Search results for "organometallic"

showing 10 items of 370 documents

The CO-releasing molecule CORM-3 protects against articular degradation in the K/BxN serum transfer arthritis model.

2010

Contains fulltext : 89015.pdf (Publisher’s version ) (Closed access) Carbon monoxide-releasing molecules can counteract inflammatory responses. The aim of this study was to investigate whether tricarbonylchloro(glycinate)ruthenium (II) (CORM-3) is able to control the effector phase of experimental arthritis. Arthritis was induced in C57Black-6 mice by an intraperitoneal injection of serum from arthritic K/BxN mice. CORM-3 was administered intraperitoneally at 10 mg/kg/day (5 mg/kg twice a day) from days 0 to 10 and animals were sacrificed on day 11. Serum levels of osteocalcin and prostanoids were measured by enzyme-linked immunosorbent assay and radioimmunoassay. Gene expression was determ…

Cartilage ArticularMaleSerummedicine.medical_specialtymedicine.medical_treatmentIntraperitoneal injectionArthritisMice TransgenicHMGB1Auto-immunity transplantation and immunotherapy [N4i 4]RutheniumMicechemistry.chemical_compoundMice Inbred NODInternal medicineOrganometallic CompoundsmedicineAnimalsPharmacologyCarbon MonoxidebiologyChemistryProstaglandin D2 synthaseRadioimmunoassaymedicine.diseaseArthritis ExperimentalMice Inbred C57BLDisease Models AnimalEndocrinologyRANKLbiology.proteinOsteocalcinProstaglandin D2Infection and autoimmunity [NCMLS 1]European Journal of Pharmacology
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Exceptional affinity of nanostructured organic-inorganic hybrid materials towards dioxygen: confinement effect of copper complexes

2007

We report the exceptional reactivity towards dioxygen of a nanostructured organic-inorganic hybrid material due to the confinement of copper cyclam within a silica matrix. The key step is the metalation reaction of the ligand, which can occur before or after xerogel formation through the sol-gel process. The incorporation of a Cu(II) center into the material after xerogel formation leads to a bridged Cu(I)/Cu(II) mixed-valence dinuclear species. This complex exhibits a very high affinity towards dioxygen, attributable to auto-organization of the active species in the solid. The remarkable properties of these copper complexes in the silica matrix demonstrate a high cooperative effect for O(2…

Cations DivalentMetalationInorganic chemistrychemistry.chemical_elementLigands010402 general chemistry01 natural sciencesCatalysischemistry.chemical_compoundAdsorptionHeterocyclic CompoundsCyclamPolymer chemistryOrganometallic CompoundsLamellar structureReactivity (chemistry)ComputingMilieux_MISCELLANEOUSdioxygen bindingBinding Sites010405 organic chemistryLigandsol-gel processesSpectrum AnalysisOrganic ChemistryTemperatureGeneral Chemistry[CHIM.MATE]Chemical Sciences/Material chemistrySilicon DioxideCopperEnzymesNanostructuresPeroxides0104 chemical sciencesOxygenchemistrytetraazamacrocyclesMultiprotein Complexescopper[ CHIM.MATE ] Chemical Sciences/Material chemistryAnisotropyAdsorptionHybrid materialGelsorganic-inorganic hybrid composites
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Enzyme-Controlled Nanodevice for Acetylcholine-Triggered Cargo Delivery Based on Janus Au–Mesoporous Silica Nanoparticles

2017

[EN] This work reports a new gated nanodevice for acetylcholine-triggered cargo delivery. We prepared and characterized Janus Au-mesoporous silica nanoparticles functionalized with acetylcholinesterase on the Au face and with supramolecular b-cyclodextrin: benzimidazole inclusion complexes as caps on the mesoporous silica face. The nanodevice is able to selectively deliver the cargo in the presence of acetylcholine via enzyme-mediated acetylcholine hydrolysis, locally lowering the pH and opening the supramolecular gate. Given the key role played by ACh and its relation with Parkinson's disease and other nervous system diseases, we believe that these findings could help design new therapeuti…

Cell SurvivalSupramolecular chemistryNanoparticleNanotechnologymacromolecular substances02 engineering and technology010402 general chemistry01 natural sciencesCatalysisQUIMICA ORGANICACIENCIA DE LOS MATERIALES E INGENIERIA METALURGICAQUIMICA ANALITICAmedicineOrganometallic CompoundsControlled releaseNanotechnologyHumansJanusNanodevicechemistry.chemical_classificationDrug CarriersChemistryHydrolysisQUIMICA INORGANICAOrganic Chemistrybeta-CyclodextrinsGeneral ChemistryMesoporous silicaHydrogen-Ion Concentration021001 nanoscience & nanotechnologyEnzymes ImmobilizedSilicon DioxideControlled releaseMesoporous materialsAcetylcholine0104 chemical sciencesEnzymeDoxorubicinAcetylcholinesteraseNanoparticlesBenzimidazolesGold0210 nano-technologyPorosityAcetylcholinemedicine.drugHeLa Cells
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An organogold compound as potential antimicrobial agent against drug resistant bacteria: Initial mechanistic insights

2021

Abstract The rise of antimicrobial resistance has necessitated novel strategies to efficiently combat pathogenic bacteria. Metal‐based compounds have been proven as a possible alternative to classical organic drugs. Here, we have assessed the antibacterial activity of seven gold complexes of different families. One compound, a cyclometalated Au(III) C^N complex, showed activity against Gram‐positive bacteria, including multi‐drug resistant clinical strains. The mechanism of action of this compound was studied in Bacillus subtilis. Overall, the studies point towards a complex mode of antibacterial action, which does not include induction of oxidative stress or cell membrane damage. A number …

Cell Survivalmedicine.drug_classAntibioticsorganometallic drugsmode of action.Microbial Sensitivity TestsGram-Positive Bacteriamedicine.disease_causeBiochemistrydrug resistant bacteriaMiceStructure-Activity RelationshipAntibioticsDrug Discoverygold compoundsmedicineAnimalsGeneral Pharmacology Toxicology and PharmaceuticsMode of actionPharmacologyFull PaperDose-Response Relationship DrugMolecular StructurebiologyChemistryOrganic ChemistryPathogenic bacteriaFull Papersbiology.organism_classificationAntimicrobialAnti-Bacterial AgentsMechanism of actionBiochemistryMolecular Medicinemedicine.symptomAntibacterial activityOrganogold CompoundsBacteriaEx vivo
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Simulations of a Graphene Nanoflake as a Nanovector To Improve ZnPc Phototherapy Toxicity: From Vacuum to Cell Membrane

2017

International audience; We propose a new approach to improving photodynamic therapy (PDT) by transporting zinc phthalocyanine (ZnPc) in biological systems via a graphene nanoflake, to increase its targeting. Indeed, by means of time-dependent density functional theory simulations, we show that the ZnPc molecule in interaction with a graphene nanoflake preserves its optical properties not only in a vacuum but also in water. Moreover, molecular dynamic simulations demonstrate that the graphene nanoflake/ZnPc association, as a carrier, permits one to stabilize the ZnPc/graphene nanoflake system on the cellular membrane, which was not possible when using ZnPc alone. We finally conclude that the…

Cellular membraneIndolesMaterials scienceVacuum[SPI.NANO] Engineering Sciences [physics]/Micro and nanotechnologies/MicroelectronicsNanotechnology02 engineering and technology[SPI.MAT] Engineering Sciences [physics]/Materials010402 general chemistry01 natural sciences[SPI.MAT]Engineering Sciences [physics]/Materialslaw.inventionCell membraneMolecular dynamicslawCell Line TumorOrganometallic CompoundsmedicineHumansMoleculeGeneral Materials Science[SPI.NANO]Engineering Sciences [physics]/Micro and nanotechnologies/Microelectronics[SPI.ACOU]Engineering Sciences [physics]/Acoustics [physics.class-ph]Zinc phthalocyanine[SPI.ACOU] Engineering Sciences [physics]/Acoustics [physics.class-ph]Photosensitizing AgentsGrapheneCell Membrane021001 nanoscience & nanotechnologyNanostructures0104 chemical sciencesmedicine.anatomical_structurePhotochemotherapyGraphiteDensity functional theory0210 nano-technology
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Sequestration of organomettalic compounds by synthetic and naturally occuring polycarboxylate ligands. Binding of monomethylmercury(II) by polyacryli…

2007

The sequestering capacity of synthetic and naturally occurring polycarboxylate ligands towards mono- methylmercury(II) was evaluated by stability quantitative data on the interaction of CH3Hgþ with different molecular weight synthetic polyacrylates (2 and 20 kDa average M.wt) and alginate (70– 100 kDa) extracted from brown algae Macrocystis pyrifera. The influence of ionic medium was evaluated by measurements on the CH3Hgþ-polyacrylate systems in NaNO3 medium at different ionic strengths (0.10, 0.25, 0.50 and 0.75mol Lÿ1), and a Debye–Hu¨ ckel type equation was used for the dependence of complex formation constants on ionic strength. Measurements on the CH3Hgþ - alginate system were carried…

Chemical Health and SafetybiologyChemistryHealth Toxicology and MutagenesisComplex formationIonic bondingmonomethylmercury; sequestration by organic matter; polyacrylic and alginic acidsToxicologybiology.organism_classificationBrown algaemonomethylmercuryBinding abilityType equationpolyacrylic and alginic acidsmonomethylmercury sequestration by organic matter polyacrylic and alginic acids speciation equilibrium analysis complex species formationIonic strengthOrganic chemistrySettore CHIM/01 - Chimica Analiticasequestration by organic matterNuclear chemistryGroup 2 organometallic chemistry
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A Rational Design for Imidazolate-Bridged Linear Trinuclear Compounds from Mononuclear Copper(II) Complexes with 2-[((Imidazol-2-ylmethylidene)amino)…

2001

Two mononuclear copper(II) complexes with the unsymmetrical tridentate ligand 2-[((imidazol-2-ylmethylidene)amino)ethyl]pyridine (HL), [Cu(HL)(H2O)](ClO4)2.2H2O (1) and [Cu(HL)Cl2] (2), have been prepared and characterized. The X-ray analysis of 2 revealed that the copper(II) ion assumes a pentacoordinated square pyramidal geometry with an N3Cl2 donor set. When 1 and 2 are treated with an equimolecular amount of potassium hydroxide, the deprotonation of the imidazole moiety promotes a self-assembled process, by coordination of the imidazolate nitrogen atom to a Cu(II) center of an adjacent unit, leading to the polynuclear complexes [[Cu(L)(H2O)](ClO4)]n (3) and [[Cu(L)Cl].2H2O]n (4). Variab…

Chemical PhenomenaPyridinesStereochemistryMolecular Conformationchemistry.chemical_elementCrystallography X-RayLigandsInorganic ChemistryMagneticschemistry.chemical_compoundDeprotonationImidazolatePyridineOrganometallic CompoundsImidazolePhysical and Theoretical ChemistryIsostructuralChemistry PhysicalChemistryLigandImidazolesHydrogen BondingCopperSquare pyramidal molecular geometryCrystallographyCopperInorganic Chemistry
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Stereoselective syntheses of piperidinones and their modification by organometallic coupling reactions

2007

Dehydropiperidinones stereoselectively obtained from N-arabinosyl imines were iodinated at the enaminone structure. Knochel iodine-magnesium exchange afforded Grignard compounds of these piperidinone derivatives which reacted, either directly or after transmetalation to zinc or copper intermediates, with alkyl-, aryl- or acylhalides to give correspondingly substituted piperidinones. Stereoselective conjugate allyl cuprate addition to a thus obtained 5-allyl dehydropiperidinone and ring-closing metathesis of the product gave a hydroquinolinone containing three stereogenic centers.

Chemistry OrganicMolecular ConformationStereoisomerismCrystallography X-RayMetathesisBiochemistryCoupling reactionStereocenterchemistry.chemical_compoundTransmetalationOrganometallic CompoundsOrganic chemistryMagnesiumPhysical and Theoretical ChemistryPiperidonesGroup 2 organometallic chemistryMolecular StructureChemistryArylOrganic ChemistryStereoisomerismZincModels ChemicalStereoselectivityIminesCopperIodineOrg. Biomol. Chem.
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Complexes of organometallic compounds XXVIII. The solution chemistry of bis(acetylacetone)ethylenediimine adducts of organotin(IV) halides

1971

Abstract The nature of methanol solutions of a series of bis(acetylacetone)ethylenediimine adducts of organotin(IV) halides has been studied by electronic and PMR spectroscopy and by osmometry and conductivity. Effectively complete dissociation to the free ligand and solvated organotin(IV) halide moieties is inferred.

ChemistryAcetylacetoneOrganic ChemistryHalideBiochemistryDissociation (chemistry)AdductInorganic Chemistrychemistry.chemical_compoundOsmometerPolymer chemistryMaterials ChemistryOrganic chemistryMethanolPhysical and Theoretical ChemistrySpectroscopyGroup 2 organometallic chemistryJournal of Organometallic Chemistry
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Hybrid Materials Formed by Two Molecular Networks. Towards Multiproperty Materials

1999

Abstract The possibilities offered by hybrid materials formed by two molecular networks in the context of the molecular magnets are illustrated. Molecule-based layered magnets are used as anionic hosts for electroactive molecules, with the aim of obtaining multiproperty materials exhibiting in addition to the cooperative magnetism other interesting properties according to the nature of the inserted molecules. In particular, hybrid molecular compounds containing molecular species giving rise to paramagnetic, conducting, or bi-stable properties are reported.

ChemistryMagnetismInorganic chemistryContext (language use)equipment and suppliesCondensed Matter PhysicsParamagnetismMolecular networkChemical physicsMagnetMoleculeHybrid materialhuman activitiesGroup 2 organometallic chemistry
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