Search results for "Sesquiterpene lactone"

showing 10 items of 21 documents

Phytochemical Studies on Ptilostemon greuteri Raimondo & Domina (Compositae)

2012

Ptilostemon greuteri Raimondo & Domina is described as a new species and its growth is limited to the area of the province of Trapani. Essential oils of aerial parts of P. greuteri were analized by gas chromatography-mass spectrometry (GC-MS). The analysis of acetonic extract of aerial parts led to identification of triterpenes components: α-amyrin, β-amyrin, α-amyrin acetate, β-amyrin acetate, lupeol, lupeol acetate and taraxasterol. CC and preparative TLC of acetonic extracts has yielded lignan lactone and a sesquiterpene lactone that have been isolated previously from other Ptilostemon species.

Ptilostemon greuterilcsh:Chemistrylcsh:QD241-441Compositaepentacyclic triterpeneslcsh:QD1-999lcsh:Organic chemistryESSENTIAL OIL AERIAL PARTS NMRlcsh:Botanysesquiterpene lactonelignan lactoneessential oillcsh:QK1-989
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Two new sesquiterpene lactones from Montanoa tomentosa ssp. microcephala

2001

Sesquiterpene lactones Antiproliferative activitySettore BIO/14 - Farmacologia
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Evaluation of the in vitro and in vivo antineoplastic effects of Parthenolide on MDA-MB231 breast cancer cells

2012

Triple-negative breast cancer refers to an aggressive subtype of breast cancer in which the tumor cells lack receptors for estrogen, progesterone and the HER2 protein on their surfaces. This type of breast cancer does not respond to treatments such as hormone therapy, like tamoxifen and aromatase inhibitors, or drugs that target HER2, like Herceptin. It is important, therefore, the identification of new selective drugs for the treatment of these tumors. Parthenolide (PN), a sesquiterpene lactone extracted from the medical plant Tanacetum parthenium, exerts anticancer activity on several tumor cell lines in culture, acting through diverse molecular mechanisms. Our previous studies have shown…

Settore BIO/10 - BiochimicaBreast cancer cells sesquiterpene lactones parthenolide DMAPT
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Structure and stereochemistry of stenophyllolide, a germacrolide from Centaurea aspera var. Stenophylla

1984

Abstract A crystalline compound, named stenophyllolide, obtained from an extract of Centaurea aspera var. stenophylla was shown to be 9β,15-dihydroxygermacra-1(10),4,11-trien-6α,12-olide by X-ray analysis. The molecular structure of stenophyllolide was solved with orthorhombic space group P2 1 2 1 2 1 , a = 11.719 (5), b = 13.389 (5), c = 8.646 (5) A for Z = 4, by direct methods and refined to a final R of 0.06 for 1198 observed reflections.

Stenophyllachemistry.chemical_classificationbiologyStereochemistryPlant ScienceGeneral MedicineHorticultureSesquiterpenebiology.organism_classificationSesquiterpene lactoneBiochemistrychemistry.chemical_compoundchemistryCentaurea asperaOrthorhombic crystal systemMolecular BiologyPhytochemistry
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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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Melampolides from Enydra anagallis

2001

The investigation of an Argentine collection of Enydra anagallis afforded sesquiterpene lactones of the melampolide type two of which were previously known. Their structures were elucidated by spectroscopic methods. Fil: Bardon, Alicia del Valle. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Tucumán. Instituto de Química del Noroeste. Universidad Nacional de Tucumán. Facultad de Bioquímica, Química y Farmacia. Instituto de Química del Noroeste; Argentina Fil: Cardona, Luis. Universidad de Valencia; España Fil: Cartagena, Elena. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Tucumán. In…

StereochemistryOtras Ciencias BiológicasCOMPOSITAEPlant ScienceHorticultureAsteraceaeSesquiterpeneBiochemistryCiencias BiológicasHeliantheaechemistry.chemical_compoundLactonesOrganic chemistryMolecular Biologychemistry.chemical_classificationbiologyChemistrySpectrum AnalysisOtras Ciencias QuímicasENYDRACiencias QuímicasSESQUITERPENE LACTONESGeneral Medicinebiology.organism_classificationAnagallisHELIANTHEAESesquiterpenesLactoneCIENCIAS NATURALES Y EXACTASMELAMPOLIDES
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Antiproliferative activity against leukemia cells of sesquiterpene lactones from the Turkish endemic plant Centaurea drabifolia subsp. detonsa

2017

The apolar organic extract obtained from aerial parts of Centaurea drabifolia Sibth. & Sm. subsp. detonsa (Bornm.) Wagenitz, growing wild in Turkey, was investigated for the first time for its secondary metabolite composition. Seven sesquiterpene lactones belonging to the guaiane class (1-7), including the new compound 4, along with a fatty acid lactone derivative (8), were isolated. The structures of these compounds were established by spectroscopic analysis, including 2D NMR spectroscopic techniques, with the stereostructure of the new guaiane 4 determined with the help of MTPA derivatization. Cytotoxic activities of compounds 1-7 were evaluated against two cancer cell lines, namely acute…

TurkeyCentaurea drabifoliaStereochemistryCynaropicrinCentaureaMultidrug-resistant cell lineSecondary metaboliteBiologySesquiterpene01 natural sciencesLactonesSesquiterpenes GuaianeStructure-Activity Relationshipchemistry.chemical_compoundCell Line TumorDrug DiscoverymedicineHumansDerivatizationPharmacologychemistry.chemical_classificationLeukemiaMolecular StructurePlant Extracts010405 organic chemistryFatty acidGeneral MedicinePlant Components AerialAntineoplastic Agents PhytogenicCynaropicrin0104 chemical sciences010404 medicinal & biomolecular chemistrychemistryDrug Resistance NeoplasmAntileukemic activityDrug Screening Assays AntitumorSesquiterpene lactonesSesquiterpenesTwo-dimensional nuclear magnetic resonance spectroscopyDerivative (chemistry)Lactonemedicine.drugFitoterapia
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<strong>Artemisinin: Tentative Mechanism of Action and Resistance</strong>

2016

The sesquiterpene lactones constitute a large class of secondary plant metabolites, which carry a‑methylene‑g‑lactone groups as common structural element and display a number of bioactivities. Every year, 1–2 million people living in the tropics and subtropics die of malaria. Lactone artemisinin is the most effective treatment vs. malaria, the most infectious disease in the world today. Artemisinins are derived from extracts of sweet wormwood (Artemisia annua) and are well established for the treatment of malaria, e.g., highly drug-resistant strains. They resulted in one of the most significant advances in the treatment of malaria since the discovery and first use of quinine over 300 years …

chemistry.chemical_classificationArtemisininsQuinineNatural productTraditional medicineArtemisia annuaBiologySesquiterpene lactonemedicine.diseasebiology.organism_classificationchemistry.chemical_compoundDrug developmentchemistryparasitic diseasesmedicineArtemisininMalariamedicine.drugProceedings of 2nd International Electronic Conference on Medicinal Chemistry
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SF002-96-1, a new drimane sesquiterpene lactone from an Aspergillus species, inhibits survivin expression

2013

Survivin, a member of the IAP (inhibitor of apoptosis) gene family, is overexpressed in virtually all human cancers and is functionally involved in the inhibition of apoptosis, regulation of cell proliferation, metastasis and resistance to therapy. Because of its upregulation in malignancy, survivin has currently attracting considerable interest as a new target for anticancer therapy. In a screening of approximately 200 strains of imperfect fungi for the production of inhibitors of survivin promoter activity, a new drimane sesquiterpene lactone, SF002-96-1, was isolated from fermentations of an Aspergillus species. The compound inhibited survivin promoter activity in transiently transfected…

chemistry.chemical_classificationCell growthnatural productsOrganic Chemistrystructure elucidationapoptosisTransfectionsecondary metabolitesurvivinInhibitor of apoptosisSesquiterpene lactoneMolecular biologyFull Research Paperinhibitorlcsh:QD241-441ChemistrychemistryDownregulation and upregulationlcsh:Organic chemistryApoptosisSurvivinImmunologyProtein biosynthesislcsh:Qlcsh:ScienceBeilstein Journal of Organic Chemistry
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Guaianolides from Centaurea babylonica

2005

chemotaxonomyCentaurea babylonicabiologyChemotaxonomyguaianolideBotanysesquiterpene lactoneCentaurea babylonicaAsteraceaeAsteraceaebiology.organism_classificationBiochemistryEcology Evolution Behavior and Systematics
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