0000000000449972

AUTHOR

Sergio Rosselli

showing 181 related works from this author

The Diterpenoids of the Genus Marrubium (Lamiaceae)

2006

The occurrence and chemical structures of labdane diterpenoids from the genus Marrubium are reviewed and the published 13C NMR spectroscopic data for these compounds is presented. The pharmacological activities and biogenesis of these diterpenoids are also reported.

Pharmacologybiology010405 organic chemistryPlant ScienceGeneral Medicinebiology.organism_classification01 natural sciences0104 chemical sciencesLabdane010404 medicinal & biomolecular chemistrychemistry.chemical_compoundComplementary and alternative medicinechemistryGenusDrug DiscoveryBotanyLamiaceaeMarrubiumNatural Product Communications
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Lipase-catalysed preparation of acyl derivatives of the germacranolide cnicin

2009

Several acyl derivatives of cnicin were obtained through lipase-catalysed acylation and alcoholysis reactions. In most reactions lipases showed a regioselective behaviour affording only one product. Longer chain acyl derivatives were prepared at lower temperature than the used in lipase-catalysed reactions, to preclude side products formation. The enzymatic approach let to prepare a family of novel acetyl and fatty acid derivatives of cnicin which are not obtainable following traditional organic synthetic procedures. Fil: Monsalve, Leandro Nicolas. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Ciudad Universitaria. Unidad de Microanálisis…

GermacranolideTriacylglycerol lipaseBioengineeringBiochemistryCnicinCatalysisEnzyme catalysisAcylationchemistry.chemical_compoundOrganic chemistryLipasechemistry.chemical_classificationbiologyENZYME CATALYSISChemistryProcess Chemistry and TechnologyCiencias QuímicasRegioselectivityALCOHOLYSISCNICINACYLATIONSESQUITERPENOIDSEnzymeQuímica Orgánicabiology.proteinCIENCIAS NATURALES Y EXACTAS
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Volatile constituents of Calamintha origanifolia boiss. Growing wild in Lebanon

2007

The essential oil of aerial parts of Calamintha origanifolia Boiss. (Lamiaceae), growing wild in Lebanon, was obtained by hydrodistillation and was analysed by GC and GC-MS. 49 compounds, representing 92.2% of the oil, were identified. The major components, belonging to the class of oxygenated monoterpenes, were pulegone (22.5%), isomenthone (12.2%) and piperitenone (9.6%). The oil showed a slight antimicrobial activity against three bacterial strains.

Pharmacology010404 medicinal & biomolecular chemistryComplementary and alternative medicine010405 organic chemistryDrug DiscoveryBotanyPlant ScienceGeneral MedicineBiologybiology.organism_classification01 natural sciencesCalamintha0104 chemical sciences
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Essential oil compositions of Teucrium fruticans, T. scordium subsp. scordioides and T. siculum growing in Sicily and Malta

2020

In the present study, the chemical composition of the essential oils from the aerial parts of Teucrium fruticans L. collected in Sicily and Malta, Teucrium scordium subsp. scordioides (Schreb.) Arcang. and Teucrium siculum (Raf.) Guss., collected in Sicily, were evaluated by GC-MS. The main volatile components of both T. fruticans collections were germacrene D (29.4% and 50.0%), (E)-β-caryophyllene (19.6% and 21.9%), and 1-octen-3-ol (19.7% and 7.4%); T. scordium subsp. scordioides essential oil was rich in caryophyllene oxide (25.8%), α-pinene (19.4%) and β-pinene (8.5%); T. siculum essential oil was rich in (E)-β-caryophyllene (30.9%), 1-octen-3-ol (9.0%), α-humulene (8.6%) and germacrene…

Teucrium ssp.Organic ChemistryVolatile componentsSettore CHIM/06 - Chimica OrganicaPlant ScienceBiology1-Octen-3-olbiology.organism_classificationBiochemistryAnalytical Chemistrylaw.inventionChemotaxonomyTeucrium(E)-β-CaryophylleneCaryophyllene oxidelawBotanyTeucrium scordiumSettore BIO/15 - Biologia FarmaceuticaGermacrene DEssential oilGermacrene DNatural Product Research
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Floral scent in Iris planifolia (Iridaceae) suggests food reward

2018

Iris species can adopt different pollination strategies to attract their pollinators, generalized shelter-mimicking, specialized deceptive sexual-mimicking or food-rewarding. As attractive stimuli, Iris flowers may use their colours, large-size, symmetry, and volatile organic compounds (VOCs). However, relatively few studies in- vestigated Iris floral olfactory cues in the context of plant-visitor/pollinator interactions. In the present study we combined the identification of the floral volatiles of the nectariferous I. planifolia with insects visiting its flowers to gather data on its biology. Floral volatiles were collected in the natural environment by dynamic headspace and analysed by g…

0106 biological sciencesHoney beeInsectaPollinationIris Plantmedia_common.quotation_subjectHover flieContext (language use)Plant ScienceInsectFlowersHorticultureBiologyAnisoles01 natural sciencesBiochemistryGas Chromatography-Mass SpectrometryIridaceaeHoney BeesPollinatorBotanyAnimalsDynamic headspacePollinationMolecular BiologyIris planifoliamedia_commonVolatile Organic CompoundsAromatic compound010405 organic chemistryfungifood and beveragesGeneral MedicineSettore CHIM/06 - Chimica OrganicaBees0104 chemical sciencesIridaceaeBumble beeItalyFloral scentSettore BIO/03 - Botanica Ambientale E ApplicataIris planifoliaGC-MS010606 plant biology & botany
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Composition and allelopathic effect of essential oils of two thistles: Cirsium creticum (Lam.) D.�Urv. ssp. triumfetti (Lacaita) Werner and Carduus n…

2007

Abstract Cirsium and Carduus are two of the main genera of true thistles. Different species in these genera share a quantity of secondary metabolites and have interesting ecological properties. The essential oils of two species, Cirsium creticum and Carduus nutans, were analysed, showing the presence as main compounds of 4-ethyl guaiacol (15%), hexadecanoic acid (10.6%), (E)-β-damascenone (7.8%), dihydroactinidiolide (6.0%) and 4-vinyl guaiacol (4.5%) for C. creticum and hexadecanoic acid (18.6%), hexahydrofarnesylacetone (7.8%), heptacosane (5.9%), 4-vinyl guaiacol (5.8%), pentacosane (3.8%) and eugenol (3.6%) for C. nutans. The oils were evaluated at different doses for their effect on ge…

biologyfood and beveragesRaphanusCarduus nutansLactucaPlant Sciencebiology.organism_classificationlaw.inventionEugenolchemistry.chemical_compoundCirsiumchemistrylawBotanyCarduusEcology Evolution Behavior and SystematicsEssential oilAllelopathy
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Chemical composition and antimicrobial activity of the essential oil from aerial parts of Micromeria fruticulosa (Bertol.) Grande (Lamiaceae) growing…

2007

The essential oil of aerial parts of Micromeria fruticulosa (Lamiaceae) growing wild in Southern Italy was obtained by hydrodistillation and analysed by GC and GC–MS. Sixty-one compounds, representing 91.3% of the oil, were identified. The major components were γ-terpinene (14.5%), β-caryophyllene (12.6%), p-cymene (8.9%), α-pinene (8.2%) and β-bisabolene (7.2%). The essential oil showed action mainly against Gram-positive bacteria. Copyright © 2007 John Wiley & Sons, Ltd.

p-CymenebiologyCaryophylleneGeneral Chemistrybiology.organism_classificationTerpenoidlaw.inventionMicromeriaSteam distillationchemistry.chemical_compoundchemistrylawBotanyLamiaceaeEssential oilFood ScienceAntibacterial agent
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Chemical composition of the essential oils of Centaurea sicana and C. giardinae growing wild in Sicily

2008

The essential oils of Centaurea sicana (S) and C. giardinae (G) were studied by GC and GC-MS. Thirty constituents for S, representing 81.5% of the total oil, and 24 compounds for G (94.2% of the total) were identified. The oils were rich in sesquiterpenoids (47.9% for S and 54.7% for G) and hydrocarbons (25.9% for S and 31.7% for G). Germacrene D (13.3%), ( E)-β-farnesene (8.3%), nonacosane (7.3%), heptacosane (6.5%) and phytol (6%) were recognized as the main constituents for S, while caryophyllene oxide (17.7%), nonacosane (14.5%), germacrene D (11.5%), caryophyllene (11.2%) and heptacosane (10.3%) were the main compounds for G.

Pharmacologyfood.ingredientbiologyChemistryPlant ScienceGeneral MedicineAsteraceaebiology.organism_classificationSicanalaw.inventionfoodComplementary and alternative medicineCaryophyllene oxideCentaurealawDrug DiscoveryBotanyCentaurea giardinaeChemical compositionEssential oilGermacrene D
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Sesquiterpene lactones of Anthemis alpestris

2002

chemistry.chemical_compoundbiologychemistryAnthemideaeBotanyAnthemidinaeAnthemisAsteraceaebiology.organism_classificationSesquiterpeneBiochemistryEcology Evolution Behavior and SystematicsBiochemical Systematics and Ecology
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Photoinduced functionalization of diterpenes: transformation of the C-20 methyl of atractyligenin into a carbomethoxymethyl or carbamoylmethyl group

2003

Abstract Irradiation of the nor-diterpene atractyligenin 1a and of its methyl ester 1b at λ=254 nm in methanol or in methanol in the presence of nitrogen nucleophiles such as ammonia or methylamine gave, besides the decarboxylation product 2, the ester 3a or the amides 3b, 3c, respectively, providing the transformation of the C-20 angular methyl into a carbomethoxymethyl or carbamoylmethyl group. A photochemical pathway involves formation of C-19/C-20 bond in the excited state, followed by a collapse into a ketene intermediate which will capture the nucleophilic reagent.

MethylamineDecarboxylationGeneral Chemical EngineeringGeneral Physics and AstronomyKeteneGeneral ChemistryMedicinal chemistrychemistry.chemical_compoundAmmoniachemistryNucleophileReagentOrganic chemistryMethanolDiterpeneJournal of Photochemistry and Photobiology A: Chemistry
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Anti-HIV Agents Derived from the ent-Kaurane Diterpenoid Linearol

2002

Twenty-six semisynthetic ent-kaurane derivatives of linearol (1) have been investigated for their anti-HIV effects. Five compounds (4, 7, 11, 25, and 26) showed significant activity against HIV replication in H9 lymphocyte cells with EC(50) values in the range <0.1-3.11 microg/mL. With TI values of 163 and 184, compounds 4 and 25 are especially promising for further development as potential anti-HIV agents.

Magnetic Resonance SpectroscopyAnti-HIV AgentsStereochemistryLymphocyteEnt kaurane diterpenoidHuman immunodeficiency virus (HIV)Pharmaceutical ScienceBiologymedicine.disease_causeAnalytical Chemistrychemistry.chemical_compoundDrug DiscoverymedicineCombinatorial Chemistry TechniquesHumansLymphocytesPharmacologyMolecular StructureAnti hivOrganic ChemistryHIVbiology.organism_classificationIn vitroTerpenoidmedicine.anatomical_structureComplementary and alternative medicinechemistryLentivirusSideritisMolecular MedicineDiterpenesDiterpeneJournal of Natural Products
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Advances on the chemistry of furano-diterpenoids from Teucrium genus

2005

This paper updates the previous reviews, reporting the results published in the last six years on the chemistry of these diterpenoids.

PharmacologyLamiaceaebiologyStereochemistryChemistryOrganic ChemistryneoclerodanediterpenoidGeneral Medicinefuroclerodanebiology.organism_classificationAnalytical ChemistryTeucriumTeucriumTerpeneGenusBotanyLamiaceae
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Volatile constituents of aerial parts ofCentaurea sibthorpii(Sect. Carduiformes, Asteraceae) from Greece and their biological activity

2008

The volatile constituents of the aerial parts of Centaurea sibthorpii [Sect. Carduiformes, Asteraceae] collected in Greece were extracted by hydrodistillation and analysed by GC and GC-MS. Altogether 63 components were identified. Fatty acids and sesquiterpenoidic compounds were the most abundant components in the oil. A study on the biological activity of the oil showed no action against Gram-positive and Gram-negative bacteria.

Chromatography GasCentaureaMicrobial Sensitivity TestsPlant ScienceGram-Positive BacteriaBiochemistryGas Chromatography-Mass SpectrometryAnalytical Chemistrylaw.inventionlawGram-Negative BacteriaCentaurea sibthorpii essential oil (E)-beta-farneseneBotanyOils VolatilePlant OilsEssential oilGreecebiologyFatty AcidsOrganic ChemistryBiological activityPlant Components AerialAsteraceaebiology.organism_classificationCentaureacyclosativene fatty acids antimicrobial activityNatural Product Research
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Volatile Components from Aerial parts of Centaurea gracilenta and C. ovina ssp. besserana Growing Wild in Bulgaria

2011

The essential oils of Centaurea gracilenta Velen. (CG) and C. ovina Pall. ex Willd. ssp. besserana (DC.) Dostál (COB) growing wild in Bulgaria, were studied by GC and GC-MS. Forty-five compounds for CG, representing the 90.1% of the oil, and 68 compounds for COB, representing the 91.9% of the oil, were identified. The oils were rich in sesquiterpenoids (33.4% for CG and 27.3% for COB), hydrocarbons (28.3% for CG and 10.7% for COB) and carbonylic compounds (12.7% for CG and 13.1% for COB). Fatty acids were abundant only for COB (31.3%). β-Eudesmol (12.8%), nonacosane (11.8%) and p-vinyl guiacol (7.5%) were recognized as the main constituents for CG, while hexadecanoic acid (21.4%), spathule…

PharmacologybiologyNonacosanePlant ScienceGeneral Medicinebiology.organism_classificationSpathulenolchemistry.chemical_compoundComplementary and alternative medicineCaryophyllene oxidechemistryCentaureaDrug DiscoveryBotanyNatural Product Communications
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Chemical composition of essential oil from Italian populations of Artemisia alba Turra (Asteraceae).

2012

The use of essential oils as chemotaxonomic markers could be useful for the classification of Artemisia species and to caracterize biodiversity in the different populations. An analysis of the chemical composition of four essential oils from Italian populations of Artemisia alba Turra (collected in Sicily, Marche and Abruzzo) was investigated. In this paper an in depth study of the significant differences observed in the composition of these oils is reported.

BiodiversityPharmaceutical ScienceGas Chromatography-Mass SpectrometryArticleessential oilAnalytical Chemistrylaw.inventionArtemisia albalawDrug DiscoveryBotanyOils VolatilePlant OilsSettore BIO/15 - Biologia FarmaceuticaPhysical and Theoretical ChemistryChemical compositionArtemisia alba; essential oil; biodiversity; α-bisabolone oxide A; davanone DEssential oilα-bisabolone oxide AbiologyEcologyOrganic Chemistryfood and beveragesdavanone DSettore CHIM/06 - Chimica OrganicaBiodiversityAsteraceaebiology.organism_classificationArtemisiaItalyChemistry (miscellaneous)MonoterpenesMolecular MedicineArtemisia<em>Artemisia alba</em>; essential oil; biodiversity; α-bisabolone oxide A; davanone DMolecules (Basel, Switzerland)
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The Essential Oil Compositions of Three Teucrium Taxa Growing Wild in Sicily: HCA and PCA Analyses

2021

The chemical composition and the qualitative and quantitative variability of the essential oils of three taxa belonging to the Teucrium genus were studied. The investigated taxa, that grow wild in Sicily, were Teucrium flavum L. (section Chamaedrys (Mill.) Scheb.), Teucrium montanum and Teucrium capitatum L. of section Polium (Mill.) Scheb. Essential oils were extracted by hydrodistillation and analyzed by GC-MS. In total, 74 compounds were identified. Sesquiterpene hydrocarbons were found to be the main group for T. flavum (48.3%). T. capitatum consisted essentially of monoterpene hydrocarbons (72.7%), with &alpha

MonoterpeneTeucrium flavum L.Pharmaceutical ScienceBiologySesquiterpene01 natural sciencesessential oilArticleGas Chromatography-Mass SpectrometryAnalytical Chemistrylaw.inventionTeucriumlcsh:QD241-441Teucriumchemistry.chemical_compoundlcsh:Organic chemistrySpecies SpecificityGenuslawDrug DiscoveryBotanyOils VolatileCluster AnalysisPlant OilsPhysical and Theoretical ChemistryTeucrium montanum L.Chemical compositionessential oilsSicilyEssential oilPCAPrincipal Component Analysis<i>Teucrium flavum</i> L.010405 organic chemistryOrganic ChemistryPlant Components Aerialbiology.organism_classification<i>Teucrium capitatum</i> L.<i>Teucrium montanum</i> L.0104 chemical sciences010404 medicinal & biomolecular chemistrychemotaxonomychemistryTeucrium capitatum L.Chemistry (miscellaneous)ChemotaxonomyMolecular MedicineComposition (visual arts)GC-MSMolecules
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Guaianolides from the Aerial Parts of Centaurea Hololeuca

2006

Seven guaianolides were isolated from the acetone extract of the aerial parts of Centaurea hololeuca Boiss. The antifeedant activity of the natural compounds (1–7) and of four chloro derivatives (8–11), synthesized from repin (1) and janerin (3) were tested against larvae of Spodoptera littoralis. Cebellin J (6) and chlorojanerin (11) showed significant antifeedant activity at 100 ppm, whereas at this concentration cebellin G (4) and 15-deschloro-15-hydroxychlorojanerin (7) stimulated feeding. Cebellin G (4) stimulated larvae of S. littoralis to feed at low concentration, but deterred feeding at high concentrations. The addition of chlorine to repin (1) resulted in an increase in antifeeda…

0106 biological sciencesPharmacologybiologyChemistryPlant ScienceGeneral Medicinebiology.organism_classification010603 evolutionary biology01 natural sciencesComplementary and alternative medicineCentaureaDrug DiscoveryBotany010606 plant biology & botanyNatural Product Communications
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The Diterpenoids of the Genus Elaeoselinum (Apiaceae) and their Biological Properties

2008

The natural kaurane, beyerane and atisane diterpenoids isolated from the genus Elaeoselinum (Apiaceae)and their semi-synthetic derivatives are reviewed. Published 13C NMR spectroscopic data and biological properties of these diterpenes are also reported.

ApiaceaebiologyGenusElaeoselinumChemistryBiological propertyOrganic ChemistryBotanyditerpenoids Eleoselinum biological propertiesSettore BIO/15 - Biologia Farmaceuticabiology.organism_classificationCurrent Organic Chemistry
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Anthemis wiedemanniana essential oil prevents LPS-induced production of NO in RAW 264.7 macrophages and exerts antiproliferative and antibacterial ac…

2012

Anthemis wiedemanniana is known in folk medicine for the treatment of microbial infections, cancer and also urinary and pulmonary problems. In this study, the chemical composition of the essential oil from A. wiedemanniana was evaluated and its antibacterial activity was tested against 10 bacterial strains. The oil was also tested for its potentiality to inhibit nitric oxide production in RAW 264.7 macrophages and for its cytotoxicity against four human cancer cell lines. A. wiedemanniana oil, rich of oxygenated monoterpenes (25.4%), showed a good antibacterial activity against Gram-positive bacteria and a good activity against the two Gram-negative bacteria, Escherichia coli and Proteus vu…

Anthemis wiedemanniana essential oil antiproliferative activity antibacterial activityLipopolysaccharidesProteus vulgarisPlant ScienceMicrobial Sensitivity Testsmedicine.disease_causeGram-Positive BacteriaBiochemistryAnalytical ChemistryNitric oxideMicrobiologylaw.inventionCell Linechemistry.chemical_compoundMicelawCell Line TumormedicineEscherichia coliOils VolatileAnimalsHumansAnthemisSettore BIO/15 - Biologia FarmaceuticaCytotoxicityEscherichia coliEssential oilNitritesCell ProliferationbiologyOrganic ChemistrySettore CHIM/06 - Chimica Organicabiology.organism_classificationProteusAntineoplastic Agents PhytogenicAnti-Bacterial AgentschemistryMonoterpenesAnthemisAntibacterial activityBacteriaNatural product research
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Acid-induced rearrangement of epoxygermacra-8,12-olides: synthesis and absolute configuration of guaiane and eudesmane derivatives from artemisiifolin

2010

A study on the acid-induced rearrangement of 4,5-epoxy- and 1,10-epoxygermacra-8,12-olides was carried out. From a 4,5-epoxy derivative, guaianes were obtained, whereas 1,10-epoxy derivatives furnished, depending on the stereochemistry of the C-1/C-10 epoxy ring, trans-5β,10α- or trans-5α,10β-eudesmanolides.

Derivative (finance)ChemistryStereochemistryvisual_artOrganic ChemistryAbsolute configurationvisual_art.visual_art_mediumsynthetic methods terpenoids rearrangement cyclization natural productsEpoxySettore CHIM/06 - Chimica OrganicaPhysical and Theoretical ChemistryRing (chemistry)Terpenoid
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Essential oil composition and antifeedant properties of Bellardia trixago (L.) All. (sin. Bartsia trixago L.) (Scrophulariaceae)

2008

biologyantifeedantScrophulariaceaeSettore CHIM/06 - Chimica Organicabiology.organism_classificationBiochemistryBellardia trixago Bartsia trixago essential oil antifeedant ovipositionEssential oillaw.inventionBartsia trixagolawBellardia trixagoBotanyBellardia trixagoComposition (visual arts)Settore BIO/15 - Biologia FarmaceuticaovipositionEcology Evolution Behavior and SystematicsEssential oilBartsia
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Antibacterial and Antifungal Activities of Acetonic Extract from Paullinia cupana Mart Seeds

2013

The antibacterial and antifungal activities of the acetone extract from Paullinia cupana var. sorbilis Mart. (Sapindaceae) seeds, commonly called guarana, were assessed against selected bacterial and fungal strains. We tested the extract against both standard American Type Culture Collection (ATCC) and clinically isolated (CI) bacterial strains and three fungal strains. Minimum inhibitory concentration (MIC) and minimum bactericidal concentration (MBC) values for bacteria and MIC and minimum fungicidal concentration for fungi were determined. The extract showed an activity against the nine bacterial strains tested, both CI and ATCC strains (MIC comprised between 32 and 128 μm/mL and MBC bet…

AntifungalAntifungal Agentsmedicine.drug_classPlant ScienceAntibacterial effectMicrobial Sensitivity TestsSapindaceaeAntifungalBiochemistryAnalytical ChemistryMicrobiologyMinimum inhibitory concentrationfoodmedicinePaulliniaPaullinia cupanaMinimum fungicidal concentrationSettore BIO/15 - Biologia FarmaceuticaPaullinia cupanaMinimum bactericidal concentrationbiologyTraditional medicinePlant ExtractsOrganic ChemistrySettore CHIM/06 - Chimica Organicabiology.organism_classificationfood.foodAnti-Bacterial AgentsAntibacterialSeedsBacteria
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Chemical Composition and Antimicrobial Activity of the Essential Oil from Flowers of Eryngium triquetrum (Apiaceae) Collected Wild in Sicily

2016

The chemical composition of the essential oil from flowers of Eringium triquetrum Vahl. collected in Sicily was evaluated by GC and GC-MS. The main components were pulegone (50.6%), piperitenone (30.5%) and menthone (7.0%). Comparison of this oil with other studied oils of Eringium species is discussed. The oil showed good antibacterial and antifungal activities against some microorganisms that infest historical art works.

EryngiumFlowersPlant Science01 natural scienceslaw.inventionchemistry.chemical_compoundAnti-Infective AgentslawPulegoneVolatile componentDrug DiscoveryBotanyOils VolatilePlant OilsEryngium triquetrumPiperitenoneSettore BIO/15 - Biologia FarmaceuticaSicilyChemical compositionEssential oilPharmacologyApiaceaeBacteriabiology010405 organic chemistryMenthone.Drug Discovery3003 Pharmaceutical ScienceFungiSettore CHIM/06 - Chimica OrganicaGeneral MedicineComplementary and Alternative Medicine2708 Dermatologybiology.organism_classificationAntimicrobialEryngium triquetrumMenthone0104 chemical sciences010404 medicinal & biomolecular chemistryComplementary and alternative medicinechemistryTriquetrumPulegoneApiaceaeNatural Product Communications
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Phytochemical analysis ofAchillea ligusticaAll. from Lipari Island (Aeolian Islands)

2016

A complete chemical investigation of Achillea ligustica All. growing at Lipari (Aeolian Island, Sicily) has been carried out. Seventeen metabolites have been isolated and characterised from dichloromethane and methanol extracts of flowers and aerial parts, and GC/MS analyses of petroleum ether extracts was carried out, revealing a composition in sesquiterpenoids similar to those reported for populations from Greece, Sicily and Algeria, showing the presence of (3RS,6RS)-2,6-dimethyl-1,7-octadiene-3,6-diol (1), 2,6-dimethyl-octa-3(E),7-diene-2,6-diol (2), iso-seco-tanapartholide (3) from DCM fraction. In addition from the methanolic extract of the aerial parts, peculiar flavonoid glucuronides…

Magnetic Resonance SpectroscopyAchilleaAchillea ligusticaPhytochemicalsFlavonoidPlant Science01 natural sciencesBiochemistryAnalytical Chemistrychemistry.chemical_compoundterpenoidsachillea ligustica; asteraceae; chemotaxonomy; flavonoids; phytochemistry; terpenoidsPetroleum etherSettore BIO/15 - Biologia FarmaceuticaApigeninSicilyIslandschemistry.chemical_classificationMolecular Structureachillea ligusticaAchilleaPhytochemicalFlowerChemotaxonomyQuercetinterpenoidfood.ingredientFlowersPhytochemicalBiologyGas Chromatography-Mass SpectrometryIslandPlant ExtractfoodBotanyasteraceaePlant Extracts010405 organic chemistryOrganic ChemistrySettore CHIM/06 - Chimica OrganicaPlant Components AerialAsteraceaebiology.organism_classificationTerpenoid0104 chemical scienceschemotaxonomy010404 medicinal & biomolecular chemistrychemistryflavonoidsFlavonoidphytochemistryNatural Product Research
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ChemInform Abstract: Further Furoclerodanes from Teucrium “maghrebinum”

2010

Two more pairs of C-12 epimeric neoclerodanes were isolated from the aerial parts of Teucrium “maghrebinum” (Teucriumpolium subspecies still unidentified). They are the known teukotschyn 1, the new 12-epi-teukotschyn 2, the new teughrebin 3 and the new 12-epi-teughrebin 4. The structures of the new products were elucidated mainly by spectroscopic methods.

TerpeneTeucriumbiologyChemistryBotanyGeneral MedicineSubspeciesbiology.organism_classificationChemInform
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Neoclerodanes from Teucrium orientale

2004

Abstract Two new neoclerodane diterpenoids, 6-deacetyl-teucrolivin A (5) and 8beta-hydroxy-teucrolivin B (6), were isolated from the aerial parts of Teucrium orientale, along with four already known neoclerodane diterpenoids, teucrolivin A (1), teucrolivin B (2), teucrolivin C (3) and teucrolivin H (4), previously isolated from Teucrium oliverianum. Their structures were elucidated on the basis of spectroscopic evidence and chemical transformations. Compounds 1-3 were assayed for antifeedant activity against Spodoptera littoralis, S. frugiperda and Heliocoverpa armigera. Teucrolivin A was the most potent of the three compounds tested.

LamiaceaeMagnetic Resonance SpectroscopyLamiaceae Teucrium orientale structure elucidation neo-clerodane diterpenoid antifeedant activityTraditional medicinebiologyStereochemistryChemistryMolecular ConformationTeucrium oliverianumGeneral ChemistryFeeding BehaviorGeneral MedicineSettore CHIM/06 - Chimica OrganicaSpodopterabiology.organism_classificationDiterpenes ClerodaneTerpeneLarvaDrug DiscoveryTeucrium orientaleAnimalsLamiaceaeChromatography Thin LayerSettore BIO/15 - Biologia FarmaceuticaSpodoptera littoralis
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Chemical composition of the essential oil from Thapsia garganica L. (Apiaceae) grown wild in Sicily and its antimicrobial activity.

2015

In this study, the chemical composition of the essential oil from flowers and leaves of Thapsia garganica L. collected in Sicily was evaluated by GC and GC-MS. The main components of T. garganica flower oil (T.f.) were chamazulene (58.3%), humulene oxide II (9.0%), tricosane (8.2%) and pentacosane (8.2%). Also the oil from leaves (T.l.) was characterised by high content of chamazulene (49.2%). Other abundant metabolites were 1,4-dimethylazulene (18.5%), (E)-phytol (6.3%) and neophytadiene (5.1%). The comparison with other studied oils of genus Thapsia is discussed. Antimicrobial activity against several micro-organisms, including some ones infesting historical art craft, was also determined.

Anti-Infective AgentAntifungal Agentshumulene oxide IIPlant Science01 natural sciencesThapsia garganicaBiochemistrylaw.inventionAnalytical Chemistrychemistry.chemical_compoundAnti-Infective AgentslawAntifungal AgentSettore BIO/15 - Biologia FarmaceuticaChemical compositionSicilyThapsia1-dimethylazulenebiologyHumuleneChemistryMicrobial Sensitivity TestchamazuleneAntimicrobialThapsia (plant)Anti-Bacterial Agentsvolatile componentFlowerPlant LeaveThapsia garganicaFlowersMicrobial Sensitivity TestsGas Chromatography-Mass SpectrometryBotanyAnti-Bacterial AgentOils VolatileEssential oilApiaceaeantimicrobial activityBacteria010405 organic chemistryChamazuleneOrganic ChemistryFungiSettore CHIM/06 - Chimica Organicabiology.organism_classification0104 chemical sciencesPlant Leaves010404 medicinal & biomolecular chemistryApiaceaeNatural product research
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Fixed oil from seeds of narrow-leaved ash (F. angustifolia subsp. angustifolia): Chemical profile, antioxidant and antiproliferative activities.

2019

Fraxinus angustifolia subsp. angustifolia is a plant with an age-old use for the production of manna. However, it is also a valuable source of fixed oil rich-seeds. In the present study we examined the chemical and biological properties of this oil in order to support a possible application in foodstuffs, nutraceuticals and cosmetics. Fatty acid composition, volatile and phenolic substances were evaluated. Oleic and linoleic acid represented 45.5% and 50.0%, respectively, of the total fatty acid composition. Among polar phenolic substances identified (secoiridoids, phenylethanoid glycosides, phenolic acids and alcohols, flavonoids, coumarins) isoverbascoside is for the first time reported i…

PolyphenolAntioxidant030309 nutrition & dieteticsLinoleic acidmedicine.medical_treatmentFixed oilAntiproliferative activityFraxinus angustifoliaAntioxidantsSettore BIO/01 - Botanica Generale03 medical and health scienceschemistry.chemical_compound0404 agricultural biotechnologyNutraceuticalAntioxidant activityGlucosidesPhenolsBiological propertymedicineHydroxybenzoatesOils VolatilePlant OilsSettore BIO/15 - Biologia FarmaceuticaFood scienceFraxinus angustifolia subsp. angustifoliachemistry.chemical_classificationFlavonoids0303 health sciencesABTSbiologyPlant ExtractsSettore BIO/02 - Botanica SistematicaFatty AcidsGlycosideMelanoma AmelanoticSettore CHIM/06 - Chimica Organica04 agricultural and veterinary sciencesPhenylethanoidFatty acidbiology.organism_classification040401 food sciencechemistrySeedsVolatile substancesFood ScienceOleic AcidFood research international (Ottawa, Ont.)
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Guaianolides and lignans from the aerial parts of Centaurea ptosimopappa.

2006

The genus Centaurea L. (Asteraceae, tribe Cardueae, subtribe Centaureinae) comprises ca. 600 species distributed in Asia, Europa, North Africa and America (Hickey and King, 1981; Heywood, 1979). Turkish flora numbers 187 species, 114 of which being endemic (Davis, 1975; Davis et al., 1988; Wagenitz et al., 1988; Guner et al., 2000; Duran and Duman, 2000; Turkoglu et al., 2003). Centaurea ptosimopappa Hayek is an endemic species distributed in the Mediterranean and South-Eastern Anatolian regions of Turkey; widespread and locally frequent in the Amanos and Casus mountains (Davis, 1975; Reeves and Adiguzel, 2004). Aerial parts of C. ptosimopappa were collected in Hatay, the Amanos Mountain ab…

Mediterranean climatebiologyGenusCentaureaBotanyCentaureinaeAsteraceaebiology.organism_classificationTribe (biology)Centaurea ptosimopappaEndemismBiochemistryEcology Evolution Behavior and Systematics
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Cytotoxic activity of some natural and syntetic sesquiterpene lactones

2006

Several natural and synthetic sesquiterpene lactones with different skeletons were tested and found to be active against nine cancer cell lines. Elemane (4), heliangolane (5) and their hydroxy analogues 9 and 10, all containing an α,β-unsaturated aldehyde substituent, were the most potent compounds.

StereochemistrySubstituentPharmaceutical ScienceCentaureaPharmacognosySesquiterpeneAldehydeANTITUMOR AGENTSAnalytical Chemistrychemistry.chemical_compoundInhibitory Concentration 50LactonesStructure-Activity RelationshipCell Line TumorDrug DiscoveryStructure–activity relationshipOrganic chemistryCytotoxic T cellHumansCENTAUREA-PAUICytotoxicityPharmacologychemistry.chemical_classificationBiological ProductsMolecular StructureDERIVATIVESOrganic ChemistryCNICINSettore CHIM/06 - Chimica OrganicaAntineoplastic Agents PhytogenicComplementary and alternative medicinechemistryMolecular MedicineSesquiterpenesLactone
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Graphene oxide-silica nanohybrids as fillers for PA6 based nanocomposites

2014

Graphene oxide (GO) was prepared by oxidation of graphite flakes by a mixture of H2SO4/H3PO4 and KMnO4 based on Marcano's method. Two different masterbatches containing GO (33.3%) and polyamide-6 (PA6) (66.7%) were prepared both via solvent casting in formic acid and by melt mixing in a mini-extruder (Haake). The two masterbatches were then used to prepare PA6-based nanocomposites with a content of 2% in GO. For comparison, a nanocomposite by direct mixing of PA6 and GO (2%) and PA6/graphite nanocomposites were prepared, too. The oxidation of graphite into GO was assessed by X-ray diffraction (XRD), Micro-Raman spectroscopy, scanning electron microscopy (SEM), X-ray photoelectron spectrosco…

Materials scienceNanocompositeScanning electron microscopeGrapheneOxideAnalytical chemistryNanoparticleCastinglaw.inventionchemistry.chemical_compoundChemical engineeringX-ray photoelectron spectroscopychemistrylawgraphene oxide silica nanohybrids PA6GraphiteAIP Conference Proceedings
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Ferulago nodosa Subsp. geniculata (Guss.) Troia &amp; Raimondo from Sicily (Italy): Isolation of Essential Oil and Evaluation of Its Bioactivity

2020

Ferulago nodosa (L.) Boiss. (Apiaceae) is a species occurring in the Balkan-Tyrrhenian area. The object of the present study is Sicilian F. nodosa subsp. geniculata (Guss.) Troia & Raimondo, classified as an endemic F. nodosa subspecies. Aerial parts of this plant species were subjected to hydrodistillation to obtain an essential oil. A total of 93 compounds were identified with 2,3,6-trimethyl benzaldehyde (19.0%), spathulenol (9.0%), (E)-caryophyllene (5.4%), and caryophyllene oxide (5.4%) as the main components. The biological activities of F. nodosa essential oil were also investigated. This oil showed an interesting antioxidant potential in a 2,2′-Azino-bis(3-ethylbenzothiazoline-6-sul…

obesityantioxidantPharmaceutical ScienceFerulago nodosaSubspeciesAntioxidant potential030226 pharmacology & pharmacy01 natural sciencesArticleessential oilAnalytical Chemistrylaw.inventionlcsh:QD241-44103 medical and health scienceschemistry.chemical_compound0302 clinical medicinelcsh:Organic chemistrylawDrug DiscoverySettore BIO/15 - Biologia FarmaceuticaPhysical and Theoretical ChemistryEssential oilApiaceaeABTSdiabetesbiologyTraditional medicineOrganic ChemistrySettore CHIM/06 - Chimica Organicabiology.organism_classificationgas chromatography-mass spectrometry0104 chemical sciences010404 medicinal & biomolecular chemistrychemistryCaryophyllene oxidediabeteChemistry (miscellaneous)Settore BIO/03 - Botanica Ambientale E ApplicataPlant speciesMolecular MedicineMolecules
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Volatile Components of Centaurea Bracteata and C. Pannonica subsp. Pannonica growing wild in Croatia

2010

This paper reports on the volatile components of oils from the aerial parts (CBA) and roots (CBR) of Centaurea bracteata Scop. and aerial parts of C. pannonica (Heuffel) Simonkai subsp. pannonica (CPA), two Asteraceae growing wild in Croatia. The volatile components, obtained by hydrodistillation, were determined by GC-MS analysis. The yields (w/w) of the dried oils were 0.10% (CBA), 0.22% (CBR) and 0.09% (CPA), respectively. A total of 91 compounds were identified accounting for 91.1%, 93.3% and 87.9% of the total oil for CBA, CBR and CPA, respectively. All the samples were characterized mainly by hydrocarbons (7.1-34.1%), fatty acids (9.7-45.9%), and oxygenated sesquiterpenes (15.2-16.6%…

PharmacologyCentaurea bracteatabiologyNonacosanePlant compositionPlant ScienceGeneral MedicineAsteraceaebiology.organism_classificationHorticulturechemistry.chemical_compoundComplementary and alternative medicinechemistryCaryophyllene oxideEnvironmental chemistryDrug DiscoveryGas chromatography–mass spectrometryChemical compositionNatural Product Communications
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Neoclerodane Diterpenoids from Teucrium maghrebinum

2000

Eight neoclerodane diterpenoids were identified in the extract of the aerial parts of Teucrium maghrebinum. Three of these, 12-epi-teucjaponin A (1), 12-epi-montanin D (2), and 12-epi-montanin B (3), are new natural products, whereas five, teucjaponin A, montanin D, 19-deacetylteuscorodol, teusalvin C (4), and montanin B, are already known. These eight compounds form four pairs of epimers at carbon C-12.

Pharmacologychemistry.chemical_classificationFolk medicineLamiaceaeMagnetic Resonance SpectroscopyMolecular StructurebiologyStereochemistryOrganic ChemistryPharmaceutical SciencePharmacognosybiology.organism_classificationMass SpectrometryTerpenoidAnalytical ChemistryTeucriumchemistry.chemical_compoundComplementary and alternative medicinechemistryDrug DiscoveryMolecular MedicineEpimerDiterpenesDiterpeneLactoneJournal of Natural Products
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ChemInform Abstract: Photoinduced Functionalization of the C-20 Methyl Group of the Nor-diterpene Atractyligenin.

2010

Abstract Irradiation of the nor-diterpene atractyligenin at λ =254 nm in methanol gave, on one hand, the decarboxylation product, and provided, on the other hand, the transformation of the C-20 angular methyl into a methylene-carbomethoxy group. A photochemical pathway involving formation of C-19/C-20 bond is suggested.

Terpenechemistry.chemical_compoundDecarboxylationChemistryStereochemistrySurface modificationGeneral MedicineMethanolDiterpeneAtractyligeninMethyl groupChemInform
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NMR-based quantification of rosmarinic and carnosic acids, GC-MS profile and bioactivity relevant to neurodegenerative disorders of Rosmarinus offici…

2013

Abstract A comparative study of phytochemicals content and biological properties of eight Rosmarinus officinalis (rosemary) populations (RO1–RO8) collected in different areas of Tunisia was carried out. Two of the main rosemary constituents, rosmarinic and carnosic acids, were quantified by an NMR technique. Carnosic acid content was higher than that of rosmarinic acid. The non-polar constituents were examined by GC and GC–MS. Total phenols and flavonoids content were also determined in order to discuss the possible correlation between these phytochemicals and bioactivity. Antioxidant activity was investigated through different in vitro assays. Sample RO3 from a sub-humid area showed the hi…

rosmarinic acidAntioxidantDPPHmedicine.medical_treatmentMedicine (miscellaneous)Rosmarinuschemistry.chemical_compoundAntioxidant activitymedicineAnticholinesterese activityTX341-641Settore BIO/15 - Biologia FarmaceuticaPhenolscarnosic acidNutrition and DieteticsABTSChromatographybiologyChemistryNutrition. Foods and food supplyRosmarinic acidCarnosic acidSettore CHIM/06 - Chimica OrganicaRosmarinic and carnosic acidsbiology.organism_classificationNMRBiochemistryRosmarinic and carnosic acidOfficinalisRosmarinus officinalisneurodegenerative disorderPhytochemicals contentFood Science
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A novel approach to prevent graphene oxide re-aggregation during the melt compounding with polymers

2015

Abstract The technology for the preparation of polymer-GO nanocomposites was investigated by studying the structure-properties relationships of two different systems, based on PA6 and EVA, fabricated by using different preparation methods, i.e. melt mixing, wet phase inversion, and the combination of the two. The morphology of nanocomposites resulted dramatically influenced by the technique adopted and showed to be the critical variable affecting the physical properties of the materials. Finally, the mechanical and dynamic-mechanical of the nanocomposites were improved by using the hybrid technique combining the two procedures.

Dynamic mechanical thermal analysis (DMTA); Graphene; Interphase; Polymer-matrix composites (PMCs); Raman spectroscopy; Engineering (all); Ceramics and CompositesPolymer-matrix composites (PMCs)Materials scienceOxidelaw.inventionchemistry.chemical_compoundsymbols.namesakeEngineering (all)lawComposite materialInterphasechemistry.chemical_classificationDynamic mechanical thermal analysis (DMTA)NanocompositeMelt mixingGrapheneGeneral EngineeringPolymerSettore ING-IND/22 - Scienza E Tecnologia Dei MaterialichemistryCompoundingRaman spectroscopyCeramics and CompositessymbolsGrapheneRaman spectroscopyPhase inversionComposites Science and Technology
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Solid state 13C-NMR methodology for the cellulose composition studies of the shells of Prunus dulcis and their derived cellulosic materials.

2020

Lignocellulosic fibers and microcellulose have been obtained by simple alkaline treatment from softwood al- mond shells. In particular, the Prunus dulcis Miller (D.A.) Webb. was considered as a agro industrial waste largely available in southern Italy. The materials before and after purification have been characterized by 13C CPMAS NMR spectroscopy methodology. A proper data analysis provided the relative composition of lignin and holo- cellulose at each purification step and the results were compared with thermogravimetric analysis and FT-IR. To value the possibility of using this material in a circular economy framework, the fibrous cellulosic material was used to manufacture a handmade c…

Thermogravimetric analysisSoftwoodMaterials sciencePolymers and PlasticsAlmond shell Cellulose13C CP MAS NMR02 engineering and technology010402 general chemistry01 natural sciencesLigninIndustrial wastechemistry.chemical_compoundMaterials ChemistrySettore ICAR/13 - Disegno IndustrialeLigninNutsSettore CHIM/01 - Chimica AnaliticaRecyclingFiberSettore BIO/15 - Biologia FarmaceuticaCelluloseCarbon-13 Magnetic Resonance SpectroscopyCelluloseWaste ProductsOrganic Chemistrycardboard021001 nanoscience & nanotechnologyPulp and paper industryPrunus dulcis0104 chemical sciencesHandmade cardboard MicrocelluloseSettore AGR/03 - Arboricoltura Generale E Coltivazioni ArboreePrunus dulcisSettore ING-IND/22 - Scienza E Tecnologia Dei MaterialichemistryCellulosic ethanolvisual_artvisual_art.visual_art_medium0210 nano-technologyCarbohydrate polymers
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Labdane Diterpenoids from Marrubium globosum ssp. libanoticum

2006

From the aerial parts of Marrubium globosum ssp. libanoticum, seven labdane diterpenoids were isolated. Three of them are new natural products [(13R)-9alpha,13alpha-epoxylabda-6beta(19),16(15)-diol dilactone (2), deacetylvitexilactone (7), marrulanic acid (8)], whereas the other four, namely, (13S)-9alpha,13alpha-epoxylabda-6beta(19),16(15)-diol dilactone (1), cyllenin A (3), 15-epi-cyllenin A (4), and marrulibanoside, are previously known compounds. The structures of 2, 7, and 8 were determined by spectroscopic and chemical methods.

StereochemistryLEONURUSPharmaceutical SciencePharmacognosyAnalytical ChemistryLabdanechemistry.chemical_compoundDrug DiscoveryBotanyLebanonNuclear Magnetic Resonance BiomolecularPharmacologychemistry.chemical_classificationFolk medicinePlants MedicinalMolecular StructurebiologyOrganic Chemistrybiology.organism_classificationTerpenoidComplementary and alternative medicinechemistryMolecular MedicineDiterpenesDiterpeneLactoneMarrubiumMarrubiumJournal of Natural Products
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Sesquiterpene lactones and other constituents of three Cardueae from Cyprus

2001

chemistry.chemical_compoundchemistrybiologyBotanyCentaurea aegialophilaCardopatium corymbosumAsteraceaeSesquiterpenebiology.organism_classificationBiochemistryEcology Evolution Behavior and SystematicsBiochemical Systematics and Ecology
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Furostanol saponins and ecdysones with cytotoxic activity from Helleborus bocconei ssp. intermedius

2009

Two furostanol saponins helleboroside A (1) and helleboroside B (2) were isolated from the methanol extract of Helleborus bocconei Ten. subsp. intermedius (Guss.) Greuter and Burdet, along with the furospirostanol saponin 4 and two ecdysones: ecdysterone (5) and polypodyne B (6). Compound 2 was enzymatically hydrolysed to give product 3. The biological activity of all compounds was tested against rat C6 glioma cells showing a significant cytotoxicity for compounds 3, 4 and 6. Copyright © 2009 John Wiley & Sons, Ltd.

EcdysoneStereochemistryHelleborusSaponinRanunculaceaePharmacognosyCell Linefurostanol saponinC6 glioma cellAnimalsSettore BIO/15 - Biologia FarmaceuticaMedicinal plantsCytotoxicitycytotoxic activityPharmacologychemistry.chemical_classificationMolecular StructureTraditional medicinebiologyPlant ExtractsGlycosideBiological activitySettore CHIM/06 - Chimica OrganicaSaponinsbiology.organism_classificationAntineoplastic Agents PhytogenicRatsHelleborusSterolschemistryH. bocconei subsp. intermediuRanunculaceae
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Cytotoxic geranylflavonoids from Bonannia graeca

2011

The analysis of the aerial parts of Bonannia graeca led to the isolation and characterization of two new polar geranylated flavonoids (6 and 7). The structure elucidation was performed by extensive spectroscopic methods (1D and 2D NMR) and comparison with literature data. All natural flavonoids isolated from B. graeca (1–7) and some synthetic derivatives (8–11) were tested for cytotoxic activity against four human tumor cell lines. Preliminary structure-activity relationship correlations are discussed.

Synthetic derivativesStereochemistryChemical structurePlant ScienceHorticultureBiochemistryArticleStructure-Activity RelationshipBonannia graecaCell Line TumorHumansCytotoxic T cellStructure–activity relationshipSettore BIO/15 - Biologia FarmaceuticaGeranylflavonoidsMolecular BiologyFlavonoidsApiaceaeMolecular StructurebiologyCytotoxic activityfungiEuphorbiaceaefood and beveragesGeneral MedicineSettore CHIM/06 - Chimica OrganicaPlant Components Aerialbiology.organism_classificationAntineoplastic Agents PhytogenicHuman tumorTwo-dimensional nuclear magnetic resonance spectroscopyApiaceae
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Chemical Composition and antimicrobial activity of the essential oils from two species of Thimus growing wild in southern Italy

2009

The volatile constituents of the aerial parts of two samples of Thymus longicaulis C. Presl, collected in Campania and in Sicily, and two samples of Thymus pulegioides L. from the same regions, were extracted by hydrodistillation and analyzed. Considering the four oils together, seventy-eight different compounds were identified: 57 for Thymus longicaulis from Sicily (91.1% of the total oil), 40 for Thymus longicaulis from Campania (91.5% of the oil), 39 for Thymus pulegioides from Sicily (92.5% of the oil) and 29 for Thymus pulegioides from Campania (90.1% of the oil). The composition of the oils is different, although the most abundant components are identical in T. pulegioides. The essent…

<em>Thymus longicaulis</em> C. Presl; <em>Thymus pulegioides </em>L.; essential oil composition; thymol; geraniol; antibacterial activityThymus pulegioidesPharmaceutical ScienceMicrobial Sensitivity TestsArticleAnalytical Chemistrylcsh:QD241-441Thymus Plantchemistry.chemical_compoundlcsh:Organic chemistryantibacterial activitythymolDrug DiscoveryBotanyOils VolatilePlant OilsThymus PlantSettore BIO/15 - Biologia FarmaceuticaPhysical and Theoretical ChemistrygeraniolThymolChemical compositionessential oil compositionThymus longicaulisbiologyBacteriaThymus pulegioides L.Organic ChemistrySettore CHIM/06 - Chimica Organicabiology.organism_classificationAntimicrobialAnti-Bacterial AgentschemistryItalyantimicrobial activity essential oils Thimus longicaulis Thimus pulegioidesChemistry (miscellaneous)Molecular MedicineComposition (visual arts)Thymus longicaulis C. PreslGeraniol
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The first example of natural cyclic carbonate in terpenoids

2006

Abstract The first natural occurring cyclic carbonate terpenoid, the guaianolide hololeucin ( 1 ), was isolated from the aerial part of Centaurea hololeuca . Its structure was elucidated on the basis of extensive proton, 13 C and two-dimensional NMR experiments, as well as by transformation in its diacetyl derivative.

StereochemistryOrganic ChemistrySESQUITERPENE LACTONESBiochemistryDiacetylTerpenoidGUAIANOLIDESchemistry.chemical_compoundchemistryDrug DiscoveryOrganic chemistryCarbonateCONSTITUENTSDerivative (chemistry)Tetrahedron Letters
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Volatile constituents of aerial parts of three endemicCentaureaspecies from Turkey:Centaurea amanicolaHub.-Mor.,CentaureaconsanguineaDC. andCentaurea…

2008

The volatile constituents of the aerial parts of Centaurea amanicola Hub.-Mor., Centaurea consanguinea DC. and Centaurea ptosimopappa Hayek were extracted by hydrodistillation and analysed by GC and GC–MS. Altogether 94 components were identified. Sesquiterpenoids, fatty acids and carbonylic compounds were the most abundant components in the oils. Hexadecanoic acid and (Z,Z )-9,12-octadecadienoic acid were the main fatty acids in all the examined samples, that showed different patterns of composition. The study on the biological activity of the oils showed an action mainly against the Gram-positive pathogens.

biologyCentaurea consanguineaOrganic ChemistryPharmacology toxicologyPlant Sciencebiology.organism_classificationBiochemistryAnalytical Chemistrylaw.inventionlawCentaureaBotanyCentaurea ptosimopappaEssential oilNatural Product Research
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Minor diterpenoids from Scutellaria polyodon.

2000

Four minor neoclerodane diterpene constituents were isolated from the aerial parts of Scutellaria polyodon. These compounds were characterized as the new scupolins J (1) and K (2) and the previously known scutalpin O (3) and scutalsin.

PharmacologybiologyMolecular StructureChemistryStereochemistrySpectrum AnalysisOrganic ChemistryPharmaceutical SciencePlantsbiology.organism_classificationTerpenoidAnalytical Chemistrychemistry.chemical_compoundComplementary and alternative medicineDrug DiscoveryScutellariaMolecular MedicineHemiacetalDiterpeneDiterpenesJournal of natural products
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Monoterpene derivatives from the flowers of Ferulago campestris, (Apiaceae).

2013

Ferulago campestris (Besser) Grec., (Ferula galbanifera (Mill) Kock. = F. campestris), finocchiazzo, is an annual or perennial herb of the Mediterranean area. In this paper the phytochemical studies of the CH2Cl2 and MeOH extracts of the flowers are described. Several ferulol derivatives and a new 10-hydroxy-verbenone ester (7) were isolated. The structure of the new compound was established by extensive NMR analysis, including HMBC and HSQC pulse sequences.

ApiaceaeMagnetic Resonance SpectroscopybiologyPlant ExtractsMonoterpeneOrganic Chemistry10-hydroxy-verbenone esterEstersPlant ScienceNuclear magnetic resonance spectroscopySettore CHIM/06 - Chimica OrganicaFlowersPerennial herbbiology.organism_classificationBiochemistryFerulago campestrisAnalytical ChemistryPhytochemicalBotanyMonoterpenesMediterranean areaSettore BIO/15 - Biologia Farmaceuticaferulol derivativeFerulago campestriApiaceaeNatural product research
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Conformational analysis and DFT calculations of 8α-hydroxy-germacradiene-6,12-olide derivatives

2005

The Systematic Conformational Search Analysis (SCSA) code was employed to study the conformational properties of the 8α-hydroxy-germacradiene-6,12-olide isomers. This procedure was extended to the trans,cis- and trans,trans-1(10),4-isomers of 8α,15-dihydroxy-germacradiene-6,12-olides and 8α-hydroxy-15-oxo-germacradiene-6,12-olides, to investigate structural and energetic analogies between these and the 8α-hydroxy-germacradiene-6,12-olide species. The calculated 13C NMR spectra, at the hybrid DFT mPW1PW91 level, showed a sound correlation with the corresponding experimental spectra, providing a valid support to the reliability of the calculated structures and to the consistence of our confor…

CrystallographyChemistryComputational chemistryOrganic ChemistryPhysical and Theoretical ChemistryCarbon-13 NMRSpectral lineJournal of Physical Organic Chemistry
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A new irregular diterpenoid of biogenetic interest from the flowers of Magydaris tomentosa (Desf.) DC. (Apiaceae)

2007

A new irregular acyclic diterpene, magytomol acetate (2), has been isolated from the light petroleum extract of the flowers of Magydaris tomentosa (Desf.) DC. (Apiaceae) and its structure has been elucidated by means of extensive spectroscopic experiments. The new compound can be considered the acetyl derivative of the biogenetic precursor of other irregular diterpenes isolated from other species belonging to the family Apiaceae.

PharmacologyApiaceaebiology010405 organic chemistryChemistryPlant ScienceGeneral Medicinebiology.organism_classification01 natural sciencesTerpenoid0104 chemical sciences010404 medicinal & biomolecular chemistryComplementary and alternative medicineDrug DiscoveryBotanyMagydaris
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Antifeedant activity of neo-clerodane diterpenoids from Teucrium fruticans and derivatives of fruticolone

1999

The antifeedant activity of three neo-clerodane diterpenoids, fruticolone, isofruticolone and fruticolide from Teucrium fruticans was assessed using larvae of Spodoptera littoralis. Isofruticolone was one of the most potent of the Teucrium derived neo-clerodanes. Chemical modification of functional groups on fruticolone showed that its activity could be enhanced.

biologyStereochemistryBiological activityPlant ScienceGeneral MedicineHorticulturebiology.organism_classificationBiochemistryTerpenoidTeucriumchemistry.chemical_compoundchemistryNoctuidaeDiterpeneSpodoptera littoralisMolecular BiologyPhytochemistry
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Cytotoxic Activity of Some Natural and Synthetic ent-Kauranes

2007

Atractyligenin (1) and several synthetic derivatives were tested and found to be active against tumor cell replication. Compound 1 was readily converted to the 2,15-diketo (3) or 15-keto (4) derivatives, which contain an alpha,beta-unsaturated ketone. Compounds 3 and 4 showed significant cytotoxic activity against all six tested cancer cell lines and were most potent against 1A9 ovarian cancer cells with EC50 values of 0.2 and 0.3 microM, respectively. These two 1-analogues are promising lead compounds for further investigation.

KetoneStereochemistryPharmaceutical ScienceAsteraceaeAtractylosideBiologyANTITUMOR AGENTSAnalytical Chemistrychemistry.chemical_compoundDrug DiscoveryTumor Cells CulturedHumansCytotoxic T cellCytotoxicityOvarian NeoplasmsPharmacologychemistry.chemical_classificationLamiaceaePlants MedicinalMolecular StructureDERIVATIVESOrganic ChemistryBiological activityAntineoplastic Agents PhytogenicTerpenoidIn vitroComplementary and alternative medicinechemistryBiochemistryCell cultureMolecular MedicineFemaleDrug Screening Assays AntitumorDiterpeneDiterpenes KauraneJournal of Natural Products
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The Diterpenoids from the Genus Hyptis (Lamiaceae)

2009

The genus Hyptis (family Lamiaceae) is known mainly for the essential oils isolated from the aerial parts of several species. Less known are the diterpenoids, extracted from a limited number of species. In consideration of the interest for the structures of this class of compounds, largely occurring in the whole Lamiaceae family, the present paper means to review and update their chemistry. Also the use of many species of Hyptis in folk-medicine is reported.

PharmacologyFamily LamiaceaebiologyHyptisOrganic ChemistrySettore CHIM/06 - Chimica Organicabiology.organism_classificationTerpenoidAnalytical ChemistryLabdanechemistry.chemical_compoundchemistryHyptis Lamiaceae diterpenoidsGenusBotanyLamiaceaeAbietaneHETEROCYCLES
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The Cytotoxic Properties of Natural Coumarins Isolated from Roots ofFerulago campestris(Apiaceae) and of Synthetic Ester Derivatives of Aegelinol

2009

Grandivittin (1), agasyllin (2), aegelinol benzoate (3) and felamidin (20), four natural coumarins isolated from Ferulago campestris, and several synthetic ester derivatives of aegelinol (4) were tested against four tumor cell lines. Some of them were shown to be marginally cytotoxic against the A549 lung cancer cell line.

PharmacologyEster derivativesfood.ingredientApiaceaeStereochemistryPlant compositionPlant ScienceGeneral MedicineBiologybiology.organism_classificationFerulago campestrisFerulagofoodComplementary and alternative medicineDrug DiscoveryCytotoxic T cellOrganic chemistryNatural Product Communications
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Metabolites from the Aerial Parts of the Sicilian Population of Artemisia alba

2013

Phytochemical investigation of the CH2Cl2 extract of the aerial parts of Artemisia alba Turra afforded one new irregular sesquiterpenoid, artemiric acid, and five known metabolites: hydroxydavanone, the coumarins isofraxidin and scopoletin, (6 S*,7 S*,10 R*)–6,10-dimethyl-7,10-epoxyocta-11-enoic acid and artalbic acid. From the MeOH extract three flavonoids were identified: chrysoeriol, quercetin and isorhamnetin. The possible biogenetic pathways of artemiric and artalbic acids are discussed.

Pharmacologyeducation.field_of_studybiologyIsofraxidinPopulationPlant ScienceGeneral MedicineAsteraceaeChrysoeriolbiology.organism_classificationchemistry.chemical_compoundComplementary and alternative medicinechemistryPhytochemicalScopoletinDrug DiscoveryBotanyArtemisiaeducationIsorhamnetinNatural Product Communications
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Volatile constituents of Scutellaria rubicunda Hornem subsp. linnaeana (Caruel) Rech. (Lamiaceae) endemic in Sicily

2006

PharmacologybiologyTraditional medicineCaryophylleneOrganic ChemistryVolatileScutellaria rubicunda HornemPharmaceutical Sciencebiology.organism_classificationBiochemistrylaw.inventionAnalytical Chemistrychemistry.chemical_compoundLinaloolchemistryComplementary and alternative medicinelawDrug DiscoveryBotanyScutellariaMolecular MedicineLamiaceaeSpodoptera littoralisEcology Evolution Behavior and SystematicsEssential oilPlanta Medica
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Essential oil composition of the fruits of Periploca laevigata Aiton subsp. angustifolia (Labill.) Markgraf (Apocynaceae – Periplocoideae)

2011

The essential oil of the fruits of Periploca laevigata Aiton subsp. angustifolia (Labill.) Markgraf (Apocynaceae) from Lampedusa Island was obtained by hydrodistillation and its composition was analysed. The analyses allowed the identification and quantification of 64 volatile compounds belonging to different classes. The most abundant compounds were nonacosane, heptacosane, hentriacontane and δ-cadinene. Among the volatile compounds identified in the fruits of P. laevigata subsp. angustifolia, 31 are present in other taxa of Apocynaceae, 19 have antimicrobial activity and four are pheromones for the butterfly Danaus chrysippus. The possible ecological role of the volatile compounds found i…

Settore BIO/07 - EcologiaNonacosanePlant ScienceBiochemistryPheromonesessential oilAnalytical Chemistrylaw.inventionchemistry.chemical_compoundpheromoneAnti-Infective AgentslawBotanyAlkanesOils VolatileDanaus chrysippusEssential oilHentriacontanePeriplocabiologyApocynaceaeOrganic ChemistrySettore CHIM/06 - Chimica Organicabiology.organism_classificationHydrocarbonsApocynaceaeTaxonSettore AGR/11 - Entomologia Generale E ApplicatachemistrySex pheromoneFruitvolatile componentsSettore BIO/03 - Botanica Ambientale E ApplicataantimicrobialPeriplocoideae
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Hand-made paper obtained by green procedure of cladode waste of Opuntia ficus indica (L.) Mill. from Sicily

2019

Cellulosic fibres have been obtained by green procedures from the cladodes of Opuntia ficus indica (L.) Mill., constituting a large agro industrial waste in our territory. The materials have been analysed for its relative composition, applying, IR and TG methodologies and it was characterised by the absence of lignin. The fibrous material allowed the manufacture of a handmade paper obtaining an ecological material suitable for packaging purposes. The authors evidenced that the simple protocol based on hot water treatment was able to decrease the amount of hemicellulose in the final material.

CactaceaeOpuntia ficusPlant Science01 natural sciencesBiochemistryIndustrial wasteAnalytical Chemistrychemistry.chemical_compoundSettore ICAR/13 - Disegno IndustrialeCladodesLigninHemicelluloseSettore BIO/15 - Biologia FarmaceuticaCelluloseOpuntia ficus indicaSettore CHIM/02 - Chimica Fisicabiology010405 organic chemistrypaperOrganic ChemistrySettore CHIM/06 - Chimica Organicabiology.organism_classificationPulp and paper industrycellulose0104 chemical sciencesSettore AGR/03 - Arboricoltura Generale E Coltivazioni Arboree010404 medicinal & biomolecular chemistrychemistryCellulosic ethanolEnvironmental science
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Flavonoids from Teucrium fruticans L.

2014

From aerial parts of &lt;em&gt;Teucrium fncticans&lt;/em&gt; L. three flavonoids were isolated and identified as 5-hydroxy-6, 7, 3', 4'-tetramethoxyflavone, 5, 4'-dihydroxy-6, 7, 3'-trimethoxyflavone (cirsilineol) and 5, 4'-dihydroxy-6, 7-dimethoxyflavone (cirsimaritin). The former compound was found to be a predominant flavone aglycone constituent of the plant material. This is the first report on the isolation of flavonoids from the plant.

chemistry.chemical_classificationLamiaceaebiologyTraditional medicinePlant Sciencebiology.organism_classificationFlavonesCirsilineollcsh:QK1-989Teucriumchemistry.chemical_compoundAglyconeflavoneschemistryTeucrium fruticansflavonoid compoundslcsh:BotanyLamiaceae
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Effects of air pollution on production of essential oil in Feijoa Sellowiana Berg. grown in the "Italian triangle of death"

2010

The composition of the essential oils of fruits from Feijoa sellowiana grown in the district of Acerra is compared with those collected from unpolluted sites. Essential oils from the fruits of F. sellowiana were analysed by GC/MS. Sixty compounds, representing 96.6% and 97.8% (unpolluted site and Acerra site, respectively) of the oils, were identified. The major constituents were β-caryophyllene (12.4% and 16.8%), ledene (9.6% and 11.1%), α-humulene (6.3% and 8.2%), β-elemene (4.9% and 5.3%) and δ-cadinene (4.7% and 5.2%) in the control site and Acerra site, respectively. The antioxidant components were increased in response to polluted condition. The acetonic extracts of F. sellowiana from…

PollutionAntioxidantAcerramedicine.medical_treatmentmedia_common.quotation_subjectair pollutionAir pollutionmedicine.disease_causeFlavoneslaw.inventionFeijoa sellowianalawBiomonitoringBotanymedicineessential oilsmetabolitesEssential oilGeneral Environmental Sciencemedia_commonchemistry.chemical_classificationbeta-caryophyllenebiologyChemistryMyrtaceaePublic Health Environmental and Occupational HealthFeijoa sellowiana essential oils oil composition beta-caryophyllene Acerra biomonitoring air pollution air quality metabolites Italy.Settore CHIM/06 - Chimica Organicabiology.organism_classificationair qualityHorticultureItalyoil compositionbiomonitoringComposition (visual arts)Feijoa sellowiana essential oil composition beta-caryophyllene
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A Review of the Phytochemistry, Traditional Uses, and Biological Activities of the Genus Ballota and Otostegia

2019

AbstractThe 2 genera Ballota and Otostegia, belonging to the Lamiaceae family, are closely related taxonomically and found mainly in the Mediterranean area, Middle East, and North Africa. Since ancient times, they have been largely employed in traditional medicine for their biological properties such as antimicrobial, anti-inflammatory, antispasmodic, insecticidal, anti-malaria, etc. Phytochemical investigations of Ballota and Otostegia species have revealed that diterpenoids are the main constituents of the genera. A large number of flavonoids and other metabolites were also identified. This review, covering literature from 1911 up to 2018, includes traditional uses, chemical profiles (bot…

OtostegiaantioxidantPhytochemistryfood.ingredientPharmaceutical Sciencesecondary metabolite01 natural sciencesAnalytical ChemistryfoodGenusBiological propertyDrug DiscoveryAnimalsHumansSettore BIO/15 - Biologia FarmaceuticaPharmacologyLamiaceaebiologyTraditional medicinePlant Extracts010405 organic chemistryOrganic ChemistrySettore CHIM/06 - Chimica OrganicaBallotabiology.organism_classification0104 chemical sciencesantibacterial010404 medicinal & biomolecular chemistryTaxonComplementary and alternative medicinePhytochemicalMolecular MedicineLamiaceaeMedicine TraditionalOtostegiaBallotaantifungalPhytotherapyPlanta Medica
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Ceiba speciosa (A. St.-Hil.) Seeds Oil: Fatty Acids Profiling by GC-MS and NMR and Bioactivity

2020

This study aimed to evaluate the chemical composition by gas chromatography-mass spectrometry (GC-MS) and Nuclear Magnetic Resonance (NMR) analyses, the antioxidant activities evaluated by different in vitro assays namely 2,2-diphenyl-1-picrylhydrazyl (DPPH), 2,2&prime

obesityAntioxidantantioxidantDPPHLinoleic acidmedicine.medical_treatmentMalvalic acidPharmaceutical Science01 natural sciencesArticleAnalytical ChemistryPalmitic acidlcsh:QD241-441chemistry.chemical_compound0404 agricultural biotechnologylcsh:Organic chemistryfixed oilDrug DiscoverymedicineSettore BIO/15 - Biologia FarmaceuticaPhysical and Theoretical ChemistryLipaseChromatographyABTSbiologydiabetesOrganic Chemistry04 agricultural and veterinary sciencesSettore CHIM/06 - Chimica Organicabiology.organism_classification040401 food scienceNMR0104 chemical sciences010404 medicinal & biomolecular chemistrychemistryChemistry (miscellaneous)diabetebiology.proteinMolecular MedicineGC-MSCeiba speciosaMolecules
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Essential oils composition of two Sicilian cultivars of Opuntia ficus-indica (L.) Mill. (Cactaceae) fruits (prickly pear).

2013

The essential oils composition of the skin, pulp and seeds from fruits of two Sicilian cultivars of Opuntia ficus-indica (cv. Sanguigna and cv. Surfarina) has been obtained by hydrodistillation and the possible antioxidant, antimicrobial and semiochemical roles have been investigated comparing the data with those reported in the literature. The presence of antioxidants and antimicrobials found in this study increases the spectrum of compounds that have beneficial properties in O. ficus-indica. In addition, several compounds identified in this study have been reported to influence the behaviour of Ceratitis capitata, a phytophagous pest which causes severe damages to several crops including …

Settore BIO/07 - EcologiaantioxidantChromatography GasPlant ScienceBiologyengineering.materialBiochemistryessential oilAntioxidantsGas Chromatography-Mass SpectrometryAnalytical ChemistryAnti-Infective AgentsBotanyOils VolatilePlant OilsCultivarSemiochemicalSicilyDistillationPEARMolecular StructurePulp (paper)fungiOrganic Chemistryfood and beverageskairomonesOpuntiaCeratitis capitataSettore CHIM/06 - Chimica OrganicaCeratitis capitataAntimicrobialbiology.organism_classificationSettore AGR/11 - Entomologia Generale E ApplicataKairomoneFruitSettore BIO/03 - Botanica Ambientale E ApplicataengineeringantimicrobialPEST analysisNatural product research
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Essential Oil Composition of Tanacetum vulgare Subsp. Siculum (Guss.) Raimondo et Spadaro (Asteraceae) from Sicily

2009

Ninety-four components of the essential oils from aerial parts and capitula of Tanacetum vulgare subsp. siculum (Guss.) Raimondo et Spadaro were detected. α-Thujone, β-thujone and 1,8-cineole were the main constituents of the oils. The analysis allows the assignment of this Tanacetum species to the thujone chemotype.

PharmacologybiologyChemotypePlant ScienceGeneral MedicineAsteraceaebiology.organism_classificationlaw.inventionchemistry.chemical_compoundEucalyptolComplementary and alternative medicinechemistrylawDrug DiscoveryBotanyBeta-thujoneComposition (visual arts)ThujoneChemical compositionEssential oilNatural Product Communications
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Artalbic acid, a sesquiterpene with an unusual skeleton from Artemisia alba (Asteraceae) from Sicily

2011

Abstract From the aerial parts of Artemisia alba (Asteraceae) artalbic acid ( 1 ), a sesquiterpene with an unusual skeleton, was isolated. Its structure was elucidated on the basis of extensive proton, 13 C and two-dimensional NMR experiments, as well as by transformation in its methyl ester derivative.

biologyStereochemistryOrganic ChemistrySettore CHIM/06 - Chimica OrganicaAsteraceaeSesquiterpenebiology.organism_classificationBiochemistrySkeleton (computer programming)chemistry.chemical_compoundchemistryDrug DiscoveryArtemisiaSesquiterpene Irregular skeleton Asteraceae Artemisia albaTetrahedron Letters
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Flavonoids in Subtribe Centaureinae (Cass.) Dumort. (Tribe Cardueae, Asteraceae): Distribution and 13C-NMR Spectral Data

2012

Abstract This review reports the occurrence of flavonoids in subtribe Centaureinae of Asteraceae family. It extensively covers the literature up to 2010 and collects all available (13)C-NMR data.

FlavonoidsMagnetic Resonance SpectroscopybiologyPlant compositionCentaureinaeBioengineeringGeneral ChemistryGeneral MedicineAsteraceaeAsteraceaebiology.organism_classificationTribe (biology)BiochemistryBotanyMolecular MedicineSpectral dataMolecular Biology
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Guaianolides from Centaurea babylonica

2005

chemotaxonomyCentaurea babylonicabiologyChemotaxonomyguaianolideBotanysesquiterpene lactoneCentaurea babylonicaAsteraceaeAsteraceaebiology.organism_classificationBiochemistryEcology Evolution Behavior and Systematics
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Further Furoclerodanes fromTeucrium “maghrebinum”

2001

Two more pairs of C-12 epimeric neoclerodanes were isolated from the aerial parts of Teucrium “maghrebinum” (Teucriumpolium subspecies still unidentified). They are the known teukotschyn 1, the new 12-epi-teukotschyn 2, the new teughrebin 3 and the new 12-epi-teughrebin 4. The structures of the new products were elucidated mainly by spectroscopic methods.

TerpeneTeucriumbiologyStereochemistryChemistryOrganic ChemistryNanotechnologyPhysical and Theoretical ChemistrySubspeciesbiology.organism_classificationEuropean Journal of Organic Chemistry
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Functional investigation and applications of the acetylesterase activity of the Citrus sinensis (L.) Osbeck peel

2020

The hydrolysis of acetyl moieties on a set of commercially relevant substrates was performed by employing the whole tissue of Citrus sinensis (L.) Osbeck peel as an efficient biocatalyst in mild reaction conditions with high degree of regioselectivity. The reaction is done in aqueous media and the product is easily recovered. Optimal reaction conditions were deduced and two practical applications were investigated: the elaboration of acetylglicerols and the preparation of vitamin K1 precursor. Peel waste (flavedo and albedo) from orange juice manufacturing was successfully employed as a biocatalyst.

genetic structures010405 organic chemistryChemistryOrganic Chemistryfood and beveragesAcetylesterase activitySettore CHIM/06 - Chimica OrganicaPlant Scienceequipment and supplies01 natural sciencesBiochemistryenzymatic biocatalysi0104 chemical sciencesAnalytical Chemistry010404 medicinal & biomolecular chemistryHydrolysisFood sciencevitamin K1Citrus × sinensisacetate hydrolysiacetinCitrus sinensiNatural Product Research
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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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Effect of Marrubium globosum ssp libanoticum on intestinal motility

2007

PharmacologyTraditional medicinebiologybusiness.industryOrganic ChemistryPharmaceutical Sciencebiology.organism_classificationAnalytical ChemistryIntestinal motilityComplementary and alternative medicineDrug DiscoveryMolecular MedicineMedicinebusinessMarrubium
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Essential Oil Composition of Alluaudia procera and in Vitro Biological Activity on Two Drug-Resistant Models

2019

Drug resistance is a major obstacle in antibiotic and antitumor chemotherapy. In response to the necessity to find new therapeutic strategies, plant secondary metabolites including essential oils (EOs) may represent one of the best sources. EOs in plants act as constitutive defenses against biotic and abiotic stress, and they play an important role in the pharmacology for their low toxicity, good pharmacokinetic and multitarget activity. In this context, natural products such as EOs are one of the most important sources of drugs used in pharmaceutical therapeutics. The aim of this paper was to identify the chemical composition of the essential oil of Alluaudia procera leaves, obtained by hy…

medicine.drug_classAntibioticsPharmaceutical ScienceContext (language use)Drug resistancePharmacologyBiologymedicine.disease_causeSettore BIO/19 - Microbiologia Generaleessential oilAnalytical Chemistrylaw.inventionDidiereaceaelcsh:QD241-44103 medical and health scienceslcsh:Organic chemistryPharmacokineticslawDrug DiscoverymedicineSettore BIO/15 - Biologia FarmaceuticaPhysical and Theoretical ChemistryEssential oilacute myeloid leukemia cell030304 developmental biology0303 health sciences030306 microbiologyAbiotic stressOrganic ChemistryBiological activitySettore CHIM/06 - Chimica Organicasucculent plantsChemistry (miscellaneous)Staphylococcus aureusSettore BIO/03 - Botanica Ambientale E ApplicataSettore BIO/14 - FarmacologiaMolecular MedicineMolecules
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Phytochemical investigation of the needles of Abies nebrodensis (Lojac.) Mattei

2019

Abies nebrodensis (Lojac.) Mattei (Pinaceae) is a species living in a very small population only in a confined area of Sicily. In this study, the dichloromethane extract of the leaves was analyzed. Apart from three already known metabolites namely dehydroabietic acid; maltol; and rheosmin, previously detected in other species of Abies, a lanostane derivative was isolated. Its chemical structure was elucidated by means of extensive spectroscopic methods.

rheosminAbies nebrodensiChemical structurePopulationMaltolPlant Science01 natural sciencesBiochemistryLanostaneAnalytical ChemistrySettore BIO/01 - Botanica Generalechemistry.chemical_compoundOrganic chemistrySettore BIO/15 - Biologia FarmaceuticaAbies nebrodensiseducationeducation.field_of_studymaltolbiology010405 organic chemistrySettore BIO/02 - Botanica SistematicaOrganic ChemistrySettore CHIM/06 - Chimica Organicabiology.organism_classification0104 chemical sciences010404 medicinal & biomolecular chemistrychemistryPhytochemicalPinaceaedehydroabietic acidlanostaneDerivative (chemistry)
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Chemical composition of volatile and fixed oils from of Salvia argentea L. (Lamiaceae) growing wild in Sicily.

2015

The chemical compositions of the essential oil and of the non-polar extracts (petroleum ether, dichloromethane) of the aerial parts (flowers, leaves and stems) of Salvia argentea L. were determined by GC-FID and gas chromatography–mass spectrometry analysis. 14-Hydroxy-α-humulene (40.1%) was recognised as the main constituents of the essential oil of S. argentea, together with 1,3,8-p-menthatriene (12.1%), globulol (7.4%) and β-sesquiphellandrene (5.8%). Tritriacontane (9.9% and 14.1%), heptacosane (8.4% and 10.5%), hentriacontane (8.3% and 10.9%), tetradecanal (8.4% and 10.2%) and methyldotriacontane (7.9% and 7.6%) were recognised as the main constituents of the extracts in petroleum …

SesquiterpeneLinolenic AcidsPlant ScienceSalvia argentea01 natural sciencesBiochemistrylaw.inventionAnalytical ChemistryFatty Acids Monounsaturatedchemistry.chemical_compoundlawfixed oilPetroleum etherSettore BIO/15 - Biologia FarmaceuticaSalviaSicilyHentriacontanebiologyTraditional medicineChemistryvolatile componentPetroleumFlowerParaffinLinolenic AcidPlant LeaveSesquiterpenesLinolenic acidFlowersSalviaGas Chromatography-Mass Spectrometry14-hydroxy-α-humulenePlant ExtractBotanyOils VolatileEssential oilLamiaceae010405 organic chemistryPlant ExtractsOrganic ChemistrySettore CHIM/06 - Chimica Organicabiology.organism_classification0104 chemical sciencesPlant Leaves010404 medicinal & biomolecular chemistrySalvia argenteaSettore BIO/03 - Botanica Ambientale E ApplicataLamiaceaefatty acidGas chromatography–mass spectrometryNatural product research
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Chemical composition and anticancer activity of essential oils of Mediterranean sage (Salvia officinalis L.) grown in different environmental conditi…

2013

Salvia officinalis L. can be found worldwide and its leaves are commonly used as ingredient in food industry. Sage essential oil is applied in the treatment of a range of diseases and has been shown to possess different biological activities. The objectives of our research were to study the effects of environment on crop, chemical composition and anticancer activity on S. officinalis essential oil. Sage was cultivated at eighteen experimental sites in south-central Italy (Molise) in different growing environments. The essential oils (S1-S18), extracted by hydrodistillation, were analyzed by GC and CG/MS. Results show that the main components were α-thujone, camphor, borneol, γ-muurolene and…

Chromatography GasAntineoplastic AgentsToxicologyMass SpectrometryBorneollaw.inventionchemistry.chemical_compoundCamphorfoodlawCell Line TumorBotanyOils VolatileHumansSalvia officinalisEssential oilbiologyTraditional medicineSclareolSAGESalvia officinalisGeneral Medicinebiology.organism_classificationfood.foodchemistryOfficinalisSalvia aethiopisFood ScienceFood and Chemical Toxicology
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Chemical composition of the essential oil from aerial parts of Stachys palustris L. (Lamiaceae) growing wild in Southern Italy

2007

The paper reports the composition of the essential oil from aerial parts of Stachys palustris L. (Lamiaceae) from Southern Italy. The essential oil was extracted by hydrodistillation from selected plants and its chemical composition was determined by the GC-MS system on two fused- silica capillary columns of different polarity. The mass fraction of oil was 0.21 % on a dry weight basis. Altogether, 92 compounds were identified accounting for 93.6 % of the total oil, which was characterized mainly by carbonylic compounds (25.4 %), fatty acids and their esters (24.2 %), along with sesquiterpenoidic compounds (16.0 %) and phenols (11.2 %). The major components of the sample were caryophyllene o…

Stachys palustris; Lamiaceae; essential oil; caryophyllene oxide; hexahydrofarnesyl acetone; GC-MS
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Potential allelopathic activity ofSideritis italica(Miller) Greuter et Burdet essential oil

2011

Sideritis italica (Miller) Greuter et Burdet is a widespread Mediterranean Lamiacea. Essential oils from S. italica flowerheads and leaves were extracted by hydrodistillation and then tested for their potential allelopathic activity against Raphanus sativus L. (Magnoliophyta) and the moss Tortula muralis (Hedw.) (Bryophyta), two organisms already tested for allelopathy, and against two bryophytes growing in the same environment as S. italica: the moss Bryum capillare Hedw. and the liverwort Lunularia cruciata (L.) Dum. For R. sativus, we considered seed germination and root and epicotyl growth. For the mosses, we used spore germination and protonemata development, while for the liverwort, w…

biologySettore CHIM/06 - Chimica OrganicaPlant Sciencebiology.organism_classificationEssential oillaw.inventionThallusRaphanus sativuGerminationlawBryophyteBotanySideritis italicaSpore germinationSideritisEpicotylAllelopathic activitySettore BIO/15 - Biologia FarmaceuticaEcology Evolution Behavior and SystematicsEssential oilAllelopathyLunulariaPlant Biosystems - An International Journal Dealing with all Aspects of Plant Biology
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Essential Oils and Pure Volatile Compounds as Potential Drugs in Alzheimer's Disease Therapy: An Updated Review of the Literature

2016

Background: The use of aromatic plants to relief different illness is not a new therapy. Actually aromatic plants have been used for many centuries by different cultures around the world. Pharmacological studies provide scientific support to the traditional use of aromatic medicinal plants and aromatherapy; nevertheless, more clinical trials are required regarding to their effectiveness in order to establish a guidance for their use in routine healthcare. Moreover, modern medicine in studies about olfactory function has attained great achievements and got Nobel Prize in 2004. These new searches have obviously fueled interest in the essential oils and volatile compounds of natural origin. Se…

Olfactory systemModern medicineBuChEiAChEiAmyloid-β peptideAlzheimer’s diseasePharmacologyBiology01 natural sciencesEssential oillaw.inventionOlfactory mucosaAlzheimer DiseaselawDrug DiscoveryOils VolatilemedicineAnimalsHumansSettore BIO/15 - Biologia FarmaceuticaMedicinal plantsEssential oilPharmacologyVolatile Organic Compounds010405 organic chemistryDrug Discovery3003 Pharmaceutical ScienceSettore CHIM/06 - Chimica Organica0104 chemical sciencesOlfactory bulb010404 medicinal & biomolecular chemistrymedicine.anatomical_structureOdorVolatile compoundAromatherapyCurrent Pharmaceutical Design
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Chemical Composition and Antibacterial Activity of Extracts of Helleborus bocconei Ten. subsp. intermedius

2007

Helleborus bocconei Ten. subsp. intermedius (Ranunculaceae) is a Sicilian medicinal plant used for the treatment of pneumonia affecting cows and horses and for the removal of human decayed molars. The goal of our study was to assess the biological activity of Helleborus bocconei subsp. intermedius by testing its extracts for their activity against bacteria known to cause respiratory diseases. The two more active extracts (light petroleum from roots and aerial parts), as well as the dichloromethane extracts, were analyzed by GC/MS and their composition is reported.

PharmacologyTraditional medicine010405 organic chemistryHelleborusRanunculaceaePlant ScienceGeneral MedicineBiologymedicine.diseasebiology.organism_classification01 natural sciences0104 chemical sciences010404 medicinal & biomolecular chemistryComplementary and alternative medicineDrug DiscoverymedicineAntibacterial activityChemical compositionPneumonia (non-human)Natural Product Communications
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GC and GC-–MS Analysis of Volatile Compounds From Ballota nigra subsp. uncinata Collected in Aeolian Islands, Sicily (Southern Italy)

2020

In the present study, the chemical composition of the essential oils from aerial parts of Ballota nigra subsp. uncinata (Bég.) Patzak collected in Sicily was evaluated by gas chromatography (GC) and GC-mass spectrometry. The main components of the oil were ( E)-phytol (20.0%), α-pinene (9.0%), hexahydrofarnesyl acetone (5.7%), and α-selinene (5.1%). Cluster analysis of the essential oil compositions of all the taxa belonging to B. nigra s.l. group was performed.

Plant Science01 natural sciencesessential oillaw.inventionlawDrug DiscoveryBotanyBallota nigraStachydeaeSettore BIO/15 - Biologia FarmaceuticaChemical compositionEssential oilPharmacologyStachydeaeLamiaceaebiology010405 organic chemistryChemistryGeneral MedicineSettore CHIM/06 - Chimica Organicabiology.organism_classification0104 chemical sciences010404 medicinal & biomolecular chemistryComplementary and alternative medicineAeolian processesLamiaceaeGas chromatographyGas chromatography–mass spectrometryBallota nigra subsp. uncinata(E)-Phytol
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Phytochemical Profile and Apoptotic Activity of Onopordum cynarocephalum.

2012

A phytochemical investigation of acetone and chloroform extracts of the aerial parts of Onopordum cynarocephalum Boiss. et Blanche was carried out. It led to the isolation of two new sesquiterpenes, the elemane aldehyde (2) and the eudesmane (11), together with 15 known compounds: two lignans (1 and 15) and 13 sesquiterpenes (3–10, 12–14, 16, 17). The structures were elucidated by spectroscopic analyses, especially 1D and 2D NMR spectra. The anti-growth effect against three human melanoma cell lines, M14, A375, and A2058, of the different extracts and compounds of O. cynarocephalum was also investigated. Among them, the chloroform extract exhibited the strongest biological activity, while t…

StereochemistryPharmaceutical ScienceApoptosisDNA FragmentationLignansAnalytical Chemistrychemistry.chemical_compoundInhibitory Concentration 50cytotoxic activity Onopordum cynarocephalum Boiss. et BlancheCell Line TumorDrug DiscoveryHumansSesquiterpenes EudesmaneHSP70 Heat-Shock ProteinsFuransArctigeninCell ProliferationPharmacologyLignanChloroformPlants MedicinalbiologyDose-Response Relationship DrugMolecular StructureCaspase 3Plant ExtractsOrganic ChemistryOnopordumPTEN PhosphohydrolaseBiological activityPlant Components AerialAntineoplastic Agents PhytogenicEnzyme assayMonocyclic SesquiterpenesComplementary and alternative medicinePhytochemicalchemistryApoptosisbiology.proteinMolecular MedicineDNA fragmentationSesquiterpenes
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Essential oils composition of Periploca laevigata Aiton subsp. angustifolia (Labill.) Markgraf (Apocynaceae – Periplocoideae)

2012

The essential oil of roots, branches, leaves, flowers and fruits of Periploca laevigata Aiton subsp. angustifolia (Apocynaceae) from Lampedusa Island has been obtained by hydrodistillation and its composition analysed. The analyses allowed the identification and quantification of 86 volatile compounds. Branches showed the higher diversity with 57 compounds followed by fruits with 33, roots with 23, flowers with 16 and leaves with six compounds, respectively. In the matrices examined three constituents, heneicosane, docosane and tricosane are in common, although with different percentages. At least the most abundant compounds found in the matrices have been reported to have several biologica…

Settore BIO/07 - EcologiaAllomoneFlowersPlant ScienceBiologyPlant RootsBiochemistryessential oilPheromonesAnalytical Chemistrylaw.inventionIngredientlawBotanyOils VolatileMedicinal plantsEssential oilsemiochemicals visitorsApocynaceaeHost (biology)Organic ChemistrySettore CHIM/06 - Chimica Organicabiology.organism_classificationApocynaceaePlant LeavesSettore AGR/11 - Entomologia Generale E ApplicataFruitKairomoneSettore BIO/03 - Botanica Ambientale E ApplicatantimicrobialPeriplocoideaeNatural Product Research
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Chemical Composition, In Vitro Antitumor and Pro-Oxidant Activities of Glandora rosmarinifolia (Boraginaceae) Essential Oil

2018

The biological properties of essential oils have been demonstrated in the treatment of several diseases and to enhance the bioavailability of other drugs. In natural habitats the essential oils compounds may play important roles in the protection of the plants as antibacterials, antivirals, antifungals, insecticides and also against herbivores by reducing their appetite for such plants or by repelling undesirable others. We analyzed by gas-chromatography mass spectrometry the chemical composition of the essential oil of aerial parts of Glandora rosmarinifolia (Ten.) D.C. Thomas obtained by hydrodistillation and verified some biological activities on a panel of hepatocellular carcinoma cell …

0301 basic medicineChemical RadicalsAntioxidantmedicine.medical_treatmentMDA-MB-231Cancer Treatmentlcsh:MedicinenaphthoquinoneChemical CompositionBiochemistryPhysical ChemistryditerpeneAntioxidantslaw.invention0302 clinical medicinelawBreast TumorsSUM 149Medicine and Health SciencesBioassaySettore BIO/15 - Biologia FarmaceuticaCytotoxicitylcsh:ScienceMultidisciplinarybiologyTraditional medicineChemistryLiver DiseasesBoraginaceaeBoraginaceaeOxidantsHep3BLipidsChemistryOncology030220 oncology & carcinogenesisPhysical SciencesResearch ArticleHepG2Free RadicalsCell SurvivalGastroenterology and HepatologyCarcinomas03 medical and health sciencesInhibitory Concentration 50Cell Line TumorAromatic HydrocarbonsGastrointestinal TumorsBreast CancermedicineOils VolatileHumansPlant OilsEssential oilcytotoxic activityHA22T/VGH; HepG2; Hep3B; SUM 149; MDA-MB-231; cytotoxic activity; diterpenes; naphthoquinones; plant secondary metabolitesVolatile Organic CompoundsDose-Response Relationship DrugCell growthPlant ExtractsHA22T/VGHlcsh:RChemical CompoundsBiology and Life SciencesCancers and NeoplasmsEpithelial CellsHepatocellular CarcinomaSettore CHIM/06 - Chimica OrganicaPlant Components Aerialbiology.organism_classificationPro-oxidantplant secondary metabolitesAntineoplastic Agents PhytogenicHydrocarbonsBioavailability030104 developmental biologySettore BIO/03 - Botanica Ambientale E ApplicataHepatocytesSettore BIO/14 - Farmacologialcsh:QOils
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Cytotoxic Activity and Composition of Petroleum Ether Extract from Magydaris tomentosa (Desf.) W. D. J. Koch (Apiaceae)

2015

The petroleum ether extract of Magydaris tomentosa flowers (Desf.) W. D. J. Koch has been analyzed by GC-MS. It is mainly constituted by furanocoumarins such as xanthotoxin, xanthotoxol, isopimpinellin, and bergaptene. Other coumarins such as 7-methoxy-8-(2-formyl-2-methylpropyl) coumarin and osthole also occurred. The antiproliferative activity of Magydaris tomentosa flower extract has been evaluated in vitro on murine monocye/macrophages (J774A.1), human melanoma (A375) and human breast cancer (MCF-7) tumor cell lines, showing a major activity against the latter.

AlkanePharmaceutical ScienceAnalytical ChemistryMicechemistry.chemical_compoundxanthotoxinDrug DiscoveryCytotoxic T cellPetroleum etherSettore BIO/15 - Biologia FarmaceuticaCell DeathbiologyTraditional medicineisopimpinellinxanthotoxolFlowerChemistry (miscellaneous)Molecular MedicineHumanIsopimpinellinFlowersCoumarinMagydaris tomentosaGas Chromatography-Mass SpectrometryArticlePlant Extractfuranocoumarinslcsh:QD241-441<i>Magydaris tomentosa</i>ostholelcsh:Organic chemistryCell Line TumorFuranocoumarinAlkanesBotanyAnimalsHumansPhysical and Theoretical Chemistryether extractMagydaris tomentosa; coumarins; furanocoumarins; xanthotoxin; xanthotoxol; isopimpinellin; osthole; bergaptene; MCF-7Cell ProliferationApiaceaecoumarinsAnimalPlant ExtractsOrganic ChemistrySettore CHIM/06 - Chimica Organicabiology.organism_classificationCoumarinIn vitrochemistryMCF-7XanthotoxolMCF-7ApiaceaebergapteneMolecules
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Secondary metabolites from Pinus mugo Turra subsp. mugo growing in the Majella National Park (Central Apennines, Italy).

2013

In this study, we examined the composition regarding secondary metabolites of P. mugo Turra ssp. mugo growing in the protected area of Majella National Park, which is the southernmost station of the habitat of this species. Both the nonpolar and polar fractions were considered. In particular, the essential-oil composition showed a high variety of compounds, and 109 compounds were detected, and 101 were identified, among which abietane-type compounds have a taxonomic relevance. Abietanes were also isolated from the polar fraction, together with an acylated flavonol and a remarkably high amount of shikimic acid.

FlavonolsBioengineeringBiochemistryEssential oilPinus mugoBotanyOils Volatileessential oilsMolecular BiologyEcosystembiologyNational parkChemistryPinus mugoflavonols; diterpenes; essential oils; abietanes; pinus mugoGeneral ChemistryGeneral MedicineSettore CHIM/06 - Chimica Organicabiology.organism_classificationPinusPinus <genus>ItalyAbietanesMolecular MedicineAbietaneDiterpenesDiterpeneFlavonolChemistrybiodiversity
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Volatile constituents of aerial parts of Lasiopogon muscoides

2009

ChemistryLasiopogon muscoides Gnaphaliinae volatile constituentsOrganic chemistrySettore CHIM/06 - Chimica OrganicaSettore BIO/15 - Biologia FarmaceuticaPlant ScienceGeneral ChemistryLasiopogon muscoidesGeneral Biochemistry Genetics and Molecular BiologyChemistry of Natural Compounds
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Phytochemical profile and insecticidal activity of Drimia pancration (Asparagaceae) against adults of Stegobium paniceum (Anobiidae)

2020

Chemical and spectroscopic investigation of the bulbs of Drimia pancration resulted in the isolation of one known flavonol (1), never isolated from this plant species, and of three previously described steroidal saponins (2–4), but whose configuration at their stereogenic centres was not clearly determined. By mean of 1H NMR, 13C NMR, nuclear overhauser effects (NOE) and two-dimensional NMR spectra the full stereochemical structures of compounds 2–4 were proved and all the 1H and 13C signals were assigned. Furthermore, the methanol and butanol extracts of D. pancration were tested against adults of Stegobium paniceum beetles. Despite the non-significant results regarding the repellent activ…

Drimiasteroidal saponinsflavonolStegobium paniceumbiologyTraditional medicine010405 organic chemistryOrganic ChemistryinsecticideSettore CHIM/06 - Chimica OrganicaPlant Sciencebiology.organism_classification01 natural sciencesBiochemistry0104 chemical sciencesAnalytical Chemistry010404 medicinal & biomolecular chemistryAsparagaceaeAnobiidaePhytochemicalDrimia pancrationPlant speciesSettore BIO/15 - Biologia Farmaceutica
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New oxidative derivatives of atractyligenin and their cytotoxic activity

2006

ent-Kauranes are naturally occurring diterpenoids isolated from several families, such as Asteraceae and Lamiaceae. These compounds have attracted interest because of their structures and their biological activities as anti-tumorals, anti-HIV and anti-bacterials [1]. Extensive chemical work [2] was carried out on the structure of atractyligenin, the nor-diterpene aglycone of the glucoside atractyloside, occurring, together with its diterpene homologous carboxy-atractyloside, in the root of Atractylis gummifera L. (Compositae). The interest for these compounds was stimulated by the high toxicity [3] of both glucosides, responsible of many deadly poisoning in past time. Due to the 15-hydroxyl…

PharmacologyChemistryOrganic ChemistryPharmaceutical ScienceOxidative phosphorylationSettore CHIM/06 - Chimica OrganicaAtractyligeninAnalytical ChemistryComplementary and alternative medicineChemical engineeringBiochemistryoxidative atractyligenin cytotoxic activityDrug DiscoveryMolecular MedicineCytotoxic T cell
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The diterpenoids from the genus Sideritis

2006

ABSTRACT: The genus Sideritis consists of 100-150 or more species, growing mainly in the countries around the Mediterranean area. The genus is particularly rich in diterpenoids, occurring in almost all the species, and shows many different carbon skeleta. Several species are still used in traditional medicine. Recent studies indicated the occurrence of interesting biological activities, like anti-inflammatory, antibacterial, antimicrobial, anti-HIV replication, antifeedant, antiulcerogenic, analgesic, and antihypoglycaemic.

biologyTraditional medicineGenusBotanyditerpenoids SideritisSideritisMediterranean areaSettore CHIM/06 - Chimica Organicabiology.organism_classificationAntimicrobial
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Synthesis of Rosmarinic Acid Amides as Antioxidative and Hypoglycemic Agents

2019

Type 2 diabetes mellitus (T2DM) is an important metabolic disorder for which there is an urgent need for new antidiabetic drugs. α-Glucosidase inhibition is an established protocol for T2DM therapy. Because hyperglycemia causes oxidative tissue damage, the development of agents with both α-glucosidase inhibition and antioxidant activity from natural or natural-derived polyphenols such derivatives of rosmarinic acid (RA) represents an attractive therapeutic option. We report a study on amides 1-10 derived from RA and their evaluation for yeast α-glucosidase inhibition and antioxidant activity (DPPH and ORAC tests). All amides showed higher inhibitory activity than that of RA, were by far mor…

3003DrugAntioxidantDPPHProton Magnetic Resonance Spectroscopymedia_common.quotation_subjectmedicine.medical_treatmentPharmaceutical ScienceOxidative phosphorylationPharmacologyDepsides01 natural sciencesAntioxidantsAnalytical Chemistrychemistry.chemical_compoundDrug DiscoverymedicineHypoglycemic AgentsSettore BIO/15 - Biologia FarmaceuticaCarbon-13 Magnetic Resonance SpectroscopyIC50media_commonAcarbosePharmacology010405 organic chemistrydiabetes mellituDrug Discovery3003 Pharmaceutical ScienceRosmarinic acidOrganic ChemistrySettore CHIM/06 - Chimica OrganicaComplementary and Alternative Medicine2708 DermatologyAmidesamide0104 chemical sciences010404 medicinal & biomolecular chemistryRosmarinic acidComplementary and alternative medicinechemistryCinnamatesPolyphenolAnalytical Chemistry; Molecular Medicine; Pharmacology; 3003; Drug Discovery3003 Pharmaceutical Science; Complementary and Alternative Medicine2708 Dermatology; Organic ChemistryMolecular Medicineα-glucosidasemedicine.drug
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Effects of solvent-free microwave extraction on the chemical composition of essential oil of Calamintha nepeta (L.) Savi compared with the convention…

2008

The essential oil of Calamintha nepeta has been obtained by solvent-free microwave extraction (SFME) and by classical hydrodistillation (HD). A comparative qualitative-quantitative study on the composition of the oils was carried out. A total of 38 compounds, constituting 97.6% of the oil, were identified in the oil obtained by SFME, whereas 46 compounds, representing 95.4% of the oil, were characterized in the HD oil. SFME-distilled oil is richer in lightly oxygenated monoterpenes (LOM) than HD oil. It also has a higher amount of sesquiterpenes and a lower quantity of hydrocarbon monoterpenes. HD oil seems to be affected by chemical changes more than SFME oil.

chemistry.chemical_classificationLamiaceaeChromatographybiologyPlant ExtractsExtraction (chemistry)TemperatureFiltration and SeparationSettore CHIM/06 - Chimica Organicabiology.organism_classificationCalamintha nepeta essential oil hydrodistillation solvent-free microwave extractionCalaminthaAnalytical Chemistrylaw.inventionSteam distillationHydrocarbonchemistrylawNepetaOils VolatileSolventsLamiaceaeMicrowavesChemical compositionEssential oil
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Two New Flavonoids fromBonannia graeca: a DFT-NMR Combined Approach in Solving Structures

2007

Two new cyclized C-geranylated flavonoids, the dihydroflavonol bonanniol C (4a) and the flavanone bonannione B (6a), were isolated as minor compounds from the aerial parts of Bonannia graeca (Umbelliferae). Their structures were elucidated by a combined approach of extensive spectroscopic means and quantum mechanical methods. (© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2007)

chemistry.chemical_compoundchemistryStereochemistryOrganic ChemistrySettore CHIM/06 - Chimica OrganicaPhysical and Theoretical ChemistryUmbelliferae Bonannia graeca Geranylated flavonoids DFTFlavanoneCombined approachEuropean Journal of Organic Chemistry
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ChemInform Abstract: Natural and Hemisynthetic Neoclerodane Diterpenoids from Scutellaria and Their Antifeedant Activity

2010

Covering: Up to June 2001. Previous review: on the clerodanes, Nat. Prod. Rep., 1992, 9, 243.

TerpeneTraditional medicinebiologyChemistryScutellariaGeneral Medicinebiology.organism_classificationChemInform
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Structure and Biological Activity of the Furan-Diterpenoids from the Genera Leonotis and Leonurus

2007

The present review, covering the literature up to 2006, reports the chemistry and the biological activities of the diterpenoids occurring in the aerial parts of species belonging to the genera Leonotis and Leonurus, family Lamiaceae.

PharmacologyFamily Lamiaceaenatural productLeonurusLeonuruNatural productbiologyOrganic Chemistrybiological activityBiological activitybiology.organism_classificationAnalytical ChemistryLabdanechemistry.chemical_compoundchemistryFuranLeonotiBotanyLabdaneLeonotisHETEROCYCLES
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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
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Antispasmodic Effects and Structure−Activity Relationships of Labdane Diterpenoids from Marrubium globosum ssp. libanoticum

2009

Marrubium globosum ssp. libanoticum is a medicinal plant used in Lebanon to reduce pain and smooth muscle spasms. A chloroform extract obtained from M. globosum aerial parts reduced acetylcholine-induced contractions in the isolated mouse ileum. The purification of this extract identified, among 12 isolated labdane diterpenoids, four new compounds, named 13-epicyllenin A (4), 13,15-diepicyllenin A (5), marrulibacetal (9), and marrulactone (11). Their structures were determined by spectroscopic methods. Compound 9, which exerted antispasmodic activity, is likely the active ingredient of the extract. Preliminary structure-activity relationships for this class of compounds are suggested.

MaleAntispasmodic effectditerpenoidPharmaceutical SciencePharmacognosyAnalytical ChemistryLabdaneMiceStructure-Activity Relationshipchemistry.chemical_compoundIleumDrug DiscoveryBotanymedicineAnimalsLebanonMedicinal plantsPharmacologyMarrubium globosum ssp. libanoticumPlants MedicinalMolecular StructurebiologyPlant ExtractsfungiOrganic ChemistryParasympatholyticsfood and beveragesMuscle SmoothSettore CHIM/06 - Chimica Organicabiology.organism_classificationAcetylcholineTerpenoidAntispasmodic AgentComplementary and alternative medicinechemistryMolecular MedicineAntispasmodicDiterpenesDiterpeneMarrubiumMarrubiummedicine.drugJournal of Natural Products
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The ethnobotany, phytochemistry and biological properties of genus Ferulago – A review

2020

Abstract Ethnopharmacological relevance The genus Ferulago, belonging to the Apiaceae family, is found mainly in the Mediterranean area, Southwest and Middle Asia, the Caucasus and North Africa. Since ancient times, species of this genus have been largely employed in traditional medicine for their biological properties such as antimicrobial, anti-inflammatory, antispasmodic, insecticidal, and anti-malaria, cholinesterase inhibition effects, etc. Aims The scope of this paper is to present a comprehensive respect review of this interesting genus including traditional uses, chemical composition of volatile and non-volatile metabolites, and in vitro and in vivo biological properties either util…

Phytochemistryfood.ingredientPhytochemicalsEthnobotanyApiaceae Bioactivity Essential oil Ferulago spp. Secondary metabolitesBiologylaw.inventionFerulago03 medical and health sciences0302 clinical medicinefoodGenuslawDrug DiscoveryAnimalsHumansSettore BIO/15 - Biologia FarmaceuticaEssential oil030304 developmental biologyPharmacology0303 health sciencesApiaceaeTraditional medicineSettore CHIM/06 - Chimica OrganicaAntimicrobialbiology.organism_classificationPhytochemical030220 oncology & carcinogenesisEthnobotanySettore BIO/03 - Botanica Ambientale E ApplicataMedicine TraditionalPlant PreparationsApiaceaeJournal of Ethnopharmacology
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Essential oils of three species of scutellaria and their influence on Spodoptera littoralis

2013

Scutellaria orientalisbiologyCaryophyllenePlant compositionSettore CHIM/06 - Chimica Organicabiology.organism_classificationBiochemistrylaw.inventionchemistry.chemical_compoundEssential oils Scutellaria Spodoptera littoralischemistrylawBotanyScutellariaScutellaria sp. Essential oil Spodoptera littoralisSettore BIO/15 - Biologia FarmaceuticaSpodoptera littoralisEcology Evolution Behavior and SystematicsEssential oil
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Photoinduced functionalization of diterpenes: photochemical behaviour of grandifloric acid in methanol and acetonitrile

2004

Abstract Irradiation of grandiflorolic acid (11) at λ=254 nm in acetonitrile gave the two epimers 13 and 14 through a photodecarboxylation reaction of the carboxylic group on C-4. Irradiation of compound 11 in methanol at λ=254 nm provided the transformation of the C-20 angular methyl into a carbomethoxymethyl group. In this case, unlike compounds 13 and 14, only one of the two possible isomers (15) was obtained (equatorial methyl at C-4). A mechanistic approach of this reaction in discussed, and the role of mutual stereochemistry between C-20 methyl and C-19 carboxylic group in determining the course of the reaction is pointed out.

PhotochemistryGeneral Chemical EngineeringCarboxylic groupGeneral Physics and AstronomyGeneral ChemistrySettore CHIM/06 - Chimica OrganicaNatural compoundPhotochemistrychemistry.chemical_compoundGrandiflorolic acidchemistrySurface modificationEpimerMethanolIrradiationGrandiflorolic acidAcetonitrileDiterpene
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Essential Oils of Chiliadenus Lopadusanus (Asteraceae)

2013

The essential oils from the leaves and flowers of Chiliadenus lopadusanus growing on Lampedusa Island were obtained by hydrodistillation and analyzed by GC-MS. The major component was camphor (39.4% in the leaves and 24.0% in the flowers), followed in the leaves by torreyol (6.7%), t-cadinol (5.2%) and 1,8-cineole (3.8%), while in the flowers by t-cadinol (15.2%), t-muurolol (5.1%) and torreyol (4.5%). Among the compounds identified, several seem to play a role in antibacterial, antifungal, allelopathic and spasmolytic activity. In addition, several compounds identified in this study seem to influence the attraction of Megachile ( Eutricharaea) apicalis (Megachilidae) and Halictus ( Selado…

PharmacologyHalictidaebiologyHalictusPlant ScienceGeneral MedicineAsteraceaebiology.organism_classificationMegachileCamphorchemistry.chemical_compoundComplementary and alternative medicinechemistryPollinatorDrug DiscoveryBotanyMegachilidaeAllelopathyNatural Product Communications
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Cytotoxic activity of some natural and synthetic guaianolides

2005

Several natural guaianolides and synthetic derivatives of repin (1) were tested and found to be active against tumor cell replication. Repin (1) and both mono- and di-halohydrin analogues (2, 7-9, 11, 12) showed significant antitumor potency. A more effective compound (17) was obtained by esterificating repin with the paclitaxel side chain.

PaclitaxelStereochemistryPharmaceutical ScienceEpoxideSesquiterpeneAnalytical Chemistrychemistry.chemical_compoundStructure-Activity RelationshipDrug DiscoveryTumor Cells CulturedPotencyHumansCytotoxicityPharmacologychemistry.chemical_classificationMolecular StructureChemistryOrganic ChemistrySettore CHIM/06 - Chimica OrganicaAntineoplastic Agents PhytogenicIn vitroTerpenoidCentaurea Asteraceae sesquiterpene lactonesComplementary and alternative medicinePaclitaxelMolecular MedicineDrug Screening Assays AntitumorSesquiterpenesLactone
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Essential oil composition of Tanacetum vulgare subsp. siculum (Guss.) Raimondo et Spadaro (Asteraceae) from Sicily

2009

Ninety-four components of the essential oils from aerial parts and capitula of Tanacetum vulgare subsp. siculum (Guss.) Raimondo et Spadaro were detected. alpha-Thujone, beta-thujone and 1,8-cineole were the main constituents of the oils. The analysis allows the assignment of this Tanacetum species to the thujone chemotype.

Tanacetum vulgare subsp. siculum (Guss.) Raimondo et Spadaro Asteraceae essential oil alpha thujone beta-thujone 18-cineoleTanacetumOils VolatileSicilyGas Chromatography-Mass Spectrometry
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Enzyme-catalysed transformations of ent-kaurane diterpenoids

2005

Several acetyl derivatives of linearol, atractyligenin and atractylitriol were obtained through enzyme-catalysed acetylation and deacetylation reactions. In most reactions lipases showed regio- and stereoselective behaviour, allowing a family of novel compounds to be prepared. Fil: Monsalve, Leandro Nicolas. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Ciudad Universitaria. Unidad de Microanálisis y Métodos Físicos en Química Orgánica. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales. Unidad de Microanálisis y Métodos Físicos en Química Orgánica; Argentina. Universidad de Buenos Aires. Facultad de Ciencias Exactas y …

Química OrgánicaACETYLATIONENZYME CATALYSISChemistryStereochemistryDEACETYLATIONOrganic ChemistryENT-KAURANESCiencias QuímicasDITERPENOIDSPhysical and Theoretical ChemistryEnt kauraneCIENCIAS NATURALES Y EXACTAS
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GC and GC/MS analysis of the essential oil of Salvia hierosolymitana boiss. Growing wild in Lebanon

2007

The essential oil of the aerial parts of Salvia hierosolymitana Boiss. (Lamiaceae), growing wild in Lebanon, was obtained by hydrodistillation and analysed by GC and GC-MS. Ninety-two compounds, representing 92.7% of the oil, were identified. The major components were hexadecanoic acid (15.5%), phytol (5.4%), hexahydrofarnesyl acetone (4.6%), (Z,Z)-9,12-octadecadienoic acid (4.5%) and 4-vinylguaiacol (4.4%).

PharmacologyTraditional medicinebiology010405 organic chemistryPlant ScienceGeneral Medicinebiology.organism_classification01 natural sciencesSalvia hierosolymitana0104 chemical scienceslaw.invention010404 medicinal & biomolecular chemistryComplementary and alternative medicinelawDrug DiscoveryGas chromatography–mass spectrometryEssential oil
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Rearrangement of Germacranolides. Synthesis and Absolute Configuration of Elemane and Heliangolane Derivatives from Cnicin

2003

A study of the Cope rearrangement of 15-oxo-germacranolides to 15-oxo-elemanolides has been carried out. The synthesis of two natural elemanolides, isolated from Centaurea paui, and an efficent isomerization of the C-4/C-5 double bond of 15-oxo-germacranolides to form heliangolides are reported. The absolute configuration of all the compounds has been ascertained. (© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2003)

chemistry.chemical_classificationchemistry.chemical_compoundchemistryDouble bondCentaurea pauiStereochemistryOrganic ChemistryAbsolute configurationPhysical and Theoretical ChemistryCnicinIsomerizationCope rearrangementEuropean Journal of Organic Chemistry
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Hastifolins A-G, antefeedant neo-clerodane diterpenoids from Scutellaria hastifolia

2010

From the aerial parts of Scutellaria hastifolia, family Lamiaceae (Labiatae), seven neo-clerodane diterpenoids (hastifolins A-G) were isolated. The products are similar to the known scuteparvin and are characterized by being trans-cinnamoyl derivatives. Structures and stereochemistry were determined by intensive NMR investigation. Six of the products form three pairs of epimers at C-13. Hastifolins A-C showed significant antifeedant activity.

Family LamiaceaeStereochemistryScutellariaChemical structurePlant ScienceHorticultureSpodopteraBiochemistryDiterpenes Clerodanechemistry.chemical_compoundFeeding behaviorAnimalsMolecular BiologyNuclear Magnetic Resonance BiomolecularbiologyMolecular StructureGeneral MedicineFeeding BehaviorSettore CHIM/06 - Chimica Organicabiology.organism_classificationTerpenoidchemistryLarvaScutellariaLamiaceaeEpimerDiterpeneScutellaria hastifolia Lamiaceae diterpenes neo-clerodanes epimers antifeedant
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Chemical composition and biological activity of Salvia verbenaca essential oil

2011

Salvia verbenaca L. (syn. S. minore) is a perennial herb known in the traditional medicine of Sicily as “spaccapetri” and is used to resolve cases of kidney stones, chewing the fresh leaves or in decoction. The chemical composition of the essential oil obtained from aerial parts of S. verbenaca collected in Piano Battaglia (Sicily) on July 2009, was analyzed by GC and GC-MS. The oil was strongly characterized by fatty acids (39.5%) and carbonylic compounds (21.2%), with hexadecanoic acid (23.1%), ( Z)-9-octadecenoic acid (11.1%) and benzaldehyde (7.3%) as the main constituents. The in vitro activity of the essential oil against some microorganisms in comparison with chloramphenicol by the …

Gram-positive bacteriaCarboxylic AcidsDecoctionMicrobial Sensitivity TestsPlant ScienceSalviaGram-Positive BacteriaGas Chromatography-Mass Spectrometrylaw.inventionfoodlaw(Z)-9-octadecenoic acidGram-Negative BacteriaDrug DiscoveryPlant OilsVolatile componeSettore BIO/15 - Biologia FarmaceuticaSalviaFood scienceSicilyChemical compositionEssential oilPharmacologyβ-phellandrene (Z)-9-octadecenoic acid Antibacterial activity Benzaldehyde Hexadecanoic acid Lamiaceae Salvia verbenaca Volatile componeLamiaceaeSalvia verbenacabiologyChemistryFatty AcidsVolatile componentsSettore CHIM/06 - Chimica OrganicaGeneral MedicineBenzaldehydePlant Components Aerialbiology.organism_classificationfood.foodAnti-Bacterial AgentsComplementary and alternative medicineβ-phellandreneSalvia verbenacaAntibacterial activityGas chromatography–mass spectrometryHexadecanoic acidBacteria
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Synthesis of β-methylfurolabdanes from (+)-sclareolide

2002

An efficient synthesis of the methylfurolabdane 3 from (+)-sclareolide (6) via the hydroxyalkenes 12 is reported. Alternative modes of cyclization of 12 allowed the synthesis of methyldihydrofuran derivatives 4 and 5 and methyltetrahydrofuran derivatives 15. (© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2002)

Terpenechemistry.chemical_compoundChemistryOrganic ChemistrySclareolidePhysical and Theoretical ChemistryCombinatorial chemistry
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Photoinduced functionalization of the C-20 methyl group of the nor-diterpene atractyligenin

2001

Abstract Irradiation of the nor-diterpene atractyligenin at λ =254 nm in methanol gave, on one hand, the decarboxylation product, and provided, on the other hand, the transformation of the C-20 angular methyl into a methylene-carbomethoxy group. A photochemical pathway involving formation of C-19/C-20 bond is suggested.

chemistry.chemical_compoundchemistryDecarboxylationOrganic ChemistryDrug DiscoverySurface modificationMethanolDiterpeneAtractyligeninBiochemistryMedicinal chemistryMethyl groupTetrahedron Letters
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Cytotoxic Effect of Eudesmanolides Isolated from Flowers of Tanacetum vulgare ssp. siculum

2012

WOS: 000306752700042

sesquiterpeneeudesmanolidePharmaceutical ScienceFlowersSesquiterpeneArticleChinese hamsterCell LineAnalytical ChemistryHuman lungInhibitory Concentration 50Tanacetumchemistry.chemical_compoundsesquiterpenesDrug DiscoveryBotanymedicineAnimalsHumansCytotoxic T cellSettore BIO/15 - Biologia FarmaceuticaPhysical and Theoretical ChemistryTanacetum vulgarecytotoxic activityCell ProliferationCell DeathbiologyTraditional medicine<em>Tanacetum vulgare</em>; sesquiterpenes; eudesmanolides; cytotoxic activityeudesmanolidesOrganic ChemistrySettore CHIM/06 - Chimica Organicabiology.organism_classificationIn vitroTanacetum vulgare; sesquiterpenes; eudesmanolides; cytotoxic activitymedicine.anatomical_structurechemistryPhytochemicalChemistry (miscellaneous)Molecular MedicineColorimetryFormazanMolecules; Volume 17; Issue 7; Pages: 8186-8195
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Volatile constituents of aerial parts of three endemic Centaurea species from Turkey: Centaurea amanicola Hub.-Mor., Centaurea consanguinea DC. and C…

2008

The volatile constituents of the aerial parts of Centaurea amanicola Hub.-Mor., Centaurea consanguinea DC. and Centaurea ptosimopappa Hayek were extracted by hydrodistillation and analysed by GC and GC-MS. Altogether 94 components were identified. Sesquiterpenoids, fatty acids and carbonylic compounds were the most abundant components in the oils. Hexadecanoic acid and (Z,Z )-9,12-octadecadienoic acid were the main fatty acids in all the examined samples, that showed different patterns of composition. The study on the biological activity of the oils showed an action mainly against the Gram-positive pathogens.

Centaurea amanicola Centaurea consanguinea Centaurea ptosimopappa essential oil GC/MS antimicrobial activityChromatography GasTurkeyOils VolatilePlant OilsCentaureaSettore CHIM/06 - Chimica OrganicaSettore BIO/15 - Biologia FarmaceuticaMicrobial Sensitivity TestsPlant Components AerialGram-Positive BacteriaGas Chromatography-Mass SpectrometryAnti-Bacterial AgentsNatural product research
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The metabolites of the genus onopordum (asteraceae): Chemistry and biological properties

2011

Onopordum is an interesting genus belonging to the tribe Cardueae (Asteraceae family), and the species of this genus are used as food and in the popular medicine of several countries. The present paper reviews all the metabolites present in all the species of this genus, reported up to 2009, and several chemotaxonomic consideration have been made. Furthermore, the occurrence in other genus, the spectral data, the synthetic approaches, the chemical modifications and the biological properties of the sesquiterpenes of genus Onopor- dum have been reviewed.

13C NMRbiologyOnopordumBiological activitySesquiterpenoidOrganic ChemistryZoologySettore CHIM/06 - Chimica OrganicaAsteraceaebiology.organism_classificationTribe (biology)Steroids and triterrpeneSynthesisGenusBiological propertyBotanyFlavonoidChemcial modificationSpectral data
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Analysis of Essential Oil from Teucrium maghrebinum Greuter et Burdet Growing Wild in Algeria

2009

The chemical composition of the essential oil obtained from aerial parts of Teucrium maghrebinum growing wild in Algeria was analyzed by GC and GC-MS. Among the 66 identified compounds, δ-cadinene (12.7%), germacrene D (11.4%), γ-cadinene (9.5%) and 4-vinyl guaiacol (4.0%) were the most abundant. The oil is strongly characterized by the presence of sesquiterpenes (61.5%), particularly hydrocarbon sesquiterpenes (49.6%).

Pharmacologychemistry.chemical_classificationbiologyChemistryPlant ScienceGeneral Medicinebiology.organism_classificationlaw.inventionTeucriumchemistry.chemical_compoundHydrocarbonComplementary and alternative medicinelawDrug DiscoveryBotanyLamiaceaeGuaiacolGas chromatography–mass spectrometryChemical compositionEssential oilGermacrene DNatural Product Communications
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A Review of the Phytochemistry, Traditional Uses and Biological Activities of the Essential Oils of Genus Teucrium

2020

AbstractThe genus Teucrium is a large and polymorphic genus of the Lamiaceae family distributed in mild climate zones, particularly in the Mediterranean basin and Central Asia. Studies of nonvolatile constituents of Teucrium species showed that they are a rich source of neo-clerodane diterpenoids, considered as chemotaxonomic markers of the genus. In addition to the nonvolatile metabolites, there has been a large interest in the essential oils of this genus. In this review, a complete survey of the chemical composition and biological properties of the essential oils isolated from Teucrium taxa is provided. In traditional medicine, since ancient times, species of this genus have been widely …

PhytochemistryPharmaceutical Science01 natural sciencesMediterranean BasinTeucriumAnalytical Chemistrylaw.inventionTeucriumGenuslawBiological propertyDrug DiscoveryBotanyOils VolatileEssential oilPharmacologyLamiaceaebiologyPlant Extracts010405 organic chemistryOrganic Chemistrybiology.organism_classification0104 chemical sciences010404 medicinal & biomolecular chemistryTaxonComplementary and alternative medicineTeucrium Lamiaceae ethnopharmacology essential oil biological propertiesMolecular MedicineLamiaceaeMedicine TraditionalPlanta Medica
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Antimicrobial and Antioxidant Activities of Coumarins from the Roots of Ferulago campestris (Apiaceae)

2009

We report the isolation of several coumarins and the stereochemical assessment of some pyranocoumarins, as well as the antibacterial and antioxidant activities of the three most abundant ones (grandivittin, agasyllin and aegelinol benzoate) isolated from the roots of Ferulago campestris collected in Sicily and of the hydrolysis product (aegelinol). Aegelinol and agasyllin showed antibacterial activity against nine ATCC and the same clinically isolated Gram-positive and Gram-negative bacterial strains. At a concentration between 16 and 125 μg/mL both coumarins showed a significant antibacterial effect against both Gram-negative and Gram-positive bacteria. In particular the ATCC strains Staph…

food.ingredientNeutrophilsPharmaceutical ScienceBiologyGram-Positive Bacteriamedicine.disease_causePlant RootsPyranocoumarinsPyranocoumarinsAntioxidantsArticleAnalytical ChemistryFerulagoMicrobiologyfoodAnti-Infective AgentsAntioxidant activityCoumarinsGram-Negative BacteriaDrug DiscoveryLeukocytesmedicineHumansAbsolute configurationPhysical and Theoretical ChemistryFerulago campestris coumarins pyranocoumarins absolute configuration antibacterial activity antioxidant activityDose-Response Relationship DrugOrganic ChemistrySettore CHIM/06 - Chimica OrganicaEnterobacterbiology.organism_classificationAntimicrobialChemistry (miscellaneous)Staphylococcus aureusMolecular MedicineFerulago campestris; Coumarins; Pyranocoumarins; Absolute configuration; Antibacterial activity; Antioxidant activityFerulago campestrisAntibacterial activityAntibacterial activityEnterobacter cloacaeBacteriaApiaceaeMolecules; Volume 14; Issue 3; Pages: 939-952
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Acid Rearrangment of Epoxy-germacranolides and Absolute Configuration of 1β,10α-Epoxy-salonitenolide

2010

The acid-catalyzed cyclization of mono epoxides of cnicin acetonide (3) was investigated. Several 6,12-eudesmanolides were obtained, and their stereochemistry established by extensive spectroscopic analyses. Chemical correlations also led to the assignment of the absolute configuration of 1β,10α-epoxy-salonitenolide (13), a previously isolated natural product. The cytotoxic activities of some compounds were determined against A549 and MCF-7 tumor cell lines. The esterified germacranolides 2–6 were selectively cytotoxic against the MCF-7 breast cancer cell line.

PharmacologyNatural productStereochemistryAbsolute configurationSalonitenolidePlant ScienceGeneral MedicineEpoxyAcetonideCnicinchemistry.chemical_compoundComplementary and alternative medicineBreast cancer cell linechemistryvisual_artDrug Discoveryvisual_art.visual_art_mediumOrganic chemistryCytotoxicityNatural Product Communications
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Chemical composition of essential oils of Anthemis secundiramea Biv. subsp. secundiramea (Asteraceae) collected wild in Sicily and their activity on …

2016

In the present study, the chemical composition of the essential oil from the aerial parts of Anthemis secundiramea Biv. subsp. secundiramea L. collected in Sicily was evaluated by GC and gas chromatography–mass spectrometry. The main components of A. secundiramea were (Z)-lyratyl acetate (14.6%), (Z)-chrysanthenyl acetate (9.9%), (Z)-chrysanthenol (8.7%) and (E)-chrysanthenyl acetate (7.7%). The comparing with other studied oils of genus Anthemis belonging to the same clade is discussed. Antibacterial and antifungal activities against some micro-organisms infesting historical art craft, were also determined.

AntifungalAntifungal Agentsmedicine.drug_classPlant compositionchrysanthenyl derivatives antibacterial and antifungal activityPlant ScienceAsteraceaeBiology01 natural sciencesBiochemistryGas Chromatography-Mass SpectrometryAnalytical Chemistrylaw.inventionBridged Bicyclo CompoundsGenuslawBotanyOils VolatilemedicinePlant OilsAnthemisSettore BIO/15 - Biologia FarmaceuticaSicilyChemical compositionEssential oilAnthemis secundiramea010405 organic chemistryOrganic ChemistrySettore CHIM/06 - Chimica OrganicaAsteraceaebiology.organism_classificationAnti-Bacterial Agents0104 chemical sciences(Z)-lyratyl acetatevolatile component010404 medicinal & biomolecular chemistryAnthemis secundiramea Biv. subsp. secundirameaMonoterpenesAnthemisArtNatural Product Research
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Floral scent in a sexually deceptive Ophrys orchid: from headspace collections to solvent extractions

2018

Sexually deceptive orchid flowers use visual, tactile and olfactory cues of female insects in order to attract males of one or a few closely related species as pollinators. Ophrys L. is the most species-rich genus of sexually deceptive orchids in the Mediterranean Basin. Despite Ophrys pollinated by Andrena male bees use alkanes and mainly alkenes with specific double-bond positions as key signals that trigger pseudocopulatory behavior, some volatile organic compounds (VOCs) with low molecular weight were found as long-range attractants non-eliciting copulatory behavior. Since floral scents in Ophrys have been extensively studied by solvent extractions here we aimed to understand which flor…

0106 biological sciences0301 basic medicineAndrenapollinationPollinationAndrenaPlant ScienceFlowers01 natural sciencesGas Chromatography-Mass Spectrometry03 medical and health sciencesPollinatorvolatile organic compoundsBotanyOphrys panormitanaOrchidaceaeOphrysOrchidaceaebiologySettore CHIM/06 - Chimica Organicabiology.organism_classificationPseudocopulation030104 developmental biologyOdorantsSettore BIO/03 - Botanica Ambientale E ApplicataKovats retention indexGas chromatography010606 plant biology & botanyResearch Paper
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Antifeedant activity of neo-clerodane diterpenoids from Teucrium arduini

2002

Traditional medicineBiologyBiochemistryEcology Evolution Behavior and SystematicsTeucrium arduiniBiochemical Systematics and Ecology
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Antibacterial and antifungal activities of Otanthus maritimus (L.) Hoffmanns.Link essential oil from Sicily.

2013

The chemical composition of the essential oil obtained from the flowers of Otanthus maritimus L., a perennial plant growing wild in maritime sands in the Mediterranean region, was investigated by GC and GC-MS analyses. Totally 66 were identified. The oil was dominated by the high content of monoterpene compounds, especially oxygenated monoterpenes which accounted for 73.1%. The most abundant components were yomogi alcohol (20.8%), camphor (15.8%), artemisyl acetate (15.3%) and artemisia alcohol (13.7%). The oil was tested against two Gram (+) and six Gram (-) bacterial strains, both American Type Culture Collection standard strains and clinically isolated (CI), one potentially pathogenic ye…

Artemisyl acetateAntifungal AgentsMonoterpenePlant ScienceFlowersMicrobial Sensitivity TestsAsteraceaeGram-Positive BacteriaBiochemistryYomogi alcoholGas Chromatography-Mass SpectrometryAnalytical Chemistrylaw.inventionRhizoctonia solaniCamphorchemistry.chemical_compoundlawBotanyCandida albicansGram-Negative BacteriaOils VolatileAntifungal activitySettore BIO/15 - Biologia FarmaceuticaSicilyEssential oilBotrytis cinereabiologyOrganic Chemistryfood and beveragesSettore CHIM/06 - Chimica Organicabiology.organism_classificationCamphorAnti-Bacterial AgentsOtanthuschemistryMonoterpenesArtemisiaAntibacterial activityOtanthus maritimuAntibacterial activityNatural product research
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Constituents of leaves and flowers essential oils of Helichrysum pallasii (Spreng.) Ledeb. growing wild in Lebanon.

2009

The chemical compositions of the essential oils obtained from leaves and flowers of Helichrysum pallasii were analyzed by gas chromatography and gas chromatography-mass spectrometry. Among the 102 identified constituents, hexadecanoic acid (16.2%), (Z,Z)-9,12-octadecadienoic acid (6.8%), tetradecanoic acid (2.6%), and (Z)-caryophyllene (4.2%) were the main constituent of the oil from leaves, while in the oil from flowers hexadecanoic acid (14.7%), (Z,Z)-9,12-octadecadienoic acid (14.2%), (Z)-caryophyllene (3.6%), and delta-cadinene (3.1%) predominated. The oils were both characterized by sesquiterpenes (33.4% for leaves and 33.7% for flowers, respectively) and fatty acids and esters (30.3% …

Helichrysum pallasii (Spreng.) Ledeb.Palmitic AcidMedicine (miscellaneous)Myristic acidFlowersMyristic Acidlaw.inventionPalmitic acidMinimum inhibitory concentrationchemistry.chemical_compoundlawBotanyOils VolatileStaphylococcus epidermidisPlant OilsFood scienceLebanonEssential oilHelichrysumPolycyclic SesquiterpenesNutrition and DieteticsbiologyBacteriaPlant ExtractsAnti-Inflammatory Agents Non-SteroidalFatty AcidsEstersAsteraceaebiology.organism_classificationAnti-Bacterial AgentsPlant LeaveschemistryHelichrysumFatty Acids UnsaturatedStearic acidGas chromatographySesquiterpenesJournal of medicinal food
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Headspace Volatile Composition of the Flowers of Caralluma europaea N.E.Br. (Apocynaceae)

2009

The volatile constituents of the flowers of Caralluma (Apteranthes) europaea (Guss.) N.E. Br. (Apocynaceae - Asclepiadoideae) from Lampedusa Island were analyzed by headspace method. The analyses allowed the identification and quantification of 41 compounds. The main components were, among the monoterpenoids, terpinolene (23.3%), a-terpinene (19.1%) and linalool (18.4%), whereas, among the carbonylic compounds the major constituents were heptanal (2.0%), octanoic acid (2.4%) and hexanoic acid (1.7%). It is worth to mention the presence of a nitrogen containing compound, indole (0.8%) and of a sulphur containing compound, dimethylsulphide (t). The compounds found in the flowers of C. europea…

IndolespollinationPharmaceutical ScienceHymenopteraAnalytical Chemistrychemistry.chemical_compoundLinaloolDrug Discovery<em>Caralluma europaea</em>; <em>Apteranthes europaea</em>; Diptera; pollination; sapromyiophily; volatilesHexanoic acidchemistry.chemical_classificationApocynaceaevolatilesChemistry (miscellaneous)Molecular MedicineComposition (visual arts)CaprylatesSettore BIO/07 - EcologiaChromatography GasAcyclic MonoterpenesCyclohexane MonoterpenesFlowersBiologySulfidesArticleSettore CHIM/12 - Chimica Dell'Ambiente E Dei Beni CulturaliLepidoptera genitalialcsh:QD241-441lcsh:Organic chemistryBotanyOrganic matterPhysical and Theoretical ChemistryCaproatesCaralluma europaea; Apteranthes europaea; Diptera; pollination; sapromyiophily; volatilesAldehydesVolatile Organic CompoundsPlant ExtractsTerpenesDipteraOrganic ChemistrySettore CHIM/06 - Chimica Organicabiology.organism_classificationApocynaceaechemistryOdorsapromyiophilyCaralluma europaeaSettore BIO/03 - Botanica Ambientale E ApplicataMonoterpenesApteranthes europaea
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In Vitro Modulation of P-Glycoprotein Activity by Euphorbia intisy Essential Oil on Acute Myeloid Leukemia Cell Line HL-60R

2021

Euphorbia species have a large spectrum of traditional medicinal uses. We tested the biological activities of the essential oil (EO) of Euphorbia intisy Drake in an acquired multidrug resistance leukemia model to assess whether the EO obtained by hydrodistillation of stems was able to reverse the resistant phenotype. HL-60R cell lines are characterized by the overexpression of P-glycoprotein (P-gp), inhibitors of apoptosis proteins (IAPs) and constitutive expression of NF-κB. EO chemical composition was determined by GC/MS analysis

lcsh:Medicinelcsh:RS1-441Pharmaceutical ScienceP-glycoprotein01 natural sciencesessential oilNF-κBFlow cytometrylcsh:Pharmacy and materia medicamultidrug resistanceDrug DiscoverymedicineChemosensitizing agentSettore BIO/15 - Biologia FarmaceuticaP-glycoproteincancer cellbiologymedicine.diagnostic_test010405 organic chemistryChemistrylcsh:RMyeloid leukemiamyeloid leukemia cellSettore CHIM/08 - Chimica FarmaceuticaMolecular biologyIn vitro0104 chemical sciencesMultiple drug resistance010404 medicinal & biomolecular chemistryApoptosisCell cultureSettore BIO/03 - Botanica Ambientale E ApplicataSettore BIO/14 - Farmacologiabiology.proteinMolecular Medicineinhibitors of apoptosis proteinsPharmaceuticals
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A study on the essential oil of Ferulago campestris : How much does extraction method influence the oil composition?

2011

The essential oil of different parts of Ferulago campestris (Bess.) collected in Sicily has been extracted by microwave-assisted hydrodistillation (MAHD) and by classic hydrodistillation (HD). A comparative qualitative-quantitative study on the composition of the oils was carried out. A total of 100 compounds were identified in the oils obtained by MAHD, whereas 88 compounds characterized the HD oils. The most prominent components were, in all different parts of F. campestris and in both extraction methods, 2,4,5-trimethylbenzaldehyde and 2,4,6-trimethylbenzaldehyde isomers; the latter was not previously found. The attempt to evaluate where the oil components are located in all parts of the…

ChromatographyChemistrylawFiltration and SeparationComposition (visual arts)Extraction methodsFerulago campestrisEssential oilAnalytical Chemistrylaw.inventionJournal of Separation Science
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Volatile components and antifeedant activity of the essential oil from Scutellaria hastifolia L.

2009

PharmacologybiologyOrganic ChemistryPharmaceutical ScienceSettore CHIM/06 - Chimica Organicabiology.organism_classificationAnalytical Chemistrylaw.inventionComplementary and alternative medicineScutellaria hastifolia L.essential oil antifeedant activitylawDrug DiscoveryBotanyScutellariaMolecular MedicineEssential oil
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ChemInform Abstract: Artalbic Acid, a Sesquiterpene with an Unusual Skeleton from Artemisia alba (Asteraceae) from Sicily.

2011

Abstract From the aerial parts of Artemisia alba (Asteraceae) artalbic acid ( 1 ), a sesquiterpene with an unusual skeleton, was isolated. Its structure was elucidated on the basis of extensive proton, 13 C and two-dimensional NMR experiments, as well as by transformation in its methyl ester derivative.

Terpenechemistry.chemical_compoundchemistrybiologyStereochemistryArtemisiaGeneral MedicineAsteraceaeSesquiterpenebiology.organism_classificationSkeleton (computer programming)ChemInform
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Natural and hemisynthetic neoclerodane diterpenoids from Scutellaria and their antifeedant activityElectronic supplementary information (ESI) availab…

2002

Covering: Up to June 2001. Previous review: on the clerodanes, Nat. Prod. Rep., 1992, 9, 243.

biologyChemistryChinese traditionalOrganic ChemistryDrug DiscoveryScutellariaOrganic chemistrybiology.organism_classificationBiochemistryNatural Product Reports
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The Essential Oil of Thymbra capitata and its Application as A Biocide on Stone and Derived Surfaces

2019

Many chemicals used nowadays for the preservation of cultural heritage pose a risk to both human health and the environment. Thus, it is desirable to find new and eco-friendly biocides that can replace the synthetic ones. In this regard, plant essential oils represent effective alternatives to synthetic substances for the preservation of historical monuments. Thymbra capitata (syn. Thymus capitatus) is a medicinal and aromatic plant growing in the Mediterranean area and endowed with important pharmacological properties related to its essential oil. Among them, the antimicrobial ones make the T. capitata essential oil an ideal candidate for industrial applications

BiocideStone surface<i>Thymbra capitata</i>02 engineering and technologyPlant Science01 natural sciencesThymbra capitataessential oillaw.inventionchemistry.chemical_compoundHuman healthfoodstone surfaceslawnatural biocideThymbra capitataCarvacrolSettore BIO/15 - Biologia FarmaceuticaEcology Evolution Behavior and SystematicsEssential oilSettore CHIM/02 - Chimica FisicaEcology010405 organic chemistryChemistrybiological inhibitionBotanySettore CHIM/06 - Chimica Organicacultural heritage021001 nanoscience & nanotechnologyPulp and paper industryfood.food0104 chemical sciencesbiodeteriogensPickering emulsionQK1-989CapitataBiodeteriogenMediterranean areaThymus capitatus0210 nano-technologyPlants
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Extremely potent antifeedant neo-clerodane derivatives of scutecyprol A

2004

Two known neo-clerodane diterpenoids, scutecyprol A (1) and scutalbin C (2), have been isolated from the acetone extract of the aerial parts of Scutellaria sieberi. The antifeedant activity of scutecyprol A (1), of its 15-oxo derivative (3), and of several halohydrins (4-9), synthesized starting from compounds 1 and 3, against Spodoptera littoralis have been determined and structure-antifeedant relationships are discussed.

InsecticidesbiologyScutellaria sieberiScutalbin CStereochemistryScutellariaGeneral ChemistryhalohydrinSpodoptera littoralisSpodopterabiology.organism_classificationantifeedant activityDiterpenes ClerodaneLepidoptera genitaliachemistry.chemical_compoundchemistryAcetoneNoctuidaeAnimalsscutecyprol ASettore BIO/15 - Biologia FarmaceuticaScutellaria sieberiGeneral Agricultural and Biological SciencesSpodoptera littoralis
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Scuteparvin, a new neoclerodane diterpenoid from Scutellaria parvula

2004

Abstract The diterpenoid fraction occurring in the acetone extract of the aerial parts of Scutellaria parvula has been investigated. Only one neoclerodane diterpenoid, scuteparvin, was isolated and its structure elucidated as 4α,18-epoxy-6α- trans -cinnamoyloxy- neo clerod-13-en-15,16-olide, a new natural product. Scuteparvin is quite similar to the already known ajugarin V from Ajuga remota , the only difference being the occurrence of a trans -cinnamoyl ester system instead of an acetate on the 6α-OH group. This finding confirms that the genera Scutellaria and Ajuga are closely related taxonomically.

biologyStereochemistryneoclerodaneScutellaria parvulabiology.organism_classificationBiochemistryditerpeneTerpenoidAjugalamiaceaeScutellaria parvulaBotanyScutellariaEcology Evolution Behavior and SystematicsBiochemical Systematics and Ecology
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Essential oil from the aerial parts of Centaurea cuneifolia Sibth. & Sm. and C. euxina Velen., two species growing wild in Bulgaria

2009

Abstract The volatile constituents of the aerial parts of Centaurea cuneifolia Sibth. & Sm. and Centaurea euxina Velen. from Bulgaria were extracted by hydrodistillation and were analyzed. The main components in C. cuneifolia were β-eudesmol (26.5%) and hexadecanoic acid (17.6%). The main components in C. euxina were hexadecanoic acid (20.3%), spathulenol (10.8%) and caryophyllene oxide (6.2%). The chemotaxonomic significances with respect to other previously studied species of the same sections ( Achrolopus and Phalolepis , respectively) are discussed.

beta-eudesmoloAsteraceaeBiochemistryCentaurea cuneifoliaessential oilSpathulenollaw.inventionPalmitic acidchemistry.chemical_compoundCentaurea cuneifolialawBotanyhexadecanoic acidSettore BIO/15 - Biologia FarmaceuticaChemical compositionEcology Evolution Behavior and SystematicsEssential oilspatulenolbiologySettore CHIM/06 - Chimica OrganicaAsteraceaechemotaxonomic significancebiology.organism_classificationchemistryChemotaxonomyCentaureaC. euxina
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Sesquiterpene lactones from Anthemis wiedemanniana

2005

Asteraceae; Anthemis wiedemanniana; sesquiterpene lactones; germacranolides; eudesmanolide

eudesmanolidebiologyTraditional medicineAsteraceaeAsteraceaebiology.organism_classificationSesquiterpeneBiochemistrychemistry.chemical_compoundchemistrysesquiterpene lactoneAnthemisgermacranolideEcology Evolution Behavior and SystematicsAnthemis wiedemannianaBiochemical Systematics and Ecology
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Photochemical reactivity of 6α-hydroxy, 7-keto neoclerodane diterpenoids

2006

Abstract The photochemical reactivity, in methanol at λ  = 254 nm, of two 6α-hydroxy-7-keto neoclerodane, isoeriocephalin ( 1 ) and teucrolivin B ( 2 ) was evaluated. From the first compound, two new products were obtained: the 6β-hydroxy epimer ( 3 ) and the ɛ-lactone ( 4 ). The second one yielded exclusively the new spiro γ-lactone ( 5 ). The formation of these new products can be explained by the well-known radical mechanism Norrish type I.

chemistry.chemical_compoundchemistryStereochemistryGeneral Chemical EngineeringGeneral Physics and AstronomyPhotochemical reactivityEpimerGeneral ChemistryMethanolSettore CHIM/06 - Chimica Organicaphotochemical reactivity Norrish type I
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Composition of essential oil of lemon thyme (Thymus × citriodorus) at different hydrodistillation times.

2018

Distillation time can both to optimise the production and to engineer the composition of essential oil in essential oil bearing plants. Purpose of this study was to evaluate the effect of duration of hydrodistillation on composition of essential oil of Thymus × citriodorus, the natural source of commercially important geraniol and citral, a component with valuable biological properties. Essential oils were isolated by hydrodistillation at different distillation times and analysed by GC/MS analytical methods. Increase in percentage of essential oil during all hydrodistillation time gradient was uneven. Elongation of hydrodistillation time decreased percentages of monoterpenes but increased p…

Time FactorsAcyclic MonoterpenesPlant ScienceCitral01 natural sciencesBiochemistryessential oilgeranialGas Chromatography-Mass Spectrometrylaw.inventionAnalytical ChemistryThymus Plantchemistry.chemical_compoundlawBiological propertyOils VolatileThymus citriodorusFood scienceSettore BIO/15 - Biologia FarmaceuticageraniolDistillationEssential oilhydrodistillation timeDistillation010405 organic chemistryChemistrynerolTerpenesOrganic ChemistrySettore CHIM/06 - Chimica Organica0104 chemical sciencesThymus × citriodoru010404 medicinal & biomolecular chemistryneralNatural sourceMonoterpenesComposition (visual arts)SesquiterpenesGeraniolNatural product research
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Assigning the C-15 configuration of 15-hydroxy-, 15-methoxy-, 15-ethoxy-hexahydrofurofuran neoclerodane diterpenoids

2004

Abstract Examination of 1 H and 13 C NMR spectra allows the establishment of rules for assigning the correct configuration at C-15 of 15-hydroxy-, 15-methoxy-, 15-ethoxy-hexahydrofurofuran neoclerodane diterpenoids. The structure of several diterpenoids has been assigned or ammended.

ChemistryStereochemistryOrganic ChemistryDrug DiscoveryAlkoxy groupCarbon-13 NMRBiochemistryTetrahedron
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Cytotoxicity of oleanolic and ursolic acid derivatives toward hepatocellular carcinoma and evaluation of NF-κB involvement.

2019

Oleanolic and ursolic acids are two ubiquitous isomeric triterpene phytochemicals known for their anticancer activity. A set of derivatives of the two compounds with a modified oxidation state and lipophylicity at C-3 and C-28 positions, were prepared and tested as anticancer agents versus the lines HepG2, Hep3B and HA22T/VGH of hepatocarcinoma, a strongly aggressive tumor that is not responsive toward the standard therapies. New derivatives containing a three carbons side chain on the C-3 position were synthetized in both stereoisomeric forms by the Barbier-Grignard procedure and three of them were found to be active toward all of the three targets. The implication of the transcriptional n…

Carcinoma HepatocellularApoptosis01 natural sciencesBiochemistrychemistry.chemical_compoundUrsolic acid Oleanolic acid HepG2 Hep3B HA22T/VGH Antitumor activity NF−κBUrsolic acidTriterpeneOleaDrug DiscoverymedicineTumor Cells CulturedHumansSettore BIO/15 - Biologia FarmaceuticaOleanolic AcidCytotoxicityMolecular BiologyCell Proliferationchemistry.chemical_classification010405 organic chemistryPlant ExtractsOrganic ChemistryLiver NeoplasmsNF-kappa BNF-κBSettore CHIM/06 - Chimica Organicamedicine.diseaseAntineoplastic Agents Phytogenicdigestive system diseasesTriterpenes0104 chemical sciences010404 medicinal & biomolecular chemistrychemistryMechanism of actionHepatocellular carcinomaMalusSettore BIO/14 - FarmacologiaCancer researchmedicine.symptomBioorganic chemistry
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Antibacterial activity of flavonoids and phenylpropanoids from Marrubium globosum ssp. libanoticum.

2006

Marrubium globosum Montbr. et Auch. ex Benth. ssp. libanoticum Boiss. (Lamiaceae) is a medicinal plant used for the treatment of inflammatory diseases, asthma, coughs and other pulmonary and urinary problems. The goal of our study was to assess the biological activity of M. globosum testing the methanol extract of aerial parts for its antibacterial activity against bacteria known to cause respiratory, gastrointestinal, skin and urinary disorders; the extract showed antibacterial effects against all the strains of bacteria used. A purification of this active extract showed the presence, as main constituents, of verbascoside, isorhamnetin 3-O-beta-D-rutinoside, quercetin 3-O-beta-D-rutinoside…

PharmacologyNaringeninAnti-Infective Agents/analysis Microbial Sensitivity TestsFlavonoidsbiologyTraditional medicineBacteriaPhenylpropionatesMicrobial Sensitivity Testsbiology.organism_classificationchemistry.chemical_compoundVerbascosidechemistryAnti-Infective AgentsApigeninBotanySettore BIO/15 - Biologia FarmaceuticaKaempferolQuercetinMarrubiumIsorhamnetinAntibacterial agentMarrubiumPhytotherapy research : PTR
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Volatile components of aerial parts of Centaurea nigrescens an C. stenolepis growing wild in the Balkans

2010

The volatile constituents of the aerial parts of Centaurea nigrescens Willd, collected in Romania and of two samples of C. stenolepis A. Kerner from Bulgaria and Romania were obtained by hydrodistillation and analyzed. The main components of C. stenolepis were caryophyllene oxide (6.9-15.6%), hexahydrofarnesyl acetone (6.5-4.4%), heptacosane (6.0-4.9%) and p-vinyl guiacol (4.3-5.0%). The main components of C. nigrescens were caryophyllene oxide (9.9%), β-eudesmol (9.5%), spathulenol (7.6%), heptacosane (6.1%) and p-vinyl guiacol (5.5%). The chemotaxonomic significance with respect to their co-location in Sections Lepteranthus and Nigrescentes, respectively, is discussed.

PharmacologybiologyCentaurea stenolepisCentaurea nigrescens Centaurea stenolepis Asteraceae volatile componentscaryophyllene oxide hexahydrofarnesyl acetone beta-eudesmol spathulenol p-vinyl guaiacolCentaureaPlant ScienceGeneral MedicineSettore CHIM/06 - Chimica OrganicaAsteraceaePlant Components Aerialbiology.organism_classificationSpathulenolComplementary and alternative medicineCaryophyllene oxideDrug DiscoveryBotanyCentaurea nigrescensOils VolatilePlant OilsSettore BIO/15 - Biologia FarmaceuticaStenolepisBeta-eudesmol
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Powerful tumor cell growth-inhibiting activity of a synthetic derivative of atractyligenin: Involvement of PI3K/Akt pathway and thioredoxin system

2014

The semi-synthetic ent-kaurane 15-ketoatractyligenin methyl ester (SC2017) has been previously reported to possess high antiproliferative activity against several solid tumor-derived cell lines. Our study was aimed at investigating SC2017 tumor growth-inhibiting activity and the underlying mechanisms in Jurkat cells (T-cell leukemia) and xenograft tumor models. METHODS: Cell viability was evaluated by MTT assay. Cell cycle progression, reactive oxygen species (ROS) elevation and apoptotic hallmarks were monitored by flow cytometry. Inhibition of thioredoxin reductase (TrxR) by biochemical assays. Levels and/or activation status of signaling proteins were assessed by western blotting. Xenogr…

CellBiophysicsAntineoplastic AgentsApoptosisAtractylosideBiologyCell cycleBiochemistryJurkat cellsMicePhosphatidylinositol 3-KinasesThioredoxinsTumor Cells CulturedmedicineAnimalsHumansMTT assayViability assaySettore BIO/15 - Biologia FarmaceuticaMolecular BiologyProtein kinase BPI3K/AKT/mTOR pathwayCell ProliferationPI3K/AktHCT 116 xenograftCytochromes cApoptosiThioredoxin systemSettore CHIM/06 - Chimica OrganicaCell cycleXenograft Model Antitumor AssaysCell biologymedicine.anatomical_structureCaspasesCancer researchThioredoxinDiterpenes KauraneProto-Oncogene Proteins c-aktEnt-kaurane
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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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Sesquiterpenes from Onopordum illyricum and their antifeedant activity

2012

Phytochemical investigation of the acetone extract of the aerial parts of Onopordum illyricum L. afforded five known sesquiterpenoids: compounds 3 and 4 already isolated from O. illirycum, and 8α-[4′-hydroxymethacryloyloxy]-sonchucarpolide (1), 8α-[4′-hydroxymethacryloyloxy]-4-epi-sonchucarpolide (2) and 8-(4′-hydroxymethacryloyl)-dehydromelitensin (5), not previously detected in this species. Compounds 4 and 5 showed moderate antifeedant activity against larvae of Spodoptera littoralis.

PharmacologybiologyTraditional medicineSesquiterpenes Onopordum illyricun antifeedant activityOnopordumPlant ScienceGeneral MedicineFeeding BehaviorSettore CHIM/06 - Chimica OrganicaAsteraceaeSpodopterabiology.organism_classificationComplementary and alternative medicinePhytochemicalLarvaDrug DiscoveryAnimalsSettore BIO/15 - Biologia FarmaceuticaSpodoptera littoralisSesquiterpenesOnopordum illyricum
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Sesquiterpene lactones and other constituents of Centaurea paniculata ssp. castellana

2002

Centaurea paniculatachemistry.chemical_classificationchemistry.chemical_compoundchemistryBotanyBiologySesquiterpeneBiochemistryFlavonesEcology Evolution Behavior and SystematicsBiochemical Systematics and Ecology
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Sesquiterpenoids in subtribe Centaureinae (Cass.) Dumort (tribe Cardueae, Asteraceae): distribution, (13)C NMR spectral data and biological propertie…

2012

Asteraceae Bercht. & J. Presl is one of the biggest and most economically important plant families. The taxonomy and phylogeny of Asteraceae is rather complex and according to the latest and most reliable taxonomic classification of Panero & Funk, based on the analysis of nine chloroplast regions, the family is divided into 12 subfamilies and 35 tribes. One of the largest tribes of Asteraceae is Cardueae Cass. with four subtribes (Carlininae, Echinopinae, Carduinae and Centaureinae) and more than 2500 species. Susanna & Garcia-Jacas have organized the genera of Centaureinae (about 800 species) into seven informal groups, which recent molecular studies have confirmed: 1. Basal genera; 2. Vol…

Magnetic Resonance Spectroscopy13C NMR spectral dataPlant ScienceHorticultureRhaponticumAsteraceaeBiochemistryElemaneSerratulaPhylogeneticsBotanySettore BIO/15 - Biologia FarmaceuticaAntiviralSpectral dataMolecular BiologyPhylogenyEffects on insectGermacranebiologyMolecular StructurePlant ExtractsCentaureinaeGeneral MedicineSettore CHIM/06 - Chimica OrganicaAsteraceaebiology.organism_classificationCentaureinaeCentaureaGuiaianesAntiprotozoalTaxonomy (biology)AntimicrobialAnti-inflammatoryEffects on plantEudesmaneAntitumor and cytotoxicSesquiterpenesPhytochemistry
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Antibacterial and anticoagulant activities of coumarins isolated from the flowers of Magydaris tomentosa.

2006

The phytochemical investigation of the acetone and methanol extracts of the flowers of Magydaris tomentosa (Desf.) DC afforded six known coumarins as well as (+)-meranzin hydrate (7), not previously reported as a natural product. The antibacterial activity of umbelliprenin (1), osthol (2), imperatorin (3), citropten (4) and (+)-meranzin hydrate (7) was tested against Gram-positive and Gram-negative bacteria. All coumarins (1-7) isolated in this study inhibited growth of all bacterial strains tested (MIC between 16 and 256 microg/mL), the most active being imperatorin (3) (MICs between 32 and 128 microg/mL) and citropten (4) (MICs between 16 and 256 microg/mL). The anticoagulant activity of …

MalePharmaceutical ScienceCitroptenFlowersMicrobial Sensitivity TestsPharmacognosyAnalytical Chemistrychemistry.chemical_compoundCoumarinsDrug DiscoveryOrganic chemistryAnimalsRats WistarAntibacterial agentPharmacologyApiaceaebiologyTraditional medicineImperatorinOrganic ChemistryAnticoagulantsbiology.organism_classificationAnti-Bacterial AgentsRatsComplementary and alternative medicinechemistryPhytochemicalMolecular MedicineAntibacterial activityOstholApiaceaePlanta medica
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Chemodiversity of the Essential Oil from Leaves of Abies nebrodensis (Lojac.) Mattei

2016

Abies nebrodensis (Lojac.) Mattei (Pinaceae) is a species occurring in a very small population only in a restricted area of Sicily. Its taxonomic classification as different species has been object of discussion. In this work the chemical composition of the essential oil from the leaves is presented for the first time and compared to the essential oils from other euroasiatic species reported in literature. Peculiar characteristics of the essential oil of A. nebrodensis are highlighted.

0106 biological sciencesAbies nebrodensiPlant compositionPopulationBioengineering01 natural sciencesPlant OilBiochemistryEssential oilGas Chromatography-Mass Spectrometrylaw.inventionSettore BIO/01 - Botanica Generalechemistry.chemical_compoundlawBotanyAbieOils VolatilePlant OilsSettore BIO/15 - Biologia FarmaceuticaAbies nebrodensiseducationMolecular BiologyEssential oilbeta-Pineneeducation.field_of_studybiologySettore BIO/02 - Botanica SistematicaChemistry (all)General ChemistryGeneral MedicineBiological classificationβ-PineneSettore CHIM/06 - Chimica Organicabiology.organism_classification0104 chemical sciencesPlant LeavesChemotaxonomy010404 medicinal & biomolecular chemistrychemistryChemotaxonomyPinaceaeMolecular MedicinePlant LeaveAbies010606 plant biology & botany
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Cytotoxic activity of diterpenoids isolated from the aerial parts of Elaeoselinum asclepium subsp. meoides.

2008

The phytochemical investigation of the acetone extract of the aerial parts of Elaeoselinum asclepium (L.) Bertol. subsp. meoides (Desf.) Fiori afforded several known diterpenoids as well as meoidic acid ( 5), new in the literature. The cytotoxic activities of elasclepic acid ( 1), ENT-atis-16-en-19-oic acid ( 2), ent-beyer-15-en-19-oic acid ( 3), ent-kaur-16-en-19-oic acid ( 4) and meoidic acid ( 5) were investigated on rat glioma C6 cells by evaluation of cell growth inhibition.

StereochemistryElaeoselinum asclepium subsp. meoides Umbelliferae diterpenoids meoidic acid cytotoxic activityPharmaceutical ScienceBiologyPharmacognosyAnalytical Chemistrychemistry.chemical_compoundCell Line TumorDrug Discoveryotorhinolaryngologic diseasesAcetoneCytotoxic T cellAnimalsCytotoxicityCell ProliferationPharmacologyMolecular StructureOrganic ChemistrySettore CHIM/06 - Chimica OrganicaElaeoselinum asclepium subsp. meoidesAntineoplastic Agents PhytogenicTerpenoidRatsComplementary and alternative medicinechemistryPhytochemicalMolecular MedicineDiterpeneDiterpenesApiaceaePlanta medica
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Assigning the C-15 configuration of 15-hydroxy-, 15-methoxy-, 15-ethoxy- hexahydrofurofuran neoclerodane diterpenoids

2004

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INDAGINE FITOCHIMICA SUGLI OLI DEI SEMI DI PTILOSTEMON GREUTERI (ASTERACEAE)

2012

Oli essenziali
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Lipase-catalysed preparation of acyl derivatives of the germacranolide sesquiterpenoid cnicin

2009

Several acyl derivatives of cnicin were obtained through lipase-catalysed acylation and alcoholysis reactions. In most reactions lipases showed a regioselective behaviour affording only one product. Longer chain acyl derivatives were prepared at lower temperature than the used in lipase-catalysed reactions, to preclude side products formation. The enzymatic approach let to prepare a family of novel acetyl and fatty acid derivatives of cnicin which are not obtainable following traditional organic synthetic procedures.

enzyme catalysis acylation alcoholysis sesquiterpenoids cnicinSettore CHIM/06 - Chimica Organica
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Indagini fitochimiche su alcune popolazioni italiane di Artemisia alba (Asteraceae)

2010

Flora Sicilia Appennino marchigiano oli essenzialiSettore BIO/15 - Biologia Farmaceutica
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Studio dell'attività biocatalitica delle piante del genere Citrus: risultati preliminari

2012

Citrus. Deacetilazione. BiocatalisiSettore CHIM/06 - Chimica Organica
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Phytochemical composition and antimicrobial activity of essential oil from different parts of Ferulago campestris growing wild in the Natural Park of…

2008

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Composition and allelopathic effect of the essential oils of two thistles: Cirsium creticum (Lam.) D.’Urv. ssp. triumfetti (Lacaita) Werner and Cardu…

2007

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Fetid odors in Caralluma europaea (Guss.) N.E.Br. (Apocynaceae-Asclepiadoideae): a chemical characterization

2008

ApocynaceaeSettore BIO/07 - EcologiapollinatorSettore BIO/03 - Botanica Ambientale E Applicatachemical volatilesfloral odorSettore CHIM/06 - Chimica OrganicaSettore CHIM/12 - Chimica Dell'Ambiente E Dei Beni Culturali
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Studio della reazione di Grignard su derivati dell'acido ursolico

2014

acido ursolico reattici di GrignardSettore CHIM/06 - Chimica Organica
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Sintesi di lattoni sesquiterpenici e loro attività citotossica

2004

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Natural products and derivatives from Ferulago campestris (Apiaceae)

2008

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Indagini fitochimiche sul galbano di Sicilia

2009

Settore BIO/15 - Biologia FarmaceuticaFerula galbaniflua botanica farmaceutica
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Citrus peels as biocatalyst for deacetylation reactions

2014

enzymatic deacetylation Citrus phitonadione
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Phytochemical investigation of the needles of Aabies nebrodensis (Lojac.) Mattei

2019

Abies nebrodensis (Lojac.) Mattei (Pinaceae) is a species living in a very small population only in a confined area of Sicily. In this study, the dichloromethane extract of the leaves was analyzed. Apart from three already known metabolites namely dehydroabietic acid; maltol; and rheosmin, previously detected in other species of Abies, a lanostane derivative was isolated. Its chemical structure was elucidated by means of extensive spectroscopic methods.

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Antibacterial and anticoagulant activities of coumarins isolated from the flowers of Magydaris tomentosa (Desf.) DC (Apiaceae)

2007

The phytochemical investigation of the acetone and methanol extracts of the flowers of Magydaris tomentosa (Desf.) DC afforded six known coumarins as well as (+)-meranzin hydrate (7), not previously reported as a natural product. The antibacterial activity of umbelliprenin (1), osthol (2), imperatorin (3), citropten (4) and (+)-meranzin hydrate (7) was tested against Gram-positive and Gram-negative bacteria. All coumarins (1-7) isolated in this study inhibited growth of all bacterial strains tested (MIC between 16 and 256 μg/mL), the most active being imperatorin (3) (MICs between 32 and 128 μg/mL) and citropten (4) (MICs between 16 and 256 μg/mL). The anticoagulant activity of compounds 1-…

Anti-Bacterial Agents/chemistry Coumarins/chemistry
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The cytotoxic activity of natural and semisynthetic sesquiterpene lactones

2004

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Conformational analysis and DFT calculations of 8 alpha-hydroxy-germacradiene-6,12-olide derivatives

2005

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Antimicrobial activity of coumarins from the roots of Ferulago campestris (Apiaceae)

2008

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Rapid and eco-friendly synthesis of graphene oxide-silica nanohybrids

2014

The increasing interest in Graphene oxide (GO) is due to many issues: the presence of both sp2-conjugated atoms and oxygen-containing functional groups provides a strong hydrophilicity and the possibility to further functionalize it with other molecules (i.e. π-π interactions covalent attachment etc.) [1]. Furthermore since the GO is biocompatible and noncytotoxic many studies have been recently focused on the development of GO-based nanodevices for bioimaging DNA detection drug delivery. Due to their low cytotoxicity and large internal surface area silica nanoparticles have been taken into account as promising material for biolabeling and drug loading/delivery. Particular consideration has recently been demonstrated for GO-silica composites because of the potentialities for electrical applications their chemical inertia and stability toward ions exposure. The possibility to combine the extraordinary properties of GO and silica offers several advantages for the realization of nanoprobes for biological applications and of biosensor [12]. The strategy for the fabrication of GO-nanosilica nanohybrids can be schematized as follows: (i) synthesis of GO by oxidizing graphite powder with the method described by Marcano et al. [3] (ii) Preparation of oxygen-loaded silica nanoparticles by thermal treatments in controlled atmosphere in order to induce high NIR emission at 1272 nm from high purity silica nanoparticles. (iii) preparation of GrO-silica nanohybrid films via rapid solvent casting in water. The nanohybrids were tested by XPS FTIR Raman analysis UV photoluminescence analysis TGA Zeta potential measurements electrical tests AFM and SEM. Several nanohybrids were prepared by combining two different typologies of GO and two different samples of silica.
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Nuovi flavonoidi da Bonannia graeca (L.) Halácsy e loro attività biologica

2006

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Metaboliti secondari in Caralluma europaea

2007

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Chemodiversity of the essential oil from leaves of Abies nebrodensis (Lojac.) Mattei

2016

As activities of the project "Preservation of Abies nebrodensis and restore of Geraci Siculo peatlands", the chemical composition of essential oils, obtained from leaves of Madonie fir, was compared with the ones of essential oils derived from Eurasian species studied up to now

Settore BIO/01 - Botanica GeneraleSettore BIO/02 - Botanica SistematicaSettore BIO/03 - Botanica Ambientale E ApplicataSettore BIO/15 - Biologia FarmaceuticaSicily Abies nebrodensis endemic essential oils
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The cytotoxic activity of natural and semisynthetic guaianolides

2004

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Indagine fitochimica sulle radici di Helleborus bocconei Ten. subsp. intermedius.

2006

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Metabolites from the aerial parts of the Sicilian population of Artemisia alba Turra

2013

Phytochemical investigation of the CH2Cl2 extract of the aerial parts of Artemisia alba Turra afforded one new irregular sesquiterpenoid, artemiric acid, and five known metabolites: hydroxydavanone, the coumarins isofraxidin and scopoletin, (6S*,7S*,10R*)-6,10-dimethyl-7,10-epoxyocta-11-enoic acid and artalbic acid. From the MeOH extract three flavonoids were identified: chrysoeriol, quercetin and isorhamnetin. The possible biogenetic pathways of artemiric and artalbic acids are discussed.

Secondary metabolites Artemisia alba TurraSettore CHIM/06 - Chimica Organica
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Sintesi e attività antitumorale di derivati dell'acido ursolico

2014

Settore CHIM/06 - Chimica Organicaacido ursolico attività antitumorale HCT116
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Chemical composition and anticancer activity of essential oil of Mediterranean sage (Salvia officinalis L.)

2013

Anticancer activity essential oil Salvia officinalis L.Settore CHIM/06 - Chimica OrganicaSettore BIO/15 - Biologia Farmaceutica
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Lignans and an unusual steroids from the seeds of Centaurea sclerolepis Boiss

2005

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Attività citotossica di derivati ent-kauranici.

2006

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Phytochemical investigation of four Teucrium species

2004

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Chemical composition of the essential oil of Centaurea sicana and C. giardinae growing wild in Sicily

2008

The essential oils of Centaurea sicana (S) and C. giardinae (G) were studied by GC and GC-MS. Thirty constituents for S, representing 81.5% of the total oil, and 24 compounds for G (94.2% of the total) were identified. The oils were rich in sesquiterpenoids (47.9% for S and 54.7% for G) and hydrocarbons (25.9% for S and 31.7% for G). Germacrene D (13.3%), (E)-β-farnesene (8.3%), nonacosane (7.3%), heptacosane (6.5%) and phytol (6%) were recognized as the main constituents for S, while caryophyllene oxide (17.7%), nonacosane (14.5%), germacrene D (11.5%), caryophyllene (11.2%) and heptacosane (10.3%) were the main compounds for G.

Centaurea sicana Centaurea giardinae asteraceae essential oil germacrene D caryophyllene oxideSettore CHIM/06 - Chimica Organica
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Biological activities of natural guaianolides from Centaurea hololeuca Boiss and their derivatives

2005

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Chemical composition of salvia argentea L. (laminaceae)

2014

laminaceae s. argentea acido ursolicoSettore CHIM/06 - Chimica Organica
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Chemical composition of the essential oil from the aerial parts of Micromeria fruticolosa (Bertol.) Grande (Lamiaceae) growing wild in Southern Italy.

2006

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Composizione chimica degli olii essenziali di due nuove specie di Centaurea (Centaureinae, Asteraceae) della Sicilia

2007

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Flavonoids in sbtribe Centaureinae (Cass.) Dumort (tribe Carduae, Asteraceae): distibution and 13C spectral data

2012

Asteraceae Bercht. & J. Presl is one of the biggest and most economically important plant families. The taxonomy and phylogeny of Asteraceae is rather complex and according to the latest and most reliable taxonomic classification of Panero & Funk, based on the analysis of nine chloroplast regions, the family is divided into 12 subfamilies and 35 tribes. One of the largest tribes of Asteraceae is Cardueae Cass. with four subtribes (Carlininae, Echinopinae, Carduinae and Centaureinae) and more than 2500 species. Susanna & Garcia-Jacas have organized the genera of Centaureinae (about 800 species) into seven informal groups, which recent molecular studies have confirmed: 1. Basal genera; 2. Vol…

Flavonoids Centaureinae (Cass.) Dumort Carduae Asteraceae 13C NMRSettore CHIM/06 - Chimica OrganicaSettore BIO/15 - Biologia Farmaceutica
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