Search results for "Farmaceutica"

showing 10 items of 582 documents

Pyrido[4′,3′:4,5]pyrrolo[2,1-d][1,2,3,5]tetrazines, a new class of Temozolomide heteroanalogues

2009

A series of derivatives of new ring system pyrido[4’,3’:4,5]pyrrolo[2,1-d] [1,2,3,5]tetrazine was obtained from moderate to excellent yields by reaction of 2-diazo-3-ethoxycarbonyl-pyrrolo[2,3- c]pyridine with alkyl- or aryl-isocyanates in dichlorometane at room temperature or at 50 °C under microwave irradiation.

Temozolomide heteroanaloguesOrganic ChemistrySettore CHIM/08 - Chimica FarmaceuticaArkivoc
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Comparative studies of the Pschorr reaction in the pyrazole series. Access to the new dibenzo[e,g]pyrazolo[1,5-a][1,3]diazocine system of pharmaceuti…

2008

The diazonium tetrafluoroborate 11 obtained from 2-amino-N-methyl-N-(1-phenyl-3- methylpyrazol-5-yl)benzamide was transformed in dry acetonitrile via an ionic or radical pathway. Differences were observed with respect to ionic or radical transformations in aqueous media of the analogous diazonium hydrogen sulfate 1 derived from the same amine. In acetonitrile solution, the ionic pathway was characterized by an increased yield of 1,4-dimethyl- 3-phenyl-pyrazolo(3,4-c)isoquinolin-5-one 4 and by the formation of its isomer, the new derivative 7,9-dimethyldibenzo(e,g)pyrazolo(1,5-a)(1,3)diazocin-10(9H)-one 12. When the reaction followed a radical pathway, the pyrazolo(3,4-c)isoquinoline derivat…

Tetrafluoroborate1Ionic bonding4-pyrazolyl transferPyrazoleMedicinal chemistrylcsh:QD241-441chemistry.chemical_compoundlcsh:Organic chemistryPyrazolo[3Organic chemistry4-c]isoquinolineIsoquinolineAcetonitrileBenzamidePyrazolodibenzodiazocinePschorr reactionpyrazolo(34-c)isoquinolinepyrazolodibenzodiazocine14-pyrazolyl transfer X-ray structure14-pyrazolyl transfer; Pschorr reaction; Pyrazolodibenzodiazocine; Pyrazolo[34-c]isoquinoline; X-ray structureOrganic ChemistryPschorr reactionSettore CHIM/08 - Chimica FarmaceuticachemistryPschor reaction pyrazolo[34-c]isoquinoline pyrazolodibenzodiazocine 14- pyrazolyl transfer X-ray structureAmine gas treatingX-ray structureDerivative (chemistry)
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Sintesi di un isostero del 3,5-dimetil-6-fenil-8-(trifluorometil)-5,6-diidropirazolo[3,4-f][1,2,3,5]tetrazepin-4(3H)-one (CF3-TZP) con potenziale att…

2018

In un precedente lavoro abbiamo mostrato i risultati relativi alla sintesi ed all’attività biologica del CF3-TZP 1[1] (Figura 1). Le attività antiproliferativa e apoptotica del composto 1 sono state testate su differenti linee cellulari, HL60 sensibili, HL60-R (MDR), K562 e K562-R (resistenti al Gleevec®), mostrando un profilo di attività biologica similare sulle cellule sensibili e resistenti nel range di 21-40 µM per l’IC50 e 36-62 µM per l’AC50. L’analisi citofluorimetrica sulle K562 sensibili ha indicato che il composto 1 determina un arresto dose-dipendente del ciclo cellulare in fase G0-G1 nelle prime 24 h di trattamento, mentre nelle successive 24 h si è notato una riduzione del picc…

Tetrazepinoni; attività antiproliferativa; attività apoptotica.attività apoptotica.TetrazepinoniSettore CHIM/08 - Chimica Farmaceuticaattività antiproliferativa
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Essential oil compositions of Teucrium fruticans, T. scordium subsp. scordioides and T. siculum growing in Sicily and Malta

2020

In the present study, the chemical composition of the essential oils from the aerial parts of Teucrium fruticans L. collected in Sicily and Malta, Teucrium scordium subsp. scordioides (Schreb.) Arcang. and Teucrium siculum (Raf.) Guss., collected in Sicily, were evaluated by GC-MS. The main volatile components of both T. fruticans collections were germacrene D (29.4% and 50.0%), (E)-β-caryophyllene (19.6% and 21.9%), and 1-octen-3-ol (19.7% and 7.4%); T. scordium subsp. scordioides essential oil was rich in caryophyllene oxide (25.8%), α-pinene (19.4%) and β-pinene (8.5%); T. siculum essential oil was rich in (E)-β-caryophyllene (30.9%), 1-octen-3-ol (9.0%), α-humulene (8.6%) and germacrene…

Teucrium ssp.Organic ChemistryVolatile componentsSettore CHIM/06 - Chimica OrganicaPlant ScienceBiology1-Octen-3-olbiology.organism_classificationBiochemistryAnalytical Chemistrylaw.inventionChemotaxonomyTeucrium(E)-β-CaryophylleneCaryophyllene oxidelawBotanyTeucrium scordiumSettore BIO/15 - Biologia FarmaceuticaGermacrene DEssential oilGermacrene DNatural Product Research
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1,4-Dimethyl-3-phenyl-3H-pyrazolo[3,4-c]isoquinolin-5(4H)-one

2008

The title compound, C18H15N3O, is the product of the thermal decomposition of the diazonium salt derived from 2-amino-N-methyl-N-(3-methyl-1-phenyl-1H-pyrazol-5-yl)benzamide. It is characterized by a trans orientation of the methyl groups with respect to the tricyclic ring system. The molecule has a nearly planar phenylpyrazolo[3,4-c]isoquinolin-5-one system, the largest deviation from the mean plane being 0.066 (2) angstrom for the O atom. The dihedral angle between the phenyl substituent and the heterotricycle is 67 (1)degrees. The packing is stabilized by C-H center dot center dot center dot N hydrogen-bond interactions, with the formation of molecular chains along the c axis.

Thermal decompositionSubstituentAtom (order theory)General ChemistryDihedral angleCondensed Matter PhysicsRing (chemistry)BioinformaticsOrganic PapersSettore CHIM/08 - Chimica Farmaceuticalcsh:Chemistrychemistry.chemical_compoundCrystallographylcsh:QD1-999chemistrysingle-crystal X-ray studyGeneral Materials ScienceBenzamideActa Crystallographica Section E Structure Reports Online
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Solid state 13C-NMR methodology for the cellulose composition studies of the shells of Prunus dulcis and their derived cellulosic materials.

2020

Lignocellulosic fibers and microcellulose have been obtained by simple alkaline treatment from softwood al- mond shells. In particular, the Prunus dulcis Miller (D.A.) Webb. was considered as a agro industrial waste largely available in southern Italy. The materials before and after purification have been characterized by 13C CPMAS NMR spectroscopy methodology. A proper data analysis provided the relative composition of lignin and holo- cellulose at each purification step and the results were compared with thermogravimetric analysis and FT-IR. To value the possibility of using this material in a circular economy framework, the fibrous cellulosic material was used to manufacture a handmade c…

Thermogravimetric analysisSoftwoodMaterials sciencePolymers and PlasticsAlmond shell Cellulose13C CP MAS NMR02 engineering and technology010402 general chemistry01 natural sciencesLigninIndustrial wastechemistry.chemical_compoundMaterials ChemistrySettore ICAR/13 - Disegno IndustrialeLigninNutsSettore CHIM/01 - Chimica AnaliticaRecyclingFiberSettore BIO/15 - Biologia FarmaceuticaCelluloseCarbon-13 Magnetic Resonance SpectroscopyCelluloseWaste ProductsOrganic Chemistrycardboard021001 nanoscience & nanotechnologyPulp and paper industryPrunus dulcis0104 chemical sciencesHandmade cardboard MicrocelluloseSettore AGR/03 - Arboricoltura Generale E Coltivazioni ArboreePrunus dulcisSettore ING-IND/22 - Scienza E Tecnologia Dei MaterialichemistryCellulosic ethanolvisual_artvisual_art.visual_art_medium0210 nano-technologyCarbohydrate polymers
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Composition of essential oil of lemon thyme (Thymus × citriodorus) at different hydrodistillation times.

2018

Distillation time can both to optimise the production and to engineer the composition of essential oil in essential oil bearing plants. Purpose of this study was to evaluate the effect of duration of hydrodistillation on composition of essential oil of Thymus × citriodorus, the natural source of commercially important geraniol and citral, a component with valuable biological properties. Essential oils were isolated by hydrodistillation at different distillation times and analysed by GC/MS analytical methods. Increase in percentage of essential oil during all hydrodistillation time gradient was uneven. Elongation of hydrodistillation time decreased percentages of monoterpenes but increased p…

Time FactorsAcyclic MonoterpenesPlant ScienceCitral01 natural sciencesBiochemistryessential oilgeranialGas Chromatography-Mass Spectrometrylaw.inventionAnalytical ChemistryThymus Plantchemistry.chemical_compoundlawBiological propertyOils VolatileThymus citriodorusFood scienceSettore BIO/15 - Biologia FarmaceuticageraniolDistillationEssential oilhydrodistillation timeDistillation010405 organic chemistryChemistrynerolTerpenesOrganic ChemistrySettore CHIM/06 - Chimica Organica0104 chemical sciencesThymus × citriodoru010404 medicinal & biomolecular chemistryneralNatural sourceMonoterpenesComposition (visual arts)SesquiterpenesGeraniolNatural product research
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Phytochemical and anti-staphylococcal biofilm assessment of Dracaena draco L. Spp. draco resin

2013

Background: Dracaena draco L. ssp. draco is known as the “dragon's blood tree” and it is endemic from the Canary Islands and Morocco. Objective: Carry out phytochemical investigation of acetonic extracts of red resin obtained from the trunk of D. draco, to obtain to the isolation of the most abundant resin constituents, belonging to the class of flavonoids: flavans, along with homoisoflavans and homoisoflavanones. Materials and Methods: The structures of the isolated compounds were established by Nuclear Magnetic Resonance (NMR) and mass spectrometry data and comparison with literature data. The acetonic extract was evaluated for its anti-staphylococcal properties against two reference stra…

Traditional medicineDracaena draco L.Antibiofilm activity Dracaena draco L. dragon blood resin flavan homoisoflavanBiofilmPharmaceutical SciencehomoisoflavanBiologySettore BIO/19 - Microbiologia Generalebiology.organism_classificationSettore CHIM/08 - Chimica FarmaceuticaDraco (constellation)dragon blood resinchemistry.chemical_compoundPhytochemicalchemistryflavanFlavanAntibiofilm activityDrug DiscoveryBotanyDracaena dracoOriginal ArticlePharmacognosy Magazine
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Sintesi ed Attività Biologica di nuovi derivati Triazenici e Triazinici

2014

Triazine.triazeniSettore CHIM/08 - Chimica Farmaceutica
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STUDIO DELL'INTERAZIONE DI DNA-NATIVO CON Zn(3-ACETIL-1-(2-NITROFENIL)PENTAN-1,4-DIONATO)2

2011

TrichetoneZincoIntercalanteSettore CHIM/03 - Chimica Generale E InorganicaDNASettore CHIM/08 - Chimica Farmaceutica
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