Search results for "Ethylenedioxy"

showing 7 items of 67 documents

CCDC 230883: Experimental Crystal Structure Determination

2004

Related Article: E.Coronado, C.Gimenez-Saiz, C.J.Gomez-Garcia, S.C.Capelli|2004|Angew.Chem.,Int.Ed.|43|3022|doi:10.1002/anie.200453985

Space GroupCrystallographyCrystal SystemDi-potassium hexakis(bis(ethylenedioxy)tetrathiafulvalene)borato-hexatriacontaoxo-dodeca-tungsten undecahydrateCrystal StructureCell ParametersExperimental 3D Coordinates
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3,4-Dihydroxy- and 3,4-methylenedioxy- phenanthrene-type alkaloids with high selectivity for D2 dopamine receptor.

2013

Abstract Dopamine-mediated neurotransmission plays an important role in relevant psychiatric and neurological disorders. Nowadays, there is an enormous interest in the development of new drugs acting at the dopamine receptors (DR) as potential new targets for the treatment of schizophrenia or Parkinson’s disease. Previous studies have revealed that isoquinoline compounds such as tetrahydroisoquinolines (THIQs) can behave as selective D 2 dopaminergic alkaloids. In the present study we have synthesized five aporphine compounds and five phenanthrene alkaloids and evaluated their potential dopaminergic activity. Binding studies on rat striatal membranes were used to evaluate their affinity and…

StereochemistryClinical BiochemistryPharmaceutical ScienceNeurotransmissionPharmacologyBiochemistryMethylenedioxychemistry.chemical_compoundAlkaloidsDrug DiscoveryAnimalsHumansAporphineIsoquinolineMolecular BiologyChemistryReceptors Dopamine D2Organic ChemistryDopaminergicParkinson DiseasePhenanthrenePhenanthrenesCorpus StriatumRatsDopamine receptorSchizophreniaMolecular MedicineSelectivityBioorganicmedicinal chemistry letters
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Synthesis of new melatoninergic hexahydroindenopyridines

2014

Hexahydroindenopyridine (HHIP) is an interesting heterocyclic framework that contains an indene core similar to ramelteon. This type of tricyclic piperidines aroused our interest as potential melatoninergic ligands. Melatonin receptor ligands have applications in insomnia and depression. We report herein an efficient two-step method to prepare new HHIP by the reaction of an enamine with 3-bromopropylamine hydrobromide. Some synthesized compounds showed moderate affinity for melatonin receptors in the nanomolar or low micromolar range. Furthermore, the methylenedioxy HHIPs 2d (N-phenylacetamide) and 2f (N,N-diethylacetamide), exhibited high selectivity at MT1 or MT2 receptors, respectively, …

StereochemistryClinical BiochemistryRamelteonPharmaceutical ScienceLigandsHeterocyclic Compounds 4 or More RingsBiochemistryMelatonin receptorMethylenedioxyEnamineMelatoninStructure-Activity Relationshipchemistry.chemical_compoundDrug DiscoverymedicineHumansIndeneMolecular Biologychemistry.chemical_classificationDose-Response Relationship DrugMolecular StructureReceptor Melatonin MT2HydrobromideReceptor Melatonin MT1Organic ChemistryHEK293 CellschemistryMolecular MedicineTricyclicmedicine.drugBioorganic & Medicinal Chemistry Letters
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Efficient synthesis of hexahydroindenopyridines and their potential as melatoninergic ligands.

2014

Hexahydroindenopyridine (HHIP) is an interesting tricyclic piperidine nucleus that is structurally related to melatonin, a serotonin-derived neurohormone. Melatonin receptor ligands have applications in several cellular, neuroendocrine and neurophysiological disorders, including depression and/or insomnia. We report herein an efficient two-step method to prepare new HHIP via enamine C-alkylation-cyclization. The influence of substituents on the benzene ring and the nitrogen atom on melatoninergic receptors has been studied. Among the 25 synthesized HHIPs, some of them containing methylenedioxy (series 2) and 8-chloro-7-methoxy substituents (series 4) on the benzene ring revealed affinity fo…

StereochemistryPyridinesRing (chemistry)LigandsMelatonin receptorMethylenedioxyEnaminechemistry.chemical_compoundStructure-Activity RelationshipDrug DiscoveryHumansReceptorCells CulturedPharmacologychemistry.chemical_classificationBinding SitesDose-Response Relationship DrugMolecular StructureReceptor Melatonin MT2Receptor Melatonin MT1Organic ChemistryGeneral MedicineHEK293 CellschemistryPiperidineAcetamideTricyclicEuropean journal of medicinal chemistry
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Spatial differences and temporal changes in illicit drug use in Europe quantified by wastewater analysis

2014

Aims To perform wastewater analyses to assess spatial differences and temporal changes of illicit drug use in a large European population. Design Analyses of raw wastewater over a 1-week period in 2012 and 2013. Setting and Participants Catchment areas of wastewater treatment plants (WWTPs) across Europe, as follows: 2012: 25 WWTPs in 11 countries (23 cities, total population 11.50 million); 2013: 47 WWTPs in 21 countries (42 cities, total population 24.74 million). Measurements Excretion products of five illicit drugs (cocaine, amphetamine, ecstasy, methamphetamine, cannabis) were quantified in wastewater samples using methods based on liquid chromatography coupled to mass spectrom…

cannabisTime FactorsEcstasyEcstasyMethamphetaminesMedicine (miscellaneous)SewageWaste Disposal FluidMass SpectrometryMethamphetamineCocaineMedicineWater treatmentDrug useAmphetamine; cannabis; cocaine; drugs of abuse; ecstasy; methamphetamine; sewagebiologySewageAmphetamine ; Cannabis ; Cocaine ; Drugs of abuse ; Ecstasy ; Methamphetamine ; Sewage6. Clean waterEuropeSubstance Abuse DetectionSubstance abusePsychiatry and Mental healthWastewaterPopulation SurveillanceDrug Abuse And AlcoholismEnvironmental Monitoringdrugs of abuseDrugs of abusemedicine.medical_specialtySubstance-Related DisordersN-Methyl-34-methylenedioxyamphetaminecocaineEnvironmental healthHumanssewageIllicit drugPsychiatryecstasyCannabisCannabinoidsIllicit Drugsbusiness.industryAmphetaminesResearch ReportsEuropean populationmedicine.diseasebiology.organism_classificationMetropolitan areaAmphetamineHuman medicineCannabisbusinessWater Pollutants ChemicalChromatography Liquid
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Optimization of Polymer Blue-Light-Emitting Devices by Introducing a Hole-Injection Layer Doped with the Molecular Nanomagnet [Mn12O12(H2O)4(C6F5COO)…

2006

chemistry.chemical_classificationMaterials scienceMolecular magnetsbusiness.industryMechanical EngineeringDopingHole injection layerPolymerNanomagnetElectron transport chainchemistry.chemical_compoundchemistryMechanics of MaterialsOptoelectronicsGeneral Materials SciencebusinessPoly(34-ethylenedioxythiophene)Blue lightAdvanced Materials
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Differential effects of MDMA and cocaine on inhibitory avoidance and object recognition tests in rodents.

2017

Introduction Drug addiction continues being a major public problem faced by modern societies with different social, health and legal consequences for the consumers. Consumption of psychostimulants, like cocaine or MDMA (known as ecstasy) are highly prevalent and cognitive and memory impairments have been related with the abuse of these drugs. Aim The aim of this work was to review the most important data of the literature in the last 10 years about the effects of cocaine and MDMA on inhibitory avoidance and object recognition tests in rodents. Development: The object recognition and the inhibitory avoidance tests are popular procedures used to assess different types of memory. We compare th…

medicine.medical_specialtyMDMACognitive Neurosciencemedia_common.quotation_subjectN-Methyl-34-methylenedioxyamphetamineEcstasyInvestigación médicaEnsayos clínicosExperimental and Cognitive PsychologyRodentiaPublic problemInhibitory postsynaptic potential03 medical and health sciencesBehavioral Neuroscience0302 clinical medicineCocaineDopamine Uptake Inhibitorsmental disordersmedicineAvoidance LearningAnimalsDrogasPsychiatrymedia_commonMemory DisordersAdrenergic Uptake InhibitorsBehavior AnimalAddictionMDMACognitionRecognition PsychologyInhibitory avoidanceAbstinenceDifferential effects030227 psychiatryEfectos fisiológicosPsychologyEstupefaciente030217 neurology & neurosurgerymedicine.drugNeurobiology of learning and memory
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