Search results for "Saponin"

showing 10 items of 132 documents

Cytotoxicity of Secondary Metabolites from Dracaena viridiflora Engl & Krause and their Semisynthetic Analogues

2017

The MeOH extract of Dracaena viridiflora was found to display significant cytotoxicity against some cancer cell lines. Systematic phytochemical investigation of this extract led to the isolation and structure elucidation of ten secondary metabolites including five spirostane (1-5) and one furostane (6) steroidal saponins. Furthermore, some acetylated spirostane analogues and three previously unreported derivatives with the 22,26-epoxycholesta-5,22-diene skeleton (15-17) were prepared from trillin (1), prosapogenin A of dioscin (2) and dioscin (4) by reaction with ZnCl 2/Ac 2O. Among the isolated and semisynthetic compounds, dioscin showed the most potent cytotoxicity against A549, Jurkat an…

Pharmacologysteroidal saponinsbiologyTraditional medicine010405 organic chemistryChemistryOrganic ChemistryPlant Sciencebiology.organism_classification01 natural sciencesDracaena viridifloralcsh:QK1-9890104 chemical scienceslcsh:Chemistrylcsh:QD241-441010404 medicinal & biomolecular chemistrylcsh:QD1-999lcsh:Organic chemistryepoxycholesta-5.22-dieneslcsh:BotanyDrug DiscoverycytotoxicityCytotoxicityDracaenaRecords of Natural Products
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Triterpenoid saponins from the cultivar “Green Elf” of Pittosporum tenuifolium

2021

Four oleanane-type glycosides were isolated from a horticultural cultivar “Green Elf” of the endemic Pittosporum tenuifolium (Pittosporaceae) from New Zealand: three acylated barringtogenol C glycosides from the leaves, with two previously undescribed 3-O-β-d-glucopyranosyl-(1→2)-[α-l-arabinopyranosyl-(1→3)]-β-d-glucuronopyranosyl-21-O-angeloyl-28-O-acetylbarringtogenol C, 3-O-β-d-galactopyranosyl-(1→2)-[α-l-arabinopyranosyl-(1→3)]-β-d-glucuronopyranosyl-21-O-angeloyl-28-O-acetylbarringtogenol C, and the known 3-O-β-d-glucopyranosyl-(1→2)-[α-l-arabinopyranosyl-(1→3)]-β-d-glucuronopyranosyl-21-O-angeloyl-28-O-acetylbarringtogenol C (Eryngioside L). From the roots, the known 3-O-β-d-glucopyra…

PittosporaceaeSaponinPittosporaceaePharmaceutical ScienceOrganic chemistry01 natural sciencesTAS1R2/TASR3Analytical ChemistryTriterpenoidTAS1R3QD241-441sweet tasteDrug Discovery[SDV.BBM]Life Sciences [q-bio]/Biochemistry Molecular BiologyCultivarPhysical and Theoretical Chemistrytaste inhibitor2. Zero hungerchemistry.chemical_classificationbiologyTraditional medicine010405 organic chemistryPittosporum tenuifoliumbarringtogenol CGlycosideSweet tastebiology.organism_classification0104 chemical sciencesPittosporum tenuifolium010404 medicinal & biomolecular chemistry<i>Pittosporum tenuifolium</i>chemistryChemistry (miscellaneous)Molecular Medicine[SDV.AEN]Life Sciences [q-bio]/Food and Nutrition
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Polymeric matrix hydrophobicity governs saponin packing-density on nanoparticle surface and the subsequent biological interactions.

2020

Abstract This study investigated the loading behavior of Quillaja saponin as a model surface-active cargo on (NP) nanoparticles prepared with various hydrophobic polymers and using different organic solvents through emulsification/solvent evaporation, and the impact of NP surface hydrophobicity upon the cytotoxic and hemolytic properties of the loaded entity. A superficial monolayered arrangement of saponins on NP was established (R2 > 0.9) for all NP, as the saponin loading values complied with the Langmuir adsorption isotherm over the entire concentration range. Next, based on the measurement of interfacial tension between formulation phases, and the subsequent use of Gibb’s adsorption is…

PolymersSurface PropertiesSaponinNanoparticle02 engineering and technology010402 general chemistry01 natural sciencesQuillaja SaponinsBiomaterialsSurface tensionsymbols.namesakeColloid and Surface ChemistryGibbs isothermAdsorptionchemistry.chemical_classificationbiologyChemistryLangmuir adsorption modelPolymerSaponins021001 nanoscience & nanotechnologybiology.organism_classification0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsChemical engineeringQuillajasymbolsNanoparticles0210 nano-technologyHydrophobic and Hydrophilic InteractionsJournal of colloid and interface science
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Olive mill wastewaters decontamination based on organo-nano-clay composites

2019

Abstract Green composites for environmental applications were successfully prepared by intercalation of the biosurfactant Quillaja saponin onto montmorillonite mineral clay on varying pH and surfactant/clay ratio. Equilibrium adsorption isotherms were constructed and the system was characterized by performing TGA and XRD analyses. The efficiency of the surfactant-modified clay in the removal of the organic content present in olive mill wastewaters (OMW) was evaluated by means of spectrophotometric measurements. The interest for this cogent issue comes from the consideration that, despite their high pollutant content, OMW can be considered as a potential resource of several organic compounds…

PolyphenolMaterials Chemistry2506 Metals and AlloysMaterials scienceHill isothermXRDIntercalation (chemistry)Surfaces Coatings and FilmQuillaja saponinCeramics and Composite02 engineering and technology01 natural sciencesCoatings and Filmschemistry.chemical_compoundAdsorptionPulmonary surfactant0103 physical sciencesMaterials ChemistryElectronicOrganoclayOptical and Magnetic MaterialsComposite materialMontmorillonite010302 applied physicsOlive mill wastewaterAdsorption; Biowaste; Hill isotherm; Montmorillonite; Olive mill wastewaters; Polyphenols; Quillaja saponin; TGA; XRD; Electronic Optical and Magnetic Materials; Ceramics and Composites; Process Chemistry and Technology; Surfaces Coatings and Films; Materials Chemistry2506 Metals and AlloysTGAbiologyElectronic Optical and Magnetic MaterialProcess Chemistry and TechnologyPolyphenolsHuman decontaminationBiowaste021001 nanoscience & nanotechnologybiology.organism_classificationSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsSurfacesSubstrate (building)MontmorillonitechemistryQuillajaCeramics and CompositesOlive mill wastewatersAdsorption0210 nano-technology
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Cytotoxic Acacic Acid Glycosides from the Roots of Albizia coriaria

2009

Two new oleanane-type saponins, coriariosides A (1) and B (2), along with a known saponin, gummiferaoside C (3), were isolated from the roots of Albizia coriaria. Their structures were established by extensive analysis of 1D and 2D NMR experiments (COSY, ROESY, TOCSY, HSQC, and HMBC) and mass spectrometry. Compounds 1 and 3 when tested for cytotoxicity against two colorectal human cancer cells showed activity against the HCT 116 (IC50 4.2 microM for 1 and 2.7 microM for 3) and HT-29 (IC50 6.7 microM for 1 and 7.9 microM for 3) cell lines.

SaponinPharmaceutical ScienceAlbizziaPharmacognosyPlant RootsAnalytical ChemistryTriterpeneCoriariaDrug DiscoveryBotanyHumansCameroonOleanolic AcidMedicinal plantsNuclear Magnetic Resonance BiomolecularPharmacologychemistry.chemical_classificationPlants MedicinalMolecular StructurebiologyOrganic ChemistryGlycosideSaponinsHCT116 Cellsbiology.organism_classificationAlbiziaAntineoplastic Agents PhytogenicTriterpenesTerpenoidComplementary and alternative medicinechemistryMolecular MedicineDrug Screening Assays AntitumorHT29 CellsJournal of Natural Products
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Arboreasides A−E, Triterpene Saponins from the Bark of Cussonia arborea

2009

Five new triterpene saponins, arboreasides A-E (1-5), and two known saponins, ciwujianoside C(3) and 23-hydroxyursolic acid 28-O-alpha-L-rhamnopyranosyl-(1--4)-beta-D-glucopyranosyl-(1--6)-beta-D-glucopyranosyl ester, were isolated from the bark of Cussonia arborea. The structures were established using extensive 1D and 2D NMR spectroscopic analyses and mass spectrometry.

SaponinPharmaceutical SciencePharmacognosyAnalytical ChemistryTriterpeneDrug DiscoveryBotanyCameroonAraliaceaeNuclear Magnetic Resonance BiomolecularPharmacologychemistry.chemical_classificationMolecular StructurebiologyOrganic ChemistryGlycosideSaponinsbiology.organism_classificationTriterpenesTerpenoidComplementary and alternative medicinechemistryvisual_artPlant Barkvisual_art.visual_art_mediumMolecular MedicineAraliaceaeBarkCussonia arboreaJournal of Natural Products
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New Acylated Triterpene Saponins from Silene fortunei that Modulate Lymphocyte Proliferation

2002

Three new acylated triterpene saponins 1-3, with a quillaic acid as aglycon, were isolated from the roots of Silene fortunei together with a known phytoecdysteroid (20-hydroxyecdysone). The compounds were characterized mainly by a combination of 2D NMR techniques, mass spectrometry, and chemical methods. Saponins 1-3, jenisseensosides C and D (4, 5), and 6 (deacylated form of 2/3 and 4/5) were found to stimulate the proliferation of the Jurkat tumor cell lines at low concentration. At high concentration, 2/3 and 4/5 inhibited the proliferation of the cells and suggested the induction of apoptosis.

SaponinPhytoecdysteroidPharmaceutical ScienceApoptosisLymphocyte proliferationPharmacognosyLymphocyte ActivationPlant RootsJurkat cellsAnalytical ChemistryJurkat CellsTriterpeneDrug DiscoveryHumansSileneNuclear Magnetic Resonance BiomolecularPharmacologychemistry.chemical_classificationSilenePlants MedicinalMolecular StructurebiologyHydrolysisOrganic ChemistryGlycosideAcetylationStereoisomerismSaponinsbiology.organism_classificationTriterpenesComplementary and alternative medicinechemistryBiochemistryMolecular MedicineJournal of Natural Products
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New triterpenoid estersaponins from the root barks of Pittosporum verticillatum subsp. verticillatum and evaluation of cytotoxicities

2013

The phytochemical investigation of the root barks of Pittosporum verticillatum Bojer subsp. verticillatum led to the isolation of three new triterpene saponins, 3-O-[β-D-glucopyranosyl-(1→2)]-[α-L-arabinopyranosyl-(1→3)]-[α-L-arabinofuranosyl-(1→4)]-β-D-glucuronopyranosyl-21-O-(2-acetoxy-2-methylbutanoyl)-R1-barrigenol (1), 3-O-[β-D-glucopyranosyl-(1→2)]-[α-L-arabinopyranosyl-(1→3)]-[α-L-arabinofuranosyl-(1→4)]-β-D-glucuronopyranosyl-21-O-(2-acetoxy-2-methylbutanoyl)-28-O-acetyl-R1-barrigenol (2), 3-O-[β-D-glucopyranosyl-(1→2)]-[α-L-arabinopyranosyl-(1→3)]-[α-L-arabinofuranosyl-(1→4)]-β-D-glucuronopyranosyl-21-O-β,β-dimethylacryloyl-22-O-angeloyl-R1-barrigenol (3), and one known saponin sen…

Senaciapittoside BStereochemistrySaponinPlant RootsCell LineTerpeneTriterpenoidTriterpeneCell Line TumorNeoplasmsDrug DiscoveryAnimalsHumansRosalesPharmacologychemistry.chemical_classificationMolecular StructurebiologyPlant ExtractsGeneral MedicineSaponinsPittosporumbiology.organism_classificationTriterpenesRatschemistryPhytochemicalPlant BarkHuman cancerFitoterapia
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Anti-inflammatory glycoterpenoids from Scrophularia auriculata.

2000

The activity of the four glycoterpenoids: two saponins, verbascosaponin A and verbascosaponin, and two iridoids, scropolioside A and scrovalentinoside, isolated from Scrophularia auriculata ssp. pseudoauriculata, were studied in different models of acute and chronic inflammation. Both saponins significantly inhibited the mouse paw edema induced by carrageenan and ear edema induced by single and multiple doses of 12-O-tetradecanoylphorbol 13-acetate (TPA). Verbascosaponin A showed a potency twice as high as that of indomethacin in the acute TPA model. Verbascosaponin A and scropolioside A were active after a long latency period against ethyl phenylpropiolate edema, as are glucocorticoids. Wh…

Serotoninmedicine.drug_classAnti-Inflammatory AgentsInflammationPharmacognosyPharmacologyAnti-inflammatoryCapillary Permeabilitychemistry.chemical_compoundMiceGlucosidesEdemaMedicineAnimalsEdemaHypersensitivity DelayedIridoidsGlycosidesPyransPharmacologyPlants Medicinalbiologybusiness.industryTerpenesBiological activityEarScrophularia auriculataSaponinsbiology.organism_classificationTriterpenesCarrageenanMechanism of actionchemistryImmunologyIridoid GlycosidesTetradecanoylphorbol AcetateFemalemedicine.symptombusinessEuropean journal of pharmacology
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Citotoxic saponins from Schefflera fagueti

2003

Settore BIO/14 - FarmacologiaTriterpene saponins Antiproliferative activity
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