Search results for "Enone"

showing 10 items of 320 documents

A putative social chemosignal elicits faster cortical responses than perceptually similar odorants.

2006

Social chemosignals, so-called pheromones, have recently attracted much attention in that effects on women's psychophysiology and cortical processing have been reported. We here tested the hypothesis that the human brain would process a putative social chemosignal, the endogenous steroid endrostadienone, faster than other odorants with perceptually matched intensity and hedonic characteristics. Chemosensory event-related potentials (ERP) were recorded in healthy women. ERP analyses indicate that androstadienone was processed significantly faster than the control odorants. Androstadienone elicited shorter latencies for all recorded ERP components but most so for the late positivity. This fin…

Olfactory systemVisual perceptionMotion PerceptionCortical processingPheromoneschemistry.chemical_compound0302 clinical medicineAttentionHydrogen SulfideEvoked PotentialsCerebral Cortex0303 health sciencesBrain MappingAndrostadienoneElectroencephalographyHuman brainOlfactory PathwaysMiddle AgedChemoreceptor CellsSmellmedicine.anatomical_structureNeurologyPattern Recognition VisualSex pheromoneSensory Thresholds[ SCCO.NEUR ] Cognitive science/NeuroscienceAndrogensFemalePsychologyERPpsychological phenomena and processesAdultCognitive NeuroscienceOlfactionAndrosterone03 medical and health sciencesmedicinePsychophysicsReaction TimeHumansSocial Behavior030304 developmental biologyCommunicationDose-Response Relationship Drugbusiness.industry[SCCO.NEUR]Cognitive science/NeuroscienceOlfactionAndrostadienesPsychophysiologychemistrybusinessNeuroscience030217 neurology & neurosurgeryPsychomotor PerformanceNeuroImage
researchProduct

The Interplay of Inverted Redox Potentials and Aromaticity in the Oxidized States of New π-Electron Donors: 9-(1,3-Dithiol-2-ylidene)fluorene and 9-(…

2006

Derivatives of 9-(1,3-dithiol-2-ylidene)fluorene (9) and 9-(1,3-dithiol-2-ylidene)thioxanthene (10) have been synthesised using Horner-Wadsworth-Emmons reactions of (1,3-dithiol-2-yl)phosphonate reagents with fluorenone and thioxanthen-9-one. X-ray crystallography, solution electrochemistry, optical spectroscopy, spectroelectrochemistry and simultaneous electrochemistry and electron paramagnetic resonance (SEEPR), combined with theoretical calculations performed at the B3P86/6-31G** level, elucidate the interplay of the electronic and structural properties in these molecules. These compounds are strong two-electron donors, and the oxidation potentials depend on the electronic structure of t…

Organic ChemistryThioxantheneDithiolAromaticitySulfoxideGeneral ChemistryFluorenePhotochemistryCatalysisDicationchemistry.chemical_compoundchemistryFluorenoneRadical ionChemistry - A European Journal
researchProduct

PPAR-γ Agonist GW1929 But Not Antagonist GW9662 Reduces TBBPA-Induced Neurotoxicity in Primary Neocortical Cells

2013

Tetrabromobisphenol A (2,2-bis(4-hydroxy-3,5-dibromophenyl)propane; TBBPA) is a widely used brominated flame retardant. TBBPA induces neuronal damage, but the mechanism by which this occurs is largely unknown. We studied the possible involvement of peroxisome proliferator-activated receptor gamma (PPAR-γ) in TBBPA-induced apoptosis and toxicity in mouse primary neuronal cell cultures. TBBPA enhanced both, caspase-3 activity and lactate dehydrogenase (LDH) release in neocortical cells after 6 and 24 h of exposition. These data were supported at the cellular level with Hoechst 33342 staining. Immunoblot analyses showed that, compared with control cells, 10 μM TBBPA decreased the expression of…

PPAR-γTime FactorsNeuroscience(all)Polybrominated BiphenylsPeroxisome proliferator-activated receptorGW1929Caspase 3ApoptosisNeocortexPharmacologyBiologyToxicologyNeuroprotectionBenzophenonesMicemedicineNeurotoxicityAnimalsAnilidesReceptorCells Culturedchemistry.chemical_classificationNeuronsDose-Response Relationship DrugL-Lactate DehydrogenaseCaspase 3General NeuroscienceNeurotoxicityApoptotic bodymedicine.diseasePPAR gammaTBBPANeuroprotective AgentschemistryCell cultureApoptosisTyrosineNeurotoxicity SyndromesOriginal ArticleCentral Nervous System AgentsNeurotoxicity Research
researchProduct

Sicilia e Grecia La conservazione dei monumenti alla fine del Settecento

2015

Fin dalla seconda metà del Settecento in Sicilia si inizia a tutelare, e dunque conservare, i monumenti dell’epoca classica della città di Taormina e perfino un gruppo di alberi secolari, chiamati il “castagno dei cento cavalli”. Inoltre, nel 1778, il governo borbonico istituì, per tutti i monumenti antichi della Sicilia, una commissione formata dai “Regi custodi” – sopraintendenti delle antichità, da un architetto esperto di monumenti antichi, da un pittore di vedute e da un capo mastro, per studiare e rilevare lo stato di conservazione dei monumenti stessi. A seguito di queste indagini, nel 1780, furono approntati i primi interventi di restauro nel tempio di Segesta e in alcuni templi di …

Parthenon (Athens) Selinunte (Sicily) T.B. Elgin S. Angell W. Harris Protection Archeological restorationSettore ICAR/19 - RestauroPartenone (Atene) Seminante (Sicilia) T.B. Elgin S. Angell W. Harris tutela restauro archeologico
researchProduct

In vitro cytotoxicity of patulin, deoxynivalenol, nivalenol and zearalenone on CHO-K1 cells

2006

Patulinchemistry.chemical_compoundchemistryIn vitro cytotoxicityGeneral MedicineToxicologyMolecular biologyZearalenoneToxicology Letters
researchProduct

Optically active titanium complexes containing a tridentate linked amido-cyclopentadienyl ligand

2000

Optically active titanium complexes Ti{η5:η1-C5R4SiMe2NC6H10 (OCH2Ph)-2}Cl2 (R = H, Me), containing a cyclopentadienyl ligand linked to the chiral trans-2-benzyloxycyclohexylamido group, were synthesized and characterized in both enantiomerically pure forms. A single crystal X-ray structure analysis of (−)-(R,R)-Ti{η5:η1-C5H4SiMe2NC6H10(OCH2Ph)-2}Cl2 shows a structure in which the benzyloxy group in the amido sidechain is not interacting with the titanium center. Upon activation with n-butyllithium, these complexes hydrogenate acetophenone N-benzylimine with low enantioselectivity. Chirality 12:472–475, 2000. © 2000 Wiley-Liss, Inc.

PharmacologyLigandOrganic ChemistryCenter (category theory)chemistry.chemical_elementOptically activeCatalysisAnalytical Chemistrychemistry.chemical_compoundCrystallographychemistryCyclopentadienyl complexDrug DiscoveryOrganic chemistryChirality (chemistry)Single crystalSpectroscopyAcetophenoneTitaniumChirality
researchProduct

Development of predictive retention-activity models of butyrophenones by biopartitioning micellar chromatography

2001

The predictive and interpretative capability of quantitative chromatographic retention-biological activity models is supported by the fact that in adequate experimental conditions the solute partitioning into the chromatographic system can emulate the solute partitioning into lipid bilayers of biological membranes, which is the basis of drug and metabolite uptake, passive transport across membranes and bioaccumulation. The use of retention data obtained in biopartitioning micellar chromatography (BMC) has been demonstrated to be helpful in describing the biological behaviour of different kinds of drugs. In this chromatographic system, polioxyethylene 23 lauryl ether Brij35 micellar mobile p…

PharmacologyNeuroleptic DrugsChromatographyPassive transportChemistryMetaboliteClinical BiochemistryBiological membraneGeneral MedicineBiochemistryMicelleAnalytical Chemistrychemistry.chemical_compoundMembraneStationary phaseDrug DiscoveryButyrophenonesMolecular BiologyBiomedical Chromatography
researchProduct

Mitochondrial (dys)function - a factor underlying the variability of efavirenz-induced hepatotoxicity?

2015

Background and Purpose The non-nucleoside analogue reverse transcriptase inhibitor efavirenz is associated with hepatic toxicity and metabolic disturbances. Although the mechanisms involved are not clear, recent evidence has pinpointed a specific mitochondrial action of efavirenz accompanied by the induction of an endoplasmic reticulum (ER) stress/unfolded protein response in human hepatic cells. The aim of this study was to further investigate the involvement of this organelle by evaluating efavirenz's effects in cells lacking functional mitochondria (rho°) and comparing them with those of the typical mitotoxic agent rotenone, a standard complex I inhibitor, and the ER stress inducer thaps…

PharmacologyThapsigarginEfavirenzReverse-transcriptase inhibitorEndoplasmic reticulumRotenoneBiologyMitochondrionPharmacologychemistry.chemical_compoundchemistryUnfolded protein responseHepatic stellate cellmedicinemedicine.drugBritish Journal of Pharmacology
researchProduct

Severe Brochostenosis by Oral Propafenone Immediately After Commencing Treatment

2011

Propafenone is a membrane-stabilizing agent belonging to a subgroup of the Vaughan Williams class I antidysrhythmic agents, structurally resembling propranolol and characterized by weaker beta-blocking activity. Despite respiratory complications having been reported as examples of side effects, very few reports have been published in the literature.We describe the case of an elderly woman with a history of hypertension and allergy to Parietaria, grass, olive, mites, and with periodic asthmatic manifestations, for whom the administration of oral propafenone for recurrent supraventricular dysrhythmia was associated with the sudden onset of severe bronchostenosis.A 78-year-old woman was freque…

Pharmacologybusiness.industryGeneral MedicinePropafenonemedicine.diseaseRhonchipropafenone broncostenosisHypoxemiaBronchospasmAnesthesiamedicineSalbutamolPharmacology (medical)Medical historyRespiratory functionSupraventricular tachycardiamedicine.symptombusinessmedicine.drugAmerican Journal of Therapeutics
researchProduct

Antiasthmatic acetophenones - an in vivo study on structure activity relationship.

1994

The recently isolated acetophenone glucoside androsin, as the major antiasthmatic principle of Picrorhiza kurroa Royle ex Benth. (Scrophulariaceae), was used as a lead compound for detailed structure-activity relationship studies. More than 25 synthesized or commercially available acetophenones with modified substitution patterns were screened in the Plethysmographic guinea pig model using PAF and/or ovalbumin as challenging agents for the generation of bronchial constriction. Whereas the aglycones in most cases were more effective than the corresponding glycosides, substitution patterns in position 3 and 4 of the phenyl ring and the keto function attached to the phenyl ring were found to b…

Pharmacologychemistry.chemical_classificationStereochemistryPicrorhiza kurroaPharmaceutical ScienceGlycosideIn vitrochemistry.chemical_compoundComplementary and alternative medicinechemistryGlucosideIn vivoDrug DiscoveryMolecular MedicineStructure–activity relationshipLead compoundAcetophenonePhytomedicine : international journal of phytotherapy and phytopharmacology
researchProduct