Search results for "Benzene Derivative"

showing 10 items of 44 documents

On the nature of organic electron density transfer complexes within molecular electron density theory.

2019

The structural features of a series of organic molecular complexes formed between the strong electrophilic tetracyanoethylene and twelve benzene derivatives with increased nucleophilic character, herein called Electron Density Transfer Complexes (EDTCs), have been studied using Molecular Electron Density Theory. The favourable nucleophilic/electrophilic interactions, which favour the global electron density transfer (GEDT) towards the electrophile, are responsible for the formation of these species. Molecular complexes presenting a GEDT above 0.05e are classified as EDTCs. Analysis of the Parr functions of the separated reagents and the topological analysis of the electron density of the ED…

Electron density010405 organic chemistryOrganic ChemistryElectronic structureTetracyanoethylene010402 general chemistry01 natural sciencesBiochemistry0104 chemical scienceschemistry.chemical_compoundNucleophilechemistryComputational chemistryReagentElectrophileBenzene derivativesPhysical and Theoretical ChemistryOrganicbiomolecular chemistry
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How amino and nitro substituents affect the aromaticity of benzene ring

2020

Abstract The effect of strongly electron-accepting and electron-donating substituents on the aromaticity of the benzene ring has been revealed based on experimental and computational data. It has been documented that the nitro group affects the π-electron structure of the ring in its benzene derivative ca. 2.8 times weaker than the amino group. However, their joint effects in the meta and para nitroaniline, compared to nitrobenzene, results in a decrease of the delocalization in the ring by a factor ca. 4.0 and 6.5, respectively.

General Physics and AstronomyAromaticity02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnologyPara-nitroanilineRing (chemistry)01 natural sciencesMedicinal chemistry0104 chemical sciencesNitrobenzenechemistry.chemical_compoundDelocalized electronchemistryBenzene derivativesNitroPhysical and Theoretical Chemistry0210 nano-technologyBenzeneChemical Physics Letters
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Identification of highly effective antitrypanosomal compounds in essential oils from the Apiaceae family

2018

The Apiaceae family encompasses aromatic plants of economic importance employed in foodstuffs, beverages, perfumery, pharmaceuticals and cosmetics. Apiaceae are rich sources of essential oils because of the wealth of secretory structures (ducts and vittae) they are endowed with. The Apiaceae essential oils are available on an industrial level because of the wide cultivation and disposability of the bulky material from which they are extracted as well as their relatively cheap price. In the fight against protozoal infections, essential oils may represent new therapeutic options. In the present work, we focused on a panel of nine Apiaceae species (Siler montamon, Sison amomum, Echinophora spi…

Human African trypanosomiasiAlkeneApiaceae; BALB/3T3; Essential oils; Human African trypanosomiasis; Trypanosoma brucei; 3T3 Cells; Alkenes; Animals; Apiaceae; Benzyl Compounds; Cyclohexenes; Dioxolanes; Inhibitory Concentration 50; Mice; Monoterpenes; Oils Volatile; Plant Oils; Pyrogallol; Terpenes; Trypanosoma brucei brucei; Trypanosomiasis; Pollution; Public Health Environmental and Occupational Health; Health Toxicology and MutagenesisHealth Toxicology and Mutagenesis[SDV]Life Sciences [q-bio]VolatileMonoterpeneAllylbenzene DerivativesPlant Oil01 natural sciencesCosmeticsEssential oilTerpenechemistry.chemical_compoundMiceTrypanosoma bruceiBALB/3T3media_commonBicyclic Monoterpenes2. Zero hungerbiologyTraditional medicineChemistryBenzyl CompoundsDioxolanesGeneral Medicine3T3 CellsPollutionHealthEssential oilsTerpeneIdentification (biology)Public HealthDioxolaneCyclohexenesmedia_common.quotation_subjectAcyclic MonoterpenesApiaceae; BALB/3T3; Essential oils; Human African trypanosomiasis; Trypanosoma brucei; 3T3 Cells; Alkenes; Animals; Apiaceae; Benzyl Compounds; Cyclohexenes; Dioxolanes; Inhibitory Concentration 50; Limonene; Mice; Monoterpenes; Oils Volatile; Plant Oils; Pyrogallol; Terpenes; Trypanosoma brucei brucei; TrypanosomiasisTrypanosoma brucei bruceiCyclohexane MonoterpenesTrypanosoma bruceiAlkenesPyrogallolInhibitory Concentration 50TrypanosomiasisBenzyl CompoundsCyclohexenesOils VolatileCyclohexeneAnimalsPlant OilsToxicology and Mutagenesis3T3 CellApiaceaeAnimal010405 organic chemistryTerpenesEnvironmental and Occupational HealthHuman African trypanosomiasisPublic Health Environmental and Occupational Healthbiology.organism_classification0104 chemical sciences010404 medicinal & biomolecular chemistryPyrogallolMonoterpenesCymenesBenzyl CompoundOilsLimoneneApiaceae
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New amide and dioxopiperazine derivatives from leaves of Breynia nivosa

2017

The first chemical investigation of leaves of Breynia nivosa from Nigeria resulted in the isolation of two new amide derivatives breynivosamides A and B (1 and 2) and two new dioxopiperazine derivatives breynivosines A and B (4 and 5) together with seven known compounds (3, 6-11). The structures of the new compounds were elucidated by 1D, 2D NMR and HRESIMS data as well as by comparison with the literature. All isolated compounds were tested for the cytotoxic and antimicrobial activities. Only cristatin A (6) showed cytotoxicity against the L5178Y mouse lymphoma cell line with an IC50 value of 13.9μM while breynivosamide A (1) exhibited moderate antimicrobial activity against Mycobacterium …

LymphomaStereochemistryMicrobial Sensitivity Tests01 natural sciencesMycobacterium tuberculosisMagnoliopsidaMicechemistry.chemical_compoundAnti-Infective AgentsCell Line TumorAmideDrug DiscoveryBenzene DerivativesAnimalsBreyniaCytotoxicityIC50PharmacologyMolecular Structurebiology010405 organic chemistryChemistryMouse LymphomaTryptophanGeneral Medicinebiology.organism_classificationAntimicrobialAmides0104 chemical sciencesPlant Leaves010404 medicinal & biomolecular chemistryTwo-dimensional nuclear magnetic resonance spectroscopyFitoterapia
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Study of the influence of temperature and precipitations on the levels of BTEX in natural waters.

2013

Assessment of seasonal changes in surface water quality is an important aspect for evaluating temporal variation of water due to natural or anthropogenic inputs of point and non-point sources. The objective of this paper was to investigate the influence of seasonal temperature fluctuations and precipitations on the levels of BTEX in natural waters. Principal component analysis (PCA) was used to evaluate the seasonal correlations of BTEX levels in water and to extract the parameters that are most important in assessing seasonal variations of water quality. This study was carried out as a part of VOCs monitoring program in natural water samples from Mediterranean coast. To carry out this proj…

Mediterranean climateEnvironmental EngineeringHealth Toxicology and MutagenesisRainBTEXlaw.inventionRiverslawBenzene DerivativesEnvironmental ChemistryFlame ionization detectorWaste Management and DisposalDetection limitPrincipal Component AnalysisChemistryMediterranean RegionTemperaturePollutionMonitoring programEnvironmental chemistryPrincipal component analysisGas chromatographyWater qualitySeasonsWater Pollutants ChemicalEnvironmental MonitoringJournal of hazardous materials
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Characterization of two Lactococcus lactis zinc membrane proteins, Llmg_0524 and Llmg_0526, and role of Llmg_0524 in cell wall integrity

2015

Background Due to its extraordinary chemical properties, the cysteine amino acid residue is often involved in protein folding, electron driving, sensing stress, and binding metals such as iron or zinc. Lactococcus lactis, a Gram-positive bacterium, houses around one hundred cysteine-rich proteins (with the CX2C motif) in the cytoplasm, but only a few in the membrane. Results In order to understand the role played by this motif we focused our work on two membrane proteins of unknown function: Llmg_0524 and Llmg_0526. Each of these proteins has two CX2C motifs separated by ten amino-acid residues (CX2CX10CX2C). Together with a short intervening gene (llmg_0525), the genes of these two protein…

Microbiology (medical)Lysozymechemistry.chemical_elementZincPlasma protein bindingGrowthMicrobiologyMembrane proteins;Growth;Cumene hydroperoxideProtein structureBacterial ProteinsCumene hydroperoxideCell Wallcystéinelactococcus lactisMembrane proteinsBenzene Derivatives[SDV.BBM]Life Sciences [q-bio]/Biochemistry Molecular BiologyCysteineBinding siteBinding SitesbiologyProtein StabilityLactococcus lactispropriété de membranebiology.organism_classificationcroissanceProtein Structure Tertiary3. Good healthZincchemistryBiochemistryMembrane proteinProtein foldingProtein BindingResearch ArticleCysteine
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Heterocyclic and Phenyl Double-Bond-Locked Combretastatin Analogues Possessing Potent Apoptosis-inducing activity in HL60 and in MDR Cell lines

2005

Two new series of combretastatin (CA-4) analogues have been prepared. The alkenyl motif of CA-4 was replaced either by a five-membered heterocyclic (isoxazoline or isoxazole) or by a six-membered ring (pyridine or benzene). The new compounds have been evaluated for their effects on tubulin assembly and for cytotoxic and apoptotic activities. Five compounds (18b, 20a, 21a, 34b, and 35b) demonstrated an attractive profile of cytotoxicity (IC501 microM) and apoptosis-inducing activity but poor antitubulin activity. The isoxazoline derivatives 18b, 20a, and 21a, demonstrated potent apoptotic activity different from that of natural CA-4. Their ability to block most cells in the G2 phase suggests…

Models MolecularA-4 ANALOGSDouble bondHL60StereochemistryPyridinesTUBULINApoptosisANTINEOPLASTIC AGENTSchemistry.chemical_compoundStructure-Activity RelationshipCell Line TumorDrug DiscoveryStilbenesBenzene DerivativesHumansIsoxazoleBIOLOGICAL EVALUATIONCytotoxicitychemistry.chemical_classificationCombretastatinbiologyCOLCHICINEDEATHIsoxazolesDrug Resistance MultipleTubulinANTIMITOTIC ANTITUMOR AGENTSMULTIDRUGchemistryApoptosisCell cultureDrug Resistance NeoplasmDISCOVERYbiology.proteinMolecular MedicineDrug Screening Assays AntitumorSOLID TUMOR-THERAPY
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Tetrathiafulvalene-Based Mixed-Valence Acceptor-Donor-Acceptor Triads: A Joint Theoretical and Experimental Approach

2013

This work presents a joint theoretical and experimental characterisation of the structural and electronic properties of two tetrathiafulvalene (TTF)-based acceptor-donor-acceptor triads (BQ-TTF-BQ and BTCNQ-TTF - BTCNQ; BQ is naphthoquinone and BTCNQ is benzotetracyano-p-quinodimethane) in their neutral and reduced states. The study is performed with the use of electrochemical, electron paramagnetic resonance (EPR), and UV/Vis/NIR spectroelectrochemical techniques guided by quantum-chemical calculations. Emphasis is placed on the mixed-valence properties of both triads in their radical anion states. The electrochemical and EPR results reveal that both BQ-TTF-BQ and BTCNQ-TTF-BTCNQ triads in…

Models MolecularElectronic structureDonor–acceptor systemsElectronsNanotechnology010402 general chemistry01 natural sciencesCatalysisElectron Transportchemistry.chemical_compoundHeterocyclic CompoundsNitrilesBenzene Derivatives010405 organic chemistryChemistryBusiness administrationOrganic ChemistryElectron Spin Resonance SpectroscopyGeneral ChemistryAcceptor3. Good health0104 chemical sciencesDensity functional calculationsFleroxacinChristian ministryMixed-valent compoundsDonor acceptorOxidation-ReductionTetrathiafulvaleneNaphthoquinonesEPR spectroscopyChemistry - A European Journal
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Simultaneous Freezing of Chirality and In−Out Conformation of a Macropentacyclic Cryptand by Protonation

2004

Compound 1, a cryptand-derived macropentacycle, is a flexible molecule that encompasses many conformations (symmetrical, unsymmetrical, and chiral ones) depending on the observation temperature (VT 1H NMR). Selective monoprotonation of this molecule leads to a totally unsymmetrical, rigidly chiral species in solution (1H NMR). Helical chirality and in-out conformation of monoprotonated 1 are observed in the solid state by X-ray diffraction analysis, as well as the proton location. The latter is bound to the endo bridgehead nitrogen atom and involved in hydrogen-bonding interactions with the three closest sulfurs. Significant induction of chirality is triggered by reaction of 1 with the opti…

Models MolecularMagnetic Resonance SpectroscopyProtonChemistryStereochemistryCryptandMolecular ConformationDiastereomerStereoisomerismProtonationGeneral ChemistryNuclear magnetic resonance spectroscopyCrystallography X-RayBiochemistryCatalysisColloid and Surface ChemistryCrown EthersBenzene DerivativesProton NMRMoleculeDisulfidesAminesProtonsChirality (chemistry)Journal of the American Chemical Society
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Orientational preferences of aromatic guests in dimeric capsules of tetraurea calix[4]arenes—MD and NMR studies

2006

Molecular dynamics (MD) simulations have been performed for complexes of a dimeric capsule of a tetraurea calixarene with a series of twelve aromatic guests. A distinct orientational preference and a restriction of the internal mobility was found which depend on the size and electronic properties of the guests. The results are in agreement with the CIS values obtained from (1)H NMR spectroscopic measurements and with complexation selectivities obtained by competition experiments.

Models MolecularMagnetic Resonance SpectroscopyPyridinesChemistryOrganic ChemistryBinding CompetitiveBiochemistrySubstrate SpecificityKineticsMolecular dynamicsCrystallographyPhenolsPyrazinesCalixareneBenzene DerivativesProton NMRThermodynamicsUreaCalixarenesPhysical and Theoretical ChemistryElectronic propertiesOrg. Biomol. Chem.
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