Search results for "ALK"

showing 10 items of 4314 documents

Sequence similarity of mammalian epoxide hydrolases to the bacterial haloalkane dehalogenase and other related proteins Implication for the potential…

1994

Direct comparison of the amino acid sequences of microsomal and soluble epoxide hydrolase superficially indicates that these enzymes are unrelated. Both proteins, however, share significant sequence similarity to a bacterial haloalkane dehalogenase that has earlier been shown to belong to the alpha/beta hydrolase fold family of enzymes. The catalytic mechanism for the dehalogenase has been elucidated in detail [Verschueren et al. (1993) Nature 363, 693-698] and proceeds via an ester intermediate where the substrate is covalently bound to the enzyme. From these observations we conclude (i) that microsomal and soluble epoxide hydrolase are distantly related enzymes that have evolved from a co…

Epoxide hydrolase 2StereochemistryHydrolasesMolecular Sequence DataBiophysicsHydrolaseEsteraseBiochemistryEsteraseCatalysisChelataseα/β Hydrolase foldBacterial ProteinsStructural BiologyMicrosomesHydrolaseGeneticsAnimalsAmino Acid SequenceEpoxide hydrolaseMolecular BiologyDehalogenasePeroxidasechemistry.chemical_classificationEpoxide HydrolasesMammalsBacteriaSequence Homology Amino AcidCell BiologyLipaseBiological EvolutionEnzymechemistryBiochemistrySolubilityEpoxide HydrolasesLuciferaseHaloalkane dehalogenaseFEBS Letters
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Anti-Eryptotic Activity of Food-Derived Phytochemicals and Natural Compounds

2022

Human red blood cells (RBCs), senescent or damaged due to particular stress, can be removed by programmed suicidal death, a process called eryptosis. There are various molecular mechanisms underlying eryptosis. The most frequent is the increase in the cytoplasmic concentration of Ca2+ ions, later exposure of erythrocytes to oxidative stress, hyperosmotic shock, ceramide formation, stimulation of caspases, and energy depletion. Phosphatidylserine (PS) exposed by eryptotic RBCs due to interaction with endothelial CXC-Motiv-Chemokin-16/Scavenger-receptor, causes the RBCs to adhere to vascular wall with consequent damage to the microcirculation. Eryptosis can be triggered by various xenobiotics…

ErythrocytesOrganic ChemistryPhytochemicalsEryptosisAnemiaGeneral MedicinePhosphatidylserinesRed blood cellsCatalysisPhenolic compoundsComputer Science ApplicationsInorganic ChemistryOxidative StressAlkaloidsSettore BIO/10 - BiochimicaFood-derived compoundAnimalsHumansCalciumPhysical and Theoretical ChemistryMolecular BiologySpectroscopy
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Conformational polymorphs of 1,1,2,2-tetrachloroethane: pressure vs. temperature.

2011

Directional Cl···Cl type I and II interactions govern the low-density aggregation of 1,1,2,2-tetrachloroethane molecules in synclinal conformation in the crystalline state at low temperature, whereas the dense molecular packing in high-pressure is achieved for the antiperiplanar conformers and electrostatically less favored Cl···Cl contacts. The mechanism of transformation between loose and dense associations involves the collapse of Cl···Cl contacts and conformational conversion.

EthaneChemistry1122-TetrachloroethaneMetals and AlloysChemieMolecular ConformationTemperatureGeneral ChemistryCrystallography X-RayCatalysisMolecular conformationSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsCrystallographychemistry.chemical_compoundChloridesAlkane stereochemistryMaterials ChemistryCeramics and CompositesHydrocarbons ChlorinatedPressureMoleculeConformational isomerismChemical communications (Cambridge, England)
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“Dumb” pH-Independent and Biocompatible Hydrogels Formed by Copolymers of Long-Chain Alkyl Glycidyl Ethers and Ethylene Oxide

2020

The formation and rheological properties of hydrogels based on amphiphilic ABA triblock polyether copolymers are described, relying solely on the hydrophobic interaction of long-chain alkyl glycidyl ether (AlkGE)- based A-blocks that are combined with a hydrophilic poly(ethylene glycol) (PEG) midblock. Via anionic ring-opening copolymerization (AROP), ethylene oxide (EO) and long-chain alkyl glycidyl ethers (AlkGEs) were copolymerized, using deprotonated poly(ethylene glycol) (PEG) macroinitiators (Mn of 10, 20 kg mol-1). The polymerization afforded amphiphilic ABA triblock copolymers with molar masses in the range of 21-32 kg mol-1 and dispersities (Đ) of Đ = 1.07-1.17. Kinetic studies rev…

Ethylene OxidePolymers and PlasticsPolymersBioengineering02 engineering and technology010402 general chemistry01 natural sciencesPolyethylene GlycolsBiomaterialsHydrophobic effectchemistry.chemical_compoundAmphiphilePolymer chemistryMaterials ChemistryCopolymerAlkylchemistry.chemical_classificationEthylene oxidetechnology industry and agricultureHydrogelsHydrogen-Ion Concentration021001 nanoscience & nanotechnology0104 chemical sciencesKineticschemistryPolymerizationSelf-healing hydrogelsEpoxy Compounds0210 nano-technologyEthylene glycolBiomacromolecules
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Long-Chain Alkyl Epoxides and Glycidyl Ethers: An Underrated Class of Monomers.

2020

Long-chain epoxides and specifically alkyl glycidyl ethers represent a class of highly hydrophobic monomers for anionic ring-opening polymerization (AROP), resulting in apolar aliphatic polyethers. In contrast, poly(ethylene glycol) is known for its high solubility in water. The combination of hydrophobic and hydrophilic monomers in block and statistical copolymerization reactions enables the synthesis of amphiphilic polyethers for a wide range of purposes, utilizing micellar interactions in aqueous solutions, e.g., viscosity enhancement of aqueous solutions, formation of supramolecular hydrogels, or for polymeric surfactants. Controlled polymerization of these highly hydrophobic long-chain…

Ethylene OxidePolymers and PlasticsPolymersEpoxide02 engineering and technologyPoloxamer010402 general chemistry01 natural sciencesPolymerizationchemistry.chemical_compoundSurface-Active AgentsAmphiphileMaterials ChemistryCopolymerAlkylMicelleschemistry.chemical_classificationEthylene oxideChemistryOrganic Chemistrytechnology industry and agriculture021001 nanoscience & nanotechnologyCombinatorial chemistry0104 chemical sciencesMonomerPolymerizationEpoxy Compounds0210 nano-technologyEthylene glycolHydrophobic and Hydrophilic InteractionsMacromolecular rapid communications
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Polymerization of Ethylene Oxide, Propylene Oxide, and Other Alkylene Oxides: Synthesis, Novel Polymer Architectures, and Bioconjugation.

2015

The review summarizes current trends and developments in the polymerization of alkylene oxides in the last two decades since 1995, with a particular focus on the most important epoxide monomers ethylene oxide (EO), propylene oxide (PO), and butylene oxide (BO). Classical synthetic pathways, i.e., anionic polymerization, coordination polymerization, and cationic polymerization of epoxides (oxiranes), are briefly reviewed. The main focus of the review lies on more recent and in some cases metal-free methods for epoxide polymerization, i.e., the activated monomer strategy, the use of organocatalysts, such as N-heterocyclic carbenes (NHCs) and N-heterocyclic olefins (NHOs) as well as phosphazen…

Ethylene OxidePolymersEpoxide02 engineering and technology010402 general chemistry01 natural sciencesPolymerizationchemistry.chemical_compoundPolymer chemistryCopolymerOrganic chemistryPropylene oxideEthylene oxideMolecular StructureCationic polymerizationOxidesGeneral Chemistry021001 nanoscience & nanotechnology0104 chemical sciencesAnionic addition polymerizationchemistryPolymerizationAlkynesCoordination polymerizationEpoxy Compounds0210 nano-technologyChemical reviews
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Reactions at Interfaces: Oxygenation of n-Butyl Ligands Anchored on Silica Surfaces with Methyl(trifluoromethyl)dioxirane

2011

The oxygenation of n-butyl and n-butoxy chains bonded to silica with methyl(trifluoromethyl)dioxirane (1) revealed the ability of the silica matrix to release electron density toward the reacting C(2)-H σ-bond through the Si-C(1) and Si-O(1) σ-bonds connecting the alkyl chain to the surface (silicon β-effect). The silica surface impedes neither the alkyl chain adopting the conformation required for the silicon β-effect nor dioxirane 1 approaching the reactive C(2) methylene group. Reaction regioselectivity is insensitive to changes in the solvation of the reacting system, the location of organic ligands on the silica surface, and the H-bonding character of the silica surface. Reaction rates…

Ethylene OxideTrimethylsilylSiliconSurface PropertiesMolecular Conformationchemistry.chemical_elementChemistry Techniques SyntheticPhotochemistryReaction ratechemistry.chemical_compoundDioxiraneMethyleneAlkylchemistry.chemical_classificationTrifluoromethylOrganic ChemistryRegioselectivityEstersHydrogen BondingStereoisomerismSilicon DioxideOxygenSolutionsKineticschemistryButanesOxidation-ReductionThe Journal of Organic Chemistry
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[N⋅⋅⋅I+⋅⋅⋅N] Halogen-Bonded Dimeric Capsules from Tetrakis(3-pyridyl)ethylene Cavitands

2016

Two [N⋅⋅⋅I+⋅⋅⋅N] halogen-bonded dimeric capsules using tetrakis(3-pyridyl)ethylene cavitands with different lower rim alkyl chains are synthesized and analyzed in solution and the gas phase. These first examples of symmetrical dimeric capsules making use of the iodonium ion (I+) as the main connecting module are characterized by 1H NMR spectroscopy, diffusion ordered NMR spectroscopy (DOSY), electrospray ionization mass spectrometry (ESI-MS), and ion mobility-mass spectrometry (TW-IMS) experiments. The synthesis and effective halogen-bonded dimerization proceeds through analogous dimeric capsules with [N⋅⋅⋅Ag+⋅⋅⋅N] binding motifs as the intermediates as evidenced by the X-ray structures of …

EthyleneElectrospray ionizationhalogen bonds010402 general chemistryMass spectrometry01 natural sciencesCatalysiscavitandsIonchemistry.chemical_compoundPolymer chemistryOrganic chemistrySpectroscopyta116Alkylmass spectrometrychemistry.chemical_classificationta114010405 organic chemistrydimeric capsulesGeneral MedicineGeneral ChemistryNuclear magnetic resonance spectroscopy0104 chemical scienceschemistryHalogenhalonium ionsANGEWANDTE CHEMIE
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Non-bridged amido cyclopentadienyl complexes of titanium: synthesis, characterization, and olefin polymerization catalysis

2000

Alkylation of Ti(η 5 -C 5 Me 5 )(NMe 2 )Cl 2 gives thermally stable, crystalline dialkyl complexes Ti(η 5 -C 5 Me 5 )(NMe 2 )R 2 (R=Me, CH 2 Ph, Ph). The molecular structure of the dibenzyl complex reveals an unprecedented conformation of the doubly bonded NMe 2 group which is turned parallel to the η 5 -C 5 Me 5 ligand, according to single-crystal X-ray diffraction studies. Treatment of the dibenzyl complex with B(C 6 F 5 ) 3 in d 5 -bromobenzene solution results in the quantitative formation of a thermally (>10°C) unstable monobenzyl cation as solvent-separated ion pair [Ti(η 5 -C 5 Me 5 )(NMe 2 )CH 2 Ph] + [PhCH 2 B(C 6 F 5 ) 3 ] − which efficiently polymerizes styrene syndiospecifically…

EthyleneLigandOrganic ChemistryAlkylationPhotochemistryBiochemistryMedicinal chemistryStyreneCatalysisInorganic Chemistrychemistry.chemical_compoundchemistryPolymerizationCyclopentadienyl complexMaterials ChemistryMoleculePhysical and Theoretical ChemistryJournal of Organometallic Chemistry
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Effective copolymerization of ethylene with α,ω-alkenols and homopolymerization of α,ω-alkenols catalyzed by aminophenolate zirconium complex

2019

Abstract A zirconium complex of diamine-bis(phenolate) ligand, [(tBu2O2NN’)ZrCl]2(μ-O) where (tBu2O2NN’) = Me2N(CH2)2N(CH2–2-O−-3,5-tBu2-C6H2)2, activated with (iBu)3Al/Ph3CB(C6F5)4, was for the first time used in copolymerization of ethylene with unsaturated alcohols (CH2 = CH(CH2)nCH2OH, where n = 7, 8, 3). The hydroxyl groups of comonomers were protected with R3-xAlClx (where x = 0 or 1, R = iBu, Et). In contrast to the formerly reported catalysts, the activity of this catalyst is much higher in ethylene/alkenols copolymerization than in ethylene homopolymerization and its lifetime is long. Moreover, the copolymers with high polar comonomer contents (up to 16.4 mol%, 52.3 wt%) were produ…

EthylenePolymers and PlasticsGeneral Chemical Engineeringαchemistry.chemical_element02 engineering and technology010402 general chemistry01 natural sciencesBiochemistryCatalysischemistry.chemical_compoundcoordination polymerizationω-alkenolsPolymer chemistryethyleneMaterials ChemistryCopolymerEnvironmental Chemistryfunctionalization of polymersZirconiumLigandComonomerGeneral Chemistry021001 nanoscience & nanotechnology0104 chemical scienceschemistryPolymerizationCoordination polymerization0210 nano-technologyReactive and Functional Polymers
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