Search results for "Gate"

showing 10 items of 1811 documents

Isomerization of 9c11t/10t12c CLA in Triacylglycerols

2010

Published version of an article in the journal: Lipids . The original publication is available at Spingerlink. http://dx.doi.org/10.1007/s11745-010-3452-x Isomers of conjugated linoleic acid from 7t9c through 12t14t can be induced by thermal treatment of triacylglycerol samples of 9c11t or 10t12c fatty acids in glass tubes. The formation of conjugated linoleic acids (CLAs) has been observed during thermal induction of the above-mentioned triacylglycerols at 250, 280 and 320A degrees C. The concentrations of isomers formed in the mixture varied depending on the temperature and duration of the heating experiments. The objective of this study was to find a suitable thermal induction temperatur…

chemistry.chemical_classificationHeptaneChromatography GasChromatographySpectrophotometry InfraredGlycerideConjugated linoleic acidOrganic Chemistryfood and beveragesFatty acidCell BiologyThermal treatmentBiochemistryAmpoulechemistry.chemical_compoundIsomerismchemistryOrganic chemistryLinoleic Acids ConjugatedGas chromatographyVDP::Mathematics and natural science: 400::Chemistry: 440::Organic chemistry: 441IsomerizationTriglycerides
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Glycoconjugate expression and cartilage development of the cranial skeleton.

1998

Only few detailed investigations have focused on the glycobiology of cranial development. The functional elements in most inductive and morphogenetic processes are not individual cells, but rather collectives of interacting populations and extracellular matrix components that give rise to specific tissues and organs. Experimental evidence strongly suggests that sugar chains not only confer morphological characteristics. Complex carbohydrate molecules and their corresponding receptors are involved in recognition processes decoding biological information during cranial morphogenesis. The distribution patterns of glycoconjugates are highly dynamic and show a clear correlation with characterist…

chemistry.chemical_classificationHistologyGlycobiologyGlycoconjugateHistocytochemistryCartilageSkullMorphogenesisCell DifferentiationBiologyEpitopeCell biologyExtracellular matrixmedicine.anatomical_structureCartilageBiochemistrychemistryIn vivoLectinsmedicineAnimalsHumansAnatomyReceptorGlycoconjugatesActa anatomica
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Self-assembly of fluorescent diimidazolium salts: tailor properties of the aggregates changing alkyl chain features

2016

Searching for new fluorescent organic salts to be used in biomedical and electrochemical field, we conjugated properties of imidazolium salts with the ones of naphthalene diimide core and we obtained some N,N′-bis-(1-alkyl-3-propylimidazolium)naphthalene diimide diiodides. We took into account alkyl chains going from hexyl to dodecyl, as well as hydrogenated and fluorinated alkyl tails. After determination of their thermal behaviour by differential scanning calorimetry, concentration-, and temperature-dependent spectroscopic studies (UV-vis and fluorescence) were performed evidencing the occurrence of isodesmic and enthalpy-driven self-assembly processes. Properties of aggregates were also …

chemistry.chemical_classificationIsodesmic reactionScanning electron microscopeGeneral Chemical EngineeringDiimidazolium salts self-assembly H-aggregatesSettore CHIM/06 - Chimica Organica02 engineering and technologyGeneral ChemistryConjugated system010402 general chemistry021001 nanoscience & nanotechnologyPhotochemistry01 natural sciencesFluorescenceFluorescence spectroscopy0104 chemical sciencesDifferential scanning calorimetrychemistrySelf-assembly0210 nano-technologyAlkylRSC Advances
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Stopped-Flow and DFT Studies of Proton Transfer and Isomerization of 5-Amino-3-imino-1,2,6,7-tetracyano-3H-pyrrolizine and Its Related Base 2-(5-Amin…

2001

International audience; A complete kinetic study of pH-dependent isomerization of 5-amino-3-imino-1,2,6,7-tetracyano-3H-pyrrolizine (HL) and 2-(5-amino-3,4-dicyano-2H-pyrrol-2-ylidene)-1,1,2-tricyanoethanide (L‘-) in the pH range from −0.5 to +13 in aqueous solution, which spans over 7 orders of magnitude for the pseudo-first-order rates (log k from −4.8 to +2.5), has revealed for the first time the existence of the corresponding conjugate species L- and HL‘. The study has allowed the determination of the acid dissociation constants of HL (pKa) and HL‘ (pKa‘), as well as all of the individual forward and reverse isomerization rates of the acidic (HL/HL‘) and basic (L-/L‘-) forms. Although L…

chemistry.chemical_classificationIsomerizationAqueous solutionBase (chemistry)ProtonStereochemistryEquilibrium[CHIM.ORGA]Chemical Sciences/Organic chemistryProtonation02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesDecompositionAcid dissociation constant0104 chemical sciences[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistryKineticschemistryOrganic reactionsKinetic parametersPhysical and Theoretical Chemistry0210 nano-technologyIsomerizationConjugate
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Effect of ewe feeding system (grass v. concentrate) on intramuscular fatty acids of lambs raised exclusively on maternal milk

2005

AbstractTwenty pregnant Comisana ewes were divided into two groups of 10. One group was allowed to graze a vetch pasture (grass). The second group of animals was housed collectively in a pen and was given hay and concentrates (concentrate). After lambing, all the ewes were allowed to stay with the respective lambs between 18:00 h and 07:00 h of the following day in two different pens. Therefore all the lambs were raised exclusively on maternal milk. The lambs were slaughtered at 38 days of age. Milk and lamb meat (longissimus dorsi muscle) fatty acids were analysed. Ewes on grass produced milk with a lower (P< 0·001) proportion of saturated fatty acids and with a higher proportion of bot…

chemistry.chemical_classificationLinolenic acidLinoleic acidConjugated linoleic acidDomestic sheep reproductionfood and beveragesBiologychemistry.chemical_compoundAnimal sciencechemistryGrazingHayAnimal Science and ZoologyIntramuscular fatFood sciencePolyunsaturated fatty acid
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Synthesis of glycosylated β3-homo-threonine conjugates for mucin-like glycopeptide antigen analogues

2010

Glycopeptides from the mucin family decorated with tumour-associated carbohydrate antigens (TACA) have proven to be important target structures for the development of molecularly defined anti-cancer vaccines. The strategic incorporation of β-amino acid building blocks into such mucin-type sequences offers the potential to create pseudo-glycopeptide antigens with improved bioavailability for tumour immunotherapy. Towards this end, TN and TF antigen conjugates O-glycosidically linked to Fmoc-β3-homo-threonine were prepared in good yield via Arndt–Eistert homologation of the corresponding glycosyl α-amino acid derivative. By incorporation of TN-Fmoc-β3hThr conjugate into the 20 amino acid tand…

chemistry.chemical_classificationMUC1 antigenssolid-phase synthesisChemistryGlycoconjugateOrganic Chemistryglycosylamino acidsβ3-homo-threonineCombinatorial chemistryGlycopeptideAmino acidlcsh:QD241-441chemistry.chemical_compoundglycopeptideSolid-phase synthesisBiochemistryAntigenlcsh:Organic chemistryGlycosyllcsh:QThreoninelcsh:ScienceMUC1Beilstein Journal of Organic Chemistry
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Controlled release of drugs: Polymers and aggregate systems. Edited byM. Rosoff, VCH Verlagsgesellschaft, Weinheim, 1989, xi, 315 pp., bound, DM 132.…

1989

chemistry.chemical_classificationMaterials scienceAggregate (composite)Polymer sciencechemistryMechanics of MaterialsMechanical EngineeringGeneral Materials SciencePolymerControlled releaseAdvanced Materials
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Synthesis of Microporous Carbon Nanofibers and Nanotubes from Conjugated Polymer Network and Evaluation in Electrochemical Capacitor

2009

One-dimensional fibers and tubes are constructed through the oriented carbon-carbon cross-linking reactions towards rigid conjugated polymer networks. As the result, a template-free and one-step synthesis of CNTs and CNFs is achieved through a simple carbonization of the as-formed carbon-rich tubular and fiberlike polyphenylene precursors under argon. Microporous CNTs and CNFs with a surface area up to 900 m2 g–1 are obtained, together with HR-TEM characterizations indicating the formation of intrinsic microporous structure in these rigid carbon-rich networks. The primary electrochemical experiments reveal their promising applications as advanced electrodes in electrochemical double-layered…

chemistry.chemical_classificationMaterials scienceCarbonizationCarbon nanofiberMicroporous materialPolymerCarbon nanotubeConjugated systemCondensed Matter PhysicsElectrochemistryElectronic Optical and Magnetic Materialslaw.inventionBiomaterialsChemical engineeringchemistrylawElectrodeElectrochemistryComposite materialAdvanced Functional Materials
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The folding of individual conjugated polymer chains during annealing.

2011

chemistry.chemical_classificationMaterials scienceChemical engineeringchemistryAnnealing (metallurgy)Polymer chemistryGeneral ChemistryPolymerConjugated systemCatalysisAngewandte Chemie (International ed. in English)
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New n-dopable thiophene based polymers

1999

Abstract New conjugated polymers containing variable amounts of thienyl and thienyl-S,S-dioxide units have been prepared by chemical or electrochemical polymerization of the appropriate substrates. The presence of the thienyl S,S-dioxide units leads to the decrease of the LUMO energies with respect to those of the ‘all thienyl’ counterparts. Electrochemical and spectro electrochemical data of n-doping of these materials are reported.

chemistry.chemical_classificationMaterials scienceElectrochemical polymerizationMechanical EngineeringMetals and AlloysPolymerConjugated systemCondensed Matter PhysicsPhotochemistryElectrochemistryElectronic Optical and Magnetic MaterialsElectrochemical dopingchemistry.chemical_compoundchemistryMechanics of MaterialsMaterials ChemistryThiopheneHOMO/LUMOSynthetic Metals
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