Search results for "Urea"

showing 10 items of 888 documents

Chemical composition of the essential oils of Centaurea formanekii and Centaurea orphanidea ssp. thessala, two Centaurea species growing wild in Gree…

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 …

Centaurea formanekiiCaryophyllene oxideC. orphanidea ssp. thessalaγ-elemeneSettore CHIM/06 - Chimica OrganicaSettore BIO/15 - Biologia FarmaceuticaAsteraceaeHexadecanoic acidMusk xyleneEssential oil
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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…

Centaurea hololeucaguaianolideAsteraceaechemosystematicantifeedant activity
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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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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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Volatile components from aerial parts of centaurea spinosociliata seenus ssp. Cristata (Bartl.) Dostál and centaurea spinosociliata seenus ssp. spino…

2010

The paper reports on the volatile components oil from aerial parts of two Asteraceae growing wild in Croatia: Centaurea spinosociliata ssp. cristata (syn. Centaurea cristata Bartl. subsp. rabenhorstiana (Sch.Bip.) Nyman) (CSC) and C. spinosociliata ssp. spinosociliata (CSS). The volatile components were obtained by hydrodistillation from selected plants and were determined by the GC-MS system on two fused-silica capillary columns of different polarity. The oil content was 0.08 % (CSC) and 0.07 % (CSS) on a dry weight basis. Altogether 73 compounds were identified accounting for 90.8 % (CSC) and 92.8 % (CSS) of the total oil, that were characterized mainly by hydrocarbons (37.9 %; 30.4 %), s…

Centaurea spinosociliata ssp. cristata; C. spinosociliata ssp. spinosociliata; Asteraceae; volatile components; heptacosane; cyclosativene; caryophyllene oxide; GC-MSSettore CHIM/06 - Chimica OrganicaCentaurea spinosociliata Seenus ssp. cristata (Bartl.) Dostál Centaurea spinosociliata Seenus ssp. spinosociliata asteraceae volatile components heptacosane cyclosativene caryophyllene oxide GC-MS
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Chemical composition of the essential oil of the local endemics Centaurea davidovii and C. parilica (Asteraceae, sect. Lepteranthus) from Bulgaria

2014

In the present study the chemical compositions of the essential oils from aerial parts of Centaurea davidovii Urum. and C. parilica Stoj. & Stef., both endemic to Bulgaria, were evaluated by GC and GC-MS. The main components of C. davidovii were β-eudesmol (13.9%), spathulenol (13.3%), caryophyllene oxide (10.1%) and ( Z)-phytol (5.4%). The main components of C parilica were hexadecanoic acid (39.2%), ( Z, Z)-9,12-octadecadienoic acid (11.9%), caryophyllene oxide (6.8%) and spathulenol (6.6%). In order to compare the essential oils composition of these taxa and of related species a PCA analysis was carried out.

CentaureaC. davidoviiPlant Scienceβ-eudesmolessential oilSpathulenollaw.inventionlawDrug DiscoveryBotanyhexadecanoic acidspathulenolOils VolatileCentaurea specieSettore BIO/15 - Biologia FarmaceuticaC. parilicaBulgariaEndemismChemical compositionessential oilsEssential oilPharmacologybiologyPlant ExtractsGeneral MedicineSettore CHIM/06 - Chimica OrganicaCentaurea davidoviiAsteraceaebiology.organism_classificationComplementary and alternative medicineCaryophyllene oxideCentaureaCentaurea parilica
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Sesquiterpene Lactones fromCentaurea paui

1994

Abstract A new elemanolide and two new heliangolides as well as (2R,3R)-(+)-3-hydroxy-2-methyl-butyrolactone have been isolated from Centaurea paui. The structures were elucidated by high field NMR techniques and chemical transformation.

Chemical transformationchemistry.chemical_compoundChemistryStereochemistryCentaurea pauiMolecular MedicineHigh fieldSesquiterpeneNatural Product Letters
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2021

We report on the thermodynamic, structural, and dynamic properties of a recently proposed deep eutectic solvent, formed by choline acetate (ChAc) and urea (U) at the stoichiometric ratio 1:2, hereinafter indicated as ChAc:U. Although the crystalline phase melts at 36–38 °C depending on the heating rate, ChAc:U can be easily supercooled at sub-ambient conditions, thus maintaining at the liquid state, with a glass–liquid transition at about −50 °C. Synchrotron high energy x-ray scattering experiments provide the experimental data for supporting a reverse Monte Carlo analysis to extract structural information at the atomistic level. This exploration of the liquid structure of ChAc:U reveals th…

ChemistryHydrogen bondGeneral Physics and AstronomyDeep eutectic solventCrystallographysymbols.namesakechemistry.chemical_compoundMolecular dynamicsPhase (matter)symbolsUreaPhysical and Theoretical Chemistryvan der Waals forceSupercoolingStoichiometryThe Journal of Chemical Physics
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Chemical Reactivity in AOT Microemulsions:  Kinetics of Water Replacement in a Square-Planar Palladium(II) Aquo Complex by Monoalkylthioureas

1998

The kinetics of water replacement in the cationic palladium(II) aquo complex [Pd(Et4dien)(H2O)]2+, where Et4dien = Et2N(CH2)2NH(CH2)2NEt2, by thiourea, methylthiourea, and ethylthiourea have been studied at 25.0 °C in heptane−AOT−water microemulsion over a wide range of the molar ratio R (=[H2O]/[AOT]) at the constant surfactant concentration of 0.13 mol dm-3. The reaction rates are significantly higher in microemulsions than in bulk water and decrease rapidly as the parameter R increases. The kinetic data, interpreted quantitatively by applying the pseudophase model to the microemulsion, indicate that there is a weak partitioning of the nucleophiles between the water core and the AOT inter…

ChemistryKineticsInorganic chemistrychemistry.chemical_elementSurfaces Coatings and FilmsPartition coefficientReaction ratechemistry.chemical_compoundThioureaPulmonary surfactantMaterials ChemistryMicroemulsionPhysical and Theoretical ChemistryMetal aquo complexPalladiumThe Journal of Physical Chemistry B
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Fatty Acid Carboxylate- and Anionic Surfactant-Controlled Delivery Systems That Use Mesoporous Silica Supports

2010

We report the preparation of a MCM-41 mesoporous material that contains the dye [Ru(bipy) 3 ]Cl 2 (bipy= bipyridine) inside the mesopores and functionalised with suitable binding groups at the entrance of the pores. Solids S1―S3 were obtained by the reaction of the mesoporous material with N-methyl-N'-propyltrimethoxysilylimidazolium chloride, N-phenyl-N'-[3-(trimethoxysilyl)propyl]thiourea, or N-phenyl-N'-[3-(trimethoxysilyl)propy1]urea, respectively. A study of the dye delivery of these systems in buffered water (pH 7.0, 2-[4-(2-hydroxyethyl)piperazin-1-yl]ethanesulfonic acid (HEPES), 10 ―3 mol dm ―3 ) in the presence of a family of carboxylate ions was carried out. In the interaction of …

ChemistryOrganic ChemistryInorganic chemistryGeneral ChemistryMesoporous silicaChlorideCatalysisBipyridinechemistry.chemical_compoundThioureaPolymer chemistrymedicineEthanesulfonic acidCarboxylateHybrid materialMesoporous materialmedicine.drugChemistry - A European Journal
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