Search results for "aromaattiset hiilivedyt"

showing 5 items of 5 documents

Retene, pyrene and phenanthrene cause distinct molecular-level changes in the cardiac tissue of rainbow trout (Oncorhynchus mykiss) larvae, Part 2 – …

2020

Polycyclic aromatic hydrocarbons (PAHs) are global contaminants of concern. Despite several decades of research, their mechanisms of toxicity are not very well understood. Early life stages of fish are particularly sensitive with the developing cardiac tissue being a main target of PAHs toxicity. The mechanisms of cardiotoxicity of the three widespread model polycyclic aromatic hydrocarbons (PAHs) retene, pyrene and phenanthrene were explored in rainbow trout (Oncorhynchus mykiss) early life stages. Newly hatched larvae were exposed to sublethal doses of each individual PAH causing no detectable morphometric alterations. Changes in the cardiac proteome and metabolome were assessed after 7 o…

Proteomicsbiologiset vaikutuksetEnvironmental Engineering010504 meteorology & atmospheric sciencestoksiinitDevelopmental toxicitycardiotoxicity010501 environmental sciencesmyrkyllisyys01 natural sciencesproteomiikkaTranscriptomechemistry.chemical_compoundMetabolomicsproteomicsMetabolomeEnvironmental ChemistryAnimalsMetabolomicsdevelopmental toxicityaquatic toxicology14. Life underwaterPolycyclic Aromatic HydrocarbonsWaste Management and Disposal0105 earth and related environmental scienceskalatRetenevesistötPyrenesbiologyChemistryPhenanthrenePhenanthrenesAryl hydrocarbon receptorPollutionmetabolomicsekotoksikologiaBiochemistryLarvaOncorhynchus mykisspolycyclic aromatic hydrocarbons (PAHs)biology.proteinPyrenearomaattiset hiilivedytepäpuhtaudet
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Effects of side chains of oxatub[4]arene on its conformational interconversion, molecular recognition and macroscopic self-assembly.

2017

A series of oxatub[4]arenes with different alkyl side chains have been synthesized. The conformational interconversion, molecular recognition and macroscopic self-assembly behaviour of oxatub[4]arene derivatives were investigated. The difference in side chains slightly changes the binding affinities, but results in different self-assembly morphologies at the solid state.

StereochemistrySolid-state010402 general chemistry01 natural sciencesCatalysisside chainsoxatubarenesMolecular recognitionMaterials ChemistrySide chainta116makromolekyylitAlkylBinding affinitieschemistry.chemical_classification010405 organic chemistryChemistryMetals and Alloysself-assemblyGeneral Chemistry0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsCeramics and CompositesSelf-assemblyaromaattiset hiilivedytChemical communications (Cambridge, England)
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Retene, pyrene and phenanthrene cause distinct molecular-level changes in the cardiac tissue of rainbow trout (Oncorhynchus mykiss) larvae, part 1 – …

2020

Polycyclic aromatic hydrocarbons (PAHs) are contaminants of concern that impact every sphere of the environment. Despite several decades of research, their mechanisms of toxicity are still poorly understood. This study explores the mechanisms of cardiotoxicity of the three widespread model PAHs retene, pyrene and phenanthrene in the rainbow trout (Oncorhynchus mykiss) early life stages. Newly hatched larvae were exposed to each individual compound at sublethal doses causing no significant increase in the prevalence of deformities. Changes in the cardiac transcriptome were assessed after 1, 3, 7 and 14 days of exposure using custom Salmo salar microarrays. The highest number of differentiall…

biologiset vaikutuksetEnvironmental Engineering010504 meteorology & atmospheric sciencestoksiinitcardiotoxicitymyrkyllisyys010501 environmental sciences01 natural sciencesRespiratory electron transport chainTranscriptometranscriptomicschemistry.chemical_compoundkirjolohiMyosinAnimalsEnvironmental Chemistryaquatic toxicology412 Animal science dairy scienceWaste Management and Disposal0105 earth and related environmental sciencesvesistötRetenePyreneslohikalatHeartPhenanthrenesPhenanthrenePollutionekotoksikologiachemistryBiochemistrypolycyclic aromatic hydrocarbons (PAHs)LarvaOncorhynchus mykissToxicityPyreneRainbow troutTranscriptomearomaattiset hiilivedytepäpuhtaudetScience of The Total Environment
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Simultaneous Endo- and Exo-Complex Formation of Pyridine[4]arene Dimer with Neutral and Anionic Guests

2017

The formation of complexes between hexafluorophosphate (PF6−) and tetraisobutyloctahydroxypyridine[4]arene has been thoroughly studied in the gas phase (ESI‐QTOF‐MS, IM‐MS, DFT calculations), in the solid state (X‐ray crystallography), and in chloroform solution (1H, 19F, and DOSY NMR spectroscopy). In all states of matter, simultaneous endo complexation of solvent molecules and exo complexation of a PF6− anion within a pyridine[4]arene dimer was observed. While similar ternary complexes are often observed in the solid state, this is a unique example of such behavior in the gas phase. peerReviewed

hexafluorophosphatecoordination complexaromaattiset hiilivedyt
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Toxicity of retene and pyrene on fish at different light conditions

2011

whitefishhaukinorthern pikelohimyrkyllisyysprotein endpointsympäristön tilaphototoxicityeleytheroembryoskirjolohipyreenitympäristömyrkytkalatfishluonnonvalotoxityrainbow troutenvironmental chemicalshiilivedytqPCRjuvenileympäristövaikutuksetsiikamikrobiologiareteenittranscriptomemicroarrayvaloaromaattiset hiilivedyt
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