Search results for " monoterpenes."

showing 10 items of 43 documents

Risk management of ochratoxigenic fungi and ochratoxin A in maize grains by bioactive EVOH films containing individual components of some essential o…

2018

Abstract Aspergillus steynii and Aspergillus tubingensis are possibly the main ochratoxin A (OTA) producing species in Aspergillus section Circumdati and section Nigri, respectively. OTA is a potent nephrotoxic, teratogenic, embryotoxic, genotoxic, neurotoxic, carcinogenic and immunosuppressive compound being cereals the first source of OTA in the diet. In this study bioactive ethylene-vinyl alcohol copolymer (EVOH) films containing cinnamaldehyde (CINHO), linalool (LIN), isoeugenol (IEG) or citral (CIT) which are major components of some plant essential oils (EOs) were produced and tested against A. steynii and A. tubingensis growth and OTA production in partly milled maize grains. Due to …

Ochratoxin AAntifungal AgentsWater activityAcyclic MonoterpenesCitralMicrobiologyZea maysCinnamaldehydechemistry.chemical_compound0404 agricultural biotechnologyLinaloolOils VolatileFood scienceAcroleinAspergillusRisk ManagementbiologyWater04 agricultural and veterinary sciencesGeneral Medicinebiology.organism_classification040401 food scienceOchratoxinsIsoeugenolAspergilluschemistryAspergillus tubingensisMonoterpenesPolyvinylsFood ScienceInternational journal of food microbiology
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Antibacterial Activity and Anticancer Activity of Rosmarinus officinalis L. Essential Oil Compared to That of Its Main Components

2012

In this study, Rosmarinus officinalis L. essential oil and three of its main components 1,8-cineole (27.23%), α-pinene (19.43%) and β-pinene (6.71%) were evaluated for their in vitro antibacterial activities and toxicology properties. R. officinalis L. essential oil possessed similar antibacterial activities to α-pinene, and a little bit better than β-pinene, while 1,8-cineole possessed the lowest antibacterial activities. R. officinalis L. essential oil exhibited the strongest cytotoxicity towards three human cancer cells. Its inhibition concentration 50% (IC50) values on SK-OV-3, HO-8910 and Bel-7402 were 0.025‰, 0.076‰ and 0.13‰ (v/v), respectively. The cytotoxicity of all the test sampl…

Pharmaceutical ScienceRosmarinusAnalytical Chemistrylaw.inventionchemistry.chemical_compoundlawDrug DiscoveryFood scienceCytotoxicityBicyclic Monoterpenesbiologyantibacterial activities18-cineoleAnti-Bacterial AgentsChemistry (miscellaneous)α-pineneOfficinaliscytotoxicityMolecular MedicineAntibacterial activityCell SurvivalMicrobial Sensitivity TestsRosmarinus officinalis L.Articlelcsh:QD241-441Bridged Bicyclo CompoundsInhibitory Concentration 50lcsh:Organic chemistryCell Line TumorBotanyOils Volatile<em>Rosmarinus officinalis </em>L.; 18-cineole; α-pinene; β-pinene; antibacterial activities; cytotoxicityHumansPhysical and Theoretical ChemistryIC50Essential oilEucalyptolBacteriaPlant ExtractsOrganic ChemistryCyclohexanolsbiology.organism_classificationAntineoplastic Agents PhytogenicRosmarinusβ-pineneEucalyptolchemistryMonoterpenesDrug Screening Assays AntitumorHuman cancerMolecules; Volume 17; Issue 3; Pages: 2704-2713
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Phytotoxic Activities of Mediterranean Essential Oils

2010

Made available in DSpace on 2013-08-28T14:12:36Z (GMT). No. of bitstreams: 1 WOS000279207300035.pdf: 281167 bytes, checksum: fc72a9258845b6d806e3ebbaf2617e52 (MD5) Made available in DSpace on 2013-09-30T18:36:30Z (GMT). No. of bitstreams: 2 WOS000279207300035.pdf: 281167 bytes, checksum: fc72a9258845b6d806e3ebbaf2617e52 (MD5) WOS000279207300035.pdf.txt: 48896 bytes, checksum: d8cd11d4997d3f23c1211486475739e1 (MD5) Previous issue date: 2010-06-01 Submitted by Vitor Silverio Rodrigues (vitorsrodrigues@reitoria.unesp.br) on 2014-05-20T13:48:46Z No. of bitstreams: 2 WOS000279207300035.pdf: 281167 bytes, checksum: fc72a9258845b6d806e3ebbaf2617e52 (MD5) WOS000279207300035.pdf.txt: 48896 bytes, ch…

PimpinellaFoeniculumPharmaceutical SciencephytotoxicityArticleLepidium sativumRaphanusseedling growthAnalytical Chemistrylcsh:QD241-441foodlcsh:Organic chemistryDrug DiscoveryBotanyOils VolatileRadiclePlant OilsPhysical and Theoretical Chemistryessential oilsLavandula angustifoliaLamiaceaebiologyOrganic ChemistrySalvia officinalisVerbena officinalismonoterpenesLettucebiology.organism_classificationfood.foodFoeniculumgerminationChemistry (miscellaneous)SeedsMolecular MedicineLamiaceaeMelissa officinalisessential oils; phytotoxicity; germination; seedling growth; monoterpenesHyssopus officinalisApiaceaeMolecules
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The endoperoxide ascaridol shows strong differential cytotoxicity in nucleotide excision repair-deficient cells

2011

Targeting synthetic lethality in DNA repair pathways has become a promising anti-cancer strategy. However little is known about such interactions with regard to the nucleotide excision repair (NER) pathway. Therefore, cell lines with a defect in the NER genes ERCC6 or XPC and their normal counterparts were screened with 53 chemically defined phytochemicals isolated from plants used in traditional Chinese medicine for differential cytotoxic effects. The screening revealed 12 drugs that killed NER-deficient cells more efficiently than proficient cells. Five drugs were further analyzed for IC50 values, effects on cell cycle distribution, and induction of DNA damage. Ascaridol was the most effe…

RAD23BDNA RepairDNA repairDNA damageCyclohexane MonoterpenesBiologyToxicologyCell LineInhibitory Concentration 50HumansCytotoxic T cellMedicine Chinese TraditionalPharmacologyDose-Response Relationship DrugCell cycleAntineoplastic Agents PhytogenicMolecular biologyPeroxidesG2 Phase Cell Cycle CheckpointsCell cultureCancer cellMonoterpenesM Phase Cell Cycle CheckpointsReactive Oxygen SpeciesDNA DamageDrugs Chinese HerbalNucleotide excision repairToxicology and Applied Pharmacology
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Chemical composition of the essential oils of three endemic species of Anthemis sect. Hiorthia (DC.) R.Fern. growing wild in Sicily and chemotaxonomi…

2014

The chemical composition of the essential oils isolated from the aerial parts of Anthemis pignattiorum Guarino, Raimondo & Domina and A. ismelia Lojac. and the aerial parts and flowers of Anthemis cupaniana Tod. ex Nyman , three endemic Sicilian species belonging to the section Hiorthia, was determined by GC-FID and GC/MS analyses. (Z)-Muurola-4(14),5-diene (27.3%) was recognized as the main constituent of the A. pignattiorum essential oil, together with isospathulenol (10.6%), sabinene (7.7%), and artemisyl acetate (6.8%), while in the oil obtained from the aerial parts of A. ismelia , geranyl propionate (8.8%), bornyl acetate (7.9%), β-thujone (7.8%), neryl propionate (6.5%), and t-muurol…

SabineneAnthemis specieBioengineeringFlowersBiologyBiochemistryEssential oillaw.inventionSettore BIO/01 - Botanica Generalechemistry.chemical_compoundlawBotanyCluster analysis (CA)Oils VolatileCluster AnalysisAnthemisEndemismMolecular BiologyChemical compositionAnthemis cupanianaSicilyEssential oilBicyclic MonoterpenesTaxonomychemistry.chemical_classificationTerpenesChemotaxisSettore BIO/02 - Botanica Sistematicafungifood and beveragesGeneral ChemistryGeneral MedicineSettore CHIM/06 - Chimica OrganicaAnthemis pignattiorumPlant Components Aerialbiology.organism_classificationchemistryAthemis ismeliaBornyl acetatePropionateMonoterpenesMolecular MedicineFernAnthemisSesquiterpenes
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Inhibitory Activity and Chemical Characterization ofDaucus carotasubsp.maximusEssential Oils

2017

The essential oils (EOs) of green seeds from Daucus carota subsp. maximus growing wild in Pantelleria Island (Sicily, Italy) were characterized. EOs were extracted by steam distillation, examined for their inhibitory properties against food-borne Gram-positive and Gram-negative bacteria and analyzed for the chemical composition by gas chromatography (GC) and mass spectrometry (MS). Undiluted EOs showed a large inhibition spectrum against Gram-positive strains and also vs. Acinetobacter spp. and Stenotrophomonas maltophilia. The minimum inhibition concentration (MIC) was in the range 1.25 – 2.50 μl/ml for the most sensitive strains. The chemical analysis indicated that D. carota subsp…

Sesquiterpene0301 basic medicineSettore AGR/05 - Assestamento Forestale E SelvicolturaMonoterpeneChemical compositionMonoterpeneSettore MED/42 - Igiene Generale E Applicata01 natural sciencesBiochemistryEssential oilCarotollaw.inventionchemistry.chemical_compoundlawFood scienceChemical compositionInhibitory activitiebiologyChemistry (all)General MedicineAnti-Bacterial AgentsDaucus carotaStenotrophomonas maltophiliaSeedsMolecular MedicineSesquiterpenes030106 microbiologyBioengineeringPyrogallolGram-Positive BacteriaSesquiterpeneSteam distillation03 medical and health sciencesAnti-Bacterial AgentGram-Negative BacteriaBotanyChemical composition; Daucus carota; Essential oils; Foodborne bacteria; Inhibitory activities; Anti-Bacterial Agents; Daucus carota; Gram-Negative Bacteria; Gram-Positive Bacteria; Monoterpenes; Oils Volatile; Pyrogallol; Seeds; Sesquiterpenes; Bioengineering; Chemistry (all); Biochemistry; Molecular Medicine; Molecular BiologyOils VolatileMolecular BiologySeed010405 organic chemistryGeneral ChemistryFoodborne bacteriabiology.organism_classification0104 chemical sciencesMonocyclic SesquiterpeneschemistryMonoterpenesGas chromatographySettore AGR/16 - Microbiologia AgrariaDaucus carotaChemistry &amp; Biodiversity
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Chemical composition of the essential oil of Moluccella spinosa L. (Lamiaceae) collected wild in Sicily and its activity on microorganisms affecting …

2015

In this study the chemical composition of the essential oil from aerial parts of Moluccella spinosa L. collected in Sicily was evaluated by GC and GC-MS. The main components of M. spinosa L. were α-pinene (26.6%), caryophyllene oxide (16.8%) and β-caryophyllene (8.6%). A comparison with other studied oils of genus Moluccella is made. Antibacterial and antifungal activities against some microorganisms infesting historical textiles were also determined.

SesquiterpeneAntifungal AgentsTextileMoluccellaMicroorganismcaryophyllene oxideMoluccella spinosaMonoterpenePlant ScienceMicrobial Sensitivity TestsPlant OilBiochemistryAnalytical Chemistrylaw.inventionGenuslawAnti-Bacterial AgentBotanyOils VolatileAntifungal AgentPlant OilsMoluccella spinosaChemical compositionSicilyEssential oilBicyclic MonoterpenesPolycyclic SesquiterpenesLamiaceaebiologyMicrobial Sensitivity TestMedicine (all)Textilesβ-caryophylleneOrganic ChemistryPlant Components Aerialbiology.organism_classificationantibacterial and antifungal activityα-pineneAnti-Bacterial Agentsvolatile componentCaryophyllene oxideMonoterpenesLamiaceaeSesquiterpenesNatural product research
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Chemical composition and herbicidal activity of the essential oil from a Cistus ladanifer population from Spain

2012

[EN] The essential oil composition of Cistus ladanifer grown in central Spain was analysed by gas chromatography and gas chromatography/mass spectrometry, revealing it to be rich in oxygenated compounds, with trans-pinocarveol (20.00%), bornyl acetate (7.03%) and terpinen-4-ol (6.37%) as the main monoterpene compounds. Viridiflorol (13.59%) and ledol (4.36%) were the main constituents of the oxygenated sesquiterpene fraction. Large amounts of-pinene (4.70%) were found in the hydrocarbonated fractions. To study its possible use as a natural herbicide, the oil was tested invitro against Amaranthus hybridus, Portulaca oleracea, Chenopodium album, Conyza canadensis and Parietaria judaica, compl…

SesquiterpeneHerbicidal activityLedolUnclassified drugAmaranthus hybridusPineneTerpinen 4 olChemical compositionAmaranthus hybridusPlant ScienceBiochemistryCistus ladaniferEssential oilAnalytical Chemistrylaw.inventionChenopodium albumchemistry.chemical_compoundLedollawBornyl acetateBicyclic MonoterpenesBIOLOGIA VEGETALeducation.field_of_studyAmaranthusbiologyGC/MSCistusPortulacaceaeConyza canadensisGerminationCistus ladaniferPinocarveolHerbicideTerpene derivativeChromatography GasPopulationBOTANICAMass fragmentographyGerminationPortulacaArticleGas Chromatography-Mass SpectrometryChenopodiumCistusBotanyOils VolatileeducationEssential oilHerbicidesOrganic ChemistryTerpinen-4-olCistaceaebiology.organism_classificationWeedParietaria judaicaParietariachemistrySpainViridiflorolMonoterpenesWeedsConyza
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Identification of aroma compounds of Vitis vinifera L. flowers by SPME GC-MS analysis

2015

Using a gas chromatographic method (GC-MSanalysis), it was possible to determine the volatile constituent of an odorous flower from Vitis vinifera varieties growing in Sicily. More than 50 compounds were identified and the technique allowed us to determine that sesquiterpenes, as well as monoterpenes such as limonene and cymene, were the principal components. The odour-profiles allowed us to distinguish between variety groups or even single varieties.

Settore AGR/03 - Arboricoltura Generale E Coltivazioni Arboreegrapevine flowering monoterpenes.Settore AGR/13 - Chimica Agraria
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Identification of aroma compaunds of Vitis Vinifera L. flowers by SPME GC-MS analysis

2014

Using a gas chromatographic method (GC-MS-analysis), it was possible to determine the volatile constituent of an odorous flower from Vitis vinifera varieties growing in Sicily. More than 50 compounds were identified and the technique allowed us to determine that sesquiterpenes, as well as monoterpenes such as limonene and cymene, were the principal components. The odour-profiles allowed us to distinguish between variety groups or even single varieties.

Settore AGR/03 - Arboricoltura Generale E Coltivazioni Arboreegrapevine flowering sesquiterpenes monoterpenesSettore AGR/13 - Chimica Agraria
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