Search results for "TERPENES"

showing 10 items of 470 documents

Volatile compounds of flowers and leaves of Sideritis italica (Miller)Greuter et Burdet (Lamiaceae), a plant used as mountain tea

2010

Sideritis italica (Miller) Greuter et Burdet (Lamiaceae), widely used in ethnopharmacological medicine, occurs in Southern Italy and Sicily. The phytochemical composition of the essential oils of S. italica flowers and leaves, harvested in Piano Battaglia (Sicily), was analysed by GC and GC-MS. Of the 51 compounds, 43 in the oil from flowers and 29 in the oil from leaves were identified. Kaur-15-ene (20.0%) was recognised as the main constituent of the oil from flowers, together with beta-cubebene (12.1%), beta-pinene (8.5%), (Z)-nuciferol (6.5%), tricyclene (4.5%) and alpha-bisabolol (4.0%). In the oil from leaves, p-methoxyacetophenone (26.0%) prevailed, as did hexadecanoic acid (21.3%), …

Chromatography GasNonanalPlant compositionPalmitatesPlant ScienceFlowersBiologyBiochemistryGas Chromatography-Mass SpectrometryAnalytical ChemistryPalmitic acidchemistry.chemical_compoundBridged Bicyclo CompoundsBotanyPhytochemical compositionOils VolatileChemical compositionBicyclic Monoterpenesbeta-PineneLamiaceaeTeaOrganic Chemistrybiology.organism_classificationMonocyclic SesquiterpenesPlant LeaveschemistrySideritisMonoterpenesLamiaceaeSesquiterpenes
researchProduct

Volatile constituents of the aerial parts of white salsify (Tragopogon porrifolius L., Asteraceae).

2010

Tragopogon porrifolius L. grows as a vegetable in southern Italy and all parts of it are edible. In the present study the volatile components of the aerial part are described. Gas chromatography and gas chromatography-mass spectrometry analysis showed the presence of 38 components in all. On the whole, the volatile fraction was constituted mainly by carbonylic compounds (24.6%), phenols (21.5%) and fatty acids and esters (19.7%). The most abundant compounds were 4-vinyl guaiacol (19.0%), hexadecanoic acid (17.9%), hexahydrofarnesylacetone (15.8%) and hentriacontane (10.7%).

Chromatography GasPalmitic AcidPlant ScienceAsteraceaeBiochemistryGas Chromatography-Mass SpectrometryAnalytical ChemistryTragopogonPalmitic acidchemistry.chemical_compoundBotanyPhenolsHentriacontaneTragopogon porrifolius Asteraceae white salsify Volatile constituents 4-vinyl guaiacol hexadecanoic acid hexahydrofarnesylacetonebiologyTerpenesOrganic ChemistryGuaiacolSettore CHIM/06 - Chimica OrganicaAsteraceaePlant Components Aerialbiology.organism_classificationchemistryGuaiacolGas chromatographyGas chromatography–mass spectrometryVolatilizationNatural product research
researchProduct

GC and GC–MS analysis of the essential oil of Nepeta cilicica Boiss. ex Benth. from Lebanon

2013

The hydrodistillation of the aerial parts of Nepeta cilicica Boiss. ex Benth., collected in Lebanon in the Horsh Ehden reserve, yielded 0.13% (w/w) of essential oil. Gas chromatography (GC) and GC-mass spectroscopy analysis enabled the identification of 75 compounds representing 96.8% of the total oil. The most abundant compounds were spathulenol (15.1%), hexadecanoic acid (14%), δ-cadinene (5.5%) and α-copaene (4.5%). On the whole, the oil was constituted mainly by sesquiterpenes (45.9%), among which sesquiterpene hydrocarbons (27.6%) slightly prevailed over oxygenated sesquiterpenes (18.3%).

Chromatography GasbiologyOrganic ChemistryPalmitic AcidPlant Sciencebiology.organism_classificationSesquiterpeneBiochemistryGas Chromatography-Mass SpectrometryAnalytical ChemistrySpathulenollaw.inventionchemistry.chemical_compoundchemistrylawNepetaδ cadineneBotanyNepetaOils VolatileGas chromatographyLebanonGas chromatography–mass spectrometrySesquiterpenesEssential oilNatural Product Research
researchProduct

Identification of diterpenes in canvas painting varnishes by gas chromatography-mass spectrometry with combined derivatisation.

2004

A derivatisation method that combines the formation of ethyl esters from the carboxylic groups and trimethylsilyl ethers from hydroxyl groups of the components of diterpenic resins is presented in this paper. This methodology involves two experimental steps: (1) formation of ethyl esters using ethyl chloroformate; and (2) the esterified compounds are lead to react with trimethylsilylimidazole to form the corresponding trimethylsilyl ethers. The main advantage of the proposed method is the possibility of performing simultaneously the analysis of amino acids from proteins, fatty acids from drying oils, and diterpenic compounds from natural resins usually found in works of art. This methodolog…

ChromatographySilylationTrimethylsilylChemistryOrganic ChemistryVarnishGeneral Medicineengineering.materialReference StandardsBiochemistryAnalytical Chemistrychemistry.chemical_compoundCanada balsamvisual_artPaintvisual_art.visual_art_mediumengineeringOrganic chemistryEthyl chloroformatePaintingsGas chromatographyGas chromatography–mass spectrometryDiterpenesAbietic acidJournal of chromatography. A
researchProduct

Kaemgalangol A: Unusual seco-isopimarane diterpenoid from aromatic ginger Kaempferia galanga.

2018

Abstract A new unusual seco-isopimarane, kaemgalangol A (1) and 12 usual analogs (2−13) were isolated from the rhizomes of Kaempferia galanga (Family: Zingiberaceae). KaemgalangolA (1) represented a rarely isolated 9,10-seco-isopimarane skeleton. The chemical structures of the isolated compounds were mainlyinvestigated by spectroscopic techniques such as 1D, 2D NMR, and HRMS. The absolute configuration of 1–3 was studied by X-ray diffraction analysis as well as experimental and TDDFT-calculated electronic circular dichroism. Among the isolated diterpenoids, 5, 6 and 9 exhibited cytotoxic activity against HeLa (IC50 75.1, 74.2 and 76.5 μM, respectively) and HSC-2 (IC50 69.9, 53.3 and 58.2 μM…

Circular dichroismStereochemistry01 natural sciencesHeLaZingiberaceaeDrug DiscoveryKaempferia galangaHumansPharmacologybiologyMolecular Structure010405 organic chemistryChemistryAbsolute configurationGeneral Medicinebiology.organism_classificationAntineoplastic Agents PhytogenicTerpenoid0104 chemical sciencesRhizome010404 medicinal & biomolecular chemistryZingiberaceaeDiterpenesTwo-dimensional nuclear magnetic resonance spectroscopyRhizomeHeLa CellsFitoterapia
researchProduct

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
researchProduct

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
researchProduct

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
researchProduct

Betulin binds to melanocortin receptors and antagonizes alpha-melanocyte stimulating hormone induced cAMP generation in mouse melanoma cells.

2007

Betulin is a principal component of birch bark and is known to possess a broad range of biological activities, including antiinflammatory, antiviral and anticancer actions. The present study was carried out in vitro to clarify the influence of betulin on melanocortin (MC) receptor-ergic signalling by using COS-7 cells transfected with corresponding human MC receptor DNA. The results showed that betulin binds to the human melanocortin MC1, three to five receptors with selectivity to the MC1 subtype (K(i) value 1.022 +/- 0.115 microM). Betulin binds to the MC receptors with the following potency order-MC > MC3 > MC5 > MC4. Betulin itself does not stimulate cAMP generation, however, it slightl…

Clinical BiochemistryBiologyBiochemistryBinding Competitivechemistry.chemical_compoundMiceBetulinic acidChlorocebus aethiopsCyclic AMPAnimalsHumansReceptorMelanomaBetulinReceptors MelanocortinCell BiologyGeneral MedicineTransfectionIn vitroalpha-Melanocyte-stimulating hormoneTriterpenesKineticsBiochemistrychemistryCell culturealpha-MSHCOS CellsMelanocortinCell biochemistry and function
researchProduct

Metabolism of polychlorinated norbornenes by Clostridium butyricum.

1972

STUDIES of the metabolism of cyclodien-insecticides, such as dieldrin, endrin, endosulphan, have revealed valuable information about their fate in the ecosystem1. With all metabolites identified so far, however, the hexachlorinated norbornene moiety remains unchanged2,3. Only from photodieldrin, a cage-like derivative of dieldrin, have dechlorinated metabolites been reported4,5.

ClostridiumMultidisciplinarybiologyChemical PhenomenaStereochemistryTerpenesMetabolismbiology.organism_classificationNorbornanesPhotodieldrinchemistry.chemical_compoundDieldrinChemistrychemistryBiochemistryEndrinMoietyChlorineDerivative (chemistry)Clostridium butyricumNorborneneNature
researchProduct