Search results for "Hexylamine"

showing 10 items of 13 documents

Performance of amines as silanol suppressors in reversed-phase liquid chromatography

2016

In reversed-phase liquid chromatography, cationic basic compounds yield broad and asymmetrical peaks, as a result of their ionic interaction with the anionic free silanol groups present in the silica-based stationary phases (commonly derivatised with C18 groups). A simple way to improve the peak shape is the addition to the hydro-organic mobile phase of a reagent (usually called additive) with cationic character. This associates with the stationary phase to prevent the access of analytes to the free silanol groups. Cationic additives may interact electrostatically with the anionic silanols. The hydrophobic region of the additive may also associate with the alkyl chains bound to the stationa…

Adrenergic beta-AntagonistsIonic Liquids010402 general chemistry01 natural sciencesBiochemistryAnalytical Chemistrychemistry.chemical_compoundHexylamineEndcappingPhase (matter)BoratesAminesChromatography Reverse-PhaseChromatography010401 analytical chemistryOrganic ChemistryImidazolesCationic polymerizationGeneral MedicineReversed-phase chromatographySilanes0104 chemical sciencesSilanolchemistryIonic liquidPentylamineHydrophobic and Hydrophilic InteractionsJournal of Chromatography A
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Tuning the selectivity of molecularly imprinted polymer extraction of arylcyclohexylamines: From class-selective to specific

2020

Abstract A molecularly imprinted polymer (MIP) has been prepared in presence of 3-hydroxy phencyclidine (3-OH PCP) as template by bulk polymerization using N,N-dimethylformamide, as porogenic solvent, for the selective solid-phase extraction (SPE) of arylcyclohexylamines from oral fluids. Experimental variables of the extraction procedure have been studied in order to increase both, extraction recovery of 3-OH PCP, used as model analyte, and imprinting factor. By modifying the composition of the washing solvent, the selectivity of the MIP extraction procedure can be tuned, moving from an arylcyclohexylamine selective method to a 3-OH PCP specific method. The applicability of the synthesized…

AnalyteArylcyclohexylamineBulk polymerizationSurface PropertiesIon-mobility spectrometry02 engineering and technology01 natural sciencesBiochemistryPolymerizationAnalytical ChemistryMolecularly Imprinted PolymersIon Mobility SpectrometrymedicineEnvironmental ChemistryParticle SizeSpectroscopyDetection limitCyclohexylaminesChromatographyMolecular StructureChemistry010401 analytical chemistryMolecularly imprinted polymer021001 nanoscience & nanotechnology0104 chemical sciencesSolvent0210 nano-technologySelectivitymedicine.drugAnalytica Chimica Acta
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1986

The aminolysis of diphenyl terephthalate by means of hexylamine was studied in dimethyl sulfoxide as a model reaction for polyamidation. The kinetic analysis showed that the two ester groups of the diphenyl ester do not react independently. Furthermore, the reaction of the first ester group was of mixed second and third order, while the reaction of the second ester group contained only a second order term. The rate constants found were used to determine the Arrhenius activation parameters.

Arrhenius equationsymbols.namesakechemistry.chemical_compoundCondensation polymerReaction rate constantAminolysisMonomerChemistryDimethyl sulfoxideHexylamineKineticsPolymer chemistrysymbolsDie Makromolekulare Chemie
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VCD studies on cyclic peptides assembled from L-α-amino acids and a trans-2-aminocyclopentane- or trans-2-aminocyclohexane carboxylic acid.

2010

The increasing interest in peptidomimetics of biological relevance prompted us to synthesize a series of cyclic peptides comprising trans-2-aminocyclohexane carboxylic acid (Achc) or trans-2-aminocyclopentane carboxylic acid (Acpc). NMR experiments in combination with MD calculations were performed to investigate the three-dimensional structure of the cyclic peptides. These data were compared to the conformational information obtained by electronic circular dichroism (ECD) and vibrational circular dichroism (VCD) spectroscopy. Experimental VCD spectra were compared to theoretical VCD spectra computed quantum chemically at B3LYP/6-31G(d) density functional theory (DFT) level. The good agreem…

Circular dichroismCyclohexanecarboxylic AcidsPeptidomimeticStereochemistryCarboxylic acidMolecular ConformationMolecular Dynamics SimulationBiochemistryelectronic circular dichroismPeptides CyclicMolecular dynamicsStructural BiologyDrug DiscoveryCycloleucineMolecular BiologyNuclear Magnetic Resonance BiomolecularPharmacologychemistry.chemical_classificationCyclohexylaminesCircular DichroismOrganic Chemistrycyclic peptidestrans-2-aminocyclopentaneGeneral Medicinevibrational circular dichroismCyclic peptideNMRAmino acidtrans-2-aminocyclohexane carboxylic acidchemistryVibrational circular dichroismMolecular MedicineDensity functional theorycarboxylic acidPeptidomimeticsJournal of peptide science : an official publication of the European Peptide Society
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Sensitive determination of aliphatic amines in water by high-performance liquid chromatography with chemiluminescence detection.

2004

A sensitive method has been developed for liquid chromatographic determination of short aliphatic amines in water samples. Analytes are preconcentrated and dansylated on solid sorbents (C18 solid-phase extraction cartridges). The dansyl derivatives are chromatographed and post-column mixed with peroxyoxalate (TCPO) and H2O2 in order to perform chemiluminescence detection. Optimal results have been obtained using a sample volume of 5 ml. The method has been applied to the quantification or screening of several aliphatic amines: methylamine, ethylamine, butylamine, diethylamine, pentylamine and hexylamine. The screening procedure has been developed including also polyamines (putrescine, cadav…

DiethylamineDetection limitChromatographyOrganic ChemistryGeneral MedicineBiochemistryHigh-performance liquid chromatographyPeroxyoxalateSensitivity and SpecificityAnalytical Chemistrylaw.inventionchemistry.chemical_compoundSpectrometry FluorescencechemistrylawHexylamineLuminescent MeasurementsSpectrophotometry UltravioletEthylaminePentylamineAminesChromatography High Pressure LiquidChemiluminescenceJournal of chromatography. A
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Artemisinin derivatives induce iron-dependent cell death (ferroptosis) in tumor cells

2015

Abstract Background Apoptosis and other forms of cell death have been intensively investigated in the past years to explain the mode of action of synthetic anticancer drugs and natural products. Recently, a new form of cell death emerged, which was termed ferroptosis, because it depends on intracellular iron. Here, the role of genes involved in iron metabolism and homeostasis for the cytotoxicity of ten artemisinin derivatives have been systematically investigated. Material and methods Log10IC50 values of 10 artemisinin derivatives (artesunate, artemether, arteether, artenimol, artemisitene, arteanuin B, another monomeric artemisinin derivative and three artemisinin dimer molecules) were co…

IronArtesunatePharmaceutical ScienceApoptosisTransferrin receptorDeferoxaminePhenylenediaminesPharmacologyBiologyInhibitory Concentration 50chemistry.chemical_compoundCell Line Tumorparasitic diseasesDrug DiscoverymedicineHumansArtemetherArtemisininCytotoxicityOligonucleotide Array Sequence AnalysisPharmacologychemistry.chemical_classificationCyclohexylaminesCell DeathMolecular StructureArtemisinin DimerArtemisininsGene Expression Regulation NeoplasticComplementary and alternative medicinechemistryApoptosisTransferrinArtesunateMolecular MedicineArtemethermedicine.drugPhytomedicine
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Bishistidyl heme hexacoordination, a key structural property in Drosophila melanogaster hemoglobin

2005

Hemoglobins at high concentration have been isolated long ago from some insect larvae living in hypoxic environments. Conversely, a monomeric hemoglobin has been discovered recently in the fruit fly Drosophila melanogaster as intracellular protein expressed both in larvae and in the adult fly. Such a finding indicates that the oxygen supply in insects may be more complex than previously thought, relying not only on O2 diffusion through the tubular tracheal system, but also on carrier-mediated transport and storage. We present here the crystal structure of recombinant D. melanogaster hemoglobin at 1.20 A resolution. Spectroscopic data show that the protein displays a hexacoordinated heme, wh…

Protein ConformationHemeMatrix (biology)BiologyCrystallography X-RayLigandsBiochemistrylaw.inventionchemistry.chemical_compoundHemoglobinslawMelanogasterAnimalsDrosophila ProteinsHistidineMolecular BiologyHemeCyclohexylaminesBinding SitesSpectrum AnalysisfungiCell BiologyHEXAbiology.organism_classificationOxygenMyoglobinchemistryBiochemistryAlkanesulfonic AcidsBiophysicsRecombinant DNAHemoglobinDrosophila melanogaster
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CCDC 220523: Experimental Crystal Structure Determination

2004

Related Article: S.Matsui, Y.Yoshida, Y.Takagi, T.P.Spaniol, J.Okuda|2004|J.Organomet.Chem.|689|1155|doi:10.1016/j.jorganchem.2003.11.041

Space GroupCrystallographyCrystal SystemCrystal StructureCell Parameters4-t-Butyl-N-(2-pyrrolylmethylene)cyclohexylamineExperimental 3D Coordinates
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Solvent-Enhanced Diastereo- and Regioselectivity in the PdII-Catalyzed Synthesis of Six- and Eight-Membered Heterocycles viacis-Aminopalladation

2009

The Pd(II)-catalyzed intramolecular oxidative cyclization of tosyl-protected cis- and trans-N-allyl-2-aminocyclohexanecarboxamides was examined, and efficient syntheses of cyclohexane-fused pyrimidin-4-ones and 1,5-diazocin-6-ones were developed. In the course of the research, a marked solvent effect was observed on both the regio- and diastereoselectivity. Additionally, a novel Pd(II)-mediated domino oxidation, oxidative amination reaction was discovered. Our experimental and theoretical findings suggest that the reactions proceed via a cis-aminopalladation mechanism.

Vinyl CompoundsCyclohexanecarboxylic AcidsStereochemistrychemistry.chemical_elementPyrimidinonesCatalysisCatalysisCyclohexanesAminationAminationCyclohexylaminesOxidative cyclizationMolecular StructureOrganic ChemistryRegioselectivityStereoisomerismGeneral ChemistryAzocinesAllyl CompoundsSolventchemistryCyclizationIntramolecular forceSolvent effectsOxidation-ReductionPalladiumPalladiumChemistry - A European Journal
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Identification and structural characterization of O-beta-ribosyl-(1"----2')-adenosine-5"-phosphate in yeast methionine initiator tRNA.

1990

We report in this paper on the complete structure determination of the modified nucleotide A*, now called Ar(p), that was previously identified in yeast methionine initiator tRNA as an isomeric form of O-ribosyl-adenosine bearing an additional phosphoryl-monoester group on its ribose2 moiety. By using the chemical procedure of periodate oxidation and subsequent beta-elimination with cyclohexylamine on mono- and dinucleotides containing Ar(p), we characterized the location of the phosphate group on the C-5" of the ribose2 moiety, and the linkage between the two riboses as a (1"----2')-glycosidic bond. Since the structural difference between phosphatase treated Ar(p) and authentic O-alpha-rib…

chemistry.chemical_classificationAdenosine monophosphateMethionineRNA Transfer MetStereochemistryChemical structurePhosphataseCyclohexylamineSaccharomyces cerevisiaeBiologyAdenosine Monophosphatechemistry.chemical_compoundchemistryBiochemistryTransfer RNAGeneticsMoietyNucleotideIndicators and ReagentsOxidation-ReductionChromatography High Pressure LiquidNucleic acids research
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