Search results for "Dox"

showing 10 items of 1345 documents

Suitability of 1-hexyl-3-methylimidazolium ionic liquids for the analysis of pharmaceutical formulations containing tricyclic antidepressants

2018

Abstract The reversed-phase chromatographic behaviour of six tricyclic antidepressants (amitryptiline, clomipramine, doxepin, imipramine, nortryptiline and maprotiline) was examined in this work with acetonitrile-water mobile phases, in the absence and presence of the ionic liquids 1-hexyl-3-methylimidazolium chloride and 1-hexyl-3-methylimidazolium tetrafluoroborate, which have interesting features for the separation of basic compounds, in terms of peak shape combined with reduced retention. Tricyclic antidepressants are low polarity drugs that strongly associate to the alkyl chains of conventional stationary phases. They are also positively charged in the usual working pH range (2–8) in r…

AmitriptylineDrug CompoundingIonic LiquidsNortriptyline02 engineering and technologyAntidepressive Agents Tricyclic01 natural sciencesBiochemistryChlorideAnalytical Chemistrychemistry.chemical_compoundLimit of DetectionBoratesmedicineSample preparationMaprotilineAcetonitrileAlkylchemistry.chemical_classificationChromatography Reverse-PhaseChromatography010401 analytical chemistryOrganic ChemistryImidazolesGeneral Medicine021001 nanoscience & nanotechnologyDoxepin0104 chemical scienceschemistryIonic liquidSpectrophotometry UltravioletDoxepin0210 nano-technologymedicine.drugTricyclicJournal of Chromatography A
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Fuciniceras paradoxus nov. sp. (Harpoceratinae, Ammonitina) du Domérien portugais. Réflexion sur le sens taxonomique d’un assemblage paradoxal de car…

2002

A new ammonite (Fuciniceras paradoxus) is described here. This Lower Domerian species is based on a recently revised collections which came from the Maria Pares section (Rabacal area, South of Coimbra, Portugal). Curiously, shell of F. paradoxus bears both diagnostic traits for the genus Protogrammoceras SPATH (e.g. acute ogival ventral area) and Fuciniceras HAAS (e.g. angulirursiradiate rib). Thus, the new species can be viewed as a morphological puzzle and as a challenge for taxonomists. The amazing collection of morphological traits previously suspected as highly improbable because of biomechanical constraints (1) confirms the inadequacy of the traditional use of the genera Protogrammoce…

AmmoniteSubfamilybiologyPaleontologyZoologybiology.organism_classificationParadoxuslanguage.human_languageSpace and Planetary ScienceGenusPhylogeneticsFuciniceraslanguageTaxonomy (biology)Geobios
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Structural analysis of copper(I) interaction with amyloid β peptide

2019

Abstract The N-terminal fragment of Aβ (β = beta) peptide is able to bind essential transition metal ions like, copper, zinc and iron. Metal binding usually occurs via the imidazole nitrogens of the three His residues which play a key role in the coordination chemistry. Among all the investigated systems, the interaction between copper and Amyloid β assume a biological relevance because of the interplay between the two copper oxidation states, Cu(II) and Cu(I), and their involvement in redox reactions. Both copper ions share the ability to bind Amyloid β. A huge number of investigations have demonstrated that Cu(II) anchors to the N-terminal amino and His6, His13/14 imidazole groups, while …

AmyloidSilverCoordination spherechemistry.chemical_elementPeptide010402 general chemistrySilver(I)01 natural sciencesBiochemistryRedoxCoordination complexInorganic ChemistryMetalchemistry.chemical_compoundCoordination ComplexesImidazoleHistidineAmino Acid SequenceHistidinechemistry.chemical_classificationAmyloid beta-Peptides010405 organic chemistryChemistryStructureCopperPeptide Fragments0104 chemical sciencesCrystallographyCoordinationvisual_artvisual_art.visual_art_mediumCopper(I)CopperProtein BindingJournal of Inorganic Biochemistry
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Spectrophotometric determination of promazine with an oxidative column in FIA manifolds

1992

Abstract A simple flow-injection spectrophotometric method for the determination of promazine is described. The two proposed procedures are based on the oxidation of analyte with a manganese dioxide column. Concentrations of promazine in the ranges 2–20 and 1–6 are determined with a relative standard deviation of 1.0%. The injection rates are 62 and 80 samples h −1 , respectively. The influence of foreign species and the determination of promazine in a pharmaceutical formulation are also reported.

AnalyteChemistry PharmaceuticalClinical BiochemistryRelative standard deviationPharmaceutical Sciencechemistry.chemical_elementManganesePharmaceutical formulationRedoxDosage formAnalytical ChemistryDrug DiscoverymedicinePromazineSpectroscopyPromazineFlow injection analysisManganeseChromatographyChemistryOxidesHydrogen-Ion ConcentrationManganese CompoundsCalibrationFlow Injection AnalysisSpectrophotometry UltravioletOxidation-Reductionmedicine.drugJournal of Pharmaceutical and Biomedical Analysis
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Theoretical Study on the Photo-Oxidation and Photoreduction of an Azetidine Derivative as a Model of DNA Repair

2021

Photocycloreversion plays a central role in the study of the repair of DNA lesions, reverting them into the original pyrimidine nucleobases. Particularly, among the proposed mechanisms for the repair of DNA (6-4) photoproducts by photolyases, it has been suggested that it takes place through an intermediate characterized by a four-membered heterocyclic oxetane or azetidine ring, whose opening requires the reduction of the fused nucleobases. The specific role of this electron transfer step and its impact on the ring opening energetics remain to be understood. These processes are studied herein by means of quantum-chemical calculations on the two azetidine stereoisomers obtained from photocyc…

AnionsAcetonitrilesPyrimidineLightPhotochemistryAzetidinePharmaceutical ScienceOrganic chemistryDNA repair010402 general chemistryRing (chemistry)PhotochemistryOxetane01 natural sciencesArticleAnalytical ChemistryNucleobaseElectron transferchemistry.chemical_compoundElectron transferQUIMICA ORGANICAQD241-441AzetidineCationsredox propertiesDrug DiscoveryPhotosensitizerPhysical and Theoretical ChemistryPhotolyasering openingdensity functional theoryphotochemistry010405 organic chemistryRing openingModels Theoreticalelectron transfer0104 chemical scienceschemistryChemistry (miscellaneous)Density functional theoryMolecular MedicineAzetidinesThermodynamicsGasesazetidineOxidation-ReductionRedox propertiesMolecules
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[3.3]Ferrocenophanes with guanidine bridging units as multisignalling receptor molecules for selective recognition of anions, cations, and amino acid…

2007

The synthesis, electrochemical, and optical properties of a new [3.3]ferrocenophane framework in which two ferrocene subunits, with similar electronic environments, are linked through two substituted guanidine moieties, are reported. The receptors 4-7 have been prepared in good yields by the reaction of bis(carbodiimide) 3 with primary amines. This architecture is exceptionally "tunable" because a variety of "legs" may be appended to the basic [3.3]ferrocenophane scaffold to give a wide range of signaling units. These receptors show remarkable ion-sensing properties, due to the presence of a redox active unit (ferrocene), and an amphoteric binding site (guanidine). In this nitrogen-rich str…

AnionsModels MolecularMetallocenesInorganic chemistryCrystallography X-RayRedoxCatalysisMetalchemistry.chemical_compoundMolecular recognitionCationsElectrochemistryMoleculeFerrous CompoundsAmino AcidsGuanidineGuanidineCarbodiimideFluorescent Dyeschemistry.chemical_classificationSpectrum AnalysisOrganic ChemistryGeneral ChemistryAmino acidCrystallographyFerrocenechemistryvisual_artvisual_art.visual_art_mediumChemistry (Weinheim an der Bergstrasse, Germany)
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The Radical Trap in Atom Transfer Radical Polymerization Need Not Be Thermodynamically Stable. A Study of the MoX3(PMe3)3 Catalysts

2005

The molybdenum(III) coordination complexes MoX(3)(PMe(3))(3) (X = Cl, Br, and I) are capable of controlling styrene polymerization under typical atom transfer radical polymerization (ATRP) conditions, in conjunction with 2-bromoethylbenzene (BEB) as an initiator. The process is accelerated by the presence of Al(OPr(i))(3) as a cocatalyst. Electrochemical and synthetic studies aimed at identifying the nature of the spin trap have been carried out. The cyclic voltammogram of MoX(3)(PMe(3))(3) (X = Cl, Br, I) shows partial reversibility (increasing in the order ClBrI) for the one-electron oxidation wave. Addition of X(-) changes the voltammogram, indicating the formation of MoX(4)(PMe(3))(3) f…

AnionsReaction mechanismRadical polymerization010402 general chemistryPhotochemistry01 natural sciencesBiochemistryRedoxCatalysisStyreneCatalysisStyreneschemistry.chemical_compoundColloid and Surface ChemistryRadical polymerizationOxidationOrganic chemistry[CHIM.COOR]Chemical Sciences/Coordination chemistryRedox reactions010405 organic chemistryAtom-transfer radical-polymerizationGeneral Chemistry[CHIM.CATA]Chemical Sciences/Catalysis0104 chemical sciences[CHIM.POLY]Chemical Sciences/PolymersPolymerizationchemistryCyclic voltammetry
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The different redox-activity of dianthrylbenzene and dianthrylbiphenyl

1989

Abstract The reduction of dianthrylbenzene and dianthrylbiphenyl to stable tetraanion salts is described by NMR spectroscopy and cyclic voltammetry. The significantly different Coulomb interactions between the anthracene units are compared with those in dianthrylalkanes.

Anthracenechemistry.chemical_compoundchemistryOrganic ChemistryDrug DiscoveryInorganic chemistryNuclear magnetic resonance spectroscopyCyclic voltammetryBiochemistryRedox ActivityTetrahedron Letters
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Electrochemistry and spectroelectrochemistry of bismanganese biscorroles dyads

2011

Three manganese biscorrole dyads were synthesized, physicochemically characterized and investigated as to their electrochemistry and spectroelectrochemistry in nonaqueous media. Each dyad contained the same two corroles linked in a face-to-face arrangement via one of the three different linking groups, 9,9-dimethylxanthene, anthracene or diphenylether, the exact nature of which determined the distance and possible interaction between the two metallomacrocycles. The initial compounds contained Mn ( III ) in their air stable form and were shown to exhibit two major redox processes, one being a Mn (III)/ Mn (IV) conversion and the other being either Mn ( III )/ Mn ( II ) or reduction at the c…

Anthracenechemistry.chemical_elementGeneral ChemistryManganeseConjugated systemElectrochemistryPhotochemistryRedoxchemistry.chemical_compoundElectron transferchemistryPyridinePolymer chemistryCorroleJournal of Porphyrins and Phthalocyanines
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Resistance of p53 knockout cells to doxorubicin is related to reduced formation of DNA strand breaks rather than impaired apoptotic signaling

2003

The anthracycline doxorubicin (adriamycin) is an important chemotherapeutic agent used in the treatment of solid epithelial and mesenchymal tumors as well as leukemias. A variety of mechanisms has been proposed to be involved in doxorubicin-induced cytotoxicity such as DNA intercalation, oxidative stress, DNA strand breakage by inhibition of topoisomerase II, activation of death receptors, and altered p53 expression. Concerning doxorubicin resistance and p53 status data reported are contradictory. Here, we show that mouse fibroblasts deficient in p53 (p53(-/-)) are more resistant to doxorubicin than p53 wild-type (p53 wt) cells. This is in contrast to other genotoxic agents (UV-light, alkyl…

AnthracyclineApoptosisIn Vitro TechniquesBiochemistryCell LineMicemedicineAnimalsTopoisomerase II InhibitorsDoxorubicinMolecular BiologyEtoposideMice KnockoutbiologyTopoisomeraseCell BiologyFas receptorMolecular biologyDoxorubicinDrug Resistance NeoplasmCell cultureApoptosisCancer researchbiology.proteinTumor Suppressor Protein p53Topoisomerase-II InhibitorDNA DamageSignal Transductionmedicine.drugDNA Repair
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