Search results for "HYDROCARBONS"

showing 10 items of 368 documents

Asymmetric synthesis of chloroisothreonine derivatives via syn-stereoselective Mannich-type additions across N-sulfinyl-α- chloroimines

2014

Mannich-type reactions of O-Boc glycolic esters across chiral N-sulfinyl-α-chloroaldimines resulted in the efficient and syn-stereoselective synthesis of new γ-chloro-α-hydroxy-β-amino esters (dr > 99:1). The α-coordinating ability of the chlorine atom was of great importance for the diastereoselectivity of the Mannich-type reaction and overruled the chelation of the sulfinyl oxygen with the lithium ion of the incoming E-enolate in the transition state model. These novel chloroisothreonine derivatives proved to be excellent building blocks in asymmetric synthesis of novel syn-β,γ-aziridino-α-hydroxy esters and biologically relevant trans-oxazolidinone carboxylic esters.

Models MolecularThreonineState modelStereochemistryOrganic ChemistryChlorine atomEnantioselective synthesischemistry.chemical_elementEstersStereoisomerismCrystallography X-RayBiochemistryOxygenMannich BaseschemistryHydrocarbons ChlorinatedSide chainLithiumStereoselectivityChelationIminesPhysical and Theoretical Chemistryta116Organic and Biomolecular Chemistry
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Organic salts and aromatic substrates in two-component gel phase formation: the study of properties and release processes

2015

To identify gel phases able to act as confined reaction media or materials for the removal of organic pollutants, we studied two-component gel phases formed by naphthalenedisulfonate diimidazolium salts in the presence of some organic guests, in 1-propanol solution. Guests differing in π-surface area, bulkiness and electronic properties were taken into account. Soft materials obtained were investigated for their thermal stability, self-repairing ability and morphology. Furthermore, two-component gel phase formation was studied using resonance light scattering (RLS) measurements. Guest release processes from the gel phase were also studied. These processes were monitored as a function of tim…

Morphology (linguistics)Chemistry PhysicalUltraviolet RaysComponent (thermodynamics)ChemistryExtraction (chemistry)ImidazolesGeneral ChemistrySettore CHIM/06 - Chimica OrganicaCondensed Matter PhysicsResonance (chemistry)Hydrocarbons AromaticDynamic Light ScatteringLight scatteringSolventChemical engineeringPhase (matter)Microscopy Electron ScanningOrganic chemistrySaltsThermal stabilityGelsOrganogels diimidazolium salts soft materials
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Brominated flame retardants and toxic elements in the meat and liver of red deer (Cervus elaphus), wild boar (Sus scrofa), and moose (Alces alces) fr…

2017

In order to evaluate the contamination status of terrestrial biota in Latvia, muscle and liver tissues of red deer (Cervus elaphus), wild boar (Sus scrofa), and moose (Alces alces) were analyzed for the content of polybrominated diphenyl ethers (PBDE), hexabromocyclododecane (HBCD), tetrabromobisphenol A (TBBPA), as well as cadmium and lead. The highest mean concentrations of PBDEs (46.6pgg-1 wet weight (w.w.)), cadmium (0.95mgkg-1 w.w.), and lead (0.22mgkg-1 w.w.) were observed in the tissues of moose, while the wild boar samples contained the highest levels of HBCD, with the mean concentration equal to 264pgg-1 w.w. in muscle tissues. Generally low mean concentrations of TBBPA from 0.52 t…

Muscle tissueEnvironmental EngineeringPolybrominated BiphenylsSus scrofa0211 other engineering and technologiesZoologychemistry.chemical_element02 engineering and technology010501 environmental sciencesBiology01 natural scienceschemistry.chemical_compoundPolybrominated diphenyl ethersWild boarbiology.animalmedicineHalogenated Diphenyl EthersEnvironmental ChemistryAnimalsWaste Management and Disposal0105 earth and related environmental sciencesFlame RetardantsHexabromocyclododecane021110 strategic defence & security studiesCadmiumDeerPollutionLatviaHydrocarbons BrominatedRed Meatmedicine.anatomical_structureCongenerchemistryLiverBioaccumulationTetrabromobisphenol AEnvironmental MonitoringThe Science of the total environment
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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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Cuticular hydrocarbon profiles in Blattella germanica: effects of halofenozide, boric acid and benfuracarb

2006

1379-1176 (Print) Journal Article; In order to complete previous studies conducted on Blattella germanica, three insecticides from different groups were evaluated: boric acid, an inorganic compound, benfuracarb, a carbamate, and halofenozide, a non-steroidal ecdysone agonist. Boric acid (8.20%, LD50) and benfuracarb (2%, LD50) were incorporated into the diet and orally administrated to newly emerged adults of both sexes, while halofenozide (0.33%, LD50) was applied topically. Hydrocarbons extracts was made on bidistilled pentane from control and treated series sampled 6 days following treatment. Extracts was analyzed by gas chromatography. Data showed that cuticular profiles of control and …

OralMaleChromatographyHydrazines/*toxicityTime Factorsintegumentary systembeta-Alanine/*analogs & derivatives/toxicityHydrocarbons/*analysisBenzofurans/*toxicityBenzoic Acids/*toxicityLethal Dose 50TopicalInsecticides/*toxicityBoric Acids/*toxicityGasAdministrationAnimalsFemaleBlattellidae/chemistry/drug effects/growth & development
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Exposure to retene, fluoranthene, and their binary mixture causes distinct transcriptomic and apical outcomes in rainbow trout (Oncorhynchus mykiss) …

2022

Polycyclic aromatic hydrocarbons (PAHs) are widely spread environmental contaminants which affect developing organisms. It is known that improper activation of the aryl hydrocarbon receptor (AhR) by some PAHs contributes to toxicity, while other PAHs can disrupt cellular membrane function. The exact downstream mechanisms of AhR activation remain unresolved, especially with regard to cardiotoxicity. By exposing newly hatched rainbow trout alevins (Oncorhynchus mykiss) semi-statically to retene (32 µg l−1; AhR agonist), fluoranthene (50 µg l−1; weak AhR agonist and CYP1a inhibitor) and their binary mixture for 1, 3, 7 and 14 days, we aimed to uncover novel mechanisms of cardiotoxicity using a…

PAH-yhdisteetFluorenesEarly life developmentHealth Toxicology and MutagenesisPAHPhenanthrenesAquatic ScienceseoksetReteneekotoksikologiakirjolohiOncorhynchus mykissMixtureAnimalsFluorantheneympäristömyrkytalkionkehitystranskriptomiPolycyclic Aromatic HydrocarbonsTranscriptomeWater Pollutants ChemicalYolk Sac
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Endogenous AhR agonist FICZ accumulates in rainbow trout (Oncorhynchus mykiss) alevins exposed to a mixture of two PAHs, retene and fluoranthene

2022

AbstractMultiple studies have reported synergized toxicity of PAH mixtures in developing fish larvae relative to the additive effect of the components. From a toxicological perspective, multiple mechanisms are known to contribute to synergism, such as altered toxicodynamics and kinetics, as well as increased oxidative stress. An understudied contributor to synergism is the accumulation of endogenous metabolites, for example: the aryl hydrocarbon receptor 2 (AhR2) agonist and tryptophan metabolite 6-Formylindolo(3,2-b)carbazole (FICZ). Fish larvae exposed to FICZ, alongside knock-down of cytochrome p450 (cyp1a), has been reported to induced symptoms of toxicity similar to those observed foll…

PAH-yhdisteetHealth Toxicology and MutagenesisGeneral MedicinePAHManagement Monitoring Policy and LawToxicologymixtureekotoksikologiaFICZReceptors Aryl HydrocarbonkirjolohiLarvasynergismOncorhynchus mykissAnimalsblue sac diseaseaineenvaihduntatuotteetympäristömyrkytalkionkehitysPolycyclic Aromatic Hydrocarbonskalat
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Polycyclic Aromatic Hydrocarbons Phenanthrene and Retene Modify the Action Potential via Multiple Ion Currents in Rainbow Trout Oncorhynchus mykiss C…

2019

Polycyclic aromatic hydrocarbons (PAHs) are ubiquitous contaminants in aqueous environments. They affect cardiovascular development and function in fishes. The 3-ring PAH phenanthrene has recently been shown to impair cardiac excitation-contraction coupling by inhibiting Ca2+ and K+ currents in marine warm-water scombrid fishes. To see if similar events take place in a boreal freshwater fish, we studied whether the PAHs phenanthrene and retene (an alkylated phenanthrene) modify the action potential (AP) via effects on Na+ (INa ), Ca2+ (ICaL ), or K+ (IKr , IK1 ) currents in the ventricular myocytes of the rainbow trout (Oncorhynchus mykiss) heart. Electrophysiological characteristics of myo…

PAH-yhdisteetHealth Toxicology and MutagenesiscardiotoxicityAction Potentialstoksikologia010501 environmental sciences01 natural sciences03 medical and health scienceschemistry.chemical_compoundmode of actionEnvironmental ChemistryMyocyteAnimalsaquatic toxicologyMyocytes CardiacPatch clampPolycyclic Aromatic HydrocarbonsMode of actionIon channelkalat030304 developmental biology0105 earth and related environmental sciencesvesistöt0303 health sciencesRetenebiologyPhenanthrenePhenanthrenesAryl hydrocarbon receptorhiilivedytchemistryReceptors Aryl Hydrocarbonpolycyclic aromatic hydrocarbons (PAHs)Oncorhynchus mykissbiology.proteinBiophysicsRainbow troutWater Pollutants ChemicalEnvironmental toxicology and chemistry
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Changes in Cardiac Proteome and Metabolome Following Exposure to the Pahs Retene and Fluoranthene and Their Mixture in Developing Rainbow Trout Alevi…

2022

Exposure to polycyclic aromatic hydrocarbons (PAHs) is known to affect developing organisms. Utilization of different omics-based technologies and approaches could therefore provide a base for the discovery of novel mechanisms of PAH induced development of toxicity. To this aim, we investigated how exposure towards two PAHs with different toxicity mechanisms: retene (an aryl hydrocarbon receptor 2 (Ahr2) agonist), and fluoranthene (a weak Ahr2 agonist and cytochrome P450 inhibitor (Cyp1a)), either alone or as a mixture, affected the cardiac proteome and metabolome in newly hatched rainbow trout alevins (Oncorhynchus mykiss). In total, we identified 65 and 82 differently expressed proteins (…

PAH-yhdisteetProteomicsHistoryEnvironmental EngineeringProteomePolymers and PlasticsDevelopmental toxicologyPharmacology and ToxicologyZoologiproteomiikkaIndustrial and Manufacturing EngineeringkirjolohiMixtureAnimalsEnvironmental ChemistryMetabolomicsPolycyclic Aromatic HydrocarbonsBusiness and International ManagementaineenvaihduntaWaste Management and DisposalFluorenessydänPAHPhenanthrenesFarmakologi och toxikologiMiljövetenskapPollutionekotoksikologiaRainbow troutOncorhynchus mykissMetabolomePROTEOMICSkehitysbiologiaZoologyEnvironmental SciencesSSRN Electronic Journal
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Photoinduced toxicity of retene to Daphnia magna under enhanced UV-B radiation.

2001

Abstract The effects of UV radiation on the acute toxicity of retene (7-isopropyl-1-methylphenanthrene) to Daphnia magna Straus were studied. Dehydroabietic acid (DHAA) from which retene is formed in the vicinity of pulp and paper industry was also studied. Pyrene, anthracene, and phenanthrene were used as model PAH compounds. The time taken for immobilization (ET50) was monitored under biologically effective UV-B dose rates of 240, 365, 565, and 650 mW m−2 (UV-A and visible light also present). Median effective concentrations (EC50) were determined after a 15-min UV exposure (565 mW m−2) followed by 24 h in the dark. Retene ( 10–320 μg l −1 ) was not acutely toxic in the dark. The inductio…

PaperEnvironmental EngineeringPhotochemistryUltraviolet RaysHealth Toxicology and MutagenesisDaphnia magnaIndustrial WasteAbsorptionLethal Dose 50chemistry.chemical_compoundEnvironmental ChemistryOrganic chemistryAnimalsPolycyclic Aromatic HydrocarbonsAnthraceneRetenebiologyPublic Health Environmental and Occupational HealthGeneral MedicineGeneral ChemistryPhenanthrenePhenanthrenesbiology.organism_classificationPollutionAcute toxicitychemistryDaphniaToxicityAbietanesPyreneDiterpenesPhototoxicityWater Pollutants ChemicalNuclear chemistryChemosphere
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