Search results for "Methylamine"

showing 10 items of 97 documents

The gut microbiota: An emerging risk factor for cardiovascular and cerebrovascular disease

2018

Commensal gut microbiota have recently been implicated in cardiovascular disease (CVD) and cerebrovascular disease. Atherosclerotic plaque formation depends on the colonization status of the host. In addition to host nutrition and the related microbiota-dependent metabolic changes, activation of innate immune pathways triggers the development of atherosclerosis and supports arterial thrombosis. Gnotobiotic mouse models have uncovered that activation of Toll-like receptor-2 by gut microbial ligands supports von Willebrand factor-integrin mediated platelet deposition to the site of vascular injury. Depending on nutritional factors, the microbiota-derived choline-metabolite trimethylamine N-ox…

Blood Platelets0301 basic medicineIntegrinsEmerging riskImmunologyDiseaseBiologyGut floradigestive systemMethylaminesMice03 medical and health sciencesVon willebrandRisk Factorsvon Willebrand FactormedicineAnimalsHumansImmunology and AllergyPlateletSymbiosisInnate immune systemInfant NewbornInfantThrombosisAtherosclerosisbiology.organism_classificationmedicine.diseaseThrombosisImmunity InnatePlaque AtheroscleroticToll-Like Receptor 2Gastrointestinal MicrobiomeCerebrovascular Disorders030104 developmental biologyCardiovascular DiseasesArterial thrombusImmunologyEuropean Journal of Immunology
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Synthesis and inhibitory activity of dimethylamino-chalcone derivatives on the induction of nitric oxide synthase.

2002

A series of nine dimethylamino-chalcone derivatives (1,3-diaryl-propenones) was synthesized and screened as potential inhibitors of NO and PGE(2) production in the RAW 264.7 macrophage cell line. 4-Dimethylamino-2',5'-dimethoxychalcone (6) was found to be the most potent and dual inhibitor (IC(50s) in the submicromolar range) of NO and PGE(2) production. 2',6'-Dimethoxylation appeared to be an effective requirement for selective and potent inhibition of nitric oxide synthase induction as it was confirmed by Western blot analysis. Chalcone (6) at 25 mg kg(-1) by oral route, inhibited significantly the formation of oedema in the carrageenan-induced model of inflammation in mice.

ChalconeAnti-Inflammatory AgentsDrug Evaluation PreclinicalAdministration OralNitric Oxide Synthase Type IIInflammationInhibitory postsynaptic potentialChemical synthesisDinoprostoneNitric oxideCell Linechemistry.chemical_compoundMiceStructure-Activity RelationshipChalconeWestern blotDrug DiscoverymedicineOral routeAnimalsEdemaPharmacologychemistry.chemical_classificationmedicine.diagnostic_testbiologyMacrophagesOrganic ChemistryDual inhibitorMacrophage cellGeneral MedicineMolecular biologyNitric oxide synthaseEnzymeBiochemistrychemistryEnzyme inhibitorCell cultureEnzyme Inductionbiology.proteinmedicine.symptomNitric Oxide SynthaseDimethylaminesEuropean journal of medicinal chemistry
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Dioxomolybdenum(VI) complexes with tri- and tetradentate aminobis(phenolate)s

2005

Abstract The reactions of tridentate ligands, bis(2-hydroxy-3,5-dimethylbenzyl)methylamine (H2ONOMe) and bis(2-hydroxy-3-tert-butyl-5-methylbenzyl)methylamine (H2ONOtBu) with [MoO2(acac)2] (1) in methanol lead to the precipitation of monomeric dioxomolybdenum(VI) complexes [MoO2(ONOMe)(MeOH)] · MeOH (2a) and [MoO2(ONOtBu)(MeOH)] · MeOH (2b), respectively. Identical reactions in acetonitrile provide dimeric complexes [Mo2O2(μ-O)2(ONOMe)2] (3a) and [Mo2O2(μ-O)2(ONOtBu)2] (3b). The reactions of 1 with tetradentate ligands, N,N′-bis(2-hydroxy-3,5-dimethylbenzyl)-N,N′-dimethylethane-1,2-diamine (H2ONNOMe) and N,N′-bis(2-hydroxy-3,5-di-tert-butylbenzyl)-N,N′-dimethylethane-1,2-diamine (H2ONNOtBu)…

ChemistryStereochemistryMethylamineCrystal structureMedicinal chemistryInorganic Chemistrychemistry.chemical_compoundMonomerBenzoinMaterials ChemistryMethanolPhysical and Theoretical ChemistryAcetonitrilePhosphineNorbornenePolyhedron
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Seafood freshness determination through vapour phase Fourier transform infrared spectroscopy.

2006

Abstract A new vapour-phase manifold has been developed to determine trimethylamine (TMA) in fish and cephalopod samples by Fourier transform infrared (FT-IR) spectroscopy. Samples were treated off-line for 1 h with trichloroacetic acid (TCA), filtered and washed. The obtained extracts were aspirated and alkalinized with NaOH 2.0 M, in an on-line system. TMA was separated from the solution in a gas phase separator and then transported by means of a nitrogen carrier into a home made 10 cm pathlength IR gas cell, where the corresponding FT-IR spectra were acquired by accumulating 30 scans per spectrum with 2 cm−1 nominal resolution. The method was applied to the determination of TMA in natura…

ChromatographyChemistryInfraredAnalytical chemistrySeparator (oil production)chemistry.chemical_elementTrimethylamineBiochemistryNitrogenAnalytical Chemistrysymbols.namesakechemistry.chemical_compoundFourier transformsymbolsEnvironmental ChemistryGas chromatographyFourier transform infrared spectroscopySpectroscopySpectroscopyAnalytica chimica acta
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Liquid chromatographic determination of aliphatic amines in water using solid support assisted derivatization with 9-fluorenylmethyl chloroformate

2002

A simple and sensitive method has been developed for the liquid chromatographic determination of short-chain aliphatic amines in water. Analytes are retained in solid-phase extraction (SPE) cartridges, and then derivatized by drawing an aliquot of the fluorogeneic reagent 9-fluorenylmethyl chloroformate (FMOC) through the cartridges. After a certain reaction time the derivatives formed are desorbed with acetonitrile. The collected extracts are then chromatographed on a LiChrospher 100 RP18 125 mm×4 mm i.d., 5 μm, column using an acetonitrile-water gradient. The influence of experimental conditions (SPE material, volume of sample, concentration of FMOC, time of reaction and pH) has been inve…

ChromatographyChemistryOrganic ChemistryClinical BiochemistryReversed-phase chromatographyChloroformateBiochemistryAnalytical Chemistrychemistry.chemical_compoundTap waterReagentSample preparationSolid phase extractionDerivatizationDimethylamine
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A microscale Kjeldahl nitrogen determination for environmental waters.

2008

A microscale Kjeldahl system has been designed which has been homemade reduced. The digestor unit of a macroKjeldahl system and a modified glassware microdistillation unit have been used. The optimal conditions for digestion and distillation have been established for ammonium and methylamine as model compound of organic amino nitrogen. The optimised procedure has been applied to the determination of Kjeldahl nitrogen in water samples. Recoveries near 100% and good precision have been achieved. This procedure combines nitrogen miniaturized system and the use of a selective ion electrode for ammonia detection. The analysis time was reduced 4.8 times and the analysis cost 6.6 times compared wi…

ChromatographyMethylamineInorganic chemistrychemistry.chemical_elementNitrogenAnalytical Chemistrylaw.inventionIon selective electrodeAmmoniachemistry.chemical_compoundchemistrylawAmmoniumKjeldahl methodDistillationMicroscale chemistryTalanta
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Detector supports: application to aliphatic amines in wastewater

2005

Abstract Solid support assisted derivatization coupled to diffuse reflectance spectroscopy (DRS) was proposed and proved useful for the detection and quantification of aliphatic amines in water as an example. Dabsyl chloride (DBS), ninhydrin and sodium 1,2-naphtoquinone 4-sulphonate (NQS) were assayed as derivatization reagents. C 18 and SDB-XC disks and C 18 cartridges were tested for amine retention and after that derivatization. The decrease of the orange colour of dabsyl chloride on SBD-XC disks produced by the formation of its derivative with methylamine in the support (10 min at 100 °C) allowed the selective determination of the amine at concentration level equal or higher than 0.5 mg…

ChromatographyMethylamineNQSPropylamineChlorideAnalytical Chemistrychemistry.chemical_compoundchemistryNinhydrinmedicineEthylaminePentylamineDerivatizationmedicine.drugTalanta
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Core Histones Are Glutaminyl Substrates for Tissue Transglutaminase

1996

Chicken erythrocyte core histones are glutaminyl substrates in the transglutaminase (TGase) reaction with monodansylcadaverine (DNC) as donor amine. The modification is very fast when compared with that of many native substrates of TGase. Out of the 18 glutamines of the four histones, nine (namely glutamine 95 of H2B; glutamines 5, 19, and 125 of H3; glutamines 27 and 93 of H4; and glutamines 24, 104, and 112 of H2A) are the amine acceptors in free histones. The use of Gln112 of H2A requires a temperature-dependent partial unfolding of the histone, showing that structural determinants are decisive for the glutamine specificity. The structures of H2A and H2B do not appreciably change upon mo…

Circular dichroismErythrocytesTissue transglutaminaseGlutamineGuinea PigsMolecular Sequence DataIn Vitro TechniquesBiochemistrySubstrate SpecificityHistoneschemistry.chemical_compoundCadaverineAnimalsNucleosomeAmino Acid SequenceMolecular BiologyPeptide sequenceTransglutaminasesMolecular StructurebiologyMethylamineCell BiologyNucleosomesChromatinGlutamineKineticsHistonechemistryBiochemistrybiology.proteinJournal of Biological Chemistry
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Separation, isolation and stereochemical assignment of imazalil enantiomers and their quantitation in an in vitro toxicity test

2016

A simple method for the separation of the enantiomers of the fungicide imazalil was developed. Racemic imazalil was separated into its enantiomers with an enantiomeric purity of 99% using HPLC-UV with an enantioselective column (permethylated cyclodextrin) operated in reversed phase mode (water with 0.2% trimethylamine and 0.08% acetic acid and methanol). The absolute configuration of the separated enantiomers was assigned and unequivocally confirmed by optical rotation as well as by vibrational circular dichroism (VCD) and electronic circular dichroism (ECD) combined with ab-initio calculations. The same enantioselective column was also used to develop an HPLC-MS/MS method for the quantifi…

Circular dichroismOptical RotationTrimethylamineIn Vitro Techniques010501 environmental sciencesTandem mass spectrometryVibration01 natural sciencesBiochemistryAnalytical Chemistrychemistry.chemical_compoundTandem Mass SpectrometryToxicity TestsImazalil Enantiomers HPLC-UV Isolation Vibrational circular dichroism HPLC–MS/MSHumansChromatography High Pressure Liquid0105 earth and related environmental scienceschemistry.chemical_classificationChromatographyCyclodextrin010405 organic chemistryCircular DichroismOrganic ChemistryImidazolesAbsolute configurationEnantioselective synthesisStereoisomerismGeneral MedicineFungicides Industrial0104 chemical scienceschemistryVibrational circular dichroismSteroidsEnantiomerJournal of Chromatography A
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Properties of trialkylamines as catalysts of resoles synthesis

2000

A series of the syntheses of phenol–formaldehyde resoles was carried out in the presence of trimethyl-, triethyl-, tripropyl-, and tributylamines and sodium hydroxide as catalysts for this process. The rate constants were calculated for the partial reactions identified in the synthesis. Also, the performance properties of the resins obtained and the hardened resin samples were estimated in simple tests. © 2000 John Wiley & Sons, Inc. J Appl Polym Sci 77: 898–902, 2000

Condensation polymerPolymers and PlasticsTertiary amineTrimethylamineGeneral ChemistryTributylamineSurfaces Coatings and FilmsCatalysischemistry.chemical_compoundReaction rate constantchemistrySodium hydroxideMaterials ChemistryOrganic chemistryJournal of Applied Polymer Science
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