Search results for "Azine"

showing 10 items of 1589 documents

Synthesis, biological evaluation, and: In silico studies of novel chalcone: In pyrazoline-based 1,3,5-triazines as potential anticancer agents

2020

A novel series of triazin-chalcones (7,8)a-g and triazin-N-(3,5-dichlorophenyl)pyrazolines (9,10)a-g were synthesized and evaluated for their anticancer activity against nine different cancer strains. Triazine ketones 5 and 6 were synthesized from the cyanuric chloride 1 by using stepwise nucleophilic substitution of the chlorine atom. These ketones were subsequently subjected to a Claisen-Schmidt condensation reaction with aromatic aldehydes affording chalcones (7,8)a-g. Then, N-(3,5-dichlorophenyl)pyrazolines (9,10)a-g were obtained by cyclocondensation reactions of the respective chalcones (7,8)a-g with 3,5-dichlorophenylhydrazine. Among all the evaluated compounds, chalcones 7d,g and 8g…

ChalconeGeneral Chemical EngineeringCyanuric chloridePyrazolineTriazine derivatives01 natural sciencesClaisen Schmidt condensation03 medical and health scienceschemistry.chemical_compoundNucleophilic substitutionNucleophilic substitution030304 developmental biologyTriazinechemistry.chemical_classification0303 health sciences010405 organic chemistryLigandBiological evaluationGeneral ChemistryCondensation reactionCombinatorial chemistryCyclocondensation reaction0104 chemical sciencesEnzymechemistryAnticancer activitieThymidylate synthasePotential anticancer agent
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Albumin binding and hydrophobic character of promazine and chlorpromazine metabolites.

1972

1. The binding of didesmethylpromazine, promazine N-oxide, 2-hydroxypromazine, promazine sulfoxide, monodesmethylpromazine sulfoxide, didesmethylchlorpromazine, chlorpromazine N-oxide, and chlorpromazine sulfoxide to bovine serum albumin was determined by means of sephadex gel filtration. 2. The albumin binding of these substances was characterized by the following parameters: the percentage α of free substance, the percentage β of bound substance, the binding constants K1, k+ and m, the number of binding sites per albumin molecule, and the free binding energy ΔFo. 3. The partition coefficients between n-octanol and buffer solution, pH 7.40, were measured for the above mentioned metabolites…

Chemical PhenomenaChlorpromazineStatistics as TopicPlasma protein bindingchemistry.chemical_compoundmedicineAnimalsBovine serum albuminChlorpromazinePromazinePromazinePharmacologyChromatographyBinding SitesbiologyAlbuminSulfoxideSerum Albumin BovineGeneral MedicineBuffer solutionChemistrychemistrySolubilitySephadexSulfoxidesbiology.proteinChromatography GelCattleNitrogen OxidesChlorinemedicine.drugProtein BindingNaunyn-Schmiedeberg's archives of pharmacology
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Nitrogen-15 NMR Studies on Hydrazines. 2— Substituent Effect Analysis inortho-Substituted Phenylhydrazines and Anilines

1996

15N and 13C NMR spectra of some ortho-substituted phenylhydrazines were measured at natural isotope abundance in DMSO-d6 solutions. The substituent present exerts a larger effect on the chemical shift of the nitrogen atom directly bound to the aromatic ring (N-1), the second one (N-2) showing an attenuated trend of similar sign. Contrary to what observed for para and meta isomers, the cross-correlation between N-1 and N-2 SCS values of ortho-substituted phenylhydrazines is not satisfactory; on the other hand, N-1 SCSs show a reasonably good linear regression with the σR− constants. As expected, no correlation was found between N-1 and C-1 or H-1 SCS values. Correlations between 13C and 15N …

Chemical shiftPhenylhydrazinesSubstituentchemistry.chemical_elementNatural abundanceGeneral ChemistryCarbon-13 NMRRing (chemistry)PhotochemistryNitrogenMedicinal chemistrySpectral linechemistry.chemical_compoundchemistryGeneral Materials ScienceMagnetic Resonance in Chemistry
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Comparison of thermal‐ and photo‐polymerization of lauryl methacrylate monolithic columns for CEC

2009

Lauryl methacrylate-based (LMA) monolithic columns for CEC, prepared using either thermal initiation or by UV-irradiation in the presence of AIBN have been compared. Thermal polymerization was carried out at 70 degrees C for 20 h. For UV initiation, the effects of the time exposure to UV light and irradiation energy were investigated. For each initiation process, the influence of composition of porogenic solvent (1,4-butanediol/1-propanol ratio) on the physical and electrochromatographic properties of the resulting monoliths was also evaluated. Photochemically lauryl methacrylate stationary phases initiated showed higher permeabilities and better efficiencies than those prepared by thermal …

Chemical substanceChromatographyMaterials scienceClinical BiochemistryBiochemistryAnalytical Chemistrylaw.inventionSolventMagazinePolymerizationlawPermeability (electromagnetism)ThermalIrradiationScience technology and societyNuclear chemistryELECTROPHORESIS
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Fluorination of Cu(001) Surface by C60F48 Molecule Adsorption

2019

Copper surface functionalization by defluorination of C60F48 molecules with submonolayer and monolayer coverages on the Cu(001) crystal is studied by X-ray photoelectron spectroscopy. At room tempe...

Chemical substanceMaterials sciencechemistry.chemical_elementPhotochemistryCopperSurfaces Coatings and FilmsElectronic Optical and Magnetic Materialslaw.inventionCrystalGeneral EnergyMagazineX-ray photoelectron spectroscopychemistrylawMonolayerSurface modificationMoleculePhysical and Theoretical ChemistryThe Journal of Physical Chemistry C
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FI-chemiluminometric study of thiazides by on-line photochemical reaction

2004

The present manuscript deals with a simple and sensitive flow-injection method for the chemiluminescent determination of thiazides. The method is based on the on-line photodegradation and chemiluminescent determination of the resulting photo-fragments. The on-line photodegradation is performed in basic medium by using a photoreactor consisting of a 550 cm long x 0.8 mm ID piece of PTFE tubing helically coiled around an 8 W low-pressure mercury lamp. The determination of the photo-irradiated thiazides is performed by a chemiluminescent oxidative reaction with Ce(IV) in sulphuric acid medium. A heterogeneous group of thiazides (indapamide, metolazone, hydroflumethiazide, chlorthalidone and be…

ChemiluminescencePhotochemistrymedicine.medical_treatmentClinical BiochemistryPharmaceutical SciencePhotochemistryAnalytical Chemistrylaw.inventionThiazidesFIAchemistry.chemical_compoundHydrochlorothiazidelawQUIMICA ANALITICADrug DiscoverymedicineBendroflumethiazidePhotodegradationSpectroscopyChemiluminescenceDetection limitHydroflumethiazideChromatographyThiadiazinesChemistryPhotochemical reactionHydrochlorothiazideFlow Injection AnalysisLuminescent MeasurementsPharmaceuticalsMetolazoneDiureticmedicine.drugJournal of Pharmaceutical and Biomedical Analysis
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Correction: Phenothiazine-based dyes for efficient dye-sensitized solar cells

2016

Correction for ‘Phenothiazine-based dyes for efficient dye-sensitized solar cells’ by Zu-Sheng Huang et al., J. Mater. Chem. C, 2016, 4, 2404–2426.

Chemistry02 engineering and technologyGeneral Chemistry010402 general chemistry021001 nanoscience & nanotechnologyPhotochemistry01 natural sciencesGeneralLiterature_MISCELLANEOUS0104 chemical scienceschemistry.chemical_compoundDye-sensitized solar cellPhenothiazineMaterials Chemistry0210 nano-technologyJournal of Materials Chemistry C
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The first excited singlet state of s‐tetrazine: A theoretical analysis of some outstanding questions

1996

The equation‐of‐motion coupled cluster method for excited electronic states (EOMEE‐CC) is applied to study the structure and selected properties of the first excited singlet state of s‐tetrazine. Adiabatic S1←S0 excitation energies obtained with large basis sets containing up to 270 functions are uniformly somewhat above the experimental 0–0 value of 2.238 eV, but nevertheless are the most accurate calculations reported to date for this quantity. The equilibrium geometry of S1 predicted in this study is in excellent agreement with another high‐level calculation, and moreover is quantitatively consistent with both the intensity of vibrational progressions observed in absorption and measured …

ChemistryAnharmonicityGeneral Physics and AstronomyElectronic structuresymbols.namesakeTetrazinechemistry.chemical_compoundCoupled clusterFranck–Condon principleExcited statesymbolsPhysical and Theoretical ChemistryAtomic physicsAdiabatic processExcitationThe Journal of Chemical Physics
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Influence of spatial arrangements of π-spacer and acceptor of phenothiazine based dyes on the performance of dye-sensitized solar cells

2013

Abstract Three phenothiazine based organic dyes PTA , PDTA and PTDA with D– π –A, π –D– π –A and A– π –D– π –A frameworks were designed and synthesized for the dye sensitized solar cells (DSSCs). Phenothiazine with octyloxyphenyl moiety acts as donor while thiophene and cyanoacetic acid units act as a π -spacer and an acceptor, respectively. The effects of the molecular structures of the dyes on the performance of the DSSCs were investigated systematically along with their photophysical and photoelectrochemical properties. The dye PTDA with A– π –D– π –A framework exhibited a better light harvesting capacity and an effective electron extraction pathway from the electron donor to the TiO 2 s…

ChemistryElectron donorGeneral ChemistryCondensed Matter PhysicsPhotochemistryAcceptorElectronic Optical and Magnetic MaterialsBiomaterialschemistry.chemical_compoundDye-sensitized solar cellCyanoacetic acidPhenothiazineOrganic dyeMaterials ChemistryThiopheneMoietyElectrical and Electronic EngineeringOrganic Electronics
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Metal-free regioselective C–C bond cleavage in 1,3,5-triazine derivatives of β-diketones

2014

Metal-free regioselective activation of a carbon–carbon bond in 1,3,5-triazine derivatives of β-diketones is easily achieved, in the absence of a catalyst, with the assistance of intramolecular hydrogen bonding.

ChemistryHydrogen bondRegioselectivityGeneral ChemistryCatalysisCatalysischemistry.chemical_compound135-TriazineMetal freeIntramolecular forcePolymer chemistryMaterials ChemistryOrganic chemistryta116Bond cleavageNew J. Chem.
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