Search results for "lcsh:QD241-441"

showing 10 items of 438 documents

A Stereocontrolled Protocol to Highly Functionalized Fluorinated Scaffolds through a Fluoride Opening of Oxiranes

2016

A novel selective and substrate-dependent synthetic protocol has been developed towards the synthesis of various fluorine-containing, highly functionalized cycloalkane derivatives. The method involves the stereoselective epoxidation of some unsaturated cyclic beta-amino acid derivatives as model compounds, followed by a regioselective fluoride opening of oxiranes under various conditions with Deoxofluor and XtalFluor-E reagents, thereby offering an insight into this new epoxide opening methodology with fluoride.

Hydrocarbons FluorinatedPharmaceutical ScienceEpoxideAlkenesstereoselectivity010402 general chemistry01 natural sciencesArticleAnalytical Chemistrylcsh:QD241-441Fluorideschemistry.chemical_compoundlcsh:Organic chemistryDrug DiscoveryOrganic chemistryPhysical and Theoretical Chemistryamino acidsSulfur Compoundsoxirane; fluorination; amino acids; stereoselectivity; regioselectivity010405 organic chemistryOrganic ChemistryRegioselectivityStereoisomerismfluorination0104 chemical sciencesCycloalkanechemistryChemistry (miscellaneous)oxiraneregioselectivityReagentEpoxy CompoundsMolecular MedicineStereoselectivityFluorideMolecules
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Conformational equilibrium in supramolecular chemistry: Dibutyltriuret case

2015

The association of substituted benzoates and naphthyridine dianions was used to study the complexation of dibutyltriuret. The title molecule is the simplest molecule able to form two intramolecular hydrogen bonds. The naphthyridine salt was used to break two intramolecular hydrogen bonds at a time while with the use of substituted benzoates the systematic approach to study association was achieved. Both, titrations and variable temperature measurements shed the light on the importance of conformational equilibrium and its influence on association in solution. Moreover, the associates were observed by mass spectrometry. The DFT-based computations for complexes and single bond rotational barr…

HydrogenScienceSupramolecular chemistrychemistry.chemical_elementFull Research Papersupramolecular chemistrylcsh:QD241-441QD241-441lcsh:Organic chemistryComputational chemistrysupramolekulaarinen kemiaSingle bondOrganic chemistryMoleculelcsh:Scienceta116ChemistryHydrogen bondQOrganic Chemistryassociationhydrogen bondingNMRBenzoatesChemistryIntramolecular forcelcsh:QrotamerismTitrationBeilstein Journal of Organic Chemistry
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Factors Affecting Polyphenol Biosynthesis in Wild and Field Grown St. John’s Wort (Hypericum perforatum L. Hypericaceae/Guttiferae)

2009

The increasing diffusion of herbal products is posing new questions: why are products so often different in their composition and efficacy? Which approach is more suitable to increase the biochemical productivity of medicinal plants with large-scale, low-cost solutions? Can the phytochemical profile of a medicinal plant be modulated in order to increase the accumulation of its most valuable constituents? Will polyphenol-rich medicinal crops ever be traded as commodities? Providing a proactive answer to such questions is an extremely hard task, due to the large number of variables involved: intraspecific chemodiversity, plant breeding, ontogenetic stage, post-harvest handling, biotic and abi…

HypericinsPharmaceutical ScienceReviewBiologyHypericaceaeAnalytical Chemistrylcsh:QD241-441Secondary metabolism optimizationlcsh:Organic chemistryPhenolsDrug DiscoveryHypericum perforatumHumansBiomassPlant breedingPhysical and Theoretical ChemistryMedicinal plantsProductivityHypericum perforatum; Hypericins; Polyphenols; Flavonoids; Secondary metabolism optimizationFlavonoidsAbiotic componentGood agricultural practicePlants MedicinalMolecular StructurePlant Extractsbusiness.industryOrganic ChemistryGenetic VariationPolyphenolsHypericum perforatumAgriculturebiology.organism_classificationBiotechnologyChemistry (miscellaneous)PolyphenolMolecular MedicineSeasonsbusinessHypericumMolecules
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In situ formation of steroidal supramolecular gels designed for drug release

2013

In this work, a steroidal gelator containing an imine bond was synthesized, and its gelation behavior as well as a sensitivity of its gels towards acids was investigated. It was shown that the gels were acid-responsive, and that the gelator molecules could be prepared either by a conventional synthesis or directly in situ during the gel forming process. The gels prepared by both methods were studied and it was found that they had very similar macroand microscopic properties. Furthermore, the possibility to use the gels as carriers for aromatic drugs such as 5-chloro-8-hydroxyquinoline, pyrazinecarboxamide, and antipyrine was investigated and the prepared two-component gels were studied with…

In situMagnetic Resonance SpectroscopykolesteroliImineSupramolecular chemistryPharmaceutical ScienceArticleChloroquinolinolsAnalytical ChemistryDelayed-Action Preparationslcsh:QD241-441chemistry.chemical_compoundgeeliDrug Delivery Systemslcsh:Organic chemistryDrug DiscoveryPolymer chemistryMoleculeddc:530Physical and Theoretical Chemistryta116drug releaseOrganic ChemistryorganogelcholesterolNuclear magnetic resonance spectroscopyacid-responsiveHydrogen-Ion ConcentrationchemistryChemistry (miscellaneous)in situ gelationDelayed-Action PreparationsDrug deliveryDrug releaseMolecular Medicineorganogel; acid-responsive; cholesterol; <i>in situ</i> gelation; drug releaseGels
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Synthesis and biological evaluation of new indazole derivatives

2010

New N-methyl and N-ethyl substitutions in the indazole nucleus are reported by reacting 3-(2-aminobenzamido)indazole and the appropriate trimethyl/triethyl orthobenzoate. Single crystal X-ray analysis confirms the N-ethylation position for the 3-(1-ethyl-1H-indazol-3-yl)-2-phenylquinazolin-4(3H)-one derivative 3f. Compounds 11a-d and 3a-d were tested to evaluate their antimicrobial, their antiproliferative activity and their COX inhibitory activities showing scarce or moderately antiproliferative activity and some inhibitory activity against COX-1 and COX-2.

IndazoleStereochemistryOrganic Chemistrybiological activityBiological activityAntimicrobialSettore CHIM/08 - Chimica Farmaceuticalcsh:QD241-441chemistry.chemical_compoundN-methyl/N-ethyl alkylationlcsh:Organic chemistry4(3H)-quinazolinonechemistryindazolecrystallographyBiological evaluationArkivoc
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A Facile Synthesis of Deaza-Analogues of the Bisindole Marine Alkaloid Topsentin

2013

A series of substituted ethyl 1-[(tert-butoxycarbonyl)amino]-2-methyl-5- (1-methyl-1H-indol-3-yl)-4-[(1-methyl-1H-indol-3-yl)carbonyl]-1H-pyrrole-3-carboxylates were prepared in excellent yields (82-98%) by one-pot reactions between β-dicarbonyl compounds 12a-e and 1,2-diaza-1,3-diene (DD) 13. Derivatives 10a,c-e, deazaanalogues of the bis-indole alkaloid topsentin, screened by the National Cancer Institute (Bethesda, MD, USA) in the in vitro one dose primary anticancer assay against a panel of about 60 human tumor cell lines, showed no significant activity, with the exception of compound 9e, which showed moderate activity against the HOP-92 cell line of the non small cell lung cancer sub-p…

IndolesStereochemistryPharmaceutical ScienceAntineoplastic AgentsModerate activityArticleAnalytical Chemistrylcsh:QD241-441Alkaloidslcsh:Organic chemistrytopsentin; bis-indole alkaloids; antitumor activity; ethyl 1-[(<i>tert</i>-butoxycarbonyl)amino]-2-methyl-5-(1-methyl-1<i>H</i>-indol-3-yl)-4-[(1-methyl-1<i>H</i>-indol-3-yl)-carbonyl]-1<i>H</i>-pyrrole-3-carboxylatesCell Line Tumortopsentin; bis-indole alkaloids; antitumor activity; ethyl 1-[(tertbutoxycarbonyl) amino]-2-methyl-5-(1-methyl-1H-indol-3-yl)-4-[(1-methyl-1H-indol-3-yl)- carbonyl]-1H-pyrrole-3-carboxylatesDrug DiscoverymedicineHumansantitumor activityethyl 1-[(tert-butoxycarbonyl)amino]-2-methyl-5-(1-methyl-1H-indol-3-yl)-4-[(1-methyl-1H-indol-3-yl)-carbonyl]-1H-pyrrole-3-carboxylatesPhysical and Theoretical ChemistryAntitumor activityethyl 1-[(tertbutoxycarbonyl) amino]-2-methyl-5-(1-methyl-1H-indol-3-yl)-4-[(1-methyl-1H-indol-3-yl)- carbonyl]-1H-pyrrole-3-carboxylatesChemistryAlkaloidOrganic ChemistryImidazolesCancermedicine.diseaseSettore CHIM/08 - Chimica FarmaceuticaIn vitroHuman tumorbis-indole alkaloidsChemistry (miscellaneous)Cell culturebis-indole alkaloidMolecular MedicineNon small cellDrug Screening Assays AntitumortopsentinMolecules; Volume 18; Issue 3; Pages: 2518-2527
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Headspace Volatile Composition of the Flowers of Caralluma europaea N.E.Br. (Apocynaceae)

2009

The volatile constituents of the flowers of Caralluma (Apteranthes) europaea (Guss.) N.E. Br. (Apocynaceae - Asclepiadoideae) from Lampedusa Island were analyzed by headspace method. The analyses allowed the identification and quantification of 41 compounds. The main components were, among the monoterpenoids, terpinolene (23.3%), a-terpinene (19.1%) and linalool (18.4%), whereas, among the carbonylic compounds the major constituents were heptanal (2.0%), octanoic acid (2.4%) and hexanoic acid (1.7%). It is worth to mention the presence of a nitrogen containing compound, indole (0.8%) and of a sulphur containing compound, dimethylsulphide (t). The compounds found in the flowers of C. europea…

IndolespollinationPharmaceutical ScienceHymenopteraAnalytical Chemistrychemistry.chemical_compoundLinaloolDrug Discovery<em>Caralluma europaea</em>; <em>Apteranthes europaea</em>; Diptera; pollination; sapromyiophily; volatilesHexanoic acidchemistry.chemical_classificationApocynaceaevolatilesChemistry (miscellaneous)Molecular MedicineComposition (visual arts)CaprylatesSettore BIO/07 - EcologiaChromatography GasAcyclic MonoterpenesCyclohexane MonoterpenesFlowersBiologySulfidesArticleSettore CHIM/12 - Chimica Dell'Ambiente E Dei Beni CulturaliLepidoptera genitalialcsh:QD241-441lcsh:Organic chemistryBotanyOrganic matterPhysical and Theoretical ChemistryCaproatesCaralluma europaea; Apteranthes europaea; Diptera; pollination; sapromyiophily; volatilesAldehydesVolatile Organic CompoundsPlant ExtractsTerpenesDipteraOrganic ChemistrySettore CHIM/06 - Chimica Organicabiology.organism_classificationApocynaceaechemistryOdorsapromyiophilyCaralluma europaeaSettore BIO/03 - Botanica Ambientale E ApplicataMonoterpenesApteranthes europaea
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Radical addition to iminium ions and cationic heterocycles

2014

Carbon-centered radicals represent highly useful reactive intermediates in organic synthesis. Their nucleophilic character is reflected by fast additions to electron deficient C=X double bonds as present in iminium ions or cationic heterocycles. This review covers diverse reactions of preformed or in situ-generated cationic substrates with various types of C-radicals, including alkyl, alkoxyalkyl, trifluoromethyl, aryl, acyl, carbamoyl, and alkoxycarbonyl species. Despite its high reactivity, the strong interaction of the radical’s SOMO with the LUMO of the cation frequently results in a high regioselectivity. Intra- and intermolecular processes such as the Minisci reaction, the Porta react…

Ionsheterocycles540 Chemistry and allied sciencesMinisci reactionphotoredox catalysisPorta reactionReviewradicalsCarbonCatalysislcsh:QD241-441transition metal catalysisModels Chemicaladdition reactionslcsh:Organic chemistryHeterocyclic CompoundsCations540 Chemieiminium saltsrearrangementslate-stage functionalization
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Bioadhesive Matrix Tablets Loaded with Lipophilic Nanoparticles as Vehicles for Drugs for Periodontitis Treatment: Development and Characterization

2019

Periodontitis treatment is usually focused on the reduction or eradication of periodontal pathogens using antibiotics against anaerobic bacteria, such as metronidazole (MTR). Moreover, recently the correlation between periodontal diseases and overexpression of reactive oxygen species (ROS) led to the introduction of antioxidant biomolecules in therapy. In this work, bioadhesive buccal tablets, consisting of a hydrophilic matrix loaded with metronidazole and lipophilic nanoparticles as a vehicle of curcumin, were developed. Curcumin (CUR)-loaded nanostructured lipid carriers (NLC) were prepared using glycyrrhetic acid, hexadecanol, isopropyl palmitate and Tween&reg

Isopropyl palmitateoral mucosal drug deliveryPolymers and PlasticsBioadhesiveSonicationbuccal matrix tabletsnanostructured lipid carriersbuccal matrix tablet02 engineering and technologynanostructured lipid carrier030226 pharmacology & pharmacyhydrophilic spongeArticlelcsh:QD241-44103 medical and health scienceschemistry.chemical_compound0302 clinical medicinemetronidazolelcsh:Organic chemistryPulmonary surfactantMucoadhesioncurcuminoral diseaseperiodontitisChromatographyChemistryGeneral ChemistryBuccal administrationPermeation021001 nanoscience & nanotechnologySettore CHIM/09 - Farmaceutico Tecnologico ApplicativoNLCAnaerobic bacteria0210 nano-technologybuccal delivery
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Biomimetic Alginate/Gelatin Cross-Linked Hydrogels Supplemented with Polyphosphate for Wound Healing Applications

2020

In the present study, the fabrication of a biomimetic wound dressing that mimics the extracellular matrix, consisting of a hydrogel matrix composed of non-oxidized and periodate-oxidized marine alginate, was prepared to which gelatin was bound via Schiff base formation. Into this alginate/oxidized-alginate-gelatin hydrogel, polyP was stably but reversibly integrated by ionic cross-linking with Zn2+ ions. Thereby, a soft hybrid material is obtained, consisting of a more rigid alginate scaffold and porous structures formed by the oxidized-alginate-gelatin hydrogel with ionically cross-linked polyP. Two forms of the Zn-polyP-containing matrices were obtained based on the property of polyP to f…

Keratinocyteszinc ionscell migrationMetal NanoparticlesPharmaceutical ScienceBiocompatible Materials02 engineering and technologyGelatinAnalytical ChemistryExtracellular matrixchemistry.chemical_compoundBiomimeticsCell MovementPolyphosphatesSpectroscopy Fourier Transform InfraredDrug DiscoveryalginateSkinchemistry.chemical_classificationcoacervate0303 health sciencesCoacervateTissue ScaffoldsHydrogelsPolymerHydrogen-Ion Concentration021001 nanoscience & nanotechnologyExtracellular MatrixZincChemistry (miscellaneous)Self-healing hydrogelsMolecular Medicine0210 nano-technologyHybrid materialPorosityinorganic polyphosphatefood.ingredientionic cross-linkingAlginatesCell Survivalperiodate oxidationArticlegelatinlcsh:QD241-44103 medical and health sciencesfoodlcsh:Organic chemistryHumansPhysical and Theoretical Chemistry030304 developmental biologyIonsWound HealingTissue EngineeringPolyphosphateOrganic Chemistryhuman epidermal keratinocytestechnology industry and agricultureChemical engineeringchemistrynanoparticlesEpidermisWound healingMolecules
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