Search results for "Hydrogen"

showing 10 items of 4254 documents

Hydrogen activation with perfluorinated organoboranes: 1,2,3-tris(pentafluorophenyl)-4,5,6,7-tetrafluoro-1-boraindene

2013

The perfluorinated boraindene was synthesized and fully characterized. Both computational and crystallographic data show that is antiaromatic. Compound was shown to react reversibly with H2 and to catalyse the hydrogenation of cyclohexene. The mechanism of catalysis was probed experimentally and computationally.

TrisHydrogenChemistryMetals and AlloysCyclohexeneCrystallographic datachemistry.chemical_elementGeneral ChemistryPhotochemistryCatalysisSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsCatalysischemistry.chemical_compoundPolymer chemistryMaterials ChemistryCeramics and Compositesta116AntiaromaticityChem. Commun.
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Darstellung einiger oligomerer Cyclo{oligo[(2-hydroxy-1,3-phenylen)methylen]}e. Spektroskopische Untersuchung ihrer Pseudorotation

1978

Es wird die Darstellung von Cyclo{tris[(2-hydroxy-5-methyl-1,3-phenylen)methylen]-(2-hydroxy-5-tert-butyl-1,3-phenylen)methylen} (4a), Cyclo{bis[(2-hydroxy-5-methyl-1,3-phenylen)methylen]-bis[(2-hydroxy-5-tert-butyl-1,3-phenylen)methylen]}(4b) und Cyclo-{pentakis[(2-hydroxy-5-methyl-1,3-phenylen)methylen]} (4c) beschrieben. Die IR-Spektren zeigen, das die phenolischen Hydroxygruppen der Vierringverbindungen 4a und 4b intramolekulare, vom Losungs(CCl4)- oder Zerteilungsmittel (KBr) weitgehend unabhangige Wasserstoffbrucken bilden, die bei der pentameren Ringverbindung 4c schwacher sind. Anhand der 1H-NMR-Spektren last sich bei diesen Verbindungen eine Pseudorotation nachweisen. Die Massenspe…

TrisPolymers and PlasticsHydrogen bondStereochemistryPentamerInfrared spectroscopyMedicinal chemistrychemistry.chemical_compoundColloid and Surface ChemistrychemistryIntramolecular forcePolymer chemistryMaterials ChemistryMoleculePseudorotationPhysical and Theoretical ChemistryMethyleneDie Makromolekulare Chemie
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Stable adducts of nerve agents sarin, soman and cyclosarin with TRIS, TES and related buffer compounds—Characterization by LC-ESI-MS/MS and NMR and i…

2009

Abstract Buffering compounds like TRIS are frequently used in chemical, biochemical and biomedical applications to control pH in solution. One of the prerequisites of a buffer compound, in addition to sufficient buffering capacity and pH stability over time, is its non-reactivity with other constituents of the solution. This is especially important in the field of analytical chemistry where analytes are to be determined quantitatively. Investigating the enzymatic hydrolysis of G-type nerve agents sarin, soman and cyclosarin in buffered solution we have identified stable buffer adducts of TRIS, TES and other buffer compounds with the nerve agents. We identified the molecular structure of the…

TrisSpectrometry Mass Electrospray IonizationMagnetic Resonance SpectroscopyBicineSomanClinical BiochemistryAnalytical chemistryCyclosarinBiochemistryAnalytical Chemistrychemistry.chemical_compoundOrganophosphorus CompoundsTandem Mass SpectrometryChemical Warfare AgentsTromethamineTE bufferTBE bufferTricineAqueous solutionChromatographyChemistryCell BiologyGeneral MedicineHydrogen-Ion ConcentrationSarinMOPSModels ChemicalChromatography LiquidJournal of Chromatography B
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Purification, isolation and characterization of a phosphoglycolate phosphatase isoenzyme from human erythrocytes.

1982

1. Preparation, purification and characterization of a phosphoglycolate phosphatase (PGP) isoenzyme from human erythrocytes was achieved by DEAE-Sepharose CL-6B chromatography and isoelectric focusing using carrier ampholytes, pH 4-6. 2. The isoenzyme has an isoelectric point of 5.00 +/- 0.05 and could be purified 33,000 fold to a specific activity of 32.7 U/mg of protein. It represents the PGP phenotype 1 consisting of a single isoenzyme. 3. The enzyme is composed of two subunits (mol. wt 35,000) which are identical and not connected by SS-bridges. 4. At 4 degrees C the isoenzyme is more stable in the pH range of 7-9 than at acid pH values. 5. Incubation at 30 and 40 degrees C for 4 hr doe…

Trischemistry.chemical_classificationChromatographyErythrocytesHot TemperatureIsoelectric focusingProtein ConformationBiologyHydrogen-Ion ConcentrationBiochemistryIsozymePhosphoric Monoester HydrolasesMOPSIsoenzymesMolecular Weightchemistry.chemical_compoundKineticsIsoelectric pointEnzymechemistryBiochemistryHumansSpecific activityIsoelectric PointPhosphoglycolate phosphataseThe International journal of biochemistry
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Selective dimerisation of tetraurea calix[4]arenes

2010

The formation of hydrogen-bonded dimeric capsules from tetraurea calix[4]arenes is controlled by loops, connecting adjacent urea functions, and more or less bulky substituents. The dimerisation is only possible if loops are not overlapping and if the respective residues can pass the loops. A sorting scheme based on small and bulky residues and one to four loops allows reducing the number of possible dimers from 35 to 6 in a stoichiometric mixture of 11 ureas. With three different loop sizes (O–(CH2) n –O chains with n = 10, 14, 20 connecting adjacent phenylurea functions via their meta positions), it is possible to distinguish four urea residues of different sizes (small, medium, bulky and …

Trischemistry.chemical_compoundResidue (chemistry)chemistryHydrogen bondStereochemistryCalixareneUreaGeneral ChemistrySelf-assemblyStoichiometrySupramolecular Chemistry
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Inhibitor-Induced Dimerization of an Essential Oxidoreductase from African Trypanosomes

2018

Trypanosomal and leishmanial infections claim tens of thousands of lives each year. The metabolism of these unicellular eukaryotic parasites differs from the human host and their enzymes thus constitute promising drug targets. Tryparedoxin (Tpx) from Trypanosoma brucei is the essential oxidoreductase in the parasite's hydroperoxide-clearance cascade. In vitro and in vivo functional assays show that a small, selective inhibitor efficiently inhibits Tpx. With X-ray crystallography, SAXS, analytical SEC, SEC-MALS, MD simulations, ITC, and NMR spectroscopy, we show how covalent binding of this monofunctional inhibitor leads to Tpx dimerization. Intra- and intermolecular inhibitor-inhibitor, pro…

TrypanosomaProtein ConformationSpermidineDimerTrypanosoma brucei bruceiAntiprotozoal AgentsMolecular Dynamics SimulationTrypanosoma brucei010402 general chemistry01 natural sciencesCatalysischemistry.chemical_compoundThioredoxinsBacterial ProteinsIn vivoOxidoreductaseAnimalsHumansEnzyme Inhibitorschemistry.chemical_classificationbiology010405 organic chemistryHydrogen PeroxideGeneral ChemistryNuclear magnetic resonance spectroscopyLigand (biochemistry)biology.organism_classificationGlutathione0104 chemical sciencesEnzymechemistryBiochemistryDrug DesignChemically induced dimerizationProtein MultimerizationOxidoreductasesOxidation-ReductionProtein BindingAngewandte Chemie International Edition
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Vomilenine Reductase — a novel Enzyme catalyzing a crucial Step in the Biosynthesis of the Therapeutically applied Antiarrhythmic Alkaloid Ajmaline

2002

Delineation of the biochemical pathway leading to the antiarrhythmic Rauvolfia alkaloid ajmaline has been an important target in biosynthetic research for many years. The biosynthetic sequence starting with tryptamine and the monoterpene secologanin consists of about 10 different steps. Most of the participating enzymes have been detected and characterized previously, except those catalyzing the reduction of the intermediate vomilenine. A novel NADPH-dependent enzyme that reduces the intermediate has been isolated from Rauvolfia serpentina cell suspension cultures. Vomilenine reductase (M(r )43 kDa, temp opt 30 degrees C, pH opt 5.7-6.2), saturates the indolenine double bond of vomilenine w…

TryptamineRauvolfiaStereochemistryClinical BiochemistryPharmaceutical ScienceReductaseBiochemistryCatalysisRauwolfiaIndole Alkaloidschemistry.chemical_compoundRauvolfia serpentinaDrug DiscoverymedicineSecologanin Tryptamine AlkaloidsMolecular BiologyCells CulturedAjmalineChromatographyMolecular StructurebiologyOrganic ChemistryTemperatureHydrogen-Ion Concentrationbiology.organism_classificationSecologanin Tryptamine AlkaloidsAjmalinechemistryBiochemistryVomilenineMolecular MedicineSecologaninOxidoreductasesAnti-Arrhythmia AgentsNADPmedicine.drugBioorganic & Medicinal Chemistry
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Acidic Environment Leads to ROS-Induced MAPK Signaling in Cancer Cells

2011

Tumor micromilieu often shows pronounced acidosis forcing cells to adapt their phenotype towards enhanced tumorigenesis induced by altered cellular signalling and transcriptional regulation. In the presents study mechanisms and potential consequences of the crosstalk between extra- and intracellular pH (pH(e), pH(i)) and mitogen-activated-protein-kinases (ERK1/2, p38) was analyzed. Data were obtained mainly in AT1 R-3327 prostate carcinoma cells, but the principle importance was confirmed in 5 other cell types. Extracellular acidosis leads to a rapid and sustained decrease of pH(i) in parallel to p38 phosphorylation in all cell types and to ERK1/2 phosphorylation in 3 of 6 cell types. Furth…

Tumor PhysiologyIntracellular Spacelcsh:MedicineSignal transductionERK signaling cascadeMolecular cell biologyNeoplasmsBasic Cancer ResearchTumor MicroenvironmentSignaling in Cellular ProcessesPhosphorylationCyclic AMP Response Element-Binding ProteinCreb Signalinglcsh:ScienceCellular Stress ResponsesMultidisciplinaryKinaseMechanisms of Signal TransductionSignaling cascadesHydrogen-Ion ConcentrationProtein-Tyrosine KinasesCell biologyOncologyMedicinePhosphorylationMitogen-Activated Protein KinasesSodium-Potassium-Exchanging ATPaseIntracellularResearch ArticleCell SurvivalMAP Kinase Signaling Systemp38 mitogen-activated protein kinasesIntracellular pHBiologyCREBModels BiologicalCell GrowthDogsCell Line TumorAnimalsHumansProtein Kinase InhibitorsBiologyPI3K/AKT/mTOR pathwaylcsh:RRatsEnzyme ActivationCancer cellbiology.proteinlcsh:QExtracellular SpaceReactive Oxygen SpeciesAcidsPLoS ONE
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Novel γ-turn mimetics with a reinforced hydrogen bond

1999

Abstract Pyridylmethylphenols 2 can mimic the geometry of γ-turns. Hydrogen bonding in 2 has been characterized by X-ray crystallography, IR and NMR spectroscopy, and molecular modeling.

Turn (biochemistry)CrystallographyMolecular modelChemistryHydrogen bondOrganic ChemistryDrug DiscoveryNuclear magnetic resonance spectroscopyBiochemistryTetrahedron Letters
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Photo Induced Radical Reactions

2012

This article discusses a number of reactions of potential synthetic interest occurring through photochemically generated organic radicals. Emphasis is placed on the nature of the resulting photoproducts, whose formation is discussed on a mechanistic basis. If available, experimental evidence (obtained by laser flash photolysis or related time-resolved techniques) is provided. The material is organized according to the reaction types, for instance, homolytic cleavage, mesolytic cleavage, radical addition, and oxidative or reductive electron transfer. In addition to the classical carboncarbon or carbonhydrogen bond breaking processes, such as the Norrish type I reaction, the hydrogen abstract…

Type I reactionElectron transferChemistryRadicalFlash photolysisBond breakingCleavage (embryo)PhotochemistryHydrogen atom abstractionBond cleavage
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