismuth as well as phenylantimony and phenylbismuth with monoanionic 2-mercaptoaniline are reported. IR spectra are consistent with chelating behaviour of the ligand but only a weak nitrogen to metal bonding interaction is advanced. The mass spectra fragmentation pattern is also presented. It can be interpreted with the loss of successive ligand units and, as a general feature, the abundance of a given ion decreases as the mass of the metal increases. Species with one or two protons less give more intense peaks possibly corresponding to ions containing the dianionic form of the ligand.

Inorganic chemistrychemistry.chemical_elementInfrared spectroscopyBismuthIonInorganic ChemistryMetalchemistryAntimonyvisual_artMaterials ChemistryMass spectrumvisual_art.visual_art_mediumChelationPhysical and Theoretical ChemistryArsenicInorganica Chimica Acta
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Study of the cytolethal distending toxin (CDT)-activated cell cycle checkpoint. Involvement of the CHK2 kinase.

2001

AbstractThe bacterial cytolethal distending toxin (CDT) triggers a G2/M cell cycle arrest in eukaryotic cells by inhibiting the CDC25C phosphatase-dependent CDK1 dephosphorylation and activation. We report that upon CDT treatment CDC25C is fully sequestered in the cytoplasmic compartment, an effect that is reminiscent of DNA damage-dependent checkpoint activation. We show that the checkpoint kinase CHK2, an upstream regulator of CDC25C, is phosphorylated and activated after CDT treatment. In contrast to what is observed with other DNA damaging agents, we demonstrate that the activation of CHK2 can only take place during S-phase. Use of wortmannin and caffeine suggests that this effect is no…

Intracellular FluidCell cycle checkpointCytolethal distending toxinCell Cycle ProteinsAtaxia Telangiectasia Mutated ProteinsBiochemistryS PhaseWortmanninchemistry.chemical_compoundStructural BiologyPhosphorylation0303 health sciences030302 biochemistry & molecular biologyCell CycleCell cycleProtein-Tyrosine Kinases3. Good healthCell biologyDNA-Binding Proteinsbiological phenomena cell phenomena and immunityWortmanninG2 PhaseCytolethal distending toxinBacterial ToxinsProto-Oncogene Proteins pp60(c-src)Biophysics[SDV.BC]Life Sciences [q-bio]/Cellular BiologyBiologyProtein Serine-Threonine KinasesCell Line03 medical and health sciencesCaffeineGeneticsHumanscdc25 PhosphatasesCHEK1Molecular Biology[SDV.BC] Life Sciences [q-bio]/Cellular Biology030304 developmental biologyCheckpoint 2 kinaseCyclin-dependent kinase 1Cell growthTumor Suppressor ProteinsCell BiologyG2-M DNA damage checkpointCDC25CAndrostadienesGenes cdcchemistryCancer researchHeLa CellsFEBS letters
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Pharmacodynamic approach to study the gene transfer process employing non-viral vectors

2000

Abstract In the present work we set out to apply pharmacodynamic concepts derived from dose–response curves (Potency and Efficacy) to characterize the gene transfer efficiency of a vector:DNA complex. We employed two widely used vectors, the cationic lipid DOTAP (N,N,N-trimethyl 1-2-3-bis (1-oxo-9-octa-decenyl)oxy-(Z,Z)-1-propanaminium methyl sulfate) and the cationic polymer PEI (polyethylenimine, 800 kDa) to transfect several constructions of the green fluorescent protein cDNA. The analysis of dose–response curves indicated that in all cases the goodness-of-fit was > 0.99. Potency is a measure that provides information on gene activity per amount of DNA. Efficacy is a measure of maximum g…

Intrinsic activityGenetic VectorsComputational biologyBiologyBiochemistryViral vectorFatty Acids MonounsaturatedMiceComplementary DNAGene expressionTumor Cells CulturedAnimalsHumansPotencyGenePharmacologyGeneticsReporter geneDose-Response Relationship DrugGenetic transferGene Transfer TechniquesDNAAnti-Bacterial AgentsQuaternary Ammonium CompoundsGentamicinsHeLa CellsPlasmidsBiochemical Pharmacology
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Drift time-specific collision energies enable deep-coverage data-independent acquisition proteomics.

2013

A data-independent acquisition (DIA) mass spectrometry approach, ultradefinition (UD)MSE, offers high reproducibility and improved proteome coverage over alternative DIA and data-dependent acquisition workflows. We present a data-independent acquisition mass spectrometry method, ultradefinition (UD) MSE. This approach utilizes ion mobility drift time-specific collision-energy profiles to enhance precursor fragmentation efficiency over current MSE and high-definition (HD) MSE data-independent acquisition techniques. UDMSE provided high reproducibility and substantially improved proteome coverage of the HeLa cell proteome compared to previous implementations of MSE, and it also outperformed a…

IonsProteomicsReproducibilityProteomeSoftware toolCoverage dataCell BiologyBiologyProteomicsCollisionBioinformaticsMass spectrometryBiochemistryPeptide Fragmentsbody regionsTandem Mass SpectrometryProteomeHumansMolecular BiologyAlgorithmSoftwareBiotechnologyChromatography LiquidHeLa CellsNature methods
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