Search results for "Xanthone"

showing 10 items of 28 documents

Non-ionic photo-acid generators for applications in two-photon lithography

2009

Non-ionic photoacid generators (PAGs) have been designed and synthesized for use in two-photon lithography (TPL). The chromophores in these new PAGs are covalently linked to the photocleavable group by a flexible joint. Their thermal stability, solubility and efficiency to produce acid under both one- and two-photon excitation were characterized. The potential of these PAGs for TPL was tested in two negative-tone resist systems relying on different mechanisms: free-radical/cationic polymerization or a cationically initiated cross-linking reaction. These PAGs needed lower threshold power for polymerization compared to a commercially available photoinitiator, isopropylthioxanthone, and a phot…

IsopropylthioxanthoneMaterials scienceCationic polymerizationGeneral ChemistryPhotochemistryMultiphoton lithographychemistry.chemical_compoundResistPolymerizationchemistryMaterials ChemistryTrifluoromethanesulfonateLithographyPhotoinitiatorJ. Mater. Chem.
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Glucuronide triterpene saponins from Bersama engleriana

2006

Five 3-O-glucuronide triterpene saponins (1-5) were isolated from the stem bark of Bersama engleriana Gurke along with two known saponins, polyscias saponin C and aralia saponin 15, and one major C-glycoside xanthone, mangiferin. The structures of the saponins were established mainly by means of spectroscopic methods (one- and two-dimensional NMR spectroscopy as well as FAB-, HRESI-mass spectrometry) as 3-O-[beta-D-glucopyranosyl-(1-->2)-beta-D-glucuronopyranosyl]-28-O-[beta-D-glucopyranosyl]-betulinic acid (1), 3-O-[beta-D-glucopyranosyl-(1-->2)-[beta-D-galactopyranosyl-(1-->3)]-beta-D-glucuronopyranosyl]-oleanolic acid (2), 3-O-[beta-D-glucopyranosyl-(1-->3)-beta-D-glucuronopyranosyl]-28-…

Magnetic Resonance SpectroscopyStereochemistryMolecular Sequence DataSaponinPlant ScienceHorticultureBiochemistrychemistry.chemical_compoundTriterpeneBetulinic acidXanthoneCarbohydrate ConformationGlycosidesMangiferinMolecular BiologyOleanolic acidchemistry.chemical_classificationPlants MedicinalPlant ExtractsGlycosideGeneral MedicineSaponinsTriterpenesCarbohydrate SequencechemistryPlant BarkGlucuronidePhytochemistry
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Evaluation of genotoxicity and DNA protective effects of mangiferin, a glucosylxanthone isolated from Mangifera indica L. stem bark extract.

2012

Abstract Mangiferin is a glucosylxantone isolated from Mangifera indica L. stem bark. Several studies have shown its pharmacological properties which make it a promising candidate for putative therapeutic use. This study was focused to investigate the in vitro genotoxic effects of mangiferin in the Ames test, SOS Chromotest and Comet assay. The genotoxic effects in bone marrow erythrocytes from NMRI mice orally treated with mangiferin (2000 mg/kg) were also evaluated. Additionally, its potential antimutagenic activity against several mutagens in the Ames test and its effects on CYP1A1 activity were assessed. Mangiferin (50–5000 μg/plate) did not increased the frequency of reverse mutations …

MaleStereochemistryDNA damageBinucleated cellsXanthonesPharmacologyToxicologymedicine.disease_causeAmes testRats Sprague-Dawleychemistry.chemical_compoundMicemedicineAnimalsMangiferinMangiferaPlant StemsChemistryMutagenicity TestsPlant ExtractsGeneral MedicineDNARatsComet assaySOS chromotestComet AssayMicronucleusGenotoxicityFood Science
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Modulation of P450 enzymes by Cuban natural products rich in polyphenolic compounds in rat hepatocytes.

2008

This paper reports cytotoxic effects and changes in the P450 system after exposing rat hepatocytes to four polyphenol-rich products widely used in Cuban traditional medicine (Mangifera indica L. (MSBE), Thalassia testudinum (Tt), Erythroxylum minutifolium and confusum extracts). Effects of mangiferin, the main polyphenol in MSBE, were also evaluated. Cytotoxicity was assayed by the MTT test after exposure of cells to the products (50-1000 microg/mL) for 24 or 72 h. The results showed that 500 microg/mL MSBE was moderately cytotoxic after 72 h, while mangiferin was not. Marked reductions in cell viability were produced by Erythroxylum extracts at concentrationsor = 200 microg/mL, whereas onl…

MaleXanthonesToxicologyRats Sprague-Dawleychemistry.chemical_compoundCytochrome P-450 Enzyme SystemmedicineAnimalsMangiferaMangiferinCells CulturedBiological ProductsMangiferabiologyTraditional medicineMolecular StructureChemistryPlant ExtractsCYP1A2CubaGeneral MedicineCYP2E1biology.organism_classificationErythroxylumRatsPolyphenolPhenacetinChlorzoxazoneHepatocytesMedicine Traditionalmedicine.drugChemico-biological interactions
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Synthesis of toxyloxanthone B

2014

A synthesis of the naturally occurring xanthone toxyloxanthone B is described, in which the key step is the regioselective addition of a methyl salicylate to a substituted benzyne, followed by cyclization of the intermediate aryl anion to form the xanthone, the regiochemistry of the aryne addition being confirmed by X-ray crystallography. Subsequent introduction of the pyran ring by [3,3]-rearrangement and deprotection completed the synthesis.

Natural products Xanthones Oxygen heterocycle Benzyne addition Claisen rearrangement.StereochemistryArylOrganic ChemistryRegioselectivitySettore CHIM/06 - Chimica OrganicaRing (chemistry)BiochemistryAryneClaisen rearrangementchemistry.chemical_compoundchemistryPyranDrug DiscoveryXanthone
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Secoiridoids and Xanthones fromGentianella nitida

1996

From Gentianella nitida twelve known metabolites were isolated and identified by HPLC-UV and/or by spectroscopic methods as secologanoside, amaroswerin, amarogentin (secoiridoids), isoorientin (C-glucosylflavone), mangiferin, demethylbellidifolin 8-O-glucoside, norswertianine 1-O-glucoside, swertianine 1-O-primeveroside, swertianine 8-O-glucoside, norswertianine, demethylbellidifolin, and swertianine (xanthone glycosides and aglycones). Secologanoside is reported here for the first time in Gentianaceae species ; the antioxidant mangiferin was obtained as the major compound in good yield.

Pharmacologychemistry.chemical_classificationGentianaceaeTraditional medicinebiologyIsoorientinOrganic ChemistryPharmaceutical ScienceGlycosidePharmacognosyAmarogentinbiology.organism_classificationAnalytical Chemistrychemistry.chemical_compoundComplementary and alternative medicinechemistryGlucosideDrug DiscoveryBotanyXanthoneMolecular MedicineMangiferinPlanta Medica
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Anticancer activities of six selected natural compounds of some Cameroonian medicinal plants.

2011

BACKGROUND: Natural products are well recognized as sources of drugs in several human ailments. In the present work, we carried out a preliminary screening of six natural compounds, xanthone V(1) (1); 2-acetylfuro-1,4-naphthoquinone (2); physcion (3); bisvismiaquinone (4); vismiaquinone (5); 1,8-dihydroxy-3-geranyloxy-6-methylanthraquinone (6) against MiaPaCa-2 pancreatic and CCRF-CEM leukemia cells and their multidrug-resistant subline, CEM/ADR5000. Compounds 1 and 2 were then tested in several other cancer cells and their possible mode of action were investigated. METHODOLOGY/FINDINGS: The tested compounds were previously isolated from the Cameroonian medicinal plants Vismia laurentii (1,…

PhytochemistryPhytopharmacologyPhytochemicalslcsh:MedicinePharmacologyToxicologyBiochemistryHeLachemistry.chemical_compoundDrug DiscoveryMolecular Cell BiologyBasic Cancer ResearchXanthoneCameroonCytotoxicitylcsh:ScienceCellular Stress ResponsesCaspase 7MultidisciplinaryCell DeathCaspase 3Cell CycleCell cycleChemistryOncologyMedicineResearch ArticleDrugs and DevicesToxic AgentsAntineoplastic AgentsBiologyQuailCaspase 7Cell GrowthComplementary and Alternative MedicineCell Line TumorChemical BiologyAnimalsHumansBiologyCell ProliferationBiological ProductsPlants MedicinalCell growthlcsh:Rbiology.organism_classificationCapillarieschemistryDoxorubicinApoptosisCancer celllcsh:QMedicinal ChemistryCytometryPLoS ONE
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Xanthone-photosensitized detoxification of the veterinary anthelmintic fenbendazole

2013

Fenbendazole (1) is a common veterinary anthelmintic, toxic to water living microorganisms. Fluorescence quantum yields of 1 were found to be 0.11 in acetonitrile, 0.068 in methanol, 0.034 in cyclohexane, and 0.013 in water. The singlet excited state energy was ca. 96 kcal mol(-1) in all solvents. The phosphorescence spectrum of 1 in ethanol at 77 K displayed a maximum at 450 nm, leading to a triplet energy of 75 kcal mol(-1). Experimental excited state energies agree well with the results of OFT calculations at the time-dependent B3LYP/6-311+G(d,p)//B3LYP/6-31G(d) level. Laser flash photolysis (LFP) of 1 at 266 nm led to transients absorbing in the 300-700 nm range, ascribed to radical cat…

Veterinary medicineToxicityChemistryGeneral Chemical EngineeringDaphnia magnaEnvironmental remediationPhotodissociationGeneral Physics and AstronomyMICROBIOLOGIAFenbendazoleGeneral ChemistryPhotochemistrychemistry.chemical_compoundQUIMICA ORGANICARadical ionExcited statePhotodegradationXanthoneBIOQUIMICA Y BIOLOGIA MOLECULARFlash photolysisSinglet statePhotodegradationPhosphorescenceJournal of Photochemistry and Photobiology A: Chemistry
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Mangiferin nanoemulsions in treatment of inflammatory disorders and skin regeneration

2018

Abstract In this paper mangiferin nanoemulsions were developed using hyaluronic acid of different molecular weight, in absence or presence of Transcutol-P. An extensive study was carried out on the physico-chemical properties of nanoemulsions. Nanosizer and transmission electron microscopy showed oil droplets average size 296 nm with monodisperses distribution (PI ≤ 0.30). The zeta potential was highly negative (−30 mV). FTIR analysis confirms the existence of physical interactions among compounds. Rheological measurements allowed to conclude that all formulations present a pseudoplastic behavior (s ∼ 0.4) in presence of the biopolymer. Moreover, mangiferin release depends on the molecular …

XanthonesAnti-Inflammatory AgentsPharmaceutical Scienceengineering.materialMicechemistry.chemical_compoundSkin Physiological PhenomenaHyaluronic acidZeta potentialAnimalsRegenerationDistribution (pharmacology)Mangiferinchemistry.chemical_classificationWound HealingChromatographyPolymerPermeationDrug LiberationchemistryPermeability (electromagnetism)engineeringNanoparticlesEmulsionsFemaleBiopolymerRheologyInternational Journal of Pharmaceutics
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Cytotoxicity and modes of action of three naturally occurring xanthones (8-hydroxycudraxanthone G, morusignin I and cudraxanthone I) against sensitiv…

2014

Abstract Background Resistance of cancer to chemotherapy remains a challenging issue for scientists as well as physicians. Naturally occurring xanthones possess a variety of biological activities such as anti-inflammatory, anti-bacterial, and anti-cancer effects. The present study was aimed at investigating the cytotoxicity and the modes of action of three naturally occurring xanthones namely, morusignin I (1), 8-hydroxycudraxanthone G (2) and cudraxanthone I (3) against a panel of nine cancer cell lines, including various sensitive and drug-resistant phenotypes. Methods The cytotoxicity of the compounds was determined using a resazurin reduction assay, whereas the caspase-Glo assay was use…

XanthonesPharmaceutical ScienceApoptosisCaspase 8Flow cytometryCell Line TumorNeoplasmsDrug DiscoverymedicineHumansCytotoxicityCaspaseMembrane Potential MitochondrialPharmacologybiologymedicine.diagnostic_testPlant ExtractsCancerCell Cycle CheckpointsHep G2 CellsCell cyclemedicine.diseaseAntineoplastic Agents PhytogenicDrug Resistance MultipleComplementary and alternative medicineDrug Resistance NeoplasmApoptosisCell cultureCaspasesImmunologybiology.proteinCancer researchMolecular MedicineGarciniaPhytotherapyPhytomedicine
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