Search results for "naphthalimide"

showing 5 items of 5 documents

Metal NHC Complexes with Naphthalimide Ligands as DNA-Interacting Antiproliferative Agents

2017

Naphthalimide-based N-heterocyclic carbene (NHC) complexes of the type [(1,5-cyclooctadiene)(NHC)RhCl)] (4 a-c), [(p-cymene)(NHC)RuCl2 )] (5 a-c), and [(NHC)CuBr] (6 a-c) were synthesized and investigated as antiproliferative agents that target DNA. The cytotoxic effects were largely driven by the naphthalimide structure, which is a DNA-intercalating moiety. Regarding the metal center, the highest activities were observed with the rhodium complexes, and cytotoxic activity was significantly lower for the ruthenium derivatives. The stable coordination of the NHC ligands of selected complexes 4 b and 5 b in solution was confirmed, and their DNA binding properties were studied by UV/Vis spectro…

Circular dichroismStereochemistryIntercalation (chemistry)Molecular Conformationchemistry.chemical_elementApoptosisCrystallography X-RayLigands010402 general chemistry01 natural sciencesBiochemistryRhodiumMetalchemistry.chemical_compoundDrug StabilityCoordination ComplexesDrug DiscoveryHumansMoietyGeneral Pharmacology Toxicology and PharmaceuticsrutheniumCell ProliferationPharmacology010405 organic chemistryChemistryCircular DichroismOrganic ChemistryDNAnaphthalimideIntercalating Agentsanticancer agent0104 chemical sciencesRutheniumcarbeneNaphthalimidesSettore CHIM/03 - Chimica Generale E Inorganicacoppervisual_artrhodiumMCF-7 CellsMonoterpenesvisual_art.visual_art_mediumCymenesMolecular MedicineSpectrophotometry UltravioletHT29 CellsMethaneCarbeneDNAChemMedChem
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Fluorescent organometallic rhodium(I) and ruthenium(II) metallodrugs with 4-ethylthio-1,8-naphthalimide ligands: Antiproliferative effects, cellular …

2018

Fluorescent 4-ethylthio-1,8-naphthalimides containing rhodium(I) N-heterocyclic carbene (NHC) and ruthenium (II) NHC fragments were synthesised and evaluated for their antiproliferative effects, cellular uptake and DNA-binding activity. Both types of organometallics triggered ligand dependent efficient cytotoxic effects against tumor cells with the rhodium(I) NHC derivatives causing stronger effects than the ruthenium (II) NHC analogues. Antiproliferative effects could also be observed against several pathogenic Gram-positive bacterial strains, whereas the growth of Gram-negative bacteria was not substantially affected. Cellular uptake was confirmed by atomic absorption spectroscopy as well…

Intercalation (chemistry)Fluorescent DyeLigands01 natural sciencesAntineoplastic Agentchemistry.chemical_compoundNeoplasmsDrug DiscoveryMoietyCell DeathBacterial InfectionsGeneral MedicineIntercalating AgentsNaphthalimideAnti-Bacterial AgentsRutheniumNaphthalimidesSettore CHIM/03 - Chimica Generale E InorganicaHumanStereochemistrychemistry.chemical_elementAntineoplastic AgentsLigandCarbene010402 general chemistryG-quadruplexBacterial InfectionRutheniumRhodiumCell Line TumorAnti-Bacterial AgentOrganometallic CompoundsG-QuadruplexeHumansRhodiumBioorganometallicFluorescent DyesGroup 2 organometallic chemistryCell ProliferationPharmacologyOrganometallic CompoundBacteria010405 organic chemistryLigandOrganic ChemistryIntercalating Agent0104 chemical sciencesG-QuadruplexeschemistryNeoplasmDrug Screening Assays AntitumorCarbene
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Naphthalimide imidazolium-based supramolecular hydrogels as bioimaging and theranostic soft materials

2020

1,8-Naphthalimide-based imidazolium salts differing for the alkyl chain length and the nature of the anion were synthesized and characterized to obtain fluorescent probes for bioimaging applications. First, their self-assembly behavior and gelling ability were investigated in water and water/dimethyl sulfoxide binary mixtures. Only salts having longer alkyl chains were able to give supramolecular hydrogels, whose properties were investigated by using a combined approach of fluorescence, resonance light scattering, and rheology measurements. Morphological information was obtained by scanning electron microscopy. In addition, conductive properties of organic salts in solution and gel state we…

Materials scienceCell SurvivalMacromolecular SubstancesSurface PropertiesScanning electron microscopeimidazolium salts010402 general chemistry01 natural sciencesTheranostic Nanomedicinechemistry.chemical_compoundbioimaging; fluorescence; imidazolium salts; naphthalimide; supramolecular hydrogelsCell Line TumorPhase (matter)HumansGeneral Materials ScienceParticle SizeSettore BIO/06 - Anatomia Comparata E CitologiabioimagingAlkylFluorescent Dyeschemistry.chemical_classificationMolecular Structure010405 organic chemistryDimethyl sulfoxideOptical ImagingImidazolesHydrogelsBiological activitySettore CHIM/06 - Chimica OrganicaResonance (chemistry)Combinatorial chemistryFluorescencenaphthalimide0104 chemical sciencesNaphthalimideschemistrySelf-healing hydrogelssupramolecular hydrogelsfluorescence
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A review of investigation on 4-substituted 1,8-naphthalimide derivatives

2020

DG acknowledges to the ERDF PostDoc project No. 1.1.1.2/VIAA/1/16/177. We are grateful to J. V. Grazulevičius for the valuable comments on the manuscript.

Materials scienceOrganic solar cell18-NaphthalimideMechanical EngineeringMetals and AlloysC-4 positionNanotechnology02 engineering and technologyElectroluminescence010402 general chemistry021001 nanoscience & nanotechnologyCondensed Matter PhysicsOptoelectronic devices01 natural sciences0104 chemical sciencesElectronic Optical and Magnetic MaterialsElectron-donatingMechanics of MaterialsMaterials ChemistryOLED:NATURAL SCIENCES:Physics [Research Subject Categories]Electron-accepting0210 nano-technologyDiode
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CCDC 206783: Experimental Crystal Structure Determination

2003

Related Article: B.Zarychta, J.Zaleski, V.Prezhdo, B.Uspenskiy|2003|Acta Crystallogr.,Sect.E:Struct.Rep.Online|59|o332|doi:10.1107/S1600536803003428

Space GroupCrystallographyCrystal SystemCrystal StructureCell ParametersN-(3-Methoxypropyl)-18-naphthalimideExperimental 3D Coordinates
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