Search results for "composition"

showing 10 items of 2675 documents

Chemical composition of the essential oils of Centaurea formanekii and C. orphanidea ssp. thessala, growing wild in Greece.

2012

The volatile constituents of the aerial parts of Centaurea formanekii Halacsy and the aerial parts, capitula and roots of C. orphanidea Heldr. & Sart. ex Boiss. ssp. thessala (Hausskn.) Dostál from Greece were extracted by hydrodistillation and analyzed. The main components in C. formanekii were hexadecanoic acid (13.6%), δ-elemene (9.1%), and spathulenol (6.9%). The main components in C. orphanidea ssp. thessala were γ-elemene (26.1%) and caryophyllene oxide (13.2%) in the aerial parts, hexadecanoic acid (33.5%) and heptacosane (6.3%) in the capitula, and hexadecanoic acid methyl ester (22.0%) and α-chamigrene (14.0%) in the roots. The chemotaxonomic significance with respect to other…

PharmacologybiologyGreeceChemistryEcologyCentaureaPlant ScienceGeneral Medicinebiology.organism_classificationGas Chromatography-Mass SpectrometrySpathulenolComplementary and alternative medicineCaryophyllene oxideCentaureaDrug DiscoveryBotanyOils VolatilePlant OilsChemical compositionNatural product communications
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Chemical Composition of the Essential Oil of Zingiber Zerumbet Var. Darcyi

2012

The chemical composition of essential oil obtained by hydrodistillation method from the rhizomes of Z. zerumbet var. darcyi was determined by GC and GC-MS. Thirty-three compounds, accounting for 93.6% of the oil were identified including twenty compounds in minor (0.1-0.6%) and eight in trace (<0.05%) amounts. The main compounds were zerumbone (69.9%) α-humulene (12.9%), humulene epoxide II (2.5%), caryophyllene oxide (1.1%) and camphene (1.9%). In this analysis, it has been found that the variety could be used as an additional new source of natural zerumbone besides Zingiber zerumbet. This is a first report on the analysis of Z. zerumbet var. darcyi oil.

PharmacologybiologyHumuleneTraditional medicinePlant ScienceGeneral Medicinebiology.organism_classificationlaw.inventionRhizomechemistry.chemical_compoundComplementary and alternative medicinechemistryZingiber zerumbetlawDrug DiscoveryBotanyCampheneZingiberaceaeGas chromatography–mass spectrometryChemical compositionEssential oilNatural Product Communications
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New Steroidal Alkaloids from Solanum Hypomalacophyllum

2010

Two new steroidal alkaloids (1-2) have been isolated from the leaves and roots of Solanum hypomalacophyllum Bitter, respectively. Their structures have been elucidated as deacetoxysolaphyllidine-3- O-β-D-glucopyranoside (1) and 4-keto-5,6-dihydro-(20 S)-verazine (2). Furthermore, two known steroidal alkaloids, 20 R-verazine and 20 S-verazine, and the common secondary metabolites oleanolic acid and β-sitosterol were isolated from the roots, whereas deacetoxysolaphyllidine was obtained from the leaves.

PharmacologybiologyPlant compositionChemical structurePlant ScienceGeneral Medicinebiology.organism_classificationchemistry.chemical_compoundComplementary and alternative medicinechemistryDrug DiscoveryBotanySolanumChemical compositionOleanolic acidSolanaceaeNatural Product Communications
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A Generalized Synthesis of 3-Amino-5-aryl-, 3-Amino-5-polyfluorophenyl-, and 3-Amino-5-alkyl-1,2,4-oxadiazoles through Ring-degenerate Rearrangements

2002

A generalized synthesis of 3-amino-5-aryl-, 3-amino-5-poly- fluorophenyl- and 3-amino-5-alkyl-1,2,4-oxadiazoles has been developed starting from the 3-amino-5-methyl-1,2,4-oxadiazole as a common synthon. Aroylation or alkanoylation of this aminooxadiazole, followed by thermally- induced ring-degenerate equilibration of resulting 3-acylamino compounds, and final acid hydrolysis of the 3-acetylamino-5-aryl- (or 5-polyfluorophenyl-), or 3- acetylamino-5-alkyl-1,2,4-oxadiazoles counterpart which is formed, gave the expected 3-amino-5-substituted 1,2,4-oxadiazoles. In the case of some 3- aroylamino compounds, yields of final 3-amino-5-aryloxadiazoles are higher than that expected on the basis of…

Pharmacologychemistry.chemical_classificationChemistryArylOrganic ChemistryDegenerate energy levelsSynthonComposition (combinatorics)Ring (chemistry)Medicinal chemistryAnalytical Chemistrychemistry.chemical_compoundAcid hydrolysisAlkylHETEROCYCLES
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Cycloartane-type Glycosides from Two Species of Astragalus (Fabaceae)

2009

Three known cycloartane-type glycosides were isolated from the roots of two different species of Astragalus, A. glycyphyllos, A. sempervirens. The identification of these compounds were mainly achieved by 2D NMR spectroscopic techniques and FAB-MS. The results of our studies confirm that triterpene saponins from the cycloartane-type skeleton might be chemotaxonomically significant to the genus Astragalus.

Pharmacologychemistry.chemical_classificationTraditional medicinebiologyChemistryPlant compositionGlycosidePlant ScienceGeneral MedicineFabaceaebiology.organism_classificationAstragalusComplementary and alternative medicineTriterpeneGenusDrug DiscoveryNatural Product Communications
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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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Triterpene Saponins from the Fruits of Phytolacca rugosa (Phytolaccaceae)

2010

Four known serjanic acid glycosides were isolated from the fruits of Phytolacca rugosa and characterized mainly by 2D NMR spectroscopy and mass spectrometry. This aglycon has a chemotaxonomic significance for the genus Phytolacca.

Pharmacologychemistry.chemical_classificationbiologyPlant compositionGlycosidePlant ScienceGeneral MedicinePhytolacca rugosabiology.organism_classificationPhytolaccaceaeComplementary and alternative medicineTriterpenechemistryChemotaxonomyDrug DiscoveryBotanyPhytolaccaNatural Product Communications
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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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Interdiffusion in blends of polystyrene and polymethylstyrene studied by light scattering after temperature jumps across the phase boundary

1992

Abstract We describe a simple light scattering set-up for measuring interdiffusion coefficients D in polymer blends by generating spinodal decomposition and subsequent dissolution after temperature jumps across the phase boundary. In blends of polystyrene and polymethylstyrene (random copolymer of 60% m-methylstyrene and 40% p-methylstyrene) D values were obtained between 10−11 and 10−15 cm2s−1 at temperatures up to 50 K above the upper critical solution temperature. The results are discussed in relation to tracer diffusion in the same system.

Phase boundaryPolymers and PlasticsChemistrySpinodal decompositionDiffusionOrganic ChemistryThermodynamicsLight scatteringchemistry.chemical_compoundUpper critical solution temperaturePolymer chemistryMaterials ChemistryPolymer blendPolystyreneDissolutionPolymer
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Characterization and Decomposition of the Natural van der Waals SnSb2Te4 under Compression

2020

[EN] High pressure X-ray diffraction, Raman scattering, and electrical measurements, together with theoretical calculations, which include the analysis of the topological electron density and electronic localization function, evidence the presence of an isostructural phase transition around 2 GPa, a Fermi resonance around 3.5 GPa, and a pressure-induced decomposition of SnSb2Te4 into the high-pressure phases of its parent binary compounds (alpha-Sb2Te3 and SnTe) above 7 GPa. The internal polyhedral compressibility, the behavior of the Raman-active modes, the electrical behavior, and the nature of its different bonds under compression have been discussed and compared with their parent binary…

Phase transitionContext (language use)[CHIM.INOR]Chemical Sciences/Inorganic chemistry010402 general chemistry01 natural sciencesInorganic Chemistrysymbols.namesakeChemical structureCationsVan der Waalselectronic topologicalPhysical and Theoretical ChemistryCompressibility010405 organic chemistryChemistryCompressionDeformation0104 chemical scienceshigh pressuremetavalent bondingChemical physicsFISICA APLICADAMolecular vibration[PHYS.COND.CM-MS]Physics [physics]/Condensed Matter [cond-mat]/Materials Science [cond-mat.mtrl-sci]symbolsCondensed Matter::Strongly Correlated ElectronsFermi resonanceSnSb2Te4pressure-induced decompositionvan der Waals forceTernary operationRaman spectroscopyRaman scatteringbonding characterInorganic Chemistry
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