Search results for "Thiocyanates"

showing 10 items of 32 documents

Microbial and chemical origins of the bactericidal activity of thermally treated yellow mustard powder toward Escherichia coli O157:H7 during dry sau…

2010

Abstract Work examines the origin of bactericidal activity in mustard flour and explores the relative contribution from starter cultures, E. coli O157:H7 itself and other sources. Bacteria can degrade naturally occurring glucosinolates in mustard and form isothiocyanates with antimicrobial activity. In the present work, 24 starter cultures (mostly from commercial mixtures) were screened for their capacity to decompose the glucosinolate, sinalbin. The most active pair, Pediococcus pentosaceus UM 121P and Staphylococcus carnosus UM 123M, were used together for the production of dry fermented sausage contaminated with E. coli O157:H7 (~ 6.5 log CFU/g). They were compared to industrial starters…

Glycoside HydrolasesStaphylococcusColony Count MicrobialFood ContaminationEscherichia coli O157medicine.disease_causeMicrobiologyCholineMicrobiologychemistry.chemical_compoundStarterIsothiocyanatesmedicinePediococcusFood scienceEscherichia coliStaphylococcus carnosusbiologyMyrosinasefood and beveragesGeneral MedicineAntimicrobialbiology.organism_classificationAnti-Bacterial AgentsSinalbinMeat ProductschemistryGlucosinolateFermentationFood MicrobiologyFermentationPowdersMustard PlantFood ScienceInternational Journal of Food Microbiology
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Novel mixed-valence Cu compounds formed by Cu(II) dimers with double oximato bridges: in situ formation of anionic layer [Cu2(SCN)3]n(n-).

2013

Two new N3O donor ketoxime Schiff bases (HL(1) and HL(2)) have been synthesized by condensing N,N-dimethylethylenediamine with diacetylmonoxime and benzilmonoxime, respectively in a 1:1 ratio. Reaction of Cu(ClO4)2·6H2O with HL(1) resulted in a discrete oximato-bridged dinuclear Cu(II) complex [Cu2(L(1))2(H2O)2](ClO4)2 (1). The same reaction in presence of NaSCN affords the complex {[Cu(II)2(L(1))2][Cu(I)4(μ(1,3)-SCN)4(μ(1,1,3)-SCN)2]}n (2), where partial Cu(II)→Cu(I) reduction is observed. In 2, arrays of [Cu(II)2(L(1))2](2+) cationic units are inserted in between 2D {[Cu(I)4(SCN)6](2-)}n layers and connected via μ(1,1,3)-SCN(-) links, thus forming a 3D network. On the other hand, reaction…

In situAnionsModels MolecularStereochemistryAnionchemistry.chemical_elementInfrared spectroscopy010402 general chemistryCrystallography X-RayAnions; Copper; Crystallography X-Ray; Dimerization; Models Molecular; Molecular Structure; Organometallic Compounds; Oximes; Thiocyanates01 natural sciencesInorganic ChemistryOximeModelsOximes[CHIM.CRIS]Chemical Sciences/CristallographyOrganometallic CompoundsMolecule[CHIM]Chemical SciencesGroup 2 organometallic chemistryOrganometallic CompoundCrystallographyValence (chemistry)Molecular Structure010405 organic chemistryCationic polymerizationMolecular[CHIM.MATE]Chemical Sciences/Material chemistryCopper0104 chemical sciencesCrystallographychemistryX-RaySingle crystalDimerizationCopperThiocyanatesDalton transactions (Cambridge, England : 2003)
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Reversible Colorimetric Probes for Mercury Sensing

2005

The selectivity and sensitivity of two colorimetric sensors based on the ruthenium complexes N719 [bis(2,2'-bipyridyl-4,4'-dicarboxylate)ruthenium(II) bis(tetrabutylammonium) bis(thiocyanate)] and N749 [(2,2':6',2' '-terpyridine-4,4',4' '-tricarboxylate)ruthenium(II) tris(tetrabutylammonium) tris(isothiocyanate)] are described. It was found that mercury ions coordinate reversibly to the sulfur atom of the dyes' NCS groups. This interaction induces a color change in the dyes at submicromolar concentrations of mercury. Furthermore, the color change of these dyes is selective for mercury(II) when compared with other ions such as lead(II), cadmium(II), zinc(II), or iron(II). The detection limit…

IronInorganic chemistrychemistry.chemical_elementBiosensing TechniquesBiochemistrySensitivity and SpecificityCatalysischemistry.chemical_compoundColloid and Surface ChemistryIsothiocyanatesOrganometallic CompoundsColoring AgentsIonsTitaniumAqueous solutionThiocyanateMolecular StructureChemistryGeneral ChemistryMercuryChemical sensorTransition metal ionsMercury (element)RutheniumZincLeadRuthenium CompoundsColorimetrySpectrophotometry UltravioletSelectivityThiocyanatesCadmium
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A Versatile Synthesis of Fluorinated Uracils in Solution and on Solid-Phase.

2004

[reaction: see text] An efficient and convenient two-step synthesis of new fluorinated uracils is described. The first step involves the condensation of an ester enolate with a fluorinated nitrile to furnish fluorinated beta-enamino esters. In turn, these compounds react with organic isocyanates or isothiocyanates to give C-6 fluorinated uracils or thiouracils, respectively, in excellent yields. This synthesis has been successfully adapted to solid-phase conditions with high diversity, thereby facilitating the creation of small (thio)uracil libraries.

NitrileHydrocarbons FluorinatedMolecular StructureChemistryOrganic ChemistryCondensationThio-UracilGeneral MedicineBiochemistryCombinatorial chemistryTurn (biochemistry)Solutionschemistry.chemical_compoundIsothiocyanatesPhase (matter)NitrilesOrganic chemistryheterocyclic compoundsPhysical and Theoretical ChemistryUracilIsocyanatesChemInform
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Development of an Antifungal and Antimycotoxigenic Device Containing Allyl Isothiocyanate for Silo Fumigation

2019

The aims of this study were to evaluate the antifungal activity of the bioactive compound allyl isothiocyanate (AITC) against Aspergillus flavus (8111 ISPA) aflatoxins (AFs) producer and Penicillium verrucosum (D-01847 VTT) ochratoxin A (OTA) producer on corn, barley, and wheat. The experiments were carried out initially in a simulated silo system for laboratory scale composed of glass jars (1 L). Barley and wheat were contaminated with P. verrucosum and corn with A. flavus. The cereals were treated with a hydroxyethylcellulose gel disk to which 500 &micro

Ochratoxin AAflatoxinAntifungal AgentsInformation siloHealth Toxicology and MutagenesisFumigationlcsh:MedicineAspergillus flavusToxicology01 natural sciencesZea maysArticleAITCchemistry.chemical_compound0404 agricultural biotechnology<i>Penicillium verrucosum</i>AflatoxinsIsothiocyanatesPenicillium verrucosumFood scienceTriticum<i>Aspergillus flavus</i>2. Zero hungerbiologyChemistrymycotoxin reduction010401 analytical chemistrylcsh:RPenicilliumfood and beveragesAgricultureHordeumPenicillium verrucosum04 agricultural and veterinary sciencesbiology.organism_classificationAllyl isothiocyanate040401 food scienceOchratoxinsBioactive compoundfungal growth reduction0104 chemical sciencesFumigationAspergillus flavusToxins
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Comparative histological, histochemical, immunohistochemical and biochemical studies on oestrogen receptors, lectin receptors, and Barr bodies in hum…

1986

The present study performed on a total of 567 cases of human female breast cancer compares the results of the biochemical assay (dextran-coated charcoal assay = DCC) for oestrogen receptor (ER) with those of several morphological methods developed for the detection of the ER or for the prediction of prognosis by use of other systems (FSA = fluorescent ligand binding assay, ER-ICA = monoclonal antibody assay for ER, LRA = lectin receptor assay using peanut agglutinin, and Barr body estimation). Whereas no correlation at all was observed among the results of the DCC and those of the FSA and Barr body estimation, the ER-ICA and the LRA showed an unanimous tendency towards higher values of ER w…

Peanut agglutininPathologymedicine.medical_specialtymedicine.drug_classBreast NeoplasmsMonoclonal antibodyPathology and Forensic MedicinePeanut AgglutininLectinsmedicineHumansLymphocytesReceptorMolecular BiologyFluorescent DyesImmunoassaybiologyHistocytochemistryLigand binding assayAssayCancerAntibodies MonoclonalDextransCell BiologyGeneral Medicinemedicine.diseaseFluoresceinsMolecular biologyReceptors EstrogenSex ChromatinCharcoalReceptors MitogenMonoclonalbiology.proteinImmunohistochemistryFemaleFluorescein-5-isothiocyanateThiocyanatesVirchows Archiv. A, Pathological anatomy and histopathology
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Blood volume and extracellular space (ECS) of the whole body and some organs of the rat.

1978

Methods are described for estimation of blood volume and extracellular space (ECS) in the whole body and in some organs with 51Cr, 14C-thiocyanate and 3H-inulin. A mean blood volume of 47 ml/kg, a thiocyanate space of 350 ml/kg and a inulin space of 288 ml/kg were determined in the rat. The corresponding values of organs are shown in figures 1--3.

PharmacologyMaleThiocyanateBlood Volume DeterminationInulinInulinBlood volumeCell BiologyAnatomyRatsCellular and Molecular Neurosciencechemistry.chemical_compoundchemistryExtracellularMolecular MedicineAnimalsWhole bodyExtracellular SpaceMolecular BiologyThiocyanatesExperientia
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Influence of the polymerization step alone on oxygen affinity and cooperativity during production of hyperpolymers from native hemoglobins with cross…

1994

The aim of this study was to find out how the polymerization per se changes oxygen affinity (P50) and cooperativity (n50) of various soluble huge hyperpolymers prepared from native hemoglobins by crosslinking. Increase of cooperativity would be expected considering natural hemoglobin networks. Those hyperpolymers with molecular weights of some 10(6) g/mol are candidates for artificial oxygen-carrying blood additives rather than volume substitutes. Human and bovine hemoglobin reacted with several crosslinkers (2,5-diisothiocyanatobenzenesulfonate (DIBS); 4,4'-diisothiocyanatostilbene-2, 2'-disulfonate (DIDS); 1,3-butadiene diepoxide (BUDE); glutaraldehyde (GDA)) in concentrated (case 1) and …

PolymersBiomedical EngineeringCooperativity44'-Diisothiocyanostilbene-22'-Disulfonic AcidIn Vitro TechniquesBlood substitutechemistry.chemical_compoundHemoglobinsBlood SubstitutesIsothiocyanatesPolymer chemistryOrganic chemistryAnimalsHumansMolecular massChemistryBenzenesulfonatesMolecular WeightOxygenSolutionsMonomerCross-Linking ReagentsPolymerizationDIDSGlutaralEpoxy CompoundsCattleGlutaraldehydeHemoglobinThiocyanatesBiotechnologyArtificial cells, blood substitutes, and immobilization biotechnology
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A study of electron transfer in Ru(dcbpy)2(NCS)2 sensitized nanocrystalline TiO2 and SnO2 films induced by red-wing excitation.

2008

Excited state dynamics and electron transfer from the Ru(dcbpy)2(NCS)2 (RuN3) sensitizer to semiconductor nanoparticles were studied using time-resolved femtosecond absorption spectroscopy. We found that excitation of the red wing of the absorption spectrum of the sensitizer populates the (3)MLCT state directly, both in solution and attached on semiconductor nanoparticle films. Electron injection is slowed down and becomes gradually less efficient as excitation moves towards red from the absorption maximum at 535 nm. At 675 nm the injection is non-exponential and characterized by 5, 30 and 180 ps time constants. The non-exponential electron injection observed is assigned to injection from a…

Time FactorsAbsorption spectroscopyPhotochemistrySurface PropertiesAnalytical chemistryGeneral Physics and AstronomyElectronsSensitivity and SpecificityRutheniumElectron transferOrganometallic CompoundsPhysical and Theoretical ChemistryTriplet stateAbsorption (electromagnetic radiation)Coloring AgentsTitaniumChemistrybusiness.industryLasersSpectrum AnalysisTin CompoundsMembranes ArtificialNanocrystalline materialNanostructuresKineticsSemiconductorSemiconductorsExcited stateFemtosecondbusinessThiocyanatesPhysical chemistry chemical physics : PCCP
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Synthesis of plagiochiline N from santonin.

2001

This article reports the transformation of O-acetylisophotosantonin, obtained by photochemical rearrangement of santonin, into plagiochiline N, an ent-2,3-secoaromadendrane isolated from Plagiochila ovalifolia. The synthesis was carried out in a sequence involving as the key steps (a) the substitution of the lactone moiety by a gem-dimethylcyclopropane ring through a synthetic intermediate having a C(6)-C(7) double bond and (b) the ozonolysis of the C(2)-C(3) bond followed by cyclization to the dihydropyran ring characteristic of plagiochiline N. Spectroscopic data of the synthetic product fully coincided with the reported data for the natural product.

chemistry.chemical_classificationNatural productOzonolysisPlants MedicinalDouble bondDihydropyranStereochemistryAntinematodal AgentsOrganic ChemistryAlkenesRing (chemistry)chemistry.chemical_compoundchemistryMoietySantoninLactoneThiocyanatesSantoninThe Journal of organic chemistry
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