Search results for "monoterpene"

showing 10 items of 145 documents

Secondary metabolites from the aerial parts of Cytisus villosus Pourr

2017

Phytochemical investigation of the aerial parts of Cytisus villosus Pourr. resulted in the isolation and characterization of a new isoflavan, (3S, 4S)-2′,4′-dihydroxy-3′-methoxy-6,7-methylenedioxyisoflavan- 4-ol (1), and a new monoterpene, (4R,6S)-4-hydroxy-2,2,6-trimethyl-9-oxabicyclo [4.2.1] non-1(8)-en-7-one (2), together with four known flavonoids: geinstein (3), chrysin (4), chrysin -7-O-β-D-glucopyranoside (5) and 2″-O-α-L-rhamnosylorientin (6). The structures of the new compounds were elucidated on the basis of extensive spectroscopic analysis, including 1D, 2D NMR ((1)H, (13)C, COSY, TOCSY, HMBC and HSQC) and HRESIMS. The absolute configurations of 1 and 2 were established by the co…

Circular dichroism010405 organic chemistryStereochemistryMonoterpeneCytisus villosusPlant Science010402 general chemistryCytisus villosus01 natural sciencesBiochemistryisoflavonoidsArticle0104 chemical scienceschemistry.chemical_compoundchemistryPhytochemicalECDChrysinmonoterpenoidsAgronomy and Crop ScienceTwo-dimensional nuclear magnetic resonance spectroscopyBiotechnologyPhytochemistry Letters
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Metal NHC Complexes with Naphthalimide Ligands as DNA-Interacting Antiproliferative Agents

2017

Naphthalimide-based N-heterocyclic carbene (NHC) complexes of the type [(1,5-cyclooctadiene)(NHC)RhCl)] (4 a-c), [(p-cymene)(NHC)RuCl2 )] (5 a-c), and [(NHC)CuBr] (6 a-c) were synthesized and investigated as antiproliferative agents that target DNA. The cytotoxic effects were largely driven by the naphthalimide structure, which is a DNA-intercalating moiety. Regarding the metal center, the highest activities were observed with the rhodium complexes, and cytotoxic activity was significantly lower for the ruthenium derivatives. The stable coordination of the NHC ligands of selected complexes 4 b and 5 b in solution was confirmed, and their DNA binding properties were studied by UV/Vis spectro…

Circular dichroismStereochemistryIntercalation (chemistry)Molecular Conformationchemistry.chemical_elementApoptosisCrystallography X-RayLigands010402 general chemistry01 natural sciencesBiochemistryRhodiumMetalchemistry.chemical_compoundDrug StabilityCoordination ComplexesDrug DiscoveryHumansMoietyGeneral Pharmacology Toxicology and PharmaceuticsrutheniumCell ProliferationPharmacology010405 organic chemistryChemistryCircular DichroismOrganic ChemistryDNAnaphthalimideIntercalating Agentsanticancer agent0104 chemical sciencesRutheniumcarbeneNaphthalimidesSettore CHIM/03 - Chimica Generale E Inorganicacoppervisual_artrhodiumMCF-7 CellsMonoterpenesvisual_art.visual_art_mediumCymenesMolecular MedicineSpectrophotometry UltravioletHT29 CellsMethaneCarbeneDNAChemMedChem
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Antiproliferative activity of hexane extract from Tunisian Cistus libanotis, Cistus monspeliensis and Cistus villosus

2013

Abstract Background As a part of our investigation on Tunisian medicinal plants, we have carried out a phytochemical investigation of the hexane extracts from leaves of Cistus libanotis, C. villosus and C. monspeliensis, evualuating also their possible antiproliferative activity in vitro. Results The major compounds of hexane extracts were identified and quantified by GC-MS. The composition of the three species, although belonging to the same genus, is completely different. The antiproliferative activity was evaluated against murine monocyte/macrophages (J774.A1), human melanoma cells (A-375), and human breast cancer cells (MCF-7), showing major activity against the human melanoma cell line…

Cistus villosuChemistry(all)MonoterpeneCistus libanotischemistry.chemical_compoundCistusCistus monspeliensiSettore BIO/15 - Biologia FarmaceuticaCistus monspeliensisMedicinal plantsHexane extractbiologyTraditional medicineC. villosuC. monspeliensiSettore CHIM/06 - Chimica OrganicaGeneral ChemistryPreliminary Communicationbiology.organism_classificationAntiproliferative activity in vitroHexanechemistryPhytochemicalCistus libanotiHuman melanomaGC-MSChemistry Central Journal
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Lemon Oils Attenuate the Pathogenicity of Pseudomonas aeruginosa by Quorum Sensing Inhibition

2021

The chemical composition of three Citrus limon oils: lemon essential oil (LEO), lemon terpenes (LT) and lemon essence (LE), and their influence in the virulence factors production and motility (swarming and swimming) of two Pseudomonas aeruginosa strains (ATCC 27853 and a multidrug-resistant HT5) were investigated. The main compound, limonene, was also tested in biological assays. Eighty-four compounds, accounting for a relative peak area of 99.23%, 98.58% and 99.64%, were identified by GC/MS. Limonene (59–60%), γ-terpinene (10–11%) and β-pinene (7–15%) were the main compounds. All lemon oils inhibited specific biofilm production and bacterial metabolic activities into biofilm in a dose-dep…

CitrusCITRUS PEELPharmaceutical ScienceSwarming motilitypyocyaninmedicine.disease_causebiofilmAnalytical Chemistrylaw.invention//purl.org/becyt/ford/1 [https]Terpenechemistry.chemical_compoundQD241-441lawDrug Resistance Multiple BacterialQUORUM SENSINGDrug DiscoveryCitrus peelFood scienceBicyclic Monoterpenes0303 health sciencesPancreatic ElastaseVirulencequorum sensing04 agricultural and veterinary sciences040401 food scienceAnti-Bacterial AgentsmotilityChemistry (miscellaneous)Pseudomonas aeruginosaMolecular MedicineBIOFILMVIRULENCE FACTORSSignal TransductionPYOCYANINVirulence FactorsCyclohexane Monoterpenes<i>Citrus</i> peelArticleGas Chromatography-Mass Spectrometry03 medical and health sciences0404 agricultural biotechnologyPyocyaninBacterial ProteinsMOTILITYOils VolatilemedicinePlant OilselastasePhysical and Theoretical Chemistry//purl.org/becyt/ford/1.6 [https]Essential oilVolatile Organic CompoundsLimonene030306 microbiologyPseudomonas aeruginosaOrganic ChemistryBiofilmQuorum sensingchemistryBiofilmsPyocyanineLimoneneELASTASEMolecules
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Genotoxicity of citrus wastewater in prokaryotic and eukaryotic cells and efficiency of heterogeneous photocatalysis by TiO(2).

2012

Abstract The presence of (±)α-pinene, (+)β-pinene, (+)3-carene, and R-(+)limonene terpenes in wastewater of a citrus transformation factory was detected and analyzed, in a previous study, by using Solid Phase Micro-extraction (SPME) followed by GC analyses. Purpose of that research was to compare the genotoxic responses of mixtures of terpenes with the genotoxicity of the individual compounds, and the biological effects of actual wastewater. Genotoxicity was evaluated in the Salmonella reversion assay (Ames test) and in V79 cells by Comet assay. Ames tests indicated that the four single terpenes did not induce an increase of revertants frequency. On the contrary, the mixtures of terpenes ca…

CitrusChromatography GasDNA damageBiophysicsPHOTOCATALYSIS TiO2 GENOTOXICITYmedicine.disease_causeWaste Disposal FluidCatalysisAmes testCell LineTerpenechemistry.chemical_compoundBridged Bicyclo CompoundsCricetulusCricetinaeCyclohexenesmedicineAnimalsRadiology Nuclear Medicine and imagingSolid Phase MicroextractionBicyclic MonoterpenesTitaniumLimoneneRadiationChromatographyPhotolysisRadiological and Ultrasound TechnologyMutagenicity TestsTerpenesComet assayTransformation (genetics)chemistryWastewaterEnvironmental chemistryMonoterpenesSettore CHIM/07 - Fondamenti Chimici Delle TecnologieComet AssayGenotoxicityLimoneneWater Pollutants ChemicalDNA DamageJournal of photochemistry and photobiology. B, Biology
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Bioactive Constituents of Juniperus turbinata Guss. from La Maddalena Archipelago.

2018

A comprehensive phytochemical study of Juniperus turbinata (Cupressaceae) collected from La Maddalena Archipelago (Sardinia, Italy) is reported. Both the essential oil and the ethanolic extract obtained from the aerial parts were analyzed. The essential oil appears to belong to a new chemotype compared to other Mediterranean juniper accessions, as it was favored by geographic isolation of the isles. It showed a low content of monoterpene hydrocarbons and -terpineol, ent-manoyl oxide, 1,10-di-epi-cubenol as the major constituents. The ethanolic fraction contained mainly diterpenoids. Among these, 15-formyloxyimbricatolic acid (7) is a new natural product since it has hitherto been obtained o…

CupressaceaeFree RadicalsDPPHMonoterpeneJuniperus turbinata; biological activity; essential oil; imbricataloic acid; polar compoundsPhytochemicalsMolecular ConformationBioengineeringbiological activityAmentoflavonePhytochemical01 natural sciencesBiochemistryessential oilimbricataloic acidAntioxidantslaw.inventionchemistry.chemical_compoundStructure-Activity RelationshiplawCell Line TumorOils VolatileHumanspolar compoundMolecular BiologyEssential oilCell ProliferationbiologyChemotypeTraditional medicineDose-Response Relationship Drug010405 organic chemistryCupressaceaeGeneral ChemistryGeneral Medicinebiology.organism_classificationAntineoplastic Agents Phytogenic0104 chemical sciences010404 medicinal & biomolecular chemistrychemistryPhytochemicalItalyMolecular MedicineTroloxAntioxidantDrug Screening Assays AntitumorFree RadicalJuniperus turbinataHumanChemistrybiodiversity
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Phytochemical Analysis and Cytotoxicity Towards Multidrug-Resistant Leukemia Cells of Essential Oils Derived from Lebanese Medicinal Plants

2012

Juniperus excelsa fruit essential oil as well as J. oxycedrus, Cedrus libani, and Pinus pinea wood essential oils have been obtained with yields between 2.2 ± 0.3 % to 3.4 ± 0.5 % and analyzed by gas chromatography. Sesquiterpenes mainly characterized C. libani and J. oxycedrus essential oils, while in P. pinea and J. excelsa, monoterpenes were the most abundant compounds. In J. oxycedrus, cis-calamenene (7.8 %), cuparene (3.8 %), and cis-thujopsenal (2.0 %) have been detected for the first time. The cytotoxic activity of these essential oils against drug-sensitive CCRF-CEM and multidrug-resistant P-glycoprotein-expressing CEM/ADR5000 leukemia cells has been investigated (IC₅₀ values: 29.46…

Cupressaceaegas chromatographyPharmaceutical ScienceAnalytical Chemistrylaw.inventionlawDrug DiscoveryTumor Cells CulturedLebanonMedicinal plantsLeukemiabiologyTraditional medicinePinaceaeWoodDrug Resistance MultiplePhytochemicalJuniperus excelsaPinaceaeMolecular MedicineSesquiterpenesJuniperus oxycedruscancer; essential oils; gas chromatography; multidrug resistance; Juniperus excelsa; Juniperus oxycedrus; Cupressaceae; Cedrus libani; Pinus pinea; PinaceaeNOmultidrug resistanceBotanyOils VolatileHumanscancerCedrusessential oilsEssential oilCedrus libaniPharmacologyPlants MedicinalOrganic ChemistryCupressaceaePinusbiology.organism_classificationCedrus libaniAntineoplastic Agents PhytogenicComplementary and alternative medicineDrug Resistance NeoplasmFruitJuniperusMonoterpenesPinus pineaJuniperus excelsaJuniperus oxycedrusPhytotherapyPlanta Medica
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Genomic instability induced by α-pinene in Chinese hamster cell line.

2012

Here, we report the effects of exposure of mammalian cells to α-pinene, a bicyclic monoterpene used in insecticides, solvents and perfumes. Morphological analysis, performed in V79-Cl3 cells exposed for 1 h to increasing concentrations (25 up to 50 μM) of α-pinene, indicated a statistically significant increase in micronucleated and multinucleated cell frequencies; apoptotic cells were seen at 40 and 50 μM. This monoterpene caused genomic instability by interfering with mitotic process; in fact, 50% of cells (versus 19% of control cells) showed irregular mitosis with multipolar or incorrectly localised spindles. Cytogenetic analysis demonstrated high-frequency hypodiploid metaphases as well…

DNA damageHealth Toxicology and MutagenesisApoptosisToxicologymedicine.disease_causeChinese hamsterGenomic InstabilityColony-Forming Units AssayImmunoenzyme TechniquesMultinucleateCricetulusGenomic instability hamster cell lines a-pineneCricetinaeGeneticsmedicineAnimalsMitosisGenetics (clinical)Cells CulturedMicronuclei Chromosome-DefectiveBicyclic MonoterpenesChromosome AberrationsMicronucleus Testsbiologybiology.organism_classificationMolecular biologyComet assaySettore BIO/18 - GeneticaOxidative StressCell cultureMicronucleus testMonoterpenesComet AssayReactive Oxygen SpeciesOxidative stressDNA DamageMutagenesis
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Herbicidal Activity of Peumus boldus and Drimys winterii Essential Oils from Chile

2011

[EN] The essential oil composition of Peumus boldus and Drimys winterii was analyzed by means of capillary GC-FID and GC-MS. More than 96% of the total oil components (43 and 54 compounds, respectively) were identified, with ascaridole (51.17 ± 9.51), p-cymene (16.31 ± 2.52) and 1,8-cineole (14.45 ± 2.99) as the main compounds in P. boldus and ¿-eudesmol (21.65 ± 0.41), followed of elemol (12.03 ± 0.34) and terpinen-4-ol (11.56 ± 1.06) in D. winterii. The herbicidal activity was tested against Amaranthus hybridus and Portulaca oleracea. P. boldus essential oil was the most phytotoxic against both weeds, inhibiting seed germination and seedling growth at all concentrations assayed (0.125-1 ¿…

DrimysChromatography GasAmaranthus hybridusBOTANICAPharmaceutical ScienceGerminationPortulacaEssential oilArticleAnalytical Chemistrylaw.inventionlcsh:QD241-441chemistry.chemical_compoundlcsh:Organic chemistrylawDrug DiscoveryBotanyOils VolatilePhysical and Theoretical ChemistryChileSeedling growthEssential oilBIOLOGIA VEGETALGas chromatographybiologyMass spectrometryHerbicidesOrganic Chemistrybiology.organism_classificationDrimysChemistrychemistryIsolation and purificationChemistry (miscellaneous)GerminationSeedlingEssential oilsPhytotoxicityPeumusMonoterpenesMolecular MedicinePhytotoxicityHerbicideAscaridoleessential oils; phytotoxicity; germination; seedling growth; monoterpenesPeumus boldus
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Chemical composition and antimicrobial activity of the essential oils of some species of Anthemis sect. Anthemis (Asteraceae) from Sicily

2017

The chemical composition of the essential oils isolated from the aerial parts of Anthemis arvensis L. subsp. arvensis, Anthemis cretica subsp. messanensis (Brullo) Giardina &amp; Raimondo and from flowers and leaves of Anthemis cretica subsp. columnae (Ten.) Frezén were determinated by GC–FID and GC–MS analyses. Torreyol (85.4%) was recognised as the main constituent of the Anthemis arvensis subsp. arvensis essential oil, while in the essential oils of Anthemis cretica subsp. messanensis, collected on the rock and cultivated in Hortus Botanicus Panormitanus, (E)-chrysanthenyl acetate (28.8 and 24.2% resp.), 14-hydroxy-α-humulene (8.1 and 5.3% resp.), santolina triene (8 and 5.8% resp.) and …

Drug Evaluation PreclinicalRaimondoAnthemis arvensisFlowersMicrobial Sensitivity TestsPlant Science01 natural sciencesBiochemistryGas Chromatography-Mass Spectrometryessential oillaw.inventionAnalytical Chemistrychemistry.chemical_compoundBridged Bicyclo CompoundsAnti-Infective Agentsantibacterial activitylawSantolinaBotanyOils VolatileAnthemisSettore BIO/15 - Biologia FarmaceuticaChemical compositionSicilyAnthemis arvensis L. subsp. arvensiEssential oiltorreyolBicyclic MonoterpenesPolycyclic Sesquiterpenesalpha-PineneEucalyptolbiology010405 organic chemistryOrganic ChemistryAnthemis cretica subsp. columnae (Ten.) FrezénAsteraceaebiology.organism_classificationCyclohexanols0104 chemical sciencesPlant Leaves010404 medicinal & biomolecular chemistryEucalyptolchemistryMonoterpenesAnthemis cretica subsp. messanensis (Brullo) Giardina &ampAnthemisSesquiterpenes
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