Search results for "Quinoline"

showing 10 items of 391 documents

Synthesis and stereochemical studies of 1- and 2-phenyl-substituted 1,3-oxazino[4,3-a]isoquinoline derivatives

2003

Abstract Starting from the 1′- or 2′-phenyl-substituted 1-(2′-hydroxyethyl)-6,7-dimethoxy-1,2,3,4-tetrahydroisoquinoline diastereomers 3 and 6 , 4-unsubstituted and 4-(p-nitrophenyl)- and 4-oxo-substituted 1-phenyl- and 2-phenyl-9,10-dimethoxy-2H,4H-1,6,7,11b-tetrahydro-1,3-oxazino[4,3-a]isoquinolines ( 7–12 ) were prepared. The relative configurations and the predominant conformations of the products were determined by NMR spectroscopy, by quantum chemical calculations and, for (2R∗,4S∗,11bR∗)-9,10-dimethoxy-4-(p-nitrophenyl)-2-phenyl-2H,4H-1,6,7,11b-tetrahydro-1,3-oxazino[4,3-a]isoquinoline ( 11 ), by X-ray diffraction.

DiffractionQuantum chemicalchemistry.chemical_classificationStereochemistryChemistryOrganic ChemistryDiastereomerOxazinesNuclear magnetic resonance spectroscopyBiochemistrychemistry.chemical_compoundComputational chemistryDrug DiscoveryIsoquinolineTetrahedron
researchProduct

The reaction betweentriazolobenzopyridinium and triazolothiazolium ylides with dimethyl acetylenedicarboxylate

1998

Abstract The reaction of some [1,2,3]triazolo[1,5- a ]quinolinium 1,2 , [1,2,3]triazolo[5,1- a ]isoquinolinium 3,4 and [1,2,3]triazolo[5,1- b ]thiazolium 5,6 ylides with dimethyl acetylenedicarboxylate is described. Compounds as dimethyl pyrrolo[1,2- a ]quinoline-1,2-dicarboxylate 19 , dimethyl pyrrolo[2,1- a ]isoquinoline-2,3-dicarboxylate 20 , 1,1-dicyano-2,3-dimethoxycarbonyl-1 H -pyrido[1,2- a ]quinoline 24 , 4,4-dicyano-2,3-dimethoxycarbonyl-4 H -pyrido[2,1- a ]isoquinoline 25 , and 7-methyl-5,6-dimethoxy-carbonylpyrrolo[2,1- a ]thiazole 14b , are formed.

Dimethyl acetylenedicarboxylatechemistry.chemical_compoundChemistryOrganic ChemistryDrug DiscoveryQuinolineIsoquinolineThiazoleBiochemistryMedicinal chemistryTetrahedron
researchProduct

In vitro activities of antimicrobial agents against Candida species

1999

Objective. Antimicrobial mouthrinses may represent a valid alternative to topical antifungal agents. However, the action of antimicrobials could be affected by the different ingredients incorporated into mouthrinse products. The purpose of the present study was to investigate the in vitro antifungal and fungicidal activities of antimicrobials alone. Study Design. A broth macrodilution method was used to determine the minimum inhibitory concentration of 4 antimicrobial agents against Candida species. Minimum fungicidal concentration was also determined. Results. All antimicrobials showed antifungal activity against all tested organisms, but cetylpyridinium chloride received significantly low…

DrugAntifungal Agentsmedia_common.quotation_subjectColony Count MicrobialMouthwashesCetylpyridiniumMicrobial Sensitivity TestsHexetidineBiologyCetylpyridinium chlorideStatistics NonparametricMicrobiologychemistry.chemical_compoundMinimum inhibitory concentrationAlkaloidsmedicineGeneral DentistryMycosisCandidamedia_commonBenzophenanthridinesAnalysis of VarianceDose-Response Relationship DrugTraditional medicineChlorhexidineHexetidineFungi imperfectiIsoquinolinesmedicine.diseasebiology.organism_classificationAntimicrobialFungicideOtorhinolaryngologychemistryAnti-Infective Agents LocalSurgeryOral SurgeryOral Surgery, Oral Medicine, Oral Pathology, Oral Radiology, and Endodontology
researchProduct

Simple and scalable electrochemical synthesis of 2,1-benzisoxazoles and quinoline N-oxides.

2019

Cathodic reduction of the nitro moiety and subsequent intramolecular cyclization affords different substituted 2,1-benzisoxazoles and quinoline N-oxides. This methodology allows the synthesis of two different types of heterocycles from common simple starting materials, using electrons as a sole reagent for this transformation. The electrolysis can be conducted in a very simple undivided electrolysis cell under constant current conditions. This permits working on a larger scale compared to other electrochemical methodologies and represents a significant advantage.

Electrolysis010405 organic chemistryElectrolytic cellQuinolineMetals and AlloysGeneral Chemistry010402 general chemistryElectrochemistry01 natural sciencesCombinatorial chemistryCatalysis0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic Materialslaw.inventionchemistry.chemical_compoundchemistrylawReagentMaterials ChemistryCeramics and CompositesNitroConstant currentMoietyChemical communications (Cambridge, England)
researchProduct

Detection of primary DNA damage in Chlamydomonas reinhardtii by means of modified microgel electrophoresis.

1997

The assessment of genotoxic potential in surface water requires test methods, among which are those that detect initial DNA damage in organisms of aquatic biocenosis. The microgel electrophoresis (MGE) "comet assay" was applied to a ubiquitous unicellular green alga (Chlamydomonas reinhardtii) to detect DNA damage caused by genotoxins. For this, the test protocol described by Singh NP et al. [Exp Cell Res 175: 184-191, 1988] was modified. Major modifications were the use of alkaline lysis buffer with ionic detergents and the reduction of preincubation and electrophoresis times. Short-time exposure of Chlamydomonas to the well-known genotoxicants 4-nitroquinoline-1-oxide (4-NQO), N-nitrosodi…

ElectrophoresisEpidemiologyDNA damageHealth Toxicology and MutagenesisChlamydomonas reinhardtiiBiologymedicine.disease_causeDimethylnitrosaminechemistry.chemical_compoundBotanymedicineAnimalsGenetics (clinical)Cell NucleusChlamydomonasDNAHydrogen PeroxideDNA Protozoanbiology.organism_classification4-Nitroquinoline-1-oxideComet assaychemistryBiophysicsDNA fragmentationAlkaline lysisGenotoxicityDNAChlamydomonas reinhardtiiWater Pollutants ChemicalDNA DamageEnvironmental and molecular mutagenesis
researchProduct

Immunochemical rapid determination of quinoxyfen, a priority hazardous pollutant

2018

In 2013, quinoxyfen was included in the list of priority hazard pollutants of the European Water Framework Directive due to its toxicity to aquatic organisms. However, few analytical methods for the analysis of this fungicide have been reported and no rapid immunochemical methods have been published so far. In the present study, immunoreagents for quinoxyfen analysis were generated for the first time and an enzyme-linked immunosorbent assay was developed. Two carboxylated derivatives of quinoxyfen were designed on the basis of the minimum energy conformation of the target compound. Active esters of those novel compounds were prepared using N,N′-disuccinimidyl carbonate, and purified for cov…

Environmental EngineeringHealth Toxicology and MutagenesisEnzyme-Linked Immunosorbent Assay010501 environmental sciencesMass spectrometry01 natural sciencesMass SpectrometryAntibodiesAquatic organismsmedicineEnvironmental ChemistryWater pollutant0105 earth and related environmental sciencesDetection limitPollutantImmunoassayChromatographyBioconjugationmedicine.diagnostic_testChemistry010401 analytical chemistryPublic Health Environmental and Occupational HealthGeneral MedicineGeneral ChemistryPollution0104 chemical sciencesFungicides IndustrialBioconjugatesHaptenImmunoassayQuinolinesImmunochemical methodsHaptenHaptensWater Pollutants ChemicalConjugate
researchProduct

Mn(II) complexes of scorpiand-like ligands. A model for the MnSOD active centre with high in vitro and in vivo activity

2015

Manganese complexes of polyamines consisting of an aza-pyridinophane macrocyclic core functionalised with side chains containing quinoline or pyridine units have been characterised by a variety of solution techniques and single crystal x-ray diffraction. Some of these compounds have proved to display interesting antioxidant capabilities in vitro and in vivo in prokaryotic (bacteria) and eukaryotic (yeast and fish embryo) organisms. In particular, the Mn complex of the ligand containing a 4-quinoline group in its side arm which, as it happens in the MnSOD enzymes, has a water molecule coordinated to the metal ion that shows the lowest toxicity and highest functional efficiency both in vitro …

Fish ProteinsSaccharomyces cerevisiae ProteinsStereochemistryOryziasSaccharomyces cerevisiaeLigandsFish embryo modelsBiochemistryAntioxidantsInorganic Chemistrychemistry.chemical_compoundAntioxidant activityIn vivoCatalytic DomainPyridineSide chainEscherichia coliAnimalschemistry.chemical_classificationManganeseBacteriaLigandSuperoxide DismutaseEscherichia coli ProteinsQuinolineYeastIn vitroYeastMn(II) complexesEnzymechemistryModels ChemicalPolyazamacrocyclic scorpiandsQuinolines
researchProduct

Isolation and Characterization of Structurally Novel Antimutagenic Flavonoids from Spinach (Spinacia oleracea)

2001

Thirteen compounds, isolated from spinach (Spinacia oleracea), acted as antimutagens against the dietary carcinogen 2-amino-3-methylimidazo[4,5-f]quinoline in Salmonella typhimurium TA 98. The antimutagens were purified by preparative and micropreparative HPLC from a methanol/water (70:30, v/v) extract of dry spinach (commercial product) after removal of lipophilic compounds such as chlorophylls and carotenoids by solid-phase extraction (SPE). Pure active compounds were identified by instrumental analysis including FT-IR, (1)H and (13)C NMR, UV-vis spectroscopy, and mass spectrometry. All of these compounds were flavonoids and related compounds that could be attributed to five groups: (A, m…

FlavonoidsSalmonella typhimuriumchemistry.chemical_classificationSpinaciaChromatographybiologyQuinolineFlavonoidExtraction (chemistry)Antimutagenic AgentsGeneral Chemistrybiology.organism_classificationHigh-performance liquid chromatographyStructure-Activity Relationshipchemistry.chemical_compoundchemistryBiochemistrySpinacia oleraceaQuinolinesSpinachGeneral Agricultural and Biological SciencesCarotenoidAntimutagenChromatography High Pressure LiquidMutagensJournal of Agricultural and Food Chemistry
researchProduct

Chromatographically separable rotamers of an unhindered amide

2014

Surprisingly stable formamide rotamers were encountered in the tetrahydroisoquinoline and morphinan series of alkaloids. We investigated the hindered rotation around the amide bond by dynamic high-performance liquid chromatography (DHPLC) and kinetic measurements of the interconversion of the rotamers which can readily be separated by HPLC as well as TLC. The experimental results of the different methods were compared to each other as well as to results obtained by DFT calculations.

FormamideMorphinanTetrahydroisoquinolinedynamic HPLCOrganic ChemistryrotamersHigh-performance liquid chromatographyFull Research Paperamideslcsh:QD241-441Chemistrythermodynamicschemistry.chemical_compoundlcsh:Organic chemistrychemistryComputational chemistryAmidedensity functional calculationsOrganic chemistryPeptide bondlcsh:Qlcsh:ScienceConformational isomerismBeilstein Journal of Organic Chemistry
researchProduct

Isomer-nonspecific action of dichlorodiphenyltrichloroethane on aryl hydrocarbon receptor and G-protein-coupled receptor 30 intracellular signaling i…

2014

Abstract Extended residual persistence of the pesticide dichlorodiphenyltrichloroethane (DDT) raises concerns about its long-term neurotoxic effects. Little is known, however, about DDT toxicity during the early stages of neural development. This study demonstrated that DDT-induced apoptosis of mouse embryonic neuronal cells is a caspase-9-, caspase-3-, and GSK-3β-dependent process, which involves p,p’ -DDT-specific impairment of classical ERs. It also provided evidence for DDT-isomer-nonspecific alterations of AhR- and GPR30-mediated intracellular signaling, including changes in the levels of the receptor and receptor-regulated mRNAs, and also changes in the protein levels of the receptors…

GPR30Time FactorsGSK-3 betaEstrogen receptorApoptosisStimulationBiochemistryReceptors G-Protein-CoupledGlycogen Synthase Kinase 3MiceEndocrinologyneurotoxicityestrogenReceptorCells CulturedNeuronsbiologyCaspase 3estrogen receptorsCaspase InhibitorsCell biologycaspasesReceptors EstrogenQuinolinesGPERNeural developmentSignal Transductionmedicine.medical_specialtyAryl hydrocarbon receptor nuclear translocatorneuronal cell culturesDDT17-beta-estradiolIsomerismbeta-NaphthoflavoneInternal medicineparasitic diseasesCytochrome P-450 CYP1A1medicineAnimalsBcl-2BenzodioxolesRNA MessengerMolecular BiologyG protein-coupled receptorBenzoflavonesGlycogen Synthase Kinase 3 betaL-Lactate DehydrogenaseAryl hydrocarbon receptorPyrimidinesEndocrinologyReceptors Aryl Hydrocarbonbiology.proteinPyrazolesMolecular and Cellular Endocrinology
researchProduct