Search results for "Cinoxacin"

showing 7 items of 7 documents

Potentiometric and spectroscopic studies of transition-metal ions complexes with a quinolone derivative (cinoxacin). Crystal structures of new Cu(II)…

1997

Abstract The interaction of cobalt(II), nickel(II), copper(II), and zinc(II) with Cinoxacin (HCx = 1-ethyl-1,4-dihydro-4-oxo(1,3)dioxolo(4,5-g)cinnoline-3-carboxylic acid), a 4-quinolone derivative, has been studied at metal/ligand ratios of 1:1-1:3 by means of pH-metric, spectrophotometric, and ESR methods. The formation constants have been determined and the stereochemistry for the metal ions in the species present in aqueous solutions (at 37 ± 0.1°C and I = 0.1 mol dm −3 NaCl) is discussed. In all the studied systems, complexes with different stoichiometric ratios, in which cinoxacin acts both as neutral and deprotonated ligand, are formed. The anomalous sequence of the stepwise stabilit…

LigandMetal ions in aqueous solutionInorganic chemistryCinoxacinchemistry.chemical_elementZincCrystal structureTriclinic crystal systemBiochemistryInorganic ChemistryCrystallographyNickelchemistryStability constants of complexesmedicinemedicine.drugJournal of Inorganic Biochemistry
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Cinoxacin complexes with divalent metal ions. Spectroscopic characterization. Crystal structure of a new dinuclear Cd(II) complex having two chelate-…

1998

Several cinoxacin (HCx) complexes with divalent metal ions have been prepared and characterized by spectroscopic techniques. The crystal structure of [Cd 2 (Cx) 4 (H 2 O) 2 ] · 10H 2 O has been determined by X-ray diffraction. The complex is triclinic, space group with unit-cell dimensions: a =10.412(2), b =11.119(2), c =13.143(6)A, α=76.78(4)°, β =74.59(3)°, γ =77.12(3)°, V =1406.0(8) A 3 . In this complex each cadmium atom is heptacoordinated; the metal environment is formed by two O keto and two O carbox atoms from two different cinoxacinate monoanions, two carboxylate oxygen atoms from a third cinoxacinate ligand and by one water oxygen atom on the seventh position. Two of the cinoxacin…

Models MolecularDenticityStereochemistryCinoxacinCarboxylic AcidsCrystal structureMicrobial Sensitivity TestsTriclinic crystal systemCrystallography X-RayBiochemistryInorganic ChemistryMetalchemistry.chemical_compoundStructure-Activity RelationshipAnti-Infective AgentsmedicineEscherichia coliOrganometallic CompoundsChelationCarboxylateChelating Agents4-QuinolonesLigandCrystallographychemistryvisual_artvisual_art.visual_art_mediumCinoxacinmedicine.drugCadmiumJournal of inorganic biochemistry
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ComparativeIn Vitroevaluation of cumulative release of the urinary antiseptics Nalidixic acid, Pipemidic acid, Cinoxacin, and norfloxacin from white …

1994

AbstractThe in vitro diffusion of nalidixic acid (1), pipemidic acid (2), cinoxacin (3), and norfloxacin (4) was studied. The transfer rate constants (kd) from simulated gastro-intestinal juices to simulated plasma, throughout artificial wall lipid membranes, were defined. The kd values suggested that the four drugs are absorbed both in gastric and intestinal environments in similar amounts. To obtain lack of gastric unwanted effects white beeswax microspheres containing 1, 2, 3, and 4 were investigated as a vehicle for the drug intestinal release; they were prepared by the meltable dispersion process using wetting agents. Discrete, reproducible free flowing microspheres were obtained. The …

PharmacologyActive ingredientChromatographyNalidixic acidChemistryOrganic ChemistryCinoxacinPharmaceutical SciencePipemidic acidAbsorption (skin)Dosage formBiochemistryDrug DiscoverymedicineNorfloxacinmedicine.drugAntibacterial agentDrug Development and Industrial Pharmacy
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CCDC 652237: Experimental Crystal Structure Determination

2007

Related Article: M.Ruiz, R.Ortiz, L.Perello, J.Latorre, J.Server-Carrio|1997|J.Inorg.Biochem.|65|87|doi:10.1016/S0162-0134(96)00092-X

Space GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D CoordinatesAqua-bis(cinoxacinato)-copper(ii) trihydrate
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Synthesis, characterization, and crystal structure of [Cu(cinoxacinate)2] · 2H2O complex: A square-planar CuO4 chromophore. Antibacterial studies

1995

The structural and spectroscopic properties of a new copper (II) complex of cinoxacin (HCx) have been investigated. The complex [Cu(Cx)2].2H2O crystallizes in the monoclinic system, space group P2(1)/c. The cell dimensions are: a = 7.998(2), b = 7.622(1), c = 18.955(6) A, beta = 94.38(2) degree, V = 1154.6(6) A3, Z = 2. The structure was refined to R = 0.051. The crystal is composed of [Cu(Cx)2] units and uncoordinated water molecules. The Cu(II) ion, at a center of symmetry, is coordinated to two cinoxacinate (Cx) ligands related by the inversion center. Each cinoxacinate acts as bidentate ligand bonded to the cation through its carboxylate oxygen atom and through its exocyclic carbonyl ox…

Spectrophotometry InfraredStereochemistryCrystal structureMicrobial Sensitivity TestsCrystallography X-RayBiochemistryInorganic ChemistryCrystalchemistry.chemical_compoundEnterobacteriaceaeOrganometallic CompoundsMoleculeCarboxylateGroup 2 organometallic chemistryGram-Negative Aerobic BacteriaMolecular StructureChemistryLigandSpectrophotometry AtomicElectron Spin Resonance SpectroscopyChromophoreGram-Positive CocciSolubilityCinoxacinSpectrophotometry UltravioletCopperMonoclinic crystal system
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CCDC 652238: Experimental Crystal Structure Determination

2007

Related Article: M.Ruiz, R.Ortiz, L.Perello, J.Latorre, J.Server-Carrio|1997|J.Inorg.Biochem.|65|87|doi:10.1016/S0162-0134(96)00092-X

bis(Cinoxacinato)-bis(dimethylsulfoxide)-nickel(ii) tetrahydrateSpace GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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Interactions of metal ions with two quinolone antimicrobial agents (cinoxacin and ciprofloxacin)

2002

Several novel metal-quinolone compounds have been synthesized and characterized by analytical, spectroscopic and X-ray diffraction methods. The crystal structure of the four compounds, Na(2)[(Cd(Cx)3)(Cd(Cx)3(H2O))].12H2O, [Co(Cp)2(H2O)2].9H2O, [Zn(Cp)2(H2O)2].8H2O and [Cd(HCp)2(Cl)2].4H2O, is presented and discussed: HCx=1-ethyl-1,4-dihydro-4-oxo(1,3)-dioxolo(4,5-g)cinnoline-3-carboxylic acid and HCp=1-cyclopropyl-6-fluoro-1,4-dihydro-4-oxo-7-(1-piperazinyl)-3-quinoline carboxylic acid. In all these compounds the quinolone acts as a bidentate chelate ligand that binds through one carboxylate oxygen atom and the exocyclic carbonyl oxygen atom. Complexes of ciprofloxacin were screened for th…

chemistry.chemical_classificationDenticityChemistryLigandStereochemistryMetal ions in aqueous solutionCarboxylic acidCinoxacinBiochemistryInorganic Chemistrychemistry.chemical_compoundmedicineMoleculeChelationCarboxylatemedicine.drugJournal of Inorganic Biochemistry
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