Search results for "lcsh:Organic chemistry"

showing 10 items of 438 documents

Novel Penicillin-Type Analogues Bearing a Variable Substituted 2-Azetidinone Ring at Position 6: Synthesis and Biological Evaluation

2015

The synthesis and the biological activity of novel semi-synthetic β-lactam compounds containing an azetidinone moiety joined to the amino-nitrogen of the (+)-6-aminopenicillanic acid (6-APA) as new antibacterial agents is reported. The synthesized compounds were screened for their in vitro antimicrobial activity against a panel of Gram positive and Gram negative pathogens and environmental bacteria. Tested compounds displayed good antimicrobial activity against all tested Gram positive bacteria and for Staphylococcus aureus and Staphylococcus epidermidis antimicrobial activity resulted higher than that of the reference antibiotic. Additionally, in vitro cytotoxic screening was also carried …

Salmonella typhimuriumCell Survivalmedicine.drug_classStereochemistryStaphylococcusGram-positive bacteriaAntibioticsPenicillanic AcidPharmaceutical ScienceBacillus6-aminopenicillanic acid (6-APA); 2-azetidinone; β-lactam antibiotics; antibacterial; Staudinger reactionMicrobial Sensitivity Testsbeta-Lactamsmedicine.disease_causeArticle6-aminopenicillanic acid (6-APA)Analytical Chemistrylcsh:QD241-441MiceStructure-Activity Relationshiplcsh:Organic chemistryStaphylococcus epidermidisPseudomonasβ-lactam antibioticsDrug DiscoveryEscherichia colimedicineAnimalsPhysical and Theoretical ChemistrybiologyChemistryOrganic ChemistryBiological activitybiology.organism_classificationAntimicrobialAnti-Bacterial AgentsPenicillinantibacterialChemistry (miscellaneous)Staphylococcus aureusNIH 3T3 Cells2-azetidinoneAzetidinesMolecular MedicineStaudinger reactionBacteriamedicine.drugMolecules
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Chemical Composition and in Vitro Antimicrobial and Mutagenic Activities of Seven Lamiaceae Essential Oils

2009

Deeper knowledge of the potentiality of aromatic plants can provide results of economic importance for food and pharmacological industry. The essential oils of seven Lamiaceae species were analyzed by gas chromatography-mass spectrometry and assayed for their antibacterial, antifungal and mutagenic activities. Monoterpenes in the oils ranged between 82.47% (hyssop oil) and 97.48% (thyme oil), being mainly represented by oxygenated compounds. The antibacterial activity was evaluated against six pathogenic and five non-pathogenic bacterial strains. Oregano and thyme oils showed the strongest antibacterial activity against the pathogenic ones. The antifungal activity was evaluated against six …

SalmonellaPharmaceutical ScienceAntimicrobial activitymedicine.disease_causeArticleGas Chromatography-Mass SpectrometryAnalytical Chemistrylcsh:QD241-441Anti-Infective Agentslcsh:Organic chemistryDrug DiscoveryBotanyOils VolatilemedicineFood sciencePhysical and Theoretical ChemistryMedicinal plantsFood PreservativesLamiaceaeBacteriabiologymutagenic activitySAGEOrganic ChemistryFungifood and beveragesLamiaceae; essential oils; antimicrobial activity; mutagenic activityAntimicrobialbiology.organism_classificationEssential oilsChemistry (miscellaneous)Molecular MedicineLamiaceaeAntibacterial activityMutagensFood contaminantMolecules
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Essential Oil Composition of Stems and Fruits of Caralluma europaea N.E.Br. (Apocynaceae)

2010

The essential oil of the stems and fruits of Caralluma europaea (Guss.) N.E.Br. (Apocynaceae) from Lampedusa Island has been obtained by hydrodistillation and its composition analyzed. The analyses allowed the identification and quantification of 74 volatile compounds, of which 16 were aromatic and 58 non-aromatic. Stems and fruits contained 1.4% and 2.7% of aromatic compounds respectively, while non-aromatic were 88.3% and 88.8%. Non-aromatic hydrocarbons were the most abundant compounds in both organs, followed by fatty acids. Data showed differences in the profiles between stems and fruits which shared only eighteen compounds; stems accounted for 38 compounds while fruits for 53. Fruits …

Settore BIO/07 - EcologiaPlant compositionantimicrobial; Apocynaceae; <i>Caralluma europaea</i>; essential oils; semiochemicalsPharmaceutical ScienceArticleessential oilSettore CHIM/12 - Chimica Dell'Ambiente E Dei Beni CulturaliAnalytical Chemistrylaw.inventionlcsh:QD241-441lcsh:Organic chemistrylawDrug DiscoveryBotanyOils VolatileAnimalsPhysical and Theoretical Chemistryessential oilsChemical compositionEssential oilOvumCaralluma europaeaGeographyPlant StemssemiochemicalsApocynaceaebiologyOrganic ChemistrySettore CHIM/06 - Chimica Organicabiology.organism_classificationApocynaceaePlant ecologyChemistry (miscellaneous)FruitLarvaCaralluma europaeaSettore BIO/03 - Botanica Ambientale E ApplicataantimicrobialMolecular MedicineComposition (visual arts)Molecules
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Two-Dimensional Carbon: A Review of Synthesis Methods, and Electronic, Optical, and Vibrational Properties of Single-Layer Graphene

2019

Graphite has been widely used by humans for a large part of their history. Nevertheless, it has only recently been possible to isolate its basic unit: carbon atoms arranged in a honeycomb structure on a single plane, namely graphene. Since its discovery, many techniques have been developed and improved to properly synthesize graphene and its derivatives which are part of the novel class of two-dimensional materials. These advanced materials have imposed themselves in nanotechnology thanks to some outstanding physical properties due to their reduced dimensions. In the case of graphene, its reduced dimension gives rise to a high electrical mobility, a large thermal conductivity, a high mechan…

Solid-state physics2D materialNanotechnology02 engineering and technology010402 general chemistry01 natural sciencesNanomaterialslaw.inventionlcsh:QD241-441symbols.namesakeThermal conductivitylcsh:Organic chemistrylawGraphiteSpectroscopyGraphenecarbongrapheneGeneral Medicine021001 nanoscience & nanotechnologymaterial science0104 chemical sciencesHoneycomb structureRaman spectroscopysymbolsnanomaterial0210 nano-technologyRaman spectroscopy
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Host–guest complexes of conformationally flexible C-hexyl-2-bromoresorcinarene and aromatic N-oxides: solid-state, solution and computational studies

2018

Host–guest complexes of C-hexyl-2-bromoresorcinarene (BrC6) with twelve potential aromatic N-oxide guests were studied using single crystal X-ray diffraction analysis and 1H NMR spectroscopy. In the solid state, of the nine obtained X-ray crystal structures, eight were consistent with the formation of BrC6-N-oxide endo complexes. The lone exception was from the association between 4-phenylpyridine N-oxide and BrC6, in that case the host forms a self-inclusion complex. BrC6, as opposed to more rigid previously studied C-ethyl-2-bromoresorcinarene and C-propyl-2-bromoresorcinarene, undergoes remarkable cavity conformational changes to host different N-oxide guests through C–H···π(host) intera…

Solid-stateCrystal structure010402 general chemistry01 natural scienceslcsh:QD241-441lcsh:Organic chemistryPolarizabilitysupramolekulaarinen kemiaresorcinareneshost–guest chemistryHost–guest chemistrylcsh:Scienceta116Biochemistry Biophysics and Structural BiologyC–H···π Interactions010405 organic chemistryChemistryOrganic Chemistryendo/exo complexationSolution phaseditopic receptors0104 chemical sciencesaromatic N-oxidesChemistryCrystallographyProton NMRPolarlcsh:QSingle crystalBeilstein Journal of Organic Chemistry
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Carbon Nanomaterial Doped Ionic Liquid Gels for the Removal of Pharmaceutically Active Compounds from Water.

2019

Due to large drug consumption, pharmaceutically active compounds (PhACs) can be found as water contaminants. The removal of PhACs is a significant issue, as they can easily overtake traditional purification methods. Because of their surface properties, carbon nanomaterials are among the most efficient materials able to adsorb PhACs. However, their limitation is their recovery after use and their possible leakage into the aquatic system. Consequently, new hybrid supramolecular ionic liquid gels (HILGs) have been designed for the adsorption of some antibiotic drugs (ciprofloxacin and nalidixic acid) from water. The chemical&ndash

SorbentSupramolecular chemistryPharmaceutical ScienceIonic Liquids02 engineering and technologyCarbon nanotube010501 environmental sciences01 natural sciencesWaste Disposal FluidArticleAnalytical Chemistrylaw.inventionWater Purificationlcsh:QD241-441chemistry.chemical_compoundColloidAdsorptionsupramolecular gelRheologylcsh:Organic chemistrylawDrug DiscoveryHumanscarbon nanotubePhysical and Theoretical Chemistryionic liquid0105 earth and related environmental sciencescarbon nanotubesGraphenepollutant adsorptionOrganic Chemistrygraphenesupramolecular gelsWaterSettore CHIM/06 - Chimica Organica021001 nanoscience & nanotechnologyCarbonNanostructureswastewater treatmentBiodegradation EnvironmentalchemistryChemical engineeringChemistry (miscellaneous)Ionic liquidMolecular MedicineAdsorption0210 nano-technologyGelsWater Pollutants ChemicalMolecules (Basel, Switzerland)
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Series of Near-IR-Absorbing Transition Metal Complexes with Redox Active Ligands

2020

New soluble and intensely near-IR-absorbing transition metal (Ti, Zr, V, Ni) complexes were synthesized using a redox non-innocent N,N&rsquo

Spectrometry Mass Electrospray IonizationMagnetic Resonance SpectroscopyElectronsChemistry Techniques SyntheticCrystallography X-RayLigandsArticlelcsh:QD241-441Magneticslcsh:Organic chemistryX-Ray DiffractionCoordination ComplexesNickelTransition Elementsorgaaniset yhdisteetSpectroscopy Near-InfraredMolecular Structureredox-active ligandnon-innocent ligandsElectrochemical Techniquesliganditkompleksiyhdisteetmetal organic complexMetalsElectronicsOxidation-Reduction
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Synthesis, Characterization, and Saccharide Binding Studies of Bile Acid − Porphyrin Conjugates

2007

Synthesis and characterization of bile acid-porphyrin conjugates (BAPs) are reported. Binding of saccharides with BAPs in aqueous methanol was studied by monitoring changes in the visible absorption spectral of the porphyrin-moieties. Although these studies clearly showed absorbance changes, suggesting quite high if non-selective binding, the mass spectral studies do not unambiguously support these results.

Spectrometry Mass Electrospray IonizationMagnetic Resonance SpectroscopyPorphyrinsmedicine.drug_classElectrospray ionizationCarbohydratesPharmaceutical ScienceESI MS.ArticleAnalytical ChemistryAbsorbanceBile Acids and Saltslcsh:QD241-441chemistry.chemical_compoundUltraviolet visible spectroscopylcsh:Organic chemistryHeterocyclic Compoundsvisible spectroscopyDrug Discoverymedicinepolycyclic compoundsOrganic chemistryPhysical and Theoretical ChemistrysaccharideAqueous solutionBile acidMolecular StructureOrganic Chemistry1H-NMRPorphyrinCombinatorial chemistryBile acidschemistryChemistry (miscellaneous)Proton NMRMolecular Medicinesense organsporphyrinConjugateMolecules
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Molecular recognition of N-acetyltryptophan enantiomers by β-cyclodextrin

2017

The enantioselectivity of β-cyclodextrin (β-CD) towards L- and D-N-acetyltryptophan (NAcTrp) has been studied in aqueous solution and the crystalline state. NMR studies in solution show that β-CD forms complexes of very similar but not identical geometry with both L- and D-NAcTrp and exhibits stronger binding with L-NAcTrp. In the crystalline state, only β-CD–L-NAcTrp crystallizes readily from aqueous solutions as a dimeric complex (two hosts enclosing two guest molecules). In contrast, crystals of the complex β-CD–D-NAcTrp were never obtained, although numerous conditions were tried. In aqueous solution, the orientation of the guest in both complexes is different than in the β-CD–L-NAcTrp …

Stereochemistry02 engineering and technology010402 general chemistry01 natural scienceslaw.inventionlcsh:QD241-441CrystalMolecular recognitionlcsh:Organic chemistrylawMoleculeCrystallizationenantiomeric discriminationlcsh:Sciencechemistry.chemical_classificationAqueous solutionCyclodextrinChemistryEstereoquímicaOrganic ChemistryN-acetyltryptophanQuímica021001 nanoscience & nanotechnologyN-acetyltryptophanNMR0104 chemical sciencesCrystallographyβ-cyclodextrinlcsh:QX-ray structureEnantiomer0210 nano-technology
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Syntheses of Four Enantiomers of 2,3-Diendo- and 3-Endo-aminobicyclo[2.2.2]oct-5-ene-2-exo-carboxylic Acid and Their Saturated Analogues

2013

Abstract: Ethyl 2,3- diendo -3-aminobicyclo[2.2.2]oct- 5-ene-2-carboxylate ((±)- 1 ) was resolved with O , O '-dibenzoyltartaric acid via diastere omeric salt formation. The efficient synthesis of the enantiomers of 2,3- diendo -3-aminobicyclo[2.2.2]oct- 5-ene-2-carboxylic acid ((+)- 7 and (–)- 7 ), 3- endo -aminobicyclo[2.2.2]oct-5-ene-2- exo -carboxylic acid ((+)- 5 and (–)- 5 ), cis - and trans -3-aminobicyclo[2.2.2]octa ne-2-carboxylic acid ((+)- 6 , (–)- 6 , (+)- 8 and (–)- 8 ) was achieved via isomerization, hydrogenation and hydrolysis of the corresponding esters (–)- 1 and (+)- 1 . The stereochemistry and relative configurations of the synthesized compounds were determined by NMR sp…

StereochemistryCarboxylic acidCarboxylic AcidsPharmaceutical ScienceArticleAnalytical Chemistrylcsh:QD241-441Hydrolysislcsh:Organic chemistryDrug DiscoveryMoleculePhysical and Theoretical Chemistryta116Nuclear Magnetic Resonance BiomolecularEne reactionchemistry.chemical_classificationMolecular StructureChemistryOrganic ChemistryDiastereomerresolutionconstrained chiral β-amino acidsEstersNuclear magnetic resonance spectroscopycontinuous flow hydrogenationsChemistry (miscellaneous)bicyclic β-amino acid derivativesMolecular MedicineEnantiomercontinuous flow hydrogenations<b> </b>bicyclic beta-amino acid derivativesIsomerizationconstrained chiral beta-amino acids
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