Search results for "Urea"

showing 10 items of 888 documents

Components from the Essential oil of Centaurea aeolica Guss. and C-diluta Aiton from Sicily, Italy

2015

Volatile components from florets, leaves and stems and branches of Centaurea aeolica Guss. harvested in Lipari, Sicily, Italy, were analysed by gas phase chomatography (GC) and gas chomatography mass spectrometry (GC-MS). The main constituents were β-eudesmol, caryophyllene oxide, ( E )-12-norcaryophyll-5-en-2-one and hexahydrofarnesylacetone in flowers, hexahydrofarnesylacetone, 2-methyloctadecane and tricosane in the leaves and hexadecanoic acid , caryophyllene oxide and β-eudesmol in the stems and branches . The analysis of the essential oil of the aerial parts of Centaurea diluta Aiton gave mainly fatty acids and derivatives, the main ones being hexadecanoic acid and (Z,Z)-9,12-octadeca…

PharmacologyDrug Discovery3003 Pharmaceutical ScienceOrganic Chemistryβ-eudesmolPlant ScienceHexahydrofarnesylacetoneβ-eudesmollcsh:QK1-989lcsh:Chemistrylcsh:QD241-441lcsh:QD1-999lcsh:Organic chemistryCaryophyllene oxideCentaurea dilutavolatile componentslcsh:BotanyVolatile componentCentaurea aeolicaGC-MSHexadecanoic acid
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Synthesis of 2H-Imidazo[2',1':2,3] [1,3]thiazolo[4,5-e]isoindol-8-yl-phenylureas with promising therapeutic features for the treatment of acute myelo…

2022

Despite progressive advances in understanding the molecular biology of acute myeloid leukemia (AML), the conventional therapeutic approach has not changed substantially, and the outcome for most patients is poor. Thus, continuous efforts on the discovery of new compounds with improved features are required. Following a multistep sequence, we have identified a new tetracyclic ring system with strong antiproliferative activity towards several haematological cell lines. The new compounds possess structural properties typical of inactive-state-binding kinase inhibitors and are structurally related to quizartinib which is known as type-II tyrosine kinase inhibitor. In particular, the high activi…

PharmacologyFMS-like tyrosine kinase 3 (FLT3)FLT3/ITD3][13]thiazolo[4Organic Chemistry2H-imidazo [2′1':23][13]thiazolo[45-e]isoindol-8-yl-phenylureas2H-imidazo [2′1':23][13]thiazolo[45-e]isoindol-8-yl-phenylureas; Acute myeloid leukemia (AML); FLT3/ITD; FMS-like tyrosine kinase 3 (FLT3); Internal tandem duplication (ITD)ApoptosisGeneral Medicine2H-imidazo [2′Leukemia Myeloid AcuteMiceInternal tandem duplication (ITD)fms-Like Tyrosine Kinase 35-e]isoindol-8-yl-phenylureasCell Line TumorDrug DiscoveryMutationAcute myeloid leukemia (AML)AnimalsHumansProtein Kinase Inhibitors1':2European journal of medicinal chemistry
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Wirkungen von Acetazolamid, Chlorothiazid und Chlormerodrin auf die Clearance von Inulin, echtem endogenen Kreatinin, PAH und Harnstoff. Abgrenzung n…

1959

PharmacologyInulin ClearanceCreatininebusiness.industryGeneral MedicinePharmacologyNephrotoxicitychemistry.chemical_compoundchemistrymedicineUreaAminohippuric acidChlormerodrinAcetazolamidebusinessChlorothiazidemedicine.drugNaunyn-Schmiedeberg's Archiv f�r Experimentelle Pathologie und Pharmakologie
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Gel-electrophoretic description of European populations ofTerellia virens (Loew) (Diptera, Tephritidae); implications for its use as an agent for the…

1991

Allozyme frequencies of 15 enzyme loci, 14 of which were polymorphic, were used to characterize sevenTerellia virens populations originating from three allopatrically distributedCentaurea species. The two populations whose origins were geographically furthest apart, from Israel (onC. iberica) and from Switzerland (onC. vallesiaca), showed relatively high values of genetic distance from the 5 populations sampled in Austria and Hungary (onC. maculosa) (Nei's D>0.07). The latter five displayed a high degree of genetic similarity. No diagnostic (fixed) allelic differences were observed between these three groups ofT. virens populations, but they could be well characterized by significant differ…

PharmacologybiologyBiological pest controlZoologyIntroduced speciesCell BiologyAsteraceaebiology.organism_classificationCellular and Molecular NeuroscienceGenetic distanceCentaureaChemotaxonomyTephritidaeBotanyMolecular MedicineWeedMolecular BiologyExperientia
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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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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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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 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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Der Einflu� von Adrenalektomie und Nebennierenrindenhormonen auf die renalen Clearancen von Inulin, p-Aminohippurat, echtem endogenen Kreatinin und H…

1959

Pharmacologymedicine.medical_specialtyPara aminohippurateAdrenal cortex hormonesAdrenalectomymedicine.medical_treatmentInulinRenal functionEndogenyGeneral Medicinechemistry.chemical_compoundEndocrinologychemistryInternal medicinemedicineCreatinine ureaClearanceNaunyn-Schmiedebergs Archiv f�r Experimentelle Pathologie und Pharmakologie
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Effect of tormentic acid on insulin secretion in isolated rat islets of langerhans

1989

Tonnentic acid was isolated as the hypoglycemic agent of Poterium ancistroides Desf. The present study reports effects of this compound on isolated islets of Langerhans. We demonstrate that tormentic acid in the presence of 1.66 mM glucose initiates insulin secretion by isolated rat islets of Langerhans in a dose-dependent fashion at concentrations ranging from 0.05 to 0.5 mM. However, the compound has no effect on the insulin-releasing capacity of 16.6 mM glucose. Similar results were obtained with the sulfonylurea glibenclamide (0.01 mM) used as a reference. These results suggest that the hypoglycemic effect of tormentic acid is due to a diect effect of the compound in vitro.

Pharmacologymedicine.medical_specialtygeographygeography.geographical_feature_categorymedicine.drug_classTormentic acidIsletSulfonylureaIn vitroGlibenclamidechemistry.chemical_compoundEndocrinologychemistryInternal medicinemedicineInsulin secretionIsolated isletsmedicine.drugPhytotherapy Research
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