Search results for "Anthracenes"

showing 10 items of 36 documents

Arbuscular mycorrhizal fungi altered the hypericin, pseudohypericin, and hyperforin content in flowers of Hypericum perforatum grown under contrastin…

2016

St. John's Wort (Hypericum perforatum) is a perennial herb able to produce water-soluble active ingredients (a.i.), mostly in flowers, with a wide range of medicinal and biotechnological uses. However, information about the ability of arbuscular mycorrhizal fungi (AMF) to affect its biomass accumulation, flower production, and concentration of a.i. under contrasting nutrient availability is still scarce. In the present experiment, we evaluated the role of AMF on growth, flower production, and concentration of bioactive secondary metabolites (hypericin, pseudohypericin, and hyperforin) of H. perforatum under contrasting P availability. AMF stimulated the production of aboveground biomass und…

0106 biological sciencesBiomassPlant Science01 natural scienceschemistry.chemical_compoundNutrientGuttiferae sensu lato; Hypericaceae; Naphthodianthrones; Phenols; Phloroglucinols; St. John’s Wort; Flowers; Hypericum; Mycorrhizae; Perylene; Phloroglucinol; Phosphorus; Plant Extracts; TerpenesMycorrhizaeGuttiferae sensu latoPerylenemedia_commonAnthracenesbiologyNaphthodianthronefood and beveragesHypericum perforatumPhosphorus04 agricultural and veterinary sciencesGeneral MedicineHypericinSettore AGR/02 - Agronomia E Coltivazioni ErbaceeHypericumHypericummedicine.drugmedia_common.quotation_subjectFlowersSecondary metabolitePhloroglucinolCompetition (biology)GeneticPhenolsBotanyGeneticsmedicinePhloroglucinolsGuttiferae sensu lato; Hypericaceae; Naphthodianthrones; Phenols; Phloroglucinols; St. John’s Wort; Ecology Evolution Behavior and Systematics; Molecular Biology; Genetics; Plant ScienceMolecular BiologyEcology Evolution Behavior and SystematicsPhenolPlant ExtractsTerpenesfungiHypericaceaebiology.organism_classificationEcology Evolution Behavior and SystematicHyperforinchemistry040103 agronomy & agriculture0401 agriculture forestry and fisheriesNaphthodianthronesSt. John’s Wort010606 plant biology & botany
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A longitudinal DTI and histological study of the spinal cord reveals early pathological alterations in G93A-SOD1 mouse model of amyotrophic lateral s…

2017

Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disease characterized by selective motor neuron degeneration in the motor cortex, brainstem and spinal cord. It is generally accepted that ALS is caused by death of motor neurons, however the exact temporal cascade of degenerative processes is not yet completely known. To identify the early pathological changes in spinal cord of G93A-SOD1 AIS mice we performed a comprehensive longitudinal analysis employing diffusion-tensor magnetic resonance imaging alongside histology and electron microscopy, in parallel with peripheral nerve histology. We showed the gradient of degeneration appearance in spinal cord white and gray matter, startin…

0301 basic medicinePathologyNeurologyTime FactorsMotor neuron diseasesSensory Receptor CellMice0302 clinical medicineImage Processing Computer-AssistedAxonAmyotrophic lateral sclerosisGray MatterAnthracenesWhite MatterMitochondriamedicine.anatomical_structureDiffusion Tensor ImagingNeurologySpinal CordG93A-SOD1 miceBrainstemHumanMotor cortexmedicine.medical_specialtyAxon degenerationTime FactorSensory Receptor CellsSOD1Mice TransgenicWhite matter03 medical and health sciencesMagnetic resonance imagingDevelopmental NeuroscienceMicroscopy Electron TransmissionmedicineElectron microscopyAnimalsHumansMotor neuron diseaseAmyotrophic lateral sclerosiAnimalbusiness.industrySuperoxide DismutaseAmyotrophic Lateral SclerosisSpinal cordmedicine.diseaseAmyotrophic lateral sclerosisMice Inbred C57BLDisease Models Animal030104 developmental biologyAnthracenebusinessNeuroscience030217 neurology & neurosurgeryExperimental neurology
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Variability of Hypericins and Hyperforin in Hypericum Species from the Sicilian Flora

2019

Within Sicilian flora, the genus Hypericum (Guttiferae) includes 10 native species, the most popular of which is H. perforatum. Hypericum's most investigated active compounds belong to naphtodianthrones (hypericin, pseudohypericin) and phloroglucinols (hyperforin, adhyperforin), and the commercial value of the drug is graded according to its total hypericin content. Ethnobotanical sources attribute the therapeutic properties recognized for H. perforatum, also to other Hypericum species. However, their smaller distribution inside the territory suggests that an industrial use of such species, when collected from the wild, would result in an unacceptable depletion of their natural stands. This…

AdhyperforinFloraBioengineeringIntroduced speciesPhloroglucinol01 natural sciencesBiochemistrychemistry.chemical_compoundSpecies SpecificityBotanyMolecular BiologyPeryleneSicilyAnthracenesCultivated plant taxonomybiology010405 organic chemistryTerpenesGeneral ChemistryGeneral Medicinebiology.organism_classification0104 chemical sciencesHypericinSettore AGR/02 - Agronomia E Coltivazioni Erbacee010404 medicinal & biomolecular chemistryHyperforinchemistryPhytochemicalMolecular MedicineHypericumHypericum
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Influence of St John's wort on catecholamine turnover and cardiovascular regulation in humans

2004

BACKGROUND: St John's wort (Hypericum perforatum) is a popular over-the-counter antidepressant. Its antidepressive effect has been attributed in part to inhibition of monoamine transporters and monoamine oxidase, on the basis of in vitro studies. METHODS: In a double-blind, randomized, placebo-controlled, crossover study, 16 healthy subjects (11 men and 5 women; mean age, 31 +/- 5 years) ingested either St John's wort (300 mg three times daily) or placebo for 7 days. Imipramine treatment (50 mg three times daily) in 7 subjects served as a positive control. After treatment, physiologic and biochemical tests included cardiovascular reflex testing, graded head-up tilt testing, and plasma catec…

AdultMaleNitroprussideImipraminemedicine.medical_specialtyPosturePharmacologyAutonomic Nervous SystemPlaceboMethoxyhydroxyphenylglycolNorepinephrine uptakeCardiovascular Physiological PhenomenaNorepinephrineCatecholaminesDouble-Blind MethodInternal medicineHeart rateSupine PositionmedicineHumansNitric Oxide DonorsPharmacology (medical)PeryleneAnthracenesPharmacologyCross-Over StudiesAdrenergic Uptake Inhibitorsbusiness.industryHemodynamicsHypericum perforatumEndocrinologyBlood pressureMonoamine neurotransmitterCatecholamine34-Dihydroxyphenylacetic AcidAntidepressantFemalebusinessHypericummedicine.drugClinical Pharmacology & Therapeutics
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Electronic Interactions in a New π-Extended Tetrathiafulvalene Dimer

2006

The first pi-extended tetrathiafulvalene (exTTF) dimer in which the two exTTF units are covalently connected by 1,3-dithiole rings has been obtained in a multistep synthetic procedure involving the Ullmann cross-coupling reaction by using copper(I) thiophene-2-carboxylate (CuTC). The electronic spectrum reveals a significant electronic interaction between the exTTF units. The electrochemical study carried out by cyclic voltammetry in solution and in thin-layer conditions, and the electrochemical simulation and spectroelectrochemical (SEC) measurements confirm the electronic communication and show that the oxidation of dimer 14 occurs as two consecutive 2 e(-) processes D(0)-D(0)-->D(2+)-D(0…

AnthracenesAnthraceneDimerOrganic Chemistrychemistry.chemical_elementStereoisomerism[CHIM.MATE]Chemical Sciences/Material chemistryGeneral ChemistryPhotochemistryElectrochemistryCopperCatalysisDelocalized electronchemistry.chemical_compoundCrystallographyModels ChemicalchemistryHeterocyclic CompoundsCovalent bondElectrochemistryElectronicsCyclic voltammetryDimerizationOxidation-ReductionTetrathiafulvaleneChemistry - A European Journal
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Dendron to central core S1-S1 and S2-S(n) (n1) energy transfers in artificial special pairs containing dendrimers with limited numbers of conformatio…

2013

Two dendrimers consisting of a cofacial free-base bisporphyrin held by a biphenylene spacer and function- alized with 4-benzeneoxomethane (5-(4-benzene)tri-10,15,20-(4-n-octyl- benzene)zinc(II)porphyrin) using either five or six of the six available meso-positions, have been synthesized and characterized as models for the an- tenna effect in Photosystems I and II. The presence of the short linkers, -CH2O-, and long C8H17 soluble side chains substantially reduces the number of conformers (foldamers) compared with classic dendrimers built with longer flexible chains. This simpli- fication assists in their spectroscopic and photophysical analysis, notably with respect to fluorescence resonance…

AnthracenesDendrimersMolecular StructureStereochemistryMetalloporphyrinsOrganic ChemistryGeneral ChemistryBiphenylenePorphyrinFluorescenceAcceptorCatalysischemistry.chemical_compoundCrystallographyFörster resonance energy transferchemistryEnergy TransferModels ChemicalDendrimerSinglet stateConformational isomerismChemistry (Weinheim an der Bergstrasse, Germany)
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Allergic contact dermatitis from anthrarobin.

1995

AnthracenesMaleAllergymedicine.medical_specialtyBalsam of PeruEmollientsbusiness.industryPlant ExtractsAnthrarobinCross sensitivityDermatologyMiddle Agedmedicine.diseaseDermatologyStyraxImmunopathologyDermatitis Allergic ContactmedicineBENZOIN TINCTUREImmunology and AllergyHumansDermatologic AgentsbusinessContact dermatitisAllergic contact dermatitisContact dermatitis
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Intramolecular electronic excitation energy transfer in donor∕acceptor dyads studied by time and frequency resolved single molecule spectroscopy

2008

Electronic excitation energy transfer has been studied by single molecule spectroscopy in donor/acceptor dyads composed of a perylenediimide donor and a terrylenediimide acceptor linked by oligo(phenylene) bridges of two different lengths. For the shorter bridge (three phenylene units) energy is transferred almost quantitatively from the donor to the acceptor, while for the longer bridge (seven phenylene units) energy transfer is less efficient as indicated by the occurrence of donor and acceptor emission. To determine energy transfer rates and efficiencies at the single molecule level, several methods have been employed. These comprise time-correlated single photon counting techniques at r…

AnthracenesTime FactorsLightMolecular StructurePhotochemistryChemistryTemperatureGeneral Physics and AstronomyElectronsP680ElectronImidesAcceptorMolecular electronic transitionSpectrometry FluorescenceEnergy TransferPhenyleneIntramolecular forceExcited statePolycyclic Aromatic HydrocarbonsPhysical and Theoretical ChemistryAtomic physicsPeryleneExcitationThe Journal of Chemical Physics
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Mucoadhesive Polymeric Films to Enhance Barbaloin Penetration Into Buccal Mucosa: a Novel Approach to Chemoprevention.

2018

Nowadays, chemoprevention by administering natural supplements is considered an attractive strategy to reverse, suppress, or prevent the evolution of premalignant oral lesions. In particular, Barbaloin exhibits anti-proliferative, anti-inflammatory, and anti-cancer properties, and it results useful in multi-therapy with classic chemotherapeutics. Therefore, in this work, mucoadhesive buccal films, as locoregional drug delivery system able to provide a targeted and efficient therapeutic delivery of Barbaloin, are proposed. Thus, Aloin extract-loaded Eudragit (R) RL100 or Eudragit (R) RS100-based buccal films were designed in order to obtain an easily self-administrable formulation capable of…

Barbaloinbuccal filmCell SurvivalPolymersSwineAcrylic ResinsPharmaceutical ScienceAloin02 engineering and technologyAquatic Science030226 pharmacology & pharmacyChemoprevention03 medical and health scienceschemistry.chemical_compound0302 clinical medicineDrug Delivery SystemsAdhesivesDrug DiscoveryMucoadhesionmedicineAnimalsHumansEcology Evolution Behavior and SystematicsCells Culturedchemistry.chemical_classificationAnthracenesEcologyDose-Response Relationship Drugex vivo permeationPlasticizerMouth MucosaAdministration BuccalGeneral MedicinePolymerBuccal administrationPenetration (firestop)021001 nanoscience & nanotechnologyDrug LiberationchemistrySettore CHIM/09 - Farmaceutico Tecnologico ApplicativoDrug deliverySwellingmedicine.symptom0210 nano-technologyAgronomy and Crop SciencemucoadhesionBiomedical engineeringAAPS PharmSciTech
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The in vitro metabolic activation of dibenz[a,h]anthracene, catalyzed by by rat liver microsomes and examined by 32P-postlabelling.

1991

DNA has been incubated in vitro with dibenz[a,h]anthracene (DB[a,H]A) and the related 5,6-diol and 3,4-diol in the presence of 3-methylcholanthrene- or Aroclor 1254-induced rat liver microsomes. After incubation, the DNA was extracted and examined for the presence of aromatic adducts using the nuclease P1 modification of the 32P-postlabelling technique. The maps of PEI-cellulose plates and autoradiography showed that 92% of the radioactivity contained in DB[a,h]A-DNA adduct spots is derived from the related 3,4-diol and that about 50% of the adducts may be formed following the conversion of this diol to the bay-region anti- and syn-3,4-diol 1,2-oxides.

Cancer ResearchAroclorsDNA damageDiolIn Vitro TechniquesAdductchemistry.chemical_compoundpolycyclic compoundsBenz(a)AnthracenesDibenz(ah)anthraceneAnimalsheterocyclic compoundsCarcinogenBiotransformationAnthraceneChromatographyintegumentary systemorganic chemicalsRatsOncologychemistryBiochemistryMethylcholanthreneMicrosomeMicrosomes LiverEpoxy CompoundsDNA DamageMethylcholanthreneCancer letters
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