Search results for "aldehydes"

showing 10 items of 86 documents

4-hydroxynonenal inhibits glutathione peroxidase: protection by glutathione

1999

Abstract 4-Hydroxy-2,3-trans-nonenal, a lipid peroxidation product, inhibits glutathione peroxidase in a concentration-dependent manner. The concentration providing 50% inhibition is 0.12 mM. This inhibition can be almost completely (89%) prevented by 1 mM glutathione added to the incubation mixture 30 min before 4-hydroxy-2,3-trans-nonenal or 2,3-trans-nonenal, but not by other thiol-containing antioxidants such as 0.5 mM dithiothreitol or β-mercaptoethanol. Again the addition of 1 mM glutathione, and not of 0.5 mM dithiothreitol or β-mercaptoethanol, to the enzyme 30 min after incubation with 4-hydroxy-2,3-trans-nonenal restores activity to the same extent as does the preincubation with G…

chemistry.chemical_classificationAldehydesGlutathione PeroxidaseGPX3Glutathione peroxidaseGlutathione reductaseGlutathioneGPX4GlutathioneBiochemistryDithiothreitol4-HydroxynonenalLipid peroxidationchemistry.chemical_compoundNeuroprotective AgentschemistryBiochemistryPhysiology (medical)HumansLipid PeroxidationEnzyme InhibitorsFree Radical Biology and Medicine
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Modular one-pot synthesis of tetrasubstituted pyrroles from alpha-(alkylideneamino)nitriles.

2007

2,3,4,5-Tetrasubstituted pyrroles have been prepared with high regioselectivity by a formal cycloaddition of alpha-(alkylideneamino)nitriles and nitroolefins followed by elimination of HCN and HNO2. The reaction allows the convergent construction of the pyrrole ring in four steps from a nitroalkane and three aldehydes.

chemistry.chemical_classificationAldehydesNitrileOrganic ChemistryOne-pot synthesisNitroalkaneRegioselectivityAlkenesNitro CompoundsAldehydeChemical synthesisCycloadditionchemistry.chemical_compoundchemistryCyclizationNitrilesOrganic chemistryPyrrolesPyrroleThe Journal of organic chemistry
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Stereoselective Synthesis of Spiro-Decalin Oxindole Derivatives via Sequential Organocatalytic Michael-Domino Michael/Aldol Reaction.

2022

A highly stereoselective procedure for the synthesis of spiro-polycyclic oxindoles bearing five contiguous stereogenic centers including two tetrasubstituted carbons has been developed. Under sequential organocatalysis performed by a pyrrolidine-based organocatalyst and DBU, a highly atom-economical Michael–domino Michael/aldol reaction sequence was optimized, yielding variously functionalized spiro-decalin oxindoles with excellent stereoselectivity (>99:1 dr, up to 92% ee). peerReviewed

kemiallinen synteesiAldehydesMolecular StructureOrganic Chemistryasymmetric organocatalysisdomino reactionssprio heterocyclesStereoisomerismNaphthalenesCatalysisOxindolesorgaaninen kemiaSpiro Compoundsasymmetric organocatalysis; oxindoles; sprio heterocycles; domino reactionsThe Journal of organic chemistry
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Comparative cytotoxic study of silica materials functionalised with essential oil components in HepG2 cells

2020

[EN] This work evaluated the cytotoxic effect of different EOCs-functionalised silica particle types. The in vitro toxicity of eugenol and vanillin-immobilised SAS, MCM-41 microparticles and MCM-41 nanoparticles was evaluated on HepG2 cells, and compared to free EOCs and pristine materials. The results revealed that free essential oil components and bare silica had a mild cytotoxic effect on HepG2 cells. However, the comparative study showed that free eugenol and vanillin had a milder cytotoxic effect than the equivalent concentrations of immobilised components on the different silica particles, while differences in cell viability between the bare and functionalised particles relied on the …

HepG2TECNOLOGIA DE ALIMENTOSCell SurvivalCytotoxicityNanoparticleToxicologyMCM-41law.invention03 medical and health scienceschemistry.chemical_compoundInhibitory Concentration 500404 agricultural biotechnologyMCM-41Microscopy Electron TransmissionlawEugenolOils VolatileCytotoxic T cellHumansCytotoxicityEssential oil030304 developmental biology0303 health sciencesDose-Response Relationship DrugVanillinCationic polymerizationSilica04 agricultural and veterinary sciencesGeneral MedicineHep G2 CellsSilicon Dioxide040401 food scienceEugenolchemistryBenzaldehydesVanillinNanoparticlesFood ScienceNuclear chemistry
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A Modular Access to (±)-Tubocurine and (±)-Curine - Formal Total Synthesis of Tubocurarine.

2017

Two consecutive Cu-catalyzed Ullmann-type C–O couplings permitted the first successful entry toward the curare alkaloids (±)-tubocurine and (±)-curine. Starting from vanillin, the synthetic sequence comprises 15 linear steps and includes a total of 24 transformations. In addition, the total synthesis of tubocurine represents a formal total synthesis of the famous arrow poison alkaloid tubocurarine.

Molecular Structure010405 organic chemistryStereochemistryChemistryAlkaloidOrganic ChemistryCurare alkaloidsChemistry OrganicTotal synthesisTubocurarine010402 general chemistryIsoquinolines01 natural sciencesCatalysis0104 chemical sciencesTubocurineBenzaldehydesCopperThe Journal of organic chemistry
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Anti-inflammatory properties of an aldehydes-enriched fraction of grapefruit essential oil

2023

Chronic inflammation is linked to the development of numerous diseases and is accompanied by increased cytokine secretion. Macrophages provide a first line of defense against pathogens that under inflammatory stimuli release pro-inflammatory cytokines. The essential oil (EO) fractions obtained from Citrus spp. rich in different compounds have gained the attention of both researchers and users during the last decades. In particular, grapefruit (Citrus paradisi) peel is rich in phenolics and flavonoids with several health benefits, including anti-inflammatory actions. Additionally, its EO consists of a large number of compounds such as monoterpenes, sesquiterpenes, alcohols, aldehydes, esters…

nutraceuticalsspray-dryinflammationSettore BIO/13 - Biologia Applicataaldehydescitralessential oilFood ScienceCitrus paradisi
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Control of N-Heterocyclic Carbene Catalyzed Reactions of Enals: Asymmetric Synthesis of Oxindole-γ-Amino Acid Derivatives.

2017

A strategy to control the switch between a non‐cycloaddition reaction and a cycloaddition reaction of enals, using N‐heterocyclic carbene (NHC) catalyisis, has been developed. The new scalable protocol leads to γ‐amino‐acid esters bearing a tetrasubstituted stereocenter in good yields and high stereoselectivities by homo‐Mannich reactions of enals and isatin‐derived ketimines. By simply changing the N‐ketimine substituent to an ortho‐hydroxy phenyl group, the corresponding spirocyclic oxindolo‐γ‐lactams are obtained. peerReviewed

StereochemistrySubstituent010402 general chemistry01 natural sciencesCatalysisStereocenterCatalysischemistry.chemical_compoundaldehyditaldehydesPhenyl groupOxindoleta116orgaaniset yhdisteetkemiallinen synteesi010405 organic chemistryEnantioselective synthesisGeneral MedicineGeneral ChemistryCycloaddition0104 chemical scienceschemistryorganic compoundsCarbenechemical synthesisAngewandte Chemie (International ed. in English)
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Representativeness of Extracts of Offset Paper Packaging and Analysis of the Main Odor-Active Compounds

2004

Packagings often carry odors due to the support and printing inks. The aim of the investigation was to define a representative solvent-free extract of paper-based packaging materials printed by the offset process, for the identification of the odor-causing volatile compounds. Static headspace and solid-phase microextraction were the two applied extraction methods. Representativeness tests showed that the odor of the PDMS fiber extract gave satisfying odor similarities with the original packaging. The sample incubation was performed at 40 degrees C for 30 min, whereas the extraction time was 3 min at 40 degrees C. Extracts of both the nonprinted and printed papers of different batches were a…

PaperPrinting inkMass spectrometry01 natural sciences0404 agricultural biotechnologyOlfactometry[SDV.IDA]Life Sciences [q-bio]/Food engineeringSolvent extractionComputingMilieux_MISCELLANEOUSAldehydesChromatographyChemistry010401 analytical chemistryExtraction (chemistry)Food Packaging04 agricultural and veterinary sciencesGeneral Chemistry[SDV.IDA] Life Sciences [q-bio]/Food engineeringKetones040401 food science0104 chemical sciencesOdorOdorantsInkExtraction methods4-PHENYLCYCLOHEXENEVolatilizationGeneral Agricultural and Biological SciencesOFFSETpsychological phenomena and processesJournal of Agricultural and Food Chemistry
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Sunlight-induced functionalisation reactions of heteroaromatic bases with aldehydes in the presence of TiO2: A hypothesis on the mechanism

2007

In previous studies we reported a new photocatalytic system involving polycrystalline TiO2 for the selective functionalisation of heteroaromatic bases with ethers and amides. In order to extend the applications of this new reaction and to better understand the mechanism involved, we have examined aromatic and aliphatic aldehydes as acyl radical sources for the nucleophilic addition to protonated N-heteroarenes in acetonitrile as the solvent and TiO2/H2O2 as the photocatalytic system. Acyl radicals may undergo decarbonylation to yield the corresponding alkyl radicals. Acyl/alkyl derivative ratios depend on the nature of the aldehydes, and present a different distribution from that obtained i…

Settore CHIM/03 - Chimica Generale e Inorganicachemistry.chemical_classificationAldehydesNucleophilic additionGeneral Chemical EngineeringRadicalDecarbonylationHeterocyclic basesGeneral Physics and AstronomyGeneral ChemistryPhotochemistryRedoxProduct distributionSunlight-induced reactions; TiO2; Heterocyclic bases; AldehydesAdductchemistryPhotocatalysisTiO2Sunlight-induced reactionsAlkylJournal of Photochemistry and Photobiology A: Chemistry
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Purification of hydroperoxide lyase from green bell pepper (Capsicum annuum L.) fruits for the generation of C6-aldehydes in vitro.

2002

The aim of this work was to compare the efficiency of different extracts of hydroperoxide lyase from green bell peppers in producing aldehydes: a crude extract, a chloroplastic fraction, and a purified enzyme were investigated. From a crude extract, the HPO lyase was purified by ion-exchange chromatography with a 22.3-fold increase in purification factor. Analysis by SDS-PAGE electrophoresis under denaturating conditions showed only one protein with a molecular weight of 55 kDa, whereas size-exclusion chromatography indicated a molecular weight of 170 kDa. A maximum of 7500 mg of aldehydes per g of protein was obtained with the purified enzyme within 20 min of bioconversion compared to 392 …

Lipid PeroxidesProtein DenaturationChloroplastsLinolenic AcidsBioconversionBiologyAldehydechemistry.chemical_compoundBiosynthesisCytochrome P-450 Enzyme SystemPolyacrylamide gel electrophoresisAldehyde-Lyaseschemistry.chemical_classificationAldehydesChromatographyPlant ExtractsGeneral ChemistryLyasebiology.organism_classificationChromatography Ion ExchangeChloroplastMolecular WeightEnzymechemistryBiochemistryLinoleic AcidsChromatography GelElectrophoresis Polyacrylamide GelGeneral Agricultural and Biological SciencesCapsicumSolanaceaeJournal of agricultural and food chemistry
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